Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 642574 |
| ensemblid | ENSG00000203499.12 |
| hgncid | 49576 |
| symbol | IQANK1 |
| name | IQ motif and ankyrin repeat containing 1 |
| refseq_nuc | NM_001381874.1 |
| refseq_prot | NP_001368803.1 |
| ensembl_nuc | ENST00000527139.7 |
| ensembl_prot | ENSP00000489685.1 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 143734139 |
| end | 143790645 |
| strand | + |
| ver | v1.2 |
| region | chr8:143734139-143790645 |
| region5000 | chr8:143729139-143795645 |
| regionname0 | IQANK1_chr8_143734139_143790645 |
| regionname5000 | IQANK1_chr8_143729139_143795645 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 560 | 107 | 9 | 12 | 66 | 3 | 16 | 44 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0002 | 0/0 | 560 | 90 | 1 | 17 | 64 | 3 | 5 | 41 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0003 | 0/0 | 560 | 38 | 36 | 1 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0004 | 0/0 | 560 | 31 | 1 | 16 | 1 | 8 | 5 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0005 | 0/0 | 560 | 16 | 3 | 1 | 8 | 1 | 3 | 5 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0006 | 0/0 | 560 | 8 | 4 | 3 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0007 | 0/0 | 560 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0008 | 0/0 | 560 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0009 | 0/0 | 560 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0010 | 0/0 | 560 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0011 | 0/0 | 561 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(556): Show |
chr8 | 143729139 | 143795645 |
| a0012 | 0/0 | 560 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0013 | 0/0 | 560 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0014 | 0/0 | 560 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0015 | 0/0 | 561 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(556): Show |
chr8 | 143729139 | 143795645 |
| a0016 | 0/0 | 560 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0017 | 0/0 | 560 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0018 | 0/0 | 560 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0019 | 0/0 | 560 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0020 | 0/0 | 560 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0021 | 0/0 | 560 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0022 | 0/0 | 560 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0023 | 0/0 | 560 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0024 | 0/0 | 560 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0025 | 0/0 | 560 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0026 | 0/0 | 560 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0027 | 0/0 | 560 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0028 | 0/0 | 560 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0029 | 0/0 | 560 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0030 | 0/0 | 560 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0031 | 0/0 | 560 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| a0032 | 0/0 | 560 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | MDSKK others(555): Show |
chr8 | 143729139 | 143795645 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1680 | 103 | 5 | 12 | 66 | 3 | 16 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0001c0010 | 0/0 | 1680 | 4 | 4 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0002c0002 | 0/0 | 1680 | 89 | 1 | 17 | 63 | 3 | 5 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0002c0035 | 0/0 | 1680 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0003c0003 | 0/0 | 1680 | 38 | 36 | 1 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0004c0004 | 0/0 | 1680 | 31 | 1 | 16 | 1 | 8 | 5 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0005c0005 | 0/0 | 1680 | 16 | 3 | 1 | 8 | 1 | 3 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0006c0006 | 0/0 | 1680 | 8 | 4 | 3 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0007c0007 | 0/0 | 1680 | 8 | 8 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0008c0008 | 0/0 | 1680 | 7 | 7 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0009c0009 | 0/0 | 1680 | 6 | 5 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0010c0011 | 0/0 | 1680 | 4 | 4 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0011c0012 | 0/0 | 1683 | 3 | 2 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1678): Show |
chr8 | 143729139 | 143795645 | ||
| a0012c0017 | 0/0 | 1680 | 2 | 2 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0012c0027 | 0/0 | 1680 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0013c0013 | 0/0 | 1680 | 3 | 0 | 0 | 0 | 0 | 3 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0014c0019 | 0/0 | 1680 | 2 | 0 | 1 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0015c0016 | 0/0 | 1683 | 2 | 1 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1678): Show |
chr8 | 143729139 | 143795645 | ||
| a0016c0018 | 0/0 | 1680 | 2 | 0 | 2 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0017c0015 | 0/0 | 1680 | 2 | 0 | 1 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0018c0014 | 0/0 | 1680 | 2 | 0 | 0 | 0 | 0 | 2 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0019c0020 | 0/0 | 1680 | 2 | 0 | 0 | 0 | 0 | 2 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0020c0023 | 0/0 | 1680 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0021c0033 | 0/0 | 1680 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0022c0028 | 0/0 | 1680 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0023c0022 | 0/0 | 1680 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0024c0030 | 0/0 | 1680 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0025c0029 | 0/0 | 1680 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0026c0034 | 0/0 | 1680 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0027c0021 | 0/0 | 1680 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0028c0032 | 0/0 | 1680 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0029c0026 | 0/0 | 1680 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0030c0024 | 0/0 | 1680 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0031c0025 | 0/0 | 1680 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 | ||
| a0032c0031 | 0/0 | 1680 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | ATGGA others(1675): Show |
chr8 | 143729139 | 143795645 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1805 | 101 | 5 | 12 | 64 | 3 | 16 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0001c0001t0002 | 0/0 | 1805 | 2 | 0 | 0 | 2 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0001c0010t0001 | 0/0 | 1805 | 4 | 4 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0002c0002t0001 | 0/0 | 1805 | 89 | 1 | 17 | 63 | 3 | 5 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0002c0035t0001 | 0/0 | 1805 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0003c0003t0001 | 0/0 | 1805 | 38 | 36 | 1 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0004c0004t0001 | 0/0 | 1805 | 31 | 1 | 16 | 1 | 8 | 5 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0005c0005t0001 | 0/0 | 1805 | 16 | 3 | 1 | 8 | 1 | 3 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0006c0006t0001 | 0/0 | 1805 | 8 | 4 | 3 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0007c0007t0001 | 0/0 | 1805 | 8 | 8 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0008c0008t0001 | 0/0 | 1805 | 7 | 7 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0009c0009t0001 | 0/0 | 1805 | 6 | 5 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0010c0011t0001 | 0/0 | 1805 | 4 | 4 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0011c0012t0001 | 0/0 | 1808 | 3 | 2 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1803): Show |
chr8 | 143729139 | 143795645 |
| a0012c0017t0001 | 0/0 | 1805 | 2 | 2 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0012c0027t0001 | 0/0 | 1805 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0013c0013t0001 | 0/0 | 1805 | 3 | 0 | 0 | 0 | 0 | 3 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0014c0019t0001 | 0/0 | 1805 | 2 | 0 | 1 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0015c0016t0001 | 0/0 | 1808 | 2 | 1 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1803): Show |
chr8 | 143729139 | 143795645 |
| a0016c0018t0001 | 0/0 | 1805 | 2 | 0 | 2 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0017c0015t0001 | 0/0 | 1805 | 2 | 0 | 1 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0018c0014t0001 | 0/0 | 1805 | 2 | 0 | 0 | 0 | 0 | 2 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0019c0020t0001 | 0/0 | 1805 | 2 | 0 | 0 | 0 | 0 | 2 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0020c0023t0001 | 0/0 | 1805 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0021c0033t0001 | 0/0 | 1805 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0022c0028t0001 | 0/0 | 1805 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0023c0022t0001 | 0/0 | 1805 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0024c0030t0001 | 0/0 | 1805 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0025c0029t0001 | 0/0 | 1805 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0026c0034t0001 | 0/0 | 1805 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0027c0021t0001 | 0/0 | 1805 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0028c0032t0001 | 0/0 | 1805 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0029c0026t0001 | 0/0 | 1805 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0030c0024t0001 | 0/0 | 1805 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0031c0025t0001 | 0/0 | 1805 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| a0032c0031t0001 | 0/0 | 1805 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | AGTCG others(1800): Show |
chr8 | 143729139 | 143795645 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0148 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0010t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0010t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0010t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0001c0010t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0002c0035t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0003c0003t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0004c0004t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0005c0005t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0005c0005t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0005c0005t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0005c0005t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0005c0005t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0005c0005t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0005c0005t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0005c0005t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0005c0005t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0005c0005t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0005c0005t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0005c0005t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0005c0005t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0005c0005t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0005c0005t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0005c0005t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0006c0006t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0006c0006t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0006c0006t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0006c0006t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0006c0006t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0006c0006t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0006c0006t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0006c0006t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0007c0007t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0007c0007t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0007c0007t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0007c0007t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0007c0007t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0007c0007t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0007c0007t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0007c0007t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0008c0008t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0008c0008t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0008c0008t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0008c0008t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0008c0008t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0008c0008t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0008c0008t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0009c0009t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0009c0009t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0009c0009t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0009c0009t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0009c0009t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0009c0009t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0010c0011t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0010c0011t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0010c0011t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0010c0011t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0011c0012t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0011c0012t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0011c0012t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0012c0017t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0012c0017t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0012c0027t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0013c0013t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0013c0013t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0013c0013t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0014c0019t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0014c0019t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0015c0016t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0015c0016t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0016c0018t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0016c0018t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0017c0015t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0017c0015t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0018c0014t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0018c0014t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0019c0020t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0019c0020t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0020c0023t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0021c0033t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0022c0028t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0023c0022t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0024c0030t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0025c0029t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0026c0034t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0027c0021t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0028c0032t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0029c0026t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0030c0024t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0031c0025t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| a0032c0031t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0004 | c0004 | t0001 | g0167 | EUR | GBR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00099 | hp2 | a0004 | c0004 | t0001 | g0184 | EUR | GBR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | GBR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0309 | EUR | GBR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0285 | EUR | FIN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00280 | hp2 | a0005 | c0005 | t0001 | g0216 | EUR | FIN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0293 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0334 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0331 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00544 | hp1 | a0005 | c0005 | t0001 | g0209 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0318 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0292 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0317 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0265 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0322 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0333 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0258 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00642 | hp1 | a0006 | c0006 | t0001 | g0176 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0301 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00733 | hp1 | a0004 | c0004 | t0001 | g0087 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00733 | hp2 | a0014 | c0019 | t0001 | g0021 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00735 | hp1 | a0005 | c0005 | t0001 | g0215 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00735 | hp2 | a0006 | c0006 | t0001 | g0174 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00738 | hp1 | a0004 | c0004 | t0001 | g0086 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG00738 | hp2 | a0004 | c0004 | t0001 | g0182 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01069 | hp1 | a0020 | c0023 | t0001 | g0055 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01071 | hp1 | a0004 | c0004 | t0001 | g0177 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01074 | hp1 | a0004 | c0004 | t0001 | g0053 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0264 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0328 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01081 | hp2 | a0004 | c0004 | t0001 | g0158 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01109 | hp1 | a0015 | c0016 | t0001 | g0345 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01109 | hp2 | a0004 | c0004 | t0001 | g0155 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01168 | hp1 | a0016 | c0018 | t0001 | g0180 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01175 | hp1 | a0011 | c0012 | t0001 | g0342 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01175 | hp2 | a0004 | c0004 | t0001 | g0173 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01192 | hp1 | a0004 | c0004 | t0001 | g0088 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01192 | hp2 | a0009 | c0009 | t0001 | g0010 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01243 | hp1 | a0004 | c0004 | t0001 | g0183 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0279 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0261 | AMR | CLM | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01261 | hp2 | a0004 | c0004 | t0001 | g0161 | AMR | CLM | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0268 | AMR | CLM | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0298 | AMR | CLM | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01358 | hp1 | a0004 | c0004 | t0001 | g0163 | AMR | CLM | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01361 | hp2 | a0006 | c0006 | t0001 | g0175 | AMR | CLM | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01496 | hp1 | a0016 | c0018 | t0001 | g0181 | AMR | CLM | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01496 | hp2 | a0004 | c0004 | t0001 | g0188 | AMR | CLM | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01515 | hp1 | a0004 | c0004 | t0001 | g0089 | EUR | IBS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01515 | hp2 | a0017 | c0015 | t0001 | g0172 | EUR | IBS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01516 | hp1 | a0004 | c0004 | t0001 | g0168 | EUR | IBS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0205 | EUR | IBS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0058 | EUR | IBS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01517 | hp2 | a0004 | c0004 | t0001 | g0090 | EUR | IBS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01884 | hp1 | a0021 | c0033 | t0001 | g0329 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01884 | hp2 | a0003 | c0003 | t0001 | g0031 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01891 | hp1 | a0008 | c0008 | t0001 | g0024 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0255 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0310 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0259 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01975 | hp2 | a0003 | c0003 | t0001 | g0242 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0269 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0324 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01981 | hp1 | a0004 | c0004 | t0001 | g0178 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0262 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02004 | hp1 | a0004 | c0004 | t0001 | g0156 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0302 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0289 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02015 | hp2 | a0004 | c0004 | t0001 | g0247 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02027 | hp1 | a0005 | c0005 | t0001 | g0211 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0305 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02055 | hp1 | a0005 | c0005 | t0001 | g0321 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02055 | hp2 | a0022 | c0028 | t0001 | g0153 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0282 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0296 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0297 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0260 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0256 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02083 | hp1 | a0006 | c0006 | t0001 | g0059 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0276 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0278 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02145 | hp1 | a0007 | c0007 | t0001 | g0204 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02145 | hp2 | a0005 | c0005 | t0001 | g0283 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CDX | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CDX | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CDX | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0290 | EAS | CDX | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0213 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02257 | hp2 | a0006 | c0006 | t0001 | g0033 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02258 | hp1 | a0003 | c0003 | t0001 | g0230 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02258 | hp2 | a0007 | c0007 | t0001 | g0045 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02280 | hp1 | a0003 | c0003 | t0001 | g0037 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02280 | hp2 | a0003 | c0003 | t0001 | g0226 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02293 | hp1 | a0017 | c0015 | t0001 | g0157 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0274 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0313 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02572 | hp1 | a0008 | c0008 | t0001 | g0032 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02572 | hp2 | a0007 | c0007 | t0001 | g0017 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02602 | hp2 | a0023 | c0022 | t0001 | g0062 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02615 | hp1 | a0003 | c0003 | t0001 | g0012 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02615 | hp2 | a0007 | c0007 | t0001 | g0044 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02622 | hp1 | a0024 | c0030 | t0001 | g0343 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02622 | hp2 | a0003 | c0003 | t0001 | g0228 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02630 | hp1 | a0003 | c0003 | t0001 | g0072 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02630 | hp2 | a0003 | c0003 | t0001 | g0232 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02647 | hp1 | a0003 | c0003 | t0001 | g0066 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02647 | hp2 | a0008 | c0008 | t0001 | g0240 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02683 | hp1 | a0018 | c0014 | t0001 | g0061 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02683 | hp2 | a0004 | c0004 | t0001 | g0187 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0007 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02698 | hp2 | a0004 | c0004 | t0001 | g0166 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02717 | hp1 | a0003 | c0003 | t0001 | g0035 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02723 | hp1 | a0009 | c0009 | t0001 | g0014 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02723 | hp2 | a0003 | c0003 | t0001 | g0144 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02809 | hp1 | a0003 | c0003 | t0001 | g0038 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02809 | hp2 | a0025 | c0029 | t0001 | g0224 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02886 | hp1 | a0010 | c0011 | t0001 | g0231 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02886 | hp2 | a0008 | c0008 | t0001 | g0239 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02895 | hp1 | a0003 | c0003 | t0001 | g0001 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02895 | hp2 | a0003 | c0003 | t0001 | g0039 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02896 | hp1 | a0003 | c0003 | t0001 | g0001 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02896 | hp2 | a0003 | c0003 | t0001 | g0236 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02897 | hp1 | a0003 | c0003 | t0001 | g0229 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02897 | hp2 | a0003 | c0003 | t0001 | g0235 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02922 | hp1 | a0026 | c0034 | t0001 | g0212 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02922 | hp2 | a0003 | c0003 | t0001 | g0202 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02965 | hp1 | a0010 | c0011 | t0001 | g0223 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02965 | hp2 | a0003 | c0003 | t0001 | g0057 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02970 | hp1 | a0010 | c0011 | t0001 | g0233 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02970 | hp2 | a0001 | c0010 | t0001 | g0041 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02976 | hp1 | a0027 | c0021 | t0001 | g0335 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02976 | hp2 | a0028 | c0032 | t0001 | g0028 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03041 | hp1 | a0003 | c0003 | t0001 | g0018 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03041 | hp2 | a0003 | c0003 | t0001 | g0036 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03098 | hp1 | a0003 | c0003 | t0001 | g0048 | AFR | MSL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03098 | hp2 | a0010 | c0011 | t0001 | g0011 | AFR | MSL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03130 | hp1 | a0007 | c0007 | t0001 | g0046 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03130 | hp2 | a0009 | c0009 | t0001 | g0027 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03139 | hp1 | a0003 | c0003 | t0001 | g0143 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03195 | hp1 | a0001 | c0010 | t0001 | g0042 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03195 | hp2 | a0003 | c0003 | t0001 | g0197 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03209 | hp1 | a0012 | c0027 | t0001 | g0016 | AFR | MSL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03209 | hp2 | a0003 | c0003 | t0001 | g0234 | AFR | MSL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03225 | hp1 | a0003 | c0003 | t0001 | g0227 | AFR | MSL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03225 | hp2 | a0003 | c0003 | t0001 | g0200 | AFR | MSL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03239 | hp2 | a0004 | c0004 | t0001 | g0171 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03453 | hp1 | a0009 | c0009 | t0001 | g0030 | AFR | MSL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03453 | hp2 | a0008 | c0008 | t0001 | g0241 | AFR | MSL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03486 | hp1 | a0003 | c0003 | t0001 | g0201 | AFR | MSL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03486 | hp2 | a0011 | c0012 | t0001 | g0344 | AFR | MSL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03490 | hp1 | a0013 | c0013 | t0001 | g0020 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03490 | hp2 | a0019 | c0020 | t0001 | g0280 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03492 | hp1 | a0013 | c0013 | t0001 | g0019 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03516 | hp1 | a0008 | c0008 | t0001 | g0135 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03516 | hp2 | a0001 | c0010 | t0001 | g0040 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03540 | hp1 | a0009 | c0009 | t0001 | g0022 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03540 | hp2 | a0003 | c0003 | t0001 | g0225 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03579 | hp1 | a0009 | c0009 | t0001 | g0029 | AFR | MSL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03579 | hp2 | a0011 | c0012 | t0001 | g0339 | AFR | MSL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03654 | hp1 | a0003 | c0003 | t0001 | g0093 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03669 | hp1 | a0013 | c0013 | t0001 | g0026 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03669 | hp2 | a0018 | c0014 | t0001 | g0060 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03704 | hp1 | a0005 | c0005 | t0001 | g0326 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03710 | hp1 | a0029 | c0026 | t0001 | g0152 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0281 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03834 | hp2 | a0005 | c0005 | t0001 | g0327 | SAS | BEB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03927 | hp1 | a0004 | c0004 | t0001 | g0185 | SAS | BEB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0314 | SAS | BEB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0270 | SAS | BEB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | STU | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0006 | SAS | STU | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG04199 | hp1 | a0004 | c0004 | t0001 | g0154 | SAS | STU | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG04199 | hp2 | a0014 | c0019 | t0001 | g0025 | SAS | STU | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | STU | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG04204 | hp2 | a0005 | c0005 | t0001 | g0214 | SAS | STU | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | STU | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG04228 | hp2 | a0019 | c0020 | t0001 | g0288 | SAS | STU | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18522 | hp1 | a0015 | c0016 | t0001 | g0238 | AFR | YRI | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18522 | hp2 | a0008 | c0008 | t0001 | g0023 | AFR | YRI | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18612 | hp1 | a0005 | c0005 | t0001 | g0219 | EAS | CHB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0306 | EAS | CHB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18906 | hp1 | a0001 | c0010 | t0001 | g0043 | AFR | YRI | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18906 | hp2 | a0012 | c0017 | t0001 | g0198 | AFR | YRI | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18939 | hp1 | a0005 | c0005 | t0001 | g0210 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0251 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0294 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18943 | hp2 | a0030 | c0024 | t0001 | g0196 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0299 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18947 | hp2 | a0005 | c0005 | t0001 | g0217 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0307 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18950 | hp1 | a0005 | c0005 | t0001 | g0218 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0332 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18968 | hp1 | a0031 | c0025 | t0001 | g0104 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0319 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0323 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0315 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0311 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0304 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0286 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18995 | hp1 | a0005 | c0005 | t0001 | g0221 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0316 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19000 | hp2 | a0005 | c0005 | t0001 | g0220 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0275 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19030 | hp1 | a0003 | c0003 | t0001 | g0237 | AFR | LWK | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19030 | hp2 | a0006 | c0006 | t0001 | g0063 | AFR | LWK | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19043 | hp1 | a0032 | c0031 | t0001 | g0245 | AFR | LWK | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19043 | hp2 | a0003 | c0003 | t0001 | g0013 | AFR | LWK | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0287 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0320 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0337 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0295 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0312 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19070 | hp2 | a0002 | c0035 | t0001 | g0303 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0325 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0308 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA20129 | hp1 | a0003 | c0003 | t0001 | g0222 | AFR | ASW | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA20129 | hp2 | a0007 | c0007 | t0001 | g0047 | AFR | ASW | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA20752 | hp1 | a0004 | c0004 | t0001 | g0179 | EUR | TSI | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA20752 | hp2 | a0004 | c0004 | t0001 | g0170 | EUR | TSI | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA20805 | hp1 | a0004 | c0004 | t0001 | g0192 | EUR | TSI | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0284 | EUR | TSI | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | GIH | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | GIH | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01123 | hp1 | a0004 | c0004 | t0001 | g0164 | AMR | CLM | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02486 | hp1 | a0003 | c0003 | t0001 | g0340 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02486 | hp2 | a0007 | c0007 | t0001 | g0015 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG02559 | hp2 | a0003 | c0003 | t0001 | g0145 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03471 | hp1 | a0007 | c0007 | t0001 | g0203 | AFR | MSL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG03471 | hp2 | a0006 | c0006 | t0001 | g0034 | AFR | MSL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG06807 | hp1 | a0005 | c0005 | t0001 | g0330 | AFR | USA | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| HG06807 | hp2 | a0006 | c0006 | t0001 | g0186 | AFR | USA | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA20300 | hp1 | a0003 | c0003 | t0001 | g0199 | AFR | USA | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | USA | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA21309 | hp1 | a0012 | c0017 | t0001 | g0067 | AFR | LWK | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| NA21309 | hp2 | a0004 | c0004 | t0001 | g0336 | AFR | LWK | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0148 | REF | REF | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:143739867 | G | T | 5 | a0002 a0005 a0019 others(2): Show |
