Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 135295 |
| ensemblid | ENSG00000154548.9 |
| hgncid | 21220 |
| symbol | SRSF12 |
| name | serine and arginine rich splicing factor 12 |
| refseq_nuc | NM_080743.5 |
| refseq_prot | NP_542781.3 |
| ensembl_nuc | ENST00000452027.3 |
| ensembl_prot | ENSP00000414302.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 89095959 |
| end | 89118071 |
| strand | - |
| ver | v1.2 |
| region | chr6:89095959-89118071 |
| region5000 | chr6:89090959-89123071 |
| regionname0 | SRSF12_chr6_89095959_89118071 |
| regionname5000 | SRSF12_chr6_89090959_89123071 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 261 | 375 | 96 | 84 | 142 | 13 | 38 | 108 | SRSF12_chr6_89090959_89123071 | SRSF12 | MSRYT others(256): Show |
chr6 | 89090959 | 89123071 |
| a0002 | 0/0 | 261 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | MSRYT others(256): Show |
chr6 | 89090959 | 89123071 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 783 | 375 | 96 | 84 | 142 | 13 | 38 | SRSF12_chr6_89090959_89123071 | SRSF12 | ATGTC others(778): Show |
chr6 | 89090959 | 89123071 | ||
| a0002c0002 | 0/0 | 783 | 1 | 0 | 0 | 0 | 1 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | ATGTC others(778): Show |
chr6 | 89090959 | 89123071 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3589 | 112 | 11 | 23 | 67 | 0 | 11 | SRSF12_chr6_89090959_89123071 | SRSF12 | AGGCT others(3584): Show |
chr6 | 89090959 | 89123071 |
| a0001c0001t0002 | 1/0 | 3589 | 87 | 22 | 28 | 30 | 3 | 3 | SRSF12_chr6_89090959_89123071 | SRSF12 | AGGCT others(3584): Show |
chr6 | 89090959 | 89123071 |
| a0001c0001t0003 | 0/0 | 3589 | 79 | 20 | 16 | 25 | 3 | 15 | SRSF12_chr6_89090959_89123071 | SRSF12 | AGGCT others(3584): Show |
chr6 | 89090959 | 89123071 |
| a0001c0001t0004 | 0/0 | 3589 | 24 | 1 | 13 | 0 | 5 | 5 | SRSF12_chr6_89090959_89123071 | SRSF12 | AGGCT others(3584): Show |
chr6 | 89090959 | 89123071 |
| a0001c0001t0005 | 0/0 | 3587 | 15 | 8 | 0 | 6 | 0 | 1 | SRSF12_chr6_89090959_89123071 | SRSF12 | AGGCT others(3582): Show |
chr6 | 89090959 | 89123071 |
| a0001c0001t0006 | 0/0 | 3588 | 11 | 11 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | AGGCT others(3583): Show |
chr6 | 89090959 | 89123071 |
| a0001c0001t0007 | 0/0 | 3588 | 10 | 0 | 1 | 8 | 0 | 1 | SRSF12_chr6_89090959_89123071 | SRSF12 | AGGCT others(3583): Show |
chr6 | 89090959 | 89123071 |
| a0001c0001t0008 | 0/0 | 3587 | 9 | 8 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | AGGCT others(3582): Show |
chr6 | 89090959 | 89123071 |
| a0001c0001t0009 | 0/0 | 3589 | 5 | 5 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | AGGCT others(3584): Show |
chr6 | 89090959 | 89123071 |
| a0001c0001t0010 | 0/0 | 3587 | 5 | 5 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | AGGCT others(3582): Show |
chr6 | 89090959 | 89123071 |
| a0001c0001t0011 | 0/0 | 3589 | 1 | 0 | 0 | 0 | 1 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | AGGCT others(3584): Show |
chr6 | 89090959 | 89123071 |
| a0001c0001t0012 | 0/0 | 3589 | 2 | 2 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | AGGCT others(3584): Show |
chr6 | 89090959 | 89123071 |
| a0001c0001t0013 | 0/1 | 3589 | 1 | 0 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | AGGCT others(3584): Show |
chr6 | 89090959 | 89123071 |
| a0001c0001t0014 | 0/0 | 3589 | 1 | 0 | 0 | 0 | 1 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | AGGCT others(3584): Show |
chr6 | 89090959 | 89123071 |
| a0001c0001t0015 | 0/0 | 3588 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | AGGCT others(3583): Show |
chr6 | 89090959 | 89123071 |
| a0001c0001t0016 | 0/0 | 3589 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | AGGCT others(3584): Show |
chr6 | 89090959 | 89123071 |
| a0001c0001t0017 | 0/0 | 3589 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | AGGCT others(3584): Show |
chr6 | 89090959 | 89123071 |
| a0001c0001t0018 | 0/0 | 3589 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | AGGCT others(3584): Show |
chr6 | 89090959 | 89123071 |
| a0001c0001t0019 | 0/0 | 3589 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | AGGCT others(3584): Show |
chr6 | 89090959 | 89123071 |
| a0001c0001t0020 | 0/0 | 6377 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | AGGCT others(6372): Show |
chr6 | 89090959 | 89123071 |
| a0001c0001t0021 | 0/0 | 3588 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF12_chr6_89090959_89123071 | SRSF12 | AGGCT others(3583): Show |
chr6 | 89090959 | 89123071 |
| a0001c0001t0022 | 0/0 | 3589 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | AGGCT others(3584): Show |
chr6 | 89090959 | 89123071 |
| a0001c0001t0023 | 0/0 | 3589 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | AGGCT others(3584): Show |
chr6 | 89090959 | 89123071 |
| a0001c0001t0024 | 0/0 | 3589 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF12_chr6_89090959_89123071 | SRSF12 | AGGCT others(3584): Show |
chr6 | 89090959 | 89123071 |
| a0001c0001t0025 | 0/0 | 3589 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | AGGCT others(3584): Show |
chr6 | 89090959 | 89123071 |
| a0001c0001t0026 | 0/0 | 3587 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | AGGCT others(3582): Show |
chr6 | 89090959 | 89123071 |
| a0001c0001t0027 | 0/0 | 3587 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | AGGCT others(3582): Show |
chr6 | 89090959 | 89123071 |
| a0002c0002t0011 | 0/0 | 3589 | 1 | 0 | 0 | 0 | 1 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | AGGCT others(3584): Show |
chr6 | 89090959 | 89123071 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 40 | 1 | 14 | 25 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0004 | 0/0 | 23 | 1 | 1 | 17 | 0 | 4 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0010 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0003 | 1/0 | 29 | 4 | 13 | 10 | 0 | 1 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0005 | 0/0 | 9 | 6 | 2 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0002 | 0/0 | 36 | 10 | 5 | 11 | 1 | 9 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0016 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0022 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0004g0006 | 0/0 | 8 | 0 | 3 | 0 | 4 | 1 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0004g0011 | 0/0 | 6 | 0 | 3 | 0 | 0 | 3 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0004g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0005g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0005g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0005g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0006g0009 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0006g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0007g0008 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0007g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0007g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0008g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0008g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0008g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0008g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0008g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0008g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0009g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0010g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0011g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0012g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0012g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0013g0045 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0014g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0015g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0016g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0017g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0018g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0019g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0020g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0021g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0022g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0023g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0024g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0025g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0026g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0001c0001t0027g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| a0002c0002t0011g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0011 | g0051 | EUR | FIN | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0006 | EUR | FIN | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG00323 | hp1 | a0002 | c0002 | t0011 | g0052 | EUR | FIN | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0006 | EUR | FIN | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG00438 | hp2 | a0001 | c0001 | t0007 | g0008 | EAS | CHS | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | CHS | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG00597 | hp1 | a0001 | c0001 | t0022 | g0133 | EAS | CHS | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG00673 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | CHS | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0157 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0159 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0068 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG00741 | hp2 | a0001 | c0001 | t0008 | g0120 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01069 | hp1 | a0001 | c0001 | t0015 | g0099 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0085 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0030 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0113 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0061 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0062 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01168 | hp2 | a0001 | c0001 | t0016 | g0084 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0066 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | CLM | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | CLM | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0026 | AMR | CLM | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01261 | hp1 | a0001 | c0001 | t0007 | g0008 | AMR | CLM | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | CLM | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0054 | AMR | CLM | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | CLM | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0022 | EUR | IBS | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0006 | EUR | IBS | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0032 | EUR | IBS | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0023 | EUR | IBS | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0032 | EUR | IBS | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0006 | EUR | IBS | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01884 | hp1 | a0001 | c0001 | t0008 | g0116 | AFR | ACB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0053 | AFR | ACB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0021 | AFR | ACB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0030 | AMR | PEL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PEL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PEL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0067 | AMR | PEL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | KHV | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0115 | AFR | ACB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0161 | AFR | ACB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | KHV | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | ACB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ACB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | CDX | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02165 