Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4922 |
| ensemblid | ENSG00000133636.11 |
| hgncid | 8038 |
| symbol | NTS |
| name | neurotensin |
| refseq_nuc | NM_006183.5 |
| refseq_prot | NP_006174.1 |
| ensembl_nuc | ENST00000256010.7 |
| ensembl_prot | ENSP00000256010.5 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 85874295 |
| end | 85882992 |
| strand | + |
| ver | v1.2 |
| region | chr12:85874295-85882992 |
| region5000 | chr12:85869295-85887992 |
| regionname0 | NTS_chr12_85874295_85882992 |
| regionname5000 | NTS_chr12_85869295_85887992 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 170 | 417 | 91 | 79 | 183 | 16 | 46 | 141 | NTS_chr12_85869295_85887992 | NTS | MMAGM others(165): Show |
chr12 | 85869295 | 85887992 |
| a0002 | 0/0 | 170 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | MMAGM others(165): Show |
chr12 | 85869295 | 85887992 |
| a0003 | 0/0 | 170 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | MMAGM others(165): Show |
chr12 | 85869295 | 85887992 |
| a0004 | 0/0 | 170 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | MMAGM others(165): Show |
chr12 | 85869295 | 85887992 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 510 | 416 | 90 | 79 | 183 | 16 | 46 | NTS_chr12_85869295_85887992 | NTS | ATGAT others(505): Show |
chr12 | 85869295 | 85887992 | ||
| a0001c0004 | 0/0 | 510 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | ATGAT others(505): Show |
chr12 | 85869295 | 85887992 | ||
| a0002c0003 | 0/0 | 510 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | ATGAT others(505): Show |
chr12 | 85869295 | 85887992 | ||
| a0003c0005 | 0/0 | 510 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | ATGAT others(505): Show |
chr12 | 85869295 | 85887992 | ||
| a0004c0002 | 0/0 | 510 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | ATGAT others(505): Show |
chr12 | 85869295 | 85887992 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1239 | 362 | 85 | 72 | 146 | 14 | 43 | NTS_chr12_85869295_85887992 | NTS | ATAGT others(1234): Show |
chr12 | 85869295 | 85887992 |
| a0001c0001t0002 | 0/0 | 1239 | 40 | 0 | 3 | 34 | 0 | 3 | NTS_chr12_85869295_85887992 | NTS | ATAGT others(1234): Show |
chr12 | 85869295 | 85887992 |
| a0001c0001t0003 | 0/0 | 1235 | 5 | 0 | 3 | 0 | 2 | 0 | NTS_chr12_85869295_85887992 | NTS | ATAGT others(1230): Show |
chr12 | 85869295 | 85887992 |
| a0001c0001t0004 | 0/0 | 1239 | 3 | 3 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | ATAGT others(1234): Show |
chr12 | 85869295 | 85887992 |
| a0001c0001t0005 | 0/0 | 1239 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | ATAGT others(1234): Show |
chr12 | 85869295 | 85887992 |
| a0001c0001t0006 | 0/0 | 1239 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | ATAGT others(1234): Show |
chr12 | 85869295 | 85887992 |
| a0001c0001t0008 | 0/0 | 1239 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | ATAGT others(1234): Show |
chr12 | 85869295 | 85887992 |
| a0001c0001t0009 | 0/0 | 1239 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | ATAGT others(1234): Show |
chr12 | 85869295 | 85887992 |
| a0001c0001t0010 | 0/0 | 1239 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | ATAGT others(1234): Show |
chr12 | 85869295 | 85887992 |
| a0001c0001t0011 | 0/0 | 1239 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | ATAGT others(1234): Show |
chr12 | 85869295 | 85887992 |
| a0001c0004t0001 | 0/0 | 1239 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | ATAGT others(1234): Show |
chr12 | 85869295 | 85887992 |
| a0002c0003t0001 | 0/0 | 1239 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | ATAGT others(1234): Show |
chr12 | 85869295 | 85887992 |
| a0003c0005t0002 | 0/0 | 1239 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | ATAGT others(1234): Show |
chr12 | 85869295 | 85887992 |
| a0004c0002t0007 | 0/0 | 1239 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | ATAGT others(1234): Show |
chr12 | 85869295 | 85887992 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 68 | 6 | 8 | 48 | 2 | 4 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0002 | 0/0 | 45 | 0 | 15 | 20 | 1 | 9 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0004 | 0/0 | 12 | 1 | 10 | 0 | 1 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0005 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0006 | 0/0 | 10 | 0 | 6 | 0 | 2 | 2 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0008 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0009 | 0/0 | 7 | 0 | 4 | 0 | 1 | 2 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0010 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0011 | 0/0 | 6 | 1 | 0 | 3 | 0 | 2 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0012 | 0/0 | 5 | 2 | 0 | 1 | 0 | 2 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0023 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0040 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0045 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0053 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0122 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0156 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0002g0003 | 0/0 | 12 | 0 | 0 | 11 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0002g0007 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0003g0018 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0004g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0006g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0008g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0009g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0010g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0001t0011g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0001c0004t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0002c0003t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0003c0005t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| a0004c0002t0007g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | FIN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | FIN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00423 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | CHS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0056 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01175 | hp1 | a0001 | c0001 | t0010 | g0106 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0018 | EUR | IBS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | IBS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0018 | EUR | IBS | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01978 | hp1 | a0002 | c0003 | t0001 | g0017 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | CDX | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CDX | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02451 | hp2 | a0001 | c0001 | t0008 | g0120 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0049 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02922 | hp2 | a0001 | c0001 | t0011 | g0163 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0135 | AFR | MSL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0049 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | STU | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | STU | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0105 | SAS | BEB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | STU | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0084 | SAS | STU | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | STU | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | STU | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18965 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | LWK | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | LWK | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19059 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19064 | hp1 | a0001 | c0001 | t0009 | g0014 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19091 | hp2 | a0003 | c0005 | t0002 | g0073 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | YRI | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | TSI | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | TSI | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0032 | EUR | TSI | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | GIH | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02559 | hp1 | a0001 | c0004 | t0001 | g0130 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | USA | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | USA | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | USA | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | USA | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | LWK | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| NA21309 | hp2 | a0004 | c0002 | t0007 | g0001 | AFR | LWK | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0156 | REF | REF | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0122 | REF | REF | NTS_chr12_85869295_85887992 | NTS | chr12 | 85869295 | 85887992 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:85874446 | C | G | 1 | a0003 | 1 | NA19091.hp2 | missense_variant | MODERATE | c.43C>G | p.Leu15Val | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/4 | 152/1239 | 43/513 | 15/170 | chr12 | 85874446 | |||
| chr12:85876677 | C | A | 1 | a0004 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.111C>A | p.Phe37Leu | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/4 | 220/1239 | 111/513 | 37/170 | chr12 | 85876677 | |||
| chr12:85878399 | C | A | 1 | a0002 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.190C>A | p.Leu64Ile | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/4 | 299/1239 | 190/513 | 64/170 | chr12 | 85878399 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:85882366 | C | T | 1 | a0001c0004 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.504C>T | p.Tyr168Tyr | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 4/4 | 613/1239 | 504/513 | 168/170 | chr12 | 85882366 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:85874401 | A | G | 3 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0011 |
7 | HG00639.hp2 HG00741.hp2 HG01175.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-3A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/4 | 3 | chr12 | 85874401 | ||||||
| chr12:85882507 | T | A | 1 | a0001c0001t0005 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*132T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 4/4 | 132 | chr12 | 85882507 | ||||||
| chr12:85882518 | A | G | 1 | a0001c0001t0009 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*143A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 4/4 | 143 | chr12 | 85882518 | ||||||
| chr12:85882569 | G | A | 3 | a0001c0001t0002 a0001c0001t0010 a0003c0005t0002 |
42 | HG01175.hp1 HG01928.hp2 HG01952.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*194G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 4/4 | 194 | chr12 | 85882569 | ||||||
| chr12:85882691 | G | A | 1 | a0001c0001t0006 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*316G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 4/4 | 316 | chr12 | 85882691 | ||||||
| chr12:85882707 | C | T | 1 | a0001c0001t0008 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*332C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 4/4 | 332 | chr12 | 85882707 | ||||||
| chr12:85882802 | G | A | 1 | a0004c0002t0007 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*427G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 4/4 | 427 | chr12 | 85882802 | ||||||
| chr12:85882875 | AGATT | A | 1 | a0001c0001t0003 | 5 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*505_*508delGATT | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 4/4 | 505 | INFO_REALIGN_3_PRIME | chr12 | 85882875 | |||||
| chr12:85882909 | T | A | 1 | a0001c0001t0004 | 3 | HG02630.hp1 HG03486.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*534T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 4/4 | 534 | chr12 | 85882909 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:85874633 | C | T | 1 | a0001c0001t0011g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.73+157C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85874633 | |||||||
| chr12:85874705 | C | T | 35 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(32): Show |
85 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.73+229C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85874705 | |||||||