110 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
missense_variant | MODERATE | c.94G>T | p.Gly32Trp | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/14 | 179/1805 | 94/1683 | 32/560 | chr8 | 143739867 | |||
| chr8:143739894 | G | A | 1 | a0027 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.121G>A | p.Ala41Thr | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/14 | 206/1805 | 121/1683 | 41/560 | chr8 | 143739894 | |||
| chr8:143739895 | C | T | 1 | a0027 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.122C>T | p.Ala41Val | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/14 | 207/1805 | 122/1683 | 41/560 | chr8 | 143739895 | |||
| chr8:143739922 | C | T | 1 | a0014 | 2 | HG00733.hp2 HG04199.hp2 |
missense_variant | MODERATE | c.149C>T | p.Ser50Leu | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/14 | 234/1805 | 149/1683 | 50/560 | chr8 | 143739922 | |||
| chr8:143739940 | C | A | 1 | a0027 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.167C>A | p.Ala56Asp | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/14 | 252/1805 | 167/1683 | 56/560 | chr8 | 143739940 | |||
| chr8:143771521 | A | G | 6 | a0008 a0009 a0013 others(3): Show |
20 | HG00733.hp2 HG01192.hp2 HG01891.hp1 others(17): Show |
missense_variant | MODERATE | c.209A>G | p.Gln70Arg | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 4/14 | 294/1805 | 209/1683 | 70/560 | chr8 | 143771521 | |||
| chr8:143771614 | A | G | 18 | a0002 a0003 a0005 others(15): Show |
181 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(178): Show |
missense_variant | MODERATE | c.302A>G | p.Lys101Arg | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 4/14 | 387/1805 | 302/1683 | 101/560 | chr8 | 143771614 | |||
| chr8:143772134 | C | T | 2 | a0007 a0027 |
9 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(6): Show |
missense_variant | MODERATE | c.554C>T | p.Ala185Val | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 6/14 | 639/1805 | 554/1683 | 185/560 | chr8 | 143772134 | |||
| chr8:143772161 | C | T | 1 | a0024 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.581C>T | p.Thr194Met | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 6/14 | 666/1805 | 581/1683 | 194/560 | chr8 | 143772161 | |||
| chr8:143772435 | G | A | 5 | a0002 a0018 a0019 others(2): Show |
96 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
missense_variant | MODERATE | c.742G>A | p.Gly248Arg | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/14 | 827/1805 | 742/1683 | 248/560 | chr8 | 143772435 | |||
| chr8:143789022 | G | C | 1 | a0020 | 1 | HG01069.hp1 | missense_variant | MODERATE | c.897G>C | p.Glu299Asp | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 8/14 | 982/1805 | 897/1683 | 299/560 | chr8 | 143789022 | |||
| chr8:143789463 | C | T | 10 | a0004 a0013 a0016 others(7): Show |
45 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(42): Show |
missense_variant | MODERATE | c.1021C>T | p.Arg341Trp | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 10/14 | 1106/1805 | 1021/1683 | 341/560 | chr8 | 143789463 | |||
| chr8:143789976 | G | C | 1 | a0026 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.1201G>C | p.Glu401Gln | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 12/14 | 1286/1805 | 1201/1683 | 401/560 | chr8 | 143789976 | |||
| chr8:143790018 | G | A | 1 | a0022 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.1243G>A | p.Asp415Asn | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 12/14 | 1328/1805 | 1243/1683 | 415/560 | chr8 | 143790018 | |||
| chr8:143790142 | C | A | 1 | a0030 | 1 | NA18943.hp2 | missense_variant | MODERATE | c.1295C>A | p.Pro432His | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 13/14 | 1380/1805 | 1295/1683 | 432/560 | chr8 | 143790142 | |||
| chr8:143790241 | C | G | 18 | a0001 a0002 a0003 others(15): Show |
288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
missense_variant | MODERATE | c.1394C>G | p.Thr465Arg | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 13/14 | 1479/1805 | 1394/1683 | 465/560 | chr8 | 143790241 | |||
| chr8:143790253 | C | T | 3 | a0008 a0010 a0032 |
12 | HG01891.hp1 HG02572.hp1 HG02647.hp2 others(9): Show |
missense_variant | MODERATE | c.1406C>T | p.Ala469Val | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 13/14 | 1491/1805 | 1406/1683 | 469/560 | chr8 | 143790253 | |||
| chr8:143790372 | G | C | 2 | a0011 a0015 |
5 | HG01109.hp1 HG01175.hp1 HG03486.hp2 others(2): Show |
missense_variant | MODERATE | c.1447G>C | p.Asp483His | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 14/14 | 1532/1805 | 1447/1683 | 483/560 | chr8 | 143790372 | |||
| chr8:143790408 | C | T | 1 | a0031 | 1 | NA18968.hp1 | missense_variant | MODERATE | c.1483C>T | p.Arg495Trp | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 14/14 | 1568/1805 | 1483/1683 | 495/560 | chr8 | 143790408 | |||
| chr8:143790424 | T | TGCA | 2 | a0011 a0015 |
5 | HG01109.hp1 HG01175.hp1 HG03486.hp2 others(2): Show |
conservative_inframe_insertion | MODERATE | c.1501_1503dupCAG | p.Gln501dup | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 14/14 | 1589/1805 | 1504/1683 | 502/560 | INFO_REALIGN_3_PRIME | chr8 | 143790424 | ||
| chr8:143790459 | G | A | 1 | a0029 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.1534G>A | p.Asp512Asn | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 14/14 | 1619/1805 | 1534/1683 | 512/560 | chr8 | 143790459 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:143772183 | A | G | 3 | a0001c0010 a0007c0007 a0027c0021 |
13 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(10): Show |
synonymous_variant | LOW | c.603A>G | p.Ala201Ala | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 6/14 | 688/1805 | 603/1683 | 201/560 | chr8 | 143772183 | |||
| chr8:143789480 | C | T | 2 | a0012c0017 a0028c0032 |
3 | HG02976.hp2 NA18906.hp2 NA21309.hp1 |
synonymous_variant | LOW | c.1038C>T | p.His346His | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 10/14 | 1123/1805 | 1038/1683 | 346/560 | chr8 | 143789480 | |||
| chr8:143789999 | C | T | 1 | a0002c0035 | 1 | NA19070.hp2 | synonymous_variant | LOW | c.1224C>T | p.Cys408Cys | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 12/14 | 1309/1805 | 1224/1683 | 408/560 | chr8 | 143789999 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:143790641 | C | T | 1 | a0001c0001t0002 | 2 | NA18957.hp2 NA19001.hp1 |
3_prime_UTR_variant | MODIFIER | c.*33C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 14/14 | 33 | chr8 | 143790641 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:143734223 | A | G | 8 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0003c0003t0001g0340 others(5): Show |
8 | HG01109.hp1 HG01175.hp1 HG02486.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.-5+4A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143734223 | |||||||
| chr8:143734255 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-5+36G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143734255 | |||||||
| chr8:143734330 | C | T | 1 | a0002c0002t0001g0337 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-5+111C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143734330 | |||||||
| chr8:143734379 | C | T | 1 | a0004c0004t0001g0336 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-5+160C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143734379 | |||||||
| chr8:143734418 | C | T | 1 | a0027c0021t0001g0335 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-5+199C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143734418 | |||||||
| chr8:143734459 | G | C | 2 | a0002c0002t0001g0006 a0002c0002t0001g0007 |
2 | HG02698.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-5+240G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143734459 | |||||||
| chr8:143734489 | T | C | 1 | a0002c0002t0001g0008 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-5+270T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143734489 | |||||||
| chr8:143734498 | G | GGACCCCG others(7): Show |
1 | a0002c0002t0001g0009 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-5+280_-5+293dupGA others(12): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr8 | 143734498 | ||||||
| chr8:143734589 | C | T | 94 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0004 others(91): Show |
97 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.-5+370C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143734589 | |||||||
| chr8:143734622 | C | T | 1 | a0002c0002t0001g0334 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-5+403C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143734622 | |||||||
| chr8:143734623 | G | A | 23 | a0003c0003t0001g0012 a0003c0003t0001g0013 a0003c0003t0001g0018 others(20): Show |
23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.-5+404G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143734623 | |||||||
| chr8:143734725 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-5+506C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143734725 | |||||||
| chr8:143734867 | C | G | 1 | a0004c0004t0001g0247 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-5+648C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143734867 | |||||||
| chr8:143735164 | G | T | 1 | a0001c0001t0001g0246 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-4-686G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143735164 | |||||||
| chr8:143735167 | T | G | 1 | a0001c0001t0001g0246 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-4-683T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143735167 | |||||||
| chr8:143735168 | G | T | 1 | a0001c0001t0001g0246 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-4-682G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143735168 | |||||||
| chr8:143735199 | C | T | 23 | a0003c0003t0001g0012 a0003c0003t0001g0013 a0003c0003t0001g0018 others(20): Show |
23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.-4-651C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143735199 | |||||||
| chr8:143735316 | G | A | 341 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(338): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.-4-534G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143735316 | |||||||
| chr8:143735351 | C | G | 1 | a0002c0002t0001g0333 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-4-499C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143735351 | |||||||
| chr8:143735483 | TGATTAC | T | 22 | a0003c0003t0001g0001 a0003c0003t0001g0222 a0003c0003t0001g0225 others(19): Show |
23 | HG01975.hp2 HG02258.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.-4-365_-4-360delAT others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr8 | 143735483 | ||||||
| chr8:143735523 | G | A | 2 | a0006c0006t0001g0033 a0006c0006t0001g0034 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-4-327G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143735523 | |||||||
| chr8:143735540 | G | A | 5 | a0003c0003t0001g0035 a0003c0003t0001g0036 a0003c0003t0001g0037 others(2): Show |
5 | HG02280.hp1 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-310G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143735540 | |||||||
| chr8:143735734 | G | A | 8 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(5): Show |
8 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4-116G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143735734 | |||||||
| chr8:143735748 | C | A | 1 | a0003c0003t0001g0048 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-4-102C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143735748 | |||||||
| chr8:143735833 | C | T | 1 | a0002c0002t0001g0332 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-4-17C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143735833 | |||||||
| chr8:143736008 | A | C | 1 | a0027c0021t0001g0335 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.85+70A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143736008 | |||||||
| chr8:143736010 | C | T | 1 | a0002c0002t0001g0334 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.85+72C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143736010 | |||||||
| chr8:143736140 | T | A | 1 | a0003c0003t0001g0222 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.85+202T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143736140 | |||||||
| chr8:143736141 | A | AT | 108 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(105): Show |
111 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.85+220dupT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr8 | 143736141 | ||||||
| chr8:143736141 | AT | A | 16 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(13): Show |
16 | HG00558.hp1 HG01069.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.85+220delT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr8 | 143736141 | ||||||
| chr8:143736177 | T | C | 23 | a0003c0003t0001g0012 a0003c0003t0001g0013 a0003c0003t0001g0018 others(20): Show |
23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.85+239T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143736177 | |||||||
| chr8:143736334 | G | C | 1 | a0002c0002t0001g0253 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.85+396G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143736334 | |||||||
| chr8:143736370 | CCTGACCT others(20): Show |
C | 1 | a0002c0002t0001g0252 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.85+433_85+459delCT others(25): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143736370 | |||||||
| chr8:143736481 | C | G | 1 | a0002c0002t0001g0253 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.85+543C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143736481 | |||||||
| chr8:143736547 | G | T | 1 | a0002c0002t0001g0253 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.85+609G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143736547 | |||||||
| chr8:143736639 | C | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0205 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.85+701C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143736639 | |||||||
| chr8:143736657 | C | A | 22 | a0003c0003t0001g0001 a0003c0003t0001g0222 a0003c0003t0001g0225 others(19): Show |
23 | HG01975.hp2 HG02258.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.85+719C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143736657 | |||||||
| chr8:143736690 | T | A | 1 | a0006c0006t0001g0059 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.85+752T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143736690 | |||||||
| chr8:143736782 | C | T | 22 | a0003c0003t0001g0001 a0003c0003t0001g0222 a0003c0003t0001g0225 others(19): Show |
23 | HG01975.hp2 HG02258.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.85+844C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143736782 | |||||||
| chr8:143736806 | C | T | 1 | a0002c0002t0001g0331 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.85+868C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143736806 | |||||||
| chr8:143736897 | C | T | 10 | a0003c0003t0001g0048 a0003c0003t0001g0057 a0003c0003t0001g0197 others(7): Show |
10 | HG02145.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.85+959C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143736897 | |||||||
| chr8:143737049 | C | T | 8 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(5): Show |
8 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.85+1111C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737049 | |||||||
| chr8:143737059 | C | T | 2 | a0001c0001t0001g0195 a0030c0024t0001g0196 |
2 | NA18943.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.85+1121C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737059 | |||||||
| chr8:143737144 | G | A | 1 | a0003c0003t0001g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.85+1206G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737144 | |||||||
| chr8:143737175 | C | G | 108 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0004 others(105): Show |
111 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.85+1237C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737175 | |||||||
| chr8:143737333 | A | G | 5 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0002g0056 others(2): Show |
5 | HG02129.hp2 NA18943.hp2 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+1395A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737333 | |||||||
| chr8:143737450 | G | C | 23 | a0003c0003t0001g0012 a0003c0003t0001g0013 a0003c0003t0001g0018 others(20): Show |
23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.85+1512G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737450 | |||||||
| chr8:143737520 | G | C | 1 | a0025c0029t0001g0224 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.85+1582G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737520 | |||||||
| chr8:143737608 | C | T | 1 | a0024c0030t0001g0343 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.85+1670C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737608 | |||||||
| chr8:143737621 | C | T | 1 | a0004c0004t0001g0192 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.85+1683C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737621 | |||||||
| chr8:143737625 | C | T | 1 | a0003c0003t0001g0242 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.85+1687C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737625 | |||||||
| chr8:143737704 | G | A | 1 | a0002c0002t0001g0254 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.85+1766G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737704 | |||||||
| chr8:143737734 | G | A | 3 | a0018c0014t0001g0060 a0018c0014t0001g0061 a0023c0022t0001g0062 |
3 | HG02602.hp2 HG02683.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.85+1796G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737734 | |||||||
| chr8:143737814 | G | A | 1 | a0002c0002t0001g0255 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.85+1876G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737814 | |||||||
| chr8:143737850 | C | G | 10 | a0003c0003t0001g0048 a0003c0003t0001g0057 a0003c0003t0001g0197 others(7): Show |
10 | HG02145.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.85+1912C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737850 | |||||||
| chr8:143737927 | G | A | 1 | a0006c0006t0001g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.86-1932G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737927 | |||||||
| chr8:143738136 | C | T | 1 | a0005c0005t0001g0330 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.86-1723C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143738136 | |||||||
| chr8:143738172 | C | T | 1 | a0027c0021t0001g0335 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.86-1687C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143738172 | |||||||
| chr8:143738324 | C | T | 3 | a0018c0014t0001g0060 a0018c0014t0001g0061 a0023c0022t0001g0062 |
3 | HG02602.hp2 HG02683.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.86-1535C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143738324 | |||||||
| chr8:143738506 | G | A | 3 | a0001c0001t0001g0206 a0001c0010t0001g0040 a0001c0010t0001g0041 |
3 | HG02970.hp2 HG03516.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.86-1353G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143738506 | |||||||
| chr8:143738519 | G | A | 1 | a0027c0021t0001g0335 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.86-1340G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143738519 | |||||||
| chr8:143738550 | C | T | 1 | a0008c0008t0001g0032 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.86-1309C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143738550 | |||||||
| chr8:143738559 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.86-1300G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143738559 | |||||||
| chr8:143738648 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.86-1211C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143738648 | |||||||
| chr8:143738738 | C | A | 8 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(5): Show |
8 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.86-1121C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143738738 | |||||||
| chr8:143738854 | C | T | 6 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0003c0003t0001g0340 others(3): Show |
6 | HG01175.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-1005C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143738854 | |||||||
| chr8:143738911 | C | T | 1 | a0003c0003t0001g0031 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.86-948C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143738911 | |||||||
| chr8:143738943 | G | T | 1 | a0001c0001t0001g0191 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.86-916G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143738943 | |||||||
| chr8:143739023 | G | A | 1 | a0027c0021t0001g0335 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.86-836G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739023 | |||||||
| chr8:143739065 | G | A | 1 | a0009c0009t0001g0010 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.86-794G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739065 | |||||||
| chr8:143739112 | C | T | 1 | a0027c0021t0001g0335 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.86-747C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739112 | |||||||
| chr8:143739148 | C | G | 1 | a0027c0021t0001g0335 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.86-711C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739148 | |||||||
| chr8:143739175 | A | G | 341 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(338): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.86-684A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739175 | |||||||
| chr8:143739253 | TG | T | 8 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(5): Show |
8 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.86-604delG | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr8 | 143739253 | ||||||
| chr8:143739268 | C | T | 192 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(189): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.86-591C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739268 | |||||||
| chr8:143739325 | G | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(2): Show |
5 | NA18942.hp2 NA18951.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.86-534G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739325 | |||||||
| chr8:143739327 | C | T | 2 | a0003c0003t0001g0066 a0012c0017t0001g0067 |
2 | HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.86-532C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739327 | |||||||
| chr8:143739332 | C | T | 1 | a0021c0033t0001g0329 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.86-527C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739332 | |||||||
| chr8:143739626 | G | C | 2 | a0002c0002t0001g0256 a0002c0002t0001g0257 |
2 | HG02080.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.86-233G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739626 | |||||||
| chr8:143739722 | C | A | 1 | a0001c0001t0001g0071 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.86-137C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739722 | |||||||
| chr8:143739774 | C | T | 1 | a0012c0017t0001g0067 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.86-85C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739774 | |||||||
| chr8:143739787 | A | G | 2 | a0007c0007t0001g0203 a0007c0007t0001g0204 |
2 | HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.86-72A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739787 | |||||||
| chr8:143739807 | A | G | 9 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0003c0003t0001g0066 others(6): Show |
9 | HG01175.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.86-52A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739807 | |||||||
| chr8:143739830 | C | G | 2 | a0003c0003t0001g0066 a0012c0017t0001g0067 |
2 | HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.86-29C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739830 | |||||||
| chr8:143740001 | A | T | 1 | a0001c0001t0001g0190 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.175+53A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740001 | |||||||
| chr8:143740004 | G | A | 22 | a0003c0003t0001g0001 a0003c0003t0001g0222 a0003c0003t0001g0225 others(19): Show |
23 | HG01975.hp2 HG02258.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.175+56G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740004 | |||||||
| chr8:143740038 | C | G | 1 | a0002c0002t0001g0252 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.175+90C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740038 | |||||||
| chr8:143740132 | A | G | 1 | a0006c0006t0001g0059 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.175+184A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740132 | |||||||
| chr8:143740160 | C | A | 6 | a0003c0003t0001g0035 a0003c0003t0001g0036 a0003c0003t0001g0037 others(3): Show |
6 | HG02280.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+212C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740160 | |||||||
| chr8:143740197 | G | T | 1 | a0001c0001t0001g0189 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.175+249G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740197 | |||||||
| chr8:143740273 | C | T | 3 | a0009c0009t0001g0010 a0009c0009t0001g0029 a0009c0009t0001g0030 |
3 | HG01192.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.175+325C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740273 | |||||||
| chr8:143740313 | C | T | 1 | a0028c0032t0001g0028 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.175+365C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740313 | |||||||
| chr8:143740340 | G | C | 2 | a0003c0003t0001g0066 a0012c0017t0001g0067 |
2 | HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.175+392G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740340 | |||||||
| chr8:143740421 | C | T | 47 | a0001c0001t0001g0054 a0001c0001t0001g0159 a0001c0001t0001g0160 others(44): Show |
47 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(44): Show |
intron_variant | MODIFIER | c.175+473C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740421 | |||||||
| chr8:143740479 | C | T | 7 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0003c0003t0001g0340 others(4): Show |
7 | HG01175.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.175+531C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740479 | |||||||
| chr8:143740550 | C | T | 1 | a0027c0021t0001g0335 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.175+602C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740550 | |||||||
| chr8:143740580 | A | G | 1 | a0010c0011t0001g0223 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.175+632A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740580 | |||||||
| chr8:143740614 | GCGGAGCC others(3): Show |
G | 1 | a0001c0001t0001g0151 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.175+667_175+676del others(10): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740614 | |||||||
| chr8:143740645 | G | A | 1 | a0012c0017t0001g0198 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.175+697G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740645 | |||||||
| chr8:143740652 | C | T | 3 | a0007c0007t0001g0045 a0007c0007t0001g0046 a0007c0007t0001g0047 |
3 | HG02258.hp2 HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.175+704C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740652 | |||||||
| chr8:143740732 | T | C | 1 | a0005c0005t0001g0209 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.175+784T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740732 | |||||||
| chr8:143740748 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.175+800G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740748 | |||||||
| chr8:143740830 | G | T | 108 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0004 others(105): Show |
111 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.175+882G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740830 | |||||||