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | CDX | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | CDX | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02257 | hp1 | a0001 | c0001 | t0008 | g0038 | AFR | ACB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0040 | AFR | ACB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ACB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02280 | hp1 | a0001 | c0001 | t0009 | g0012 | AFR | ACB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0121 | AFR | ACB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02451 | hp2 | a0001 | c0001 | t0010 | g0013 | AFR | ACB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | KHV | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02523 | hp2 | a0001 | c0001 | t0018 | g0090 | EAS | KHV | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02572 | hp1 | a0001 | c0001 | t0012 | g0109 | AFR | GWD | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0112 | AFR | GWD | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02630 | hp2 | a0001 | c0001 | t0010 | g0013 | AFR | GWD | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02647 | hp1 | a0001 | c0001 | t0017 | g0048 | AFR | GWD | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0057 | SAS | PJL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0011 | SAS | PJL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0063 | SAS | PJL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | GWD | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02723 | hp2 | a0001 | c0001 | t0008 | g0038 | AFR | GWD | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0160 | SAS | PJL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | GWD | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | GWD | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | GWD | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | GWD | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02895 | hp2 | a0001 | c0001 | t0027 | g0117 | AFR | GWD | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | GWD | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | ESN | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | ESN | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ESN | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | ESN | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0036 | AFR | ESN | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | ESN | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0036 | AFR | ESN | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03017 | hp1 | a0001 | c0001 | t0024 | g0135 | SAS | PJL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0110 | SAS | PJL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | GWD | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03041 | hp2 | a0001 | c0001 | t0010 | g0013 | AFR | GWD | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0127 | AFR | MSL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03098 | hp2 | a0001 | c0001 | t0012 | g0108 | AFR | MSL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03139 | hp1 | a0001 | c0001 | t0008 | g0021 | AFR | ESN | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | ESN | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | ESN | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03209 | hp1 | a0001 | c0001 | t0009 | g0012 | AFR | MSL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0040 | AFR | MSL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | MSL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | MSL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0065 | SAS | PJL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03453 | hp1 | a0001 | c0001 | t0009 | g0012 | AFR | MSL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | MSL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | MSL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0119 | AFR | MSL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0107 | AFR | ESN | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | MSL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | MSL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0028 | SAS | PJL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0011 | SAS | PJL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03831 | hp2 | a0001 | c0001 | t0007 | g0102 | SAS | BEB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0011 | SAS | BEB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03834 | hp2 | a0001 | c0001 | t0021 | g0101 | SAS | BEB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0091 | SAS | BEB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0023 | SAS | STU | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | STU | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0111 | SAS | BEB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | STU | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG04199 | hp2 | a0001 | c0001 | t0005 | g0124 | SAS | STU | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | STU | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | STU | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | STU | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | STU | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18522 | hp1 | a0001 | c0001 | t0010 | g0013 | AFR | YRI | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0114 | AFR | YRI | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0050 | AFR | YRI | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | YRI | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18942 | hp2 | a0001 | c0001 | t0005 | g0126 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18977 | hp1 | a0001 | c0001 | t0005 | g0118 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18979 | hp2 | a0001 | c0001 | t0007 | g0018 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18982 | hp2 | a0001 | c0001 | t0005 | g0125 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18984 | hp1 | a0001 | c0001 | t0023 | g0155 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18986 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19002 | hp1 | a0001 | c0001 | t0025 | g0075 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19005 | hp1 | a0001 | c0001 | t0005 | g0123 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19011 | hp1 | a0001 | c0001 | t0007 | g0018 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | LWK | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | LWK | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | LWK | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19056 | hp1 | a0001 | c0001 | t0019 | g0158 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19082 | hp2 | a0001 | c0001 | t0007 | g0018 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19085 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19085 | hp2 | a0001 | c0001 | t0005 | g0039 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | YRI | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA20129 | hp1 | a0001 | c0001 | t0009 | g0012 | AFR | ASW | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ASW | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0002 | EUR | TSI | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0034 | EUR | TSI | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0069 | EUR | TSI | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA20805 | hp2 | a0001 | c0001 | t0014 | g0079 | EUR | TSI | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | CLM | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02109 | hp2 | a0001 | c0001 | t0026 | g0122 | AFR | ACB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | ACB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ACB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | ACB | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03471 | hp1 | a0001 | c0001 | t0010 | g0013 | AFR | MSL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | MSL | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | USA | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0021 | AFR | USA | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18955 | hp1 | a0001 | c0001 | t0020 | g0144 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA18955 | hp2 | a0001 | c0001 | t0005 | g0039 | EAS | JPT | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA20300 | hp1 | a0001 | c0001 | t0009 | g0012 | AFR | USA | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | USA | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0100 | AFR | LWK | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0013 | g0045 | REF | REF | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0003 | REF | REF | SRSF12_chr6_89090959_89123071 | SRSF12 | chr6 | 89090959 | 89123071 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:89098631 | G | C | 1 | a0002 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.733C>G | p.His245Asp | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 917/3589 | 733/786 | 245/261 | chr6 | 89098631 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:89096043 | T | C | 1 | a0001c0001t0006 | 11 | HG02486.hp1 HG02717.hp2 HG02922.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2535A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 2535 | chr6 | 89096043 | ||||||
| chr6:89096114 | G | C | 1 | a0001c0001t0022 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2464C>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 2464 | chr6 | 89096114 | ||||||
| chr6:89096157 | AT | A | 4 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0015 others(1): Show |
23 | HG00438.hp2 HG00673.hp1 HG01069.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2420delA | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 2420 | chr6 | 89096157 | ||||||
| chr6:89096169 | C | T | 10 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(7): Show |
144 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*2409G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 2409 | chr6 | 89096169 | ||||||
| chr6:89096366 | A | G | 1 | a0001c0001t0021 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2212T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 2212 | chr6 | 89096366 | ||||||
| chr6:89096423 | T | C | 1 | a0001c0001t0019 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2155A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 2155 | chr6 | 89096423 | ||||||
| chr6:89096429 | C | T | 2 | a0001c0001t0011 a0002c0002t0011 |
2 | HG00280.hp1 HG00323.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2149G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 2149 | chr6 | 89096429 | ||||||
| chr6:89096511 | G | A | 1 | a0001c0001t0003 | 79 | HG00558.hp1 HG00609.hp2 HG01074.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*2067C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 2067 | chr6 | 89096511 | ||||||
| chr6:89096596 | G | T | 12 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(9): Show |
169 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*1982C>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 1982 | chr6 | 89096596 | ||||||
| chr6:89096663 | GTTA | G | 5 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0010 others(2): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1912_*1914delTAA | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 1912 | chr6 | 89096663 | ||||||
| chr6:89096799 | C | A | 1 | a0001c0001t0023 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1779G>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 1779 | chr6 | 89096799 | ||||||
| chr6:89096951 | G | A | 1 | a0001c0001t0026 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1627C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 1627 | chr6 | 89096951 | ||||||
| chr6:89096970 | T | C | 12 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(9): Show |
