Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84305 |
| ensemblid | ENSG00000170473.17 |
| hgncid | 30258 |
| symbol | PYM1 |
| name | PYM homolog 1, exon junction complex associated factor |
| refseq_nuc | NM_032345.3 |
| refseq_prot | NP_115721.1 |
| ensembl_nuc | ENST00000408946.7 |
| ensembl_prot | ENSP00000386156.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 55901413 |
| end | 55927894 |
| strand | - |
| ver | v1.2 |
| region | chr12:55901413-55927894 |
| region5000 | chr12:55896413-55932894 |
| regionname0 | PYM1_chr12_55901413_55927894 |
| regionname5000 | PYM1_chr12_55896413_55932894 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 204 | 339 | 78 | 74 | 135 | 16 | 34 | 103 | PYM1_chr12_55896413_55932894 | PYM1 | MEAAG others(199): Show |
chr12 | 55896413 | 55932894 |
| a0002 | 0/0 | 204 | 5 | 0 | 0 | 5 | 0 | 0 | 3 | PYM1_chr12_55896413_55932894 | PYM1 | MEAAG others(199): Show |
chr12 | 55896413 | 55932894 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 612 | 312 | 58 | 73 | 130 | 16 | 34 | PYM1_chr12_55896413_55932894 | PYM1 | ATGGA others(607): Show |
chr12 | 55896413 | 55932894 | ||
| a0001c0002 | 1/0 | 612 | 22 | 20 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | ATGGA others(607): Show |
chr12 | 55896413 | 55932894 | ||
| a0001c0004 | 0/0 | 612 | 5 | 0 | 0 | 5 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | ATGGA others(607): Show |
chr12 | 55896413 | 55932894 | ||
| a0002c0003 | 0/0 | 612 | 5 | 0 | 0 | 5 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | ATGGA others(607): Show |
chr12 | 55896413 | 55932894 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1203 | 201 | 28 | 52 | 85 | 8 | 28 | PYM1_chr12_55896413_55932894 | PYM1 | ACTCA others(1198): Show |
chr12 | 55896413 | 55932894 |
| a0001c0001t0002 | 0/1 | 1207 | 62 | 13 | 15 | 24 | 6 | 3 | PYM1_chr12_55896413_55932894 | PYM1 | ACTCA others(1202): Show |
chr12 | 55896413 | 55932894 |
| a0001c0001t0003 | 0/0 | 1202 | 22 | 3 | 3 | 12 | 2 | 2 | PYM1_chr12_55896413_55932894 | PYM1 | ACTCA others(1197): Show |
chr12 | 55896413 | 55932894 |
| a0001c0001t0004 | 0/0 | 1208 | 10 | 8 | 1 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | ACTCA others(1203): Show |
chr12 | 55896413 | 55932894 |
| a0001c0001t0005 | 0/0 | 1206 | 7 | 0 | 2 | 5 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | ACTCA others(1201): Show |
chr12 | 55896413 | 55932894 |
| a0001c0001t0006 | 0/0 | 1203 | 3 | 3 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | ACTCA others(1198): Show |
chr12 | 55896413 | 55932894 |
| a0001c0001t0007 | 0/0 | 1207 | 2 | 2 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | ACTCA others(1202): Show |
chr12 | 55896413 | 55932894 |
| a0001c0001t0008 | 0/0 | 1204 | 2 | 1 | 0 | 0 | 0 | 1 | PYM1_chr12_55896413_55932894 | PYM1 | ACTCA others(1199): Show |
chr12 | 55896413 | 55932894 |
| a0001c0001t0009 | 0/0 | 1203 | 2 | 0 | 0 | 2 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | ACTCA others(1198): Show |
chr12 | 55896413 | 55932894 |
| a0001c0001t0011 | 0/0 | 1202 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | ACTCA others(1197): Show |
chr12 | 55896413 | 55932894 |
| a0001c0002t0002 | 1/0 | 1207 | 19 | 17 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | ACTCA others(1202): Show |
chr12 | 55896413 | 55932894 |
| a0001c0002t0005 | 0/0 | 1206 | 2 | 2 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | ACTCA others(1201): Show |
chr12 | 55896413 | 55932894 |
| a0001c0002t0010 | 0/0 | 1207 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | ACTCA others(1202): Show |
chr12 | 55896413 | 55932894 |
| a0001c0004t0001 | 0/0 | 1203 | 5 | 0 | 0 | 5 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | ACTCA others(1198): Show |
chr12 | 55896413 | 55932894 |
| a0002c0003t0001 | 0/0 | 1203 | 4 | 0 | 0 | 4 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | ACTCA others(1198): Show |
chr12 | 55896413 | 55932894 |
| a0002c0003t0003 | 0/0 | 1202 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | ACTCA others(1197): Show |
chr12 | 55896413 | 55932894 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 14 | 4 | 1 | 6 | 0 | 3 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0003 | 0/0 | 10 | 3 | 2 | 4 | 1 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0004 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0005 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0017 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0026 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0007 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0041 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0196 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0003g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0004g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0004g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0004g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0005g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0005g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0005g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0005g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0006g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0007g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0008g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0008g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0009g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0001t0011g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0002t0002g0002 | 0/0 | 11 | 11 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0002t0002g0012 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0002t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0002t0002g0208 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0002t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0002t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0002t0010g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0004t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0004t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0004t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0001c0004t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0002c0003t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0002c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0002c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| a0002c0003t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0227 | EUR | GBR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | GBR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | GBR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | FIN | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0044 | EUR | FIN | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0077 | EUR | FIN | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0204 | EUR | FIN | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | CHS | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | CHS | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | CHS | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00558 | hp1 | a0002 | c0003 | t0003 | g0173 | EAS | CHS | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | CHS | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | CHS | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00673 | hp2 | a0001 | c0004 | t0001 | g0180 | EAS | CHS | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0211 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0065 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0068 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01256 | hp1 | a0001 | c0001 | t0005 | g0096 | AMR | CLM | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | CLM | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0206 | AMR | CLM | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0210 | EUR | IBS | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0187 | EUR | IBS | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | ACB | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0070 | AFR | ACB | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0234 | AMR | PEL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0232 | AMR | PEL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0150 | AMR | PEL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PEL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | KHV | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | KHV | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | ACB | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02071 | hp2 | a0002 | c0003 | t0001 | g0168 | EAS | KHV | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0212 | EAS | KHV | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | KHV | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | ACB | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0047 | AFR | ACB | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02155 | hp2 | a0001 | c0001 | t0005 | g0226 | EAS | CDX | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | ACB | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | ACB | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0128 | AFR | ACB | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | ACB | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | GWD | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0022 | AFR | GWD | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0049 | AFR | GWD | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | GWD | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0022 | AFR | GWD | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | GWD | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0089 | AFR | GWD | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02897 | hp1 | a0001 | c0002 | t0005 | g0048 | AFR | GWD | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0121 | AFR | ESN | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | ESN | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | GWD | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03041 | hp2 | a0001 | c0002 | t0005 | g0046 | AFR | GWD | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | ESN | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | ESN | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | MSL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | MSL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03225 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | MSL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | MSL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03453 | hp2 | a0001 | c0002 | t0010 | g0050 | AFR | MSL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0153 | SAS | PJL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0198 | SAS | PJL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | ESN | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | MSL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | STU | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0220 | SAS | STU | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0109 | SAS | PJL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0223 | SAS | BEB | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | STU | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | STU | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | STU | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG04228 | hp1 | a0001 | c0001 | t0008 | g0084 | SAS | STU | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | STU | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | YRI | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | YRI | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | YRI | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0021 | AFR | YRI | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18942 | hp2 | a0001 | c0001 | t0005 | g0218 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18954 | hp1 | a0001 | c0001 | t0005 | g0201 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18954 | hp2 | a0001 | c0001 | t0011 | g0193 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18960 | hp1 | a0001 | c0001 | t0009 | g0039 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18963 | hp1 | a0001 | c0001 | t0009 | g0039 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18969 | hp1 | a0002 | c0003 | t0001 | g0034 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18977 | hp1 | a0001 | c0004 | t0001 | g0176 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19011 | hp2 | a0001 | c0004 | t0001 | g0035 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19057 | hp2 | a0002 | c0003 | t0001 | g0160 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19058 | hp1 | a0001 | c0004 | t0001 | g0181 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19062 | hp1 | a0001 | c0001 | t0005 | g0224 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19074 | hp1 | a0001 | c0001 | t0005 | g0213 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19085 | hp2 | a0002 | c0003 | t0001 | g0034 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19088 | hp1 | a0001 | c0004 | t0001 | g0035 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | ASW | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | ASW | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | TSI | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0044 | EUR | TSI | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0215 | EUR | TSI | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0027 | EUR | TSI | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | GIH | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | GIH | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0221 | AFR | ACB | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | ACB | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | ACB | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | MSL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | MSL | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | USA | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0021 | AFR | USA | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | USA | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA20300 | hp2 | a0001 | c0001 | t0008 | g0085 | AFR | USA | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | LWK | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | LWK | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0196 | REF | REF | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0208 | REF | REF | PYM1_chr12_55896413_55932894 | PYM1 | chr12 | 55896413 | 55932894 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:55902291 | C | G | 1 | a0002 | 5 | HG00558.hp1 HG02071.hp2 NA18969.hp1 others(2): Show |
missense_variant | MODERATE | c.196G>C | p.Glu66Gln | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 3/3 | 329/1207 | 196/615 | 66/204 | chr12 | 55902291 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:55901923 | T | C | 1 | a0001c0004 | 5 | HG00673.hp2 NA18977.hp1 NA19011.hp2 others(2): Show |
synonymous_variant | LOW | c.564A>G | p.Ala188Ala | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 3/3 | 697/1207 | 564/615 | 188/204 | chr12 | 55901923 | |||
| chr12:55901950 | A | G | 3 | a0001c0001 a0001c0004 a0002c0003 |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
synonymous_variant | LOW | c.537T>C | p.Pro179Pro | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 3/3 | 670/1207 | 537/615 | 179/204 | chr12 | 55901950 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:55901452 | T | A | 2 | a0001c0001t0006 a0001c0001t0007 |
5 | HG02451.hp1 HG03041.hp1 HG06807.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*420A>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 3/3 | 420 | chr12 | 55901452 | ||||||
| chr12:55901452 | T | TA | 2 | a0001c0001t0004 a0001c0001t0008 |
12 | HG01169.hp2 HG01891.hp1 HG02080.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*419dupT | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 3/3 | 419 | chr12 | 55901452 | ||||||
| chr12:55901452 | TA | T | 5 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0011 others(2): Show |
33 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*419delT | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 3/3 | 419 | chr12 | 55901452 | ||||||
| chr12:55901453 | A | T | 1 | a0001c0001t0001 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*419T>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 3/3 | 419 | chr12 | 55901453 | ||||||
| chr12:55901503 | G | A | 1 | a0001c0002t0010 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*369C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 3/3 | 369 | chr12 | 55901503 | ||||||
| chr12:55901760 | GAAGT | G | 9 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(6): Show |
241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
3_prime_UTR_variant | MODIFIER | c.*108_*111delACTT | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 3/3 | 108 | chr12 | 55901760 | ||||||
| chr12:55901779 | G | T | 1 | a0001c0001t0007 | 2 | HG06807.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*93C>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 3/3 | 93 | chr12 | 55901779 | ||||||
| chr12:55901783 | C | A | 2 | a0001c0001t0009 a0001c0001t0011 |
3 | NA18954.hp2 NA18960.hp1 NA18963.hp1 |
3_prime_UTR_variant | MODIFIER | c.*89G>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 3/3 | 89 | chr12 | 55901783 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:55902502 | G | C | 13 | a0001c0001t0002g0041 a0001c0001t0002g0042 a0001c0001t0002g0043 others(10): Show |
16 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.132-147C>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 2/2 | chr12 | 55902502 | |||||||
| chr12:55902515 | T | C | 1 | a0001c0001t0003g0077 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.132-160A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 2/2 | chr12 | 55902515 | |||||||
| chr12:55902530 | T | C | 1 | a0001c0001t0007g0021 | 2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.132-175A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 2/2 | chr12 | 55902530 | |||||||
| chr12:55902563 | C | T | 49 | a0001c0001t0001g0195 a0001c0001t0002g0007 a0001c0001t0002g0020 others(46): Show |
60 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.132-208G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 2/2 | chr12 | 55902563 | |||||||
| chr12:55902597 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.132-242G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 2/2 | chr12 | 55902597 | |||||||
| chr12:55902635 | G | T | 1 | a0001c0001t0001g0053 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.132-280C>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 2/2 | chr12 | 55902635 | |||||||
| chr12:55902982 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0003g0121 |
7 | HG01243.hp1 HG02451.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.131+405G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 2/2 | chr12 | 55902982 | |||||||
| chr12:55903800 | TAA | T | 6 | a0001c0001t0002g0067 a0001c0001t0004g0013 a0001c0001t0004g0023 others(3): Show |
10 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.38-322_38-321delTT | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55903800 | |||||||
| chr12:55903841 | C | T | 49 | a0001c0001t0001g0195 a0001c0001t0002g0007 a0001c0001t0002g0020 others(46): Show |
60 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.38-361G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55903841 | |||||||
| chr12:55903857 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.38-377C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55903857 | |||||||
| chr12:55904032 | A | T | 1 | a0001c0001t0001g0101 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.38-552T>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55904032 | |||||||
| chr12:55904209 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0185 a0001c0001t0001g0186 others(1): Show |
6 | NA18948.hp2 NA18971.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.38-729G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55904209 | |||||||
| chr12:55904218 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.38-738G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55904218 | |||||||
| chr12:55904415 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.38-935T>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55904415 | |||||||
| chr12:55904539 | T | C | 1 | a0001c0001t0007g0021 | 2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.38-1059A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55904539 | |||||||
| chr12:55904566 | A | G | 7 | a0001c0001t0001g0104 a0001c0001t0002g0067 a0001c0001t0004g0013 others(4): Show |
11 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.38-1086T>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55904566 | |||||||
| chr12:55904595 | CA | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.38-1116delT | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55904595 | |||||||
| chr12:55904595 | CAA | C | 12 | a0001c0001t0001g0071 a0001c0001t0001g0075 a0001c0001t0001g0083 others(9): Show |
12 | HG00558.hp1 HG01070.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.38-1117_38-1116del others(2): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55904595 | |||||||
| chr12:55904595 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0097 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.38-1126_38-1116del others(11): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55904595 | |||||||
| chr12:55904595 | CAAAAAAA others(7): Show |
C | 7 | a0001c0001t0001g0104 a0001c0001t0002g0067 a0001c0001t0004g0013 others(4): Show |
11 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.38-1129_38-1116del others(14): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55904595 | |||||||
| chr12:55904612 | A | G | 49 | a0001c0001t0001g0188 a0001c0001t0001g0195 a0001c0001t0002g0007 others(46): Show |
60 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.38-1132T>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55904612 | |||||||
| chr12:55904615 | A | G | 1 | a0001c0001t0003g0121 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.38-1135T>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55904615 | |||||||