| chr12:85874881 | G | A | 3 | a0001c0001t0003g0018 a0001c0001t0003g0055 a0001c0001t0003g0056 |
5 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.73+405G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85874881 | |||||||
| chr12:85874896 | C | G | 1 | a0001c0001t0001g0139 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.73+420C>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85874896 | |||||||
| chr12:85875060 | C | T | 5 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(2): Show |
6 | HG02055.hp1 HG02630.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.73+584C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85875060 | |||||||
| chr12:85875163 | T | G | 4 | a0001c0001t0003g0018 a0001c0001t0003g0055 a0001c0001t0003g0056 others(1): Show |
6 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.73+687T>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85875163 | |||||||
| chr12:85875217 | G | A | 4 | a0001c0001t0003g0018 a0001c0001t0003g0055 a0001c0001t0003g0056 others(1): Show |
6 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.73+741G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85875217 | |||||||
| chr12:85875224 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.73+748C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85875224 | |||||||
| chr12:85875268 | C | T | 5 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0132 others(2): Show |
7 | HG02109.hp1 HG02486.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.73+792C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85875268 | |||||||
| chr12:85875391 | G | C | 1 | a0001c0001t0001g0057 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.73+915G>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85875391 | |||||||
| chr12:85875662 | A | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0131 a0001c0001t0009g0014 |
6 | NA18954.hp2 NA18973.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.74-978A>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85875662 | |||||||
| chr12:85875692 | T | C | 2 | a0001c0001t0002g0058 a0001c0001t0002g0059 |
2 | HG01928.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.74-948T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85875692 | |||||||
| chr12:85876074 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(148): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.74-566G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85876074 | |||||||
| chr12:85876106 | C | CA | 52 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
108 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.74-532dupA | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 85876106 | ||||||
| chr12:85876140 | AC | A | 5 | a0001c0001t0001g0026 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
7 | HG01192.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.74-499delC | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85876140 | |||||||
| chr12:85876173 | T | C | 3 | a0001c0001t0003g0018 a0001c0001t0003g0055 a0001c0001t0003g0056 |
5 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.74-467T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85876173 | |||||||
| chr12:85876231 | T | C | 3 | a0001c0001t0003g0018 a0001c0001t0003g0055 a0001c0001t0003g0056 |
5 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.74-409T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85876231 | |||||||
| chr12:85876244 | A | T | 1 | a0001c0001t0001g0161 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.74-396A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85876244 | |||||||
| chr12:85876271 | A | G | 1 | a0001c0001t0001g0024 | 3 | NA18990.hp1 NA19057.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.74-369A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85876271 | |||||||
| chr12:85876405 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.74-235T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85876405 | |||||||
| chr12:85876469 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.74-171A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 1/3 | chr12 | 85876469 | |||||||
| chr12:85876722 | A | G | 3 | a0001c0001t0003g0018 a0001c0001t0003g0055 a0001c0001t0003g0056 |
5 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+21A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85876722 | |||||||
| chr12:85876831 | G | GA | 46 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(43): Show |
99 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.135+140dupA | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 85876831 | ||||||
| chr12:85876851 | GT | G | 35 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(32): Show |
85 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.135+152delT | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 85876851 | ||||||
| chr12:85877031 | T | A | 1 | a0001c0001t0011g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.135+330T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85877031 | |||||||
| chr12:85877053 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.135+352C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85877053 | |||||||
| chr12:85877072 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.135+371G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85877072 | |||||||
| chr12:85877077 | T | C | 16 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(13): Show |
77 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.135+376T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85877077 | |||||||
| chr12:85877272 | G | A | 1 | a0001c0001t0011g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.135+571G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85877272 | |||||||
| chr12:85877285 | G | A | 49 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
104 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.135+584G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85877285 | |||||||
| chr12:85877311 | A | T | 1 | a0001c0004t0001g0130 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.135+610A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85877311 | |||||||
| chr12:85877336 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.135+635T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85877336 | |||||||
| chr12:85877401 | CT | C | 51 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
104 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.135+717delT | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 85877401 | ||||||
| chr12:85877401 | CTT | C | 7 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(4): Show |
8 | HG02055.hp1 HG02630.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.135+716_135+717del others(2): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 85877401 | ||||||
| chr12:85877688 | G | A | 1 | a0001c0001t0004g0135 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.136-657G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85877688 | |||||||
| chr12:85877719 | A | G | 2 | a0001c0001t0004g0049 a0001c0001t0004g0135 |
3 | HG02630.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.136-626A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85877719 | |||||||
| chr12:85877781 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | HG00621.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.136-564G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85877781 | |||||||
| chr12:85877796 | A | T | 1 | a0001c0001t0001g0054 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.136-549A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85877796 | |||||||
| chr12:85877891 | T | TAACAATT others(25): Show |
1 | a0001c0001t0001g0146 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.136-453_136-422dup others(32): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 85877891 | ||||||
| chr12:85878038 | T | A | 1 | a0001c0001t0001g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.136-307T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85878038 | |||||||
| chr12:85878124 | C | T | 2 | a0001c0001t0004g0049 a0001c0001t0004g0135 |
3 | HG02630.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.136-221C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85878124 | |||||||
| chr12:85878133 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.136-212G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85878133 | |||||||
| chr12:85878325 | G | T | 1 | a0001c0001t0003g0056 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.136-20G>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 2/3 | chr12 | 85878325 | |||||||
| chr12:85878573 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG02922.hp1 | splice_region_variant&intron_variant | LOW | c.360+4T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85878573 | |||||||
| chr12:85878600 | A | T | 35 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(32): Show |
85 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.360+31A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85878600 | |||||||
| chr12:85878795 | T | A | 1 | a0001c0001t0001g0147 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.360+226T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85878795 | |||||||
| chr12:85879036 | T | TTTTATGT others(24): Show |
1 | a0001c0001t0001g0141 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.360+475_360+476ins others(31): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879036 | ||||||
| chr12:85879039 | T | TATGTATA others(5): Show |
3 | a0001c0001t0003g0018 a0001c0001t0003g0055 a0001c0001t0003g0056 |
5 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.360+475_360+476ins others(12): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879039 | ||||||
| chr12:85879045 | C | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(40): Show |
97 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.360+476C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879045 | |||||||
| chr12:85879071 | TA | T | 5 | a0001c0001t0001g0044 a0001c0001t0001g0078 a0001c0001t0001g0117 others(2): Show |
6 | HG02132.hp2 NA18947.hp2 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+504delA | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879071 | ||||||
| chr12:85879079 | A | G | 7 | a0001c0001t0001g0023 a0001c0001t0001g0044 a0001c0001t0001g0078 others(4): Show |
10 | HG01168.hp1 HG02132.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.360+510A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879079 | |||||||
| chr12:85879089 | T | TTTTTATG others(151): Show |
1 | a0001c0001t0011g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.360+536_360+537ins others(158): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879089 | ||||||
| chr12:85879089 | T | TTTTTATG others(363): Show |
1 | a0001c0001t0001g0133 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.360+540_360+541ins others(370): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879089 | ||||||
| chr12:85879098 | A | ATGTACGT others(49): Show |
1 | a0001c0001t0001g0128 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.360+530_360+531ins others(56): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879098 | ||||||
| chr12:85879100 | A | G | 1 | a0001c0001t0001g0043 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.360+531A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879100 | |||||||
| chr12:85879110 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.360+541C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879110 | |||||||
| chr12:85879111 | G | A | 4 | a0001c0001t0001g0015 a0001c0001t0003g0018 a0001c0001t0003g0055 others(1): Show |
9 | HG00323.hp1 HG00639.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.360+542G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879111 | |||||||
| chr12:85879121 | T | TTTTATGT others(54): Show |
1 | a0001c0001t0001g0118 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.360+555_360+556ins others(61): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879121 | ||||||
| chr12:85879121 | T | TTTTTATG others(55): Show |
3 | a0001c0001t0001g0136 a0001c0001t0004g0049 a0001c0001t0004g0135 |
4 | HG02055.hp1 HG02630.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+587_360+588ins others(62): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879121 | ||||||
| chr12:85879143 | G | A | 3 | a0001c0001t0003g0018 a0001c0001t0003g0055 a0001c0001t0003g0056 |
5 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.360+574G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879143 | |||||||