169 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*1608A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 1608 | chr6 | 89096970 | ||||||
| chr6:89097049 | C | G | 5 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0010 others(2): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1529G>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 1529 | chr6 | 89097049 | ||||||
| chr6:89097061 | G | A | 1 | a0001c0001t0014 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1517C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 1517 | chr6 | 89097061 | ||||||
| chr6:89097083 | T | C | 1 | a0001c0001t0024 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1495A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 1495 | chr6 | 89097083 | ||||||
| chr6:89097273 | A | C | 9 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(6): Show |
139 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*1305T>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 1305 | chr6 | 89097273 | ||||||
| chr6:89097495 | G | GA | 5 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0010 others(2): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1082dupT | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 1082 | chr6 | 89097495 | ||||||
| chr6:89097521 | C | CTTTTTTT others(2781): Show |
1 | a0001c0001t0020 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1056_*1057insAGGC others(2784): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 1056 | chr6 | 89097521 | ||||||
| chr6:89097601 | G | A | 10 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(7): Show |
144 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*977C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 977 | chr6 | 89097601 | ||||||
| chr6:89097695 | A | G | 1 | a0001c0001t0003 | 79 | HG00558.hp1 HG00609.hp2 HG01074.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*883T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 883 | chr6 | 89097695 | ||||||
| chr6:89097709 | A | G | 1 | a0001c0001t0018 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*869T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 869 | chr6 | 89097709 | ||||||
| chr6:89097857 | G | C | 1 | a0001c0001t0025 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*721C>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 721 | chr6 | 89097857 | ||||||
| chr6:89097896 | A | C | 2 | a0001c0001t0008 a0001c0001t0027 |
10 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*682T>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 682 | chr6 | 89097896 | ||||||
| chr6:89097898 | C | T | 1 | a0001c0001t0017 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*680G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 680 | chr6 | 89097898 | ||||||
| chr6:89098107 | C | A | 1 | a0001c0001t0027 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*471G>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 471 | chr6 | 89098107 | ||||||
| chr6:89098222 | A | T | 1 | a0001c0001t0016 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*356T>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 356 | chr6 | 89098222 | ||||||
| chr6:89098292 | T | C | 5 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0010 others(2): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*286A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 286 | chr6 | 89098292 | ||||||
| chr6:89098304 | A | G | 1 | a0001c0001t0015 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*274T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 274 | chr6 | 89098304 | ||||||
| chr6:89098500 | C | T | 1 | a0001c0001t0014 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*78G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 78 | chr6 | 89098500 | ||||||
| chr6:89098536 | T | C | 1 | a0001c0001t0012 | 2 | HG02572.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*42A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 42 | chr6 | 89098536 | ||||||
| chr6:89098576 | G | C | 1 | a0001c0001t0010 | 5 | HG02451.hp2 HG02630.hp2 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2C>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 5/5 | 2 | chr6 | 89098576 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:89099186 | A | G | 1 | a0001c0001t0004g0030 | 2 | HG01081.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.417-239T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099186 | |||||||
| chr6:89099206 | A | G | 1 | a0001c0001t0005g0124 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.417-259T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099206 | |||||||
| chr6:89099218 | A | G | 21 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(18): Show |
36 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.417-271T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099218 | |||||||
| chr6:89099224 | A | G | 1 | a0001c0001t0004g0068 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.417-277T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099224 | |||||||
| chr6:89099387 | T | G | 5 | a0001c0001t0008g0021 a0001c0001t0008g0038 a0001c0001t0008g0116 others(2): Show |
8 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.417-440A>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099387 | |||||||
| chr6:89099396 | CT | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(89): Show |
247 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.417-450delA | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099396 | |||||||
| chr6:89099399 | T | C | 2 | a0001c0001t0005g0040 a0001c0001t0005g0127 |
3 | HG02258.hp1 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.417-452A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099399 | |||||||
| chr6:89099400 | C | A | 2 | a0001c0001t0005g0040 a0001c0001t0005g0127 |
3 | HG02258.hp1 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.417-453G>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099400 | |||||||
| chr6:89099402 | C | A | 2 | a0001c0001t0005g0040 a0001c0001t0005g0127 |
3 | HG02258.hp1 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.417-455G>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099402 | |||||||
| chr6:89099403 | C | CAT | 5 | a0001c0001t0005g0039 a0001c0001t0005g0123 a0001c0001t0005g0124 others(2): Show |
6 | HG04199.hp2 NA18942.hp2 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.417-458_417-457dup others(2): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099403 | |||||||
| chr6:89099403 | C | T | 2 | a0001c0001t0005g0040 a0001c0001t0005g0127 |
3 | HG02258.hp1 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.417-456G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099403 | |||||||
| chr6:89099406 | A | ATATATAC others(43): Show |
2 | a0001c0001t0005g0040 a0001c0001t0005g0127 |
3 | HG02258.hp1 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.417-460_417-459ins others(50): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099406 | |||||||
| chr6:89099406 | A | ATATATAT others(73): Show |
2 | a0001c0001t0005g0020 a0001c0001t0005g0115 |
4 | HG02055.hp1 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.417-460_417-459ins others(80): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099406 | |||||||
| chr6:89099408 | ATATATAC others(15): Show |
A | 1 | a0001c0001t0026g0122 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.417-483_417-462del others(22): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099408 | |||||||
| chr6:89099413 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(90): Show |
246 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.417-466A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099413 | |||||||
| chr6:89099413 | T | TATAC | 2 | a0001c0001t0008g0114 a0001c0001t0010g0013 |
6 | HG02451.hp2 HG02630.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.417-467_417-466ins others(4): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099413 | |||||||
| chr6:89099413 | T | TATACACA others(49): Show |
2 | a0001c0001t0008g0021 a0001c0001t0008g0120 |
2 | HG00741.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.417-467_417-466ins others(56): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099413 | |||||||
| chr6:89099413 | T | TATACACA others(75): Show |
3 | a0001c0001t0008g0021 a0001c0001t0008g0116 a0001c0001t0008g0119 |
4 | HG01884.hp1 HG03139.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.417-467_417-466ins others(82): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099413 | |||||||
| chr6:89099413 | T | TATACACA others(23): Show |
1 | a0001c0001t0027g0117 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.417-467_417-466ins others(30): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099413 | |||||||
| chr6:89099413 | T | TATACACA others(49): Show |
1 | a0001c0001t0005g0121 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.417-467_417-466ins others(56): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099413 | |||||||
| chr6:89099413 | T | TATACACA others(75): Show |
1 | a0001c0001t0008g0038 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.417-467_417-466ins others(82): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099413 | |||||||
| chr6:89099415 | C | CACAT | 2 | a0001c0001t0004g0011 a0001c0001t0007g0008 |
3 | HG01070.hp1 HG01071.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.417-469_417-468ins others(4): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099415 | |||||||
| chr6:89099415 | C | CAT | 55 | a0001c0001t0001g0134 a0001c0001t0003g0002 a0001c0001t0003g0016 others(52): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.417-470_417-469dup others(2): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099415 | |||||||
| chr6:89099415 | C | T | 1 | a0001c0001t0007g0008 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.417-468G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099415 | |||||||
| chr6:89099417 | T | C | 19 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(16): Show |
30 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.417-470A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099417 | |||||||
| chr6:89099426 | G | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(100): Show |
264 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.417-479C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099426 | |||||||
| chr6:89099428 | G | A | 35 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(32): Show |
111 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.417-481C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099428 | |||||||
| chr6:89099432 | A | G | 35 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(32): Show |
112 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.417-485T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099432 | |||||||
| chr6:89099439 | T | C | 14 | a0001c0001t0005g0020 a0001c0001t0005g0040 a0001c0001t0005g0115 others(11): Show |
24 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.417-492A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099439 | |||||||
| chr6:89099441 | C | T | 35 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(32): Show |
112 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.417-494G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099441 | |||||||
| chr6:89099443 | C | T | 1 | a0001c0001t0026g0122 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.417-496G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099443 | |||||||
| chr6:89099443 | CAT | C | 8 | a0001c0001t0001g0141 a0001c0001t0001g0145 a0001c0001t0001g0149 others(5): Show |
10 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.417-498_417-497del others(2): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099443 | |||||||
| chr6:89099444 | ATATATAT others(5): Show |
A | 6 | a0001c0001t0005g0039 a0001c0001t0005g0118 a0001c0001t0005g0123 others(3): Show |
