Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 124404 |
| ensemblid | ENSG00000140623.14 |
| hgncid | 26348 |
| symbol | SEPTIN12 |
| name | septin 12 |
| refseq_nuc | NM_144605.5 |
| refseq_prot | NP_653206.2 |
| ensembl_nuc | ENST00000268231.13 |
| ensembl_prot | ENSP00000268231.8 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 4777606 |
| end | 4788345 |
| strand | - |
| ver | v1.2 |
| region | chr16:4777606-4788345 |
| region5000 | chr16:4772606-4793345 |
| regionname0 | SEPTIN12_chr16_4777606_4788345 |
| regionname5000 | SEPTIN12_chr16_4772606_4793345 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 358 | 412 | 87 | 78 | 183 | 16 | 46 | 135 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | MDPLR others(353): Show |
chr16 | 4772606 | 4793345 |
| a0002 | 0/0 | 358 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | MDPLR others(353): Show |
chr16 | 4772606 | 4793345 |
| a0003 | 0/0 | 358 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | MDPLR others(353): Show |
chr16 | 4772606 | 4793345 |
| a0004 | 0/0 | 358 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | MDPLR others(353): Show |
chr16 | 4772606 | 4793345 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1074 | 262 | 71 | 51 | 103 | 11 | 25 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | ATGGA others(1069): Show |
chr16 | 4772606 | 4793345 | ||
| a0001c0002 | 0/1 | 1074 | 135 | 11 | 26 | 71 | 5 | 21 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | ATGGA others(1069): Show |
chr16 | 4772606 | 4793345 | ||
| a0001c0003 | 0/0 | 1074 | 8 | 4 | 1 | 3 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | ATGGA others(1069): Show |
chr16 | 4772606 | 4793345 | ||
| a0001c0004 | 0/0 | 1074 | 7 | 1 | 0 | 6 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | ATGGA others(1069): Show |
chr16 | 4772606 | 4793345 | ||
| a0002c0005 | 0/0 | 1074 | 7 | 7 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | ATGGA others(1069): Show |
chr16 | 4772606 | 4793345 | ||
| a0003c0006 | 0/0 | 1074 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | ATGGA others(1069): Show |
chr16 | 4772606 | 4793345 | ||
| a0004c0007 | 0/0 | 1074 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | ATGGA others(1069): Show |
chr16 | 4772606 | 4793345 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1356 | 256 | 67 | 50 | 103 | 11 | 24 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | ACACA others(1351): Show |
chr16 | 4772606 | 4793345 |
| a0001c0001t0003 | 0/0 | 1356 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | ACACA others(1351): Show |
chr16 | 4772606 | 4793345 |
| a0001c0001t0004 | 0/0 | 1356 | 2 | 0 | 1 | 0 | 0 | 1 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | ACACA others(1351): Show |
chr16 | 4772606 | 4793345 |
| a0001c0002t0002 | 0/1 | 1356 | 135 | 11 | 26 | 71 | 5 | 21 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | ACACA others(1351): Show |
chr16 | 4772606 | 4793345 |
| a0001c0003t0001 | 0/0 | 1356 | 8 | 4 | 1 | 3 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | ACACA others(1351): Show |
chr16 | 4772606 | 4793345 |
| a0001c0004t0002 | 0/0 | 1356 | 7 | 1 | 0 | 6 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | ACACA others(1351): Show |
chr16 | 4772606 | 4793345 |
| a0002c0005t0001 | 0/0 | 1356 | 7 | 7 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | ACACA others(1351): Show |
chr16 | 4772606 | 4793345 |
| a0003c0006t0001 | 0/0 | 1356 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | ACACA others(1351): Show |
chr16 | 4772606 | 4793345 |
| a0004c0007t0002 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | ACACA others(1351): Show |
chr16 | 4772606 | 4793345 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 42 | 5 | 9 | 22 | 1 | 5 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0002 | 1/0 | 28 | 4 | 3 | 13 | 2 | 5 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0005 | 0/0 | 10 | 1 | 1 | 6 | 0 | 2 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0006 | 0/0 | 9 | 0 | 2 | 6 | 0 | 1 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0007 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0008 | 0/0 | 7 | 0 | 1 | 2 | 2 | 2 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0009 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0033 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0003 | 0/0 | 15 | 0 | 5 | 8 | 0 | 2 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0004 | 0/0 | 14 | 0 | 7 | 4 | 0 | 3 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0010 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0015 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0026 | 0/1 | 3 | 0 | 0 | 0 | 0 | 2 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0043 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0046 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0047 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0050 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0055 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0003t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0003t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0003t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0003t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0003t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0003t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0004t0002g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0004t0002g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0004t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0004t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0001c0004t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0002c0005t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0002c0005t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0002c0005t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0002c0005t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0002c0005t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0003c0006t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| a0004c0007t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | GBR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0015 | EUR | GBR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | CHS | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | CHS | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0204 | EAS | CHS | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | CHS | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0163 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0210 | EAS | CHS | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00735 | hp2 | a0001 | c0003 | t0001 | g0089 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0053 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0053 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0046 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0055 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0200 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0185 | AMR | CLM | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0047 | AMR | CLM | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0015 | AMR | CLM | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0166 | AMR | CLM | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0183 | EUR | IBS | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0046 | EUR | IBS | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0135 | AMR | PEL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0197 | AMR | PEL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0182 | EAS | KHV | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02055 | hp1 | a0002 | c0005 | t0001 | g0160 | AFR | ACB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0193 | EAS | KHV | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0194 | EAS | KHV | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0171 | EAS | KHV | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0172 | EAS | KHV | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0213 | EAS | KHV | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | KHV | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02145 | hp1 | a0002 | c0005 | t0001 | g0065 | AFR | ACB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | CDX | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CDX | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0203 | EAS | CDX | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0215 | EAS | CDX | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0169 | AFR | ACB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | ACB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02280 | hp2 | a0003 | c0006 | t0001 | g0040 | AFR | ACB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02451 | hp1 | a0002 | c0005 | t0001 | g0141 | AFR | ACB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0048 | AFR | ACB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0184 | AFR | GWD | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0153 | AFR | GWD | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0042 | SAS | PJL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0042 | SAS | PJL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0154 | AFR | GWD | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0187 | SAS | PJL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02818 | hp2 | a0001 | c0002 | t0002 | g0189 | AFR | GWD | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02965 | hp2 | a0001 | c0003 | t0001 | g0159 | AFR | ESN | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03041 | hp1 | a0002 | c0005 | t0001 | g0148 | AFR | GWD | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03098 | hp2 | a0003 | c0006 | t0001 | g0040 | AFR | MSL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03130 | hp2 | a0001 | c0002 | t0002 | g0161 | AFR | ESN | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0170 | AFR | ESN | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03209 | hp1 | a0002 | c0005 | t0001 | g0023 | AFR | MSL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03225 | hp2 | a0001 | c0002 | t0002 | g0049 | AFR | MSL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03453 | hp2 | a0002 | c0005 | t0001 | g0023 | AFR | MSL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0157 | AFR | MSL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0050 | SAS | PJL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0178 | SAS | PJL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0050 | SAS | PJL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0049 | AFR | GWD | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0043 | SAS | PJL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0132 | SAS | PJL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0026 | SAS | STU | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0211 | SAS | PJL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0168 | SAS | BEB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0026 | SAS | BEB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0174 | SAS | BEB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | STU | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | STU | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0180 | SAS | STU | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0055 | SAS | STU | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0188 | SAS | STU | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | STU | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | YRI | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0014 | EAS | CHB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | CHB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0048 | AFR | YRI | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | YRI | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18943 | hp2 | a0001 | c0002 | t0002 | g0176 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18944 | hp1 | a0001 | c0004 | t0002 | g0052 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18945 | hp1 | a0001 | c0003 | t0001 | g0017 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0214 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18946 | hp1 | a0001 | c0002 | t0002 | g0056 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0173 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18957 | hp2 | a0001 | c0003 | t0001 | g0017 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18963 | hp1 | a0001 | c0004 | t0002 | g0052 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0165 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0195 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0207 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0164 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0191 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18988 | hp2 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0175 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18989 | hp2 | a0001 | c0004 | t0002 | g0051 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0181 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19006 | hp2 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | LWK | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | LWK | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0190 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19056 | hp1 | a0004 | c0007 | t0002 | g0208 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19065 | hp1 | a0001 | c0004 | t0002 | g0209 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0201 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0206 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19077 | hp2 | a0001 | c0004 | t0002 | g0212 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19078 | hp2 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0056 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19087 | hp1 | a0001 | c0003 | t0001 | g0017 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0177 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19089 | hp2 | a0001 | c0004 | t0002 | g0051 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA19240 | hp2 | a0002 | c0005 | t0001 | g0023 | AFR | YRI | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ASW | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0084 | AFR | ASW | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0047 | EUR | TSI | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | TSI | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | TSI | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0015 | EUR | TSI | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0167 | SAS | GIH | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0179 | AMR | CLM | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0186 | AFR | ACB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0192 | AFR | ACB | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | USA | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | USA | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA20300 | hp1 | a0001 | c0004 | t0002 | g0162 | AFR | USA | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0158 | AFR | USA | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | LWK | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | LWK | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0026 | REF | REF | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | SEPTIN12_chr16_4772606_4793345 | SEPTIN12 | chr16 | 4772606 | 4793345 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:4783524 | C | T | 1 | a0004 | 1 | NA19056.hp1 | missense_variant | MODERATE | c.664G>A | p.Val222Ile | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/10 | 752/1356 | 664/1077 | 222/358 | chr16 | 4783524 | |||
