Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9933 |
| ensemblid | ENSG00000080608.10 |
| hgncid | 29676 |
| symbol | PUM3 |
| name | pumilio RNA binding family member 3 |
| refseq_nuc | NM_014878.5 |
| refseq_prot | NP_055693.4 |
| ensembl_nuc | ENST00000397885.3 |
| ensembl_prot | ENSP00000380982.2 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 2804152 |
| end | 2844095 |
| strand | - |
| ver | v1.2 |
| region | chr9:2804152-2844095 |
| region5000 | chr9:2799152-2849095 |
| regionname0 | PUM3_chr9_2804152_2844095 |
| regionname5000 | PUM3_chr9_2799152_2849095 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 648 | 189 | 44 | 29 | 87 | 6 | 22 | 66 | PUM3_chr9_2799152_2849095 | PUM3 | MEVKG others(643): Show |
chr9 | 2799152 | 2849095 |
| a0002 | 1/0 | 648 | 158 | 28 | 28 | 79 | 5 | 17 | 62 | PUM3_chr9_2799152_2849095 | PUM3 | MEVKG others(643): Show |
chr9 | 2799152 | 2849095 |
| a0003 | 0/0 | 648 | 31 | 1 | 5 | 23 | 1 | 1 | 19 | PUM3_chr9_2799152_2849095 | PUM3 | MEVKG others(643): Show |
chr9 | 2799152 | 2849095 |
| a0004 | 0/0 | 648 | 10 | 0 | 6 | 4 | 0 | 0 | 4 | PUM3_chr9_2799152_2849095 | PUM3 | MEVKG others(643): Show |
chr9 | 2799152 | 2849095 |
| a0005 | 0/0 | 648 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | MEVKG others(643): Show |
chr9 | 2799152 | 2849095 |
| a0006 | 0/0 | 648 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | PUM3_chr9_2799152_2849095 | PUM3 | MEVKG others(643): Show |
chr9 | 2799152 | 2849095 |
| a0007 | 0/0 | 648 | 3 | 0 | 2 | 1 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | MEVKG others(643): Show |
chr9 | 2799152 | 2849095 |
| a0008 | 0/0 | 648 | 3 | 2 | 0 | 1 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | MEVKG others(643): Show |
chr9 | 2799152 | 2849095 |
| a0009 | 0/0 | 648 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | MEVKG others(643): Show |
chr9 | 2799152 | 2849095 |
| a0010 | 0/0 | 648 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | MEVKG others(643): Show |
chr9 | 2799152 | 2849095 |
| a0011 | 0/0 | 648 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | MEVKG others(643): Show |
chr9 | 2799152 | 2849095 |
| a0012 | 0/0 | 648 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | MEVKG others(643): Show |
chr9 | 2799152 | 2849095 |
| a0013 | 0/0 | 648 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | MEVKG others(643): Show |
chr9 | 2799152 | 2849095 |
| a0014 | 0/0 | 648 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | MEVKG others(643): Show |
chr9 | 2799152 | 2849095 |
| a0015 | 0/0 | 648 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | MEVKG others(643): Show |
chr9 | 2799152 | 2849095 |
| a0016 | 0/0 | 648 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | MEVKG others(643): Show |
chr9 | 2799152 | 2849095 |
| a0017 | 0/0 | 648 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | MEVKG others(643): Show |
chr9 | 2799152 | 2849095 |
| a0018 | 0/0 | 648 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | MEVKG others(643): Show |
chr9 | 2799152 | 2849095 |
| a0019 | 0/0 | 648 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | MEVKG others(643): Show |
chr9 | 2799152 | 2849095 |
| a0020 | 0/0 | 648 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | MEVKG others(643): Show |
chr9 | 2799152 | 2849095 |
| a0021 | 0/0 | 648 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | MEVKG others(643): Show |
chr9 | 2799152 | 2849095 |
| a0022 | 0/0 | 648 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | MEVKG others(643): Show |
chr9 | 2799152 | 2849095 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1944 | 156 | 22 | 25 | 83 | 3 | 22 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 | ||
| a0001c0005 | 0/0 | 1944 | 29 | 19 | 4 | 3 | 3 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 | ||
| a0001c0010 | 0/0 | 1944 | 3 | 3 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 | ||
| a0001c0019 | 0/0 | 1944 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 | ||
| a0002c0002 | 1/0 | 1944 | 111 | 13 | 25 | 56 | 5 | 11 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 | ||
| a0002c0003 | 0/0 | 1944 | 36 | 15 | 2 | 14 | 0 | 5 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 | ||
| a0002c0007 | 0/0 | 1944 | 9 | 0 | 0 | 9 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 | ||
| a0002c0013 | 0/0 | 1944 | 2 | 0 | 1 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 | ||
| a0003c0004 | 0/0 | 1944 | 31 | 1 | 5 | 23 | 1 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 | ||
| a0004c0006 | 0/0 | 1944 | 10 | 0 | 6 | 4 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 | ||
| a0005c0008 | 0/0 | 1944 | 5 | 5 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 | ||
| a0006c0009 | 0/0 | 1944 | 4 | 0 | 0 | 4 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 | ||
| a0007c0014 | 0/0 | 1944 | 2 | 0 | 2 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 | ||
| a0007c0024 | 0/0 | 1944 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 | ||
| a0008c0012 | 0/0 | 1944 | 3 | 2 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 | ||
| a0009c0011 | 0/0 | 1944 | 3 | 3 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 | ||
| a0010c0015 | 0/0 | 1944 | 2 | 2 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 | ||
| a0011c0023 | 0/0 | 1944 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 | ||
| a0012c0028 | 0/0 | 1944 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 | ||
| a0013c0020 | 0/0 | 1944 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 | ||
| a0014c0016 | 0/0 | 1944 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 | ||
| a0015c0029 | 0/0 | 1944 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 | ||
| a0016c0022 | 0/0 | 1944 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 | ||
| a0017c0025 | 0/0 | 1944 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 | ||
| a0018c0021 | 0/0 | 1944 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 | ||
| a0019c0027 | 0/0 | 1944 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 | ||
| a0020c0026 | 0/0 | 1944 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 | ||
| a0021c0018 | 0/0 | 1944 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 | ||
| a0022c0017 | 0/0 | 1944 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | ATGGA others(1939): Show |
chr9 | 2799152 | 2849095 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2187 | 153 | 19 | 25 | 83 | 3 | 22 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0001c0001t0003 | 0/0 | 2187 | 3 | 3 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0001c0005t0001 | 0/0 | 2187 | 29 | 19 | 4 | 3 | 3 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0001c0010t0001 | 0/0 | 2187 | 3 | 3 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0001c0019t0001 | 0/0 | 2187 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0002c0002t0001 | 1/0 | 2187 | 107 | 11 | 24 | 56 | 4 | 11 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0002c0002t0002 | 0/0 | 2187 | 3 | 2 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0002c0002t0006 | 0/0 | 2187 | 1 | 0 | 0 | 0 | 1 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0002c0003t0001 | 0/0 | 2187 | 36 | 15 | 2 | 14 | 0 | 5 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0002c0007t0001 | 0/0 | 2187 | 9 | 0 | 0 | 9 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0002c0013t0001 | 0/0 | 2187 | 2 | 0 | 1 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0003c0004t0001 | 0/0 | 2187 | 31 | 1 | 5 | 23 | 1 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0004c0006t0001 | 0/0 | 2187 | 10 | 0 | 6 | 4 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0005c0008t0001 | 0/0 | 2187 | 5 | 5 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0006c0009t0001 | 0/0 | 2187 | 4 | 0 | 0 | 4 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0007c0014t0001 | 0/0 | 2187 | 2 | 0 | 2 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0007c0024t0001 | 0/0 | 2187 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0008c0012t0001 | 0/0 | 2187 | 3 | 2 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0009c0011t0001 | 0/0 | 2187 | 3 | 3 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0010c0015t0004 | 0/0 | 2187 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0010c0015t0005 | 0/0 | 2187 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0011c0023t0001 | 0/0 | 2187 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0012c0028t0001 | 0/0 | 2187 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0013c0020t0001 | 0/0 | 2187 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0014c0016t0001 | 0/0 | 2187 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0015c0029t0001 | 0/0 | 2187 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0016c0022t0001 | 0/0 | 2187 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0017c0025t0004 | 0/0 | 2187 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0018c0021t0007 | 0/0 | 2187 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0019c0027t0001 | 0/0 | 2187 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0020c0026t0001 | 0/0 | 2187 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0021c0018t0001 | 0/0 | 2187 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| a0022c0017t0001 | 0/0 | 2187 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | GGAGA others(2182): Show |
chr9 | 2799152 | 2849095 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 1 | 4 | 1 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0208 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0005t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0005t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0005t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0005t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0005t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0005t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0005t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0005t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0005t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0005t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0005t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0005t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0005t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0005t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0005t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0005t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0005t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0005t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0005t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0005t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0005t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0005t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0005t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0005t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0005t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0005t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0010t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0010t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0010t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0001c0019t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0001 | 0/0 | 23 | 4 | 6 | 8 | 1 | 4 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0008 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0024 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0002g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0002t0006g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0003t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0003t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0003t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0003t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0003t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0003t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0003t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0003t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0003t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0003t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0007t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0007t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0007t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0007t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0007t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0007t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0007t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0007t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0013t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0002c0013t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0003c0004t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0003c0004t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0003c0004t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0003c0004t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0003c0004t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0003c0004t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0003c0004t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0003c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0003c0004t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0003c0004t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0003c0004t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0003c0004t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0003c0004t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0003c0004t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0003c0004t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0003c0004t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0003c0004t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0003c0004t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0003c0004t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0003c0004t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0003c0004t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0003c0004t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0003c0004t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0004c0006t0001g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0004c0006t0001g0015 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0004c0006t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0004c0006t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0004c0006t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0004c0006t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0005c0008t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0005c0008t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0005c0008t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0006c0009t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0006c0009t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0006c0009t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0007c0014t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0007c0014t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0007c0024t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0008c0012t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0008c0012t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0008c0012t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0009c0011t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0009c0011t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0009c0011t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0010c0015t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0010c0015t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0011c0023t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0012c0028t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0013c0020t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0014c0016t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0015c0029t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0016c0022t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0017c0025t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0018c0021t0007g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0019c0027t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0020c0026t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0021c0018t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| a0022c0017t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0006 | g0051 | EUR | GBR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0104 | EUR | GBR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0114 | EUR | GBR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0200 | EUR | FIN | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0008 | EUR | FIN | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | CHS | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00408 | hp2 | a0001 | c0005 | t0001 | g0084 | EAS | CHS | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | CHS | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | CHS | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00544 | hp1 | a0003 | c0004 | t0001 | g0010 | EAS | CHS | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00558 | hp2 | a0003 | c0004 | t0001 | g0175 | EAS | CHS | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | CHS | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00673 | hp1 | a0002 | c0003 | t0001 | g0062 | EAS | CHS | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00735 | hp2 | a0002 | c0013 | t0001 | g0145 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0086 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0052 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0166 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0164 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0157 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01074 | hp2 | a0003 | c0004 | t0001 | g0169 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01099 | hp2 | a0003 | c0004 | t0001 | g0180 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01109 | hp1 | a0002 | c0003 | t0001 | g0080 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0094 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01168 | hp2 | a0003 | c0004 | t0001 | g0170 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01169 | hp2 | a0003 | c0004 | t0001 | g0171 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0250 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01243 | hp1 | a0001 | c0005 | t0001 | g0137 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01243 | hp2 | a0002 | c0002 | t0002 | g0018 | AMR | PUR | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01255 | hp1 | a0011 | c0023 | t0001 | g0284 | AMR | CLM | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0091 | AMR | CLM | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0099 | AMR | CLM | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01256 | hp2 | a0007 | c0014 | t0001 | g0119 | AMR | CLM | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01257 | hp1 | a0001 | c0005 | t0001 | g0041 | AMR | CLM | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0106 | AMR | CLM | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01258 | hp1 | a0001 | c0005 | t0001 | g0041 | AMR | CLM | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01258 | hp2 | a0007 | c0014 | t0001 | g0066 | AMR | CLM | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01346 | hp2 | a0004 | c0006 | t0001 | g0015 | AMR | CLM | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01358 | hp2 | a0004 | c0006 | t0001 | g0155 | AMR | CLM | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01496 | hp2 | a0004 | c0006 | t0001 | g0014 | AMR | CLM | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01515 | hp1 | a0001 | c0005 | t0001 | g0040 | EUR | IBS | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | IBS | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01517 | hp1 | a0001 | c0005 | t0001 | g0040 | EUR | IBS | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0044 | EUR | IBS | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0194 | AFR | ACB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01891 | hp1 | a0001 | c0005 | t0001 | g0059 | AFR | ACB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01891 | hp2 | a0002 | c0003 | t0001 | g0055 | AFR | ACB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01928 | hp1 | a0012 | c0028 | t0001 | g0128 | AMR | PEL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01928 | hp2 | a0002 | c0003 | t0001 | g0111 | AMR | PEL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01952 | hp2 | a0001 | c0005 | t0001 | g0290 | AMR | PEL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0100 | AMR | PEL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01981 | hp2 | a0004 | c0006 | t0001 | g0153 | AMR | PEL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01993 | hp2 | a0004 | c0006 | t0001 | g0014 | AMR | PEL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02015 | hp1 | a0013 | c0020 | t0001 | g0299 | EAS | KHV | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02015 | hp2 | a0002 | c0007 | t0001 | g0245 | EAS | KHV | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0158 | EAS | KHV | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02056 | hp1 | a0003 | c0004 | t0001 | g0163 | EAS | KHV | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0129 | EAS | KHV | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | KHV | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | KHV | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02129 | hp1 | a0014 | c0016 | t0001 | g0174 | EAS | KHV | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | KHV | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02145 | hp1 | a0009 | c0011 | t0001 | g0307 | AFR | ACB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0022 | AMR | PEL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0063 | AMR | PEL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | CDX | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02257 | hp1 | a0001 | c0005 | t0001 | g0073 | AFR | ACB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02257 | hp2 | a0002 | c0003 | t0001 | g0028 | AFR | ACB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02258 | hp1 | a0001 | c0005 | t0001 | g0058 | AFR | ACB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02258 | hp2 | a0005 | c0008 | t0001 | g0131 | AFR | ACB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02273 | hp1 | a0003 | c0004 | t0001 | g0032 | AMR | PEL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0022 | AMR | PEL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02280 | hp1 | a0009 | c0011 | t0001 | g0309 | AFR | ACB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0193 | AFR | ACB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0121 | AMR | PEL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0113 | AMR | PEL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02451 | hp1 | a0015 | c0029 | t0001 | g0310 | AFR | ACB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02451 | hp2 | a0005 | c0008 | t0001 | g0027 | AFR | ACB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | KHV | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | KHV | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02572 | hp1 | a0008 | c0012 | t0001 | g0167 | AFR | GWD | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02572 | hp2 | a0016 | c0022 | t0001 | g0308 | AFR | GWD | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02615 | hp2 | a0001 | c0005 | t0001 | g0074 | AFR | GWD | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02622 | hp1 | a0002 | c0002 | t0002 | g0050 | AFR | GWD | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02630 | hp1 | a0001 | c0005 | t0001 | g0069 | AFR | GWD | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02630 | hp2 | a0001 | c0005 | t0001 | g0019 | AFR | GWD | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02647 | hp1 | a0001 | c0005 | t0001 | g0070 | AFR | GWD | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02647 | hp2 | a0002 | c0003 | t0001 | g0072 | AFR | GWD | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0083 | SAS | PJL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0301 | SAS | PJL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0008 | SAS | PJL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02738 | hp1 | a0002 | c0003 | t0001 | g0182 | SAS | PJL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0023 | SAS | PJL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02809 | hp1 | a0001 | c0005 | t0001 | g0216 | AFR | GWD | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02809 | hp2 | a0005 | c0008 | t0001 | g0048 | AFR | GWD | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02818 | hp1 | a0001 | c0005 | t0001 | g0019 | AFR | GWD | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02886 | hp1 | a0002 | c0003 | t0001 | g0078 | AFR | GWD | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0053 | AFR | GWD | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02896 | hp1 | a0002 | c0003 | t0001 | g0028 | AFR | GWD | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02896 | hp2 | a0010 | c0015 | t0004 | g0056 | AFR | GWD | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02922 | hp1 | a0017 | c0025 | t0004 | g0138 | AFR | ESN | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ESN | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02965 | hp2 | a0002 | c0003 | t0001 | g0013 | AFR | ESN | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02970 | hp1 | a0001 | c0010 | t0001 | g0226 | AFR | ESN | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02970 | hp2 | a0001 | c0005 | t0001 | g0187 | AFR | ESN | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02976 | hp1 | a0001 | c0005 | t0001 | g0232 | AFR | ESN | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0120 | SAS | PJL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03041 | hp1 | a0001 | c0005 | t0001 | g0206 | AFR | GWD | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03041 | hp2 | a0001 | c0005 | t0001 | g0068 | AFR | GWD | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0103 | AFR | MSL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0195 | AFR | MSL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03130 | hp1 | a0002 | c0003 | t0001 | g0013 | AFR | ESN | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0108 | AFR | ESN | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03139 | hp1 | a0002 | c0003 | t0001 | g0144 | AFR | ESN | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03139 | hp2 | a0010 | c0015 | t0005 | g0049 | AFR | ESN | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ESN | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03209 | hp1 | a0005 | c0008 | t0001 | g0048 | AFR | MSL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03209 | hp2 | a0001 | c0005 | t0001 | g0079 | AFR | MSL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03225 | hp1 | a0001 | c0005 | t0001 | g0235 | AFR | MSL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03225 | hp2 | a0002 | c0003 | t0001 | g0151 | AFR | MSL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0181 | SAS | PJL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03453 | hp1 | a0002 | c0003 | t0001 | g0148 | AFR | MSL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03453 | hp2 | a0005 | c0008 | t0001 | g0027 | AFR | MSL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0023 | SAS | PJL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03516 | hp2 | a0018 | c0021 | t0007 | g0312 | AFR | ESN | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03540 | hp2 | a0002 | c0003 | t0001 | g0149 | AFR | GWD | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03579 | hp1 | a0001 | c0010 | t0001 | g0229 | AFR | MSL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | STU | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | STU | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03704 | hp1 | a0002 | c0003 | t0001 | g0140 | SAS | PJL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03710 | hp1 | a0002 | c0003 | t0001 | g0141 | SAS | PJL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03710 | hp2 | a0003 | c0004 | t0001 | g0173 | SAS | PJL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03831 | hp2 | a0002 | c0013 | t0001 | g0143 | SAS | BEB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | BEB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | BEB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03942 | hp1 | a0002 | c0003 | t0001 | g0142 | SAS | BEB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | BEB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG04184 | hp2 | a0002 | c0003 | t0001 | g0139 | SAS | BEB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | STU | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | STU | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18522 | hp1 | a0002 | c0002 | t0002 | g0018 | AFR | YRI | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18522 | hp2 | a0003 | c0004 | t0001 | g0311 | AFR | YRI | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CHB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18747 | hp1 | a0003 | c0004 | t0001 | g0179 | EAS | CHB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18906 | hp1 | a0009 | c0011 | t0001 | g0185 | AFR | YRI | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18906 | hp2 | a0001 | c0005 | t0001 | g0071 | AFR | YRI | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18940 | hp1 | a0002 | c0003 | t0001 | g0064 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18941 | hp1 | a0003 | c0004 | t0001 | g0029 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18943 | hp2 | a0002 | c0003 | t0001 | g0042 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18945 | hp2 | a0003 | c0004 | t0001 | g0033 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18947 | hp2 | a0006 | c0009 | t0001 | g0306 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18948 | hp2 | a0004 | c0006 | t0001 | g0015 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18950 | hp1 | a0019 | c0027 | t0001 | g0127 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18951 | hp1 | a0008 | c0012 | t0001 | g0093 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18951 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18952 | hp1 | a0001 | c0005 | t0001 | g0295 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18953 | hp1 | a0003 | c0004 | t0001 | g0176 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18959 | hp2 | a0002 | c0007 | t0001 | g0130 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18960 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18964 | hp1 | a0007 | c0024 | t0001 | g0125 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18965 | hp1 | a0001 | c0019 | t0001 | g0254 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18968 | hp2 | a0002 | c0007 | t0001 | g0244 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18970 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18971 | hp1 | a0002 | c0003 | t0001 | g0011 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18972 | hp1 | a0002 | c0007 | t0001 | g0184 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18972 | hp2 | a0002 | c0003 | t0001 | g0165 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18973 | hp1 | a0003 | c0004 | t0001 | g0178 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18975 | hp1 | a0020 | c0026 | t0001 | g0246 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18975 | hp2 | a0004 | c0006 | t0001 | g0015 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18978 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18979 | hp1 | a0003 | c0004 | t0001 | g0029 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18982 | hp2 | a0002 | c0007 | t0001 | g0039 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18984 | hp1 | a0003 | c0004 | t0001 | g0010 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18985 | hp2 | a0002 | c0007 | t0001 | g0242 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18987 | hp1 | a0006 | c0009 | t0001 | g0047 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18988 | hp2 | a0003 | c0004 | t0001 | g0010 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18989 | hp1 | a0002 | c0007 | t0001 | g0241 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18992 | hp2 | a0003 | c0004 | t0001 | g0010 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0243 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18995 | hp1 | a0001 | c0005 | t0001 | g0253 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18997 | hp1 | a0006 | c0009 | t0001 | g0249 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18997 | hp2 | a0002 | c0007 | t0001 | g0238 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA18999 | hp2 | a0004 | c0006 | t0001 | g0154 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19003 | hp1 | a0004 | c0006 | t0001 | g0156 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19004 | hp1 | a0003 | c0004 | t0001 | g0030 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19006 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19007 | hp2 | a0006 | c0009 | t0001 | g0047 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | LWK | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19043 | hp2 | a0001 | c0005 | t0001 | g0060 | AFR | LWK | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19054 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19055 | hp1 | a0002 | c0003 | t0001 | g0011 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19056 | hp2 | a0021 | c0018 | t0001 | g0196 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19060 | hp2 | a0003 | c0004 | t0001 | g0161 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19063 | hp2 | a0003 | c0004 | t0001 | g0030 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19065 | hp2 | a0002 | c0007 | t0001 | g0039 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19067 | hp1 | a0003 | c0004 | t0001 | g0160 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19070 | hp2 | a0003 | c0004 | t0001 | g0032 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19072 | hp1 | a0002 | c0003 | t0001 | g0011 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19072 | hp2 | a0003 | c0004 | t0001 | g0159 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19077 | hp1 | a0003 | c0004 | t0001 | g0177 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19078 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19080 | hp2 | a0003 | c0004 | t0001 | g0031 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19081 | hp1 | a0003 | c0004 | t0001 | g0033 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19087 | hp1 | a0003 | c0004 | t0001 | g0031 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19088 | hp2 | a0002 | c0003 | t0001 | g0042 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19091 | hp2 | a0003 | c0004 | t0001 | g0162 | EAS | JPT | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19240 | hp1 | a0022 | c0017 | t0001 | g0168 | AFR | YRI | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | YRI | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA20129 | hp1 | a0002 | c0003 | t0001 | g0150 | AFR | ASW | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA20129 | hp2 | a0002 | c0003 | t0001 | g0147 | AFR | ASW | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA20805 | hp1 | a0003 | c0004 | t0001 | g0172 | EUR | TSI | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA20805 | hp2 | a0001 | c0005 | t0001 | g0061 | EUR | TSI | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0109 | SAS | GIH | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | GIH | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01123 | hp1 | a0004 | c0006 | t0001 | g0014 | AMR | CLM | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02109 | hp1 | a0002 | c0003 | t0001 | g0013 | AFR | ACB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02109 | hp2 | a0008 | c0012 | t0001 | g0088 | AFR | ACB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0077 | AFR | ACB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0117 | AFR | ACB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG02559 | hp2 | a0002 | c0003 | t0001 | g0146 | AFR | ACB | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03471 | hp1 | a0001 | c0010 | t0001 | g0224 | AFR | MSL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG03471 | hp2 | a0001 | c0005 | t0001 | g0075 | AFR | MSL | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | USA | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0054 | AFR | USA | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | LWK | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| NA21309 | hp2 | a0001 | c0005 | t0001 | g0057 | AFR | LWK | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0208 | REF | REF | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0024 | REF | REF | PUM3_chr9_2799152_2849095 | PUM3 | chr9 | 2799152 | 2849095 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:2807875 | C | T | 1 | a0018 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.1753G>A | p.Val585Ile | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/18 | 1814/2187 | 1753/1947 | 585/648 | chr9 | 2807875 | |||
| chr9:2811522 | T | A | 3 | a0009 a0015 a0016 |
5 | HG02145.hp1 HG02280.hp1 HG02451.hp1 others(2): Show |
missense_variant | MODERATE | c.1474A>T | p.Ser492Cys | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 15/18 | 1535/2187 | 1474/1947 | 492/648 | chr9 | 2811522 | |||
| chr9:2811557 | C | T | 1 | a0006 | 4 | NA18947.hp2 NA18987.hp1 NA18997.hp1 others(1): Show |
missense_variant | MODERATE | c.1439G>A | p.Arg480Gln | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 15/18 | 1500/2187 | 1439/1947 | 480/648 | chr9 | 2811557 | |||
| chr9:2811570 | C | T | 1 | a0013 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.1426G>A | p.Glu476Lys | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 15/18 | 1487/2187 | 1426/1947 | 476/648 | chr9 | 2811570 | |||
| chr9:2812337 | A | G | 1 | a0021 | 1 | NA19056.hp2 | missense_variant | MODERATE | c.1295T>C | p.Ile432Thr | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 14/18 | 1356/2187 | 1295/1947 | 432/648 | chr9 | 2812337 | |||
| chr9:2820046 | G | C | 1 | a0004 | 10 | HG01123.hp1 HG01346.hp2 HG01358.hp2 others(7): Show |
missense_variant | MODERATE | c.1241C>G | p.Thr414Ser | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/18 | 1302/2187 | 1241/1947 | 414/648 | chr9 | 2820046 | |||
| chr9:2820052 | T | C | 1 | a0007 | 2 | HG01256.hp2 HG01258.hp2 |
missense_variant | MODERATE | c.1235A>G | p.Asp412Gly | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/18 | 1296/2187 | 1235/1947 | 412/648 | chr9 | 2820052 | |||
| chr9:2820053 | C | T | 1 | a0007 | 1 | NA18964.hp1 | missense_variant | MODERATE | c.1234G>A | p.Asp412Asn | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/18 | 1295/2187 | 1234/1947 | 412/648 | chr9 | 2820053 | |||