7 | HG04199.hp2 NA18942.hp2 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.417-509_417-498del others(12): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099444 | |||||||
| chr6:89099445 | T | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(34): Show |
116 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.417-498A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099445 | |||||||
| chr6:89099457 | T | C | 6 | a0001c0001t0005g0039 a0001c0001t0005g0118 a0001c0001t0005g0123 others(3): Show |
7 | HG04199.hp2 NA18942.hp2 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.417-510A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099457 | |||||||
| chr6:89099464 | G | A | 6 | a0001c0001t0005g0039 a0001c0001t0005g0118 a0001c0001t0005g0123 others(3): Show |
7 | HG04199.hp2 NA18942.hp2 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.417-517C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099464 | |||||||
| chr6:89099472 | A | G | 1 | a0001c0001t0017g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.417-525T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099472 | |||||||
| chr6:89099476 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(89): Show |
247 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.417-529T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099476 | |||||||
| chr6:89099479 | T | C | 6 | a0001c0001t0005g0039 a0001c0001t0005g0118 a0001c0001t0005g0123 others(3): Show |
7 | HG04199.hp2 NA18942.hp2 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.417-532A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099479 | |||||||
| chr6:89099480 | ATGTGTG | A | 1 | a0001c0001t0009g0012 | 5 | HG02280.hp1 HG03209.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.417-539_417-534del others(6): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099480 | |||||||
| chr6:89099490 | A | G | 30 | a0001c0001t0003g0002 a0001c0001t0003g0016 a0001c0001t0003g0017 others(27): Show |
78 | HG00558.hp1 HG00609.hp2 HG01099.hp2 others(75): Show |
intron_variant | MODIFIER | c.417-543T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099490 | |||||||
| chr6:89099506 | A | G | 2 | a0001c0001t0005g0020 a0001c0001t0005g0115 |
4 | HG02055.hp1 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.417-559T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099506 | |||||||
| chr6:89099508 | A | G | 1 | a0001c0001t0005g0020 | 3 | HG02559.hp2 HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.417-561T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099508 | |||||||
| chr6:89099515 | TAC | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(125): Show |
302 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.417-570_417-569del others(2): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099515 | |||||||
| chr6:89099517 | C | T | 1 | a0001c0001t0017g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.417-570G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099517 | |||||||
| chr6:89099537 | T | G | 1 | a0001c0001t0003g0060 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.417-590A>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099537 | |||||||
| chr6:89099538 | G | GT | 88 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(85): Show |
242 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.417-592dupA | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099538 | |||||||
| chr6:89099538 | G | T | 1 | a0001c0001t0003g0060 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.417-591C>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099538 | |||||||
| chr6:89099539 | T | TA | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.417-593_417-592ins others(1): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099539 | |||||||
| chr6:89099557 | C | T | 1 | a0001c0001t0017g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.417-610G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099557 | |||||||
| chr6:89099604 | C | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(89): Show |
247 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.417-657G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099604 | |||||||
| chr6:89099692 | C | T | 1 | a0001c0001t0004g0067 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.417-745G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099692 | |||||||
| chr6:89099708 | T | C | 1 | a0001c0001t0002g0089 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.417-761A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099708 | |||||||
| chr6:89099714 | C | T | 2 | a0001c0001t0002g0077 a0001c0001t0002g0078 |
2 | HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.417-767G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099714 | |||||||
| chr6:89099887 | G | A | 1 | a0001c0001t0001g0043 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.417-940C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099887 | |||||||
| chr6:89099937 | C | A | 3 | a0001c0001t0002g0019 a0001c0001t0002g0046 a0001c0001t0002g0047 |
5 | HG01175.hp1 HG02109.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.417-990G>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099937 | |||||||
| chr6:89099983 | A | T | 1 | a0001c0001t0017g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.417-1036T>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099983 | |||||||
| chr6:89099984 | G | A | 2 | a0001c0001t0011g0051 a0002c0002t0011g0052 |
2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.417-1037C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89099984 | |||||||
| chr6:89100185 | C | A | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.417-1238G>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89100185 | |||||||
| chr6:89100405 | A | C | 1 | a0001c0001t0003g0026 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.417-1458T>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89100405 | |||||||
| chr6:89100427 | G | A | 1 | a0001c0001t0025g0075 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.417-1480C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89100427 | |||||||
| chr6:89100491 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(89): Show |
247 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.417-1544T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89100491 | |||||||
| chr6:89100522 | TA | T | 18 | a0001c0001t0002g0106 a0001c0001t0003g0061 a0001c0001t0005g0039 others(15): Show |
26 | HG00280.hp1 HG00323.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.417-1576delT | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89100522 | |||||||
| chr6:89100522 | TAA | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(95): Show |
256 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(253): Show |
intron_variant | MODIFIER | c.417-1577_417-1576d others(4): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89100522 | |||||||
| chr6:89100626 | T | C | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.417-1679A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89100626 | |||||||
| chr6:89100668 | A | G | 3 | a0001c0001t0002g0034 a0001c0001t0002g0089 a0001c0001t0002g0091 |
4 | HG01123.hp2 HG01433.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.417-1721T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89100668 | |||||||
| chr6:89100692 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(89): Show |
247 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.417-1745C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89100692 | |||||||
| chr6:89100697 | G | T | 1 | a0001c0001t0017g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.417-1750C>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89100697 | |||||||
| chr6:89100708 | C | G | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.417-1761G>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89100708 | |||||||
| chr6:89100845 | T | C | 21 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(18): Show |
32 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.417-1898A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89100845 | |||||||
| chr6:89100943 | A | G | 1 | a0001c0001t0005g0115 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.417-1996T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89100943 | |||||||
| chr6:89100979 | C | A | 3 | a0001c0001t0005g0040 a0001c0001t0005g0127 a0001c0001t0026g0122 |
4 | HG02109.hp2 HG02258.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.417-2032G>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89100979 | |||||||
| chr6:89100982 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(112): Show |
281 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.417-2035T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89100982 | |||||||
| chr6:89101046 | T | C | 1 | a0001c0001t0002g0047 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.417-2099A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89101046 | |||||||
| chr6:89101058 | A | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(110): Show |
279 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(276): Show |
intron_variant | MODIFIER | c.417-2111T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89101058 | |||||||
| chr6:89101109 | CAA | C | 21 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(18): Show |
32 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.417-2164_417-2163d others(4): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89101109 | |||||||
| chr6:89101192 | A | C | 1 | a0001c0001t0004g0067 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.417-2245T>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89101192 | |||||||
| chr6:89101364 | T | C | 1 | a0001c0001t0002g0083 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.417-2417A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89101364 | |||||||
| chr6:89101373 | A | G | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.417-2426T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89101373 | |||||||
| chr6:89101539 | T | A | 1 | a0001c0001t0002g0088 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.417-2592A>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89101539 | |||||||
| chr6:89101613 | G | C | 1 | a0001c0001t0017g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.417-2666C>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89101613 | |||||||
| chr6:89101697 | C | CA | 4 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0005g0040 others(1): Show |
5 | HG02258.hp1 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.417-2751dupT | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89101697 | |||||||
| chr6:89101697 | CA | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(89): Show |
247 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.417-2751delT | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89101697 | |||||||
| chr6:89101707 | T | A | 5 | a0001c0001t0005g0020 a0001c0001t0005g0040 a0001c0001t0005g0115 others(2): Show |
8 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.417-2760A>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89101707 | |||||||
| chr6:89102001 | C | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(89): Show |
247 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.417-3054G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89102001 | |||||||
| chr6:89102112 | A | G | 1 | a0001c0001t0017g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.416+3007T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89102112 | |||||||
| chr6:89102130 | T | G | 1 | a0001c0001t0003g0028 | 2 | HG01346.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.416+2989A>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89102130 | |||||||
| chr6:89102144 | TTTTG | T | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.416+2971_416+2974d others(6): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89102144 | |||||||