| chr8:143740833 | G | A | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0004 others(116): Show |
122 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.175+885G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740833 | |||||||
| chr8:143741013 | G | A | 1 | a0029c0026t0001g0152 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.175+1065G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741013 | |||||||
| chr8:143741139 | C | T | 23 | a0003c0003t0001g0012 a0003c0003t0001g0013 a0003c0003t0001g0018 others(20): Show |
23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.175+1191C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741139 | |||||||
| chr8:143741228 | C | T | 1 | a0006c0006t0001g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175+1280C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741228 | |||||||
| chr8:143741245 | G | A | 1 | a0027c0021t0001g0335 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.175+1297G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741245 | |||||||
| chr8:143741249 | G | T | 341 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(338): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.175+1301G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741249 | |||||||
| chr8:143741355 | G | A | 10 | a0003c0003t0001g0048 a0003c0003t0001g0057 a0003c0003t0001g0197 others(7): Show |
10 | HG02145.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+1407G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741355 | |||||||
| chr8:143741566 | C | T | 3 | a0018c0014t0001g0060 a0018c0014t0001g0061 a0023c0022t0001g0062 |
3 | HG02602.hp2 HG02683.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.175+1618C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741566 | |||||||
| chr8:143741629 | C | T | 1 | a0004c0004t0001g0188 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.175+1681C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741629 | |||||||
| chr8:143741662 | G | A | 1 | a0022c0028t0001g0153 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.175+1714G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741662 | |||||||
| chr8:143741724 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | NA18986.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.175+1776C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741724 | |||||||
| chr8:143741725 | G | A | 10 | a0003c0003t0001g0048 a0003c0003t0001g0057 a0003c0003t0001g0197 others(7): Show |
10 | HG02145.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+1777G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741725 | |||||||
| chr8:143741741 | C | T | 150 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(147): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.175+1793C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741741 | |||||||
| chr8:143741778 | A | T | 109 | a0001c0001t0001g0065 a0002c0002t0001g0002 a0002c0002t0001g0003 others(106): Show |
112 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.175+1830A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741778 | |||||||
| chr8:143741857 | T | C | 1 | a0002c0002t0001g0258 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.175+1909T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741857 | |||||||
| chr8:143741877 | G | A | 12 | a0002c0002t0001g0259 a0002c0002t0001g0260 a0002c0002t0001g0261 others(9): Show |
12 | HG00609.hp1 HG00639.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.175+1929G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741877 | |||||||
| chr8:143741888 | T | G | 1 | a0001c0001t0001g0338 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.175+1940T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741888 | |||||||
| chr8:143741930 | T | A | 1 | a0002c0002t0001g0270 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.175+1982T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741930 | |||||||
| chr8:143742037 | C | T | 1 | a0002c0002t0001g0328 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.175+2089C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742037 | |||||||
| chr8:143742040 | C | G | 2 | a0006c0006t0001g0033 a0006c0006t0001g0034 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.175+2092C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742040 | |||||||
| chr8:143742063 | C | T | 1 | a0027c0021t0001g0335 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.175+2115C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742063 | |||||||
| chr8:143742064 | G | A | 1 | a0004c0004t0001g0154 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.175+2116G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742064 | |||||||
| chr8:143742119 | G | A | 1 | a0027c0021t0001g0335 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.175+2171G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742119 | |||||||
| chr8:143742229 | GGTGTCCG others(3641): Show |
G | 1 | a0004c0004t0001g0247 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.175+2284_175+5931d others(2): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143742229 | ||||||
| chr8:143742304 | C | T | 1 | a0003c0003t0001g0035 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.175+2356C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742304 | |||||||
| chr8:143742309 | G | C | 5 | a0004c0004t0001g0086 a0004c0004t0001g0087 a0004c0004t0001g0088 others(2): Show |
5 | HG00733.hp1 HG00738.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.175+2361G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742309 | |||||||
| chr8:143742470 | C | T | 10 | a0003c0003t0001g0048 a0003c0003t0001g0057 a0003c0003t0001g0197 others(7): Show |
10 | HG02145.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+2522C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742470 | |||||||
| chr8:143742497 | C | T | 1 | a0006c0006t0001g0174 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.175+2549C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742497 | |||||||
| chr8:143742510 | C | CCCCACAA others(3): Show |
1 | a0001c0001t0001g0151 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.175+2565_175+2574d others(12): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143742510 | ||||||
| chr8:143742571 | G | A | 1 | a0012c0017t0001g0067 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.175+2623G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742571 | |||||||
| chr8:143742595 | C | T | 1 | a0024c0030t0001g0343 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.175+2647C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742595 | |||||||
| chr8:143742671 | C | T | 1 | a0002c0002t0001g0269 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.175+2723C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742671 | |||||||
| chr8:143742681 | A | G | 1 | a0002c0002t0001g0319 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.175+2733A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742681 | |||||||
| chr8:143742682 | G | A | 1 | a0002c0002t0001g0319 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.175+2734G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742682 | |||||||
| chr8:143742728 | A | C | 340 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(337): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.175+2780A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742728 | |||||||
| chr8:143742767 | A | G | 1 | a0002c0002t0001g0255 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.175+2819A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742767 | |||||||
| chr8:143742770 | G | GTGGC | 22 | a0003c0003t0001g0001 a0003c0003t0001g0222 a0003c0003t0001g0225 others(19): Show |
23 | HG01975.hp2 HG02258.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.175+2823_175+2826d others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143742770 | ||||||
| chr8:143742865 | T | C | 1 | a0002c0002t0001g0282 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.175+2917T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742865 | |||||||
| chr8:143742865 | T | G | 149 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(146): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.175+2917T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742865 | |||||||
| chr8:143742896 | G | A | 1 | a0002c0002t0001g0317 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.175+2948G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742896 | |||||||
| chr8:143742977 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.175+3029C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742977 | |||||||
| chr8:143743102 | A | G | 162 | a0001c0001t0001g0065 a0001c0001t0001g0338 a0001c0001t0001g0341 others(159): Show |
166 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.175+3154A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143743102 | |||||||
| chr8:143743115 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.175+3167G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143743115 | |||||||
| chr8:143743120 | T | C | 109 | a0001c0001t0001g0065 a0002c0002t0001g0002 a0002c0002t0001g0003 others(106): Show |
112 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.175+3172T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143743120 | |||||||
| chr8:143743282 | A | T | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0208 |
3 | NA18966.hp1 NA18998.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.175+3334A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143743282 | |||||||
| chr8:143743497 | C | T | 4 | a0001c0001t0001g0085 a0001c0001t0001g0105 a0001c0001t0001g0106 others(1): Show |
4 | HG02040.hp2 HG02132.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+3549C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143743497 | |||||||
| chr8:143743611 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.175+3663A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143743611 | |||||||
| chr8:143743705 | G | A | 1 | a0013c0013t0001g0026 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.175+3757G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143743705 | |||||||
| chr8:143743846 | C | G | 1 | a0027c0021t0001g0335 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.175+3898C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143743846 | |||||||
| chr8:143744053 | C | T | 8 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(5): Show |
8 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.175+4105C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744053 | |||||||
| chr8:143744329 | C | T | 1 | a0027c0021t0001g0335 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.175+4381C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744329 | |||||||
| chr8:143744330 | A | G | 6 | a0003c0003t0001g0035 a0003c0003t0001g0036 a0003c0003t0001g0037 others(3): Show |
6 | HG02280.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+4382A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744330 | |||||||
| chr8:143744352 | A | G | 109 | a0001c0001t0001g0065 a0002c0002t0001g0002 a0002c0002t0001g0003 others(106): Show |
112 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.175+4404A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744352 | |||||||
| chr8:143744411 | T | G | 23 | a0003c0003t0001g0012 a0003c0003t0001g0013 a0003c0003t0001g0018 others(20): Show |
23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.175+4463T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744411 | |||||||
| chr8:143744443 | A | C | 6 | a0003c0003t0001g0035 a0003c0003t0001g0036 a0003c0003t0001g0037 others(3): Show |
6 | HG02280.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+4495A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744443 | |||||||
| chr8:143744482 | G | A | 1 | a0007c0007t0001g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.175+4534G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744482 | |||||||
| chr8:143744495 | G | A | 2 | a0007c0007t0001g0046 a0007c0007t0001g0047 |
2 | HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.175+4547G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744495 | |||||||
| chr8:143744501 | A | G | 220 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(217): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.175+4553A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744501 | |||||||
| chr8:143744519 | G | A | 1 | a0011c0012t0001g0339 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.175+4571G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744519 | |||||||
| chr8:143744723 | T | C | 22 | a0003c0003t0001g0001 a0003c0003t0001g0222 a0003c0003t0001g0225 others(19): Show |
23 | HG01975.hp2 HG02258.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.175+4775T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744723 | |||||||
| chr8:143744792 | C | T | 1 | a0027c0021t0001g0335 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.175+4844C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744792 | |||||||
| chr8:143744932 | G | T | 1 | a0006c0006t0001g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175+4984G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744932 | |||||||
| chr8:143744976 | G | A | 1 | a0003c0003t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.175+5028G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744976 | |||||||
| chr8:143744993 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.175+5045C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744993 | |||||||
| chr8:143745035 | C | CTT | 109 | a0001c0001t0001g0065 a0002c0002t0001g0002 a0002c0002t0001g0003 others(106): Show |
112 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.175+5087_175+5088i others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745035 | |||||||
| chr8:143745107 | C | T | 109 | a0001c0001t0001g0065 a0002c0002t0001g0002 a0002c0002t0001g0003 others(106): Show |
112 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.175+5159C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745107 | |||||||
| chr8:143745151 | C | T | 3 | a0009c0009t0001g0010 a0009c0009t0001g0029 a0009c0009t0001g0030 |
3 | HG01192.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.175+5203C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745151 | |||||||
| chr8:143745259 | C | T | 1 | a0004c0004t0001g0173 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.175+5311C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745259 | |||||||
| chr8:143745309 | A | G | 109 | a0001c0001t0001g0065 a0002c0002t0001g0002 a0002c0002t0001g0003 others(106): Show |
112 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.175+5361A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745309 | |||||||
| chr8:143745316 | A | G | 9 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(6): Show |
9 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.175+5368A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745316 | |||||||
| chr8:143745321 | G | A | 1 | a0002c0002t0001g0328 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.175+5373G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745321 | |||||||
| chr8:143745411 | C | T | 8 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(5): Show |
8 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.175+5463C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745411 | |||||||
| chr8:143745412 | G | A | 1 | a0006c0006t0001g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175+5464G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745412 | |||||||
| chr8:143745509 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.175+5561G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745509 | |||||||
| chr8:143745512 | T | G | 3 | a0018c0014t0001g0060 a0018c0014t0001g0061 a0023c0022t0001g0062 |
3 | HG02602.hp2 HG02683.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.175+5564T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745512 | |||||||
| chr8:143745550 | G | A | 1 | a0004c0004t0001g0187 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.175+5602G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745550 | |||||||
| chr8:143745579 | T | C | 341 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(338): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.175+5631T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745579 | |||||||
| chr8:143745592 | T | C | 1 | a0006c0006t0001g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175+5644T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745592 | |||||||
| chr8:143745596 | T | C | 2 | a0001c0001t0001g0243 a0032c0031t0001g0245 |
2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.175+5648T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745596 | |||||||
| chr8:143745785 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.175+5837G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745785 | |||||||
| chr8:143745813 | C | T | 10 | a0003c0003t0001g0048 a0003c0003t0001g0057 a0003c0003t0001g0197 others(7): Show |
10 | HG02145.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+5865C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745813 | |||||||
| chr8:143745966 | A | C | 341 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(338): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.175+6018A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745966 | |||||||
| chr8:143746000 | C | T | 2 | a0009c0009t0001g0027 a0011c0012t0001g0342 |
2 | HG01175.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.175+6052C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143746000 | |||||||
| chr8:143746026 | G | A | 2 | a0006c0006t0001g0033 a0006c0006t0001g0034 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.175+6078G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143746026 | |||||||
| chr8:143746045 | T | G | 237 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.175+6097T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143746045 | |||||||
| chr8:143746074 | A | G | 8 | a0003c0003t0001g0235 a0003c0003t0001g0236 a0003c0003t0001g0237 others(5): Show |
8 | HG01975.hp2 HG02647.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.175+6126A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143746074 | |||||||
| chr8:143746342 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.175+6394G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143746342 | |||||||
| chr8:143746354 | T | G | 2 | a0006c0006t0001g0033 a0006c0006t0001g0034 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.175+6406T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143746354 | |||||||
| chr8:143746426 | A | G | 23 | a0003c0003t0001g0012 a0003c0003t0001g0013 a0003c0003t0001g0018 others(20): Show |
23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.175+6478A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143746426 | |||||||
| chr8:143746513 | G | C | 6 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0003c0003t0001g0340 others(3): Show |
6 | HG01175.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+6565G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143746513 | |||||||
| chr8:143746758 | T | G | 5 | a0001c0001t0001g0064 a0001c0001t0001g0075 a0001c0001t0001g0076 others(2): Show |
5 | HG01358.hp2 HG01981.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.175+6810T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143746758 | |||||||
| chr8:143746980 | C | T | 19 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0003c0003t0001g0048 others(16): Show |
19 | HG01175.hp1 HG02145.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.175+7032C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143746980 | |||||||
| chr8:143747023 | G | A | 2 | a0003c0003t0001g0066 a0012c0017t0001g0067 |
2 | HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.175+7075G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143747023 | |||||||
| chr8:143747168 | C | G | 2 | a0003c0003t0001g0066 a0012c0017t0001g0067 |
2 | HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.175+7220C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143747168 | |||||||
| chr8:143747230 | G | A | 8 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(5): Show |
8 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.175+7282G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143747230 | |||||||
| chr8:143747237 | T | G | 82 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0001c0010t0001g0040 others(79): Show |
83 | HG00733.hp2 HG01175.hp1 HG01192.hp2 others(80): Show |
intron_variant | MODIFIER | c.175+7289T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143747237 | |||||||
| chr8:143747493 | C | T | 1 | a0002c0002t0001g0251 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.175+7545C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143747493 | |||||||
| chr8:143747598 | CT | C | 10 | a0003c0003t0001g0048 a0003c0003t0001g0057 a0003c0003t0001g0197 others(7): Show |
10 | HG02145.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+7653delT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747598 | ||||||
| chr8:143747601 | T | G | 1 | a0007c0007t0001g0045 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.175+7653T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143747601 | |||||||
| chr8:143747638 | G | GT | 166 | a0001c0001t0001g0065 a0002c0002t0001g0002 a0002c0002t0001g0003 others(163): Show |
170 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.175+7699dupT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747638 | ||||||
| chr8:143747638 | G | GTT | 13 | a0001c0001t0001g0338 a0001c0010t0001g0040 a0001c0010t0001g0041 others(10): Show |
13 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.175+7698_175+7699d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747638 | ||||||
| chr8:143747647 | T | A | 1 | a0001c0001t0001g0248 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.175+7699T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143747647 | |||||||
| chr8:143747647 | T | TA | 6 | a0002c0002t0001g0259 a0003c0003t0001g0235 a0003c0003t0001g0236 others(3): Show |
6 | HG01975.hp1 HG01975.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+7705dupA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747647 | ||||||
| chr8:143747648 | A | T | 2 | a0001c0001t0001g0147 a0006c0006t0001g0063 |
2 | HG02071.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.175+7700A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143747648 | |||||||
| chr8:143747753 | G | A | 1 | a0002c0002t0001g0272 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.175+7805G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143747753 | |||||||
| chr8:143747802 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.175+7854A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143747802 | |||||||
| chr8:143747910 | G | GTCCTT | 60 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0065 others(57): Show |
60 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.175+8021_175+8025d others(7): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747910 | ||||||
| chr8:143747910 | G | GTCCTTTC others(3): Show |
39 | a0001c0001t0001g0005 a0001c0001t0001g0052 a0001c0001t0001g0054 others(36): Show |
39 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.175+8016_175+8025d others(12): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747910 | ||||||
| chr8:143747910 | G | GTCCTTTC others(8): Show |
26 | a0001c0001t0001g0073 a0001c0001t0001g0134 a0001c0001t0001g0136 others(23): Show |
26 | HG00099.hp2 HG00738.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.175+8011_175+8025d others(17): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747910 | ||||||
| chr8:143747910 | G | GTCCTTTC others(13): Show |
10 | a0001c0001t0001g0142 a0003c0003t0001g0143 a0004c0004t0001g0154 others(7): Show |
10 | HG00733.hp2 HG01891.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+8006_175+8025d others(22): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747910 | ||||||
| chr8:143747910 | G | GTCCTTTC others(18): Show |
3 | a0003c0003t0001g0144 a0014c0019t0001g0025 a0028c0032t0001g0028 |
3 | HG02723.hp2 HG02976.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.175+8001_175+8025d others(27): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747910 | ||||||
| chr8:143747910 | G | GTCCTTTC others(23): Show |
1 | a0003c0003t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.175+7996_175+8025d others(32): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747910 | ||||||
| chr8:143747910 | G | GTCCTTTC others(28): Show |
1 | a0013c0013t0001g0026 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.175+7991_175+8025d others(37): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747910 | ||||||
| chr8:143747910 | GTCCTT | G | 26 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(23): Show |
26 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.175+8021_175+8025d others(7): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747910 | ||||||
| chr8:143747910 | GTCCTTTC others(3): Show |
G | 33 | a0002c0002t0001g0259 a0002c0002t0001g0272 a0002c0002t0001g0322 others(30): Show |
34 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.175+8016_175+8025d others(12): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747910 | ||||||
| chr8:143747910 | GTCCTTTC others(8): Show |
G | 80 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0002c0002t0001g0002 others(77): Show |
83 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.175+8011_175+8025d others(17): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747910 | ||||||
| chr8:143747910 | GTCCTTTC others(13): Show |
G | 13 | a0002c0002t0001g0009 a0002c0002t0001g0270 a0002c0002t0001g0273 others(10): Show |
13 | HG01081.hp1 HG01243.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.175+8006_175+8025d others(22): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747910 | ||||||
| chr8:143747910 | GTCCTTTC others(18): Show |
G | 1 | a0003c0003t0001g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.175+8001_175+8025d others(27): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747910 | ||||||
| chr8:143747961 | T | TC | 4 | a0001c0010t0001g0042 a0007c0007t0001g0045 a0007c0007t0001g0046 others(1): Show |
4 | HG02258.hp2 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+8015dupC | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747961 | ||||||
| chr8:143747966 | T | TCCTTTCC others(22): Show |
2 | a0008c0008t0001g0032 a0009c0009t0001g0030 |
2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.175+8025_175+8026i others(31): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747966 | ||||||
| chr8:143747966 | T | TCCTTTCC others(28): Show |
2 | a0003c0003t0001g0013 a0003c0003t0001g0031 |
2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.175+8025_175+8026i others(37): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747966 | ||||||
| chr8:143747966 | T | TCCTTTCC others(21): Show |
1 | a0009c0009t0001g0010 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.175+8025_175+8026i others(30): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747966 | ||||||
| chr8:143747966 | T | TCCTTTCC others(33): Show |
1 | a0012c0027t0001g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.175+8025_175+8026i others(42): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747966 | ||||||
| chr8:143747966 | T | TCCTTTCC others(38): Show |
1 | a0003c0003t0001g0018 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.175+8025_175+8026i others(47): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747966 | ||||||
| chr8:143747977 | T | TC | 7 | a0003c0003t0001g0013 a0003c0003t0001g0018 a0003c0003t0001g0031 others(4): Show |
7 | HG01192.hp2 HG01884.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.175+8031dupC | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747977 | ||||||
| chr8:143747977 | T | TCCCTTTC others(18): Show |
1 | a0009c0009t0001g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.175+8031_175+8032i others(27): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747977 | ||||||
| chr8:143747977 | T | TCCCTTTC others(24): Show |
1 | a0003c0003t0001g0012 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.175+8031_175+8032i others(33): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747977 | ||||||
| chr8:143747977 | T | TCCCTTTC others(30): Show |
1 | a0010c0011t0001g0011 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.175+8031_175+8032i others(39): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747977 | ||||||
| chr8:143747985 | CTTTCCTT others(3): Show |
C | 5 | a0001c0010t0001g0041 a0001c0010t0001g0042 a0007c0007t0001g0045 others(2): Show |
5 | HG02258.hp2 HG02970.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.175+8052_175+8061d others(12): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747985 | ||||||
| chr8:143747993 | T | TC | 5 | a0001c0010t0001g0040 a0001c0010t0001g0043 a0006c0006t0001g0063 others(2): Show |
5 | HG02615.hp2 HG02976.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+8046dupC | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747993 | ||||||
| chr8:143747995 | T | C | 5 | a0001c0010t0001g0040 a0001c0010t0001g0043 a0006c0006t0001g0063 others(2): Show |
5 | HG02615.hp2 HG02976.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+8047T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143747995 | |||||||
| chr8:143748449 | A | G | 1 | a0006c0006t0001g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175+8501A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748449 | |||||||
| chr8:143748465 | C | CATGATAT others(26): Show |
3 | a0001c0001t0001g0123 a0002c0002t0001g0250 a0004c0004t0001g0177 |
3 | HG01071.hp1 NA18955.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.175+8577_175+8609d others(35): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748465 | ||||||
| chr8:143748555 | GAT | G | 5 | a0001c0001t0001g0243 a0006c0006t0001g0033 a0006c0006t0001g0034 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+8616_175+8617d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748555 | ||||||
| chr8:143748564 | A | G | 23 | a0003c0003t0001g0012 a0003c0003t0001g0013 a0003c0003t0001g0018 others(20): Show |
23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.175+8616A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748564 | |||||||
| chr8:143748622 | T | G | 1 | a0006c0006t0001g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175+8674T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748622 | |||||||
| chr8:143748630 | CATATATA others(1): Show |
C | 3 | a0008c0008t0001g0023 a0008c0008t0001g0024 a0009c0009t0001g0010 |
3 | HG01192.hp2 HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.175+8698_175+8705d others(10): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748630 | ||||||
| chr8:143748642 | TATAAATA others(35): Show |
T | 20 | a0003c0003t0001g0012 a0003c0003t0001g0013 a0003c0003t0001g0018 others(17): Show |
20 | HG00733.hp2 HG01884.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.175+8698_175+8739d others(44): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748642 | ||||||
| chr8:143748655 | C | A | 1 | a0006c0006t0001g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175+8707C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748655 | |||||||
| chr8:143748656 | A | AATCATAT others(27): Show |
3 | a0001c0001t0001g0122 a0001c0001t0001g0126 a0002c0002t0001g0279 |
3 | HG00544.hp2 HG01243.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.175+8776_175+8809d others(36): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748656 | ||||||
| chr8:143748656 | A | T | 1 | a0006c0006t0001g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175+8708A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748656 | |||||||
| chr8:143748656 | AATCATAT others(27): Show |
A | 57 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0001c0010t0001g0040 others(54): Show |
58 | HG01175.hp1 HG01975.hp2 HG02145.hp1 others(55): Show |
intron_variant | MODIFIER | c.175+8776_175+8809d others(36): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748656 | ||||||
| chr8:143748675 | AATATATA others(31): Show |
A | 1 | a0027c0021t0001g0335 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.175+8732_175+8769d others(40): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748675 | ||||||