| chr12:55904621 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.38-1141T>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55904621 | |||||||
| chr12:55904767 | C | T | 2 | a0001c0002t0002g0012 a0001c0002t0010g0050 |
4 | HG01109.hp1 HG02109.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.38-1287G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55904767 | |||||||
| chr12:55904777 | C | T | 1 | a0001c0001t0002g0232 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.38-1297G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55904777 | |||||||
| chr12:55904997 | A | T | 40 | a0001c0001t0001g0195 a0001c0001t0002g0007 a0001c0001t0002g0020 others(37): Show |
51 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.38-1517T>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55904997 | |||||||
| chr12:55905040 | C | T | 221 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(218): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.38-1560G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905040 | |||||||
| chr12:55905056 | C | G | 6 | a0001c0001t0001g0010 a0001c0001t0001g0094 a0001c0001t0001g0106 others(3): Show |
9 | HG00140.hp2 HG01069.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.38-1576G>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905056 | |||||||
| chr12:55905079 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.38-1599C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905079 | |||||||
| chr12:55905087 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.38-1607A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905087 | |||||||
| chr12:55905111 | C | G | 1 | a0001c0001t0002g0205 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.38-1631G>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905111 | |||||||
| chr12:55905299 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.38-1819C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905299 | |||||||
| chr12:55905579 | G | A | 1 | a0001c0001t0002g0051 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.38-2099C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905579 | |||||||
| chr12:55905581 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.38-2101T>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905581 | |||||||
| chr12:55905645 | G | A | 1 | a0001c0001t0005g0218 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.38-2165C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905645 | |||||||
| chr12:55905649 | G | A | 1 | a0001c0001t0004g0023 | 2 | HG02818.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.38-2169C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905649 | |||||||
| chr12:55905713 | T | A | 58 | a0001c0001t0001g0195 a0001c0001t0002g0007 a0001c0001t0002g0020 others(55): Show |
73 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.38-2233A>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905713 | |||||||
| chr12:55905724 | G | GTA | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.38-2246_38-2245dup others(2): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905724 | |||||||
| chr12:55905724 | G | GTATA | 12 | a0001c0001t0001g0045 a0001c0001t0001g0120 a0001c0001t0001g0143 others(9): Show |
16 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.38-2248_38-2245dup others(4): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905724 | |||||||
| chr12:55905748 | A | C | 1 | a0001c0001t0001g0142 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.38-2268T>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905748 | |||||||
| chr12:55905791 | TATATAAA others(189): Show |
T | 2 | a0001c0001t0002g0221 a0001c0001t0002g0222 |
2 | HG02109.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.38-2507_38-2312del | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905791 | |||||||
| chr12:55905796 | AAAAT | A | 1 | a0001c0001t0004g0013 | 3 | HG03139.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.38-2320_38-2317del others(4): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905796 | |||||||
| chr12:55905834 | A | ATATTAGA others(32): Show |
1 | a0001c0001t0001g0076 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.38-2393_38-2355dup others(39): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905834 | |||||||
| chr12:55905854 | A | ATATTAGA others(12): Show |
4 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0115 others(1): Show |
6 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.38-2393_38-2375dup others(19): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905854 | |||||||
| chr12:55905854 | A | C | 1 | a0001c0001t0001g0191 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.38-2374T>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905854 | |||||||
| chr12:55905860 | GAT | G | 5 | a0001c0001t0002g0067 a0001c0001t0004g0023 a0001c0001t0004g0024 others(2): Show |
6 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.38-2382_38-2381del others(2): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905860 | |||||||
| chr12:55905863 | A | ATATATAT others(41): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0148 a0001c0001t0001g0188 |
3 | HG00099.hp2 HG01099.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.38-2384_38-2383ins others(48): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905863 | |||||||
| chr12:55905863 | A | ATATATAT others(70): Show |
1 | a0001c0001t0001g0155 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.38-2384_38-2383ins others(77): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905863 | |||||||
| chr12:55905863 | A | ATATATAT others(99): Show |
1 | a0001c0001t0001g0001 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.38-2384_38-2383ins others(106): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905863 | |||||||
| chr12:55905863 | A | ATATATAT others(22): Show |
18 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(15): Show |
24 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.38-2412_38-2384dup others(29): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905863 | |||||||
| chr12:55905863 | A | ATATATAT others(116): Show |
4 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(1): Show |
4 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.38-2384_38-2383ins others(123): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905863 | |||||||
| chr12:55905863 | A | ATATATAT others(175): Show |
1 | a0001c0001t0002g0059 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.38-2384_38-2383ins others(182): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905863 | |||||||
| chr12:55905863 | A | ATATATAT others(99): Show |
1 | a0001c0001t0003g0153 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.38-2384_38-2383ins others(106): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905863 | |||||||
| chr12:55905863 | A | ATATATAT others(51): Show |
15 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(12): Show |
20 | HG00140.hp2 HG01069.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.38-2384_38-2383ins others(58): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905863 | |||||||
| chr12:55905863 | A | ATATATAT others(80): Show |
9 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0052 others(6): Show |
9 | HG01261.hp2 HG01361.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.38-2384_38-2383ins others(87): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905863 | |||||||
| chr12:55905863 | A | ATATATAT others(109): Show |
3 | a0001c0001t0001g0016 a0001c0001t0001g0083 a0001c0001t0001g0093 |
3 | HG01168.hp2 HG02273.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.38-2384_38-2383ins others(116): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905863 | |||||||
| chr12:55905863 | A | ATATATAT others(138): Show |
1 | a0001c0001t0001g0119 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.38-2384_38-2383ins others(145): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905863 | |||||||
| chr12:55905863 | A | ATATATAT others(223): Show |
2 | a0001c0001t0002g0041 a0001c0001t0002g0216 |
2 | NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.38-2384_38-2383ins others(230): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905863 | |||||||
| chr12:55905863 | A | ATATATAT others(252): Show |
1 | a0001c0001t0002g0203 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.38-2384_38-2383ins others(259): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905863 | |||||||
| chr12:55905863 | A | ATATATAT others(310): Show |
1 | a0001c0001t0002g0207 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.38-2384_38-2383ins others(317): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905863 | |||||||
| chr12:55905863 | A | ATATATAT others(223): Show |
1 | a0001c0001t0002g0206 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.38-2384_38-2383ins others(230): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905863 | |||||||
| chr12:55905863 | A | ATATATAT others(252): Show |
3 | a0001c0001t0002g0042 a0001c0001t0002g0230 a0001c0001t0002g0232 |
3 | HG00738.hp2 HG01978.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.38-2384_38-2383ins others(259): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905863 | |||||||
| chr12:55905863 | A | ATATATAT others(281): Show |
2 | a0001c0001t0002g0041 a0001c0001t0002g0043 |
2 | HG02004.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.38-2384_38-2383ins others(288): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905863 | |||||||
| chr12:55905863 | A | ATATATAT others(339): Show |
2 | a0001c0001t0002g0042 a0001c0001t0002g0234 |
2 | HG00735.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.38-2384_38-2383ins others(346): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905863 | |||||||
| chr12:55905863 | A | ATATATAT others(368): Show |
1 | a0001c0001t0002g0043 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.38-2384_38-2383ins others(375): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905863 | |||||||
| chr12:55905863 | A | ATATATAT others(281): Show |
1 | a0001c0001t0002g0233 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.38-2384_38-2383ins others(288): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905863 | |||||||
| chr12:55905863 | A | ATATATAT others(252): Show |
1 | a0001c0001t0004g0013 | 3 | HG03139.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.38-2384_38-2383ins others(259): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905863 | |||||||
| chr12:55905863 | A | ATATATAT others(422): Show |
1 | a0001c0001t0004g0024 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.38-2384_38-2383ins others(429): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905863 | |||||||
| chr12:55905863 | A | ATATATAT others(32): Show |
1 | a0001c0001t0001g0191 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.38-2384_38-2383ins others(39): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905863 | |||||||
| chr12:55905876 | T | A | 12 | a0001c0001t0002g0041 a0001c0001t0002g0042 a0001c0001t0002g0043 others(9): Show |
15 | HG00735.hp2 HG00738.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.38-2396A>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(12): Show |