| chr6:89102246 | C | T | 1 | a0001c0001t0017g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.416+2873G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89102246 | |||||||
| chr6:89102270 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.416+2849T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89102270 | |||||||
| chr6:89102291 | G | C | 1 | a0001c0001t0001g0044 | 2 | NA18971.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.416+2828C>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89102291 | |||||||
| chr6:89102295 | C | A | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.416+2824G>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89102295 | |||||||
| chr6:89102317 | T | C | 1 | a0001c0001t0024g0135 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.416+2802A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89102317 | |||||||
| chr6:89102340 | C | T | 1 | a0001c0001t0017g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.416+2779G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89102340 | |||||||
| chr6:89102604 | G | A | 1 | a0001c0001t0003g0037 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.416+2515C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89102604 | |||||||
| chr6:89102647 | G | A | 1 | a0001c0001t0008g0120 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.416+2472C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89102647 | |||||||
| chr6:89102748 | A | AATTT | 21 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(18): Show |
32 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.416+2367_416+2370d others(6): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89102748 | |||||||
| chr6:89102757 | A | G | 1 | a0001c0001t0009g0012 | 5 | HG02280.hp1 HG03209.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.416+2362T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89102757 | |||||||
| chr6:89102933 | T | G | 1 | a0001c0001t0006g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.416+2186A>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89102933 | |||||||
| chr6:89102987 | A | G | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.416+2132T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89102987 | |||||||
| chr6:89102998 | C | G | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.416+2121G>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89102998 | |||||||
| chr6:89103055 | C | T | 1 | a0001c0001t0001g0042 | 2 | NA19004.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.416+2064G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89103055 | |||||||
| chr6:89103095 | T | G | 21 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(18): Show |
32 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.416+2024A>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89103095 | |||||||
| chr6:89103206 | G | A | 3 | a0001c0001t0005g0040 a0001c0001t0005g0127 a0001c0001t0026g0122 |
4 | HG02109.hp2 HG02258.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.416+1913C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89103206 | |||||||
| chr6:89103331 | CT | C | 23 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0062 others(20): Show |
34 | HG00741.hp2 HG01168.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.416+1787delA | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89103331 | |||||||
| chr6:89103360 | G | A | 1 | a0001c0001t0007g0018 | 3 | NA18979.hp2 NA19011.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.416+1759C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89103360 | |||||||
| chr6:89103376 | T | C | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.416+1743A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89103376 | |||||||
| chr6:89103519 | G | A | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.416+1600C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89103519 | |||||||
| chr6:89103522 | T | G | 2 | a0001c0001t0005g0040 a0001c0001t0005g0127 |
3 | HG02258.hp1 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.416+1597A>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89103522 | |||||||
| chr6:89103525 | C | T | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.416+1594G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89103525 | |||||||
| chr6:89103669 | A | G | 2 | a0001c0001t0011g0051 a0002c0002t0011g0052 |
2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.416+1450T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89103669 | |||||||
| chr6:89103711 | T | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(128): Show |
307 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.416+1408A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89103711 | |||||||
| chr6:89103749 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(112): Show |
281 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.416+1370A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89103749 | |||||||
| chr6:89103750 | G | A | 2 | a0001c0001t0011g0051 a0002c0002t0011g0052 |
2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.416+1369C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89103750 | |||||||
| chr6:89103885 | A | G | 1 | a0001c0001t0003g0058 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.416+1234T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89103885 | |||||||
| chr6:89103964 | C | T | 12 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0030 others(9): Show |
25 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.416+1155G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89103964 | |||||||
| chr6:89103991 | C | CT | 17 | a0001c0001t0002g0031 a0001c0001t0002g0033 a0001c0001t0002g0077 others(14): Show |
26 | HG00280.hp1 HG00741.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.416+1127dupA | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89103991 | |||||||
| chr6:89103991 | CTTTT | C | 7 | a0001c0001t0001g0015 a0001c0001t0001g0152 a0001c0001t0003g0016 others(4): Show |
13 | HG01192.hp2 HG01257.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.416+1124_416+1127d others(6): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89103991 | |||||||
| chr6:89103991 | CTTTTT | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(80): Show |
232 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.416+1123_416+1127d others(7): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89103991 | |||||||
| chr6:89103991 | CTTTTTTT others(4): Show |
C | 6 | a0001c0001t0002g0019 a0001c0001t0002g0046 a0001c0001t0002g0047 others(3): Show |
8 | HG01175.hp1 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.416+1117_416+1127d others(13): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89103991 | |||||||
| chr6:89104026 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(89): Show |
247 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.416+1093C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89104026 | |||||||
| chr6:89104053 | T | C | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.416+1066A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89104053 | |||||||
| chr6:89104102 | G | A | 5 | a0001c0001t0008g0021 a0001c0001t0008g0038 a0001c0001t0008g0116 others(2): Show |
8 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.416+1017C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89104102 | |||||||
| chr6:89104144 | C | T | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.416+975G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89104144 | |||||||
| chr6:89104168 | G | A | 2 | a0001c0001t0011g0051 a0002c0002t0011g0052 |
2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.416+951C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89104168 | |||||||
| chr6:89104223 | C | CT | 21 | a0001c0001t0002g0087 a0001c0001t0002g0093 a0001c0001t0005g0020 others(18): Show |
32 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.416+895dupA | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89104223 | |||||||
| chr6:89104223 | CTTTT | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(89): Show |
247 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.416+892_416+895del others(4): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89104223 | |||||||
| chr6:89104276 | G | A | 14 | a0001c0001t0005g0039 a0001c0001t0005g0118 a0001c0001t0005g0123 others(11): Show |
22 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.416+843C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89104276 | |||||||
| chr6:89104297 | C | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(89): Show |
247 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.416+822G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89104297 | |||||||
| chr6:89104384 | G | A | 1 | a0001c0001t0003g0063 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.416+735C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89104384 | |||||||
| chr6:89104457 | T | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(89): Show |
247 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.416+662A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89104457 | |||||||
| chr6:89104510 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.416+609T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89104510 | |||||||
| chr6:89104529 | C | T | 1 | a0001c0001t0003g0110 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.416+590G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89104529 | |||||||
| chr6:89104531 | C | T | 22 | a0001c0001t0003g0025 a0001c0001t0004g0066 a0001c0001t0005g0020 others(19): Show |
34 | HG00741.hp2 HG01192.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.416+588G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89104531 | |||||||
| chr6:89104602 | AAGTT | A | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.416+513_416+516del others(4): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89104602 | |||||||
| chr6:89104703 | G | A | 14 | a0001c0001t0005g0039 a0001c0001t0005g0118 a0001c0001t0005g0123 others(11): Show |
22 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.416+416C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89104703 | |||||||
| chr6:89104739 | G | T | 1 | a0001c0001t0017g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.416+380C>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89104739 | |||||||
| chr6:89104859 | C | G | 2 | a0001c0001t0002g0105 a0001c0001t0002g0106 |
2 | NA18962.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.416+260G>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89104859 | |||||||
| chr6:89104914 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(111): Show |
280 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.416+205T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89104914 | |||||||
| chr6:89104958 | A | C | 1 | a0001c0001t0001g0142 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.416+161T>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89104958 | |||||||
| chr6:89104992 | T | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(112): Show |
281 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.416+127A>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89104992 | |||||||
| chr6:89105053 | CA | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(89): Show |
247 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.416+65delT | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89105053 | |||||||
| chr6:89105111 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(112): Show |
281 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(278): Show |
splice_region_variant&intron_variant | LOW | c.416+8T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 4/4 | chr6 | 89105111 | |||||||
| chr6:89105337 | A | G | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.275-77T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 3/4 | chr6 | 89105337 | |||||||