| chr8:143748689 | A | C | 20 | a0003c0003t0001g0012 a0003c0003t0001g0013 a0003c0003t0001g0018 others(17): Show |
20 | HG00733.hp2 HG01884.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.175+8741A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748689 | |||||||
| chr8:143748690 | T | A | 20 | a0003c0003t0001g0012 a0003c0003t0001g0013 a0003c0003t0001g0018 others(17): Show |
20 | HG00733.hp2 HG01884.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.175+8742T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748690 | |||||||
| chr8:143748693 | CATATATA others(29): Show |
C | 2 | a0008c0008t0001g0023 a0008c0008t0001g0024 |
2 | HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.175+8751_175+8786d others(38): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748693 | ||||||
| chr8:143748720 | TATATATC others(31): Show |
T | 1 | a0009c0009t0001g0010 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.175+8779_175+8816d others(40): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748720 | ||||||
| chr8:143748724 | T | A | 11 | a0002c0002t0001g0004 a0002c0002t0001g0249 a0002c0002t0001g0251 others(8): Show |
12 | HG00558.hp2 HG00597.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.175+8776T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748724 | |||||||
| chr8:143748726 | TC | T | 11 | a0002c0002t0001g0004 a0002c0002t0001g0249 a0002c0002t0001g0251 others(8): Show |
12 | HG00558.hp2 HG00597.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.175+8779delC | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748726 | |||||||
| chr8:143748733 | TA | T | 11 | a0002c0002t0001g0004 a0002c0002t0001g0249 a0002c0002t0001g0251 others(8): Show |
12 | HG00558.hp2 HG00597.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.175+8788delA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748733 | ||||||
| chr8:143748749 | TATCATAT others(1): Show |
T | 11 | a0002c0002t0001g0004 a0002c0002t0001g0249 a0002c0002t0001g0251 others(8): Show |
12 | HG00558.hp2 HG00597.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.175+8803_175+8810d others(10): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748749 | ||||||
| chr8:143748758 | A | C | 11 | a0002c0002t0001g0004 a0002c0002t0001g0249 a0002c0002t0001g0251 others(8): Show |
12 | HG00558.hp2 HG00597.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.175+8810A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748758 | |||||||
| chr8:143748758 | A | T | 2 | a0002c0002t0001g0006 a0002c0002t0001g0007 |
2 | HG02698.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.175+8810A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748758 | |||||||
| chr8:143748762 | T | A | 1 | a0009c0009t0001g0010 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.175+8814T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748762 | |||||||
| chr8:143748765 | AT | A | 11 | a0002c0002t0001g0004 a0002c0002t0001g0249 a0002c0002t0001g0251 others(8): Show |
12 | HG00558.hp2 HG00597.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.175+8818delT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748765 | |||||||
| chr8:143748782 | C | A | 11 | a0002c0002t0001g0004 a0002c0002t0001g0249 a0002c0002t0001g0251 others(8): Show |
12 | HG00558.hp2 HG00597.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.175+8834C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748782 | |||||||
| chr8:143748783 | A | T | 11 | a0002c0002t0001g0004 a0002c0002t0001g0249 a0002c0002t0001g0251 others(8): Show |
12 | HG00558.hp2 HG00597.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.175+8835A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748783 | |||||||
| chr8:143748784 | T | C | 11 | a0002c0002t0001g0004 a0002c0002t0001g0249 a0002c0002t0001g0251 others(8): Show |
12 | HG00558.hp2 HG00597.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.175+8836T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748784 | |||||||
| chr8:143748788 | T | A | 2 | a0002c0002t0001g0006 a0002c0002t0001g0007 |
2 | HG02698.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.175+8840T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748788 | |||||||
| chr8:143748803 | A | T | 1 | a0001c0001t0001g0122 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.175+8855A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748803 | |||||||
| chr8:143748805 | A | C | 3 | a0001c0001t0001g0122 a0002c0002t0001g0006 a0002c0002t0001g0007 |
3 | HG02698.hp1 HG04115.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.175+8857A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748805 | |||||||
| chr8:143748806 | T | A | 3 | a0001c0001t0001g0122 a0002c0002t0001g0006 a0002c0002t0001g0007 |
3 | HG02698.hp1 HG04115.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.175+8858T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748806 | |||||||
| chr8:143748806 | T | TTTCA | 13 | a0002c0002t0001g0004 a0002c0002t0001g0249 a0002c0002t0001g0251 others(10): Show |
14 | HG00558.hp2 HG00597.hp2 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.175+8858_175+8859i others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748806 | |||||||
| chr8:143748807 | C | A | 1 | a0002c0002t0001g0282 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.175+8859C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748807 | |||||||
| chr8:143748807 | C | CATATAAA others(20): Show |
9 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0004c0004t0001g0154 others(6): Show |
9 | HG01123.hp1 HG01358.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.175+8881_175+8882i others(29): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748807 | ||||||
| chr8:143748807 | C | CATATAAA others(20): Show |
2 | a0001c0001t0001g0098 a0001c0001t0001g0121 |
2 | NA18951.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.175+8882_175+8908d others(29): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748807 | ||||||
| chr8:143748807 | C | CATATAAA others(47): Show |
2 | a0002c0002t0001g0312 a0002c0002t0001g0313 |
2 | HG02523.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.175+8908_175+8909i others(56): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748807 | ||||||
| chr8:143748807 | C | T | 16 | a0001c0001t0001g0122 a0002c0002t0001g0004 a0002c0002t0001g0006 others(13): Show |
17 | HG00558.hp2 HG00597.hp2 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.175+8859C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748807 | |||||||
| chr8:143748813 | A | T | 1 | a0002c0002t0001g0282 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.175+8865A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748813 | |||||||
| chr8:143748815 | T | A | 1 | a0002c0002t0001g0282 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.175+8867T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748815 | |||||||
| chr8:143748821 | A | C | 1 | a0002c0002t0001g0282 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.175+8873A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748821 | |||||||
| chr8:143748828 | ATT | A | 3 | a0007c0007t0001g0045 a0007c0007t0001g0046 a0007c0007t0001g0047 |
3 | HG02258.hp2 HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.175+8882_175+8883d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748828 | ||||||
| chr8:143748830 | T | A | 19 | a0001c0001t0001g0122 a0001c0001t0001g0136 a0001c0001t0001g0137 others(16): Show |
19 | HG01123.hp1 HG01358.hp1 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.175+8882T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748830 | |||||||
| chr8:143748830 | T | TTCATATA others(20): Show |
132 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(129): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.175+8915_175+8941d others(29): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748830 | ||||||
| chr8:143748830 | T | TTCATATA others(47): Show |
1 | a0001c0001t0001g0124 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.175+8888_175+8941d others(56): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748830 | ||||||
| chr8:143748832 | C | A | 1 | a0002c0002t0001g0282 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.175+8884C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748832 | |||||||
| chr8:143748840 | A | AATATATA others(16): Show |
1 | a0002c0002t0001g0315 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.175+8908_175+8909i others(25): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748840 | ||||||
| chr8:143748840 | AATAT | A | 10 | a0003c0003t0001g0048 a0003c0003t0001g0057 a0003c0003t0001g0197 others(7): Show |
10 | HG02145.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+8896_175+8899d others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748840 | ||||||
| chr8:143748848 | A | AATATATA others(22): Show |
3 | a0004c0004t0001g0177 a0004c0004t0001g0179 a0006c0006t0001g0186 |
3 | HG01071.hp1 HG06807.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.175+8909_175+8937d others(31): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748848 | ||||||
| chr8:143748848 | AAT | A | 6 | a0003c0003t0001g0035 a0003c0003t0001g0036 a0003c0003t0001g0037 others(3): Show |
6 | HG02280.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+8909_175+8910d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748848 | ||||||
| chr8:143748850 | T | TATATATA others(18): Show |
1 | a0006c0006t0001g0174 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.175+8911_175+8935d others(27): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748850 | ||||||
| chr8:143748857 | A | T | 89 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0008 others(86): Show |
91 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.175+8909A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748857 | |||||||
| chr8:143748884 | A | T | 1 | a0002c0002t0001g0314 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.175+8936A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748884 | |||||||
| chr8:143748886 | C | CATAT | 97 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0001c0010t0001g0040 others(94): Show |
99 | HG00558.hp2 HG00597.hp2 HG00733.hp2 others(96): Show |
intron_variant | MODIFIER | c.175+8941_175+8942i others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748886 | ||||||
| chr8:143748886 | C | CATATATA others(24): Show |
78 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0008 others(75): Show |
80 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.175+8941_175+8942i others(33): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748886 | ||||||
| chr8:143748886 | C | CATATATA others(51): Show |
1 | a0002c0002t0001g0314 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.175+8941_175+8942i others(60): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748886 | ||||||
| chr8:143748886 | C | T | 2 | a0002c0002t0001g0251 a0003c0003t0001g0072 |
2 | HG02630.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.175+8938C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748886 | |||||||
| chr8:143748890 | A | T | 11 | a0005c0005t0001g0209 a0005c0005t0001g0210 a0005c0005t0001g0211 others(8): Show |
11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+8942A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748890 | |||||||
| chr8:143748891 | ATACT | A | 11 | a0005c0005t0001g0209 a0005c0005t0001g0210 a0005c0005t0001g0211 others(8): Show |
11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+8946_175+8949d others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748891 | ||||||
| chr8:143748900 | A | T | 11 | a0005c0005t0001g0209 a0005c0005t0001g0210 a0005c0005t0001g0211 others(8): Show |
11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+8952A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748900 | |||||||
| chr8:143748906 | C | A | 11 | a0005c0005t0001g0209 a0005c0005t0001g0210 a0005c0005t0001g0211 others(8): Show |
11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+8958C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748906 | |||||||
| chr8:143748912 | T | C | 1 | a0032c0031t0001g0245 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.175+8964T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748912 | |||||||
| chr8:143748915 | C | A | 11 | a0005c0005t0001g0209 a0005c0005t0001g0210 a0005c0005t0001g0211 others(8): Show |
11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+8967C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748915 | |||||||
| chr8:143748916 | T | TC | 11 | a0005c0005t0001g0209 a0005c0005t0001g0210 a0005c0005t0001g0211 others(8): Show |
11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+8968_175+8969i others(3): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748916 | |||||||
| chr8:143748928 | T | C | 11 | a0005c0005t0001g0209 a0005c0005t0001g0210 a0005c0005t0001g0211 others(8): Show |
11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+8980T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748928 | |||||||
| chr8:143748929 | A | T | 11 | a0005c0005t0001g0209 a0005c0005t0001g0210 a0005c0005t0001g0211 others(8): Show |
11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+8981A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748929 | |||||||
| chr8:143748940 | T | C | 11 | a0005c0005t0001g0209 a0005c0005t0001g0210 a0005c0005t0001g0211 others(8): Show |
11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+8992T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748940 | |||||||
| chr8:143748942 | C | T | 11 | a0005c0005t0001g0209 a0005c0005t0001g0210 a0005c0005t0001g0211 others(8): Show |
11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+8994C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748942 | |||||||
| chr8:143748960 | TATATATC others(8): Show |
T | 1 | a0001c0001t0001g0083 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.175+9034_175+9048d others(17): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748960 | ||||||
| chr8:143748964 | T | TA | 11 | a0005c0005t0001g0209 a0005c0005t0001g0210 a0005c0005t0001g0211 others(8): Show |
11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+9017dupA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748964 | ||||||
| chr8:143748966 | T | A | 11 | a0005c0005t0001g0209 a0005c0005t0001g0210 a0005c0005t0001g0211 others(8): Show |
11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+9018T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748966 | |||||||
| chr8:143748967 | C | A | 11 | a0005c0005t0001g0209 a0005c0005t0001g0210 a0005c0005t0001g0211 others(8): Show |
11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+9019C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748967 | |||||||
| chr8:143748975 | A | C | 11 | a0005c0005t0001g0209 a0005c0005t0001g0210 a0005c0005t0001g0211 others(8): Show |
11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+9027A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748975 | |||||||
| chr8:143748982 | C | CT | 11 | a0005c0005t0001g0209 a0005c0005t0001g0210 a0005c0005t0001g0211 others(8): Show |
11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+9034_175+9035i others(3): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748982 | |||||||
| chr8:143748986 | TATAAATA others(6): Show |
T | 102 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0002c0002t0001g0002 others(99): Show |
105 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.175+9055_175+9067d others(15): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748986 | ||||||
| chr8:143748999 | C | CATAT | 11 | a0005c0005t0001g0209 a0005c0005t0001g0210 a0005c0005t0001g0211 others(8): Show |
11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+9054_175+9055i others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748999 | ||||||
| chr8:143749115 | C | T | 3 | a0002c0002t0001g0006 a0002c0002t0001g0007 a0006c0006t0001g0059 |
3 | HG02083.hp1 HG02698.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.175+9167C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749115 | |||||||
| chr8:143749166 | CAA | C | 43 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0003c0003t0001g0001 others(40): Show |
44 | HG01175.hp1 HG01975.hp2 HG02145.hp1 others(41): Show |
intron_variant | MODIFIER | c.175+9219_175+9220d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749166 | |||||||
| chr8:143749172 | A | G | 151 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.175+9224A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749172 | |||||||
| chr8:143749219 | TATATAA | T | 23 | a0003c0003t0001g0012 a0003c0003t0001g0013 a0003c0003t0001g0018 others(20): Show |
23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.175+9277_175+9282d others(8): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143749219 | ||||||
| chr8:143749249 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.175+9301G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749249 | |||||||
| chr8:143749257 | T | G | 10 | a0001c0001t0001g0058 a0001c0001t0001g0064 a0001c0001t0001g0075 others(7): Show |
10 | HG00544.hp2 HG01358.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+9309T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749257 | |||||||
| chr8:143749284 | TA | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0133 a0001c0001t0001g0140 others(1): Show |
4 | NA18948.hp1 NA18970.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+9341delA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143749284 | ||||||
| chr8:143749346 | C | CAT | 335 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(332): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.175+9400_175+9401d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143749346 | ||||||
| chr8:143749346 | C | T | 1 | a0002c0002t0001g0311 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.175+9398C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749346 | |||||||
| chr8:143749353 | A | T | 151 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.175+9405A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749353 | |||||||
| chr8:143749365 | A | G | 1 | a0002c0002t0001g0324 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.175+9417A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749365 | |||||||
| chr8:143749428 | ATC | A | 9 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0003c0003t0001g0066 others(6): Show |
9 | HG01175.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.175+9483_175+9484d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143749428 | ||||||
| chr8:143749432 | CAT | C | 23 | a0003c0003t0001g0012 a0003c0003t0001g0013 a0003c0003t0001g0018 others(20): Show |
23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.175+9490_175+9491d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143749432 | ||||||
| chr8:143749441 | T | G | 1 | a0001c0001t0001g0100 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.175+9493T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749441 | |||||||
| chr8:143749485 | TATATAAA others(8): Show |
T | 1 | a0004c0004t0001g0166 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.175+9551_175+9565d others(17): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143749485 | ||||||
| chr8:143749500 | CAT | C | 32 | a0003c0003t0001g0001 a0003c0003t0001g0048 a0003c0003t0001g0057 others(29): Show |
33 | HG01975.hp2 HG02145.hp1 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.175+9556_175+9557d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143749500 | ||||||
| chr8:143749510 | TATAAAAA others(10): Show |
T | 3 | a0018c0014t0001g0060 a0018c0014t0001g0061 a0023c0022t0001g0062 |
3 | HG02602.hp2 HG02683.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.175+9575_175+9591d others(19): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143749510 | ||||||
| chr8:143749527 | CAT | C | 5 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(2): Show |
5 | HG02615.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.175+9581_175+9582d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143749527 | ||||||
| chr8:143749538 | A | G | 1 | a0001c0001t0001g0206 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.175+9590A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749538 | |||||||
| chr8:143749548 | TGATATAT others(4): Show |
T | 4 | a0003c0003t0001g0036 a0003c0003t0001g0037 a0003c0003t0001g0038 others(1): Show |
4 | HG02280.hp1 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+9601_175+9611d others(13): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749548 | |||||||
| chr8:143749558 | C | G | 1 | a0006c0006t0001g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175+9610C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749558 | |||||||
| chr8:143749560 | T | C | 4 | a0003c0003t0001g0036 a0003c0003t0001g0037 a0003c0003t0001g0038 others(1): Show |
4 | HG02280.hp1 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+9612T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749560 | |||||||
| chr8:143749571 | C | CAT | 108 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0004 others(105): Show |
111 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.175+9634_175+9635d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143749571 | ||||||
| chr8:143749581 | TA | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0122 a0001c0001t0001g0132 |
3 | NA18947.hp1 NA18964.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.175+9634delA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749581 | |||||||
| chr8:143749582 | A | T | 109 | a0001c0001t0001g0005 a0001c0001t0001g0050 a0001c0001t0001g0051 others(106): Show |
109 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.175+9634A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749582 | |||||||
| chr8:143749584 | T | A | 176 | a0001c0001t0001g0121 a0001c0001t0001g0338 a0001c0001t0001g0341 others(173): Show |
179 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.175+9636T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749584 | |||||||
| chr8:143749587 | A | T | 334 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(331): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.175+9639A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749587 | |||||||
| chr8:143749599 | A | AT | 7 | a0004c0004t0001g0053 a0004c0004t0001g0161 a0004c0004t0001g0185 others(4): Show |
7 | HG00642.hp1 HG00735.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.175+9665dupT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143749599 | ||||||
| chr8:143749602 | T | TA | 6 | a0002c0002t0001g0253 a0002c0002t0001g0306 a0002c0002t0001g0307 others(3): Show |
6 | HG00438.hp1 HG02976.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+9654_175+9655i others(3): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749602 | |||||||
| chr8:143749603 | T | A | 183 | a0001c0001t0001g0078 a0001c0001t0001g0134 a0001c0001t0001g0194 others(180): Show |
187 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.175+9655T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749603 | |||||||
| chr8:143749604 | T | A | 1 | a0002c0002t0001g0255 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.175+9656T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749604 | |||||||
| chr8:143749607 | T | A | 9 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0003c0003t0001g0340 others(6): Show |
9 | HG01175.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.175+9659T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749607 | |||||||
| chr8:143750067 | C | T | 2 | a0006c0006t0001g0033 a0006c0006t0001g0034 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.175+10119C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750067 | |||||||
| chr8:143750130 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.175+10182C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750130 | |||||||
| chr8:143750147 | C | T | 1 | a0003c0003t0001g0340 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.175+10199C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750147 | |||||||
| chr8:143750155 | C | T | 8 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(5): Show |
8 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.175+10207C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750155 | |||||||
| chr8:143750199 | T | A | 1 | a0001c0001t0001g0101 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.175+10251T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750199 | |||||||
| chr8:143750218 | G | A | 1 | a0015c0016t0001g0345 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.175+10270G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750218 | |||||||
| chr8:143750245 | G | A | 1 | a0024c0030t0001g0343 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.175+10297G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750245 | |||||||
| chr8:143750522 | A | G | 12 | a0007c0007t0001g0015 a0007c0007t0001g0017 a0008c0008t0001g0023 others(9): Show |
12 | HG00733.hp2 HG01891.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.175+10574A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750522 | |||||||
| chr8:143750574 | G | A | 23 | a0003c0003t0001g0012 a0003c0003t0001g0013 a0003c0003t0001g0018 others(20): Show |
23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.175+10626G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750574 | |||||||
| chr8:143750610 | A | G | 1 | a0030c0024t0001g0196 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.175+10662A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750610 | |||||||
| chr8:143750717 | G | A | 107 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0004 others(104): Show |
110 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.175+10769G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750717 | |||||||
| chr8:143750771 | A | C | 22 | a0003c0003t0001g0001 a0003c0003t0001g0222 a0003c0003t0001g0225 others(19): Show |
23 | HG01975.hp2 HG02258.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.175+10823A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750771 | |||||||
| chr8:143750786 | C | A | 1 | a0003c0003t0001g0225 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.175+10838C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750786 | |||||||
| chr8:143750798 | A | G | 1 | a0028c0032t0001g0028 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.175+10850A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750798 | |||||||
| chr8:143750944 | T | TTG | 5 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0003c0003t0001g0012 others(2): Show |
5 | HG02145.hp2 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+11018_175+1101 others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143750944 | ||||||
| chr8:143750944 | T | TTGTG | 144 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0052 others(141): Show |
144 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.175+11016_175+1101 others(8): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143750944 | ||||||
| chr8:143750944 | T | TTGTGTG | 4 | a0001c0001t0001g0190 a0004c0004t0001g0154 a0016c0018t0001g0180 others(1): Show |
4 | HG00408.hp1 HG01168.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+11014_175+1101 others(10): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143750944 | ||||||
| chr8:143750944 | T | TTGTGTGT others(3): Show |
1 | a0001c0001t0001g0084 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.175+11010_175+1101 others(14): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143750944 | ||||||
| chr8:143750961 | T | TGG | 9 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0003c0003t0001g0066 others(6): Show |
9 | HG01175.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.175+11014_175+1101 others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143750961 | ||||||
| chr8:143750968 | T | G | 134 | a0001c0001t0001g0058 a0001c0001t0001g0096 a0001c0001t0001g0205 others(131): Show |
138 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.175+11020T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750968 | |||||||
| chr8:143751064 | C | T | 1 | a0027c0021t0001g0335 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.175+11116C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751064 | |||||||
| chr8:143751073 | C | T | 1 | a0002c0002t0001g0320 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.175+11125C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751073 | |||||||
| chr8:143751383 | C | T | 10 | a0003c0003t0001g0048 a0003c0003t0001g0057 a0003c0003t0001g0197 others(7): Show |
10 | HG02145.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+11435C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751383 | |||||||
| chr8:143751568 | T | C | 9 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0003c0003t0001g0066 others(6): Show |
9 | HG01175.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.175+11620T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751568 | |||||||
| chr8:143751611 | CA | C | 6 | a0001c0001t0001g0131 a0001c0010t0001g0040 a0001c0010t0001g0041 others(3): Show |
6 | HG02970.hp2 HG03195.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+11677delA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751611 | ||||||
| chr8:143751625 | A | AT | 4 | a0001c0001t0001g0074 a0002c0002t0001g0282 a0003c0003t0001g0066 others(1): Show |
4 | HG02056.hp1 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+11677_175+1167 others(5): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751625 | |||||||
| chr8:143751625 | A | T | 2 | a0001c0001t0001g0130 a0003c0003t0001g0035 |
2 | HG02717.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.175+11677A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751625 | |||||||
| chr8:143751625 | AGT | A | 4 | a0001c0001t0001g0244 a0002c0002t0001g0250 a0005c0005t0001g0215 others(1): Show |
4 | HG00280.hp2 HG00735.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+11716_175+1171 others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751625 | ||||||
| chr8:143751625 | AGTGTGTG others(1): Show |
A | 6 | a0003c0003t0001g0232 a0003c0003t0001g0237 a0010c0011t0001g0223 others(3): Show |
6 | HG02630.hp2 HG02809.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+11710_175+1171 others(12): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751625 | ||||||
| chr8:143751625 | AGTGTGTG others(3): Show |
A | 10 | a0003c0003t0001g0222 a0003c0003t0001g0225 a0003c0003t0001g0228 others(7): Show |
10 | HG01975.hp2 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+11708_175+1171 others(14): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751625 | ||||||
| chr8:143751625 | AGTGTGTG others(5): Show |
A | 6 | a0003c0003t0001g0001 a0003c0003t0001g0226 a0003c0003t0001g0227 others(3): Show |
7 | HG02258.hp1 HG02280.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.175+11706_175+1171 others(16): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751625 | ||||||
| chr8:143751640 | G | C | 1 | a0001c0001t0001g0054 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.175+11692G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751640 | |||||||
| chr8:143751650 | G | GTA | 8 | a0003c0003t0001g0012 a0003c0003t0001g0013 a0009c0009t0001g0010 others(5): Show |
8 | HG01192.hp2 HG02615.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.175+11703_175+1170 others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751650 | ||||||
| chr8:143751652 | G | A | 18 | a0003c0003t0001g0012 a0003c0003t0001g0013 a0003c0003t0001g0018 others(15): Show |
18 | HG01192.hp2 HG01884.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.175+11704G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751652 | |||||||
| chr8:143751652 | G | GTA | 10 | a0007c0007t0001g0015 a0007c0007t0001g0017 a0008c0008t0001g0023 others(7): Show |
10 | HG00733.hp2 HG01891.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+11705_175+1170 others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751652 | ||||||
| chr8:143751654 | G | A | 36 | a0003c0003t0001g0012 a0003c0003t0001g0013 a0003c0003t0001g0018 others(33): Show |
36 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.175+11706G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751654 | |||||||
| chr8:143751654 | G | GTATATAT others(17): Show |
1 | a0001c0001t0001g0133 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.175+11707_175+1170 others(28): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751654 | ||||||