37 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(34): Show |
53 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.38-2397_38-2396ins others(19): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(226): Show |
1 | a0001c0001t0002g0229 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.38-2397_38-2396ins others(233): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(167): Show |
1 | a0001c0001t0005g0224 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.38-2397_38-2396ins others(174): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(138): Show |
1 | a0001c0001t0002g0225 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.38-2397_38-2396ins others(145): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(164): Show |
1 | a0001c0001t0002g0020 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.38-2397_38-2396ins others(171): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(167): Show |
1 | a0001c0001t0005g0226 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.38-2397_38-2396ins others(174): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(193): Show |
1 | a0001c0001t0002g0223 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.38-2397_38-2396ins others(200): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(196): Show |
2 | a0001c0001t0002g0007 a0001c0001t0002g0020 |
2 | HG02083.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.38-2397_38-2396ins others(203): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(225): Show |
1 | a0001c0001t0002g0194 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.38-2397_38-2396ins others(232): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(254): Show |
2 | a0001c0001t0002g0209 a0001c0001t0002g0227 |
2 | HG00099.hp1 HG00408.hp2 |
intron_variant | MODIFIER | c.38-2397_38-2396ins others(261): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(283): Show |
1 | a0001c0001t0002g0210 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.38-2397_38-2396ins others(290): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(341): Show |
1 | a0001c0001t0002g0007 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.38-2397_38-2396ins others(348): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(370): Show |
1 | a0001c0001t0002g0020 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.38-2397_38-2396ins others(377): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(80): Show |
1 | a0001c0001t0001g0003 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.38-2397_38-2396ins others(87): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(109): Show |
1 | a0001c0001t0004g0212 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.38-2397_38-2396ins others(116): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(138): Show |
1 | a0001c0001t0002g0007 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.38-2397_38-2396ins others(145): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(167): Show |
4 | a0001c0001t0002g0007 a0001c0001t0002g0204 a0001c0001t0002g0205 others(1): Show |
4 | HG00323.hp2 HG01081.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.38-2397_38-2396ins others(174): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(196): Show |
5 | a0001c0001t0002g0007 a0001c0001t0002g0197 a0001c0001t0002g0199 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.38-2397_38-2396ins others(203): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(225): Show |
3 | a0001c0001t0002g0040 a0001c0001t0002g0202 a0001c0001t0002g0231 |
3 | HG00621.hp2 NA18972.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.38-2397_38-2396ins others(232): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(254): Show |
4 | a0001c0001t0002g0219 a0001c0001t0002g0228 a0001c0001t0002g0235 others(1): Show |
4 | NA18954.hp1 NA18972.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-2397_38-2396ins others(261): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(167): Show |
1 | a0001c0001t0002g0217 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.38-2397_38-2396ins others(174): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(109): Show |
3 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0154 |
3 | NA18940.hp2 NA18951.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.38-2397_38-2396ins others(116): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(198): Show |
1 | a0001c0001t0002g0198 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.38-2397_38-2396ins others(205): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(225): Show |
1 | a0001c0001t0002g0220 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.38-2397_38-2396ins others(232): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(254): Show |
2 | a0001c0001t0002g0044 a0001c0001t0002g0215 |
2 | NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.38-2397_38-2396ins others(261): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(283): Show |
1 | a0001c0001t0001g0195 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.38-2397_38-2396ins others(290): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(138): Show |
2 | a0001c0001t0001g0016 a0001c0001t0001g0080 |
2 | HG01255.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.38-2397_38-2396ins others(145): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(167): Show |
1 | a0001c0001t0001g0016 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.38-2397_38-2396ins others(174): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(283): Show |
1 | a0001c0001t0005g0213 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.38-2397_38-2396ins others(290): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(254): Show |
1 | a0001c0001t0002g0044 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.38-2397_38-2396ins others(261): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | T | TTAGATAT others(192): Show |
2 | a0001c0001t0002g0040 a0001c0001t0002g0200 |
2 | NA18994.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.38-2397_38-2396ins others(199): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905876 | TTAGATAT others(22): Show |
T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0138 a0001c0001t0008g0084 others(1): Show |
4 | HG01928.hp1 HG02040.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.38-2425_38-2397del others(29): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905876 | |||||||
| chr12:55905882 | ATATATAT others(3): Show |
A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0026 others(1): Show |
6 | HG01069.hp2 HG02080.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.38-2412_38-2403del others(10): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905882 | |||||||
| chr12:55905886 | ATAT | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0149 a0001c0001t0001g0152 others(1): Show |
7 | HG00642.hp2 HG01361.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.38-2409_38-2407del others(3): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905886 | |||||||
| chr12:55905889 | T | TTATATAT others(42): Show |
1 | a0001c0001t0001g0069 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.38-2410_38-2409ins others(49): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905889 | |||||||
| chr12:55905892 | T | TATATTAG others(116): Show |
1 | a0001c0001t0002g0061 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.38-2413_38-2412ins others(123): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905892 | |||||||
| chr12:55905892 | T | TTATATAT others(30): Show |
1 | a0001c0001t0001g0182 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.38-2413_38-2412ins others(37): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905892 | |||||||
| chr12:55905892 | T | TTATATAT others(32): Show |
5 | a0001c0001t0001g0017 a0001c0001t0001g0158 a0001c0001t0001g0163 others(2): Show |
6 | HG00423.hp2 HG01928.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.38-2413_38-2412ins others(39): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905892 | |||||||
| chr12:55905905 | A | T | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.38-2425T>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905905 | |||||||
| chr12:55905911 | ATATATAT others(3): Show |
A | 2 | a0001c0002t0002g0012 a0001c0002t0010g0050 |
4 | HG01109.hp1 HG02109.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.38-2441_38-2432del others(10): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905911 | |||||||
| chr12:55905911 | ATATATAT others(32): Show |
A | 1 | a0001c0001t0007g0021 | 2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.38-2470_38-2432del others(39): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905911 | |||||||
| chr12:55905921 | T | TATATTAG others(3): Show |
17 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(14): Show |
22 | HG01175.hp2 HG03486.hp2 HG03704.hp2 others(19): Show |
intron_variant | MODIFIER | c.38-2442_38-2441ins others(10): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905921 | |||||||
| chr12:55905921 | T | TTATATAT others(32): Show |
2 | a0001c0001t0001g0164 a0001c0001t0001g0169 |
2 | HG03834.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.38-2442_38-2441ins others(39): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905921 | |||||||
| chr12:55905921 | TTA | T | 2 | a0001c0001t0004g0013 a0001c0001t0004g0024 |
4 | HG03130.hp1 HG03139.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.38-2443_38-2442del others(2): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905921 | |||||||
| chr12:55905923 | A | ATATATAT others(455): Show |
2 | a0001c0001t0002g0067 a0001c0001t0004g0068 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.38-2444_38-2443ins others(462): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905923 | |||||||
| chr12:55905923 | A | ATATATAT others(426): Show |
1 | a0001c0001t0004g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.38-2444_38-2443ins others(433): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905923 | |||||||
| chr12:55905923 | A | ATATATAT others(484): Show |
1 | a0001c0001t0004g0024 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.38-2444_38-2443ins others(491): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905923 | |||||||
| chr12:55905924 | TATATATC others(56): Show |
T | 6 | a0001c0002t0002g0002 a0001c0002t0002g0022 a0001c0002t0002g0047 others(3): Show |
17 | HG02145.hp2 HG02257.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.38-2507_38-2445del others(63): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905924 | |||||||
| chr12:55905933 | A | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0086 |
5 | HG00544.hp2 HG02135.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.38-2453T>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905933 | |||||||
| chr12:55905934 | A | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.38-2454T>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905934 | |||||||
| chr12:55905937 | G | GATATATA others(53): Show |
1 | a0001c0001t0001g0003 | 2 | HG00735.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.38-2458_38-2457ins others(60): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905937 | |||||||
