Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84164 |
| ensemblid | ENSG00000100325.15 |
| hgncid | 24103 |
| symbol | ASCC2 |
| name | activating signal cointegrator 1 complex subunit 2 |
| refseq_nuc | NM_032204.5 |
| refseq_prot | NP_115580.2 |
| ensembl_nuc | ENST00000307790.8 |
| ensembl_prot | ENSP00000305502.3 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 29788611 |
| end | 29838274 |
| strand | - |
| ver | v1.2 |
| region | chr22:29788611-29838274 |
| region5000 | chr22:29783611-29843274 |
| regionname0 | ASCC2_chr22_29788611_29838274 |
| regionname5000 | ASCC2_chr22_29783611_29843274 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 757 | 219 | 62 | 56 | 71 | 9 | 19 | 51 | ASCC2_chr22_29783611_29843274 | ASCC2 | MPALP others(752): Show |
chr22 | 29783611 | 29843274 |
| a0002 | 0/0 | 757 | 62 | 4 | 0 | 52 | 1 | 5 | 36 | ASCC2_chr22_29783611_29843274 | ASCC2 | MPALP others(752): Show |
chr22 | 29783611 | 29843274 |
| a0003 | 0/0 | 757 | 45 | 6 | 9 | 22 | 1 | 7 | 18 | ASCC2_chr22_29783611_29843274 | ASCC2 | MPALP others(752): Show |
chr22 | 29783611 | 29843274 |
| a0004 | 0/0 | 757 | 18 | 0 | 3 | 12 | 0 | 3 | 9 | ASCC2_chr22_29783611_29843274 | ASCC2 | MPALP others(752): Show |
chr22 | 29783611 | 29843274 |
| a0005 | 0/0 | 757 | 9 | 2 | 5 | 1 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | MPALP others(752): Show |
chr22 | 29783611 | 29843274 |
| a0006 | 0/0 | 757 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | MPALP others(752): Show |
chr22 | 29783611 | 29843274 |
| a0007 | 0/0 | 757 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | MPALP others(752): Show |
chr22 | 29783611 | 29843274 |
| a0008 | 0/0 | 757 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | MPALP others(752): Show |
chr22 | 29783611 | 29843274 |
| a0009 | 0/0 | 757 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | MPALP others(752): Show |
chr22 | 29783611 | 29843274 |
| a0010 | 0/0 | 757 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | MPALP others(752): Show |
chr22 | 29783611 | 29843274 |
| a0011 | 0/0 | 757 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | MPALP others(752): Show |
chr22 | 29783611 | 29843274 |
| a0012 | 0/0 | 757 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | MPALP others(752): Show |
chr22 | 29783611 | 29843274 |
| a0013 | 0/0 | 757 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | MPALP others(752): Show |
chr22 | 29783611 | 29843274 |
| a0014 | 0/0 | 757 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | MPALP others(752): Show |
chr22 | 29783611 | 29843274 |
| a0015 | 0/0 | 757 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | MPALP others(752): Show |
chr22 | 29783611 | 29843274 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2271 | 216 | 62 | 55 | 70 | 9 | 18 | ASCC2_chr22_29783611_29843274 | ASCC2 | ATGCC others(2266): Show |
chr22 | 29783611 | 29843274 | ||
| a0001c0011 | 0/0 | 2271 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | ATGCC others(2266): Show |
chr22 | 29783611 | 29843274 | ||
| a0001c0013 | 0/0 | 2271 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | ATGCC others(2266): Show |
chr22 | 29783611 | 29843274 | ||
| a0001c0015 | 0/0 | 2271 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | ATGCC others(2266): Show |
chr22 | 29783611 | 29843274 | ||
| a0002c0002 | 0/0 | 2271 | 61 | 4 | 0 | 52 | 0 | 5 | ASCC2_chr22_29783611_29843274 | ASCC2 | ATGCC others(2266): Show |
chr22 | 29783611 | 29843274 | ||
| a0002c0019 | 0/0 | 2271 | 1 | 0 | 0 | 0 | 1 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | ATGCC others(2266): Show |
chr22 | 29783611 | 29843274 | ||
| a0003c0003 | 0/0 | 2271 | 45 | 6 | 9 | 22 | 1 | 7 | ASCC2_chr22_29783611_29843274 | ASCC2 | ATGCC others(2266): Show |
chr22 | 29783611 | 29843274 | ||
| a0004c0004 | 0/0 | 2271 | 18 | 0 | 3 | 12 | 0 | 3 | ASCC2_chr22_29783611_29843274 | ASCC2 | ATGCC others(2266): Show |
chr22 | 29783611 | 29843274 | ||
| a0005c0005 | 0/0 | 2271 | 9 | 2 | 5 | 1 | 1 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | ATGCC others(2266): Show |
chr22 | 29783611 | 29843274 | ||
| a0006c0006 | 0/0 | 2271 | 4 | 3 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | ATGCC others(2266): Show |
chr22 | 29783611 | 29843274 | ||
| a0007c0007 | 0/0 | 2271 | 4 | 4 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | ATGCC others(2266): Show |
chr22 | 29783611 | 29843274 | ||
| a0008c0008 | 0/0 | 2271 | 3 | 3 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | ATGCC others(2266): Show |
chr22 | 29783611 | 29843274 | ||
| a0009c0009 | 0/0 | 2271 | 2 | 2 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | ATGCC others(2266): Show |
chr22 | 29783611 | 29843274 | ||
| a0010c0017 | 0/0 | 2271 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | ATGCC others(2266): Show |
chr22 | 29783611 | 29843274 | ||
| a0011c0012 | 0/0 | 2271 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | ATGCC others(2266): Show |
chr22 | 29783611 | 29843274 | ||
| a0012c0010 | 0/0 | 2271 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | ATGCC others(2266): Show |
chr22 | 29783611 | 29843274 | ||
| a0013c0018 | 0/0 | 2271 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | ATGCC others(2266): Show |
chr22 | 29783611 | 29843274 | ||
| a0014c0016 | 0/0 | 2271 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | ATGCC others(2266): Show |
chr22 | 29783611 | 29843274 | ||
| a0015c0014 | 0/0 | 2271 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | ATGCC others(2266): Show |
chr22 | 29783611 | 29843274 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2790 | 95 | 17 | 27 | 31 | 4 | 14 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2785): Show |
chr22 | 29783611 | 29843274 |