| chr16:4783550 | T | C | 2 | a0002 a0003 |
9 | HG02055.hp1 HG02145.hp1 HG02280.hp2 others(6): Show |
missense_variant | MODERATE | c.638A>G | p.Gln213Arg | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/10 | 726/1356 | 638/1077 | 213/358 | chr16 | 4783550 | |||
| chr16:4787573 | C | T | 1 | a0003 | 2 | HG02280.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.73G>A | p.Glu25Lys | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 2/10 | 161/1356 | 73/1077 | 25/358 | chr16 | 4787573 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:4783537 | G | C | 1 | a0004c0007 | 1 | NA19056.hp1 | synonymous_variant | LOW | c.651C>G | p.Thr217Thr | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/10 | 739/1356 | 651/1077 | 217/358 | chr16 | 4783537 | |||
| chr16:4783969 | C | T | 3 | a0001c0002 a0001c0003 a0004c0007 |
143 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(140): Show |
synonymous_variant | LOW | c.474G>A | p.Val158Val | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 5/10 | 562/1356 | 474/1077 | 158/358 | chr16 | 4783969 | |||
| chr16:4787544 | A | G | 3 | a0001c0002 a0001c0004 a0004c0007 |
142 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(139): Show |
synonymous_variant | LOW | c.102T>C | p.Ala34Ala | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 2/10 | 190/1356 | 102/1077 | 34/358 | chr16 | 4787544 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:4777617 | C | G | 1 | a0001c0001t0003 | 4 | HG02257.hp2 HG02630.hp1 HG02717.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*180G>C | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 10/10 | 180 | chr16 | 4777617 | ||||||
| chr16:4777644 | T | G | 1 | a0001c0001t0004 | 2 | HG01943.hp2 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*153A>C | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 10/10 | 153 | chr16 | 4777644 | ||||||
| chr16:4788322 | G | A | 3 | a0001c0002t0002 a0001c0004t0002 a0004c0007t0002 |
142 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(139): Show |
5_prime_UTR_variant | MODIFIER | c.-65C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 1/10 | 677 | chr16 | 4788322 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:4778316 | G | A | 1 | a0001c0002t0002g0181 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.824-179C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4778316 | |||||||
| chr16:4778425 | G | C | 2 | a0001c0002t0002g0049 a0001c0002t0002g0189 |
3 | HG02818.hp2 HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.824-288C>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4778425 | |||||||
| chr16:4778472 | C | A | 83 | a0001c0001t0001g0037 a0001c0001t0001g0059 a0001c0001t0001g0081 others(80): Show |
144 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.824-335G>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4778472 | |||||||
| chr16:4778476 | T | C | 2 | a0001c0001t0003g0153 a0001c0001t0003g0154 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.824-339A>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4778476 | |||||||
| chr16:4778503 | A | G | 1 | a0001c0002t0002g0214 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.824-366T>C | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4778503 | |||||||
| chr16:4778658 | G | A | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0031 others(2): Show |
8 | HG00738.hp2 HG01081.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.824-521C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4778658 | |||||||
| chr16:4778805 | A | T | 103 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0059 others(100): Show |
168 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.824-668T>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4778805 | |||||||
| chr16:4778807 | T | A | 1 | a0001c0001t0001g0133 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.824-670A>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4778807 | |||||||
| chr16:4778809 | T | C | 89 | a0001c0001t0001g0037 a0001c0001t0001g0059 a0001c0001t0001g0081 others(86): Show |
150 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.824-672A>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4778809 | |||||||
| chr16:4778865 | C | G | 1 | a0001c0001t0001g0118 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.824-728G>C | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4778865 | |||||||
| chr16:4778905 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0016 others(7): Show |
25 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.824-768G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4778905 | |||||||
| chr16:4778965 | C | T | 1 | a0001c0002t0002g0211 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.823+725G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4778965 | |||||||
| chr16:4778966 | G | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0016 others(7): Show |
25 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.823+724C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4778966 | |||||||
| chr16:4778998 | C | T | 11 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0016 others(8): Show |
27 | HG01074.hp2 HG01515.hp2 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.823+692G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4778998 | |||||||
| chr16:4779071 | G | A | 1 | a0001c0002t0002g0181 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.823+619C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4779071 | |||||||
| chr16:4779121 | C | G | 99 | a0001c0001t0001g0041 a0001c0001t0001g0059 a0001c0001t0001g0069 others(96): Show |
163 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.823+569G>C | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4779121 | |||||||
| chr16:4779162 | A | AATAATAC others(308): Show |
1 | a0001c0004t0002g0162 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.823+527_823+528ins others(315): Show |
SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4779162 | |||||||
| chr16:4779228 | G | C | 5 | a0002c0005t0001g0023 a0002c0005t0001g0065 a0002c0005t0001g0141 others(2): Show |
8 | HG02055.hp1 HG02145.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.823+462C>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4779228 | |||||||
| chr16:4779254 | C | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0155 |
4 | HG02615.hp2 HG02886.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.823+436G>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4779254 | |||||||
| chr16:4779364 | G | C | 14 | a0001c0001t0001g0041 a0001c0001t0001g0069 a0001c0001t0001g0085 others(11): Show |
18 | HG01099.hp1 HG02055.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.823+326C>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4779364 | |||||||
| chr16:4779433 | A | G | 1 | a0001c0002t0002g0185 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.823+257T>C | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4779433 | |||||||
| chr16:4779447 | C | T | 2 | a0001c0002t0002g0054 a0001c0002t0002g0195 |
3 | NA18950.hp1 NA18968.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.823+243G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4779447 | |||||||
| chr16:4779475 | C | A | 1 | a0004c0007t0002g0208 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.823+215G>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4779475 | |||||||
| chr16:4779570 | G | A | 4 | a0002c0005t0001g0023 a0002c0005t0001g0065 a0002c0005t0001g0141 others(1): Show |
7 | HG02145.hp1 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.823+120C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4779570 | |||||||
| chr16:4779595 | T | C | 1 | a0001c0001t0001g0074 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.823+95A>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4779595 | |||||||
| chr16:4779601 | T | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0077 a0001c0001t0001g0119 others(1): Show |