| chr12:55905947 | T | TTATTATA others(22): Show |
1 | a0001c0001t0002g0102 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.38-2468_38-2467ins others(29): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905947 | |||||||
| chr12:55905952 | A | ATATATAT others(364): Show |
1 | a0001c0001t0004g0023 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.38-2473_38-2472ins others(371): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905952 | |||||||
| chr12:55905952 | A | ATATATAT others(393): Show |
1 | a0001c0001t0004g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.38-2473_38-2472ins others(400): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905952 | |||||||
| chr12:55905963 | A | T | 33 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0025 others(30): Show |
47 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(44): Show |
intron_variant | MODIFIER | c.38-2483T>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905963 | |||||||
| chr12:55905969 | A | C | 1 | a0001c0001t0003g0108 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.38-2489T>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905969 | |||||||
| chr12:55905982 | TATATA | T | 3 | a0001c0001t0007g0021 a0001c0002t0002g0012 a0001c0002t0010g0050 |
6 | HG01109.hp1 HG02109.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.38-2507_38-2503del others(5): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55905982 | |||||||
| chr12:55906133 | T | C | 9 | a0001c0001t0007g0021 a0001c0002t0002g0002 a0001c0002t0002g0012 others(6): Show |
23 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.38-2653A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55906133 | |||||||
| chr12:55906199 | T | A | 7 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(4): Show |
7 | HG00323.hp1 NA18942.hp1 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.38-2719A>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55906199 | |||||||
| chr12:55906652 | T | G | 18 | a0001c0001t0001g0078 a0001c0001t0001g0125 a0001c0001t0002g0067 others(15): Show |
36 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.38-3172A>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55906652 | |||||||
| chr12:55906656 | G | T | 6 | a0001c0001t0002g0051 a0001c0001t0002g0056 a0001c0001t0002g0057 others(3): Show |
6 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.38-3176C>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55906656 | |||||||
| chr12:55906751 | T | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.38-3271A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55906751 | |||||||
| chr12:55906964 | T | C | 6 | a0001c0002t0002g0002 a0001c0002t0002g0022 a0001c0002t0002g0047 others(3): Show |
17 | HG02145.hp2 HG02257.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.38-3484A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55906964 | |||||||
| chr12:55907064 | C | T | 3 | a0001c0001t0001g0162 a0001c0001t0001g0166 a0001c0001t0001g0170 |
3 | NA18965.hp2 NA19001.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.38-3584G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55907064 | |||||||
| chr12:55907070 | T | C | 1 | a0001c0001t0002g0102 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.38-3590A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55907070 | |||||||
| chr12:55907097 | CAT | C | 17 | a0001c0001t0001g0094 a0001c0001t0001g0103 a0001c0001t0001g0105 others(14): Show |
31 | HG00408.hp2 HG00639.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.38-3619_38-3618del others(2): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55907097 | |||||||
| chr12:55907097 | CATAT | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.38-3621_38-3618del others(4): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55907097 | |||||||
| chr12:55907166 | G | GA | 9 | a0001c0001t0007g0021 a0001c0002t0002g0002 a0001c0002t0002g0012 others(6): Show |
23 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.38-3687dupT | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55907166 | |||||||
| chr12:55907220 | T | C | 1 | a0001c0001t0002g0051 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.38-3740A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55907220 | |||||||
| chr12:55907251 | T | G | 10 | a0001c0001t0002g0051 a0001c0001t0007g0021 a0001c0002t0002g0002 others(7): Show |
24 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.38-3771A>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55907251 | |||||||
| chr12:55907301 | T | G | 1 | a0001c0001t0001g0099 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.38-3821A>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55907301 | |||||||
| chr12:55907463 | C | CA | 17 | a0001c0001t0001g0031 a0001c0001t0001g0064 a0001c0001t0001g0080 others(14): Show |
19 | HG00140.hp1 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.38-3984dupT | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55907463 | |||||||
| chr12:55907463 | C | CAAAAA | 2 | a0001c0002t0002g0002 a0001c0002t0005g0048 |
12 | HG02257.hp2 HG02559.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.38-3988_38-3984dup others(5): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55907463 | |||||||
| chr12:55907463 | CA | C | 19 | a0001c0001t0001g0026 a0001c0001t0001g0091 a0001c0001t0001g0093 others(16): Show |
22 | HG00609.hp2 HG01433.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.38-3984delT | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55907463 | |||||||
| chr12:55907526 | T | C | 9 | a0001c0001t0007g0021 a0001c0002t0002g0002 a0001c0002t0002g0012 others(6): Show |
23 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.38-4046A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55907526 | |||||||
| chr12:55907634 | G | GA | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.38-4155dupT | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55907634 | |||||||
| chr12:55907634 | G | GAA | 12 | a0001c0001t0001g0088 a0001c0001t0001g0100 a0001c0001t0001g0115 others(9): Show |
15 | HG01109.hp1 HG01175.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.38-4156_38-4155dup others(2): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55907634 | |||||||
| chr12:55907648 | AAAATTGG others(5): Show |
A | 5 | a0001c0002t0002g0002 a0001c0002t0002g0022 a0001c0002t0002g0047 others(2): Show |
16 | HG02145.hp2 HG02257.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.38-4180_38-4169del others(12): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55907648 | |||||||
| chr12:55907649 | AAATTGGA others(4): Show |
A | 1 | a0001c0002t0002g0049 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.38-4180_38-4170del others(11): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55907649 | |||||||
| chr12:55907709 | T | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.38-4229A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55907709 | |||||||
| chr12:55907710 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.38-4230C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55907710 | |||||||
| chr12:55907722 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.38-4242A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55907722 | |||||||
| chr12:55907924 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0003g0121 |
7 | HG01243.hp1 HG02451.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.38-4444G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55907924 | |||||||
| chr12:55907952 | T | A | 10 | a0001c0001t0002g0051 a0001c0001t0007g0021 a0001c0002t0002g0002 others(7): Show |
24 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.38-4472A>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55907952 | |||||||
| chr12:55908202 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.38-4722G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55908202 | |||||||
| chr12:55908335 | A | G | 1 | a0001c0001t0001g0131 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.38-4855T>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55908335 | |||||||
| chr12:55908420 | A | G | 1 | a0001c0001t0007g0021 | 2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.38-4940T>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55908420 | |||||||
| chr12:55908428 | C | CA | 7 | a0001c0001t0001g0029 a0001c0001t0001g0134 a0001c0001t0001g0135 others(4): Show |
8 | NA18940.hp1 NA18940.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.38-4949dupT | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55908428 | |||||||
| chr12:55908479 | T | C | 1 | a0001c0001t0002g0215 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.38-4999A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55908479 | |||||||
| chr12:55908504 | T | C | 3 | a0001c0001t0002g0042 a0001c0001t0002g0206 a0001c0001t0002g0207 |
4 | HG00735.hp2 HG00738.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.38-5024A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55908504 | |||||||
| chr12:55908512 | T | A | 3 | a0001c0001t0002g0042 a0001c0001t0002g0206 a0001c0001t0002g0207 |
4 | HG00735.hp2 HG00738.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.38-5032A>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55908512 | |||||||
| chr12:55908882 | T | C | 1 | a0001c0001t0002g0220 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.38-5402A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55908882 | |||||||
| chr12:55909176 | CAAGAATA others(7): Show |
C | 3 | a0001c0001t0001g0028 a0001c0001t0001g0045 a0001c0001t0003g0089 |
4 | HG02615.hp2 HG02717.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.38-5710_38-5697del others(14): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55909176 | |||||||
| chr12:55909384 | CA | C | 10 | a0001c0001t0002g0051 a0001c0001t0007g0021 a0001c0002t0002g0002 others(7): Show |
24 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.38-5905delT | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55909384 | |||||||
| chr12:55909487 | C | T | 9 | a0001c0001t0007g0021 a0001c0002t0002g0002 a0001c0002t0002g0012 others(6): Show |
23 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.38-6007G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55909487 | |||||||
| chr12:55909576 | T | C | 1 | a0001c0001t0001g0170 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.38-6096A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55909576 | |||||||
| chr12:55909583 | GA | G | 8 | a0001c0001t0006g0015 a0001c0001t0007g0021 a0001c0002t0002g0002 others(5): Show |
22 | HG02145.hp2 HG02257.hp2 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.38-6104delT | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55909583 | |||||||
| chr12:55909972 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.38-6492C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55909972 | |||||||
| chr12:55909988 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0003g0130 |
3 | NA18986.hp2 NA19012.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.38-6508G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55909988 | |||||||
| chr12:55910167 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.38-6687T>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55910167 | |||||||