| chr6:89105729 | G | A | 1 | a0001c0001t0002g0091 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.171-199C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 2/4 | chr6 | 89105729 | |||||||
| chr6:89105758 | A | G | 1 | a0001c0001t0014g0079 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.171-228T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 2/4 | chr6 | 89105758 | |||||||
| chr6:89105794 | G | A | 2 | a0001c0001t0005g0040 a0001c0001t0005g0127 |
3 | HG02258.hp1 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.171-264C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 2/4 | chr6 | 89105794 | |||||||
| chr6:89106070 | T | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(89): Show |
247 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.171-540A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 2/4 | chr6 | 89106070 | |||||||
| chr6:89106118 | TTA | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(89): Show |
247 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.171-590_171-589del others(2): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 2/4 | chr6 | 89106118 | |||||||
| chr6:89106136 | T | C | 1 | a0001c0001t0026g0122 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.171-606A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 2/4 | chr6 | 89106136 | |||||||
| chr6:89106284 | TG | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(89): Show |
247 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.171-755delC | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 2/4 | chr6 | 89106284 | |||||||
| chr6:89106360 | G | A | 2 | a0001c0001t0005g0020 a0001c0001t0005g0115 |
4 | HG02055.hp1 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.170+794C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 2/4 | chr6 | 89106360 | |||||||
| chr6:89106402 | C | T | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.170+752G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 2/4 | chr6 | 89106402 | |||||||
| chr6:89106561 | T | C | 2 | a0001c0001t0005g0039 a0001c0001t0005g0126 |
3 | NA18942.hp2 NA18955.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.170+593A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 2/4 | chr6 | 89106561 | |||||||
| chr6:89106819 | T | G | 1 | a0001c0001t0002g0092 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.170+335A>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 2/4 | chr6 | 89106819 | |||||||
| chr6:89106858 | T | C | 1 | a0001c0001t0004g0159 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.170+296A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 2/4 | chr6 | 89106858 | |||||||
| chr6:89106866 | T | C | 1 | a0001c0001t0004g0160 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.170+288A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 2/4 | chr6 | 89106866 | |||||||
| chr6:89107100 | G | A | 12 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0030 others(9): Show |
25 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.170+54C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 2/4 | chr6 | 89107100 | |||||||
| chr6:89107110 | G | A | 1 | a0001c0001t0015g0099 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.170+44C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 2/4 | chr6 | 89107110 | |||||||
| chr6:89107110 | G | C | 2 | a0001c0001t0008g0114 a0001c0001t0010g0013 |
6 | HG02451.hp2 HG02630.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.170+44C>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 2/4 | chr6 | 89107110 | |||||||
| chr6:89107316 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.66-58G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89107316 | |||||||
| chr6:89107391 | A | C | 1 | a0001c0001t0002g0096 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.66-133T>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89107391 | |||||||
| chr6:89107460 | T | G | 1 | a0001c0001t0001g0128 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.66-202A>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89107460 | |||||||
| chr6:89107502 | T | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(110): Show |
279 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(276): Show |
intron_variant | MODIFIER | c.66-244A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89107502 | |||||||
| chr6:89107558 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.66-300G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89107558 | |||||||
| chr6:89107559 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.66-301C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89107559 | |||||||
| chr6:89107574 | T | A | 1 | a0001c0001t0005g0121 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.66-316A>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89107574 | |||||||
| chr6:89107584 | A | T | 1 | a0001c0001t0002g0086 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.66-326T>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89107584 | |||||||
| chr6:89107646 | A | C | 4 | a0001c0001t0003g0024 a0001c0001t0003g0037 a0001c0001t0003g0112 others(1): Show |
6 | HG01109.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.66-388T>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89107646 | |||||||
| chr6:89107659 | T | G | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.66-401A>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89107659 | |||||||
| chr6:89107671 | G | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(89): Show |
247 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.66-413C>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89107671 | |||||||
| chr6:89107844 | A | G | 1 | a0001c0001t0017g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.66-586T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89107844 | |||||||
| chr6:89108322 | C | T | 2 | a0001c0001t0003g0023 a0001c0001t0003g0055 |
3 | HG01257.hp2 HG01516.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.66-1064G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89108322 | |||||||
| chr6:89108366 | C | G | 1 | a0001c0001t0005g0121 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.66-1108G>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89108366 | |||||||
| chr6:89108470 | A | T | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.66-1212T>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89108470 | |||||||
| chr6:89108537 | T | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(91): Show |
249 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.66-1279A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89108537 | |||||||
| chr6:89108721 | G | GCAGTATT others(16): Show |
1 | a0001c0001t0002g0094 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.66-1486_66-1464dup others(23): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89108721 | |||||||
| chr6:89108725 | T | A | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.66-1467A>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89108725 | |||||||
| chr6:89108745 | C | T | 1 | a0001c0001t0017g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.66-1487G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89108745 | |||||||
| chr6:89108759 | C | T | 1 | a0001c0001t0017g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.66-1501G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89108759 | |||||||
| chr6:89108787 | T | C | 5 | a0001c0001t0008g0021 a0001c0001t0008g0038 a0001c0001t0008g0116 others(2): Show |
8 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.66-1529A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89108787 | |||||||
| chr6:89109032 | C | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(89): Show |
247 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.66-1774G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89109032 | |||||||
| chr6:89109065 | G | A | 1 | a0001c0001t0002g0032 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.66-1807C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89109065 | |||||||
| chr6:89109086 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.66-1828T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89109086 | |||||||
| chr6:89109129 | T | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(112): Show |
281 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.66-1871A>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89109129 | |||||||
| chr6:89109295 | A | C | 1 | a0001c0001t0003g0057 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.66-2037T>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89109295 | |||||||
| chr6:89109489 | G | T | 1 | a0001c0001t0006g0036 | 2 | HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.66-2231C>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89109489 | |||||||
| chr6:89109603 | A | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0153 |
2 | NA19063.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.66-2345T>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89109603 | |||||||
| chr6:89109629 | G | C | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.66-2371C>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89109629 | |||||||
| chr6:89109784 | G | T | 1 | a0001c0001t0001g0130 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.66-2526C>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89109784 | |||||||
| chr6:89109895 | T | A | 1 | a0001c0001t0017g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.66-2637A>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89109895 | |||||||
| chr6:89109922 | T | A | 1 | a0001c0001t0003g0064 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.66-2664A>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89109922 | |||||||
| chr6:89109949 | G | A | 1 | a0001c0001t0003g0065 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.66-2691C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89109949 | |||||||
| chr6:89110090 | CA | C | 14 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0030 others(11): Show |
31 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.66-2833delT | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89110090 | |||||||
| chr6:89110114 | G | A | 1 | a0001c0001t0005g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.66-2856C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89110114 | |||||||
| chr6:89110179 | T | C | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.66-2921A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89110179 | |||||||
| chr6:89110213 | G | T | 1 | a0001c0001t0004g0157 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.66-2955C>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89110213 | |||||||
| chr6:89110214 | G | T | 1 | a0001c0001t0004g0157 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.66-2956C>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89110214 | |||||||
| chr6:89110392 | T | G | 1 | a0001c0001t0027g0117 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.66-3134A>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89110392 | |||||||
| chr6:89110758 | T | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(110): Show |
279 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(276): Show |
intron_variant | MODIFIER | c.66-3500A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89110758 | |||||||
| chr6:89110845 | G | A | 1 | a0001c0001t0024g0135 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.66-3587C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89110845 | |||||||
| chr6:89110856 | C | T | 1 | a0001c0001t0008g0021 | 3 | HG01891.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.66-3598G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89110856 | |||||||
| chr6:89110901 | A | G | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.66-3643T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89110901 | |||||||
| chr6:89110931 | CAT | C | 2 | a0001c0001t0002g0007 a0001c0001t0002g0093 |