| chr9:2824722 | G | C | 1 | a0016 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.1129C>G | p.Pro377Ala | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 11/18 | 1190/2187 | 1129/1947 | 377/648 | chr9 | 2824722 | |||
| chr9:2827074 | G | A | 1 | a0011 | 1 | HG01255.hp1 | missense_variant&splice_region_variant | MODERATE | c.1034C>T | p.Ser345Leu | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/18 | 1095/2187 | 1034/1947 | 345/648 | chr9 | 2827074 | |||
| chr9:2828742 | C | A | 4 | a0003 a0008 a0014 others(1): Show |
36 | HG00544.hp1 HG00558.hp2 HG01074.hp2 others(33): Show |
missense_variant | MODERATE | c.889G>T | p.Val297Leu | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 9/18 | 950/2187 | 889/1947 | 297/648 | chr9 | 2828742 | |||
| chr9:2828765 | C | G | 16 | a0001 a0003 a0004 others(13): Show |
254 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(251): Show |
missense_variant | MODERATE | c.866G>C | p.Arg289Pro | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 9/18 | 927/2187 | 866/1947 | 289/648 | chr9 | 2828765 | |||
| chr9:2828767 | G | C | 1 | a0010 | 2 | HG02896.hp2 HG03139.hp2 |
missense_variant | MODERATE | c.864C>G | p.His288Gln | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 9/18 | 925/2187 | 864/1947 | 288/648 | chr9 | 2828767 | |||
| chr9:2829836 | T | C | 1 | a0005 | 5 | HG02258.hp2 HG02451.hp2 HG02809.hp2 others(2): Show |
missense_variant | MODERATE | c.790A>G | p.Ile264Val | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 8/18 | 851/2187 | 790/1947 | 264/648 | chr9 | 2829836 | |||
| chr9:2829857 | A | T | 1 | a0022 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.769T>A | p.Tyr257Asn | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 8/18 | 830/2187 | 769/1947 | 257/648 | chr9 | 2829857 | |||
| chr9:2834101 | T | C | 1 | a0017 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.370A>G | p.Arg124Gly | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 4/18 | 431/2187 | 370/1947 | 124/648 | chr9 | 2834101 | |||
| chr9:2837233 | G | C | 1 | a0020 | 1 | NA18975.hp1 | missense_variant | MODERATE | c.251C>G | p.Pro84Arg | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/18 | 312/2187 | 251/1947 | 84/648 | chr9 | 2837233 | |||
| chr9:2837280 | G | C | 1 | a0019 | 1 | NA18950.hp1 | missense_variant | MODERATE | c.204C>G | p.Phe68Leu | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/18 | 265/2187 | 204/1947 | 68/648 | chr9 | 2837280 | |||
| chr9:2837281 | A | C | 1 | a0014 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.203T>G | p.Phe68Cys | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/18 | 264/2187 | 203/1947 | 68/648 | chr9 | 2837281 | |||
| chr9:2837344 | T | A | 1 | a0012 | 1 | HG01928.hp1 | missense_variant | MODERATE | c.140A>T | p.Lys47Ile | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/18 | 201/2187 | 140/1947 | 47/648 | chr9 | 2837344 | |||
| chr9:2837369 | T | G | 1 | a0015 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.115A>C | p.Lys39Gln | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/18 | 176/2187 | 115/1947 | 39/648 | chr9 | 2837369 | |||
| chr9:2838470 | C | T | 2 | a0003 a0014 |
32 | HG00544.hp1 HG00558.hp2 HG01074.hp2 others(29): Show |
missense_variant | MODERATE | c.38G>A | p.Ser13Asn | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 2/18 | 99/2187 | 38/1947 | 13/648 | chr9 | 2838470 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:2804393 | A | G | 4 | a0001c0010 a0002c0003 a0002c0013 others(1): Show |
42 | HG00673.hp1 HG00735.hp2 HG01109.hp1 others(39): Show |
synonymous_variant | LOW | c.1885T>C | p.Leu629Leu | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 18/18 | 1946/2187 | 1885/1947 | 629/648 | chr9 | 2804393 | |||
| chr9:2811505 | G | A | 9 | a0001c0001 a0001c0010 a0001c0019 others(6): Show |
183 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(180): Show |
synonymous_variant | LOW | c.1491C>T | p.His497His | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 15/18 | 1552/2187 | 1491/1947 | 497/648 | chr9 | 2811505 | |||
| chr9:2811574 | A | G | 1 | a0001c0019 | 1 | NA18965.hp1 | synonymous_variant | LOW | c.1422T>C | p.Asp474Asp | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 15/18 | 1483/2187 | 1422/1947 | 474/648 | chr9 | 2811574 | |||
| chr9:2834072 | G | A | 1 | a0007c0024 | 1 | NA18964.hp1 | synonymous_variant | LOW | c.399C>T | p.Asp133Asp | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 4/18 | 460/2187 | 399/1947 | 133/648 | chr9 | 2834072 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:2804168 | T | C | 2 | a0010c0015t0004 a0017c0025t0004 |
2 | HG02896.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*163A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 18/18 | 163 | chr9 | 2804168 | ||||||
| chr9:2804272 | T | C | 2 | a0001c0001t0003 a0010c0015t0005 |
4 | HG01884.hp2 HG02280.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*59A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 18/18 | 59 | chr9 | 2804272 | ||||||
| chr9:2844056 | G | T | 1 | a0002c0002t0006 | 1 | HG00099.hp1 | 5_prime_UTR_variant | MODIFIER | c.-22C>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/18 | 5549 | chr9 | 2844056 | ||||||
| chr9:2844059 | C | T | 1 | a0002c0002t0002 | 3 | HG01243.hp2 HG02622.hp1 NA18522.hp1 |
5_prime_UTR_variant | MODIFIER | c.-25G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/18 | 5552 | chr9 | 2844059 | ||||||
| chr9:2844064 | C | T | 1 | a0010c0015t0005 | 1 | HG03139.hp2 | 5_prime_UTR_variant | MODIFIER | c.-30G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/18 | 5557 | chr9 | 2844064 | ||||||
| chr9:2844077 | G | A | 1 | a0018c0021t0007 | 1 | HG03516.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-43C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/18 | chr9 | 2844077 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:2804649 | G | A | 3 | a0001c0005t0001g0057 a0001c0005t0001g0058 a0001c0005t0001g0059 |
3 | HG01891.hp1 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1815-186C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2804649 | |||||||
| chr9:2804740 | C | T | 2 | a0008c0012t0001g0167 a0022c0017t0001g0168 |
2 | HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1815-277G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2804740 | |||||||
| chr9:2804821 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1815-358T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2804821 | |||||||
| chr9:2804918 | C | G | 1 | a0022c0017t0001g0168 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1815-455G>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2804918 | |||||||
| chr9:2804977 | T | C | 10 | a0001c0005t0001g0019 a0001c0005t0001g0060 a0002c0007t0001g0039 others(7): Show |
12 | HG02015.hp2 HG02630.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.1815-514A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2804977 | |||||||
| chr9:2804990 | C | T | 2 | a0001c0001t0001g0301 a0001c0001t0001g0304 |
2 | HG02602.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1815-527G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2804990 | |||||||
| chr9:2805048 | G | T | 8 | a0005c0008t0001g0027 a0005c0008t0001g0048 a0005c0008t0001g0131 others(5): Show |
10 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1815-585C>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2805048 | |||||||
| chr9:2805228 | G | C | 1 | a0018c0021t0007g0312 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1815-765C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2805228 | |||||||
| chr9:2805409 | C | G | 28 | a0002c0002t0001g0243 a0003c0004t0001g0010 a0003c0004t0001g0029 others(25): Show |
36 | HG00544.hp1 HG00558.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.1815-946G>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2805409 | |||||||
| chr9:2805552 | G | A | 2 | a0001c0001t0001g0256 a0001c0001t0001g0262 |
2 | HG01496.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.1815-1089C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2805552 | |||||||
| chr9:2805719 | G | A | 1 | a0003c0004t0001g0311 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1815-1256C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2805719 | |||||||
| chr9:2805787 | A | G | 2 | a0001c0005t0001g0019 a0001c0005t0001g0060 |
3 | HG02630.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1815-1324T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2805787 | |||||||
| chr9:2805826 | A | G | 2 | a0007c0014t0001g0066 a0007c0014t0001g0119 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1815-1363T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2805826 | |||||||
| chr9:2805829 | A | G | 6 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0205 others(3): Show |
9 | HG00642.hp2 HG01169.hp1 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.1815-1366T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2805829 | |||||||
| chr9:2805946 | C | T | 3 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0278 |
3 | HG02132.hp2 NA19009.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1815-1483G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2805946 | |||||||
| chr9:2805972 | A | G | 6 | a0001c0001t0001g0046 a0001c0001t0001g0259 a0001c0001t0001g0285 others(3): Show |
7 | NA18981.hp1 NA18994.hp2 NA19004.hp2 others(4): Show |
intron_variant | MODIFIER | c.1815-1509T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2805972 | |||||||
| chr9:2805998 | A | G | 6 | a0001c0001t0001g0046 a0001c0001t0001g0259 a0001c0001t0001g0285 others(3): Show |
7 | NA18981.hp1 NA18994.hp2 NA19004.hp2 others(4): Show |
intron_variant | MODIFIER | c.1815-1535T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2805998 | |||||||
| chr9:2806144 | C | T | 1 | a0002c0007t0001g0241 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1814+1670G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2806144 | |||||||
| chr9:2806291 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1814+1523A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2806291 | |||||||
| chr9:2806426 | G | A | 1 | a0002c0002t0001g0021 | 2 | NA18957.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1814+1388C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2806426 | |||||||
| chr9:2806448 | A | C | 8 | a0001c0005t0001g0019 a0001c0005t0001g0060 a0001c0005t0001g0079 others(5): Show |
11 | HG02258.hp2 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1814+1366T>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2806448 | |||||||
| chr9:2806470 | AGATT | A | 5 | a0009c0011t0001g0185 a0009c0011t0001g0307 a0009c0011t0001g0309 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1814+1340_1814+134 others(8): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2806470 | |||||||
| chr9:2806990 | C | T | 1 | a0010c0015t0004g0056 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1814+824G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2806990 | |||||||
| chr9:2807056 | A | T | 2 | a0001c0001t0001g0303 a0001c0001t0001g0305 |
2 | HG03834.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1814+758T>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2807056 | |||||||
| chr9:2807174 | C | T | 1 | a0002c0002t0001g0099 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1814+640G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2807174 | |||||||
| chr9:2807211 | A | C | 1 | a0001c0005t0001g0061 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1814+603T>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2807211 | |||||||
| chr9:2807212 | A | T | 1 | a0001c0005t0001g0061 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1814+602T>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2807212 | |||||||
| chr9:2807247 | G | A | 2 | a0001c0001t0001g0188 a0001c0001t0001g0191 |
2 | HG00673.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.1814+567C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2807247 | |||||||
| chr9:2807597 | T | G | 1 | a0004c0006t0001g0153 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1814+217A>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2807597 | |||||||
| chr9:2807600 | C | CA | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(232): Show |
330 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.1814+213dupT | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2807600 | |||||||
| chr9:2807600 | C | CAA | 38 | a0001c0001t0001g0124 a0001c0001t0001g0258 a0001c0001t0001g0260 others(35): Show |
42 | HG00280.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1814+212_1814+213d others(4): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2807600 | |||||||
| chr9:2807600 | CA | C | 7 | a0003c0004t0001g0162 a0003c0004t0001g0177 a0009c0011t0001g0185 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1814+213delT | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2807600 | |||||||
| chr9:2807627 | T | C | 2 | a0003c0004t0001g0161 a0003c0004t0001g0179 |
2 | NA18747.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1814+187A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2807627 | |||||||
| chr9:2807718 | C | T | 7 | a0008c0012t0001g0167 a0009c0011t0001g0185 a0009c0011t0001g0307 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1814+96G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 17/17 | chr9 | 2807718 | |||||||
| chr9:2807924 | T | G | 1 | a0017c0025t0004g0138 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1724-20A>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 16/17 | chr9 | 2807924 | |||||||
| chr9:2807983 | T | A | 1 | a0002c0003t0001g0142 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1724-79A>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 16/17 | chr9 | 2807983 | |||||||
| chr9:2808159 | A | T | 1 | a0002c0003t0001g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1724-255T>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 16/17 | chr9 | 2808159 | |||||||
| chr9:2808275 | G | T | 1 | a0002c0002t0001g0108 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1724-371C>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 16/17 | chr9 | 2808275 | |||||||
| chr9:2808536 | G | C | 28 | a0002c0002t0001g0243 a0003c0004t0001g0010 a0003c0004t0001g0029 others(25): Show |
36 | HG00544.hp1 HG00558.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.1724-632C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 16/17 | chr9 | 2808536 | |||||||
| chr9:2808667 | A | C | 1 | a0003c0004t0001g0180 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1724-763T>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 16/17 | chr9 | 2808667 | |||||||
| chr9:2808733 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1724-829T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 16/17 | chr9 | 2808733 | |||||||
| chr9:2809010 | T | C | 5 | a0005c0008t0001g0027 a0005c0008t0001g0048 a0005c0008t0001g0131 others(2): Show |
7 | HG02258.hp2 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1724-1106A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 16/17 | chr9 | 2809010 | |||||||
| chr9:2809060 | T | A | 26 | a0002c0002t0001g0243 a0003c0004t0001g0010 a0003c0004t0001g0029 others(23): Show |
34 | HG00544.hp1 HG00558.hp2 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.1724-1156A>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 16/17 | chr9 | 2809060 | |||||||
| chr9:2809203 | A | G | 3 | a0002c0003t0001g0028 a0002c0003t0001g0146 a0002c0003t0001g0151 |
4 | HG02257.hp2 HG02559.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1723+1141T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 16/17 | chr9 | 2809203 | |||||||
| chr9:2809260 | G | C | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(111): Show |
155 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.1723+1084C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 16/17 | chr9 | 2809260 | |||||||
| chr9:2809457 | T | C | 1 | a0002c0002t0001g0112 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1723+887A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 16/17 | chr9 | 2809457 | |||||||
| chr9:2809537 | T | C | 2 | a0001c0001t0001g0263 a0001c0001t0001g0268 |
2 | NA18939.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1723+807A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 16/17 | chr9 | 2809537 | |||||||
| chr9:2809548 | A | C | 225 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(222): Show |
292 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(289): Show |
intron_variant | MODIFIER | c.1723+796T>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 16/17 | chr9 | 2809548 | |||||||
| chr9:2809736 | G | C | 2 | a0008c0012t0001g0167 a0022c0017t0001g0168 |
2 | HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1723+608C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 16/17 | chr9 | 2809736 | |||||||
| chr9:2809902 | G | A | 1 | a0002c0003t0001g0144 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1723+442C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 16/17 | chr9 | 2809902 | |||||||
| chr9:2810039 | T | C | 1 | a0001c0005t0001g0071 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1723+305A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 16/17 | chr9 | 2810039 | |||||||
| chr9:2810117 | C | CG | 31 | a0001c0001t0001g0263 a0001c0005t0001g0057 a0001c0005t0001g0058 others(28): Show |
39 | HG00544.hp1 HG00558.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.1723+226dupC | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 16/17 | chr9 | 2810117 | |||||||
| chr9:2810142 | T | A | 1 | a0001c0001t0001g0269 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1723+202A>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 16/17 | chr9 | 2810142 | |||||||
| chr9:2810188 | C | T | 1 | a0002c0002t0001g0120 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1723+156G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 16/17 | chr9 | 2810188 | |||||||
| chr9:2810326 | T | A | 5 | a0001c0005t0001g0061 a0002c0002t0001g0008 a0002c0002t0001g0023 others(2): Show |
9 | HG00099.hp2 HG00280.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.1723+18A>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 16/17 | chr9 | 2810326 | |||||||
| chr9:2810443 | C | A | 26 | a0002c0002t0001g0243 a0003c0004t0001g0010 a0003c0004t0001g0029 others(23): Show |
34 | HG00544.hp1 HG00558.hp2 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.1636-12G>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 15/17 | chr9 | 2810443 | |||||||
| chr9:2810505 | T | A | 31 | a0002c0002t0001g0243 a0003c0004t0001g0010 a0003c0004t0001g0029 others(28): Show |
41 | HG00544.hp1 HG00558.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.1636-74A>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 15/17 | chr9 | 2810505 | |||||||
| chr9:2810788 | G | T | 1 | a0001c0001t0001g0183 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1636-357C>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 15/17 | chr9 | 2810788 | |||||||
| chr9:2810854 | G | T | 1 | a0002c0002t0001g0109 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1636-423C>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 15/17 | chr9 | 2810854 | |||||||
| chr9:2810870 | C | T | 1 | a0008c0012t0001g0088 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1636-439G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 15/17 | chr9 | 2810870 | |||||||
| chr9:2810915 | G | T | 2 | a0008c0012t0001g0167 a0022c0017t0001g0168 |
2 | HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1635+446C>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 15/17 | chr9 | 2810915 | |||||||