| chr12:55910169 | A | G | 9 | a0001c0001t0007g0021 a0001c0002t0002g0002 a0001c0002t0002g0012 others(6): Show |
23 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.38-6689T>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55910169 | |||||||
| chr12:55910252 | C | CAT | 8 | a0001c0001t0002g0041 a0001c0001t0002g0042 a0001c0001t0002g0204 others(5): Show |
10 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.38-6774_38-6773dup others(2): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55910252 | |||||||
| chr12:55910252 | C | CATAT | 4 | a0001c0001t0002g0203 a0001c0001t0002g0216 a0001c0001t0002g0234 others(1): Show |
4 | HG01975.hp1 HG01993.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.38-6776_38-6773dup others(4): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55910252 | |||||||
| chr12:55910252 | C | CATATATA others(5): Show |
1 | a0001c0001t0002g0222 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.38-6784_38-6773dup others(12): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55910252 | |||||||
| chr12:55910252 | C | CATATATA others(11): Show |
1 | a0001c0001t0002g0221 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.38-6790_38-6773dup others(18): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55910252 | |||||||
| chr12:55910252 | CAT | C | 10 | a0001c0001t0002g0040 a0001c0001t0002g0200 a0001c0001t0002g0202 others(7): Show |
11 | HG00099.hp1 HG00621.hp2 HG03688.hp2 others(8): Show |
intron_variant | MODIFIER | c.38-6774_38-6773del others(2): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55910252 | |||||||
| chr12:55910252 | CATAT | C | 19 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0044 others(16): Show |
26 | HG00280.hp2 HG00673.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.38-6776_38-6773del others(4): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55910252 | |||||||
| chr12:55910252 | CATATATA others(3): Show |
C | 4 | a0001c0001t0001g0093 a0001c0001t0001g0120 a0001c0001t0001g0143 others(1): Show |
6 | HG02280.hp2 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.38-6782_38-6773del others(10): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55910252 | |||||||
| chr12:55910252 | CATATATA others(5): Show |
C | 2 | a0001c0001t0001g0107 a0001c0001t0001g0165 |
2 | HG00423.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.38-6784_38-6773del others(12): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55910252 | |||||||
| chr12:55910252 | CATATATA others(7): Show |
C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.38-6786_38-6773del others(14): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55910252 | |||||||
| chr12:55910252 | CATATATA others(11): Show |
C | 9 | a0001c0001t0007g0021 a0001c0002t0002g0002 a0001c0002t0002g0012 others(6): Show |
23 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.38-6790_38-6773del others(18): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55910252 | |||||||
| chr12:55910314 | T | G | 3 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0001g0182 |
3 | HG01928.hp2 HG01943.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.38-6834A>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55910314 | |||||||
| chr12:55910453 | T | C | 1 | a0001c0001t0004g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.38-6973A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55910453 | |||||||
| chr12:55910496 | G | A | 1 | a0001c0001t0002g0102 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.38-7016C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55910496 | |||||||
| chr12:55910704 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0003g0157 |
3 | NA18952.hp1 NA18955.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.38-7224T>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55910704 | |||||||
| chr12:55910946 | AC | A | 8 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(5): Show |
8 | HG01074.hp2 HG01496.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.38-7467delG | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55910946 | |||||||
| chr12:55910952 | G | A | 6 | a0001c0002t0002g0002 a0001c0002t0002g0022 a0001c0002t0002g0047 others(3): Show |
17 | HG02145.hp2 HG02257.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.38-7472C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55910952 | |||||||
| chr12:55911042 | T | A | 1 | a0001c0001t0001g0137 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.38-7562A>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55911042 | |||||||
| chr12:55911130 | T | C | 9 | a0001c0001t0007g0021 a0001c0002t0002g0002 a0001c0002t0002g0012 others(6): Show |
23 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.38-7650A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55911130 | |||||||
| chr12:55911183 | A | G | 6 | a0001c0001t0002g0040 a0001c0001t0002g0200 a0001c0001t0002g0202 others(3): Show |
7 | HG00621.hp2 NA18954.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.38-7703T>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55911183 | |||||||
| chr12:55911233 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0171 |
2 | HG01175.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.38-7753G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55911233 | |||||||
| chr12:55911408 | G | A | 9 | a0001c0001t0007g0021 a0001c0002t0002g0002 a0001c0002t0002g0012 others(6): Show |
23 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.38-7928C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55911408 | |||||||
| chr12:55911770 | G | C | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.38-8290C>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55911770 | |||||||
| chr12:55911772 | G | T | 10 | a0001c0001t0002g0051 a0001c0001t0007g0021 a0001c0002t0002g0002 others(7): Show |
24 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.38-8292C>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55911772 | |||||||
| chr12:55911790 | G | A | 1 | a0001c0001t0002g0044 | 2 | HG00280.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.38-8310C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55911790 | |||||||
| chr12:55911848 | A | AGAAGG | 5 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(2): Show |
5 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.38-8373_38-8369dup others(5): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55911848 | |||||||
| chr12:55911878 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.38-8398C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55911878 | |||||||
| chr12:55912117 | G | C | 1 | a0001c0001t0001g0082 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.38-8637C>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55912117 | |||||||
| chr12:55912209 | G | A | 1 | a0001c0001t0002g0216 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.38-8729C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55912209 | |||||||
| chr12:55912333 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.38-8853A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55912333 | |||||||
| chr12:55912516 | A | G | 9 | a0001c0001t0007g0021 a0001c0002t0002g0002 a0001c0002t0002g0012 others(6): Show |
23 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.38-9036T>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55912516 | |||||||
| chr12:55912592 | A | C | 6 | a0001c0002t0002g0002 a0001c0002t0002g0022 a0001c0002t0002g0047 others(3): Show |
17 | HG02145.hp2 HG02257.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.38-9112T>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55912592 | |||||||
| chr12:55912592 | A | G | 1 | a0001c0001t0003g0128 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.38-9112T>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55912592 | |||||||
| chr12:55912729 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.38-9249G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55912729 | |||||||
| chr12:55912871 | G | A | 1 | a0001c0001t0007g0021 | 2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.38-9391C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55912871 | |||||||
| chr12:55912920 | C | T | 1 | a0001c0001t0002g0227 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.38-9440G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55912920 | |||||||
| chr12:55912959 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
4 | HG00280.hp1 HG01069.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-9479G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55912959 | |||||||
| chr12:55913148 | T | A | 5 | a0001c0001t0002g0199 a0001c0001t0002g0217 a0001c0001t0002g0229 others(2): Show |
5 | HG02027.hp1 NA18942.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.38-9668A>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55913148 | |||||||
| chr12:55913160 | G | A | 1 | a0001c0001t0004g0024 | 2 | HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.38-9680C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55913160 | |||||||
| chr12:55913455 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0080 |
4 | HG01255.hp2 HG01433.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.38-9975A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55913455 | |||||||
| chr12:55913926 | T | TA | 3 | a0001c0001t0001g0028 a0001c0001t0001g0045 a0001c0001t0003g0089 |
4 | HG02615.hp2 HG02717.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.38-10447dupT | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55913926 | |||||||
| chr12:55914091 | T | C | 9 | a0001c0001t0007g0021 a0001c0002t0002g0002 a0001c0002t0002g0012 others(6): Show |
23 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.38-10611A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55914091 | |||||||
| chr12:55914139 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.38-10659A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55914139 | |||||||
| chr12:55914194 | A | G | 5 | a0001c0001t0002g0067 a0001c0001t0004g0023 a0001c0001t0004g0024 others(2): Show |
7 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.38-10714T>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55914194 | |||||||
| chr12:55914325 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.38-10845C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55914325 | |||||||
| chr12:55914357 | G | C | 1 | a0001c0001t0001g0139 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.38-10877C>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55914357 | |||||||
| chr12:55914439 | T | C | 3 | a0001c0002t0002g0047 a0001c0002t0002g0049 a0001c0002t0005g0046 |
3 | HG02145.hp2 HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.38-10959A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55914439 | |||||||
| chr12:55914506 | C | T | 1 | a0001c0001t0006g0015 | 3 | HG02451.hp1 HG03041.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.38-11026G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55914506 | |||||||
| chr12:55914778 | G | T | 9 | a0001c0001t0007g0021 a0001c0002t0002g0002 a0001c0002t0002g0012 others(6): Show |