| chr12:85879152 | AT | A | 7 | a0001c0001t0001g0044 a0001c0001t0001g0117 a0001c0001t0001g0118 others(4): Show |
8 | HG03130.hp1 HG03139.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.360+588delT | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879152 | ||||||
| chr12:85879153 | T | TTTTATGT others(85): Show |
2 | a0001c0001t0001g0119 a0001c0001t0001g0132 |
2 | HG02132.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.360+587_360+588ins others(92): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879153 | ||||||
| chr12:85879153 | T | TTTTATGT others(147): Show |
1 | a0001c0001t0001g0110 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.360+587_360+588ins others(154): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879153 | ||||||
| chr12:85879153 | T | TTTTTATG others(86): Show |
1 | a0001c0001t0002g0061 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.360+605_360+606ins others(93): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879153 | ||||||
| chr12:85879153 | T | TTTTTATG others(106): Show |
1 | a0001c0001t0001g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.360+619_360+620ins others(113): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879153 | ||||||
| chr12:85879153 | T | TTTTTATG others(117): Show |
1 | a0001c0001t0001g0108 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.360+619_360+620ins others(124): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879153 | ||||||
| chr12:85879153 | T | TTTTTATG others(117): Show |
1 | a0001c0001t0001g0116 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.360+619_360+620ins others(124): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879153 | ||||||
| chr12:85879153 | T | TTTTTATG others(97): Show |
1 | a0001c0001t0001g0015 | 4 | HG00323.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+619_360+620ins others(104): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879153 | ||||||
| chr12:85879156 | T | A | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.360+587T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879156 | |||||||
| chr12:85879160 | G | A | 4 | a0001c0001t0001g0136 a0001c0001t0001g0150 a0001c0001t0004g0049 others(1): Show |
5 | HG02055.hp1 HG02630.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+591G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879160 | |||||||
| chr12:85879162 | A | C | 1 | a0001c0001t0001g0133 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.360+593A>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879162 | |||||||
| chr12:85879163 | T | TATTTTAT others(4): Show |
3 | a0001c0001t0003g0018 a0001c0001t0003g0055 a0001c0001t0003g0056 |
5 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.360+595_360+605dup others(11): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879163 | ||||||
| chr12:85879174 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.360+605C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879174 | |||||||
| chr12:85879175 | G | A | 4 | a0001c0001t0001g0150 a0001c0001t0003g0018 a0001c0001t0003g0055 others(1): Show |
6 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.360+606G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879175 | |||||||
| chr12:85879184 | AT | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(97): Show |
293 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(290): Show |
intron_variant | MODIFIER | c.360+620delT | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879184 | ||||||
| chr12:85879185 | T | TTTTATGT others(54): Show |
1 | a0001c0001t0002g0041 | 2 | NA19058.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.360+619_360+620ins others(61): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879185 | ||||||
| chr12:85879185 | T | TTTTATGT others(116): Show |
2 | a0001c0001t0001g0042 a0001c0001t0001g0077 |
3 | NA19005.hp1 NA19074.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.360+619_360+620ins others(123): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879185 | ||||||
| chr12:85879188 | T | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0150 |
2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.360+619T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879188 | |||||||
| chr12:85879192 | G | A | 15 | a0001c0001t0001g0015 a0001c0001t0001g0108 a0001c0001t0001g0109 others(12): Show |
19 | HG00323.hp1 HG01256.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.360+623G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879192 | |||||||
| chr12:85879195 | T | TATTTTAT others(4): Show |
1 | a0001c0001t0003g0055 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.360+627_360+637dup others(11): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879195 | ||||||
| chr12:85879206 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.360+637C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879206 | |||||||
| chr12:85879206 | CGTAAAAT others(13): Show |
C | 2 | a0001c0001t0003g0018 a0001c0001t0003g0056 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+638_360+657del others(20): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879206 | |||||||
| chr12:85879207 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0003g0055 |
2 | HG00639.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.360+638G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879207 | |||||||
| chr12:85879216 | A | AT | 27 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(24): Show |
55 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.360+649dupT | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | ||||||
| chr12:85879216 | A | ATTTTATG others(139): Show |
1 | a0001c0001t0002g0081 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.360+649_360+650ins others(146): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | ||||||
| chr12:85879216 | A | ATTTTATG others(88): Show |
1 | a0001c0001t0001g0128 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.360+649_360+650ins others(95): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | ||||||
| chr12:85879216 | A | ATTTTATG others(181): Show |
1 | a0001c0001t0001g0037 | 2 | HG00738.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.360+649_360+650ins others(188): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | ||||||
| chr12:85879216 | A | ATTTTATG others(150): Show |
13 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0045 others(10): Show |
22 | HG01175.hp2 HG01928.hp1 HG01978.hp1 others(19): Show |
intron_variant | MODIFIER | c.360+649_360+650ins others(157): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | ||||||
| chr12:85879216 | A | ATTTTATG others(150): Show |
1 | a0001c0001t0001g0113 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.360+649_360+650ins others(157): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | ||||||
| chr12:85879216 | A | ATTTTATG others(119): Show |
38 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(35): Show |
128 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.360+649_360+650ins others(126): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | ||||||
| chr12:85879216 | A | ATTTTATG others(88): Show |
11 | a0001c0001t0001g0044 a0001c0001t0001g0103 a0001c0001t0001g0104 others(8): Show |
21 | HG01175.hp1 HG01928.hp2 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.360+649_360+650ins others(95): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | ||||||
| chr12:85879216 | A | ATTTTATG others(120): Show |
1 | a0001c0001t0002g0101 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.360+649_360+650ins others(127): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | ||||||
| chr12:85879216 | A | ATTTTATG others(130): Show |
2 | a0001c0001t0001g0009 a0001c0001t0001g0069 |
8 | HG00140.hp2 HG01123.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.360+649_360+650ins others(137): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | ||||||
| chr12:85879216 | A | ATTTTATG others(99): Show |
10 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(7): Show |
59 | HG00099.hp1 HG00408.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.360+649_360+650ins others(106): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | ||||||
| chr12:85879216 | A | ATTTTATG others(131): Show |
1 | a0001c0001t0001g0019 | 3 | HG01069.hp1 HG01071.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.360+649_360+650ins others(138): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | ||||||
| chr12:85879216 | A | ATTTTTAT others(150): Show |
4 | a0001c0001t0001g0025 a0001c0001t0001g0046 a0001c0001t0001g0126 others(1): Show |
7 | HG02257.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.360+649_360+650ins others(157): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | ||||||
| chr12:85879216 | A | ATTTTTAT others(120): Show |
1 | a0001c0001t0001g0160 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.360+649_360+650ins others(127): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | ||||||
| chr12:85879216 | A | ATTTTTAT others(182): Show |
1 | a0001c0001t0001g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.360+649_360+650ins others(189): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879216 | ||||||
| chr12:85879217 | T | TTTTATGT others(121): Show |
2 | a0001c0001t0001g0050 a0001c0001t0001g0161 |
3 | HG02109.hp2 HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.360+649_360+650ins others(128): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879217 | ||||||
| chr12:85879219 | A | T | 62 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(59): Show |
136 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.360+650A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879219 | |||||||
| chr12:85879223 | A | G | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(56): Show |
133 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.360+654A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879223 | |||||||
| chr12:85879237 | T | C | 61 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(58): Show |
135 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.360+668T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879237 | |||||||
| chr12:85879238 | G | A | 3 | a0001c0001t0001g0150 a0001c0001t0003g0018 a0001c0001t0003g0056 |
5 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+669G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879238 | |||||||
| chr12:85879238 | G | T | 1 | a0001c0001t0003g0055 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.360+669G>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879238 | |||||||
| chr12:85879240 | A | T | 1 | a0001c0001t0003g0055 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.360+671A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879240 | |||||||
| chr12:85879241 | A | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0145 |
2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.360+672A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879241 | |||||||
| chr12:85879242 | A | ATATATTT others(4): Show |
1 | a0001c0001t0001g0128 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.360+673_360+674ins others(11): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879242 | |||||||
| chr12:85879242 | A | T | 1 | a0001c0001t0003g0055 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.360+673A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879242 | |||||||
| chr12:85879243 | A | G | 1 | a0001c0001t0003g0055 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.360+674A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879243 | |||||||
| chr12:85879243 | A | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0145 |
2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.360+674A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879243 | |||||||
| chr12:85879245 | A | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0145 |
2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.360+676A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879245 | |||||||
| chr12:85879246 | TATTATAC others(3): Show |
T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0150 |
2 | HG03471.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.360+681_360+690del others(10): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879246 | ||||||
| chr12:85879247 | A | AT | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0025 others(12): Show |
20 | HG01081.hp1 HG01175.hp2 HG01978.hp1 others(17): Show |