8 | NA18612.hp1 NA18946.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.66-3675_66-3674del others(2): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89110931 | |||||||
| chr6:89110980 | G | A | 2 | a0001c0001t0002g0096 a0001c0001t0002g0097 |
2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.66-3722C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89110980 | |||||||
| chr6:89110993 | T | A | 1 | a0002c0002t0011g0052 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.66-3735A>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89110993 | |||||||
| chr6:89111036 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.66-3778G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89111036 | |||||||
| chr6:89111107 | G | GTT | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.66-3850_66-3849ins others(2): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89111107 | |||||||
| chr6:89111109 | C | G | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.66-3851G>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89111109 | |||||||
| chr6:89111111 | T | C | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.66-3853A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89111111 | |||||||
| chr6:89111190 | C | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(89): Show |
247 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.66-3932G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89111190 | |||||||
| chr6:89111225 | C | T | 2 | a0001c0001t0005g0020 a0001c0001t0005g0115 |
4 | HG02055.hp1 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.66-3967G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89111225 | |||||||
| chr6:89111470 | A | G | 1 | a0001c0001t0005g0123 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.66-4212T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89111470 | |||||||
| chr6:89111565 | T | G | 1 | a0001c0001t0001g0148 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.66-4307A>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89111565 | |||||||
| chr6:89111732 | T | A | 10 | a0001c0001t0006g0009 a0001c0001t0006g0036 a0001c0001t0006g0050 others(7): Show |
23 | HG00438.hp2 HG00673.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.66-4474A>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89111732 | |||||||
| chr6:89111817 | CTCACACG others(6): Show |
C | 1 | a0001c0001t0002g0094 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.66-4572_66-4560del others(13): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89111817 | |||||||
| chr6:89111841 | T | G | 1 | a0001c0001t0002g0094 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.66-4583A>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89111841 | |||||||
| chr6:89111848 | A | C | 1 | a0001c0001t0003g0056 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.66-4590T>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89111848 | |||||||
| chr6:89111872 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.66-4614C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89111872 | |||||||
| chr6:89111929 | T | C | 1 | a0001c0001t0026g0122 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.66-4671A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89111929 | |||||||
| chr6:89111968 | T | TTCATCTT others(5): Show |
1 | a0001c0001t0002g0094 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.66-4711_66-4710ins others(12): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89111968 | |||||||
| chr6:89111969 | A | C | 1 | a0001c0001t0002g0094 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.66-4711T>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89111969 | |||||||
| chr6:89112076 | C | T | 2 | a0001c0001t0005g0020 a0001c0001t0005g0115 |
4 | HG02055.hp1 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.66-4818G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89112076 | |||||||
| chr6:89112117 | C | G | 1 | a0001c0001t0002g0094 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.66-4859G>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89112117 | |||||||
| chr6:89112132 | C | T | 1 | a0001c0001t0008g0114 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.66-4874G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89112132 | |||||||
| chr6:89112197 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(109): Show |
278 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(275): Show |
intron_variant | MODIFIER | c.66-4939A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89112197 | |||||||
| chr6:89112447 | CT | C | 17 | a0001c0001t0003g0029 a0001c0001t0005g0039 a0001c0001t0005g0040 others(14): Show |
27 | HG00741.hp2 HG01167.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.66-5190delA | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89112447 | |||||||
| chr6:89112468 | A | T | 1 | a0001c0001t0003g0071 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.66-5210T>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89112468 | |||||||
| chr6:89112557 | C | T | 1 | a0001c0001t0003g0085 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.65+5266G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89112557 | |||||||
| chr6:89112580 | C | CT | 21 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(18): Show |
32 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.65+5242dupA | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89112580 | |||||||
| chr6:89112613 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.65+5210A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89112613 | |||||||
| chr6:89112634 | A | C | 6 | a0001c0001t0002g0005 a0001c0001t0002g0094 a0001c0001t0002g0095 others(3): Show |
14 | HG00738.hp2 HG01358.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.65+5189T>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89112634 | |||||||
| chr6:89112735 | C | T | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.65+5088G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89112735 | |||||||
| chr6:89112806 | T | C | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.65+5017A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89112806 | |||||||
| chr6:89113031 | G | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(112): Show |
281 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.65+4792C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89113031 | |||||||
| chr6:89113149 | A | G | 1 | a0001c0001t0016g0084 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.65+4674T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89113149 | |||||||
| chr6:89113236 | C | T | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.65+4587G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89113236 | |||||||
| chr6:89113309 | G | T | 1 | a0001c0001t0017g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.65+4514C>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89113309 | |||||||
| chr6:89113323 | G | A | 2 | a0001c0001t0011g0051 a0002c0002t0011g0052 |
2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.65+4500C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89113323 | |||||||
| chr6:89113407 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0041 a0001c0001t0001g0128 others(1): Show |
10 | HG01081.hp1 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.65+4416G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89113407 | |||||||
| chr6:89113454 | G | A | 1 | a0001c0001t0005g0020 | 3 | HG02559.hp2 HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.65+4369C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89113454 | |||||||
| chr6:89113463 | C | T | 1 | a0001c0001t0017g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.65+4360G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89113463 | |||||||
| chr6:89113480 | T | C | 14 | a0001c0001t0005g0039 a0001c0001t0005g0118 a0001c0001t0005g0123 others(11): Show |
22 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.65+4343A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89113480 | |||||||
| chr6:89113543 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(112): Show |
281 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.65+4280T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89113543 | |||||||
| chr6:89113560 | C | T | 1 | a0001c0001t0003g0055 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.65+4263G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89113560 | |||||||
| chr6:89113692 | G | A | 2 | a0001c0001t0007g0102 a0001c0001t0021g0101 |
2 | HG03831.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.65+4131C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89113692 | |||||||
| chr6:89113705 | G | A | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.65+4118C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89113705 | |||||||
| chr6:89113728 | C | T | 1 | a0001c0001t0017g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.65+4095G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89113728 | |||||||
| chr6:89113925 | G | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(89): Show |
247 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.65+3898C>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89113925 | |||||||
| chr6:89114134 | C | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(110): Show |
279 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(276): Show |
intron_variant | MODIFIER | c.65+3689G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89114134 | |||||||
| chr6:89114248 | T | C | 1 | a0001c0001t0002g0076 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.65+3575A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89114248 | |||||||
| chr6:89114256 | C | T | 1 | a0001c0001t0008g0116 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.65+3567G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89114256 | |||||||
| chr6:89114257 | G | A | 1 | a0001c0001t0017g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.65+3566C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89114257 | |||||||
| chr6:89114301 | A | T | 4 | a0001c0001t0002g0032 a0001c0001t0002g0072 a0001c0001t0002g0082 others(1): Show |
5 | HG00639.hp2 HG00733.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.65+3522T>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89114301 | |||||||
| chr6:89114319 | T | C | 1 | a0001c0001t0005g0121 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.65+3504A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89114319 | |||||||
| chr6:89114352 | C | T | 1 | a0001c0001t0002g0081 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.65+3471G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89114352 | |||||||
| chr6:89114355 | G | C | 1 | a0001c0001t0004g0161 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.65+3468C>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89114355 | |||||||
| chr6:89114475 | T | C | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.65+3348A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89114475 | |||||||
| chr6:89114554 | T | C | 1 | a0001c0001t0017g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.65+3269A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89114554 | |||||||
| chr6:89114588 | T | C | 2 | a0001c0001t0002g0080 a0001c0001t0014g0079 |
2 | HG01496.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.65+3235A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89114588 | |||||||
| chr6:89114603 | TA | T | 40 | a0001c0001t0002g0005 a0001c0001t0002g0019 a0001c0001t0002g0046 others(37): Show |
62 | HG00280.hp1 HG00323.hp1 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.65+3219delT | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89114603 | |||||||
| chr6:89114689 | A | G | 1 | a0001c0001t0002g0076 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.65+3134T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89114689 | |||||||