23 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.38-11298C>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55914778 | |||||||
| chr12:55914953 | C | T | 9 | a0001c0001t0007g0021 a0001c0002t0002g0002 a0001c0002t0002g0012 others(6): Show |
23 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.38-11473G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55914953 | |||||||
| chr12:55915005 | C | G | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.38-11525G>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55915005 | |||||||
| chr12:55915071 | C | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.38-11591G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55915071 | |||||||
| chr12:55915201 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.38-11721G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55915201 | |||||||
| chr12:55915213 | T | TA | 12 | a0001c0001t0002g0067 a0001c0001t0002g0219 a0001c0001t0002g0220 others(9): Show |
18 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.38-11734dupT | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55915213 | |||||||
| chr12:55915213 | T | TAA | 18 | a0001c0001t0001g0091 a0001c0001t0001g0142 a0001c0001t0001g0148 others(15): Show |
30 | HG01433.hp2 HG01884.hp2 HG01943.hp1 others(27): Show |
intron_variant | MODIFIER | c.38-11735_38-11734d others(4): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55915213 | |||||||
| chr12:55915213 | T | TAAA | 148 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(145): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.38-11736_38-11734d others(5): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55915213 | |||||||
| chr12:55915213 | T | TAAAA | 12 | a0001c0001t0001g0069 a0001c0001t0001g0079 a0001c0001t0001g0105 others(9): Show |
12 | HG00597.hp1 HG00673.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.38-11737_38-11734d others(6): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55915213 | |||||||
| chr12:55915294 | T | G | 1 | a0001c0001t0002g0051 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.38-11814A>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55915294 | |||||||
| chr12:55915348 | T | C | 1 | a0001c0001t0003g0118 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.38-11868A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55915348 | |||||||
| chr12:55915366 | C | T | 1 | a0001c0001t0002g0051 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.38-11886G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55915366 | |||||||
| chr12:55915420 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.38-11940A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55915420 | |||||||
| chr12:55915559 | T | TA | 42 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(39): Show |
66 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.38-12080dupT | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55915559 | |||||||
| chr12:55915559 | TA | T | 11 | a0001c0001t0001g0090 a0001c0001t0001g0158 a0001c0001t0001g0161 others(8): Show |
11 | HG01099.hp2 HG01515.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.38-12080delT | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55915559 | |||||||
| chr12:55915664 | G | A | 9 | a0001c0001t0007g0021 a0001c0002t0002g0002 a0001c0002t0002g0012 others(6): Show |
23 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.37+12061C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55915664 | |||||||
| chr12:55915720 | C | T | 4 | a0001c0001t0001g0195 a0001c0001t0002g0194 a0001c0001t0002g0197 others(1): Show |
4 | HG00099.hp1 HG01099.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.37+12005G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55915720 | |||||||
| chr12:55915774 | A | G | 1 | a0001c0001t0002g0231 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.37+11951T>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55915774 | |||||||
| chr12:55915826 | T | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0148 |
3 | NA18945.hp2 NA18971.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.37+11899A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55915826 | |||||||
| chr12:55915947 | T | A | 9 | a0001c0001t0007g0021 a0001c0002t0002g0002 a0001c0002t0002g0012 others(6): Show |
23 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.37+11778A>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55915947 | |||||||
| chr12:55916109 | C | T | 2 | a0001c0001t0008g0084 a0001c0001t0008g0085 |
2 | HG04228.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.37+11616G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55916109 | |||||||
| chr12:55916241 | A | G | 1 | a0001c0001t0002g0051 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.37+11484T>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55916241 | |||||||
| chr12:55916304 | T | C | 9 | a0001c0001t0007g0021 a0001c0002t0002g0002 a0001c0002t0002g0012 others(6): Show |
23 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.37+11421A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55916304 | |||||||
| chr12:55916410 | C | T | 1 | a0001c0001t0007g0021 | 2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.37+11315G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55916410 | |||||||
| chr12:55916455 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.37+11270C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55916455 | |||||||
| chr12:55916494 | A | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0086 others(3): Show |
10 | HG00544.hp2 HG02135.hp2 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.37+11231T>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55916494 | |||||||
| chr12:55916569 | G | A | 1 | a0001c0001t0004g0013 | 3 | HG03139.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.37+11156C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55916569 | |||||||
| chr12:55916759 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.37+10966A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55916759 | |||||||
| chr12:55916844 | T | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.37+10881A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55916844 | |||||||
| chr12:55917032 | G | A | 1 | a0001c0001t0002g0227 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.37+10693C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55917032 | |||||||
| chr12:55917044 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.37+10681C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55917044 | |||||||
| chr12:55917107 | T | TA | 18 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0045 others(15): Show |
28 | HG00673.hp2 HG01243.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.37+10617dupT | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55917107 | |||||||
| chr12:55917117 | T | A | 5 | a0001c0001t0002g0020 a0001c0001t0002g0223 a0001c0001t0002g0225 others(2): Show |
7 | HG00673.hp1 HG02015.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.37+10608A>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55917117 | |||||||
| chr12:55917278 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.37+10447C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55917278 | |||||||
| chr12:55917425 | C | CA | 11 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(8): Show |
11 | HG01074.hp1 HG01074.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.37+10299dupT | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55917425 | |||||||
| chr12:55917741 | C | T | 1 | a0002c0003t0001g0160 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.37+9984G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55917741 | |||||||
| chr12:55917978 | C | A | 1 | a0001c0001t0001g0127 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.37+9747G>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55917978 | |||||||
| chr12:55917982 | A | C | 9 | a0001c0001t0007g0021 a0001c0002t0002g0002 a0001c0002t0002g0012 others(6): Show |
23 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.37+9743T>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55917982 | |||||||
| chr12:55918092 | C | CT | 9 | a0001c0001t0007g0021 a0001c0002t0002g0002 a0001c0002t0002g0012 others(6): Show |
23 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.37+9632dupA | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55918092 | |||||||
| chr12:55918259 | G | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.37+9466C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55918259 | |||||||
| chr12:55918343 | G | T | 1 | a0001c0001t0002g0051 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.37+9382C>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55918343 | |||||||
| chr12:55918359 | C | G | 2 | a0001c0002t0002g0047 a0001c0002t0005g0046 |
2 | HG02145.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.37+9366G>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55918359 | |||||||
| chr12:55918442 | C | A | 29 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0029 others(26): Show |
45 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.37+9283G>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55918442 | |||||||
| chr12:55918495 | G | A | 1 | a0001c0002t0010g0050 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.37+9230C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55918495 | |||||||
| chr12:55918806 | C | T | 1 | a0001c0001t0001g0014 | 3 | NA18969.hp2 NA18990.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.37+8919G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55918806 | |||||||
| chr12:55918812 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0080 a0001c0001t0001g0140 others(1): Show |
6 | HG01255.hp2 HG01361.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.37+8913C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55918812 | |||||||
| chr12:55918858 | C | A | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.37+8867G>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55918858 | |||||||
| chr12:55919080 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.37+8645T>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55919080 | |||||||
| chr12:55919204 | A | G | 9 | a0001c0001t0007g0021 a0001c0002t0002g0002 a0001c0002t0002g0012 others(6): Show |
23 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.37+8521T>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55919204 | |||||||
| chr12:55919508 | A | G | 2 | a0001c0001t0008g0084 a0001c0001t0008g0085 |
2 | HG04228.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.37+8217T>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55919508 | |||||||
| chr12:55919883 | A | T | 1 | a0001c0001t0001g0158 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.37+7842T>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55919883 | |||||||
| chr12:55919892 | C | CA | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.37+7832dupT | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55919892 | |||||||
| chr12:55919974 | T | C | 9 | a0001c0001t0007g0021 a0001c0002t0002g0002 a0001c0002t0002g0012 others(6): Show |
23 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.37+7751A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55919974 | |||||||