intron_variant | MODIFIER | c.360+680dupT | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879247 | ||||||
| chr12:85879247 | A | ATTT | 6 | a0001c0001t0001g0008 a0001c0001t0001g0054 a0001c0001t0001g0137 others(3): Show |
13 | HG00639.hp1 HG01884.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.360+680_360+681ins others(3): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879247 | ||||||
| chr12:85879248 | T | TTTA | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(88): Show |
261 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.360+680_360+681ins others(3): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879248 | ||||||
| chr12:85879248 | TTATACAT others(2): Show |
T | 2 | a0001c0001t0003g0018 a0001c0001t0003g0056 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+681_360+689del others(9): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879248 | ||||||
| chr12:85879249 | T | A | 1 | a0001c0001t0003g0055 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.360+680T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879249 | |||||||
| chr12:85879249 | T | TTTATGTA others(46): Show |
1 | a0001c0001t0001g0036 | 2 | HG02135.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.360+680_360+681ins others(53): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879249 | |||||||
| chr12:85879249 | T | TTTTATAT others(16): Show |
1 | a0001c0001t0001g0152 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.360+680_360+681ins others(23): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879249 | |||||||
| chr12:85879250 | A | T | 48 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(45): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.360+681A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879250 | |||||||
| chr12:85879251 | T | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0152 a0001c0001t0003g0055 |
4 | HG00639.hp2 HG02135.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+682T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879251 | |||||||
| chr12:85879253 | C | T | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(159): Show |
412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
intron_variant | MODIFIER | c.360+684C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879253 | |||||||
| chr12:85879254 | A | G | 49 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.360+685A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879254 | |||||||
| chr12:85879255 | T | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0145 |
2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.360+686T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879255 | |||||||
| chr12:85879256 | A | AT | 41 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(38): Show |
85 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.360+687_360+688ins others(1): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | |||||||
| chr12:85879256 | A | ATATTTTA others(161): Show |
1 | a0001c0001t0001g0012 | 2 | HG02602.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.360+687_360+688ins others(168): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | |||||||
| chr12:85879256 | A | ATATTTTA others(307): Show |
1 | a0001c0001t0001g0047 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.360+687_360+688ins others(314): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | |||||||
| chr12:85879256 | A | ATATTTTA others(205): Show |
1 | a0001c0001t0001g0048 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.360+687_360+688ins others(212): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | |||||||
| chr12:85879256 | A | ATATTTTA others(205): Show |
1 | a0001c0001t0001g0048 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.360+687_360+688ins others(212): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | |||||||
| chr12:85879256 | A | ATATTTTA others(100): Show |
3 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0035 |
8 | HG02280.hp1 HG02647.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.360+687_360+688ins others(107): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | |||||||
| chr12:85879256 | A | ATATTTTA others(183): Show |
1 | a0001c0001t0001g0089 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.360+687_360+688ins others(190): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | |||||||
| chr12:85879256 | A | ATATTTTA others(163): Show |
4 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0043 others(1): Show |
6 | HG00323.hp2 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+687_360+688ins others(170): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | |||||||
| chr12:85879256 | A | ATATTTTA others(229): Show |
1 | a0001c0001t0001g0008 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.360+687_360+688ins others(236): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | |||||||
| chr12:85879256 | A | ATATTTTA others(163): Show |
1 | a0001c0001t0001g0072 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.360+687_360+688ins others(170): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | |||||||
| chr12:85879256 | A | ATATTTTA others(103): Show |
1 | a0001c0001t0001g0140 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.360+687_360+688ins others(110): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | |||||||
| chr12:85879256 | A | ATATTTTA others(100): Show |
1 | a0001c0001t0002g0060 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.360+687_360+688ins others(107): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | |||||||
| chr12:85879256 | A | ATATTTTA others(101): Show |
3 | a0001c0001t0002g0003 a0001c0001t0002g0086 a0001c0001t0002g0087 |
3 | NA18940.hp1 NA19081.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.360+687_360+688ins others(108): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | |||||||
| chr12:85879256 | A | ATATTTTA others(100): Show |
1 | a0001c0001t0002g0003 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.360+687_360+688ins others(107): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | |||||||
| chr12:85879256 | A | ATATTTTA others(132): Show |
4 | a0001c0001t0002g0003 a0001c0001t0002g0085 a0001c0001t0002g0088 others(1): Show |
13 | HG02015.hp1 HG02135.hp2 NA18942.hp1 others(10): Show |
intron_variant | MODIFIER | c.360+687_360+688ins others(139): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | |||||||
| chr12:85879256 | A | ATATTTTA others(135): Show |
1 | a0001c0001t0001g0146 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.360+687_360+688ins others(142): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | |||||||
| chr12:85879256 | A | ATATTTTA others(166): Show |
2 | a0001c0001t0001g0027 a0001c0001t0001g0155 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.360+687_360+688ins others(173): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | |||||||
| chr12:85879256 | A | ATATTTTA others(197): Show |
3 | a0001c0001t0001g0027 a0001c0001t0001g0144 a0001c0001t0001g0147 |
4 | HG02559.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+687_360+688ins others(204): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | |||||||
| chr12:85879256 | A | ATATTTTA others(36): Show |
2 | a0001c0001t0001g0002 a0001c0001t0002g0081 |
2 | HG03704.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.360+687_360+688ins others(43): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | |||||||
| chr12:85879256 | A | ATTTTATG others(67): Show |
1 | a0001c0001t0001g0137 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.360+687_360+688ins others(74): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | |||||||
| chr12:85879256 | A | ATTTTATG others(101): Show |
1 | a0001c0001t0001g0151 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.360+687_360+688ins others(108): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | |||||||
| chr12:85879256 | A | ATTTTATG others(112): Show |
1 | a0001c0001t0001g0008 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.360+687_360+688ins others(119): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | |||||||
| chr12:85879256 | A | ATTTTATG others(132): Show |
4 | a0001c0001t0001g0008 a0001c0001t0001g0054 a0001c0001t0001g0148 others(1): Show |
10 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.360+687_360+688ins others(139): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | |||||||
| chr12:85879256 | A | ATTTTATG others(3): Show |
88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(85): Show |
257 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.360+687_360+688ins others(10): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879256 | |||||||
| chr12:85879257 | A | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0152 a0001c0001t0003g0055 |
4 | HG00639.hp2 HG02135.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+688A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879257 | |||||||
| chr12:85879264 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0152 |
3 | HG02135.hp1 HG02572.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.360+695G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879264 | |||||||
| chr12:85879264 | G | GTACGTAA others(2): Show |
13 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0051 others(10): Show |
37 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.360+697_360+698ins others(9): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879264 | ||||||
| chr12:85879264 | G | GTACGTAA others(67): Show |
1 | a0001c0001t0001g0153 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.360+697_360+698ins others(74): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879264 | ||||||
| chr12:85879264 | G | GTACGTAA others(68): Show |
4 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0141 others(1): Show |
15 | HG00099.hp2 HG01099.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.360+697_360+698ins others(75): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879264 | ||||||
| chr12:85879264 | G | GTACGTAA others(80): Show |
3 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0143 |
7 | HG01106.hp1 HG01192.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.360+697_360+698ins others(87): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879264 | ||||||
| chr12:85879264 | G | GTACGTAA others(66): Show |
1 | a0001c0001t0002g0084 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.360+697_360+698ins others(73): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879264 | ||||||
| chr12:85879266 | A | ACGTAAAA others(136): Show |
1 | a0001c0001t0002g0058 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.360+697_360+698ins others(143): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879266 | |||||||
| chr12:85879267 | T | A | 1 | a0001c0001t0002g0058 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.360+698T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879267 | |||||||
| chr12:85879268 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.360+699A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879268 | |||||||
| chr12:85879269 | T | TAAAA | 2 | a0001c0001t0001g0050 a0001c0001t0001g0161 |
3 | HG02109.hp2 HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.360+700_360+701ins others(4): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879269 | |||||||
| chr12:85879271 | T | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0161 |
3 | HG02109.hp2 HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.360+702T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879271 | |||||||
| chr12:85879271 | T | TA | 6 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0141 others(3): Show |
17 | HG00099.hp2 HG01099.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.360+702_360+703ins others(1): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879271 | |||||||
| chr12:85879275 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0132 others(6): Show |
20 | HG00099.hp2 HG01099.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.360+706G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879275 | |||||||
| chr12:85879275 | G | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0161 |
3 | HG02109.hp2 HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.360+706G>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879275 | |||||||
| chr12:85879278 | T | C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0115 a0001c0001t0001g0152 |
4 | HG02135.hp1 HG02572.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+709T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879278 | |||||||