| chr8:143751656 | G | A | 47 | a0001c0001t0001g0133 a0003c0003t0001g0001 a0003c0003t0001g0012 others(44): Show |
48 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(45): Show |
intron_variant | MODIFIER | c.175+11708G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751656 | |||||||
| chr8:143751658 | G | A | 49 | a0001c0001t0001g0133 a0003c0003t0001g0001 a0003c0003t0001g0012 others(46): Show |
50 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(47): Show |
intron_variant | MODIFIER | c.175+11710G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751658 | |||||||
| chr8:143751658 | G | GTATATAT others(7): Show |
2 | a0004c0004t0001g0188 a0022c0028t0001g0153 |
2 | HG01496.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.175+11711_175+1171 others(18): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751658 | ||||||
| chr8:143751658 | G | GTATATAT others(9): Show |
2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | NA19011.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.175+11711_175+1171 others(20): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751658 | ||||||
| chr8:143751658 | G | GTATATAT others(13): Show |
2 | a0004c0004t0001g0173 a0027c0021t0001g0335 |
2 | HG01175.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.175+11711_175+1171 others(24): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751658 | ||||||
| chr8:143751660 | G | A | 61 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0133 others(58): Show |
62 | HG00733.hp2 HG01175.hp2 HG01192.hp2 others(59): Show |
intron_variant | MODIFIER | c.175+11712G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751660 | |||||||
| chr8:143751660 | G | GTATATAT others(11): Show |
2 | a0001c0001t0001g0162 a0004c0004t0001g0178 |
2 | HG01981.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.175+11713_175+1171 others(22): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751660 | ||||||
| chr8:143751660 | G | GTATATAT others(17): Show |
1 | a0001c0010t0001g0043 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.175+11713_175+1171 others(28): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751660 | ||||||
| chr8:143751660 | G | GTATATAT others(19): Show |
3 | a0004c0004t0001g0167 a0004c0004t0001g0182 a0008c0008t0001g0135 |
3 | HG00099.hp1 HG00738.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.175+11713_175+1171 others(30): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751660 | ||||||
| chr8:143751660 | G | GTATATAT others(21): Show |
1 | a0001c0010t0001g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.175+11713_175+1171 others(32): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751660 | ||||||
| chr8:143751660 | G | GTATATAT others(23): Show |
1 | a0007c0007t0001g0045 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.175+11713_175+1171 others(34): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751660 | ||||||
| chr8:143751660 | G | GTATATAT others(31): Show |
1 | a0007c0007t0001g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.175+11713_175+1171 others(42): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751660 | ||||||
| chr8:143751662 | G | A | 82 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0133 others(79): Show |
83 | HG00099.hp1 HG00544.hp1 HG00733.hp2 others(80): Show |
intron_variant | MODIFIER | c.175+11714G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751662 | |||||||
| chr8:143751662 | G | GTA | 20 | a0002c0002t0001g0259 a0002c0002t0001g0261 a0002c0002t0001g0262 others(17): Show |
20 | HG00609.hp1 HG00639.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.175+11715_175+1171 others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751662 | ||||||
| chr8:143751662 | G | GTATATA | 4 | a0003c0003t0001g0048 a0003c0003t0001g0057 a0003c0003t0001g0199 others(1): Show |
4 | HG02965.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+11715_175+1171 others(10): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751662 | ||||||
| chr8:143751662 | G | GTATATAT others(11): Show |
7 | a0001c0001t0001g0146 a0001c0001t0001g0248 a0004c0004t0001g0155 others(4): Show |
7 | HG01109.hp2 HG01123.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.175+11715_175+1171 others(22): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751662 | ||||||
| chr8:143751662 | G | GTATATAT others(13): Show |
12 | a0001c0001t0001g0134 a0001c0001t0001g0142 a0001c0001t0001g0160 others(9): Show |
12 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.175+11715_175+1171 others(24): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751662 | ||||||
| chr8:143751662 | G | GTATATAT others(15): Show |
9 | a0001c0001t0001g0068 a0001c0001t0001g0073 a0001c0001t0001g0085 others(6): Show |
9 | HG01261.hp2 HG02004.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.175+11715_175+1171 others(26): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751662 | ||||||
| chr8:143751662 | G | GTATATAT others(17): Show |
8 | a0001c0001t0001g0069 a0001c0001t0001g0107 a0001c0001t0001g0165 others(5): Show |
8 | HG01069.hp1 HG02148.hp2 HG03710.hp1 others(5): Show |
intron_variant | MODIFIER | c.175+11715_175+1171 others(28): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751662 | ||||||
| chr8:143751662 | G | GTATATAT others(19): Show |
3 | a0001c0001t0001g0070 a0004c0004t0001g0170 a0004c0004t0001g0187 |
3 | HG02683.hp2 NA18995.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.175+11715_175+1171 others(30): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751662 | ||||||
| chr8:143751662 | G | GTATATAT others(21): Show |
1 | a0001c0001t0001g0149 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.175+11715_175+1171 others(32): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751662 | ||||||
| chr8:143751662 | G | GTATATAT others(23): Show |
2 | a0001c0001t0001g0150 a0001c0010t0001g0040 |
2 | HG03516.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.175+11715_175+1171 others(34): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751662 | ||||||
| chr8:143751662 | G | GTATATAT others(25): Show |
1 | a0001c0010t0001g0041 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.175+11715_175+1171 others(36): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751662 | ||||||
| chr8:143751664 | G | A | 155 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(152): Show |
156 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.175+11716G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751664 | |||||||
| chr8:143751664 | G | GTA | 4 | a0002c0002t0001g0285 a0002c0002t0001g0306 a0002c0002t0001g0337 others(1): Show |
4 | HG00280.hp1 HG02055.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+11729_175+1173 others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTATA | 51 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0004 others(48): Show |
54 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.175+11727_175+1173 others(8): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTATATAT others(1): Show |
4 | a0001c0001t0001g0338 a0003c0003t0001g0201 a0007c0007t0001g0203 others(1): Show |
4 | HG01109.hp1 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+11723_175+1173 others(12): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTATATAT others(11): Show |
3 | a0001c0001t0001g0079 a0001c0001t0001g0108 a0001c0001t0001g0130 |
3 | HG02602.hp1 NA18939.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.175+11730_175+1173 others(22): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTATATAT others(13): Show |
10 | a0001c0001t0001g0080 a0001c0001t0001g0083 a0001c0001t0001g0127 others(7): Show |
10 | HG00099.hp2 HG00738.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.175+11730_175+1173 others(24): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTATATAT others(15): Show |
26 | a0001c0001t0001g0052 a0001c0001t0001g0064 a0001c0001t0001g0075 others(23): Show |
26 | HG00544.hp2 HG00558.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.175+11730_175+1173 others(26): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTATATAT others(17): Show |
9 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0114 others(6): Show |
9 | HG02132.hp1 HG03491.hp1 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.175+11730_175+1173 others(28): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTATATAT others(19): Show |
7 | a0001c0001t0001g0050 a0001c0001t0001g0058 a0001c0001t0001g0074 others(4): Show |
7 | HG01516.hp2 HG01517.hp1 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.175+11730_175+1173 others(30): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTATATAT others(21): Show |
4 | a0001c0001t0001g0051 a0001c0001t0001g0138 a0001c0001t0001g0140 others(1): Show |
4 | HG01361.hp1 NA18955.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+11730_175+1173 others(32): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTATATAT others(23): Show |
2 | a0001c0001t0001g0065 a0001c0001t0001g0071 |
2 | HG03654.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.175+11730_175+1173 others(34): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTGTA | 4 | a0002c0002t0001g0007 a0002c0002t0001g0279 a0002c0002t0001g0301 others(1): Show |
4 | HG00642.hp2 HG01243.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+11717_175+1171 others(8): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTGTATA | 12 | a0002c0002t0001g0009 a0002c0002t0001g0256 a0002c0002t0001g0257 others(9): Show |
12 | HG00140.hp2 HG01928.hp2 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.175+11717_175+1171 others(10): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTGTATAT others(3): Show |
6 | a0001c0001t0001g0341 a0003c0003t0001g0197 a0003c0003t0001g0340 others(3): Show |
6 | HG01175.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+11717_175+1171 others(14): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTGTATAT others(5): Show |
1 | a0011c0012t0001g0344 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.175+11717_175+1171 others(16): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTGTATAT others(11): Show |
3 | a0001c0001t0001g0116 a0001c0001t0001g0124 a0001c0001t0001g0190 |
3 | HG00408.hp1 HG00621.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.175+11717_175+1171 others(22): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTGTATAT others(13): Show |
4 | a0001c0001t0001g0054 a0001c0001t0001g0117 a0003c0003t0001g0093 others(1): Show |
4 | HG03491.hp2 HG03654.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+11717_175+1171 others(24): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTGTATAT others(15): Show |
5 | a0001c0001t0001g0081 a0001c0001t0001g0094 a0001c0001t0001g0128 others(2): Show |
5 | HG00438.hp2 HG01981.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.175+11717_175+1171 others(26): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTGTATAT others(17): Show |
7 | a0001c0001t0001g0049 a0001c0001t0001g0082 a0001c0001t0001g0131 others(4): Show |
7 | HG01069.hp2 HG01071.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.175+11717_175+1171 others(28): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTGTATAT others(19): Show |
9 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0100 others(6): Show |
9 | HG00673.hp1 HG02027.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.175+11717_175+1171 others(30): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTGTATAT others(21): Show |
1 | a0001c0001t0001g0097 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.175+11717_175+1171 others(32): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTGTATAT others(23): Show |
1 | a0007c0007t0001g0047 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.175+11717_175+1171 others(34): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTGTATAT others(25): Show |
1 | a0001c0001t0001g0141 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.175+11717_175+1171 others(36): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTGTATAT others(27): Show |
1 | a0006c0006t0001g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175+11717_175+1171 others(38): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTGTGTAT others(13): Show |
1 | a0004c0004t0001g0177 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.175+11717_175+1171 others(24): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTGTGTAT others(15): Show |
1 | a0001c0001t0001g0005 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.175+11717_175+1171 others(26): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTGTGTAT others(17): Show |
2 | a0001c0001t0001g0077 a0001c0001t0001g0119 |
2 | HG02300.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.175+11717_175+1171 others(28): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTGTGTAT others(19): Show |
1 | a0006c0006t0001g0059 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.175+11717_175+1171 others(30): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTGTGTAT others(29): Show |
1 | a0003c0003t0001g0144 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.175+11717_175+1171 others(40): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTGTGTAT others(37): Show |
1 | a0003c0003t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.175+11717_175+1171 others(48): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTGTGTAT others(47): Show |
1 | a0003c0003t0001g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.175+11717_175+1171 others(58): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751664 | G | GTGTGTGT others(3): Show |
1 | a0002c0002t0001g0311 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.175+11717_175+1171 others(14): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | ||||||
| chr8:143751666 | A | G | 3 | a0001c0001t0001g0243 a0021c0033t0001g0329 a0032c0031t0001g0245 |
3 | HG01884.hp1 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.175+11718A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751666 | |||||||
| chr8:143751668 | A | G | 3 | a0001c0001t0001g0243 a0021c0033t0001g0329 a0032c0031t0001g0245 |
3 | HG01884.hp1 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.175+11720A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751668 | |||||||
| chr8:143751670 | A | G | 1 | a0032c0031t0001g0245 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.175+11722A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751670 | |||||||
| chr8:143751679 | A | T | 12 | a0002c0002t0001g0259 a0002c0002t0001g0260 a0002c0002t0001g0261 others(9): Show |
12 | HG00609.hp1 HG00639.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.175+11731A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751679 | |||||||
| chr8:143751683 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.175+11735C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751683 | |||||||
| chr8:143751930 | GT | G | 339 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(336): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.175+11992delT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751930 | ||||||
| chr8:143752005 | G | T | 1 | a0001c0001t0001g0100 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.175+12057G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752005 | |||||||
| chr8:143752043 | G | A | 10 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(7): Show |
10 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+12095G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752043 | |||||||
| chr8:143752090 | C | T | 107 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0004 others(104): Show |
110 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.175+12142C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752090 | |||||||
| chr8:143752106 | T | C | 2 | a0003c0003t0001g0013 a0010c0011t0001g0011 |
2 | HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.175+12158T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752106 | |||||||
| chr8:143752111 | G | A | 2 | a0003c0003t0001g0013 a0010c0011t0001g0011 |
2 | HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.175+12163G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752111 | |||||||
| chr8:143752113 | C | T | 2 | a0003c0003t0001g0013 a0010c0011t0001g0011 |
2 | HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.175+12165C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752113 | |||||||
| chr8:143752114 | T | C | 2 | a0003c0003t0001g0013 a0010c0011t0001g0011 |
2 | HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.175+12166T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752114 | |||||||
| chr8:143752215 | C | G | 1 | a0007c0007t0001g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.175+12267C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752215 | |||||||
| chr8:143752245 | C | T | 1 | a0015c0016t0001g0345 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.175+12297C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752245 | |||||||
| chr8:143752246 | G | A | 10 | a0003c0003t0001g0048 a0003c0003t0001g0057 a0003c0003t0001g0197 others(7): Show |
10 | HG02145.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+12298G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752246 | |||||||
| chr8:143752312 | CAAGTTTC others(17): Show |
C | 1 | a0002c0002t0001g0250 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.175+12365_175+1238 others(28): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752312 | |||||||
| chr8:143752510 | A | G | 1 | a0006c0006t0001g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175+12562A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752510 | |||||||
| chr8:143752744 | G | A | 6 | a0003c0003t0001g0035 a0003c0003t0001g0036 a0003c0003t0001g0037 others(3): Show |
6 | HG02280.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+12796G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752744 | |||||||
| chr8:143752810 | A | G | 72 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0003c0003t0001g0001 others(69): Show |
73 | HG00733.hp2 HG01175.hp1 HG01192.hp2 others(70): Show |
intron_variant | MODIFIER | c.175+12862A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752810 | |||||||
| chr8:143752852 | G | A | 1 | a0002c0002t0001g0325 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.175+12904G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752852 | |||||||
| chr8:143752995 | CG | C | 4 | a0003c0003t0001g0197 a0003c0003t0001g0202 a0007c0007t0001g0203 others(1): Show |
4 | HG02145.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+13048delG | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752995 | |||||||
| chr8:143752996 | G | A | 5 | a0003c0003t0001g0048 a0003c0003t0001g0057 a0003c0003t0001g0200 others(2): Show |
5 | HG02965.hp2 HG03098.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+13048G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752996 | |||||||
| chr8:143752996 | G | GGT | 3 | a0003c0003t0001g0340 a0011c0012t0001g0339 a0024c0030t0001g0343 |
3 | HG02486.hp1 HG02622.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.175+13048_175+1304 others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752996 | |||||||
| chr8:143752996 | G | GT | 145 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(142): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.175+13073dupT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143752996 | ||||||
| chr8:143752996 | G | GTT | 29 | a0001c0001t0001g0005 a0001c0001t0001g0068 a0001c0001t0001g0074 others(26): Show |
29 | HG00642.hp1 HG00735.hp2 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.175+13072_175+1307 others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143752996 | ||||||
| chr8:143752996 | G | GTTTT | 6 | a0001c0001t0001g0124 a0003c0003t0001g0001 a0003c0003t0001g0237 others(3): Show |
6 | HG01975.hp2 HG02071.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+13070_175+1307 others(8): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143752996 | ||||||
| chr8:143752996 | G | GTTTTT | 14 | a0003c0003t0001g0001 a0003c0003t0001g0222 a0003c0003t0001g0225 others(11): Show |
14 | HG02258.hp1 HG02280.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.175+13069_175+1307 others(9): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143752996 | ||||||
| chr8:143752996 | G | T | 1 | a0003c0003t0001g0199 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.175+13048G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752996 | |||||||
| chr8:143752996 | GT | G | 75 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0006 others(72): Show |
76 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.175+13073delT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143752996 | ||||||
| chr8:143752996 | GTT | G | 8 | a0002c0002t0001g0264 a0002c0002t0001g0275 a0002c0002t0001g0308 others(5): Show |
8 | HG00544.hp1 HG01074.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.175+13072_175+1307 others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143752996 | ||||||
| chr8:143752996 | GTTTTTTT others(3): Show |
G | 1 | a0010c0011t0001g0011 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.175+13064_175+1307 others(14): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143752996 | ||||||
| chr8:143752997 | T | A | 4 | a0003c0003t0001g0197 a0003c0003t0001g0202 a0007c0007t0001g0203 others(1): Show |
4 | HG02145.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+13049T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752997 | |||||||
| chr8:143753002 | T | G | 1 | a0001c0001t0001g0341 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.175+13054T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143753002 | |||||||
| chr8:143753009 | T | G | 1 | a0027c0021t0001g0335 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.175+13061T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143753009 | |||||||
| chr8:143753110 | C | T | 107 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0004 others(104): Show |
110 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.175+13162C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143753110 | |||||||
| chr8:143753124 | C | T | 3 | a0001c0001t0001g0243 a0021c0033t0001g0329 a0032c0031t0001g0245 |
3 | HG01884.hp1 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.175+13176C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143753124 | |||||||
| chr8:143753177 | T | C | 1 | a0002c0002t0001g0309 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.175+13229T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143753177 | |||||||
| chr8:143753267 | G | T | 1 | a0002c0002t0001g0328 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.175+13319G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143753267 | |||||||
| chr8:143753303 | C | T | 1 | a0006c0006t0001g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175+13355C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143753303 | |||||||
| chr8:143753304 | G | A | 1 | a0005c0005t0001g0210 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.175+13356G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143753304 | |||||||
| chr8:143753458 | C | CT | 25 | a0001c0001t0001g0115 a0002c0002t0001g0300 a0003c0003t0001g0001 others(22): Show |
26 | HG01975.hp2 HG02055.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.175+13527dupT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143753458 | ||||||
| chr8:143753458 | CT | C | 14 | a0001c0001t0001g0054 a0001c0001t0001g0108 a0001c0001t0001g0341 others(11): Show |
14 | HG01175.hp1 HG01243.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.175+13527delT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143753458 | ||||||
| chr8:143753489 | G | A | 2 | a0003c0003t0001g0066 a0012c0017t0001g0067 |
2 | HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.175+13541G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143753489 | |||||||
| chr8:143753497 | A | G | 2 | a0006c0006t0001g0033 a0006c0006t0001g0034 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.175+13549A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143753497 | |||||||
| chr8:143753515 | A | G | 1 | a0003c0003t0001g0031 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.175+13567A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143753515 | |||||||
| chr8:143753566 | G | A | 22 | a0003c0003t0001g0001 a0003c0003t0001g0222 a0003c0003t0001g0225 others(19): Show |
23 | HG01975.hp2 HG02258.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.175+13618G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143753566 | |||||||
| chr8:143753699 | C | A | 1 | a0015c0016t0001g0238 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.175+13751C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143753699 | |||||||
| chr8:143753711 | T | TCCTAAGC others(17): Show |
1 | a0002c0002t0001g0250 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.175+13765_175+1376 others(28): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143753711 | ||||||
| chr8:143753975 | C | T | 1 | a0005c0005t0001g0218 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.175+14027C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143753975 | |||||||
| chr8:143754006 | G | T | 1 | a0027c0021t0001g0335 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.175+14058G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143754006 | |||||||
| chr8:143754051 | TCC | T | 151 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.175+14106_175+1410 others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143754051 | ||||||
| chr8:143754305 | G | A | 10 | a0003c0003t0001g0048 a0003c0003t0001g0057 a0003c0003t0001g0197 others(7): Show |
10 | HG02145.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+14357G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143754305 | |||||||
| chr8:143754309 | G | A | 43 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0003c0003t0001g0001 others(40): Show |
44 | HG01175.hp1 HG01975.hp2 HG02145.hp1 others(41): Show |
intron_variant | MODIFIER | c.175+14361G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143754309 | |||||||
| chr8:143754379 | C | T | 2 | a0003c0003t0001g0066 a0012c0017t0001g0067 |
2 | HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.175+14431C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143754379 | |||||||
| chr8:143754380 | G | A | 1 | a0008c0008t0001g0032 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.175+14432G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143754380 | |||||||
| chr8:143754438 | C | T | 151 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.175+14490C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143754438 | |||||||
| chr8:143754526 | A | G | 22 | a0003c0003t0001g0001 a0003c0003t0001g0222 a0003c0003t0001g0225 others(19): Show |
23 | HG01975.hp2 HG02258.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.175+14578A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143754526 | |||||||
| chr8:143754636 | T | A | 109 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0004 others(106): Show |
112 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.175+14688T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143754636 | |||||||
| chr8:143754837 | A | G | 1 | a0003c0003t0001g0035 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.175+14889A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143754837 | |||||||
| chr8:143754868 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.175+14920C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143754868 | |||||||
| chr8:143754878 | G | A | 1 | a0028c0032t0001g0028 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.175+14930G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143754878 | |||||||
| chr8:143754916 | G | A | 6 | a0003c0003t0001g0035 a0003c0003t0001g0036 a0003c0003t0001g0037 others(3): Show |
6 | HG02280.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+14968G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143754916 | |||||||
| chr8:143755160 | G | C | 47 | a0001c0001t0001g0054 a0001c0001t0001g0159 a0001c0001t0001g0160 others(44): Show |
47 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(44): Show |
intron_variant | MODIFIER | c.175+15212G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143755160 | |||||||
| chr8:143755578 | G | C | 6 | a0003c0003t0001g0035 a0003c0003t0001g0036 a0003c0003t0001g0037 others(3): Show |
6 | HG02280.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+15630G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143755578 | |||||||
| chr8:143755629 | G | T | 1 | a0015c0016t0001g0345 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.175+15681G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143755629 | |||||||
| chr8:143755759 | G | A | 1 | a0002c0002t0001g0328 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.176-15729G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143755759 | |||||||
| chr8:143755899 | G | C | 6 | a0003c0003t0001g0035 a0003c0003t0001g0036 a0003c0003t0001g0037 others(3): Show |
6 | HG02280.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.176-15589G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143755899 | |||||||
| chr8:143755984 | C | T | 1 | a0003c0003t0001g0200 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.176-15504C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143755984 | |||||||
| chr8:143755987 | G | A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0084 |
2 | NA18612.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.176-15501G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143755987 | |||||||
| chr8:143756009 | G | C | 6 | a0003c0003t0001g0035 a0003c0003t0001g0036 a0003c0003t0001g0037 others(3): Show |
6 | HG02280.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.176-15479G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143756009 | |||||||
| chr8:143756222 | T | G | 1 | a0003c0003t0001g0199 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.176-15266T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143756222 | |||||||
| chr8:143756332 | C | T | 3 | a0002c0002t0001g0256 a0002c0002t0001g0257 a0002c0002t0001g0299 |
3 | HG02080.hp2 NA18944.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.176-15156C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143756332 | |||||||
| chr8:143756382 | C | T | 10 | a0003c0003t0001g0048 a0003c0003t0001g0057 a0003c0003t0001g0197 others(7): Show |
10 | HG02145.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.176-15106C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143756382 | |||||||
| chr8:143756420 | T | G | 82 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0001c0010t0001g0040 others(79): Show |
83 | HG00733.hp2 HG01175.hp1 HG01192.hp2 others(80): Show |
intron_variant | MODIFIER | c.176-15068T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143756420 | |||||||
| chr8:143756519 | C | T | 5 | a0001c0001t0001g0341 a0003c0003t0001g0340 a0011c0012t0001g0339 others(2): Show |
5 | HG01175.hp1 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.176-14969C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143756519 | |||||||
| chr8:143756638 | A | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0205 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.176-14850A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143756638 | |||||||
| chr8:143756812 | T | TA | 84 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(81): Show |
84 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.176-14660dupA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143756812 | ||||||
| chr8:143756812 | TA | T | 10 | a0001c0001t0001g0085 a0002c0002t0001g0009 a0002c0002t0001g0306 others(7): Show |
10 | HG01069.hp1 HG01516.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.176-14660delA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143756812 | ||||||
| chr8:143756976 | T | TA | 120 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0004 others(117): Show |
123 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.176-14500dupA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143756976 | ||||||
| chr8:143756977 | A | G | 151 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.176-14511A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143756977 | |||||||