6 | HG00099.hp2 HG00639.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+89A>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4779601 | |||||||
| chr16:4779639 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.823+51A>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4779639 | |||||||
| chr16:4779640 | G | A | 9 | a0001c0001t0001g0041 a0001c0001t0001g0069 a0001c0001t0001g0085 others(6): Show |
10 | HG01099.hp1 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.823+50C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4779640 | |||||||
| chr16:4779681 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0117 |
2 | NA18988.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.823+9G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4779681 | |||||||
| chr16:4779683 | C | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0092 a0001c0004t0002g0209 |
4 | NA18944.hp2 NA18973.hp1 NA19065.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.823+7G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 8/9 | chr16 | 4779683 | |||||||
| chr16:4779827 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0088 |
2 | HG01952.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.727-41C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4779827 | |||||||
| chr16:4779896 | G | T | 4 | a0001c0001t0003g0147 a0001c0001t0003g0149 a0001c0001t0003g0153 others(1): Show |
4 | HG02257.hp2 HG02630.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.727-110C>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4779896 | |||||||
| chr16:4779955 | C | G | 2 | a0001c0001t0001g0083 a0001c0001t0001g0156 |
2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.727-169G>C | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4779955 | |||||||
| chr16:4780038 | T | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0062 |
12 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.727-252A>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4780038 | |||||||
| chr16:4780067 | G | C | 98 | a0001c0001t0001g0041 a0001c0001t0001g0069 a0001c0001t0001g0077 others(95): Show |
162 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.727-281C>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4780067 | |||||||
| chr16:4780107 | A | C | 5 | a0002c0005t0001g0023 a0002c0005t0001g0065 a0002c0005t0001g0141 others(2): Show |
8 | HG02055.hp1 HG02145.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.727-321T>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4780107 | |||||||
| chr16:4780230 | G | A | 1 | a0001c0002t0002g0211 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.727-444C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4780230 | |||||||
| chr16:4780315 | T | C | 4 | a0001c0001t0001g0144 a0002c0005t0001g0023 a0002c0005t0001g0065 others(1): Show |
7 | HG02145.hp1 HG02280.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.727-529A>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4780315 | |||||||
| chr16:4780507 | G | A | 1 | a0001c0002t0002g0180 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.727-721C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4780507 | |||||||
| chr16:4780542 | T | C | 9 | a0001c0001t0001g0041 a0001c0001t0001g0069 a0001c0001t0001g0085 others(6): Show |
10 | HG01099.hp1 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.727-756A>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4780542 | |||||||
| chr16:4780546 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.727-760G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4780546 | |||||||
| chr16:4780715 | A | G | 1 | a0002c0005t0001g0160 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.727-929T>C | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4780715 | |||||||
| chr16:4780796 | T | G | 1 | a0001c0002t0002g0174 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.727-1010A>C | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4780796 | |||||||
| chr16:4780915 | G | A | 81 | a0001c0001t0001g0081 a0001c0001t0001g0124 a0001c0001t0001g0144 others(78): Show |
141 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.727-1129C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4780915 | |||||||
| chr16:4780925 | A | G | 105 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0016 others(102): Show |
184 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.727-1139T>C | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4780925 | |||||||
| chr16:4780926 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0016 others(7): Show |
25 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.727-1140G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4780926 | |||||||
| chr16:4780952 | C | G | 9 | a0001c0001t0001g0041 a0001c0001t0001g0069 a0001c0001t0001g0085 others(6): Show |
10 | HG01099.hp1 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.727-1166G>C | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4780952 | |||||||
| chr16:4780989 | G | A | 5 | a0001c0001t0001g0032 a0001c0001t0001g0071 a0001c0001t0001g0072 others(2): Show |
6 | HG00741.hp2 HG01167.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.727-1203C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4780989 | |||||||
| chr16:4781096 | C | T | 105 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0016 others(102): Show |
184 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.727-1310G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781096 | |||||||
| chr16:4781215 | C | T | 1 | a0001c0002t0002g0215 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.727-1429G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781215 | |||||||
| chr16:4781216 | G | A | 3 | a0001c0002t0002g0048 a0001c0002t0002g0184 a0001c0002t0002g0186 |
4 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.727-1430C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781216 | |||||||
| chr16:4781216 | G | C | 1 | a0001c0002t0002g0204 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.727-1430C>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781216 | |||||||
| chr16:4781284 | T | TA | 13 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0016 others(10): Show |
28 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.727-1499dupT | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781284 | |||||||
| chr16:4781287 | A | G | 4 | a0001c0002t0002g0194 a0001c0002t0002g0205 a0001c0002t0002g0206 others(1): Show |
4 | HG00673.hp1 HG02071.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.727-1501T>C | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781287 | |||||||
| chr16:4781321 | T | C | 1 | a0001c0001t0001g0038 | 2 | HG00735.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.727-1535A>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781321 | |||||||
| chr16:4781401 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.727-1615G>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781401 | |||||||
| chr16:4781409 | C | CA | 7 | a0001c0001t0001g0081 a0001c0001t0001g0099 a0001c0001t0001g0124 others(4): Show |
8 | HG01175.hp2 HG02056.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.727-1624dupT | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781409 | |||||||
| chr16:4781551 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0066 |
2 | HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.727-1765C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781551 | |||||||
| chr16:4781569 | C | T | 1 | a0001c0002t0002g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.727-1783G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781569 | |||||||
| chr16:4781645 | A | AT | 16 | a0001c0001t0001g0008 a0001c0001t0001g0075 a0001c0001t0001g0087 others(13): Show |
22 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.726+1816dupA | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781645 | |||||||