| chr12:85879279 | A | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0115 a0001c0001t0001g0152 |
4 | HG02135.hp1 HG02572.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+710A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879279 | |||||||
| chr12:85879280 | T | TTTTATGT others(82): Show |
1 | a0001c0001t0001g0159 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.360+711_360+712ins others(89): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879280 | |||||||
| chr12:85879280 | TACC | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0161 |
3 | HG02109.hp2 HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.360+713_360+715del others(3): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879280 | ||||||
| chr12:85879281 | A | ATTTT | 3 | a0001c0001t0001g0132 a0001c0001t0001g0138 a0001c0001t0001g0160 |
3 | HG02071.hp2 HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.360+712_360+713ins others(4): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879281 | |||||||
| chr12:85879281 | A | T | 22 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(19): Show |
61 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.360+712A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879281 | |||||||
| chr12:85879282 | C | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(140): Show |
353 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(350): Show |
intron_variant | MODIFIER | c.360+713C>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879282 | |||||||
| chr12:85879282 | C | T | 21 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(18): Show |
60 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.360+713C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879282 | |||||||
| chr12:85879283 | C | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(136): Show |
349 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(346): Show |
intron_variant | MODIFIER | c.360+714C>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879283 | |||||||
| chr12:85879283 | C | T | 25 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(22): Show |
64 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.360+714C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879283 | |||||||
| chr12:85879284 | A | ATG | 9 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0028 others(6): Show |
24 | HG00099.hp2 HG01099.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.360+716_360+717ins others(2): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879284 | ||||||
| chr12:85879284 | A | ATGTACGT others(61): Show |
1 | a0001c0001t0001g0154 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.360+716_360+717ins others(68): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879284 | ||||||
| chr12:85879284 | A | ATGTACGT others(122): Show |
1 | a0001c0001t0001g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.360+716_360+717ins others(129): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879284 | ||||||
| chr12:85879284 | A | ATGTACGT others(93): Show |
8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0051 others(5): Show |
32 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.360+716_360+717ins others(100): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879284 | ||||||
| chr12:85879284 | A | ATGTACGT others(91): Show |
1 | a0001c0001t0001g0083 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.360+716_360+717ins others(98): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879284 | ||||||
| chr12:85879284 | A | ATGTACGT others(123): Show |
1 | a0001c0001t0001g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.360+716_360+717ins others(130): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879284 | ||||||
| chr12:85879284 | A | G | 3 | a0001c0001t0001g0132 a0001c0001t0001g0138 a0001c0001t0001g0160 |
3 | HG02071.hp2 HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.360+715A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879284 | |||||||
| chr12:85879295 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0152 |
3 | HG02135.hp1 HG02572.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.360+726G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879295 | |||||||
| chr12:85879295 | G | GTATATAA others(2): Show |
4 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0140 others(1): Show |
8 | HG01106.hp1 HG01192.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.360+731_360+732ins others(9): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879295 | ||||||
| chr12:85879303 | TATGTATA others(13): Show |
T | 1 | a0001c0001t0001g0159 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.360+743_360+762del others(20): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879303 | ||||||
| chr12:85879309 | T | C | 2 | a0001c0001t0001g0115 a0001c0001t0002g0058 |
2 | HG02148.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.360+740T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879309 | |||||||
| chr12:85879310 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0115 |
3 | HG02135.hp1 NA18987.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.360+741A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879310 | |||||||
| chr12:85879312 | A | T | 1 | a0001c0001t0011g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.360+743A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879312 | |||||||
| chr12:85879313 | A | T | 1 | a0001c0001t0011g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.360+744A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879313 | |||||||
| chr12:85879314 | A | T | 1 | a0001c0001t0011g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.360+745A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879314 | |||||||
| chr12:85879315 | ATATATTT others(4): Show |
A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0111 a0001c0001t0001g0137 |
3 | HG03453.hp2 HG03471.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.360+754_360+764del others(11): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879315 | ||||||
| chr12:85879317 | A | G | 2 | a0001c0001t0001g0136 a0001c0001t0011g0163 |
2 | HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.360+748A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879317 | |||||||
| chr12:85879321 | T | A | 1 | a0001c0001t0011g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.360+752T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879321 | |||||||
| chr12:85879323 | A | AT | 2 | a0001c0001t0001g0036 a0001c0001t0001g0152 |
3 | HG02135.hp1 HG02572.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.360+754_360+755ins others(1): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879323 | |||||||
| chr12:85879323 | A | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(155): Show |
408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.360+754A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879323 | |||||||
| chr12:85879325 | T | A | 1 | a0001c0001t0011g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.360+756T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879325 | |||||||
| chr12:85879326 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0152 a0001c0001t0011g0163 |
4 | HG02135.hp1 HG02572.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+757G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879326 | |||||||
| chr12:85879326 | G | GTATATAA others(2): Show |
16 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(13): Show |
51 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.360+762_360+763ins others(9): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879326 | ||||||
| chr12:85879326 | G | GTATATTT others(13): Show |
2 | a0001c0001t0001g0138 a0001c0001t0002g0102 |
2 | HG02074.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.360+773_360+774ins others(20): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879326 | ||||||
| chr12:85879327 | T | C | 1 | a0001c0001t0011g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.360+758T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879327 | |||||||
| chr12:85879331 | T | A | 1 | a0001c0001t0002g0058 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.360+762T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879331 | |||||||
| chr12:85879332 | T | A | 1 | a0001c0001t0002g0058 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.360+763T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879332 | |||||||
| chr12:85879337 | G | GTACGTAA others(78): Show |
1 | a0001c0001t0001g0115 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.360+770_360+771ins others(85): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879337 | ||||||
| chr12:85879337 | G | GTATATAA others(2): Show |
4 | a0001c0001t0001g0082 a0001c0001t0001g0145 a0001c0001t0001g0150 others(1): Show |
4 | HG02572.hp2 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+773_360+774ins others(9): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879337 | ||||||
| chr12:85879338 | T | TATATAAA others(2): Show |
3 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0143 |
7 | HG01106.hp1 HG01192.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.360+773_360+774ins others(9): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879338 | ||||||
| chr12:85879343 | T | A | 6 | a0001c0001t0001g0027 a0001c0001t0001g0144 a0001c0001t0001g0146 others(3): Show |
8 | HG00639.hp2 HG02559.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.360+774T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879343 | |||||||
| chr12:85879344 | T | A | 6 | a0001c0001t0001g0027 a0001c0001t0001g0144 a0001c0001t0001g0146 others(3): Show |
8 | HG00639.hp2 HG02559.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.360+775T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879344 | |||||||
| chr12:85879345 | T | A | 6 | a0001c0001t0001g0027 a0001c0001t0001g0144 a0001c0001t0001g0146 others(3): Show |
8 | HG00639.hp2 HG02559.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.360+776T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879345 | |||||||
| chr12:85879348 | G | A | 6 | a0001c0001t0001g0027 a0001c0001t0001g0144 a0001c0001t0001g0146 others(3): Show |
8 | HG00639.hp2 HG02559.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.360+779G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879348 | |||||||
| chr12:85879349 | TATATAAA others(2): Show |
T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0152 |
3 | HG02135.hp1 HG02572.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.360+785_360+793del others(9): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879349 | ||||||
| chr12:85879351 | T | C | 1 | a0001c0001t0002g0058 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.360+782T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879351 | |||||||
| chr12:85879352 | A | ATT | 6 | a0001c0001t0001g0082 a0001c0001t0001g0089 a0001c0001t0001g0115 others(3): Show |
6 | HG02572.hp2 HG02896.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+784_360+785ins others(2): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879352 | ||||||
| chr12:85879352 | A | T | 6 | a0001c0001t0001g0027 a0001c0001t0001g0144 a0001c0001t0001g0146 others(3): Show |
8 | HG00639.hp2 HG02559.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.360+783A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879352 | |||||||
| chr12:85879354 | A | T | 12 | a0001c0001t0001g0027 a0001c0001t0001g0082 a0001c0001t0001g0089 others(9): Show |
14 | HG00639.hp2 HG02559.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.360+785A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879354 | |||||||
| chr12:85879356 | A | T | 12 | a0001c0001t0001g0027 a0001c0001t0001g0082 a0001c0001t0001g0089 others(9): Show |
14 | HG00639.hp2 HG02559.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.360+787A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879356 | |||||||
| chr12:85879357 | A | ATATATTT others(4): Show |
3 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0143 |
7 | HG01106.hp1 HG01192.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.360+788_360+789ins others(11): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879357 | |||||||
| chr12:85879357 | A | G | 12 | a0001c0001t0001g0027 a0001c0001t0001g0082 a0001c0001t0001g0089 others(9): Show |
14 | HG00639.hp2 HG02559.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.360+788A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879357 | |||||||