| chr9:2810928 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1635+433G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 15/17 | chr9 | 2810928 | |||||||
| chr9:2811059 | G | C | 1 | a0001c0001t0001g0265 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1635+302C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 15/17 | chr9 | 2811059 | |||||||
| chr9:2811201 | A | G | 4 | a0001c0005t0001g0068 a0001c0005t0001g0070 a0010c0015t0004g0056 others(1): Show |
4 | HG02647.hp1 HG02896.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1635+160T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 15/17 | chr9 | 2811201 | |||||||
| chr9:2811298 | G | A | 1 | a0003c0004t0001g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1635+63C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 15/17 | chr9 | 2811298 | |||||||
| chr9:2811624 | C | T | 2 | a0008c0012t0001g0167 a0022c0017t0001g0168 |
2 | HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1413-41G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 14/17 | chr9 | 2811624 | |||||||
| chr9:2811731 | A | G | 45 | a0001c0005t0001g0019 a0001c0005t0001g0057 a0001c0005t0001g0058 others(42): Show |
56 | HG00544.hp1 HG00558.hp2 HG01074.hp2 others(53): Show |
intron_variant | MODIFIER | c.1413-148T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 14/17 | chr9 | 2811731 | |||||||
| chr9:2811732 | A | T | 1 | a0001c0005t0001g0216 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1413-149T>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 14/17 | chr9 | 2811732 | |||||||
| chr9:2811737 | T | C | 4 | a0002c0003t0001g0013 a0002c0003t0001g0072 a0002c0003t0001g0147 others(1): Show |
6 | HG02109.hp1 HG02647.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1413-154A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 14/17 | chr9 | 2811737 | |||||||
| chr9:2811803 | C | G | 6 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0205 others(3): Show |
9 | HG00642.hp2 HG01169.hp1 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.1413-220G>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 14/17 | chr9 | 2811803 | |||||||
| chr9:2811831 | G | C | 1 | a0001c0001t0003g0193 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1413-248C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 14/17 | chr9 | 2811831 | |||||||
| chr9:2811840 | C | CA | 53 | a0001c0001t0001g0186 a0001c0001t0001g0191 a0001c0001t0001g0202 others(50): Show |
64 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1413-258dupT | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 14/17 | chr9 | 2811840 | |||||||
| chr9:2811840 | C | CAA | 6 | a0001c0005t0001g0057 a0001c0005t0001g0058 a0001c0005t0001g0059 others(3): Show |
6 | HG01099.hp2 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1413-259_1413-258d others(4): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 14/17 | chr9 | 2811840 | |||||||
| chr9:2811840 | CA | C | 6 | a0001c0001t0001g0272 a0009c0011t0001g0185 a0009c0011t0001g0307 others(3): Show |
6 | HG02080.hp2 HG02145.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1413-258delT | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 14/17 | chr9 | 2811840 | |||||||
| chr9:2811924 | T | C | 1 | a0017c0025t0004g0138 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1412+296A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 14/17 | chr9 | 2811924 | |||||||
| chr9:2812036 | G | A | 2 | a0001c0001t0001g0303 a0001c0001t0001g0305 |
2 | HG03834.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1412+184C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 14/17 | chr9 | 2812036 | |||||||
| chr9:2812125 | G | C | 1 | a0002c0003t0001g0078 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1412+95C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 14/17 | chr9 | 2812125 | |||||||
| chr9:2812127 | G | C | 4 | a0002c0003t0001g0013 a0002c0003t0001g0072 a0002c0003t0001g0147 others(1): Show |
6 | HG02109.hp1 HG02647.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1412+93C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 14/17 | chr9 | 2812127 | |||||||
| chr9:2812139 | G | A | 1 | a0002c0002t0001g0181 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1412+81C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 14/17 | chr9 | 2812139 | |||||||
| chr9:2812200 | G | A | 2 | a0010c0015t0004g0056 a0010c0015t0005g0049 |
2 | HG02896.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1412+20C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 14/17 | chr9 | 2812200 | |||||||
| chr9:2812211 | T | C | 5 | a0001c0005t0001g0057 a0001c0005t0001g0058 a0001c0005t0001g0059 others(2): Show |
5 | HG01891.hp1 HG02258.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1412+9A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 14/17 | chr9 | 2812211 | |||||||
| chr9:2812374 | T | C | 1 | a0002c0002t0001g0106 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1270-12A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2812374 | |||||||
| chr9:2812425 | G | A | 1 | a0018c0021t0007g0312 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1270-63C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2812425 | |||||||
| chr9:2812457 | T | A | 1 | a0002c0002t0001g0181 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1270-95A>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2812457 | |||||||
| chr9:2812678 | A | T | 5 | a0001c0005t0001g0057 a0001c0005t0001g0058 a0001c0005t0001g0059 others(2): Show |
5 | HG01891.hp1 HG02258.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1270-316T>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2812678 | |||||||
| chr9:2812842 | T | G | 1 | a0005c0008t0001g0131 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1270-480A>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2812842 | |||||||
| chr9:2812859 | G | C | 2 | a0003c0004t0001g0311 a0008c0012t0001g0088 |
2 | HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1270-497C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2812859 | |||||||
| chr9:2812870 | T | A | 4 | a0001c0005t0001g0040 a0001c0005t0001g0041 a0002c0002t0002g0018 others(1): Show |
7 | HG01243.hp2 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1270-508A>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2812870 | |||||||
| chr9:2812943 | T | A | 2 | a0008c0012t0001g0167 a0022c0017t0001g0168 |
2 | HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1270-581A>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2812943 | |||||||
| chr9:2813028 | T | C | 2 | a0010c0015t0004g0056 a0010c0015t0005g0049 |
2 | HG02896.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1270-666A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2813028 | |||||||
| chr9:2813410 | C | G | 1 | a0001c0001t0001g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1270-1048G>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2813410 | |||||||
| chr9:2813439 | G | A | 2 | a0002c0003t0001g0139 a0002c0003t0001g0142 |
2 | HG03942.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1270-1077C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2813439 | |||||||
| chr9:2813726 | C | A | 1 | a0001c0005t0001g0084 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1270-1364G>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2813726 | |||||||
| chr9:2813773 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1270-1411G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2813773 | |||||||
| chr9:2813994 | A | G | 1 | a0002c0002t0001g0102 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1270-1632T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2813994 | |||||||
| chr9:2814057 | T | TCTAACCA others(194): Show |
2 | a0008c0012t0001g0167 a0022c0017t0001g0168 |
2 | HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1270-1696_1270-169 others(205): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2814057 | |||||||
| chr9:2814057 | T | TCTAACCA others(192): Show |
1 | a0001c0001t0001g0132 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1270-1696_1270-169 others(203): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2814057 | |||||||
| chr9:2814057 | T | TCTAACCA others(193): Show |
171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(168): Show |
224 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.1270-1696_1270-169 others(204): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2814057 | |||||||
| chr9:2814057 | T | TCTAACCA others(194): Show |
2 | a0010c0015t0004g0056 a0010c0015t0005g0049 |
2 | HG02896.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1270-1696_1270-169 others(205): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2814057 | |||||||
| chr9:2814057 | T | TCTAACCA others(194): Show |
34 | a0002c0002t0001g0243 a0002c0007t0001g0238 a0003c0004t0001g0010 others(31): Show |
44 | HG00544.hp1 HG00558.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.1270-1696_1270-169 others(205): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2814057 | |||||||
| chr9:2814057 | T | TCTAACCA others(195): Show |
8 | a0001c0005t0001g0019 a0001c0005t0001g0057 a0001c0005t0001g0058 others(5): Show |
9 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1270-1696_1270-169 others(206): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2814057 | |||||||
| chr9:2814214 | A | AT | 24 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0038 others(21): Show |
30 | HG00639.hp2 HG01169.hp1 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.1270-1853dupA | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2814214 | |||||||
| chr9:2814245 | T | A | 1 | a0001c0001t0001g0209 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1270-1883A>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2814245 | |||||||
| chr9:2814431 | G | A | 2 | a0008c0012t0001g0167 a0022c0017t0001g0168 |
2 | HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1270-2069C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2814431 | |||||||
| chr9:2814610 | C | A | 1 | a0002c0003t0001g0072 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1270-2248G>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2814610 | |||||||
| chr9:2814615 | A | T | 193 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(190): Show |
250 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(247): Show |
intron_variant | MODIFIER | c.1270-2253T>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2814615 | |||||||
| chr9:2814717 | C | A | 7 | a0001c0005t0001g0079 a0005c0008t0001g0027 a0005c0008t0001g0048 others(4): Show |
9 | HG02258.hp2 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1270-2355G>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2814717 | |||||||
| chr9:2814744 | G | A | 1 | a0003c0004t0001g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1270-2382C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2814744 | |||||||
| chr9:2814769 | AAT | A | 13 | a0001c0005t0001g0057 a0001c0005t0001g0058 a0001c0005t0001g0059 others(10): Show |
15 | HG01891.hp1 HG02258.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1270-2409_1270-240 others(6): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2814769 | |||||||
| chr9:2814777 | A | C | 2 | a0010c0015t0004g0056 a0010c0015t0005g0049 |
2 | HG02896.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1270-2415T>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2814777 | |||||||
| chr9:2814809 | C | A | 15 | a0001c0005t0001g0019 a0001c0005t0001g0057 a0001c0005t0001g0058 others(12): Show |
18 | HG01891.hp1 HG02258.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1270-2447G>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2814809 | |||||||
| chr9:2814820 | C | G | 1 | a0001c0001t0001g0281 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1270-2458G>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2814820 | |||||||
| chr9:2814840 | T | C | 46 | a0001c0005t0001g0019 a0001c0005t0001g0057 a0001c0005t0001g0058 others(43): Show |
57 | HG00544.hp1 HG00558.hp2 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.1270-2478A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2814840 | |||||||
| chr9:2814977 | C | T | 6 | a0001c0005t0001g0057 a0001c0005t0001g0058 a0001c0005t0001g0059 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1270-2615G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2814977 | |||||||
| chr9:2815042 | A | G | 1 | a0018c0021t0007g0312 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1270-2680T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2815042 | |||||||
| chr9:2815103 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1270-2741A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2815103 | |||||||
| chr9:2815335 | A | G | 32 | a0001c0005t0001g0084 a0002c0002t0001g0243 a0003c0004t0001g0010 others(29): Show |
40 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.1270-2973T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2815335 | |||||||
| chr9:2815417 | A | G | 1 | a0001c0001t0001g0263 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1270-3055T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2815417 | |||||||
| chr9:2815440 | A | G | 47 | a0001c0005t0001g0019 a0001c0005t0001g0057 a0001c0005t0001g0058 others(44): Show |
58 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.1270-3078T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2815440 | |||||||
| chr9:2815483 | T | G | 1 | a0001c0005t0001g0206 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1270-3121A>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2815483 | |||||||
| chr9:2815496 | T | A | 6 | a0004c0006t0001g0014 a0004c0006t0001g0015 a0004c0006t0001g0153 others(3): Show |
10 | HG01123.hp1 HG01346.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.1270-3134A>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2815496 | |||||||
| chr9:2815542 | T | C | 2 | a0001c0001t0001g0210 a0001c0001t0001g0266 |
2 | HG03688.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1270-3180A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2815542 | |||||||
| chr9:2815601 | C | T | 46 | a0001c0005t0001g0019 a0001c0005t0001g0057 a0001c0005t0001g0058 others(43): Show |
57 | HG00544.hp1 HG00558.hp2 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.1270-3239G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2815601 | |||||||
| chr9:2815650 | T | C | 47 | a0001c0005t0001g0019 a0001c0005t0001g0057 a0001c0005t0001g0058 others(44): Show |
58 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.1270-3288A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2815650 | |||||||
| chr9:2815866 | G | C | 2 | a0001c0005t0001g0019 a0001c0005t0001g0060 |
3 | HG02630.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1270-3504C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2815866 | |||||||
| chr9:2815966 | C | T | 47 | a0001c0005t0001g0019 a0001c0005t0001g0057 a0001c0005t0001g0058 others(44): Show |
58 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.1270-3604G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2815966 | |||||||
| chr9:2816002 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1270-3640C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2816002 | |||||||
| chr9:2816024 | A | G | 47 | a0001c0005t0001g0019 a0001c0005t0001g0057 a0001c0005t0001g0058 others(44): Show |
58 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.1270-3662T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2816024 | |||||||
| chr9:2816067 | G | A | 2 | a0001c0001t0001g0303 a0001c0001t0001g0305 |
2 | HG03834.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1270-3705C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2816067 | |||||||
| chr9:2816114 | GCTGAAGA | G | 6 | a0001c0005t0001g0057 a0001c0005t0001g0058 a0001c0005t0001g0059 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1270-3759_1270-375 others(11): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2816114 | |||||||
| chr9:2816141 | T | G | 47 | a0001c0005t0001g0019 a0001c0005t0001g0057 a0001c0005t0001g0058 others(44): Show |
58 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.1270-3779A>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2816141 | |||||||
| chr9:2816147 | G | A | 1 | a0003c0004t0001g0175 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1270-3785C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2816147 | |||||||
| chr9:2816152 | T | C | 5 | a0001c0005t0001g0057 a0001c0005t0001g0058 a0001c0005t0001g0059 others(2): Show |
5 | HG01891.hp1 HG02258.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1270-3790A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2816152 | |||||||
| chr9:2816201 | G | C | 2 | a0001c0005t0001g0019 a0001c0005t0001g0060 |
3 | HG02630.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1269+3817C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2816201 | |||||||
| chr9:2816203 | T | C | 1 | a0010c0015t0005g0049 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1269+3815A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2816203 | |||||||
| chr9:2816213 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1269+3805C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2816213 | |||||||
| chr9:2816377 | G | T | 1 | a0010c0015t0004g0056 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1269+3641C>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2816377 | |||||||
| chr9:2816396 | G | A | 2 | a0002c0003t0001g0148 a0002c0003t0001g0150 |
2 | HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1269+3622C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2816396 | |||||||
| chr9:2816455 | T | C | 2 | a0001c0005t0001g0019 a0001c0005t0001g0060 |
3 | HG02630.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1269+3563A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2816455 | |||||||
| chr9:2816473 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1269+3545A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2816473 | |||||||
| chr9:2816628 | C | T | 1 | a0001c0005t0001g0079 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1269+3390G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2816628 | |||||||
| chr9:2816686 | T | A | 3 | a0001c0005t0001g0057 a0001c0005t0001g0058 a0001c0005t0001g0059 |
3 | HG01891.hp1 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1269+3332A>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2816686 | |||||||
| chr9:2816817 | G | C | 5 | a0009c0011t0001g0185 a0009c0011t0001g0307 a0009c0011t0001g0309 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1269+3201C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2816817 | |||||||
| chr9:2816898 | G | A | 1 | a0004c0006t0001g0153 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1269+3120C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2816898 | |||||||
| chr9:2816928 | G | A | 17 | a0001c0005t0001g0057 a0001c0005t0001g0058 a0001c0005t0001g0059 others(14): Show |
19 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1269+3090C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2816928 | |||||||
| chr9:2817115 | T | C | 2 | a0001c0005t0001g0019 a0001c0005t0001g0060 |
3 | HG02630.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1269+2903A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2817115 | |||||||
| chr9:2817121 | C | A | 1 | a0002c0002t0001g0107 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1269+2897G>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2817121 | |||||||
| chr9:2817345 | T | C | 1 | a0002c0002t0001g0108 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1269+2673A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2817345 | |||||||