| chr16:4781645 | A | ATT | 10 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0016 others(7): Show |
25 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.726+1815_726+1816d others(4): Show |
SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781645 | |||||||
| chr16:4781645 | AT | A | 8 | a0001c0001t0001g0076 a0001c0001t0001g0113 a0001c0001t0001g0121 others(5): Show |
8 | HG00673.hp1 HG01168.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.726+1816delA | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781645 | |||||||
| chr16:4781772 | G | A | 35 | a0001c0001t0001g0124 a0001c0002t0002g0014 a0001c0002t0002g0015 others(32): Show |
50 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.726+1690C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781772 | |||||||
| chr16:4781832 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0131 |
2 | HG00408.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.726+1630G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781832 | |||||||
| chr16:4781842 | C | A | 1 | a0001c0001t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.726+1620G>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781842 | |||||||
| chr16:4781935 | T | C | 124 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0016 others(121): Show |
210 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(207): Show |
intron_variant | MODIFIER | c.726+1527A>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781935 | |||||||
| chr16:4781936 | G | A | 1 | a0001c0002t0002g0170 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.726+1526C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781936 | |||||||
| chr16:4781943 | C | CT | 35 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(32): Show |
56 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.726+1518dupA | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781943 | |||||||
| chr16:4781943 | C | CTT | 6 | a0001c0001t0001g0036 a0001c0001t0001g0095 a0001c0001t0001g0129 others(3): Show |
7 | HG02071.hp2 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.726+1517_726+1518d others(4): Show |
SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781943 | |||||||
| chr16:4781943 | C | CTTT | 9 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0061 others(6): Show |
17 | HG01074.hp2 HG01891.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.726+1516_726+1518d others(5): Show |
SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781943 | |||||||
| chr16:4781943 | C | CTTTT | 3 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0063 |
10 | HG02109.hp2 HG02486.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.726+1515_726+1518d others(6): Show |
SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781943 | |||||||
| chr16:4781943 | C | CTTTTTTT | 29 | a0001c0001t0001g0112 a0001c0001t0001g0124 a0001c0001t0001g0144 others(26): Show |
54 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.726+1512_726+1518d others(9): Show |
SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781943 | |||||||
| chr16:4781943 | C | CTTTTTTT others(1): Show |
45 | a0001c0001t0001g0083 a0001c0001t0001g0150 a0001c0001t0001g0151 others(42): Show |
74 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.726+1511_726+1518d others(10): Show |
SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781943 | |||||||
| chr16:4781943 | C | CTTTTTTT others(2): Show |
12 | a0001c0001t0001g0022 a0001c0001t0001g0081 a0001c0002t0002g0025 others(9): Show |
18 | HG00558.hp2 HG02129.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.726+1510_726+1518d others(11): Show |
SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781943 | |||||||
| chr16:4781943 | C | CTTTTTTT others(3): Show |
8 | a0001c0001t0001g0032 a0001c0001t0001g0070 a0001c0001t0001g0071 others(5): Show |
10 | HG01081.hp2 HG01167.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.726+1509_726+1518d others(12): Show |
SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781943 | |||||||
| chr16:4781943 | C | CTTTTTTT others(4): Show |
10 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
15 | HG00642.hp1 HG00738.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.726+1508_726+1518d others(13): Show |
SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781943 | |||||||
| chr16:4781943 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG01109.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.726+1507_726+1518d others(14): Show |
SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781943 | |||||||
| chr16:4781943 | CTTTTTTT others(4): Show |
C | 1 | a0001c0003t0001g0017 | 3 | NA18945.hp1 NA18957.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.726+1508_726+1518d others(13): Show |
SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4781943 | |||||||
| chr16:4782025 | A | C | 9 | a0001c0001t0001g0041 a0001c0001t0001g0069 a0001c0001t0001g0085 others(6): Show |
10 | HG01099.hp1 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.726+1437T>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4782025 | |||||||
| chr16:4782097 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0128 |
4 | HG00423.hp1 NA18953.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.726+1365G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4782097 | |||||||
| chr16:4782104 | C | G | 10 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0016 others(7): Show |
25 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.726+1358G>C | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4782104 | |||||||
| chr16:4782105 | C | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0016 others(7): Show |
25 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.726+1357G>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4782105 | |||||||
| chr16:4782141 | A | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0152 |
2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.726+1321T>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4782141 | |||||||
| chr16:4782169 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0016 others(7): Show |
25 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.726+1293G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4782169 | |||||||
| chr16:4782250 | T | G | 1 | a0001c0001t0001g0100 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.726+1212A>C | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4782250 | |||||||
| chr16:4782346 | T | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.726+1116A>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4782346 | |||||||
| chr16:4782415 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0016 others(7): Show |
25 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.726+1047G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4782415 | |||||||
| chr16:4782423 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.726+1039A>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4782423 | |||||||
| chr16:4782471 | G | A | 1 | a0001c0001t0004g0135 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.726+991C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4782471 | |||||||
| chr16:4782475 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.726+987T>C | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4782475 | |||||||
| chr16:4782574 | G | A | 3 | a0001c0002t0002g0045 a0001c0002t0002g0176 a0001c0002t0002g0181 |
4 | NA18943.hp2 NA18994.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.726+888C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4782574 | |||||||
| chr16:4782610 | C | CT | 6 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0094 others(3): Show |
11 | HG02523.hp2 NA18950.hp2 NA18962.hp1 others(8): Show |
intron_variant | MODIFIER | c.726+851dupA | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4782610 | |||||||