| chr12:85879358 | C | CATATTTT others(4): Show |
6 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0054 others(3): Show |
15 | HG00639.hp1 HG00738.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.360+794_360+804dup others(11): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879358 | ||||||
| chr12:85879358 | C | T | 18 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0028 others(15): Show |
26 | HG00639.hp2 HG00741.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.360+789C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879358 | |||||||
| chr12:85879374 | A | T | 2 | a0001c0001t0003g0018 a0001c0001t0003g0056 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+805A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879374 | |||||||
| chr12:85879375 | A | T | 2 | a0001c0001t0003g0018 a0001c0001t0003g0056 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+806A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879375 | |||||||
| chr12:85879376 | A | T | 2 | a0001c0001t0003g0018 a0001c0001t0003g0056 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+807A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879376 | |||||||
| chr12:85879378 | T | C | 4 | a0001c0001t0001g0082 a0001c0001t0001g0145 a0001c0001t0001g0150 others(1): Show |
4 | HG02572.hp2 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+809T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879378 | |||||||
| chr12:85879379 | A | G | 2 | a0001c0001t0003g0018 a0001c0001t0003g0056 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+810A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879379 | |||||||
| chr12:85879381 | A | T | 1 | a0001c0001t0001g0128 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.360+812A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879381 | |||||||
| chr12:85879381 | AT | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(154): Show |
406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.360+817delT | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879381 | ||||||
| chr12:85879382 | T | A | 1 | a0001c0001t0001g0128 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.360+813T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879382 | |||||||
| chr12:85879382 | T | TTTTATGT others(3): Show |
5 | a0001c0001t0001g0027 a0001c0001t0001g0137 a0001c0001t0001g0138 others(2): Show |
7 | HG02559.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.360+816_360+817ins others(10): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879382 | ||||||
| chr12:85879384 | T | A | 2 | a0001c0001t0003g0018 a0001c0001t0003g0056 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+815T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879384 | |||||||
| chr12:85879386 | T | A | 2 | a0001c0001t0003g0018 a0001c0001t0003g0056 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+817T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879386 | |||||||
| chr12:85879386 | TA | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0089 a0001c0001t0001g0115 |
4 | HG02135.hp1 HG02896.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+818delA | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879386 | |||||||
| chr12:85879388 | T | A | 2 | a0001c0001t0003g0018 a0001c0001t0003g0056 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+819T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879388 | |||||||
| chr12:85879389 | G | A | 2 | a0001c0001t0003g0018 a0001c0001t0003g0056 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+820G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879389 | |||||||
| chr12:85879406 | A | T | 1 | a0001c0001t0011g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.360+837A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879406 | |||||||
| chr12:85879407 | A | T | 1 | a0001c0001t0011g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.360+838A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879407 | |||||||
| chr12:85879408 | A | T | 1 | a0001c0001t0011g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.360+839A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879408 | |||||||
| chr12:85879409 | ATATATTT others(5): Show |
A | 2 | a0001c0001t0003g0018 a0001c0001t0003g0056 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+849_360+860del others(12): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879409 | ||||||
| chr12:85879410 | T | C | 3 | a0001c0001t0001g0027 a0001c0001t0001g0144 a0001c0001t0001g0147 |
5 | HG02559.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+841T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879410 | |||||||
| chr12:85879411 | A | G | 1 | a0001c0001t0011g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.360+842A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879411 | |||||||
| chr12:85879413 | AT | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.360+849delT | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879413 | ||||||
| chr12:85879414 | T | TTTTATGT others(14): Show |
1 | a0001c0001t0001g0132 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.360+848_360+849ins others(21): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879414 | ||||||
| chr12:85879414 | T | TTTTATGT others(25): Show |
2 | a0001c0001t0001g0037 a0001c0001t0001g0047 |
4 | HG00738.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+848_360+849ins others(32): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879414 | ||||||
| chr12:85879414 | T | TTTTATGT others(87): Show |
1 | a0001c0001t0001g0069 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.360+848_360+849ins others(94): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879414 | ||||||
| chr12:85879414 | T | TTTTATGT others(118): Show |
2 | a0001c0001t0001g0100 a0001c0001t0008g0120 |
2 | HG02451.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.360+848_360+849ins others(125): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879414 | ||||||
| chr12:85879418 | TA | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0089 a0001c0001t0001g0115 |
4 | HG02135.hp1 HG02896.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+850delA | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879418 | |||||||
| chr12:85879419 | A | T | 3 | a0001c0001t0001g0069 a0001c0001t0001g0100 a0001c0001t0008g0120 |
3 | HG02451.hp2 HG03688.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.360+850A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879419 | |||||||
| chr12:85879429 | T | A | 1 | a0001c0001t0001g0047 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.360+860T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879429 | |||||||
| chr12:85879436 | A | ATT | 4 | a0001c0001t0001g0048 a0001c0001t0001g0119 a0001c0001t0001g0133 others(1): Show |
5 | HG02109.hp1 HG02132.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+868_360+869ins others(2): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879436 | ||||||
| chr12:85879438 | A | T | 4 | a0001c0001t0001g0048 a0001c0001t0001g0119 a0001c0001t0001g0133 others(1): Show |
5 | HG02109.hp1 HG02132.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+869A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879438 | |||||||
| chr12:85879440 | A | T | 4 | a0001c0001t0001g0048 a0001c0001t0001g0119 a0001c0001t0001g0133 others(1): Show |
5 | HG02109.hp1 HG02132.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+871A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879440 | |||||||
| chr12:85879441 | A | G | 4 | a0001c0001t0001g0048 a0001c0001t0001g0119 a0001c0001t0001g0133 others(1): Show |
5 | HG02109.hp1 HG02132.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+872A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879441 | |||||||
| chr12:85879450 | A | T | 9 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0069 others(6): Show |
11 | HG00738.hp2 HG02135.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.360+881A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879450 | |||||||
| chr12:85879461 | A | ATGTATAT others(44): Show |
1 | a0001c0001t0001g0136 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.360+899_360+900ins others(51): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879461 | ||||||
| chr12:85879463 | G | GTATATAA others(2): Show |
19 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0026 others(16): Show |
49 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.360+899_360+900ins others(9): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879463 | ||||||
| chr12:85879463 | G | GTATATAA others(33): Show |
1 | a0001c0001t0001g0157 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.360+899_360+900ins others(40): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879463 | ||||||
| chr12:85879463 | G | GTATATAA others(95): Show |
2 | a0001c0001t0004g0049 a0001c0001t0004g0135 |
3 | HG02630.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.360+899_360+900ins others(102): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879463 | ||||||
| chr12:85879463 | G | GTATATTT others(13): Show |
2 | a0001c0001t0001g0050 a0001c0001t0001g0161 |
3 | HG02109.hp2 HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.360+910_360+911ins others(20): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879463 | ||||||
| chr12:85879467 | ATT | A | 8 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0069 others(5): Show |
10 | HG00639.hp2 HG00738.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.360+901_360+902del others(2): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879467 | ||||||
| chr12:85879471 | T | A | 8 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0069 others(5): Show |
10 | HG00639.hp2 HG00738.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.360+902T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879471 | |||||||
| chr12:85879472 | A | T | 4 | a0001c0001t0003g0018 a0001c0001t0003g0056 a0001c0001t0004g0049 others(1): Show |
7 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.360+903A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879472 | |||||||
| chr12:85879473 | T | A | 8 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0069 others(5): Show |
10 | HG00639.hp2 HG00738.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.360+904T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879473 | |||||||
| chr12:85879474 | G | A | 8 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0069 others(5): Show |
10 | HG00639.hp2 HG00738.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.360+905G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879474 | |||||||
| chr12:85879474 | G | GTATATAA others(2): Show |
19 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0029 others(16): Show |
39 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.360+910_360+911ins others(9): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879474 | ||||||
| chr12:85879474 | G | GTATATAA others(33): Show |
1 | a0001c0001t0001g0047 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.360+910_360+911ins others(40): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879474 | ||||||
| chr12:85879474 | G | GTATATAA others(95): Show |
1 | a0001c0001t0001g0119 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.360+910_360+911ins others(102): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879474 | ||||||
| chr12:85879474 | G | GTATATTT others(117): Show |
4 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0062 others(1): Show |
8 | HG01361.hp1 HG02293.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.360+913_360+914ins others(124): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879474 | ||||||
| chr12:85879483 | A | ATGTATAT others(13): Show |
2 | a0001c0001t0004g0049 a0001c0001t0004g0135 |
3 | HG02630.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.360+921_360+922ins others(20): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879483 | ||||||
| chr12:85879483 | A | ATGTATAT others(106): Show |
4 | a0001c0001t0001g0066 a0001c0001t0001g0080 a0001c0001t0001g0091 others(1): Show |
4 | HG02735.hp1 HG03471.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+921_360+922ins others(113): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879483 | ||||||
| chr12:85879483 | A | ATGTATAT others(168): Show |
1 | a0001c0001t0001g0079 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.360+921_360+922ins others(175): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879483 | ||||||