| chr9:2817380 | G | T | 3 | a0002c0002t0001g0114 a0002c0002t0001g0250 a0012c0028t0001g0128 |
3 | HG00140.hp2 HG01192.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.1269+2638C>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2817380 | |||||||
| chr9:2817417 | G | C | 1 | a0002c0002t0001g0109 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1269+2601C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2817417 | |||||||
| chr9:2817422 | G | A | 1 | a0002c0002t0001g0110 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1269+2596C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2817422 | |||||||
| chr9:2817510 | C | A | 6 | a0004c0006t0001g0014 a0004c0006t0001g0015 a0004c0006t0001g0153 others(3): Show |
10 | HG01123.hp1 HG01346.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.1269+2508G>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2817510 | |||||||
| chr9:2817545 | A | C | 1 | a0008c0012t0001g0167 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1269+2473T>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2817545 | |||||||
| chr9:2817546 | C | T | 1 | a0008c0012t0001g0167 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1269+2472G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2817546 | |||||||
| chr9:2817547 | A | T | 1 | a0008c0012t0001g0167 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1269+2471T>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2817547 | |||||||
| chr9:2817549 | G | T | 1 | a0008c0012t0001g0167 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1269+2469C>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2817549 | |||||||
| chr9:2817551 | A | T | 1 | a0008c0012t0001g0167 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1269+2467T>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2817551 | |||||||
| chr9:2817552 | A | C | 1 | a0008c0012t0001g0167 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1269+2466T>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2817552 | |||||||
| chr9:2817553 | G | T | 1 | a0008c0012t0001g0167 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1269+2465C>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2817553 | |||||||
| chr9:2817554 | A | G | 1 | a0008c0012t0001g0167 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1269+2464T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2817554 | |||||||
| chr9:2817854 | T | C | 2 | a0002c0002t0001g0025 a0002c0002t0001g0090 |
3 | NA19007.hp1 NA19054.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1269+2164A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2817854 | |||||||
| chr9:2817868 | C | A | 3 | a0005c0008t0001g0027 a0005c0008t0001g0048 a0005c0008t0001g0131 |
5 | HG02258.hp2 HG02451.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1269+2150G>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2817868 | |||||||
| chr9:2817887 | A | G | 73 | a0001c0001t0001g0239 a0001c0005t0001g0019 a0001c0005t0001g0057 others(70): Show |
92 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.1269+2131T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2817887 | |||||||
| chr9:2817938 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1269+2080A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2817938 | |||||||
| chr9:2818038 | G | A | 7 | a0001c0005t0001g0079 a0005c0008t0001g0027 a0005c0008t0001g0048 others(4): Show |
9 | HG02258.hp2 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1269+1980C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2818038 | |||||||
| chr9:2818045 | A | G | 1 | a0002c0002t0001g0081 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1269+1973T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2818045 | |||||||
| chr9:2818109 | C | T | 2 | a0001c0005t0001g0057 a0001c0005t0001g0059 |
2 | HG01891.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1269+1909G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2818109 | |||||||
| chr9:2818113 | G | A | 2 | a0010c0015t0004g0056 a0010c0015t0005g0049 |
2 | HG02896.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1269+1905C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2818113 | |||||||
| chr9:2818169 | G | A | 7 | a0001c0005t0001g0079 a0005c0008t0001g0027 a0005c0008t0001g0048 others(4): Show |
9 | HG02258.hp2 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1269+1849C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2818169 | |||||||
| chr9:2818194 | C | G | 9 | a0002c0002t0001g0020 a0002c0002t0001g0095 a0002c0002t0001g0100 others(6): Show |
10 | HG01975.hp2 NA18941.hp2 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.1269+1824G>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2818194 | |||||||
| chr9:2818241 | T | C | 2 | a0010c0015t0004g0056 a0010c0015t0005g0049 |
2 | HG02896.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1269+1777A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2818241 | |||||||
| chr9:2818272 | G | A | 3 | a0010c0015t0004g0056 a0010c0015t0005g0049 a0017c0025t0004g0138 |
3 | HG02896.hp2 HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1269+1746C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2818272 | |||||||
| chr9:2818601 | A | G | 1 | a0002c0003t0001g0139 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1269+1417T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2818601 | |||||||
| chr9:2818682 | C | T | 3 | a0001c0005t0001g0057 a0001c0005t0001g0058 a0001c0005t0001g0059 |
3 | HG01891.hp1 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1269+1336G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2818682 | |||||||
| chr9:2818697 | G | A | 2 | a0001c0005t0001g0019 a0001c0005t0001g0060 |
3 | HG02630.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1269+1321C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2818697 | |||||||
| chr9:2818700 | A | G | 2 | a0001c0005t0001g0019 a0001c0005t0001g0060 |
3 | HG02630.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1269+1318T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2818700 | |||||||
| chr9:2818736 | C | T | 1 | a0017c0025t0004g0138 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1269+1282G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2818736 | |||||||
| chr9:2818827 | G | A | 35 | a0002c0002t0001g0243 a0003c0004t0001g0010 a0003c0004t0001g0029 others(32): Show |
45 | HG00544.hp1 HG00558.hp2 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.1269+1191C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2818827 | |||||||
| chr9:2818859 | A | G | 2 | a0010c0015t0004g0056 a0010c0015t0005g0049 |
2 | HG02896.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1269+1159T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2818859 | |||||||
| chr9:2818929 | C | T | 1 | a0002c0003t0001g0182 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1269+1089G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2818929 | |||||||
| chr9:2818972 | T | C | 1 | a0010c0015t0004g0056 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1269+1046A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2818972 | |||||||
| chr9:2819126 | G | C | 6 | a0004c0006t0001g0014 a0004c0006t0001g0015 a0004c0006t0001g0153 others(3): Show |
10 | HG01123.hp1 HG01346.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.1269+892C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2819126 | |||||||
| chr9:2819230 | T | A | 30 | a0003c0004t0001g0010 a0003c0004t0001g0029 a0003c0004t0001g0030 others(27): Show |
38 | HG00544.hp1 HG00558.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.1269+788A>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2819230 | |||||||
| chr9:2819406 | G | C | 3 | a0001c0005t0001g0057 a0001c0005t0001g0058 a0001c0005t0001g0059 |
3 | HG01891.hp1 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1269+612C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2819406 | |||||||
| chr9:2819422 | T | C | 5 | a0002c0002t0001g0052 a0002c0002t0001g0053 a0002c0002t0001g0054 others(2): Show |
5 | HG00741.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1269+596A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2819422 | |||||||
| chr9:2819501 | T | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0230 a0001c0001t0001g0231 |
5 | HG01169.hp1 HG03239.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.1269+517A>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2819501 | |||||||
| chr9:2819699 | T | G | 1 | a0001c0005t0001g0040 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1269+319A>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2819699 | |||||||
| chr9:2819720 | G | C | 1 | a0001c0001t0001g0189 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1269+298C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2819720 | |||||||
| chr9:2819732 | G | A | 18 | a0001c0005t0001g0019 a0001c0005t0001g0057 a0001c0005t0001g0058 others(15): Show |
21 | HG00741.hp2 HG01891.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1269+286C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2819732 | |||||||
| chr9:2819907 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1269+111A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2819907 | |||||||
| chr9:2819919 | C | A | 26 | a0001c0005t0001g0084 a0003c0004t0001g0010 a0003c0004t0001g0029 others(23): Show |
34 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1269+99G>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2819919 | |||||||
| chr9:2819981 | G | A | 3 | a0001c0005t0001g0057 a0001c0005t0001g0058 a0001c0005t0001g0059 |
3 | HG01891.hp1 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1269+37C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2819981 | |||||||
| chr9:2820009 | A | T | 2 | a0003c0004t0001g0311 a0008c0012t0001g0088 |
2 | HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1269+9T>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 13/17 | chr9 | 2820009 | |||||||
| chr9:2820201 | C | CA | 30 | a0001c0001t0001g0186 a0001c0001t0001g0200 a0001c0001t0001g0211 others(27): Show |
33 | HG00280.hp1 HG00423.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.1189-104dupT | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2820201 | |||||||
| chr9:2820201 | CA | C | 13 | a0001c0001t0001g0292 a0001c0001t0001g0296 a0001c0001t0001g0304 others(10): Show |
13 | HG01070.hp1 HG01168.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1189-104delT | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2820201 | |||||||
| chr9:2820221 | G | T | 5 | a0001c0005t0001g0057 a0001c0005t0001g0058 a0010c0015t0004g0056 others(2): Show |
5 | HG02258.hp1 HG02896.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1189-123C>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2820221 | |||||||
| chr9:2820346 | C | A | 17 | a0001c0005t0001g0019 a0001c0005t0001g0057 a0001c0005t0001g0058 others(14): Show |
20 | HG00741.hp2 HG01891.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.1189-248G>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2820346 | |||||||
| chr9:2820482 | T | A | 25 | a0003c0004t0001g0010 a0003c0004t0001g0029 a0003c0004t0001g0030 others(22): Show |
33 | HG00544.hp1 HG00558.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.1189-384A>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2820482 | |||||||
| chr9:2820558 | A | G | 1 | a0001c0005t0001g0040 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1189-460T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2820558 | |||||||
| chr9:2820949 | G | A | 1 | a0010c0015t0004g0056 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1189-851C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2820949 | |||||||
| chr9:2820988 | A | G | 1 | a0010c0015t0005g0049 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1189-890T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2820988 | |||||||
| chr9:2821102 | C | T | 2 | a0007c0014t0001g0066 a0007c0014t0001g0119 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1189-1004G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821102 | |||||||
| chr9:2821171 | G | A | 3 | a0001c0005t0001g0057 a0001c0005t0001g0058 a0001c0005t0001g0059 |
3 | HG01891.hp1 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1189-1073C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821171 | |||||||
| chr9:2821249 | C | G | 1 | a0014c0016t0001g0174 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1189-1151G>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821249 | |||||||
| chr9:2821294 | A | ATTAGG | 6 | a0001c0005t0001g0216 a0009c0011t0001g0185 a0009c0011t0001g0307 others(3): Show |
6 | HG02145.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1189-1197_1189-119 others(9): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821294 | |||||||
| chr9:2821316 | C | T | 1 | a0001c0005t0001g0290 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1189-1218G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821316 | |||||||
| chr9:2821443 | C | CAAAAAAA others(3): Show |
5 | a0001c0001t0001g0262 a0001c0001t0001g0274 a0001c0005t0001g0057 others(2): Show |
5 | HG01891.hp1 HG01975.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1189-1355_1189-134 others(14): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821443 | |||||||
| chr9:2821443 | C | CAAAAAAA others(4): Show |
52 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(49): Show |
76 | HG00280.hp1 HG00558.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1189-1356_1189-134 others(15): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821443 | |||||||
| chr9:2821443 | C | CAAAAAAA others(5): Show |
50 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0034 others(47): Show |
64 | HG00140.hp1 HG00438.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1189-1357_1189-134 others(16): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821443 | |||||||
| chr9:2821443 | C | CAAAAAAA others(6): Show |
15 | a0001c0001t0001g0037 a0001c0001t0001g0152 a0001c0001t0001g0202 others(12): Show |
18 | HG00438.hp1 HG00544.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1189-1358_1189-134 others(17): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821443 | |||||||
| chr9:2821443 | C | CAAAAAAA others(7): Show |
5 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0283 others(2): Show |
5 | HG02080.hp2 HG02155.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1189-1359_1189-134 others(18): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821443 | |||||||
| chr9:2821443 | C | CAAAAAAA others(8): Show |
2 | a0001c0001t0001g0252 a0001c0005t0001g0074 |
2 | HG02615.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1189-1360_1189-134 others(19): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821443 | |||||||
| chr9:2821443 | C | CAAAAAAA others(9): Show |
4 | a0001c0005t0001g0068 a0001c0005t0001g0069 a0001c0005t0001g0070 others(1): Show |
4 | HG02630.hp1 HG02647.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1189-1361_1189-134 others(20): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821443 | |||||||
| chr9:2821443 | C | CAAAAAAA others(10): Show |
3 | a0001c0005t0001g0071 a0001c0005t0001g0073 a0001c0005t0001g0075 |
3 | HG02257.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1189-1362_1189-134 others(21): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821443 | |||||||
| chr9:2821443 | C | CAAAAAAA others(11): Show |
2 | a0001c0005t0001g0137 a0002c0002t0001g0054 |
2 | HG01243.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1189-1363_1189-134 others(22): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821443 | |||||||
| chr9:2821443 | C | CAAAAAAA others(12): Show |
4 | a0003c0004t0001g0010 a0003c0004t0001g0160 a0003c0004t0001g0175 others(1): Show |
7 | HG00544.hp1 HG00558.hp2 NA18522.hp2 others(4): Show |
intron_variant | MODIFIER | c.1189-1364_1189-134 others(23): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821443 | |||||||
| chr9:2821443 | C | CAAAAAAA others(13): Show |
9 | a0002c0002t0001g0052 a0003c0004t0001g0031 a0003c0004t0001g0159 others(6): Show |
10 | HG00741.hp2 HG02129.hp1 NA18747.hp1 others(7): Show |
intron_variant | MODIFIER | c.1189-1346_1189-134 others(24): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821443 | |||||||
| chr9:2821443 | C | CAAAAAAA others(14): Show |
11 | a0003c0004t0001g0029 a0003c0004t0001g0032 a0003c0004t0001g0161 others(8): Show |
13 | HG01074.hp2 HG01168.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1189-1346_1189-134 others(25): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821443 | |||||||
| chr9:2821443 | C | CAAAAAAA others(15): Show |
5 | a0002c0002t0001g0243 a0003c0004t0001g0030 a0003c0004t0001g0172 others(2): Show |
6 | HG01099.hp2 HG01358.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1189-1346_1189-134 others(26): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821443 | |||||||
| chr9:2821443 | C | CAAAAAAA others(16): Show |
1 | a0003c0004t0001g0033 | 2 | NA18945.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1189-1346_1189-134 others(27): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821443 | |||||||
| chr9:2821443 | C | CAAAAAAA others(37): Show |
1 | a0018c0021t0007g0312 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1189-1346_1189-134 others(48): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821443 | |||||||
| chr9:2821443 | CA | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0188 a0001c0001t0001g0189 others(3): Show |
12 | HG00609.hp1 HG00673.hp2 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.1189-1346delT | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821443 | |||||||
| chr9:2821463 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1189-1365C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821463 | |||||||
| chr9:2821498 | A | C | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(140): Show |
190 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.1189-1400T>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821498 | |||||||
| chr9:2821529 | T | G | 1 | a0001c0001t0001g0261 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1189-1431A>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821529 | |||||||
| chr9:2821644 | C | T | 5 | a0002c0002t0001g0052 a0002c0002t0001g0053 a0002c0002t0001g0054 others(2): Show |
5 | HG00741.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1189-1546G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821644 | |||||||
| chr9:2821696 | T | G | 1 | a0002c0003t0001g0055 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1189-1598A>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821696 | |||||||
| chr9:2821805 | T | C | 1 | a0002c0003t0001g0064 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1189-1707A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821805 | |||||||
| chr9:2821908 | G | A | 25 | a0003c0004t0001g0010 a0003c0004t0001g0029 a0003c0004t0001g0030 others(22): Show |
33 | HG00544.hp1 HG00558.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.1189-1810C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821908 | |||||||
| chr9:2821917 | T | C | 2 | a0010c0015t0004g0056 a0010c0015t0005g0049 |
2 | HG02896.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1189-1819A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2821917 | |||||||
| chr9:2822001 | A | G | 1 | a0008c0012t0001g0088 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1188+1780T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2822001 | |||||||
| chr9:2822015 | C | G | 1 | a0001c0001t0001g0261 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1188+1766G>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2822015 | |||||||