| chr16:4782750 | C | A | 1 | a0001c0002t0002g0202 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.726+712G>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4782750 | |||||||
| chr16:4782774 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0016 others(7): Show |
25 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.726+688G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4782774 | |||||||
| chr16:4782822 | C | G | 1 | a0001c0001t0001g0140 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.726+640G>C | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4782822 | |||||||
| chr16:4783019 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.726+443G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4783019 | |||||||
| chr16:4783022 | T | C | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.726+440A>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4783022 | |||||||
| chr16:4783030 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.726+432G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4783030 | |||||||
| chr16:4783052 | C | T | 1 | a0001c0002t0002g0169 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.726+410G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4783052 | |||||||
| chr16:4783168 | C | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0016 others(7): Show |
25 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.726+294G>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4783168 | |||||||
| chr16:4783184 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0093 a0001c0001t0001g0113 |
6 | HG01106.hp1 HG01168.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.726+278G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4783184 | |||||||
| chr16:4783204 | C | T | 1 | a0001c0001t0003g0153 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.726+258G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4783204 | |||||||
| chr16:4783218 | C | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0016 others(7): Show |
25 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.726+244G>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4783218 | |||||||
| chr16:4783219 | T | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0016 others(7): Show |
25 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.726+243A>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4783219 | |||||||
| chr16:4783221 | T | C | 84 | a0001c0001t0001g0078 a0001c0001t0001g0110 a0001c0001t0001g0111 others(81): Show |
144 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.726+241A>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4783221 | |||||||
| chr16:4783241 | C | T | 1 | a0001c0002t0002g0197 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.726+221G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4783241 | |||||||
| chr16:4783409 | G | T | 2 | a0001c0002t0002g0042 a0001c0002t0002g0166 |
3 | HG01261.hp1 HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.726+53C>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4783409 | |||||||
| chr16:4783420 | A | G | 78 | a0001c0001t0001g0112 a0001c0001t0001g0144 a0001c0002t0002g0003 others(75): Show |
138 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.726+42T>C | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4783420 | |||||||
| chr16:4783434 | G | A | 2 | a0001c0002t0002g0190 a0001c0002t0002g0203 |
2 | HG02165.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.726+28C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 7/9 | chr16 | 4783434 | |||||||
| chr16:4783614 | C | T | 40 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0024 others(37): Show |
56 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.630+35G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 6/9 | chr16 | 4783614 | |||||||
| chr16:4783818 | C | T | 3 | a0001c0002t0002g0178 a0001c0002t0002g0179 a0001c0002t0002g0187 |
3 | HG01123.hp2 HG02735.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.513-52G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 5/9 | chr16 | 4783818 | |||||||
| chr16:4783860 | T | C | 23 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(20): Show |
30 | HG00642.hp1 HG00738.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.512+71A>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 5/9 | chr16 | 4783860 | |||||||
| chr16:4784164 | C | T | 79 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0010 others(76): Show |
138 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.375-96G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784164 | |||||||
| chr16:4784167 | C | T | 79 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0010 others(76): Show |
138 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.375-99G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784167 | |||||||
| chr16:4784172 | C | T | 2 | a0002c0005t0001g0141 a0002c0005t0001g0160 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.375-104G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784172 | |||||||
| chr16:4784288 | G | C | 1 | a0001c0001t0001g0144 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.375-220C>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784288 | |||||||
| chr16:4784294 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.375-226T>C | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784294 | |||||||
| chr16:4784317 | A | C | 10 | a0001c0001t0001g0022 a0001c0001t0001g0083 a0001c0001t0001g0150 others(7): Show |
15 | HG01243.hp2 HG02145.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.375-249T>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784317 | |||||||
| chr16:4784321 | G | A | 1 | a0001c0002t0002g0202 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.375-253C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784321 | |||||||
| chr16:4784323 | G | A | 79 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0010 others(76): Show |
139 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.375-255C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784323 | |||||||
| chr16:4784341 | A | G | 80 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0010 others(77): Show |
140 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.375-273T>C | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784341 | |||||||
| chr16:4784377 | A | C | 124 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0029 others(121): Show |
197 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.375-309T>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784377 | |||||||
| chr16:4784379 | C | T | 1 | a0001c0002t0002g0050 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.375-311G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784379 | |||||||
| chr16:4784380 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.375-312C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784380 | |||||||
| chr16:4784383 | C | T | 78 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0010 others(75): Show |
137 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.375-315G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784383 | |||||||
| chr16:4784403 | C | G | 1 | a0001c0002t0002g0201 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.375-335G>C | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784403 | |||||||
| chr16:4784553 | C | T | 2 | a0001c0002t0002g0214 a0001c0002t0002g0215 |
2 | HG02165.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.375-485G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784553 | |||||||
| chr16:4784589 | G | GGGAAACG others(21): Show |
79 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0010 others(76): Show |
139 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.375-549_375-522dup others(28): Show |
SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784589 | |||||||
| chr16:4784600 | A | ACTCTACA others(22): Show |
1 | a0001c0002t0002g0177 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.375-533_375-532ins others(29): Show |
SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784600 | |||||||
| chr16:4784613 | T | A | 3 | a0001c0001t0001g0101 a0001c0001t0001g0126 a0001c0001t0001g0136 |
3 | NA18939.hp2 NA18949.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.375-545A>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784613 | |||||||
| chr16:4784637 | G | C | 2 | a0001c0002t0002g0049 a0001c0002t0002g0189 |
3 | HG02818.hp2 HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.375-569C>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784637 | |||||||
| chr16:4784769 | C | CTAAA | 22 | a0001c0001t0001g0039 a0001c0001t0001g0102 a0001c0001t0001g0137 others(19): Show |
36 | HG00140.hp1 HG01081.hp1 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.375-705_375-702dup others(4): Show |
SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784769 | |||||||
| chr16:4784769 | C | CTAAATAA others(5): Show |
1 | a0001c0002t0002g0182 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.375-713_375-702dup others(12): Show |
SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784769 | |||||||
| chr16:4784769 | CTAAA | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(115): Show |
239 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.375-705_375-702del others(4): Show |
SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784769 | |||||||
| chr16:4784769 | CTAAATAA others(1): Show |
C | 5 | a0001c0001t0001g0028 a0001c0001t0001g0068 a0001c0001t0001g0070 others(2): Show |
6 | HG00738.hp2 HG01081.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.375-709_375-702del others(8): Show |
SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784769 | |||||||
| chr16:4784769 | CTAAATAA others(5): Show |
C | 15 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0016 others(12): Show |
33 | HG01074.hp2 HG01884.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.375-713_375-702del others(12): Show |
SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784769 | |||||||
| chr16:4784769 | CTAAATAA others(9): Show |
C | 3 | a0001c0001t0001g0107 a0001c0001t0003g0153 a0001c0001t0003g0154 |
3 | HG02040.hp1 HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.375-717_375-702del others(16): Show |
SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784769 | |||||||
| chr16:4784769 | CTAAATAA others(13): Show |
C | 1 | a0001c0002t0002g0050 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.375-721_375-702del others(20): Show |
SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784769 | |||||||
| chr16:4784837 | C | T | 1 | a0001c0002t0002g0200 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.375-769G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784837 | |||||||
| chr16:4784889 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.375-821G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784889 | |||||||
| chr16:4784922 | C | T | 15 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0016 others(12): Show |
30 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.375-854G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784922 | |||||||
| chr16:4784934 | A | C | 1 | a0001c0001t0001g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.375-866T>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784934 | |||||||
| chr16:4784939 | C | T | 2 | a0001c0002t0002g0046 a0001c0002t0002g0183 |
3 | HG01081.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.374+868G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784939 | |||||||
| chr16:4784940 | G | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0016 others(9): Show |
27 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.374+867C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784940 | |||||||
| chr16:4784956 | C | T | 1 | a0001c0002t0002g0199 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.374+851G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4784956 | |||||||
| chr16:4785021 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0092 |
3 | NA18944.hp2 NA18973.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.374+786G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4785021 | |||||||
| chr16:4785111 | G | A | 1 | a0001c0002t0002g0026 | 2 | HG03688.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.374+696C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4785111 | |||||||
| chr16:4785187 | G | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0106 |
2 | HG00738.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.374+620C>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4785187 | |||||||
| chr16:4785229 | T | C | 120 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0029 others(117): Show |
193 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.374+578A>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4785229 | |||||||
| chr16:4785230 | G | A | 10 | a0001c0002t0002g0015 a0001c0002t0002g0046 a0001c0002t0002g0047 others(7): Show |
16 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.374+577C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4785230 | |||||||
| chr16:4785238 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0090 a0001c0001t0001g0105 |
7 | HG01884.hp1 HG02622.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+569G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4785238 | |||||||
| chr16:4785249 | TA | T | 110 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0029 others(107): Show |
183 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.374+557delT | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4785249 | |||||||
| chr16:4785495 | C | T | 2 | a0001c0001t0001g0104 a0002c0005t0001g0160 |
2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.374+312G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4785495 | |||||||
| chr16:4785634 | G | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0016 others(9): Show |
27 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.374+173C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4785634 | |||||||
| chr16:4785694 | C | G | 1 | a0001c0001t0001g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.374+113G>C | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4785694 | |||||||
| chr16:4785750 | C | G | 1 | a0002c0005t0001g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.374+57G>C | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4785750 | |||||||
| chr16:4785792 | A | G | 2 | a0001c0002t0002g0165 a0001c0002t0002g0198 |
2 | NA18968.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.374+15T>C | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4785792 | |||||||
| chr16:4785793 | G | A | 5 | a0001c0002t0002g0165 a0001c0002t0002g0188 a0001c0002t0002g0196 others(2): Show |
5 | HG03710.hp1 HG04228.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.374+14C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4785793 | |||||||
| chr16:4785793 | G | GA | 109 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0029 others(106): Show |
181 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.374+13dupT | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 4/9 | chr16 | 4785793 | |||||||
| chr16:4785892 | T | C | 1 | a0002c0005t0001g0160 | 1 | HG02055.hp1 | splice_region_variant&intron_variant | LOW | c.293-4A>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 3/9 | chr16 | 4785892 | |||||||
| chr16:4786120 | C | G | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01243.hp2 HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.167-15G>C | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 2/9 | chr16 | 4786120 | |||||||
| chr16:4786154 | G | GT | 123 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(120): Show |
212 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.167-50dupA | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 2/9 | chr16 | 4786154 | |||||||