| chr8:143757002 | A | G | 5 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(2): Show |
5 | HG02615.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.176-14486A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143757002 | |||||||
| chr8:143757040 | C | G | 2 | a0018c0014t0001g0061 a0023c0022t0001g0062 |
2 | HG02602.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.176-14448C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143757040 | |||||||
| chr8:143757044 | G | A | 1 | a0015c0016t0001g0238 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.176-14444G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143757044 | |||||||
| chr8:143757127 | A | T | 72 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0003c0003t0001g0001 others(69): Show |
73 | HG00733.hp2 HG01175.hp1 HG01192.hp2 others(70): Show |
intron_variant | MODIFIER | c.176-14361A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143757127 | |||||||
| chr8:143757205 | C | T | 1 | a0002c0002t0001g0279 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.176-14283C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143757205 | |||||||
| chr8:143757221 | C | T | 5 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(2): Show |
5 | HG02615.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.176-14267C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143757221 | |||||||
| chr8:143757238 | A | G | 22 | a0003c0003t0001g0001 a0003c0003t0001g0222 a0003c0003t0001g0225 others(19): Show |
23 | HG01975.hp2 HG02258.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.176-14250A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143757238 | |||||||
| chr8:143757337 | T | G | 1 | a0002c0002t0001g0002 | 2 | HG00621.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.176-14151T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143757337 | |||||||
| chr8:143757338 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.176-14150T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143757338 | |||||||
| chr8:143757339 | CTTTT | C | 12 | a0007c0007t0001g0015 a0007c0007t0001g0017 a0008c0008t0001g0023 others(9): Show |
12 | HG00733.hp2 HG01891.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.176-14137_176-1413 others(8): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143757339 | ||||||
| chr8:143757422 | C | T | 1 | a0005c0005t0001g0216 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.176-14066C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143757422 | |||||||
| chr8:143757647 | T | C | 2 | a0006c0006t0001g0033 a0006c0006t0001g0034 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.176-13841T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143757647 | |||||||
| chr8:143757952 | TG | T | 6 | a0003c0003t0001g0035 a0003c0003t0001g0036 a0003c0003t0001g0037 others(3): Show |
6 | HG02280.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.176-13535delG | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143757952 | |||||||
| chr8:143758061 | T | C | 1 | a0002c0002t0001g0287 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.176-13427T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143758061 | |||||||
| chr8:143758176 | C | G | 1 | a0002c0002t0001g0322 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.176-13312C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143758176 | |||||||
| chr8:143758414 | G | T | 8 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(5): Show |
8 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.176-13074G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143758414 | |||||||
| chr8:143758469 | G | A | 1 | a0002c0002t0001g0275 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.176-13019G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143758469 | |||||||
| chr8:143758519 | C | T | 2 | a0003c0003t0001g0227 a0003c0003t0001g0230 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.176-12969C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143758519 | |||||||
| chr8:143758697 | T | C | 82 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0001c0010t0001g0040 others(79): Show |
83 | HG00733.hp2 HG01175.hp1 HG01192.hp2 others(80): Show |
intron_variant | MODIFIER | c.176-12791T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143758697 | |||||||
| chr8:143758725 | C | T | 1 | a0029c0026t0001g0152 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.176-12763C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143758725 | |||||||
| chr8:143758735 | C | T | 3 | a0002c0002t0001g0265 a0002c0002t0001g0266 a0002c0002t0001g0267 |
3 | HG00609.hp1 NA18971.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.176-12753C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143758735 | |||||||
| chr8:143758752 | A | T | 6 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0111 others(3): Show |
6 | HG02071.hp2 NA18747.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.176-12736A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143758752 | |||||||
| chr8:143758883 | C | T | 1 | a0002c0002t0001g0311 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.176-12605C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143758883 | |||||||
| chr8:143758966 | G | A | 3 | a0007c0007t0001g0045 a0007c0007t0001g0046 a0007c0007t0001g0047 |
3 | HG02258.hp2 HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.176-12522G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143758966 | |||||||
| chr8:143758975 | G | A | 2 | a0002c0002t0001g0304 a0002c0035t0001g0303 |
2 | NA18989.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.176-12513G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143758975 | |||||||
| chr8:143759040 | G | A | 1 | a0004c0004t0001g0087 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.176-12448G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143759040 | |||||||
| chr8:143759104 | C | T | 3 | a0002c0002t0001g0256 a0002c0002t0001g0257 a0002c0002t0001g0299 |
3 | HG02080.hp2 NA18944.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.176-12384C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143759104 | |||||||
| chr8:143759238 | G | C | 4 | a0004c0004t0001g0155 a0004c0004t0001g0170 a0004c0004t0001g0188 others(1): Show |
4 | HG01109.hp2 HG01496.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-12250G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143759238 | |||||||
| chr8:143759269 | G | T | 23 | a0003c0003t0001g0012 a0003c0003t0001g0013 a0003c0003t0001g0018 others(20): Show |
23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.176-12219G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143759269 | |||||||
| chr8:143759270 | C | T | 23 | a0003c0003t0001g0012 a0003c0003t0001g0013 a0003c0003t0001g0018 others(20): Show |
23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.176-12218C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143759270 | |||||||
| chr8:143759281 | C | T | 23 | a0003c0003t0001g0012 a0003c0003t0001g0013 a0003c0003t0001g0018 others(20): Show |
23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.176-12207C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143759281 | |||||||
| chr8:143759380 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.176-12108G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143759380 | |||||||
| chr8:143759552 | A | G | 1 | a0007c0007t0001g0046 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.176-11936A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143759552 | |||||||
| chr8:143759572 | A | G | 11 | a0003c0003t0001g0012 a0003c0003t0001g0013 a0003c0003t0001g0018 others(8): Show |
11 | HG01192.hp2 HG01884.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.176-11916A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143759572 | |||||||
| chr8:143759576 | G | T | 4 | a0002c0002t0001g0253 a0002c0002t0001g0307 a0002c0002t0001g0308 others(1): Show |
4 | HG00438.hp1 NA18948.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.176-11912G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143759576 | |||||||
| chr8:143759648 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.176-11840C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143759648 | |||||||
| chr8:143759660 | TCCAAGGA others(3): Show |
T | 1 | a0005c0005t0001g0210 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.176-11825_176-1181 others(14): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143759660 | ||||||
| chr8:143759793 | T | C | 38 | a0001c0010t0001g0041 a0003c0003t0001g0001 a0003c0003t0001g0035 others(35): Show |
39 | HG01975.hp2 HG02055.hp1 HG02145.hp1 others(36): Show |
intron_variant | MODIFIER | c.176-11695T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143759793 | |||||||
| chr8:143760120 | G | A | 2 | a0002c0002t0001g0009 a0002c0002t0001g0276 |
2 | HG02083.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.176-11368G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143760120 | |||||||
| chr8:143760134 | T | C | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(2): Show |
5 | NA18942.hp2 NA18951.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.176-11354T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143760134 | |||||||
| chr8:143760512 | C | CA | 228 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(225): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.176-10959dupA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143760512 | ||||||
| chr8:143760512 | C | CAA | 25 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0095 others(22): Show |
25 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.176-10960_176-1095 others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143760512 | ||||||
| chr8:143760512 | CA | C | 39 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0003c0003t0001g0001 others(36): Show |
40 | HG01175.hp1 HG01975.hp2 HG02145.hp1 others(37): Show |
intron_variant | MODIFIER | c.176-10959delA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143760512 | ||||||
| chr8:143760637 | G | A | 70 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0003c0003t0001g0001 others(67): Show |
71 | HG00733.hp2 HG01175.hp1 HG01192.hp2 others(68): Show |
intron_variant | MODIFIER | c.176-10851G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143760637 | |||||||
| chr8:143760663 | C | G | 1 | a0002c0002t0001g0276 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.176-10825C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143760663 | |||||||
| chr8:143760728 | A | C | 1 | a0002c0002t0001g0332 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.176-10760A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143760728 | |||||||
| chr8:143760770 | C | G | 2 | a0001c0001t0001g0134 a0001c0001t0001g0142 |
2 | HG01123.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.176-10718C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143760770 | |||||||
| chr8:143760904 | C | A | 11 | a0003c0003t0001g0012 a0003c0003t0001g0013 a0003c0003t0001g0018 others(8): Show |
11 | HG01192.hp2 HG01884.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.176-10584C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143760904 | |||||||
| chr8:143760932 | G | A | 1 | a0021c0033t0001g0329 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.176-10556G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143760932 | |||||||
| chr8:143760965 | C | G | 1 | a0005c0005t0001g0210 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.176-10523C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143760965 | |||||||
| chr8:143761034 | C | A | 271 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(268): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.176-10454C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143761034 | |||||||
| chr8:143761053 | T | G | 340 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(337): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.176-10435T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143761053 | |||||||
| chr8:143761085 | G | A | 82 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0001c0010t0001g0040 others(79): Show |
83 | HG00733.hp2 HG01175.hp1 HG01192.hp2 others(80): Show |
intron_variant | MODIFIER | c.176-10403G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143761085 | |||||||
| chr8:143761278 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.176-10210G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143761278 | |||||||
| chr8:143761808 | G | GT | 155 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(152): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.176-9668dupT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143761808 | ||||||
| chr8:143761808 | G | GTT | 19 | a0001c0001t0001g0078 a0001c0001t0001g0101 a0001c0001t0001g0123 others(16): Show |
19 | HG00408.hp1 HG00733.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.176-9669_176-9668d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143761808 | ||||||
| chr8:143761886 | CAT | C | 151 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.176-9597_176-9596d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143761886 | ||||||
| chr8:143761939 | A | C | 1 | a0002c0002t0001g0281 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.176-9549A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143761939 | |||||||
| chr8:143762060 | G | A | 2 | a0006c0006t0001g0033 a0006c0006t0001g0034 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.176-9428G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143762060 | |||||||
| chr8:143762172 | G | A | 3 | a0006c0006t0001g0174 a0006c0006t0001g0175 a0006c0006t0001g0176 |
3 | HG00642.hp1 HG00735.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.176-9316G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143762172 | |||||||
| chr8:143762224 | G | A | 8 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(5): Show |
8 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.176-9264G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143762224 | |||||||
| chr8:143762263 | C | T | 1 | a0004c0004t0001g0171 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.176-9225C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143762263 | |||||||
| chr8:143762326 | A | AAGGG | 15 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(12): Show |
15 | HG01123.hp2 HG01361.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.176-9148_176-9145d others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143762326 | ||||||
| chr8:143762326 | A | G | 1 | a0005c0005t0001g0327 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.176-9162A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143762326 | |||||||
| chr8:143762341 | G | GGAAAA | 28 | a0003c0003t0001g0001 a0003c0003t0001g0035 a0003c0003t0001g0036 others(25): Show |
29 | HG01975.hp2 HG02258.hp1 HG02280.hp1 others(26): Show |
intron_variant | MODIFIER | c.176-9132_176-9128d others(7): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143762341 | ||||||
| chr8:143762361 | G | C | 1 | a0001c0001t0001g0109 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.176-9127G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143762361 | |||||||
| chr8:143762364 | T | C | 5 | a0013c0013t0001g0019 a0013c0013t0001g0020 a0013c0013t0001g0026 others(2): Show |
5 | HG00733.hp2 HG03490.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.176-9124T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143762364 | |||||||
| chr8:143762394 | C | A | 3 | a0013c0013t0001g0019 a0013c0013t0001g0020 a0013c0013t0001g0026 |
3 | HG03490.hp1 HG03492.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.176-9094C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143762394 | |||||||
| chr8:143762522 | A | G | 1 | a0015c0016t0001g0345 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.176-8966A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143762522 | |||||||
| chr8:143762785 | A | G | 151 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.176-8703A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143762785 | |||||||
| chr8:143762868 | G | T | 2 | a0003c0003t0001g0066 a0012c0017t0001g0067 |
2 | HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.176-8620G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143762868 | |||||||
| chr8:143762940 | C | CT | 10 | a0003c0003t0001g0048 a0003c0003t0001g0057 a0003c0003t0001g0197 others(7): Show |
10 | HG02145.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.176-8539dupT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143762940 | ||||||
| chr8:143762955 | CTCTTT | C | 8 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(5): Show |
8 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.176-8522_176-8518d others(7): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143762955 | ||||||
| chr8:143762970 | T | G | 1 | a0002c0002t0001g0277 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.176-8518T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143762970 | |||||||
| chr8:143763024 | TTTC | T | 9 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0003c0003t0001g0066 others(6): Show |
9 | HG01175.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.176-8461_176-8459d others(5): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143763024 | ||||||
| chr8:143763051 | C | G | 1 | a0001c0001t0001g0071 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.176-8437C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143763051 | |||||||
| chr8:143763145 | A | G | 1 | a0002c0002t0001g0286 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.176-8343A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143763145 | |||||||
| chr8:143763245 | A | C | 30 | a0003c0003t0001g0001 a0003c0003t0001g0035 a0003c0003t0001g0036 others(27): Show |
31 | HG01975.hp2 HG02258.hp1 HG02280.hp1 others(28): Show |
intron_variant | MODIFIER | c.176-8243A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143763245 | |||||||
| chr8:143763466 | A | G | 1 | a0006c0006t0001g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.176-8022A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143763466 | |||||||
| chr8:143763778 | C | G | 108 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0004 others(105): Show |
111 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.176-7710C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143763778 | |||||||
| chr8:143763892 | C | T | 1 | a0002c0002t0001g0002 | 2 | HG00621.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.176-7596C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143763892 | |||||||
| chr8:143763899 | A | G | 6 | a0003c0003t0001g0035 a0003c0003t0001g0036 a0003c0003t0001g0037 others(3): Show |
6 | HG02280.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.176-7589A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143763899 | |||||||
| chr8:143763943 | T | C | 1 | a0028c0032t0001g0028 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.176-7545T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143763943 | |||||||
| chr8:143764095 | CT | C | 8 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(5): Show |
8 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.176-7392delT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143764095 | |||||||
| chr8:143764175 | C | A | 8 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(5): Show |
8 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.176-7313C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143764175 | |||||||
| chr8:143764360 | A | G | 28 | a0003c0003t0001g0001 a0003c0003t0001g0035 a0003c0003t0001g0036 others(25): Show |
29 | HG01975.hp2 HG02258.hp1 HG02280.hp1 others(26): Show |
intron_variant | MODIFIER | c.176-7128A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143764360 | |||||||
| chr8:143764431 | A | G | 3 | a0007c0007t0001g0045 a0007c0007t0001g0046 a0007c0007t0001g0047 |
3 | HG02258.hp2 HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.176-7057A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143764431 | |||||||
| chr8:143764451 | C | CA | 190 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(187): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.176-7020dupA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143764451 | ||||||
| chr8:143764451 | C | CAA | 21 | a0001c0001t0001g0079 a0001c0001t0001g0094 a0001c0001t0001g0108 others(18): Show |
21 | HG00438.hp2 HG00642.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.176-7021_176-7020d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143764451 | ||||||
| chr8:143764551 | G | A | 6 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0003c0003t0001g0340 others(3): Show |
6 | HG01175.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.176-6937G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143764551 | |||||||
| chr8:143764661 | A | G | 187 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0001c0010t0001g0040 others(184): Show |
191 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.176-6827A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143764661 | |||||||
| chr8:143764769 | A | G | 8 | a0001c0001t0001g0159 a0004c0004t0001g0171 a0004c0004t0001g0177 others(5): Show |
8 | HG00099.hp2 HG01071.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.176-6719A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143764769 | |||||||
| chr8:143764959 | T | C | 3 | a0006c0006t0001g0033 a0006c0006t0001g0034 a0027c0021t0001g0335 |
3 | HG02257.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.176-6529T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143764959 | |||||||
| chr8:143764974 | A | G | 1 | a0003c0003t0001g0222 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.176-6514A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143764974 | |||||||
| chr8:143765075 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.176-6413G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143765075 | |||||||
| chr8:143765226 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0189 |
2 | NA18939.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.176-6262G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143765226 | |||||||
| chr8:143765242 | C | T | 1 | a0004c0004t0001g0164 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.176-6246C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143765242 | |||||||
| chr8:143765315 | C | G | 8 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(5): Show |
8 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.176-6173C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143765315 | |||||||
| chr8:143765356 | C | CA | 11 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.176-6120dupA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143765356 | ||||||
| chr8:143766448 | A | G | 1 | a0004c0004t0001g0178 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.176-5040A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143766448 | |||||||
| chr8:143766457 | G | A | 1 | a0002c0002t0001g0317 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.176-5031G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143766457 | |||||||
| chr8:143766477 | C | T | 148 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(145): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.176-5011C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143766477 | |||||||
| chr8:143766516 | C | CA | 3 | a0003c0003t0001g0066 a0012c0017t0001g0067 a0024c0030t0001g0343 |
3 | HG02622.hp1 HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.176-4967dupA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143766516 | ||||||
| chr8:143766562 | C | T | 193 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0001c0010t0001g0040 others(190): Show |
197 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.176-4926C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143766562 | |||||||
| chr8:143766586 | G | A | 48 | a0001c0001t0001g0054 a0001c0001t0001g0159 a0001c0001t0001g0160 others(45): Show |
48 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(45): Show |
intron_variant | MODIFIER | c.176-4902G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143766586 | |||||||
| chr8:143766643 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.176-4845C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143766643 | |||||||
| chr8:143766657 | C | T | 110 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0004 others(107): Show |
113 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.176-4831C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143766657 | |||||||
| chr8:143766769 | T | C | 3 | a0006c0006t0001g0033 a0006c0006t0001g0034 a0027c0021t0001g0335 |
3 | HG02257.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.176-4719T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143766769 | |||||||
| chr8:143766953 | C | T | 1 | a0004c0004t0001g0158 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.176-4535C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143766953 | |||||||
| chr8:143766993 | C | T | 28 | a0003c0003t0001g0001 a0003c0003t0001g0035 a0003c0003t0001g0036 others(25): Show |
29 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(26): Show |
intron_variant | MODIFIER | c.176-4495C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143766993 | |||||||
| chr8:143767292 | A | G | 13 | a0003c0003t0001g0048 a0003c0003t0001g0057 a0003c0003t0001g0066 others(10): Show |
13 | HG02145.hp1 HG02622.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.176-4196A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143767292 | |||||||
| chr8:143767345 | A | AGTGT | 3 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0094 |
3 | HG00438.hp2 NA18955.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.176-4130_176-4127d others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143767345 | ||||||
| chr8:143767379 | G | A | 15 | a0001c0001t0001g0341 a0001c0010t0001g0040 a0001c0010t0001g0041 others(12): Show |
15 | HG01175.hp1 HG02258.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.176-4109G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143767379 | |||||||
| chr8:143767432 | T | C | 341 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(338): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.176-4056T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143767432 | |||||||
| chr8:143767477 | T | A | 2 | a0001c0001t0001g0243 a0021c0033t0001g0329 |
2 | HG01884.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.176-4011T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143767477 | |||||||
| chr8:143767515 | G | A | 1 | a0002c0002t0001g0009 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.176-3973G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143767515 | |||||||
| chr8:143767742 | G | T | 1 | a0028c0032t0001g0028 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.176-3746G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143767742 | |||||||
| chr8:143767877 | C | CT | 71 | a0001c0001t0001g0005 a0001c0001t0001g0050 a0001c0001t0001g0064 others(68): Show |
72 | HG00544.hp2 HG00642.hp1 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.176-3589dupT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143767877 | ||||||
| chr8:143767877 | C | CTT | 11 | a0003c0003t0001g0035 a0003c0003t0001g0038 a0003c0003t0001g0039 others(8): Show |
11 | HG02258.hp1 HG02622.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.176-3590_176-3589d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143767877 | ||||||
| chr8:143767877 | CT | C | 90 | a0001c0001t0001g0246 a0002c0002t0001g0003 a0002c0002t0001g0004 others(87): Show |
92 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.176-3589delT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143767877 | ||||||
| chr8:143767970 | T | A | 341 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(338): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.176-3518T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143767970 | |||||||
| chr8:143768032 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.176-3456G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768032 | |||||||
| chr8:143768088 | G | A | 3 | a0003c0003t0001g0066 a0012c0017t0001g0067 a0024c0030t0001g0343 |
3 | HG02622.hp1 HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.176-3400G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768088 | |||||||
| chr8:143768134 | C | T | 3 | a0006c0006t0001g0033 a0006c0006t0001g0034 a0027c0021t0001g0335 |
3 | HG02257.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.176-3354C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768134 | |||||||
| chr8:143768238 | T | C | 1 | a0002c0002t0001g0279 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.176-3250T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768238 | |||||||
| chr8:143768380 | C | A | 1 | a0002c0002t0001g0313 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.176-3108C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768380 | |||||||
| chr8:143768381 | G | A | 12 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(9): Show |
12 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.176-3107G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768381 | |||||||
| chr8:143768505 | C | T | 3 | a0006c0006t0001g0033 a0006c0006t0001g0034 a0027c0021t0001g0335 |
3 | HG02257.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.176-2983C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768505 | |||||||
| chr8:143768517 | C | T | 1 | a0024c0030t0001g0343 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.176-2971C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768517 | |||||||
| chr8:143768540 | C | T | 1 | a0015c0016t0001g0345 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.176-2948C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768540 | |||||||
| chr8:143768595 | A | G | 3 | a0006c0006t0001g0033 a0006c0006t0001g0034 a0027c0021t0001g0335 |
3 | HG02257.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.176-2893A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768595 | |||||||
| chr8:143768664 | G | A | 341 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(338): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.176-2824G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768664 | |||||||
| chr8:143768711 | A | C | 3 | a0006c0006t0001g0033 a0006c0006t0001g0034 a0027c0021t0001g0335 |
3 | HG02257.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.176-2777A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768711 | |||||||
| chr8:143768740 | TTC | T | 3 | a0006c0006t0001g0033 a0006c0006t0001g0034 a0027c0021t0001g0335 |
3 | HG02257.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.176-2746_176-2745d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143768740 | ||||||
| chr8:143768744 | G | T | 3 | a0006c0006t0001g0033 a0006c0006t0001g0034 a0027c0021t0001g0335 |
3 | HG02257.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.176-2744G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768744 | |||||||
| chr8:143768748 | C | T | 3 | a0006c0006t0001g0033 a0006c0006t0001g0034 a0027c0021t0001g0335 |
3 | HG02257.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.176-2740C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768748 | |||||||
| chr8:143768944 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.176-2544C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768944 | |||||||
| chr8:143769095 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.176-2393C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143769095 | |||||||
| chr8:143769150 | C | G | 2 | a0006c0006t0001g0033 a0006c0006t0001g0034 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.176-2338C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143769150 | |||||||
| chr8:143769209 | G | A | 3 | a0009c0009t0001g0010 a0009c0009t0001g0029 a0009c0009t0001g0030 |
3 | HG01192.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.176-2279G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143769209 | |||||||
| chr8:143769262 | G | A | 1 | a0012c0017t0001g0067 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.176-2226G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143769262 | |||||||
| chr8:143769370 | T | A | 122 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0004 others(119): Show |