| chr6:89114743 | G | A | 12 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0030 others(9): Show |
25 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.65+3080C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89114743 | |||||||
| chr6:89114763 | C | T | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.65+3060G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89114763 | |||||||
| chr6:89114865 | C | T | 1 | a0001c0001t0015g0099 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.65+2958G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89114865 | |||||||
| chr6:89115031 | C | T | 2 | a0001c0001t0002g0074 a0001c0001t0025g0075 |
2 | HG02015.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.65+2792G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89115031 | |||||||
| chr6:89115047 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.65+2776G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89115047 | |||||||
| chr6:89115087 | C | T | 2 | a0001c0001t0011g0051 a0002c0002t0011g0052 |
2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.65+2736G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89115087 | |||||||
| chr6:89115168 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA18964.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.65+2655C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89115168 | |||||||
| chr6:89115207 | C | T | 1 | a0001c0001t0011g0051 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.65+2616G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89115207 | |||||||
| chr6:89115410 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.65+2413C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89115410 | |||||||
| chr6:89115427 | C | T | 1 | a0001c0001t0003g0070 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.65+2396G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89115427 | |||||||
| chr6:89115502 | G | C | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.65+2321C>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89115502 | |||||||
| chr6:89115528 | G | C | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.65+2295C>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89115528 | |||||||
| chr6:89115552 | G | C | 2 | a0001c0001t0011g0051 a0002c0002t0011g0052 |
2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.65+2271C>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89115552 | |||||||
| chr6:89115614 | G | A | 1 | a0001c0001t0017g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.65+2209C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89115614 | |||||||
| chr6:89115631 | C | CT | 7 | a0001c0001t0002g0031 a0001c0001t0002g0072 a0001c0001t0002g0073 others(4): Show |
8 | HG00280.hp1 HG00323.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.65+2191dupA | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89115631 | |||||||
| chr6:89115631 | CT | C | 19 | a0001c0001t0001g0137 a0001c0001t0001g0153 a0001c0001t0002g0005 others(16): Show |
33 | HG00558.hp1 HG00738.hp2 HG01358.hp2 others(30): Show |
intron_variant | MODIFIER | c.65+2191delA | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89115631 | |||||||
| chr6:89115636 | T | C | 5 | a0001c0001t0002g0005 a0001c0001t0002g0094 a0001c0001t0002g0095 others(2): Show |
13 | HG00738.hp2 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.65+2187A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89115636 | |||||||
| chr6:89115637 | T | C | 1 | a0001c0001t0002g0098 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.65+2186A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89115637 | |||||||
| chr6:89115647 | T | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(88): Show |
246 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.65+2176A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89115647 | |||||||
| chr6:89115798 | G | A | 6 | a0001c0001t0002g0005 a0001c0001t0002g0094 a0001c0001t0002g0095 others(3): Show |
14 | HG00738.hp2 HG01358.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.65+2025C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89115798 | |||||||
| chr6:89115809 | T | TG | 113 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(110): Show |
279 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(276): Show |
intron_variant | MODIFIER | c.65+2013_65+2014ins others(1): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89115809 | |||||||
| chr6:89115932 | G | A | 2 | a0001c0001t0005g0040 a0001c0001t0005g0127 |
3 | HG02258.hp1 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.65+1891C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89115932 | |||||||
| chr6:89115937 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(89): Show |
247 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.65+1886C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89115937 | |||||||
| chr6:89115967 | G | GCTAA | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.65+1855_65+1856ins others(4): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89115967 | |||||||
| chr6:89116063 | G | A | 2 | a0001c0001t0005g0040 a0001c0001t0005g0127 |
3 | HG02258.hp1 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.65+1760C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89116063 | |||||||
| chr6:89116182 | C | G | 2 | a0001c0001t0008g0114 a0001c0001t0010g0013 |
6 | HG02451.hp2 HG02630.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.65+1641G>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89116182 | |||||||
| chr6:89116183 | T | G | 2 | a0001c0001t0008g0114 a0001c0001t0010g0013 |
6 | HG02451.hp2 HG02630.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.65+1640A>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89116183 | |||||||
| chr6:89116213 | C | T | 1 | a0001c0001t0008g0114 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.65+1610G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89116213 | |||||||
| chr6:89116308 | C | G | 1 | a0001c0001t0003g0053 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.65+1515G>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89116308 | |||||||
| chr6:89116444 | A | G | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.65+1379T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89116444 | |||||||
| chr6:89116527 | C | T | 10 | a0001c0001t0001g0004 a0001c0001t0001g0130 a0001c0001t0001g0131 others(7): Show |
32 | HG00558.hp2 HG00597.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.65+1296G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89116527 | |||||||
| chr6:89116672 | T | G | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.65+1151A>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89116672 | |||||||
| chr6:89116774 | T | TA | 11 | a0001c0001t0001g0154 a0001c0001t0002g0019 a0001c0001t0002g0046 others(8): Show |
13 | HG01175.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.65+1048dupT | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89116774 | |||||||
| chr6:89116774 | TA | T | 47 | a0001c0001t0001g0059 a0001c0001t0001g0129 a0001c0001t0003g0002 others(44): Show |
112 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.65+1048delT | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89116774 | |||||||
| chr6:89116782 | A | AT | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.65+1040_65+1041ins others(1): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89116782 | |||||||
| chr6:89116788 | A | T | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.65+1035T>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89116788 | |||||||
| chr6:89116791 | C | A | 2 | a0001c0001t0012g0108 a0001c0001t0012g0109 |
2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.65+1032G>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89116791 | |||||||
| chr6:89116834 | T | C | 1 | a0001c0001t0017g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.65+989A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89116834 | |||||||
| chr6:89116844 | T | G | 1 | a0001c0001t0003g0113 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.65+979A>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89116844 | |||||||
| chr6:89116851 | C | T | 2 | a0001c0001t0011g0051 a0002c0002t0011g0052 |
2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.65+972G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89116851 | |||||||
| chr6:89116923 | T | C | 1 | a0001c0001t0023g0155 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.65+900A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89116923 | |||||||
| chr6:89116970 | G | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0128 |
3 | HG02886.hp1 NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.65+853C>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89116970 | |||||||
| chr6:89116992 | G | GAAGT | 21 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(18): Show |
32 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.65+830_65+831insAC others(2): Show |
SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89116992 | |||||||
| chr6:89117101 | G | A | 19 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(16): Show |
29 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.65+722C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89117101 | |||||||
| chr6:89117145 | G | A | 1 | a0001c0001t0003g0110 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.65+678C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89117145 | |||||||
| chr6:89117234 | A | G | 1 | a0001c0001t0006g0050 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.65+589T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89117234 | |||||||
| chr6:89117407 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.65+416C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89117407 | |||||||
| chr6:89117523 | G | C | 3 | a0001c0001t0003g0037 a0001c0001t0003g0112 a0001c0001t0003g0113 |
4 | HG01109.hp1 HG02630.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.65+300C>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89117523 | |||||||
| chr6:89117550 | C | A | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.65+273G>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89117550 | |||||||
| chr6:89117602 | G | A | 20 | a0001c0001t0005g0020 a0001c0001t0005g0039 a0001c0001t0005g0040 others(17): Show |
31 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.65+221C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89117602 | |||||||
| chr6:89117612 | T | C | 39 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(36): Show |
116 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.65+211A>G | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89117612 | |||||||
| chr6:89117669 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.65+154C>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89117669 | |||||||
| chr6:89117686 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.65+137G>A | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89117686 | |||||||
| chr6:89117734 | A | G | 1 | a0001c0001t0017g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.65+89T>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89117734 | |||||||
| chr6:89117736 | C | A | 6 | a0001c0001t0004g0011 a0001c0001t0004g0157 a0001c0001t0004g0159 others(3): Show |
11 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.65+87G>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89117736 | |||||||
| chr6:89117754 | C | A | 1 | a0001c0001t0001g0014 | 5 | HG00609.hp1 HG00673.hp2 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.65+69G>T | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89117754 | |||||||
| chr6:89117754 | C | G | 2 | a0001c0001t0002g0046 a0001c0001t0002g0047 |
2 | HG01175.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.65+69G>C | SRSF12 | ENSG00000154548.9 | transcript | ENST00000452027.3 | protein_coding | 1/4 | chr6 | 89117754 |