| chr16:4786267 | C | T | 1 | a0001c0002t0002g0197 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.167-162G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 2/9 | chr16 | 4786267 | |||||||
| chr16:4786278 | G | T | 1 | a0001c0001t0001g0035 | 2 | HG00621.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.167-173C>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 2/9 | chr16 | 4786278 | |||||||
| chr16:4786314 | G | A | 4 | a0001c0001t0001g0041 a0001c0003t0001g0157 a0001c0003t0001g0158 others(1): Show |
5 | HG02896.hp2 HG02897.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.167-209C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 2/9 | chr16 | 4786314 | |||||||
| chr16:4786353 | C | CT | 28 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0034 others(25): Show |
37 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.167-249dupA | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 2/9 | chr16 | 4786353 | |||||||
| chr16:4786353 | CT | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0041 others(19): Show |
32 | HG00323.hp1 HG00544.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.167-249delA | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 2/9 | chr16 | 4786353 | |||||||
| chr16:4786385 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.167-280G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 2/9 | chr16 | 4786385 | |||||||
| chr16:4786436 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.167-331C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 2/9 | chr16 | 4786436 | |||||||
| chr16:4786504 | G | A | 2 | a0001c0002t0002g0049 a0001c0002t0002g0189 |
3 | HG02818.hp2 HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.167-399C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 2/9 | chr16 | 4786504 | |||||||
| chr16:4786511 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.167-406G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 2/9 | chr16 | 4786511 | |||||||
| chr16:4786545 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0062 others(2): Show |
14 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.167-440G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 2/9 | chr16 | 4786545 | |||||||
| chr16:4786564 | C | T | 3 | a0001c0001t0003g0147 a0001c0001t0003g0149 a0002c0005t0001g0148 |
3 | HG02257.hp2 HG03041.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.167-459G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 2/9 | chr16 | 4786564 | |||||||
| chr16:4786606 | C | T | 79 | a0001c0001t0001g0146 a0001c0002t0002g0003 a0001c0002t0002g0004 others(76): Show |
138 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.167-501G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 2/9 | chr16 | 4786606 | |||||||
| chr16:4786612 | C | T | 11 | a0001c0001t0001g0022 a0001c0001t0001g0150 a0001c0001t0001g0151 others(8): Show |
13 | HG01243.hp2 HG02257.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.167-507G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 2/9 | chr16 | 4786612 | |||||||
| chr16:4786789 | G | C | 1 | a0002c0005t0001g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.167-684C>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 2/9 | chr16 | 4786789 | |||||||
| chr16:4786801 | A | T | 3 | a0001c0001t0003g0147 a0001c0001t0003g0149 a0002c0005t0001g0148 |
3 | HG02257.hp2 HG03041.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.166+679T>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 2/9 | chr16 | 4786801 | |||||||
| chr16:4786901 | G | C | 1 | a0001c0001t0001g0142 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.166+579C>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 2/9 | chr16 | 4786901 | |||||||
| chr16:4786911 | G | A | 3 | a0001c0003t0001g0157 a0001c0003t0001g0158 a0001c0003t0001g0159 |
3 | HG02965.hp2 HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.166+569C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 2/9 | chr16 | 4786911 | |||||||
| chr16:4786982 | C | T | 1 | a0001c0002t0002g0163 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.166+498G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 2/9 | chr16 | 4786982 | |||||||
| chr16:4787003 | T | C | 13 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0016 others(10): Show |
28 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.166+477A>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 2/9 | chr16 | 4787003 | |||||||
| chr16:4787020 | C | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.166+460G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 2/9 | chr16 | 4787020 | |||||||
| chr16:4787051 | T | A | 1 | a0001c0001t0001g0144 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.166+429A>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 2/9 | chr16 | 4787051 | |||||||
| chr16:4787095 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.166+385G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 2/9 | chr16 | 4787095 | |||||||
| chr16:4787361 | T | C | 100 | a0001c0001t0001g0022 a0001c0001t0001g0041 a0001c0001t0001g0146 others(97): Show |
166 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.166+119A>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 2/9 | chr16 | 4787361 | |||||||
| chr16:4787469 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.166+11G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 2/9 | chr16 | 4787469 | |||||||
| chr16:4787727 | C | T | 1 | a0001c0002t0002g0216 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-22-60G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 1/9 | chr16 | 4787727 | |||||||
| chr16:4787770 | C | G | 1 | a0001c0002t0002g0161 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-22-103G>C | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 1/9 | chr16 | 4787770 | |||||||
| chr16:4787946 | G | A | 2 | a0001c0002t0002g0214 a0001c0002t0002g0215 |
2 | HG02165.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.-22-279C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 1/9 | chr16 | 4787946 | |||||||
| chr16:4787964 | T | C | 44 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0002t0002g0003 others(41): Show |
88 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.-22-297A>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 1/9 | chr16 | 4787964 | |||||||
| chr16:4788015 | T | C | 4 | a0001c0002t0002g0057 a0001c0002t0002g0058 a0001c0002t0002g0216 others(1): Show |
6 | NA18970.hp1 NA18973.hp2 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+265A>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 1/9 | chr16 | 4788015 | |||||||
| chr16:4788064 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-23+216G>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 1/9 | chr16 | 4788064 | |||||||
| chr16:4788143 | G | A | 1 | a0002c0005t0001g0160 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-23+137C>T | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 1/9 | chr16 | 4788143 | |||||||
| chr16:4788165 | A | C | 37 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(34): Show |
65 | HG00323.hp1 HG00544.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.-23+115T>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 1/9 | chr16 | 4788165 | |||||||
| chr16:4788171 | C | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0016 others(9): Show |
27 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.-23+109G>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 1/9 | chr16 | 4788171 | |||||||
| chr16:4788197 | T | C | 100 | a0001c0001t0001g0022 a0001c0001t0001g0041 a0001c0001t0001g0150 others(97): Show |
166 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.-23+83A>G | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 1/9 | chr16 | 4788197 | |||||||
| chr16:4788244 | G | T | 1 | a0001c0001t0001g0059 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-23+36C>A | SEPTIN12 | ENSG00000140623.14 | transcript | ENST00000268231.13 | protein_coding | 1/9 | chr16 | 4788244 |