| chr9:2822059 | C | T | 3 | a0006c0009t0001g0047 a0006c0009t0001g0249 a0006c0009t0001g0306 |
4 | NA18947.hp2 NA18987.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1188+1722G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2822059 | |||||||
| chr9:2822060 | A | C | 1 | a0002c0002t0001g0085 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1188+1721T>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2822060 | |||||||
| chr9:2822263 | T | C | 10 | a0001c0001t0001g0003 a0001c0001t0001g0212 a0001c0001t0001g0257 others(7): Show |
16 | HG02132.hp2 HG03490.hp1 NA18940.hp2 others(13): Show |
intron_variant | MODIFIER | c.1188+1518A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2822263 | |||||||
| chr9:2822270 | A | T | 3 | a0002c0002t0001g0022 a0002c0002t0001g0091 a0002c0002t0001g0099 |
4 | HG01255.hp2 HG01256.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.1188+1511T>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2822270 | |||||||
| chr9:2822280 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1188+1501G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2822280 | |||||||
| chr9:2822384 | A | C | 3 | a0001c0005t0001g0057 a0001c0005t0001g0058 a0001c0005t0001g0059 |
3 | HG01891.hp1 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1188+1397T>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2822384 | |||||||
| chr9:2822450 | G | A | 2 | a0002c0002t0001g0157 a0002c0002t0001g0166 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1188+1331C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2822450 | |||||||
| chr9:2822527 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1188+1254C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2822527 | |||||||
| chr9:2822622 | T | C | 12 | a0001c0005t0001g0019 a0001c0005t0001g0060 a0001c0005t0001g0061 others(9): Show |
13 | HG01243.hp1 HG02257.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1188+1159A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2822622 | |||||||
| chr9:2822728 | CAT | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(133): Show |
180 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.1188+1051_1188+105 others(6): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2822728 | |||||||
| chr9:2822734 | AATATAAT others(3): Show |
A | 5 | a0002c0002t0001g0052 a0002c0002t0001g0053 a0002c0002t0001g0054 others(2): Show |
5 | HG00741.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1188+1037_1188+104 others(14): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2822734 | |||||||
| chr9:2822736 | TATA | T | 12 | a0001c0005t0001g0019 a0001c0005t0001g0060 a0001c0005t0001g0061 others(9): Show |
13 | HG01243.hp1 HG02257.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1188+1042_1188+104 others(7): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2822736 | |||||||
| chr9:2822758 | CATT | C | 3 | a0001c0005t0001g0057 a0001c0005t0001g0058 a0001c0005t0001g0059 |
3 | HG01891.hp1 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1188+1020_1188+102 others(7): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2822758 | |||||||
| chr9:2822782 | G | A | 6 | a0004c0006t0001g0014 a0004c0006t0001g0015 a0004c0006t0001g0153 others(3): Show |
10 | HG01123.hp1 HG01346.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.1188+999C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2822782 | |||||||
| chr9:2822855 | T | C | 1 | a0002c0002t0001g0135 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1188+926A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2822855 | |||||||
| chr9:2822862 | G | A | 2 | a0005c0008t0001g0048 a0005c0008t0001g0131 |
3 | HG02258.hp2 HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1188+919C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2822862 | |||||||
| chr9:2822897 | C | A | 25 | a0003c0004t0001g0010 a0003c0004t0001g0029 a0003c0004t0001g0030 others(22): Show |
33 | HG00544.hp1 HG00558.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.1188+884G>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2822897 | |||||||
| chr9:2823007 | G | T | 24 | a0001c0005t0001g0019 a0001c0005t0001g0057 a0001c0005t0001g0058 others(21): Show |
25 | HG00741.hp2 HG01243.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.1188+774C>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2823007 | |||||||
| chr9:2823022 | T | A | 25 | a0003c0004t0001g0010 a0003c0004t0001g0029 a0003c0004t0001g0030 others(22): Show |
33 | HG00544.hp1 HG00558.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.1188+759A>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2823022 | |||||||
| chr9:2823157 | C | G | 25 | a0003c0004t0001g0010 a0003c0004t0001g0029 a0003c0004t0001g0030 others(22): Show |
33 | HG00544.hp1 HG00558.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.1188+624G>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2823157 | |||||||
| chr9:2823176 | A | G | 1 | a0002c0002t0001g0098 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1188+605T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2823176 | |||||||
| chr9:2823220 | C | A | 1 | a0004c0006t0001g0156 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1188+561G>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2823220 | |||||||
| chr9:2823233 | T | C | 6 | a0001c0005t0001g0216 a0009c0011t0001g0185 a0009c0011t0001g0307 others(3): Show |
6 | HG02145.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1188+548A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2823233 | |||||||
| chr9:2823316 | A | G | 3 | a0006c0009t0001g0047 a0006c0009t0001g0249 a0006c0009t0001g0306 |
4 | NA18947.hp2 NA18987.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1188+465T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2823316 | |||||||
| chr9:2823358 | C | A | 1 | a0002c0003t0001g0078 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1188+423G>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2823358 | |||||||
| chr9:2823380 | G | A | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(127): Show |
174 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.1188+401C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2823380 | |||||||
| chr9:2823388 | C | G | 39 | a0001c0005t0001g0019 a0001c0005t0001g0057 a0001c0005t0001g0058 others(36): Show |
48 | HG00544.hp1 HG00558.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.1188+393G>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2823388 | |||||||
| chr9:2823606 | T | C | 1 | a0002c0002t0001g0113 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1188+175A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2823606 | |||||||
| chr9:2823683 | G | A | 6 | a0002c0002t0001g0052 a0002c0002t0001g0053 a0002c0002t0001g0054 others(3): Show |
6 | HG00741.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1188+98C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2823683 | |||||||
| chr9:2823733 | C | T | 3 | a0006c0009t0001g0047 a0006c0009t0001g0249 a0006c0009t0001g0306 |
4 | NA18947.hp2 NA18987.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1188+48G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2823733 | |||||||
| chr9:2823736 | C | A | 6 | a0002c0002t0001g0052 a0002c0002t0001g0053 a0002c0002t0001g0054 others(3): Show |
6 | HG00741.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1188+45G>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2823736 | |||||||
| chr9:2823766 | T | A | 1 | a0010c0015t0005g0049 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1188+15A>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 12/17 | chr9 | 2823766 | |||||||
| chr9:2823850 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1135-16A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 11/17 | chr9 | 2823850 | |||||||
| chr9:2823877 | T | C | 1 | a0001c0001t0003g0195 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1135-43A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 11/17 | chr9 | 2823877 | |||||||
| chr9:2823881 | G | C | 1 | a0001c0001t0001g0280 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1135-47C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 11/17 | chr9 | 2823881 | |||||||
| chr9:2824000 | A | G | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(173): Show |
229 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.1135-166T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 11/17 | chr9 | 2824000 | |||||||
| chr9:2824038 | T | A | 1 | a0002c0002t0001g0087 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1135-204A>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 11/17 | chr9 | 2824038 | |||||||
| chr9:2824044 | A | ATAGGGT | 22 | a0001c0001t0001g0239 a0001c0001t0001g0255 a0002c0003t0001g0004 others(19): Show |
30 | HG00735.hp2 HG00741.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.1135-216_1135-211d others(8): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 11/17 | chr9 | 2824044 | |||||||
| chr9:2824184 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1135-350C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 11/17 | chr9 | 2824184 | |||||||
| chr9:2824378 | C | T | 8 | a0001c0005t0001g0068 a0001c0005t0001g0069 a0001c0005t0001g0070 others(5): Show |
8 | HG01243.hp1 HG02257.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1134+339G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 11/17 | chr9 | 2824378 | |||||||
| chr9:2824585 | C | A | 1 | a0002c0003t0001g0078 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1134+132G>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 11/17 | chr9 | 2824585 | |||||||
| chr9:2824588 | T | C | 4 | a0005c0008t0001g0027 a0005c0008t0001g0048 a0005c0008t0001g0131 others(1): Show |
6 | HG02258.hp2 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1134+129A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 11/17 | chr9 | 2824588 | |||||||
| chr9:2824677 | G | A | 3 | a0001c0005t0001g0057 a0001c0005t0001g0058 a0001c0005t0001g0059 |
3 | HG01891.hp1 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1134+40C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 11/17 | chr9 | 2824677 | |||||||
| chr9:2824849 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1036-34C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2824849 | |||||||
| chr9:2824902 | T | C | 58 | a0001c0001t0001g0046 a0001c0001t0001g0285 a0001c0001t0001g0286 others(55): Show |
70 | HG00544.hp1 HG00558.hp2 HG00741.hp2 others(67): Show |
intron_variant | MODIFIER | c.1036-87A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2824902 | |||||||
| chr9:2825014 | A | G | 26 | a0001c0001t0001g0239 a0001c0005t0001g0057 a0001c0005t0001g0058 others(23): Show |
34 | HG00735.hp2 HG01099.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1036-199T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2825014 | |||||||
| chr9:2825181 | G | C | 1 | a0002c0002t0006g0051 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1036-366C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2825181 | |||||||
| chr9:2825216 | C | A | 7 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(4): Show |
7 | HG01884.hp2 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1036-401G>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2825216 | |||||||
| chr9:2825239 | A | G | 3 | a0005c0008t0001g0027 a0005c0008t0001g0048 a0005c0008t0001g0131 |
5 | HG02258.hp2 HG02451.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1036-424T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2825239 | |||||||
| chr9:2825271 | C | T | 13 | a0001c0005t0001g0019 a0001c0005t0001g0060 a0001c0005t0001g0061 others(10): Show |
14 | HG01243.hp1 HG02257.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1036-456G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2825271 | |||||||
| chr9:2825318 | C | A | 5 | a0002c0002t0001g0114 a0002c0002t0001g0157 a0002c0002t0001g0166 others(2): Show |
5 | HG00140.hp2 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1036-503G>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2825318 | |||||||
| chr9:2825489 | C | CT | 7 | a0002c0002t0001g0052 a0002c0002t0001g0053 a0002c0002t0001g0054 others(4): Show |
7 | HG00741.hp2 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1036-675dupA | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2825489 | |||||||
| chr9:2825641 | C | T | 12 | a0001c0005t0001g0019 a0001c0005t0001g0060 a0001c0005t0001g0061 others(9): Show |
13 | HG01243.hp1 HG02257.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1036-826G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2825641 | |||||||
| chr9:2825683 | T | C | 1 | a0001c0001t0001g0288 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1036-868A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2825683 | |||||||
| chr9:2825720 | T | A | 5 | a0002c0002t0001g0012 a0002c0002t0001g0065 a0002c0002t0001g0115 others(2): Show |
7 | NA18946.hp1 NA18959.hp2 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1036-905A>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2825720 | |||||||
| chr9:2825732 | G | A | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(88): Show |
124 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.1036-917C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2825732 | |||||||
| chr9:2825889 | T | C | 1 | a0002c0002t0001g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1036-1074A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2825889 | |||||||
| chr9:2825965 | T | G | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(153): Show |
209 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(206): Show |
intron_variant | MODIFIER | c.1035+1108A>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2825965 | |||||||
| chr9:2826050 | G | C | 8 | a0001c0001t0001g0045 a0001c0001t0001g0220 a0001c0001t0001g0221 others(5): Show |
9 | HG00438.hp1 HG02129.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1035+1023C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2826050 | |||||||
| chr9:2826066 | T | C | 3 | a0005c0008t0001g0027 a0005c0008t0001g0048 a0005c0008t0001g0131 |
5 | HG02258.hp2 HG02451.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1035+1007A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2826066 | |||||||
| chr9:2826099 | G | GT | 7 | a0002c0002t0001g0021 a0002c0002t0001g0082 a0002c0002t0001g0095 others(4): Show |
8 | HG00673.hp1 HG02080.hp1 NA18957.hp1 others(5): Show |
intron_variant | MODIFIER | c.1035+973dupA | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2826099 | |||||||
| chr9:2826099 | GT | G | 9 | a0001c0005t0001g0216 a0002c0002t0002g0018 a0002c0002t0002g0050 others(6): Show |
10 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1035+973delA | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2826099 | |||||||
| chr9:2826283 | T | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(131): Show |
180 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.1035+790A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2826283 | |||||||
| chr9:2826344 | C | G | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(153): Show |
203 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.1035+729G>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2826344 | |||||||
| chr9:2826381 | C | G | 1 | a0001c0001t0001g0222 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1035+692G>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2826381 | |||||||
| chr9:2826409 | T | C | 10 | a0001c0005t0001g0057 a0001c0005t0001g0058 a0001c0005t0001g0059 others(7): Show |
10 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1035+664A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2826409 | |||||||
| chr9:2826428 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1035+645C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2826428 | |||||||
| chr9:2826460 | GT | G | 19 | a0001c0005t0001g0019 a0001c0005t0001g0060 a0001c0005t0001g0068 others(16): Show |
20 | HG01243.hp1 HG02145.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1035+612delA | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2826460 | |||||||
| chr9:2826519 | A | G | 1 | a0001c0001t0001g0034 | 2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1035+554T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2826519 | |||||||
| chr9:2826674 | C | T | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(208): Show |
270 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(267): Show |
intron_variant | MODIFIER | c.1035+399G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2826674 | |||||||
| chr9:2826727 | T | G | 2 | a0010c0015t0004g0056 a0010c0015t0005g0049 |
2 | HG02896.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1035+346A>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2826727 | |||||||
| chr9:2826817 | G | A | 10 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0005t0001g0068 others(7): Show |
10 | HG01081.hp2 HG01243.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1035+256C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2826817 | |||||||
| chr9:2826985 | C | T | 2 | a0010c0015t0004g0056 a0010c0015t0005g0049 |
2 | HG02896.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1035+88G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 10/17 | chr9 | 2826985 | |||||||
| chr9:2827271 | A | G | 6 | a0001c0001t0001g0043 a0001c0001t0001g0197 a0001c0001t0001g0198 others(3): Show |
7 | HG00621.hp2 NA18612.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.957-120T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 9/17 | chr9 | 2827271 | |||||||
| chr9:2827279 | T | C | 1 | a0003c0004t0001g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.957-128A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 9/17 | chr9 | 2827279 | |||||||
| chr9:2827316 | A | C | 1 | a0001c0001t0001g0257 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.957-165T>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 9/17 | chr9 | 2827316 | |||||||
| chr9:2827394 | G | A | 1 | a0018c0021t0007g0312 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.957-243C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 9/17 | chr9 | 2827394 | |||||||
| chr9:2827468 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.957-317A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 9/17 | chr9 | 2827468 | |||||||
| chr9:2827513 | A | G | 2 | a0010c0015t0004g0056 a0010c0015t0005g0049 |
2 | HG02896.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.957-362T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 9/17 | chr9 | 2827513 | |||||||
| chr9:2827684 | G | C | 2 | a0002c0002t0001g0082 a0002c0002t0001g0118 |
2 | NA19065.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.957-533C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 9/17 | chr9 | 2827684 | |||||||
| chr9:2827701 | C | G | 3 | a0005c0008t0001g0027 a0005c0008t0001g0048 a0005c0008t0001g0131 |
5 | HG02258.hp2 HG02451.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.957-550G>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 9/17 | chr9 | 2827701 | |||||||
| chr9:2827725 | G | A | 1 | a0002c0003t0001g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.957-574C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 9/17 | chr9 | 2827725 | |||||||
| chr9:2827752 | T | C | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(113): Show |
158 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.957-601A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 9/17 | chr9 | 2827752 | |||||||