| chr12:85879483 | A | ATGTATAT others(24): Show |
2 | a0001c0001t0001g0099 a0001c0001t0002g0107 |
2 | NA18612.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.360+995_360+1025du others(32): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879483 | ||||||
| chr12:85879483 | A | ATGTATAT others(116): Show |
2 | a0001c0001t0001g0038 a0001c0001t0001g0103 |
3 | HG02622.hp1 HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.360+976_360+977ins others(123): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879483 | ||||||
| chr12:85879483 | A | ATGTATAT others(86): Show |
5 | a0001c0001t0001g0013 a0001c0001t0001g0068 a0001c0001t0001g0076 others(2): Show |
9 | HG00408.hp1 HG01175.hp1 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.360+933_360+1025du others(94): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879483 | ||||||
| chr12:85879483 | A | ATGTATAT others(117): Show |
58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(55): Show |
223 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.360+1025_360+1026i others(126): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879483 | ||||||
| chr12:85879483 | A | ATGTATAT others(148): Show |
14 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0034 others(11): Show |
25 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.360+1025_360+1026i others(157): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879483 | ||||||
| chr12:85879483 | A | ATGTATAT others(179): Show |
1 | a0001c0001t0001g0025 | 3 | HG02257.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.360+1025_360+1026i others(188): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879483 | ||||||
| chr12:85879483 | A | ATGTATAT others(139): Show |
1 | a0001c0001t0001g0090 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.360+932_360+933ins others(146): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879483 | ||||||
| chr12:85879483 | A | T | 18 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0036 others(15): Show |
25 | HG00738.hp2 HG01361.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.360+914A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879483 | |||||||
| chr12:85879493 | T | TATGTATA others(117): Show |
1 | a0001c0001t0001g0092 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.360+1025_360+1026i others(126): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879493 | ||||||
| chr12:85879514 | T | A | 18 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0026 others(15): Show |
45 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.360+945T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879514 | |||||||
| chr12:85879516 | G | GTATATTT others(13): Show |
1 | a0001c0001t0003g0055 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.360+956_360+975dup others(20): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879516 | ||||||
| chr12:85879518 | A | ATATTTTA others(115): Show |
1 | a0001c0001t0002g0060 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.360+1025_360+1026i others(124): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879518 | ||||||
| chr12:85879533 | A | T | 1 | a0001c0001t0001g0146 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.360+964A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879533 | |||||||
| chr12:85879535 | A | T | 1 | a0001c0001t0001g0146 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.360+966A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879535 | |||||||
| chr12:85879536 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.360+967A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879536 | |||||||
| chr12:85879545 | T | A | 4 | a0001c0001t0001g0142 a0001c0001t0001g0146 a0001c0001t0001g0152 others(1): Show |
4 | HG00639.hp2 HG02257.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+976T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879545 | |||||||
| chr12:85879545 | T | TTGTATAT others(159): Show |
2 | a0001c0001t0001g0016 a0001c0001t0001g0098 |
5 | HG02027.hp1 HG03130.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+1025_360+1026i others(168): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879545 | ||||||
| chr12:85879550 | T | C | 1 | a0001c0001t0001g0052 | 2 | HG00733.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.360+981T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879550 | |||||||
| chr12:85879562 | A | ATAAAATA others(118): Show |
1 | a0001c0001t0002g0087 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.360+1025_360+1026i others(127): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879562 | ||||||
| chr12:85879569 | ATATTTTT others(1): Show |
A | 2 | a0001c0001t0003g0018 a0001c0001t0003g0056 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+1001_360+1008d others(10): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879569 | |||||||
| chr12:85879571 | A | ATTTTTTG others(150): Show |
1 | a0001c0001t0001g0128 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.360+1017_360+1018i others(159): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879571 | ||||||
| chr12:85879576 | T | A | 1 | a0001c0001t0001g0152 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.360+1007T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879576 | |||||||
| chr12:85879576 | T | TGTATATT others(3): Show |
1 | a0001c0001t0001g0158 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.360+1007_360+1008i others(12): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879576 | |||||||
| chr12:85879576 | TTGTATAT others(4): Show |
T | 1 | a0001c0001t0001g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.360+1026_360+1036d others(13): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879576 | ||||||
| chr12:85879578 | G | A | 2 | a0001c0001t0003g0018 a0001c0001t0003g0056 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+1009G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879578 | |||||||
| chr12:85879587 | A | ATGTATAT others(13): Show |
27 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0026 others(24): Show |
58 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.360+1025_360+1026i others(22): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879587 | ||||||
| chr12:85879587 | A | ATGTATAT others(44): Show |
5 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0136 others(2): Show |
6 | HG00642.hp2 HG00735.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.360+1025_360+1026i others(53): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879587 | ||||||
| chr12:85879587 | A | ATGTATAT others(75): Show |
7 | a0001c0001t0001g0024 a0001c0001t0001g0039 a0001c0001t0001g0075 others(4): Show |
10 | HG02148.hp2 NA18955.hp2 NA18990.hp1 others(7): Show |
intron_variant | MODIFIER | c.360+1025_360+1026i others(84): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879587 | ||||||
| chr12:85879587 | A | ATGTATAT others(106): Show |
2 | a0001c0001t0001g0053 a0001c0001t0001g0125 |
2 | HG00280.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.360+1025_360+1026i others(115): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879587 | ||||||
| chr12:85879587 | A | ATGTATAT others(137): Show |
1 | a0001c0001t0001g0161 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.360+1025_360+1026i others(146): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879587 | ||||||
| chr12:85879587 | A | ATGTATAT others(148): Show |
1 | a0001c0001t0001g0035 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.360+1025_360+1026i others(157): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879587 | ||||||
| chr12:85879587 | A | ATGTATAT others(86): Show |
1 | a0001c0001t0011g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.360+1025_360+1026i others(95): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879587 | ||||||
| chr12:85879587 | A | T | 3 | a0001c0001t0001g0158 a0001c0001t0003g0018 a0001c0001t0003g0056 |
5 | HG00741.hp2 HG01261.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.360+1018A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879587 | |||||||
| chr12:85879589 | G | GTATATAA others(2): Show |
11 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0027 others(8): Show |
31 | HG00408.hp2 HG00639.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.360+1025_360+1026i others(11): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879589 | ||||||
| chr12:85879589 | G | GTATATAA others(95): Show |
1 | a0001c0001t0001g0093 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.360+1025_360+1026i others(104): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879589 | ||||||
| chr12:85879598 | A | T | 12 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0027 others(9): Show |
32 | HG00408.hp2 HG00639.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.360+1029A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879598 | |||||||
| chr12:85879606 | A | T | 11 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0027 others(8): Show |
31 | HG00408.hp2 HG00639.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.360+1037A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879606 | |||||||
| chr12:85879607 | A | T | 11 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0027 others(8): Show |
31 | HG00408.hp2 HG00639.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.360+1038A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879607 | |||||||
| chr12:85879608 | A | T | 11 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0027 others(8): Show |
31 | HG00408.hp2 HG00639.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.360+1039A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879608 | |||||||
| chr12:85879611 | A | G | 11 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0027 others(8): Show |
31 | HG00408.hp2 HG00639.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.360+1042A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879611 | |||||||
| chr12:85879611 | ATATTTTT others(1): Show |
A | 2 | a0001c0001t0003g0018 a0001c0001t0003g0056 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+1043_360+1050d others(10): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879611 | |||||||
| chr12:85879615 | T | A | 11 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0027 others(8): Show |
31 | HG00408.hp2 HG00639.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.360+1046T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879615 | |||||||
| chr12:85879617 | T | A | 11 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0027 others(8): Show |
31 | HG00408.hp2 HG00639.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.360+1048T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879617 | |||||||
| chr12:85879618 | T | A | 12 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0027 others(9): Show |
32 | HG00408.hp2 HG00639.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.360+1049T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879618 | |||||||
| chr12:85879618 | TTGTATAT others(4): Show |
T | 1 | a0001c0001t0001g0151 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.360+1068_360+1078d others(13): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879618 | ||||||
| chr12:85879619 | T | A | 11 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0027 others(8): Show |
31 | HG00408.hp2 HG00639.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.360+1050T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879619 | |||||||
| chr12:85879620 | G | A | 13 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0027 others(10): Show |
35 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.360+1051G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879620 | |||||||
| chr12:85879629 | A | ATGTATAT others(13): Show |
23 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0026 others(20): Show |
53 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.360+1067_360+1068i others(22): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879629 | ||||||
| chr12:85879629 | A | ATGTATAT others(75): Show |
1 | a0001c0001t0001g0152 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.360+1067_360+1068i others(84): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879629 | ||||||
| chr12:85879629 | A | ATGTATAT others(128): Show |
1 | a0001c0001t0001g0040 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.360+1067_360+1068i others(137): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879629 | ||||||
| chr12:85879629 | A | ATGTATAT others(24): Show |