125 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.176-2118T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143769370 | |||||||
| chr8:143769445 | T | C | 86 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(83): Show |
86 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.176-2043T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143769445 | |||||||
| chr8:143769481 | T | C | 194 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0001c0010t0001g0040 others(191): Show |
198 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.176-2007T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143769481 | |||||||
| chr8:143769482 | G | A | 2 | a0005c0005t0001g0215 a0005c0005t0001g0216 |
2 | HG00280.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.176-2006G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143769482 | |||||||
| chr8:143769500 | A | T | 1 | a0002c0002t0001g0296 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.176-1988A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143769500 | |||||||
| chr8:143769536 | G | A | 1 | a0007c0007t0001g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.176-1952G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143769536 | |||||||
| chr8:143769652 | C | T | 3 | a0006c0006t0001g0033 a0006c0006t0001g0034 a0027c0021t0001g0335 |
3 | HG02257.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.176-1836C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143769652 | |||||||
| chr8:143769754 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.176-1734C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143769754 | |||||||
| chr8:143769784 | T | C | 1 | a0006c0006t0001g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.176-1704T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143769784 | |||||||
| chr8:143769857 | A | C | 1 | a0002c0002t0001g0276 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.176-1631A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143769857 | |||||||
| chr8:143770320 | C | T | 3 | a0006c0006t0001g0033 a0006c0006t0001g0034 a0027c0021t0001g0335 |
3 | HG02257.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.176-1168C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143770320 | |||||||
| chr8:143770395 | G | T | 173 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0004 others(170): Show |
177 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.176-1093G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143770395 | |||||||
| chr8:143770516 | T | C | 341 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(338): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.176-972T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143770516 | |||||||
| chr8:143770564 | C | T | 2 | a0003c0003t0001g0048 a0003c0003t0001g0202 |
2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.176-924C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143770564 | |||||||
| chr8:143770624 | G | A | 1 | a0002c0002t0001g0269 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.176-864G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143770624 | |||||||
| chr8:143770638 | G | A | 121 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0004 others(118): Show |
124 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.176-850G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143770638 | |||||||
| chr8:143770709 | G | A | 46 | a0001c0001t0001g0054 a0001c0001t0001g0159 a0001c0001t0001g0160 others(43): Show |
46 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(43): Show |
intron_variant | MODIFIER | c.176-779G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143770709 | |||||||
| chr8:143770721 | C | G | 1 | a0001c0001t0001g0169 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.176-767C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143770721 | |||||||
| chr8:143770746 | G | T | 1 | a0027c0021t0001g0335 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.176-742G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143770746 | |||||||
| chr8:143770848 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.176-640C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143770848 | |||||||
| chr8:143771090 | G | C | 2 | a0006c0006t0001g0033 a0006c0006t0001g0034 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.176-398G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143771090 | |||||||
| chr8:143771166 | C | A | 1 | a0002c0002t0001g0289 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.176-322C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143771166 | |||||||
| chr8:143771175 | G | A | 7 | a0001c0001t0001g0091 a0001c0001t0001g0095 a0001c0001t0001g0107 others(4): Show |
7 | HG02080.hp1 HG02129.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.176-313G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143771175 | |||||||
| chr8:143771311 | C | G | 1 | a0024c0030t0001g0343 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.176-177C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143771311 | |||||||
| chr8:143771360 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.176-128G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143771360 | |||||||
| chr8:143771390 | C | G | 170 | a0001c0001t0001g0082 a0001c0001t0001g0096 a0001c0001t0001g0097 others(167): Show |
173 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.176-98C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143771390 | |||||||
| chr8:143771644 | G | T | 121 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0004 others(118): Show |
124 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.306+26G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 4/13 | chr8 | 143771644 | |||||||
| chr8:143771645 | G | A | 1 | a0002c0002t0001g0290 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.306+27G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 4/13 | chr8 | 143771645 | |||||||
| chr8:143771709 | G | A | 8 | a0003c0003t0001g0048 a0003c0003t0001g0057 a0003c0003t0001g0197 others(5): Show |
8 | HG02922.hp2 HG02965.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.306+91G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 4/13 | chr8 | 143771709 | |||||||
| chr8:143771710 | A | G | 1 | a0027c0021t0001g0335 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.307-91A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 4/13 | chr8 | 143771710 | |||||||
| chr8:143771743 | C | CCTCGGGG | 3 | a0006c0006t0001g0033 a0006c0006t0001g0034 a0006c0006t0001g0063 |
3 | HG02257.hp2 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.307-49_307-43dupTC others(5): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr8 | 143771743 | ||||||
| chr8:143771983 | G | A | 2 | a0006c0006t0001g0033 a0006c0006t0001g0034 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.471+18G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 5/13 | chr8 | 143771983 | |||||||
| chr8:143772315 | A | G | 1 | a0003c0003t0001g0199 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.664-42A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 6/13 | chr8 | 143772315 | |||||||
| chr8:143772494 | AGAGGTGT others(25): Show |
A | 1 | a0012c0017t0001g0198 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.789+25_789+56delCC others(30): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143772494 | ||||||
| chr8:143772507 | CCGGGAGG others(25): Show |
C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0147 |
2 | HG02071.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.789+55_789+86delCC others(30): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143772507 | ||||||
| chr8:143772508 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.789+26C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143772508 | |||||||
| chr8:143772539 | T | C | 160 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(157): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.789+57T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143772539 | |||||||
| chr8:143772628 | C | CTG | 15 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(12): Show |
15 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.789+148_789+149dup others(2): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143772628 | ||||||
| chr8:143772646 | A | G | 23 | a0003c0003t0001g0001 a0003c0003t0001g0035 a0003c0003t0001g0036 others(20): Show |
24 | HG02258.hp1 HG02280.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.789+164A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143772646 | |||||||
| chr8:143772875 | T | C | 15 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(12): Show |
15 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.789+393T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143772875 | |||||||
| chr8:143772884 | T | C | 1 | a0021c0033t0001g0329 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.789+402T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143772884 | |||||||
| chr8:143772904 | C | T | 14 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(11): Show |
14 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.789+422C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143772904 | |||||||
| chr8:143772909 | C | T | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0208 |
3 | NA18966.hp1 NA18998.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.789+427C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143772909 | |||||||
| chr8:143772936 | T | G | 15 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(12): Show |
15 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.789+454T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143772936 | |||||||
| chr8:143772956 | C | T | 15 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(12): Show |
15 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.789+474C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143772956 | |||||||
| chr8:143773015 | T | C | 15 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(12): Show |
15 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.789+533T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773015 | |||||||
| chr8:143773044 | A | G | 15 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(12): Show |
15 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.789+562A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773044 | |||||||
| chr8:143773175 | C | T | 1 | a0003c0003t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.789+693C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773175 | |||||||
| chr8:143773251 | G | A | 2 | a0006c0006t0001g0033 a0006c0006t0001g0034 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.789+769G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773251 | |||||||
| chr8:143773261 | G | T | 15 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(12): Show |
15 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.789+779G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773261 | |||||||
| chr8:143773300 | C | CA | 8 | a0001c0001t0001g0051 a0001c0001t0001g0091 a0001c0001t0001g0097 others(5): Show |
8 | HG00735.hp2 HG01168.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.789+834dupA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143773300 | ||||||
| chr8:143773307 | A | AAACAAAA others(5): Show |
11 | a0001c0010t0001g0043 a0006c0006t0001g0033 a0006c0006t0001g0034 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+827_789+828ins others(12): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143773307 | ||||||
| chr8:143773308 | A | AC | 8 | a0003c0003t0001g0048 a0003c0003t0001g0057 a0003c0003t0001g0197 others(5): Show |
8 | HG02922.hp2 HG02965.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.789+826_789+827ins others(1): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773308 | |||||||
| chr8:143773310 | A | C | 10 | a0002c0002t0001g0255 a0002c0002t0001g0274 a0002c0002t0001g0278 others(7): Show |
10 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.789+828A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773310 | |||||||
| chr8:143773314 | A | AC | 9 | a0002c0002t0001g0004 a0002c0002t0001g0249 a0002c0002t0001g0251 others(6): Show |
10 | HG00558.hp2 HG02622.hp1 NA18942.hp1 others(7): Show |
intron_variant | MODIFIER | c.789+832_789+833ins others(1): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773314 | |||||||
| chr8:143773314 | A | C | 113 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0006 others(110): Show |
115 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.789+832A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773314 | |||||||
| chr8:143773316 | ACAAAAAA others(3): Show |
A | 21 | a0003c0003t0001g0001 a0003c0003t0001g0035 a0003c0003t0001g0036 others(18): Show |
22 | HG02258.hp1 HG02280.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.789+835_789+844del others(10): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773316 | |||||||
| chr8:143773317 | C | A | 141 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0004 others(138): Show |
144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.789+835C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773317 | |||||||
| chr8:143773318 | A | C | 142 | a0001c0010t0001g0043 a0002c0002t0001g0002 a0002c0002t0001g0003 others(139): Show |
145 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.789+836A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773318 | |||||||
| chr8:143773320 | A | C | 1 | a0024c0030t0001g0343 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.789+838A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773320 | |||||||
| chr8:143773322 | A | C | 122 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0004 others(119): Show |
125 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.789+840A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773322 | |||||||
| chr8:143773325 | AC | A | 17 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0003c0003t0001g0048 others(14): Show |
17 | HG01175.hp1 HG02559.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.789+844delC | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773325 | |||||||
| chr8:143773326 | C | A | 22 | a0001c0010t0001g0043 a0008c0008t0001g0023 a0008c0008t0001g0024 others(19): Show |
22 | HG00733.hp2 HG01192.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.789+844C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773326 | |||||||
| chr8:143773326 | C | CCAAAAAA others(2): Show |
4 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(1): Show |
4 | HG02615.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.789+844_789+845ins others(9): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773326 | |||||||
| chr8:143773326 | CA | C | 10 | a0006c0006t0001g0033 a0006c0006t0001g0034 a0007c0007t0001g0015 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.789+845delA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773326 | |||||||
| chr8:143773327 | A | C | 1 | a0007c0007t0001g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.789+845A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773327 | |||||||
| chr8:143773328 | C | A | 123 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0004 others(120): Show |
126 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.789+846C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773328 | |||||||
| chr8:143773330 | A | C | 2 | a0001c0001t0001g0118 a0002c0002t0001g0255 |
2 | HG01928.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.789+848A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773330 | |||||||
| chr8:143773454 | G | T | 8 | a0003c0003t0001g0048 a0003c0003t0001g0057 a0003c0003t0001g0197 others(5): Show |
8 | HG02922.hp2 HG02965.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.789+972G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773454 | |||||||
| chr8:143773470 | A | G | 5 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0011c0012t0001g0339 others(2): Show |
5 | HG01175.hp1 HG02559.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.789+988A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773470 | |||||||
| chr8:143773797 | G | C | 1 | a0001c0001t0002g0056 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.789+1315G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773797 | |||||||
| chr8:143773867 | G | T | 124 | a0001c0001t0001g0169 a0002c0002t0001g0002 a0002c0002t0001g0003 others(121): Show |
127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.789+1385G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773867 | |||||||
| chr8:143774164 | A | G | 14 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(11): Show |
14 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.789+1682A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143774164 | |||||||
| chr8:143774177 | CA | C | 280 | a0001c0001t0001g0005 a0001c0001t0001g0050 a0001c0001t0001g0052 others(277): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.789+1710delA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143774177 | ||||||
| chr8:143774189 | A | C | 122 | a0001c0001t0001g0169 a0002c0002t0001g0002 a0002c0002t0001g0003 others(119): Show |
125 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.789+1707A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143774189 | |||||||
| chr8:143774232 | T | C | 8 | a0003c0003t0001g0048 a0003c0003t0001g0057 a0003c0003t0001g0197 others(5): Show |
8 | HG02922.hp2 HG02965.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.789+1750T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143774232 | |||||||
| chr8:143774273 | G | T | 34 | a0003c0003t0001g0001 a0003c0003t0001g0035 a0003c0003t0001g0036 others(31): Show |
35 | HG02258.hp1 HG02280.hp1 HG02280.hp2 others(32): Show |
intron_variant | MODIFIER | c.789+1791G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143774273 | |||||||
| chr8:143774345 | G | A | 2 | a0004c0004t0001g0089 a0004c0004t0001g0090 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.789+1863G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143774345 | |||||||
| chr8:143774611 | T | C | 15 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(12): Show |
15 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.789+2129T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143774611 | |||||||
| chr8:143774739 | G | C | 1 | a0014c0019t0001g0025 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.789+2257G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143774739 | |||||||
| chr8:143774744 | C | T | 3 | a0003c0003t0001g0066 a0012c0017t0001g0067 a0024c0030t0001g0343 |
3 | HG02622.hp1 HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.789+2262C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143774744 | |||||||
| chr8:143774821 | A | C | 2 | a0004c0004t0001g0167 a0004c0004t0001g0182 |
2 | HG00099.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.789+2339A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143774821 | |||||||
| chr8:143774890 | G | T | 16 | a0001c0001t0001g0341 a0001c0010t0001g0040 a0001c0010t0001g0041 others(13): Show |
16 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.789+2408G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143774890 | |||||||
| chr8:143774965 | G | A | 2 | a0006c0006t0001g0033 a0006c0006t0001g0034 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.789+2483G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143774965 | |||||||
| chr8:143774975 | G | GGGGGCAG others(17): Show |
2 | a0005c0005t0001g0283 a0005c0005t0001g0330 |
2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.789+2499_789+2522d others(26): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143774975 | ||||||
| chr8:143774989 | C | T | 16 | a0003c0003t0001g0001 a0003c0003t0001g0222 a0003c0003t0001g0225 others(13): Show |
17 | HG02258.hp1 HG02280.hp2 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.789+2507C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143774989 | |||||||
| chr8:143774993 | G | C | 8 | a0003c0003t0001g0048 a0003c0003t0001g0057 a0003c0003t0001g0197 others(5): Show |
8 | HG02922.hp2 HG02965.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.789+2511G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143774993 | |||||||
| chr8:143775184 | T | G | 1 | a0002c0002t0001g0268 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.789+2702T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143775184 | |||||||
| chr8:143775324 | G | A | 11 | a0001c0001t0001g0341 a0006c0006t0001g0033 a0006c0006t0001g0034 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+2842G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143775324 | |||||||
| chr8:143775335 | T | TAC | 45 | a0001c0001t0001g0054 a0001c0001t0001g0159 a0001c0001t0001g0160 others(42): Show |
45 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(42): Show |
intron_variant | MODIFIER | c.789+2871_789+2872d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775335 | ||||||
| chr8:143775335 | T | TACAC | 5 | a0001c0001t0001g0338 a0006c0006t0001g0186 a0011c0012t0001g0339 others(2): Show |
5 | HG01175.hp1 HG03139.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.789+2869_789+2872d others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775335 | ||||||
| chr8:143775335 | TAC | T | 4 | a0002c0002t0001g0003 a0002c0002t0001g0252 a0002c0002t0001g0287 others(1): Show |
5 | NA18964.hp2 NA18970.hp1 NA19055.hp2 others(2): Show |
intron_variant | MODIFIER | c.789+2871_789+2872d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775335 | ||||||
| chr8:143775353 | C | CACAG | 11 | a0001c0001t0001g0341 a0006c0006t0001g0033 a0006c0006t0001g0034 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+2872_789+2873i others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775353 | ||||||
| chr8:143775355 | G | C | 11 | a0001c0001t0001g0341 a0006c0006t0001g0033 a0006c0006t0001g0034 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+2873G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143775355 | |||||||
| chr8:143775526 | C | T | 8 | a0003c0003t0001g0048 a0003c0003t0001g0057 a0003c0003t0001g0197 others(5): Show |
8 | HG02922.hp2 HG02965.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.789+3044C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143775526 | |||||||
| chr8:143775622 | C | T | 1 | a0024c0030t0001g0343 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.789+3140C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143775622 | |||||||
| chr8:143775673 | A | G | 11 | a0001c0001t0001g0341 a0006c0006t0001g0033 a0006c0006t0001g0034 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+3191A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143775673 | |||||||
| chr8:143775747 | G | A | 1 | a0002c0002t0001g0320 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.789+3265G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143775747 | |||||||
| chr8:143775787 | T | TAC | 36 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0054 others(33): Show |
36 | HG00558.hp1 HG00673.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.789+3340_789+3341d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775787 | ||||||
| chr8:143775787 | T | TACAC | 10 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0146 others(7): Show |
10 | HG02165.hp1 HG02647.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.789+3338_789+3341d others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775787 | ||||||
| chr8:143775787 | T | TACACAC | 18 | a0001c0001t0001g0119 a0001c0001t0001g0243 a0002c0002t0001g0002 others(15): Show |
19 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.789+3336_789+3341d others(8): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775787 | ||||||
| chr8:143775787 | T | TACACACA others(1): Show |
34 | a0001c0001t0001g0162 a0002c0002t0001g0006 a0002c0002t0001g0007 others(31): Show |
34 | HG00609.hp1 HG01123.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.789+3334_789+3341d others(10): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775787 | ||||||
| chr8:143775787 | T | TACACACA others(3): Show |
71 | a0001c0001t0001g0139 a0001c0001t0001g0169 a0002c0002t0001g0004 others(68): Show |
72 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.789+3332_789+3341d others(12): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775787 | ||||||
| chr8:143775787 | T | TACACACA others(5): Show |
41 | a0001c0010t0001g0040 a0002c0002t0001g0003 a0002c0002t0001g0008 others(38): Show |
42 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.789+3330_789+3341d others(14): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775787 | ||||||
| chr8:143775787 | T | TACACACA others(7): Show |
6 | a0001c0010t0001g0041 a0001c0010t0001g0042 a0002c0002t0001g0313 others(3): Show |
6 | HG00423.hp2 HG02523.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.789+3328_789+3341d others(16): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775787 | ||||||
| chr8:143775787 | T | TACACACA others(9): Show |
4 | a0002c0002t0001g0291 a0002c0002t0001g0297 a0002c0002t0001g0302 others(1): Show |
4 | HG02004.hp2 HG02074.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.789+3326_789+3341d others(18): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775787 | ||||||
| chr8:143775787 | T | TACACACA others(13): Show |
1 | a0001c0010t0001g0043 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.789+3322_789+3341d others(22): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775787 | ||||||
| chr8:143775787 | T | TACACACA others(17): Show |
1 | a0002c0002t0001g0271 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.789+3318_789+3341d others(26): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775787 | ||||||
| chr8:143775787 | T | TACACGCA others(11): Show |
2 | a0003c0003t0001g0001 a0003c0003t0001g0229 |
3 | HG02895.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.789+3309_789+3310i others(20): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775787 | ||||||
| chr8:143775787 | TAC | T | 6 | a0001c0001t0001g0120 a0001c0001t0001g0122 a0001c0001t0001g0132 others(3): Show |
6 | HG01081.hp2 HG02004.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.789+3340_789+3341d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775787 | ||||||
| chr8:143775816 | ACACACAC | A | 3 | a0001c0001t0001g0341 a0007c0007t0001g0045 a0027c0021t0001g0335 |
3 | HG02258.hp2 HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.789+3337_789+3343d others(9): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775816 | ||||||
| chr8:143775818 | ACACAC | A | 4 | a0007c0007t0001g0046 a0007c0007t0001g0047 a0007c0007t0001g0203 others(1): Show |
4 | HG02145.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.789+3339_789+3343d others(7): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775818 | ||||||
| chr8:143775869 | T | C | 3 | a0003c0003t0001g0066 a0012c0017t0001g0067 a0024c0030t0001g0343 |
3 | HG02622.hp1 HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.789+3387T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143775869 | |||||||
| chr8:143775877 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.789+3395T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143775877 | |||||||
| chr8:143775887 | G | A | 1 | a0005c0005t0001g0210 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.789+3405G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143775887 | |||||||
| chr8:143775919 | A | G | 4 | a0001c0001t0001g0338 a0011c0012t0001g0339 a0011c0012t0001g0342 others(1): Show |
4 | HG01175.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.789+3437A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143775919 | |||||||
| chr8:143775961 | A | C | 11 | a0001c0001t0001g0341 a0006c0006t0001g0033 a0006c0006t0001g0034 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+3479A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143775961 | |||||||
| chr8:143775980 | G | A | 195 | a0001c0001t0001g0169 a0001c0001t0001g0338 a0001c0001t0001g0341 others(192): Show |
199 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.789+3498G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143775980 | |||||||
| chr8:143776004 | GGGCCGGG others(28): Show |
G | 5 | a0001c0001t0001g0338 a0007c0007t0001g0015 a0011c0012t0001g0339 others(2): Show |
5 | HG01175.hp1 HG02486.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.789+3535_789+3569d others(37): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143776004 | ||||||
| chr8:143776009 | G | T | 10 | a0001c0001t0001g0341 a0006c0006t0001g0033 a0006c0006t0001g0034 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.789+3527G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776009 | |||||||
| chr8:143776017 | T | C | 10 | a0001c0001t0001g0341 a0006c0006t0001g0033 a0006c0006t0001g0034 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.789+3535T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776017 | |||||||
| chr8:143776044 | G | T | 11 | a0001c0001t0001g0341 a0006c0006t0001g0033 a0006c0006t0001g0034 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+3562G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776044 | |||||||
| chr8:143776052 | C | T | 10 | a0001c0001t0001g0341 a0006c0006t0001g0033 a0006c0006t0001g0034 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.789+3570C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776052 | |||||||
| chr8:143776088 | G | A | 5 | a0013c0013t0001g0019 a0013c0013t0001g0020 a0013c0013t0001g0026 others(2): Show |
5 | HG00733.hp2 HG03490.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.789+3606G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776088 | |||||||
| chr8:143776096 | C | G | 11 | a0001c0001t0001g0341 a0006c0006t0001g0033 a0006c0006t0001g0034 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+3614C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776096 | |||||||
| chr8:143776097 | A | G | 11 | a0001c0001t0001g0341 a0006c0006t0001g0033 a0006c0006t0001g0034 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+3615A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776097 | |||||||
| chr8:143776101 | T | C | 11 | a0001c0001t0001g0341 a0006c0006t0001g0033 a0006c0006t0001g0034 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+3619T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776101 | |||||||
| chr8:143776105 | G | A | 11 | a0001c0001t0001g0341 a0006c0006t0001g0033 a0006c0006t0001g0034 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+3623G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776105 | |||||||
| chr8:143776118 | A | G | 11 | a0001c0001t0001g0341 a0006c0006t0001g0033 a0006c0006t0001g0034 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+3636A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776118 | |||||||
| chr8:143776121 | C | A | 11 | a0001c0001t0001g0341 a0006c0006t0001g0033 a0006c0006t0001g0034 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+3639C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776121 | |||||||
| chr8:143776137 | C | A | 11 | a0001c0001t0001g0341 a0006c0006t0001g0033 a0006c0006t0001g0034 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+3655C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776137 | |||||||
| chr8:143776149 | G | T | 2 | a0003c0003t0001g0066 a0012c0017t0001g0067 |
2 | HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.789+3667G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776149 | |||||||
| chr8:143776177 | C | T | 4 | a0001c0001t0001g0338 a0011c0012t0001g0339 a0011c0012t0001g0342 others(1): Show |
4 | HG01175.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.789+3695C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776177 | |||||||
| chr8:143776182 | G | A | 1 | a0003c0003t0001g0222 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.789+3700G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776182 | |||||||
| chr8:143776213 | C | T | 11 | a0001c0001t0001g0341 a0006c0006t0001g0033 a0006c0006t0001g0034 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+3731C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776213 | |||||||
| chr8:143776259 | T | C | 8 | a0001c0001t0001g0341 a0007c0007t0001g0015 a0007c0007t0001g0017 others(5): Show |
8 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.789+3777T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776259 | |||||||