| chr9:2827790 | A | T | 1 | a0003c0004t0001g0169 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.957-639T>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 9/17 | chr9 | 2827790 | |||||||
| chr9:2827861 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.957-710A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 9/17 | chr9 | 2827861 | |||||||
| chr9:2827920 | G | A | 2 | a0001c0001t0001g0285 a0001c0001t0001g0286 |
2 | NA18981.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.956+755C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 9/17 | chr9 | 2827920 | |||||||
| chr9:2828049 | T | A | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | NA19006.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.956+626A>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 9/17 | chr9 | 2828049 | |||||||
| chr9:2828060 | A | G | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(193): Show |
254 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(251): Show |
intron_variant | MODIFIER | c.956+615T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 9/17 | chr9 | 2828060 | |||||||
| chr9:2828141 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.956+534C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 9/17 | chr9 | 2828141 | |||||||
| chr9:2828152 | G | C | 2 | a0010c0015t0004g0056 a0010c0015t0005g0049 |
2 | HG02896.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.956+523C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 9/17 | chr9 | 2828152 | |||||||
| chr9:2828224 | G | A | 21 | a0002c0002t0001g0052 a0002c0002t0001g0053 a0002c0002t0001g0054 others(18): Show |
24 | HG00735.hp2 HG00741.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.956+451C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 9/17 | chr9 | 2828224 | |||||||
| chr9:2828249 | C | G | 4 | a0002c0003t0001g0139 a0002c0003t0001g0140 a0002c0003t0001g0141 others(1): Show |
4 | HG03704.hp1 HG03710.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.956+426G>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 9/17 | chr9 | 2828249 | |||||||
| chr9:2828358 | A | G | 4 | a0005c0008t0001g0027 a0005c0008t0001g0048 a0005c0008t0001g0131 others(1): Show |
6 | HG02258.hp2 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.956+317T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 9/17 | chr9 | 2828358 | |||||||
| chr9:2828462 | G | A | 1 | a0002c0007t0001g0244 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.956+213C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 9/17 | chr9 | 2828462 | |||||||
| chr9:2828492 | T | C | 2 | a0007c0014t0001g0066 a0007c0014t0001g0119 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.956+183A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 9/17 | chr9 | 2828492 | |||||||
| chr9:2828548 | C | T | 3 | a0001c0005t0001g0057 a0001c0005t0001g0058 a0001c0005t0001g0059 |
3 | HG01891.hp1 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.956+127G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 9/17 | chr9 | 2828548 | |||||||
| chr9:2828557 | T | G | 1 | a0001c0005t0001g0290 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.956+118A>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 9/17 | chr9 | 2828557 | |||||||
| chr9:2828835 | G | A | 8 | a0001c0005t0001g0019 a0001c0005t0001g0060 a0001c0005t0001g0061 others(5): Show |
11 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.853-57C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 8/17 | chr9 | 2828835 | |||||||
| chr9:2828841 | A | T | 8 | a0001c0005t0001g0019 a0001c0005t0001g0060 a0001c0005t0001g0061 others(5): Show |
11 | HG02258.hp2 HG02451.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.853-63T>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 8/17 | chr9 | 2828841 | |||||||
| chr9:2829086 | A | C | 1 | a0018c0021t0007g0312 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.853-308T>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 8/17 | chr9 | 2829086 | |||||||
| chr9:2829183 | T | C | 1 | a0002c0007t0001g0245 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.853-405A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 8/17 | chr9 | 2829183 | |||||||
| chr9:2829195 | G | A | 1 | a0002c0002t0001g0120 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.853-417C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 8/17 | chr9 | 2829195 | |||||||
| chr9:2829308 | A | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(183): Show |
244 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(241): Show |
intron_variant | MODIFIER | c.852+466T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 8/17 | chr9 | 2829308 | |||||||
| chr9:2829408 | C | A | 1 | a0001c0001t0001g0219 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.852+366G>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 8/17 | chr9 | 2829408 | |||||||
| chr9:2829966 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.678-18T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 7/17 | chr9 | 2829966 | |||||||
| chr9:2829988 | G | A | 2 | a0010c0015t0004g0056 a0010c0015t0005g0049 |
2 | HG02896.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.678-40C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 7/17 | chr9 | 2829988 | |||||||
| chr9:2830072 | T | G | 2 | a0002c0002t0001g0081 a0002c0002t0001g0136 |
2 | HG02083.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.678-124A>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 7/17 | chr9 | 2830072 | |||||||
| chr9:2830253 | T | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0188 a0001c0001t0001g0189 others(3): Show |
11 | HG00609.hp1 HG00673.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.678-305A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 7/17 | chr9 | 2830253 | |||||||
| chr9:2830341 | T | A | 1 | a0018c0021t0007g0312 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.678-393A>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 7/17 | chr9 | 2830341 | |||||||
| chr9:2830494 | C | T | 1 | a0019c0027t0001g0127 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.677+468G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 7/17 | chr9 | 2830494 | |||||||
| chr9:2830726 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.677+236T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 7/17 | chr9 | 2830726 | |||||||
| chr9:2830808 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.677+154C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 7/17 | chr9 | 2830808 | |||||||
| chr9:2830813 | T | C | 5 | a0002c0003t0001g0080 a0005c0008t0001g0027 a0005c0008t0001g0048 others(2): Show |
7 | HG01109.hp1 HG02109.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.677+149A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 7/17 | chr9 | 2830813 | |||||||
| chr9:2830902 | T | C | 2 | a0008c0012t0001g0167 a0022c0017t0001g0168 |
2 | HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.677+60A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 7/17 | chr9 | 2830902 | |||||||
| chr9:2830915 | C | T | 22 | a0002c0002t0001g0052 a0002c0002t0001g0053 a0002c0002t0001g0054 others(19): Show |
25 | HG00735.hp2 HG00741.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.677+47G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 7/17 | chr9 | 2830915 | |||||||
| chr9:2830940 | T | C | 2 | a0001c0001t0001g0289 a0001c0001t0001g0294 |
2 | HG02027.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.677+22A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 7/17 | chr9 | 2830940 | |||||||
| chr9:2831035 | A | C | 1 | a0002c0002t0001g0094 | 1 | HG01168.hp1 | splice_region_variant&intron_variant | LOW | c.611-7T>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 6/17 | chr9 | 2831035 | |||||||
| chr9:2831054 | G | A | 1 | a0002c0002t0001g0121 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.611-26C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 6/17 | chr9 | 2831054 | |||||||
| chr9:2831147 | C | T | 22 | a0002c0002t0001g0052 a0002c0002t0001g0053 a0002c0002t0001g0054 others(19): Show |
25 | HG00735.hp2 HG00741.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.610+104G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 6/17 | chr9 | 2831147 | |||||||
| chr9:2831149 | A | C | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(200): Show |
262 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(259): Show |
intron_variant | MODIFIER | c.610+102T>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 6/17 | chr9 | 2831149 | |||||||
| chr9:2831604 | G | C | 2 | a0002c0002t0001g0122 a0019c0027t0001g0127 |
2 | NA18950.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.517-260C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 5/17 | chr9 | 2831604 | |||||||
| chr9:2831652 | T | C | 12 | a0001c0005t0001g0068 a0001c0005t0001g0069 a0001c0005t0001g0070 others(9): Show |
13 | HG01243.hp1 HG02257.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.517-308A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 5/17 | chr9 | 2831652 | |||||||
| chr9:2831678 | C | T | 5 | a0001c0005t0001g0057 a0001c0005t0001g0058 a0001c0005t0001g0059 others(2): Show |
5 | HG01891.hp1 HG01891.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-334G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 5/17 | chr9 | 2831678 | |||||||
| chr9:2831809 | A | G | 2 | a0001c0005t0001g0019 a0001c0005t0001g0061 |
3 | HG02630.hp2 HG02818.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.517-465T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 5/17 | chr9 | 2831809 | |||||||
| chr9:2831839 | T | C | 1 | a0001c0005t0001g0290 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.517-495A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 5/17 | chr9 | 2831839 | |||||||
| chr9:2831891 | T | C | 195 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(192): Show |
251 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.517-547A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 5/17 | chr9 | 2831891 | |||||||
| chr9:2832011 | C | T | 1 | a0002c0002t0001g0092 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.517-667G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 5/17 | chr9 | 2832011 | |||||||
| chr9:2832213 | T | C | 1 | a0001c0019t0001g0254 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.517-869A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 5/17 | chr9 | 2832213 | |||||||
| chr9:2832224 | T | C | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0291 |
3 | HG00438.hp1 HG02129.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.517-880A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 5/17 | chr9 | 2832224 | |||||||
| chr9:2832414 | C | G | 3 | a0001c0005t0001g0019 a0001c0005t0001g0060 a0001c0005t0001g0061 |
4 | HG02630.hp2 HG02818.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+943G>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 5/17 | chr9 | 2832414 | |||||||
| chr9:2832539 | G | A | 1 | a0002c0002t0001g0077 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.516+818C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 5/17 | chr9 | 2832539 | |||||||
| chr9:2832651 | G | T | 2 | a0008c0012t0001g0167 a0022c0017t0001g0168 |
2 | HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.516+706C>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 5/17 | chr9 | 2832651 | |||||||
| chr9:2832663 | C | T | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(109): Show |
148 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.516+694G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 5/17 | chr9 | 2832663 | |||||||
| chr9:2832875 | A | C | 3 | a0001c0005t0001g0019 a0001c0005t0001g0060 a0001c0005t0001g0061 |
4 | HG02630.hp2 HG02818.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+482T>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 5/17 | chr9 | 2832875 | |||||||
| chr9:2832877 | G | C | 1 | a0022c0017t0001g0168 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.516+480C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 5/17 | chr9 | 2832877 | |||||||
| chr9:2832914 | G | C | 228 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(225): Show |
294 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(291): Show |
intron_variant | MODIFIER | c.516+443C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 5/17 | chr9 | 2832914 | |||||||
| chr9:2832981 | G | A | 2 | a0010c0015t0004g0056 a0010c0015t0005g0049 |
2 | HG02896.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.516+376C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 5/17 | chr9 | 2832981 | |||||||
| chr9:2833070 | C | T | 1 | a0001c0019t0001g0254 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.516+287G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 5/17 | chr9 | 2833070 | |||||||
| chr9:2833107 | A | G | 183 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(180): Show |
241 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.516+250T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 5/17 | chr9 | 2833107 | |||||||
| chr9:2833255 | C | T | 1 | a0005c0008t0001g0027 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.516+102G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 5/17 | chr9 | 2833255 | |||||||
| chr9:2833267 | T | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(189): Show |
250 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(247): Show |
intron_variant | MODIFIER | c.516+90A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 5/17 | chr9 | 2833267 | |||||||
| chr9:2833303 | G | C | 4 | a0002c0003t0001g0080 a0008c0012t0001g0088 a0010c0015t0004g0056 others(1): Show |
4 | HG01109.hp1 HG02109.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+54C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 5/17 | chr9 | 2833303 | |||||||
| chr9:2833485 | A | G | 1 | a0018c0021t0007g0312 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.441-53T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 4/17 | chr9 | 2833485 | |||||||
| chr9:2833568 | T | G | 1 | a0014c0016t0001g0174 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.441-136A>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 4/17 | chr9 | 2833568 | |||||||
| chr9:2833692 | AT | A | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(142): Show |
191 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.441-261delA | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 4/17 | chr9 | 2833692 | |||||||
| chr9:2833693 | T | A | 3 | a0005c0008t0001g0027 a0005c0008t0001g0048 a0005c0008t0001g0131 |
5 | HG02258.hp2 HG02451.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.441-261A>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 4/17 | chr9 | 2833693 | |||||||
| chr9:2833866 | C | T | 2 | a0003c0004t0001g0029 a0003c0004t0001g0030 |
4 | NA18941.hp1 NA18979.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.440+165G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 4/17 | chr9 | 2833866 | |||||||
| chr9:2834185 | A | G | 1 | a0002c0002t0001g0091 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.305-19T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2834185 | |||||||
| chr9:2834355 | T | C | 1 | a0001c0005t0001g0059 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.305-189A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2834355 | |||||||
| chr9:2834592 | G | C | 1 | a0014c0016t0001g0174 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.305-426C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2834592 | |||||||
| chr9:2834628 | G | C | 24 | a0001c0005t0001g0073 a0002c0002t0001g0052 a0002c0002t0001g0053 others(21): Show |
27 | HG00735.hp2 HG00741.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.305-462C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2834628 | |||||||
| chr9:2834682 | G | A | 1 | a0002c0002t0001g0083 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.305-516C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2834682 | |||||||
| chr9:2834721 | G | T | 1 | a0002c0002t0001g0090 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.305-555C>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2834721 | |||||||
| chr9:2834811 | A | T | 1 | a0001c0005t0001g0253 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.305-645T>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2834811 | |||||||
| chr9:2834833 | A | ATCTT | 182 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(179): Show |
239 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.305-668_305-667ins others(4): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2834833 | |||||||
| chr9:2834850 | T | G | 2 | a0002c0002t0001g0081 a0002c0002t0001g0136 |
2 | HG02083.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.305-684A>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2834850 | |||||||
| chr9:2834914 | A | C | 1 | a0009c0011t0001g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.305-748T>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2834914 | |||||||
| chr9:2834926 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.305-760A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2834926 | |||||||
| chr9:2835011 | T | C | 3 | a0005c0008t0001g0027 a0005c0008t0001g0048 a0005c0008t0001g0131 |
5 | HG02258.hp2 HG02451.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.305-845A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2835011 | |||||||
| chr9:2835013 | C | CA | 148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(145): Show |
196 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.305-848dupT | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2835013 | |||||||
| chr9:2835013 | C | CAA | 5 | a0001c0001t0001g0192 a0001c0001t0001g0292 a0001c0001t0001g0293 others(2): Show |
6 | HG02630.hp2 HG02818.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.305-849_305-848dup others(2): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2835013 | |||||||
| chr9:2835074 | T | G | 1 | a0002c0002t0001g0126 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.305-908A>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2835074 | |||||||
| chr9:2835137 | C | G | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(209): Show |
271 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.305-971G>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2835137 | |||||||
| chr9:2835181 | A | G | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(223): Show |
288 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.305-1015T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2835181 | |||||||
| chr9:2835204 | G | A | 6 | a0004c0006t0001g0014 a0004c0006t0001g0015 a0004c0006t0001g0153 others(3): Show |
10 | HG01123.hp1 HG01346.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.305-1038C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2835204 | |||||||
| chr9:2835374 | C | T | 1 | a0001c0005t0001g0079 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.305-1208G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2835374 | |||||||
| chr9:2835419 | A | G | 1 | a0002c0007t0001g0238 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.305-1253T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2835419 | |||||||
| chr9:2835562 | TATTC | T | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(223): Show |
288 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.305-1400_305-1397d others(6): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2835562 | |||||||
| chr9:2835579 | G | A | 148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(145): Show |
196 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.305-1413C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2835579 | |||||||