| chr12:55920102 | A | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.37+7623T>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55920102 | |||||||
| chr12:55920103 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0080 a0001c0001t0001g0141 |
5 | HG01255.hp2 HG01433.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.37+7622C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55920103 | |||||||
| chr12:55920506 | T | G | 1 | a0001c0004t0001g0181 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.37+7219A>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55920506 | |||||||
| chr12:55920575 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.37+7150A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55920575 | |||||||
| chr12:55920593 | G | A | 1 | a0001c0001t0002g0227 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.37+7132C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55920593 | |||||||
| chr12:55920661 | AAAAAGAA others(33): Show |
A | 1 | a0001c0001t0002g0235 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.37+7024_37+7063del others(40): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55920661 | |||||||
| chr12:55920700 | A | T | 2 | a0001c0002t0002g0012 a0001c0002t0010g0050 |
4 | HG01109.hp1 HG02109.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.37+7025T>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55920700 | |||||||
| chr12:55921333 | A | G | 1 | a0001c0001t0001g0025 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.37+6392T>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55921333 | |||||||
| chr12:55921799 | A | C | 9 | a0001c0001t0007g0021 a0001c0002t0002g0002 a0001c0002t0002g0012 others(6): Show |
23 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.37+5926T>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55921799 | |||||||
| chr12:55922011 | C | G | 1 | a0001c0001t0001g0083 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.37+5714G>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55922011 | |||||||
| chr12:55922040 | G | A | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.37+5685C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55922040 | |||||||
| chr12:55922083 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.37+5642A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55922083 | |||||||
| chr12:55922375 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0082 |
2 | HG01952.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.37+5350G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55922375 | |||||||
| chr12:55922445 | C | CA | 10 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(7): Show |
10 | HG01433.hp2 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.37+5279dupT | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55922445 | |||||||
| chr12:55922445 | C | CAA | 17 | a0001c0001t0001g0008 a0001c0001t0001g0066 a0001c0001t0001g0071 others(14): Show |
20 | HG00323.hp1 HG00741.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.37+5278_37+5279dup others(2): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55922445 | |||||||
| chr12:55922445 | C | CAAA | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.37+5277_37+5279dup others(3): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55922445 | |||||||
| chr12:55922445 | C | CAAAA | 15 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0055 others(12): Show |
21 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.37+5276_37+5279dup others(4): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55922445 | |||||||
| chr12:55922659 | T | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0183 a0001c0001t0003g0184 |
5 | NA18952.hp2 NA18955.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.37+5066A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55922659 | |||||||
| chr12:55922661 | T | C | 9 | a0001c0001t0007g0021 a0001c0002t0002g0002 a0001c0002t0002g0012 others(6): Show |
23 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.37+5064A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55922661 | |||||||
| chr12:55922932 | A | G | 2 | a0001c0001t0001g0066 a0001c0001t0003g0065 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.37+4793T>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55922932 | |||||||
| chr12:55922934 | T | C | 4 | a0001c0001t0001g0019 a0001c0001t0001g0185 a0001c0001t0001g0186 others(1): Show |
6 | NA18948.hp2 NA18971.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.37+4791A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55922934 | |||||||
| chr12:55923235 | T | C | 2 | a0001c0001t0001g0010 a0001c0001t0003g0153 |
5 | HG00140.hp2 HG01069.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.37+4490A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55923235 | |||||||
| chr12:55923262 | T | G | 1 | a0001c0001t0001g0154 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.37+4463A>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55923262 | |||||||
| chr12:55923392 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.37+4333G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55923392 | |||||||
| chr12:55923564 | G | GA | 6 | a0001c0001t0001g0155 a0001c0001t0002g0231 a0001c0001t0002g0232 others(3): Show |
6 | HG00408.hp1 HG01978.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.37+4160dupT | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55923564 | |||||||
| chr12:55923574 | A | C | 1 | a0001c0001t0001g0052 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.37+4151T>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55923574 | |||||||
| chr12:55924196 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0003g0157 |
3 | NA18952.hp1 NA18955.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.37+3529C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55924196 | |||||||
| chr12:55924229 | C | T | 1 | a0001c0001t0002g0063 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.37+3496G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55924229 | |||||||
| chr12:55924259 | C | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.37+3466G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55924259 | |||||||
| chr12:55924374 | T | G | 9 | a0001c0001t0007g0021 a0001c0002t0002g0002 a0001c0002t0002g0012 others(6): Show |
23 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.37+3351A>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55924374 | |||||||
| chr12:55924427 | A | G | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.37+3298T>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55924427 | |||||||
| chr12:55924445 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.37+3280G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55924445 | |||||||
| chr12:55924707 | C | T | 6 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 others(3): Show |
6 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.37+3018G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55924707 | |||||||
| chr12:55924771 | G | A | 39 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0018 others(36): Show |
51 | HG00423.hp2 HG00558.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.37+2954C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55924771 | |||||||
| chr12:55924786 | C | G | 9 | a0001c0001t0007g0021 a0001c0002t0002g0002 a0001c0002t0002g0012 others(6): Show |
23 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.37+2939G>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55924786 | |||||||
| chr12:55924812 | G | C | 1 | a0001c0001t0002g0235 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.37+2913C>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55924812 | |||||||
| chr12:55924826 | G | A | 9 | a0001c0001t0007g0021 a0001c0002t0002g0002 a0001c0002t0002g0012 others(6): Show |
23 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.37+2899C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55924826 | |||||||
| chr12:55924926 | C | T | 1 | a0001c0001t0002g0051 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.37+2799G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55924926 | |||||||
| chr12:55924974 | C | T | 1 | a0001c0001t0002g0051 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.37+2751G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55924974 | |||||||
| chr12:55924990 | T | A | 7 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(4): Show |
10 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.37+2735A>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55924990 | |||||||
| chr12:55925068 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.37+2657G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55925068 | |||||||
| chr12:55925128 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.37+2597A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55925128 | |||||||
| chr12:55925316 | T | C | 1 | a0001c0001t0002g0234 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.37+2409A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55925316 | |||||||
| chr12:55925850 | A | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | HG01074.hp2 HG01496.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.37+1875T>C | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55925850 | |||||||
| chr12:55925976 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.37+1749C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55925976 | |||||||
| chr12:55926111 | T | C | 2 | a0001c0001t0009g0039 a0001c0001t0011g0193 |
3 | NA18954.hp2 NA18960.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.37+1614A>G | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55926111 | |||||||
| chr12:55926542 | G | A | 9 | a0001c0001t0007g0021 a0001c0002t0002g0002 a0001c0002t0002g0012 others(6): Show |
23 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.37+1183C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55926542 | |||||||
| chr12:55926733 | G | T | 1 | a0001c0001t0002g0051 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.37+992C>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55926733 | |||||||
| chr12:55926736 | C | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.37+989G>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55926736 | |||||||
| chr12:55926829 | G | GTGTTGTG others(34): Show |
1 | a0001c0001t0002g0235 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.37+895_37+896insGG others(39): Show |
PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55926829 | |||||||
| chr12:55926962 | G | T | 9 | a0001c0001t0007g0021 a0001c0002t0002g0002 a0001c0002t0002g0012 others(6): Show |
23 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.37+763C>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55926962 | |||||||
| chr12:55927627 | G | T | 1 | a0001c0001t0001g0045 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.37+98C>A | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55927627 | |||||||
| chr12:55927712 | G | A | 1 | a0001c0001t0001g0236 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.37+13C>T | PYM1 | ENSG00000170473.17 | transcript | ENST00000408946.7 | protein_coding | 1/2 | chr12 | 55927712 |