6 | a0001c0001t0001g0017 a0001c0001t0001g0032 a0001c0001t0001g0040 others(3): Show |
9 | HG01175.hp2 HG01978.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.360+1164_360+1194d others(33): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879629 | ||||||
| chr12:85879629 | A | T | 13 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0027 others(10): Show |
35 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.360+1060A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879629 | |||||||
| chr12:85879643 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.360+1074T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879643 | |||||||
| chr12:85879651 | A | ATATATTT others(4): Show |
1 | a0001c0001t0002g0058 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.360+1091_360+1101d others(13): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879651 | ||||||
| chr12:85879656 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.360+1087T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879656 | |||||||
| chr12:85879660 | T | TTGTATAT others(4): Show |
11 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0053 others(8): Show |
14 | HG00438.hp2 HG00738.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.360+1099_360+1109d others(13): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879660 | ||||||
| chr12:85879660 | T | TTGTATAT others(35): Show |
8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
25 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(22): Show |
intron_variant | MODIFIER | c.360+1099_360+1140d others(44): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879660 | ||||||
| chr12:85879687 | T | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0161 |
2 | HG00280.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.360+1118T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879687 | |||||||
| chr12:85879687 | T | TTTTTTGT others(24): Show |
1 | a0001c0001t0001g0053 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.360+1148_360+1149i others(33): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879687 | ||||||
| chr12:85879691 | T | TTGTATAT others(4): Show |
27 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(24): Show |
53 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.360+1130_360+1140d others(13): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879691 | ||||||
| chr12:85879718 | T | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(8): Show |
28 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(25): Show |
intron_variant | MODIFIER | c.360+1149T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879718 | |||||||
| chr12:85879718 | T | TTTTTTGT others(24): Show |
13 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(10): Show |
29 | HG00423.hp2 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.360+1179_360+1180i others(33): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879718 | ||||||
| chr12:85879718 | T | TTTTTTGT others(97): Show |
1 | a0001c0001t0001g0050 | 2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.360+1171_360+1172i others(106): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879718 | ||||||
| chr12:85879733 | A | ATGTATAT others(23): Show |
2 | a0001c0001t0001g0048 a0001c0001t0001g0133 |
3 | HG02109.hp1 HG02723.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.360+1215_360+1244d others(32): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879733 | ||||||
| chr12:85879749 | T | C | 14 | a0001c0001t0001g0008 a0001c0001t0001g0027 a0001c0001t0001g0054 others(11): Show |
24 | HG00639.hp1 HG01261.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.360+1180T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879749 | |||||||
| chr12:85879756 | T | TATATTTT others(25): Show |
1 | a0001c0001t0001g0158 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.360+1194_360+1195i others(34): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879756 | ||||||
| chr12:85879759 | A | C | 2 | a0001c0001t0003g0018 a0001c0001t0003g0056 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+1190A>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879759 | |||||||
| chr12:85879763 | T | TA | 4 | a0001c0001t0001g0024 a0001c0001t0001g0094 a0001c0001t0001g0132 others(1): Show |
6 | HG02486.hp2 HG03139.hp1 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+1194_360+1195i others(3): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879763 | |||||||
| chr12:85879763 | T | TATGTATA others(25): Show |
1 | a0001c0001t0003g0055 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.360+1194_360+1195i others(34): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879763 | |||||||
| chr12:85879767 | A | T | 2 | a0001c0001t0003g0018 a0001c0001t0003g0056 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+1198A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879767 | |||||||
| chr12:85879780 | TTTTTGTA others(2): Show |
T | 2 | a0001c0001t0003g0018 a0001c0001t0003g0056 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+1216_360+1224d others(11): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879780 | ||||||
| chr12:85879789 | A | C | 1 | a0001c0001t0003g0055 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.360+1220A>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879789 | |||||||
| chr12:85879793 | T | A | 2 | a0001c0001t0003g0018 a0001c0001t0003g0056 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+1224T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879793 | |||||||
| chr12:85879797 | A | T | 1 | a0001c0001t0003g0055 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.360+1228A>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879797 | |||||||
| chr12:85879799 | ATAAAATA others(3): Show |
A | 2 | a0001c0001t0003g0018 a0001c0001t0003g0056 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+1232_360+1241d others(12): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879799 | ||||||
| chr12:85879813 | TA | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0094 a0001c0001t0001g0132 others(1): Show |
6 | HG02486.hp2 HG03139.hp1 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+1245delA | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879813 | |||||||
| chr12:85879824 | TA | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0094 a0001c0001t0001g0132 others(1): Show |
6 | HG02486.hp2 HG03139.hp1 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+1256delA | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879824 | |||||||
| chr12:85879841 | T | TTTTTATG others(4): Show |
2 | a0001c0001t0001g0024 a0001c0001t0001g0094 |
4 | NA18990.hp1 NA19000.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+1276_360+1286d others(13): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879841 | ||||||
| chr12:85879841 | T | TTTTTTGT others(34): Show |
2 | a0001c0001t0001g0132 a0001c0001t0001g0134 |
2 | HG02486.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.360+1276_360+1277i others(43): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85879841 | ||||||
| chr12:85879907 | A | G | 1 | a0001c0001t0001g0097 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.360+1338A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85879907 | |||||||
| chr12:85880000 | C | T | 2 | a0001c0001t0003g0018 a0001c0001t0003g0056 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+1431C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880000 | |||||||
| chr12:85880045 | C | T | 3 | a0001c0001t0003g0018 a0001c0001t0003g0055 a0001c0001t0003g0056 |
5 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.360+1476C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880045 | |||||||
| chr12:85880117 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.360+1548T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880117 | |||||||
| chr12:85880364 | T | C | 3 | a0001c0001t0003g0018 a0001c0001t0003g0055 a0001c0001t0003g0056 |
5 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.360+1795T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880364 | |||||||
| chr12:85880365 | C | T | 6 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0132 others(3): Show |
8 | HG02109.hp1 HG02486.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.360+1796C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880365 | |||||||
| chr12:85880379 | T | A | 1 | a0001c0001t0001g0136 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.360+1810T>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880379 | |||||||
| chr12:85880517 | TAAG | T | 3 | a0001c0001t0003g0018 a0001c0001t0003g0055 a0001c0001t0003g0056 |
5 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.361-1699_361-1697d others(5): Show |
NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85880517 | ||||||
| chr12:85880552 | T | G | 1 | a0001c0001t0001g0158 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.361-1671T>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880552 | |||||||
| chr12:85880719 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.361-1504G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880719 | |||||||
| chr12:85880759 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.361-1464C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880759 | |||||||
| chr12:85880760 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.361-1463G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880760 | |||||||
| chr12:85880772 | G | T | 1 | a0001c0001t0001g0158 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.361-1451G>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880772 | |||||||
| chr12:85880773 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.361-1450A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880773 | |||||||
| chr12:85880776 | C | A | 1 | a0001c0001t0001g0158 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.361-1447C>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880776 | |||||||
| chr12:85880808 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.361-1415C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880808 | |||||||
| chr12:85880809 | G | T | 1 | a0001c0001t0001g0080 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.361-1414G>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85880809 | |||||||
| chr12:85880989 | GA | G | 3 | a0001c0001t0003g0018 a0001c0001t0003g0055 a0001c0001t0003g0056 |
5 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.361-1229delA | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 85880989 | ||||||
| chr12:85881302 | A | G | 3 | a0001c0001t0003g0018 a0001c0001t0003g0055 a0001c0001t0003g0056 |
5 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.361-921A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85881302 | |||||||
| chr12:85881318 | C | T | 2 | a0001c0001t0004g0049 a0001c0001t0004g0135 |
3 | HG02630.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.361-905C>T | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85881318 | |||||||
| chr12:85881503 | T | C | 1 | a0001c0001t0001g0047 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.361-720T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85881503 | |||||||
| chr12:85881569 | T | C | 2 | a0001c0001t0003g0018 a0001c0001t0003g0056 |
4 | HG00741.hp2 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.361-654T>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85881569 | |||||||
| chr12:85881643 | C | A | 1 | a0001c0001t0001g0063 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.361-580C>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85881643 | |||||||
| chr12:85881679 | G | A | 1 | a0001c0001t0003g0055 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.361-544G>A | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85881679 | |||||||
| chr12:85881878 | A | G | 3 | a0001c0001t0003g0018 a0001c0001t0003g0055 a0001c0001t0003g0056 |
5 | HG00639.hp2 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.361-345A>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85881878 | |||||||
| chr12:85881965 | A | C | 56 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(53): Show |
127 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.361-258A>C | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85881965 | |||||||
| chr12:85882041 | T | G | 1 | a0001c0001t0001g0158 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.361-182T>G | NTS | ENSG00000133636.11 | transcript | ENST00000256010.7 | protein_coding | 3/3 | chr12 | 85882041 |