| chr9:2835730 | AGTACATT others(15): Show |
A | 1 | a0001c0005t0001g0074 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.304+1428_304+1449d others(24): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2835730 | |||||||
| chr9:2835911 | T | C | 4 | a0001c0005t0001g0057 a0001c0005t0001g0058 a0001c0005t0001g0059 others(1): Show |
4 | HG01891.hp1 HG01891.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.304+1269A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2835911 | |||||||
| chr9:2835933 | A | G | 4 | a0001c0005t0001g0057 a0001c0005t0001g0058 a0001c0005t0001g0059 others(1): Show |
4 | HG01891.hp1 HG01891.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.304+1247T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2835933 | |||||||
| chr9:2835973 | T | C | 182 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(179): Show |
239 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.304+1207A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2835973 | |||||||
| chr9:2835981 | T | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(194): Show |
257 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.304+1199A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2835981 | |||||||
| chr9:2836061 | A | C | 27 | a0001c0005t0001g0084 a0003c0004t0001g0010 a0003c0004t0001g0029 others(24): Show |
35 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.304+1119T>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2836061 | |||||||
| chr9:2836086 | G | C | 5 | a0009c0011t0001g0185 a0009c0011t0001g0307 a0009c0011t0001g0309 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.304+1094C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2836086 | |||||||
| chr9:2836291 | C | T | 5 | a0009c0011t0001g0185 a0009c0011t0001g0307 a0009c0011t0001g0309 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.304+889G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2836291 | |||||||
| chr9:2836563 | T | C | 7 | a0008c0012t0001g0167 a0009c0011t0001g0185 a0009c0011t0001g0307 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.304+617A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2836563 | |||||||
| chr9:2836692 | G | A | 2 | a0002c0003t0001g0080 a0008c0012t0001g0088 |
2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.304+488C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2836692 | |||||||
| chr9:2836759 | T | C | 3 | a0005c0008t0001g0027 a0005c0008t0001g0048 a0005c0008t0001g0131 |
5 | HG02258.hp2 HG02451.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.304+421A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2836759 | |||||||
| chr9:2836783 | T | A | 1 | a0001c0005t0001g0075 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.304+397A>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2836783 | |||||||
| chr9:2836810 | C | CGT | 4 | a0001c0001t0001g0252 a0001c0005t0001g0019 a0001c0005t0001g0060 others(1): Show |
5 | HG02630.hp2 HG02818.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.304+368_304+369dup others(2): Show |
PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2836810 | |||||||
| chr9:2837029 | T | A | 1 | a0002c0003t0001g0151 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.304+151A>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2837029 | |||||||
| chr9:2837034 | G | C | 2 | a0008c0012t0001g0167 a0022c0017t0001g0168 |
2 | HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.304+146C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2837034 | |||||||
| chr9:2837140 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.304+40C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 3/17 | chr9 | 2837140 | |||||||
| chr9:2837413 | A | G | 12 | a0001c0005t0001g0057 a0001c0005t0001g0058 a0001c0005t0001g0059 others(9): Show |
12 | HG01109.hp1 HG01891.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.83-12T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 2/17 | chr9 | 2837413 | |||||||
| chr9:2837572 | A | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0188 a0001c0001t0001g0189 others(3): Show |
11 | HG00609.hp1 HG00673.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.83-171T>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 2/17 | chr9 | 2837572 | |||||||
| chr9:2837619 | G | T | 1 | a0010c0015t0005g0049 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.83-218C>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 2/17 | chr9 | 2837619 | |||||||
| chr9:2838107 | G | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(131): Show |
179 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.82+319C>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 2/17 | chr9 | 2838107 | |||||||
| chr9:2838258 | A | T | 1 | a0001c0001t0001g0251 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.82+168T>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 2/17 | chr9 | 2838258 | |||||||
| chr9:2838283 | T | C | 4 | a0001c0001t0001g0046 a0001c0001t0001g0296 a0001c0001t0001g0297 others(1): Show |
5 | NA18994.hp2 NA19004.hp2 NA19055.hp2 others(2): Show |
intron_variant | MODIFIER | c.82+143A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 2/17 | chr9 | 2838283 | |||||||
| chr9:2838295 | C | T | 2 | a0001c0005t0001g0019 a0001c0005t0001g0060 |
3 | HG02630.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.82+131G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 2/17 | chr9 | 2838295 | |||||||
| chr9:2838419 | A | G | 2 | a0001c0005t0001g0019 a0001c0005t0001g0060 |
3 | HG02630.hp2 HG02818.hp1 NA19043.hp2 |
splice_region_variant&intron_variant | LOW | c.82+7T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 2/17 | chr9 | 2838419 | |||||||
| chr9:2838767 | T | C | 1 | a0002c0002t0001g0129 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-10-250A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2838767 | |||||||
| chr9:2838771 | G | A | 4 | a0005c0008t0001g0027 a0005c0008t0001g0048 a0005c0008t0001g0131 others(1): Show |
6 | HG02258.hp2 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-254C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2838771 | |||||||
| chr9:2838901 | G | A | 2 | a0002c0003t0001g0080 a0008c0012t0001g0088 |
2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-10-384C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2838901 | |||||||
| chr9:2838971 | A | G | 1 | a0002c0002t0001g0020 | 2 | NA18945.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-10-454T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2838971 | |||||||
| chr9:2839017 | C | G | 1 | a0002c0002t0001g0089 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-10-500G>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2839017 | |||||||
| chr9:2839216 | G | C | 1 | a0013c0020t0001g0299 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-10-699C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2839216 | |||||||
| chr9:2839273 | C | T | 1 | a0008c0012t0001g0088 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-10-756G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2839273 | |||||||
| chr9:2839394 | G | C | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-10-877C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2839394 | |||||||
| chr9:2839608 | C | G | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(193): Show |
255 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.-10-1091G>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2839608 | |||||||
| chr9:2839736 | G | T | 1 | a0002c0002t0001g0087 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-10-1219C>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2839736 | |||||||
| chr9:2839826 | T | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(148): Show |
200 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.-10-1309A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2839826 | |||||||
| chr9:2839827 | G | C | 18 | a0003c0004t0001g0010 a0003c0004t0001g0029 a0003c0004t0001g0030 others(15): Show |
26 | HG00544.hp1 HG00558.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.-10-1310C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2839827 | |||||||
| chr9:2839860 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-10-1343C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2839860 | |||||||
| chr9:2839934 | G | A | 28 | a0001c0005t0001g0079 a0003c0004t0001g0010 a0003c0004t0001g0029 others(25): Show |
36 | HG00544.hp1 HG00558.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.-10-1417C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2839934 | |||||||
| chr9:2840119 | C | T | 1 | a0003c0004t0001g0311 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-10-1602G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2840119 | |||||||
| chr9:2840340 | G | A | 2 | a0008c0012t0001g0167 a0022c0017t0001g0168 |
2 | HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-10-1823C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2840340 | |||||||
| chr9:2840829 | T | G | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(147): Show |
199 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.-10-2312A>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2840829 | |||||||
| chr9:2840864 | G | C | 3 | a0005c0008t0001g0027 a0005c0008t0001g0048 a0005c0008t0001g0131 |
5 | HG02258.hp2 HG02451.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-2347C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2840864 | |||||||
| chr9:2841067 | A | T | 1 | a0002c0002t0001g0086 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-10-2550T>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2841067 | |||||||
| chr9:2841166 | T | C | 4 | a0001c0001t0001g0132 a0002c0002t0001g0133 a0002c0002t0001g0134 others(1): Show |
4 | NA18941.hp2 NA18986.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-2649A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2841166 | |||||||
| chr9:2841213 | C | T | 1 | a0001c0005t0001g0187 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-10-2696G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2841213 | |||||||
| chr9:2841345 | G | A | 2 | a0002c0002t0001g0081 a0002c0002t0001g0136 |
2 | HG02083.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.-11+2700C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2841345 | |||||||
| chr9:2841351 | G | A | 31 | a0001c0005t0001g0068 a0001c0005t0001g0069 a0001c0005t0001g0070 others(28): Show |
39 | HG00735.hp2 HG00741.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.-11+2694C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2841351 | |||||||
| chr9:2841423 | G | C | 157 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(154): Show |
206 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.-11+2622C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2841423 | |||||||
| chr9:2841493 | A | G | 183 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(180): Show |
240 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.-11+2552T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2841493 | |||||||
| chr9:2841536 | C | G | 6 | a0001c0005t0001g0057 a0001c0005t0001g0058 a0001c0005t0001g0059 others(3): Show |
6 | HG01891.hp1 HG01891.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+2509G>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2841536 | |||||||
| chr9:2841546 | C | A | 5 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0001g0303 others(2): Show |
5 | HG02602.hp1 HG02698.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11+2499G>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2841546 | |||||||
| chr9:2841551 | G | A | 3 | a0006c0009t0001g0047 a0006c0009t0001g0249 a0006c0009t0001g0306 |
4 | NA18947.hp2 NA18987.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+2494C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2841551 | |||||||
| chr9:2841615 | T | C | 1 | a0002c0002t0001g0009 | 4 | NA18944.hp1 NA18965.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+2430A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2841615 | |||||||
| chr9:2841700 | T | C | 157 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(154): Show |
206 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.-11+2345A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2841700 | |||||||
| chr9:2841714 | CA | C | 11 | a0002c0002t0001g0082 a0002c0002t0001g0083 a0003c0004t0001g0159 others(8): Show |
11 | HG02145.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11+2330delT | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2841714 | |||||||
| chr9:2841815 | T | A | 2 | a0002c0002t0001g0157 a0002c0002t0001g0166 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-11+2230A>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2841815 | |||||||
| chr9:2841861 | T | C | 24 | a0003c0004t0001g0010 a0003c0004t0001g0029 a0003c0004t0001g0030 others(21): Show |
32 | HG00544.hp1 HG00558.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.-11+2184A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2841861 | |||||||
| chr9:2841896 | G | A | 24 | a0003c0004t0001g0010 a0003c0004t0001g0029 a0003c0004t0001g0030 others(21): Show |
32 | HG00544.hp1 HG00558.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.-11+2149C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2841896 | |||||||
| chr9:2842370 | C | A | 1 | a0001c0005t0001g0040 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-11+1675G>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2842370 | |||||||
| chr9:2842383 | G | C | 31 | a0003c0004t0001g0010 a0003c0004t0001g0029 a0003c0004t0001g0030 others(28): Show |
39 | HG00544.hp1 HG00558.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.-11+1662C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2842383 | |||||||
| chr9:2842515 | A | C | 1 | a0002c0002t0001g0081 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-11+1530T>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2842515 | |||||||
| chr9:2842562 | G | A | 6 | a0001c0005t0001g0057 a0001c0005t0001g0058 a0001c0005t0001g0059 others(3): Show |
6 | HG01891.hp1 HG01891.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+1483C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2842562 | |||||||
| chr9:2842672 | G | C | 26 | a0003c0004t0001g0010 a0003c0004t0001g0029 a0003c0004t0001g0030 others(23): Show |
34 | HG00544.hp1 HG00558.hp2 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.-11+1373C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2842672 | |||||||
| chr9:2842811 | G | A | 2 | a0008c0012t0001g0167 a0022c0017t0001g0168 |
2 | HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-11+1234C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2842811 | |||||||
| chr9:2842819 | T | C | 1 | a0002c0002t0001g0158 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-11+1226A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2842819 | |||||||
| chr9:2842901 | T | A | 1 | a0002c0002t0001g0076 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-11+1144A>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2842901 | |||||||
| chr9:2842997 | C | T | 1 | a0002c0003t0001g0080 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-11+1048G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2842997 | |||||||
| chr9:2843178 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0186 |
3 | HG02717.hp1 HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-11+867G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2843178 | |||||||
| chr9:2843201 | T | C | 23 | a0003c0004t0001g0010 a0003c0004t0001g0029 a0003c0004t0001g0030 others(20): Show |
31 | HG00544.hp1 HG00558.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.-11+844A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2843201 | |||||||
| chr9:2843326 | A | G | 13 | a0001c0005t0001g0057 a0001c0005t0001g0058 a0001c0005t0001g0059 others(10): Show |
13 | HG01891.hp1 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-11+719T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2843326 | |||||||
| chr9:2843488 | G | A | 2 | a0010c0015t0004g0056 a0010c0015t0005g0049 |
2 | HG02896.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-11+557C>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2843488 | |||||||
| chr9:2843502 | G | T | 1 | a0002c0003t0001g0078 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-11+543C>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2843502 | |||||||
| chr9:2843531 | C | T | 1 | a0018c0021t0007g0312 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-11+514G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2843531 | |||||||
| chr9:2843567 | G | T | 1 | a0002c0002t0001g0077 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-11+478C>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2843567 | |||||||
| chr9:2843573 | C | CT | 22 | a0001c0001t0001g0183 a0001c0005t0001g0019 a0001c0005t0001g0060 others(19): Show |
23 | HG00673.hp1 HG00738.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.-11+471dupA | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2843573 | |||||||
| chr9:2843573 | CT | C | 98 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(95): Show |
134 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.-11+471delA | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2843573 | |||||||
| chr9:2843618 | T | G | 1 | a0002c0002t0001g0181 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-11+427A>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2843618 | |||||||
| chr9:2843633 | T | C | 1 | a0002c0002t0001g0181 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-11+412A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2843633 | |||||||
| chr9:2843640 | A | G | 1 | a0002c0002t0001g0181 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-11+405T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2843640 | |||||||
| chr9:2843647 | T | C | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(146): Show |
195 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.-11+398A>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2843647 | |||||||
| chr9:2843654 | C | A | 1 | a0001c0005t0001g0061 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-11+391G>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2843654 | |||||||
| chr9:2843664 | C | T | 10 | a0001c0005t0001g0057 a0001c0005t0001g0058 a0001c0005t0001g0059 others(7): Show |
10 | HG01891.hp1 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11+381G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2843664 | |||||||
| chr9:2843704 | A | G | 9 | a0001c0005t0001g0019 a0001c0005t0001g0057 a0001c0005t0001g0058 others(6): Show |
10 | HG01891.hp1 HG01891.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11+341T>C | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2843704 | |||||||
| chr9:2843764 | G | C | 4 | a0009c0011t0001g0307 a0009c0011t0001g0309 a0015c0029t0001g0310 others(1): Show |
4 | HG02145.hp1 HG02280.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+281C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2843764 | |||||||
| chr9:2843862 | G | C | 1 | a0003c0004t0001g0311 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-11+183C>G | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2843862 | |||||||
| chr9:2843993 | C | T | 3 | a0002c0002t0001g0052 a0002c0002t0001g0053 a0002c0002t0001g0054 |
3 | HG00741.hp2 HG02886.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-11+52G>A | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2843993 | |||||||
| chr9:2844020 | C | A | 1 | a0005c0008t0001g0048 | 2 | HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-11+25G>T | PUM3 | ENSG00000080608.10 | transcript | ENST00000397885.3 | protein_coding | 1/17 | chr9 | 2844020 |