| chr8:143776283 | TGCAGTCC | T | 12 | a0001c0001t0001g0341 a0002c0002t0001g0316 a0006c0006t0001g0033 others(9): Show |
12 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.789+3810_789+3816d others(9): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143776283 | ||||||
| chr8:143776294 | G | C | 12 | a0001c0001t0001g0341 a0002c0002t0001g0316 a0006c0006t0001g0033 others(9): Show |
12 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.789+3812G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776294 | |||||||
| chr8:143776298 | G | A | 34 | a0001c0001t0001g0341 a0002c0002t0001g0316 a0003c0003t0001g0001 others(31): Show |
35 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(32): Show |
intron_variant | MODIFIER | c.789+3816G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776298 | |||||||
| chr8:143776327 | C | CA | 262 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(259): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.789+3863dupA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143776327 | ||||||
| chr8:143776327 | C | CAA | 32 | a0001c0001t0001g0005 a0001c0001t0001g0052 a0001c0001t0001g0065 others(29): Show |
32 | HG00438.hp2 HG00558.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.789+3862_789+3863d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143776327 | ||||||
| chr8:143776381 | C | G | 2 | a0005c0005t0001g0215 a0005c0005t0001g0216 |
2 | HG00280.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.789+3899C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776381 | |||||||
| chr8:143776425 | A | G | 122 | a0001c0001t0001g0169 a0002c0002t0001g0002 a0002c0002t0001g0003 others(119): Show |
125 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.789+3943A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776425 | |||||||
| chr8:143776578 | G | A | 1 | a0002c0002t0001g0260 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.789+4096G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776578 | |||||||
| chr8:143776578 | G | C | 11 | a0001c0001t0001g0341 a0006c0006t0001g0033 a0006c0006t0001g0034 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+4096G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776578 | |||||||
| chr8:143777143 | T | C | 11 | a0001c0001t0001g0341 a0006c0006t0001g0033 a0006c0006t0001g0034 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+4661T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143777143 | |||||||
| chr8:143777164 | G | A | 1 | a0005c0005t0001g0327 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.789+4682G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143777164 | |||||||
| chr8:143777261 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.789+4779A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143777261 | |||||||
| chr8:143777288 | C | G | 11 | a0001c0001t0001g0341 a0006c0006t0001g0033 a0006c0006t0001g0034 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+4806C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143777288 | |||||||
| chr8:143777388 | C | T | 5 | a0001c0001t0001g0065 a0001c0001t0001g0092 a0002c0002t0001g0270 others(2): Show |
5 | HG03490.hp2 HG03654.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.789+4906C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143777388 | |||||||
| chr8:143777520 | T | TA | 38 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0064 others(35): Show |
38 | HG00558.hp1 HG00642.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.789+5057dupA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143777520 | ||||||
| chr8:143777520 | TA | T | 114 | a0001c0001t0001g0169 a0002c0002t0001g0002 a0002c0002t0001g0003 others(111): Show |
117 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.789+5057delA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143777520 | ||||||
| chr8:143777537 | A | C | 9 | a0001c0001t0001g0341 a0007c0007t0001g0015 a0007c0007t0001g0017 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.789+5055A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143777537 | |||||||
| chr8:143777539 | AC | A | 8 | a0001c0001t0001g0082 a0001c0001t0001g0151 a0001c0001t0001g0208 others(5): Show |
8 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.789+5058delC | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143777539 | |||||||
| chr8:143777540 | C | A | 148 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(145): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.789+5058C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143777540 | |||||||
| chr8:143777544 | C | A | 1 | a0023c0022t0001g0062 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.789+5062C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143777544 | |||||||
| chr8:143777548 | T | TA | 12 | a0001c0001t0002g0193 a0006c0006t0001g0033 a0008c0008t0001g0032 others(9): Show |
12 | HG01192.hp2 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.789+5075dupA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143777548 | ||||||
| chr8:143777718 | G | T | 121 | a0001c0001t0001g0169 a0002c0002t0001g0002 a0002c0002t0001g0003 others(118): Show |
124 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.789+5236G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143777718 | |||||||
| chr8:143777870 | T | C | 2 | a0006c0006t0001g0033 a0006c0006t0001g0034 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.789+5388T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143777870 | |||||||
| chr8:143778197 | AAC | A | 11 | a0001c0001t0001g0341 a0006c0006t0001g0033 a0006c0006t0001g0034 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+5717_789+5718d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143778197 | ||||||
| chr8:143778199 | CA | C | 329 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(326): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.789+5729delA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143778199 | ||||||
| chr8:143778349 | G | A | 7 | a0007c0007t0001g0015 a0007c0007t0001g0017 a0007c0007t0001g0045 others(4): Show |
7 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.789+5867G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143778349 | |||||||
| chr8:143778582 | C | T | 11 | a0001c0001t0001g0341 a0006c0006t0001g0033 a0006c0006t0001g0034 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+6100C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143778582 | |||||||
| chr8:143778627 | G | A | 50 | a0001c0001t0001g0054 a0001c0001t0001g0159 a0001c0001t0001g0160 others(47): Show |
50 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(47): Show |
intron_variant | MODIFIER | c.789+6145G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143778627 | |||||||
| chr8:143778707 | A | G | 146 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(143): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.789+6225A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143778707 | |||||||
| chr8:143778747 | ATTATC | A | 8 | a0005c0005t0001g0209 a0005c0005t0001g0210 a0005c0005t0001g0211 others(5): Show |
8 | HG00544.hp1 HG02027.hp1 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.789+6270_789+6274d others(7): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143778747 | ||||||
| chr8:143778827 | C | T | 25 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(22): Show |
25 | HG00733.hp2 HG01192.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.789+6345C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143778827 | |||||||
| chr8:143778843 | C | A | 11 | a0001c0001t0001g0341 a0006c0006t0001g0033 a0006c0006t0001g0034 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+6361C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143778843 | |||||||
| chr8:143778871 | C | A | 26 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(23): Show |
26 | HG00733.hp2 HG01192.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.789+6389C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143778871 | |||||||
| chr8:143778918 | C | T | 11 | a0001c0001t0001g0341 a0006c0006t0001g0033 a0006c0006t0001g0034 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+6436C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143778918 | |||||||
| chr8:143779114 | A | G | 1 | a0002c0002t0001g0008 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.789+6632A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143779114 | |||||||
| chr8:143779569 | CTCAT | C | 45 | a0001c0001t0001g0054 a0001c0001t0001g0159 a0001c0001t0001g0160 others(42): Show |
45 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(42): Show |
intron_variant | MODIFIER | c.789+7096_789+7099d others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143779569 | ||||||
| chr8:143779862 | C | T | 8 | a0001c0001t0001g0341 a0007c0007t0001g0015 a0007c0007t0001g0017 others(5): Show |
8 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.789+7380C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143779862 | |||||||
| chr8:143780023 | A | G | 1 | a0001c0001t0002g0056 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.789+7541A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143780023 | |||||||
| chr8:143780076 | A | G | 4 | a0001c0001t0001g0338 a0011c0012t0001g0339 a0011c0012t0001g0342 others(1): Show |
4 | HG01175.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.789+7594A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143780076 | |||||||
| chr8:143780217 | C | T | 1 | a0002c0002t0001g0263 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.789+7735C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143780217 | |||||||
| chr8:143780357 | G | A | 1 | a0024c0030t0001g0343 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.789+7875G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143780357 | |||||||
| chr8:143780395 | T | C | 25 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(22): Show |
25 | HG00733.hp2 HG01192.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.789+7913T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143780395 | |||||||
| chr8:143780426 | C | G | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0208 |
3 | NA18966.hp1 NA18998.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.789+7944C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143780426 | |||||||
| chr8:143780505 | C | G | 2 | a0003c0003t0001g0001 a0003c0003t0001g0229 |
3 | HG02895.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.789+8023C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143780505 | |||||||
| chr8:143780787 | A | G | 1 | a0003c0003t0001g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.790-8128A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143780787 | |||||||
| chr8:143780790 | C | G | 146 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(143): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.790-8125C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143780790 | |||||||
| chr8:143780946 | G | A | 1 | a0012c0017t0001g0198 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.790-7969G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143780946 | |||||||
| chr8:143781063 | A | G | 4 | a0001c0001t0001g0338 a0011c0012t0001g0339 a0011c0012t0001g0342 others(1): Show |
4 | HG01175.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.790-7852A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143781063 | |||||||
| chr8:143781171 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.790-7744G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143781171 | |||||||
| chr8:143781173 | G | A | 4 | a0001c0001t0001g0338 a0011c0012t0001g0339 a0011c0012t0001g0342 others(1): Show |
4 | HG01175.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.790-7742G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143781173 | |||||||
| chr8:143781193 | A | G | 22 | a0003c0003t0001g0001 a0003c0003t0001g0035 a0003c0003t0001g0036 others(19): Show |
23 | HG02258.hp1 HG02280.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.790-7722A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143781193 | |||||||
| chr8:143781280 | A | G | 4 | a0002c0002t0001g0253 a0002c0002t0001g0307 a0002c0002t0001g0308 others(1): Show |
4 | HG00438.hp1 NA18948.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.790-7635A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143781280 | |||||||
| chr8:143781358 | T | G | 341 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(338): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.790-7557T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143781358 | |||||||
| chr8:143781561 | C | A | 1 | a0002c0002t0001g0302 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.790-7354C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143781561 | |||||||
| chr8:143781697 | A | G | 1 | a0003c0003t0001g0035 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.790-7218A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143781697 | |||||||
| chr8:143781842 | T | A | 1 | a0002c0002t0001g0008 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.790-7073T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143781842 | |||||||
| chr8:143781873 | T | C | 4 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(1): Show |
4 | HG02970.hp2 HG03195.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.790-7042T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143781873 | |||||||
| chr8:143781945 | G | A | 341 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(338): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.790-6970G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143781945 | |||||||
| chr8:143782061 | T | C | 22 | a0003c0003t0001g0001 a0003c0003t0001g0035 a0003c0003t0001g0036 others(19): Show |
23 | HG02258.hp1 HG02280.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.790-6854T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143782061 | |||||||
| chr8:143782167 | T | A | 1 | a0001c0001t0001g0243 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.790-6748T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143782167 | |||||||
| chr8:143782316 | G | A | 1 | a0003c0003t0001g0035 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.790-6599G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143782316 | |||||||
| chr8:143782380 | C | T | 2 | a0003c0003t0001g0066 a0012c0017t0001g0067 |
2 | HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.790-6535C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143782380 | |||||||
| chr8:143782454 | GCTTA | G | 145 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(142): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.790-6457_790-6454d others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143782454 | ||||||
| chr8:143782665 | C | T | 1 | a0005c0005t0001g0326 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.790-6250C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143782665 | |||||||
| chr8:143782766 | G | A | 1 | a0002c0002t0001g0261 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.790-6149G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143782766 | |||||||
| chr8:143782971 | T | A | 11 | a0001c0001t0001g0341 a0006c0006t0001g0033 a0006c0006t0001g0034 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.790-5944T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143782971 | |||||||
| chr8:143782972 | A | G | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(2): Show |
5 | NA18942.hp2 NA18951.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.790-5943A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143782972 | |||||||
| chr8:143783134 | A | G | 8 | a0003c0003t0001g0048 a0003c0003t0001g0057 a0003c0003t0001g0197 others(5): Show |
8 | HG02922.hp2 HG02965.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.790-5781A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143783134 | |||||||
| chr8:143783161 | T | C | 2 | a0006c0006t0001g0033 a0006c0006t0001g0034 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.790-5754T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143783161 | |||||||
| chr8:143783171 | T | C | 1 | a0003c0003t0001g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.790-5744T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143783171 | |||||||
| chr8:143783304 | T | G | 4 | a0001c0001t0001g0338 a0011c0012t0001g0339 a0011c0012t0001g0342 others(1): Show |
4 | HG01175.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.790-5611T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143783304 | |||||||
| chr8:143783433 | CTGATT | C | 6 | a0007c0007t0001g0015 a0007c0007t0001g0017 a0007c0007t0001g0046 others(3): Show |
6 | HG02145.hp1 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.790-5480_790-5476d others(7): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143783433 | ||||||
| chr8:143783472 | A | G | 2 | a0001c0001t0001g0134 a0001c0001t0001g0142 |
2 | HG01123.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.790-5443A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143783472 | |||||||
| chr8:143783479 | A | G | 1 | a0007c0007t0001g0017 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.790-5436A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143783479 | |||||||
| chr8:143783524 | C | G | 3 | a0009c0009t0001g0010 a0009c0009t0001g0029 a0009c0009t0001g0030 |
3 | HG01192.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.790-5391C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143783524 | |||||||
| chr8:143783656 | A | G | 3 | a0008c0008t0001g0239 a0008c0008t0001g0240 a0008c0008t0001g0241 |
3 | HG02647.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.790-5259A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143783656 | |||||||
| chr8:143783802 | T | C | 1 | a0009c0009t0001g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.790-5113T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143783802 | |||||||
| chr8:143783839 | C | T | 1 | a0015c0016t0001g0238 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.790-5076C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143783839 | |||||||
| chr8:143783925 | T | A | 122 | a0001c0001t0001g0146 a0001c0001t0001g0169 a0002c0002t0001g0002 others(119): Show |
125 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.790-4990T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143783925 | |||||||
| chr8:143784005 | C | T | 26 | a0001c0010t0001g0040 a0001c0010t0001g0041 a0001c0010t0001g0042 others(23): Show |
26 | HG00733.hp2 HG01192.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.790-4910C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143784005 | |||||||
| chr8:143784202 | A | T | 2 | a0005c0005t0001g0326 a0005c0005t0001g0327 |
2 | HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.790-4713A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143784202 | |||||||
| chr8:143784295 | T | A | 16 | a0003c0003t0001g0001 a0003c0003t0001g0222 a0003c0003t0001g0225 others(13): Show |
17 | HG02258.hp1 HG02280.hp2 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.790-4620T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143784295 | |||||||
| chr8:143784613 | A | G | 8 | a0001c0001t0001g0341 a0007c0007t0001g0015 a0007c0007t0001g0017 others(5): Show |
8 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.790-4302A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143784613 | |||||||
| chr8:143784709 | A | C | 1 | a0012c0017t0001g0198 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.790-4206A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143784709 | |||||||
| chr8:143784748 | AACACTTC others(1): Show |
A | 122 | a0001c0001t0001g0146 a0001c0001t0001g0169 a0002c0002t0001g0002 others(119): Show |
125 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.790-4164_790-4157d others(10): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143784748 | ||||||
| chr8:143784948 | A | G | 3 | a0003c0003t0001g0235 a0003c0003t0001g0236 a0003c0003t0001g0242 |
3 | HG01975.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.790-3967A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143784948 | |||||||
| chr8:143785107 | CTCTT | C | 22 | a0003c0003t0001g0001 a0003c0003t0001g0035 a0003c0003t0001g0036 others(19): Show |
23 | HG02258.hp1 HG02280.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.790-3806_790-3803d others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143785107 | ||||||
| chr8:143785118 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.790-3797C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143785118 | |||||||
| chr8:143785253 | C | CT | 7 | a0003c0003t0001g0072 a0003c0003t0001g0237 a0006c0006t0001g0033 others(4): Show |
7 | HG01175.hp1 HG02257.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.790-3641dupT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143785253 | ||||||
| chr8:143785253 | CT | C | 146 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(143): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.790-3641delT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143785253 | ||||||
| chr8:143785253 | CTT | C | 124 | a0001c0001t0001g0130 a0001c0001t0001g0149 a0001c0001t0001g0169 others(121): Show |
127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.790-3642_790-3641d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143785253 | ||||||
| chr8:143785253 | CTTT | C | 7 | a0001c0001t0001g0108 a0002c0002t0001g0250 a0002c0002t0001g0275 others(4): Show |
7 | HG02040.hp1 NA18948.hp2 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.790-3643_790-3641d others(5): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143785253 | ||||||
| chr8:143785466 | G | C | 8 | a0001c0001t0001g0341 a0007c0007t0001g0015 a0007c0007t0001g0017 others(5): Show |
8 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.790-3449G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143785466 | |||||||
| chr8:143785513 | C | T | 1 | a0003c0003t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.790-3402C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143785513 | |||||||
| chr8:143785725 | A | AT | 152 | a0001c0001t0001g0005 a0001c0001t0001g0050 a0001c0001t0001g0051 others(149): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.790-3175dupT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143785725 | ||||||
| chr8:143785725 | AT | A | 36 | a0002c0002t0001g0004 a0002c0002t0001g0252 a0002c0002t0001g0253 others(33): Show |
38 | HG02258.hp1 HG02280.hp1 HG02280.hp2 others(35): Show |
intron_variant | MODIFIER | c.790-3175delT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143785725 | ||||||
| chr8:143785874 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.790-3041G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143785874 | |||||||
| chr8:143785985 | A | G | 4 | a0001c0001t0001g0085 a0001c0001t0001g0105 a0001c0001t0001g0106 others(1): Show |
4 | HG02040.hp2 HG02132.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.790-2930A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143785985 | |||||||
| chr8:143786115 | A | G | 342 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(339): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.790-2800A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143786115 | |||||||
| chr8:143786196 | A | G | 31 | a0001c0001t0001g0243 a0001c0010t0001g0040 a0001c0010t0001g0041 others(28): Show |
31 | HG00099.hp1 HG00733.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.790-2719A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143786196 | |||||||
| chr8:143786266 | C | T | 2 | a0004c0004t0001g0053 a0004c0004t0001g0161 |
2 | HG01074.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.790-2649C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143786266 | |||||||
| chr8:143786411 | C | T | 2 | a0003c0003t0001g0066 a0012c0017t0001g0067 |
2 | HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.790-2504C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143786411 | |||||||
| chr8:143786451 | A | C | 1 | a0027c0021t0001g0335 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.790-2464A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143786451 | |||||||
| chr8:143786456 | T | G | 1 | a0028c0032t0001g0028 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.790-2459T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143786456 | |||||||
| chr8:143786577 | G | A | 2 | a0002c0002t0001g0268 a0002c0002t0001g0290 |
2 | HG01346.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.790-2338G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143786577 | |||||||
| chr8:143786594 | C | A | 2 | a0009c0009t0001g0014 a0009c0009t0001g0027 |
2 | HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.790-2321C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143786594 | |||||||
| chr8:143786798 | T | G | 1 | a0002c0002t0001g0250 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.790-2117T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143786798 | |||||||
| chr8:143786812 | T | G | 31 | a0001c0001t0001g0244 a0003c0003t0001g0001 a0003c0003t0001g0012 others(28): Show |
32 | HG02055.hp1 HG02280.hp2 HG02300.hp2 others(29): Show |
intron_variant | MODIFIER | c.790-2103T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143786812 | |||||||
| chr8:143786816 | G | A | 1 | a0027c0021t0001g0335 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.790-2099G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143786816 | |||||||
| chr8:143786827 | C | T | 77 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0073 others(74): Show |
78 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.790-2088C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143786827 | |||||||
| chr8:143786838 | T | C | 205 | a0001c0001t0001g0005 a0001c0001t0001g0050 a0001c0001t0001g0054 others(202): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.790-2077T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143786838 | |||||||
| chr8:143786970 | G | A | 15 | a0001c0001t0001g0244 a0003c0003t0001g0072 a0005c0005t0001g0283 others(12): Show |
15 | HG01109.hp1 HG01175.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.790-1945G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143786970 | |||||||
| chr8:143787114 | G | GGGTTTGT others(6): Show |
1 | a0002c0002t0001g0320 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.790-1800_790-1788d others(15): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143787114 | ||||||
| chr8:143787141 | C | T | 26 | a0001c0001t0001g0243 a0003c0003t0001g0035 a0003c0003t0001g0036 others(23): Show |
26 | HG01192.hp2 HG01884.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.790-1774C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143787141 | |||||||
| chr8:143787177 | GGGTC | G | 201 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(198): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.790-1733_790-1730d others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143787177 | ||||||
| chr8:143787372 | G | A | 5 | a0007c0007t0001g0045 a0007c0007t0001g0046 a0007c0007t0001g0047 others(2): Show |
5 | HG02145.hp1 HG02258.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.790-1543G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143787372 | |||||||
| chr8:143787381 | T | C | 3 | a0001c0001t0001g0080 a0002c0002t0001g0265 a0002c0002t0001g0273 |
3 | HG00609.hp1 NA18952.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.790-1534T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143787381 | |||||||
| chr8:143787488 | G | T | 1 | a0002c0002t0001g0250 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.790-1427G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143787488 | |||||||
| chr8:143787627 | G | C | 5 | a0011c0012t0001g0339 a0011c0012t0001g0342 a0011c0012t0001g0344 others(2): Show |
5 | HG01109.hp1 HG01175.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.790-1288G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143787627 | |||||||
| chr8:143787665 | G | A | 2 | a0003c0003t0001g0012 a0003c0003t0001g0013 |
2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.790-1250G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143787665 | |||||||
| chr8:143787692 | C | G | 1 | a0001c0001t0001g0080 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.790-1223C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143787692 | |||||||
| chr8:143787827 | C | T | 1 | a0011c0012t0001g0339 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.790-1088C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143787827 | |||||||
| chr8:143787846 | G | A | 2 | a0012c0017t0001g0067 a0012c0017t0001g0198 |
2 | NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.790-1069G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143787846 | |||||||
| chr8:143787872 | C | T | 331 | a0001c0001t0001g0005 a0001c0001t0001g0050 a0001c0001t0001g0051 others(328): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.790-1043C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143787872 | |||||||
| chr8:143787940 | A | G | 329 | a0001c0001t0001g0005 a0001c0001t0001g0050 a0001c0001t0001g0051 others(326): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.790-975A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143787940 | |||||||
| chr8:143788008 | C | T | 1 | a0004c0004t0001g0177 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.790-907C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143788008 | |||||||
| chr8:143788365 | C | T | 169 | a0001c0001t0001g0058 a0001c0001t0001g0064 a0001c0001t0001g0069 others(166): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.790-550C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143788365 | |||||||
| chr8:143788374 | T | C | 3 | a0006c0006t0001g0033 a0006c0006t0001g0034 a0012c0017t0001g0067 |
3 | HG02257.hp2 HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.790-541T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143788374 | |||||||
| chr8:143788483 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.790-432T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143788483 | |||||||
| chr8:143788516 | G | A | 1 | a0003c0003t0001g0031 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.790-399G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143788516 | |||||||
| chr8:143788531 | G | A | 48 | a0004c0004t0001g0053 a0004c0004t0001g0086 a0004c0004t0001g0087 others(45): Show |
48 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.790-384G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143788531 | |||||||
| chr8:143788577 | C | T | 1 | a0001c0001t0001g0341 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.790-338C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143788577 | |||||||
| chr8:143788636 | G | T | 1 | a0001c0001t0001g0341 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.790-279G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143788636 | |||||||
| chr8:143789080 | A | AGGTGCTG others(6): Show |
1 | a0002c0002t0001g0271 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.938+27_938+39dupGA others(11): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr8 | 143789080 | ||||||
| chr8:143789134 | G | T | 1 | a0012c0017t0001g0067 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.939-55G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 8/13 | chr8 | 143789134 | |||||||
| chr8:143789147 | C | T | 1 | a0003c0003t0001g0039 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.939-42C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 8/13 | chr8 | 143789147 | |||||||
| chr8:143789148 | G | A | 10 | a0001c0001t0001g0049 a0001c0001t0001g0068 a0001c0001t0001g0149 others(7): Show |
10 | HG00733.hp2 HG01884.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.939-41G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 8/13 | chr8 | 143789148 | |||||||
| chr8:143789891 | G | A | 1 | a0003c0003t0001g0038 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1195+22G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 11/13 | chr8 | 143789891 | |||||||
| chr8:143789924 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1196-47G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 11/13 | chr8 | 143789924 | |||||||
| chr8:143789936 | G | T | 1 | a0001c0001t0001g0094 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1196-35G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 11/13 | chr8 | 143789936 |