| a0001c0001t0002 | 0/0 | 2787 | 15 | 12 | 3 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2782): Show |
chr22 | 29783611 | 29843274 |
| a0001c0001t0003 | 0/0 | 2796 | 61 | 2 | 19 | 31 | 5 | 4 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2791): Show |
chr22 | 29783611 | 29843274 |
| a0001c0001t0004 | 0/0 | 2796 | 20 | 18 | 2 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2791): Show |
chr22 | 29783611 | 29843274 |
| a0001c0001t0005 | 0/0 | 2805 | 6 | 2 | 1 | 3 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2800): Show |
chr22 | 29783611 | 29843274 |
| a0001c0001t0006 | 0/0 | 2793 | 7 | 1 | 2 | 4 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2788): Show |
chr22 | 29783611 | 29843274 |
| a0001c0001t0007 | 0/0 | 2799 | 6 | 6 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2794): Show |
chr22 | 29783611 | 29843274 |
| a0001c0001t0009 | 0/0 | 2799 | 2 | 0 | 1 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2794): Show |
chr22 | 29783611 | 29843274 |
| a0001c0001t0011 | 0/0 | 2793 | 2 | 2 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2788): Show |
chr22 | 29783611 | 29843274 |
| a0001c0001t0012 | 0/0 | 2790 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2785): Show |
chr22 | 29783611 | 29843274 |
| a0001c0001t0014 | 0/0 | 2793 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2788): Show |
chr22 | 29783611 | 29843274 |
| a0001c0011t0009 | 0/0 | 2799 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2794): Show |
chr22 | 29783611 | 29843274 |
| a0001c0013t0001 | 0/0 | 2790 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2785): Show |
chr22 | 29783611 | 29843274 |
| a0001c0015t0001 | 0/0 | 2790 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2785): Show |
chr22 | 29783611 | 29843274 |
| a0002c0002t0002 | 0/0 | 2787 | 58 | 4 | 0 | 51 | 0 | 3 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2782): Show |
chr22 | 29783611 | 29843274 |
| a0002c0002t0003 | 0/0 | 2796 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2791): Show |
chr22 | 29783611 | 29843274 |
| a0002c0002t0010 | 0/0 | 2787 | 2 | 0 | 0 | 0 | 0 | 2 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2782): Show |
chr22 | 29783611 | 29843274 |
| a0002c0019t0002 | 0/0 | 2787 | 1 | 0 | 0 | 0 | 1 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2782): Show |
chr22 | 29783611 | 29843274 |
| a0003c0003t0001 | 0/0 | 2790 | 45 | 6 | 9 | 22 | 1 | 7 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2785): Show |
chr22 | 29783611 | 29843274 |
| a0004c0004t0001 | 0/0 | 2790 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2785): Show |
chr22 | 29783611 | 29843274 |
| a0004c0004t0004 | 0/0 | 2796 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2791): Show |
chr22 | 29783611 | 29843274 |
| a0004c0004t0005 | 0/0 | 2805 | 12 | 0 | 2 | 9 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2800): Show |
chr22 | 29783611 | 29843274 |
| a0004c0004t0008 | 0/0 | 2802 | 3 | 0 | 0 | 2 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2797): Show |
chr22 | 29783611 | 29843274 |
| a0004c0004t0013 | 0/0 | 2808 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2803): Show |
chr22 | 29783611 | 29843274 |
| a0005c0005t0002 | 0/0 | 2787 | 9 | 2 | 5 | 1 | 1 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2782): Show |
chr22 | 29783611 | 29843274 |
| a0006c0006t0002 | 0/0 | 2787 | 4 | 3 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2782): Show |
chr22 | 29783611 | 29843274 |
| a0007c0007t0004 | 0/0 | 2796 | 4 | 4 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2791): Show |
chr22 | 29783611 | 29843274 |
| a0008c0008t0001 | 0/0 | 2790 | 3 | 3 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2785): Show |
chr22 | 29783611 | 29843274 |
| a0009c0009t0002 | 0/0 | 2787 | 2 | 2 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2782): Show |
chr22 | 29783611 | 29843274 |
| a0010c0017t0001 | 0/0 | 2790 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2785): Show |
chr22 | 29783611 | 29843274 |
| a0011c0012t0003 | 0/0 | 2796 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2791): Show |
chr22 | 29783611 | 29843274 |
| a0012c0010t0002 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2782): Show |
chr22 | 29783611 | 29843274 |
| a0013c0018t0001 | 0/0 | 2790 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2785): Show |
chr22 | 29783611 | 29843274 |
| a0014c0016t0001 | 0/0 | 2790 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2785): Show |
chr22 | 29783611 | 29843274 |
| a0015c0014t0001 | 0/0 | 2790 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | AGTTT others(2785): Show |
chr22 | 29783611 | 29843274 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0196 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0199 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0002g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0001 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0004g0002 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0004g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0005g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0006g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0006g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0006g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0006g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0006g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0006g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0006g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0007g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0007g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0009g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0009g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0011g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0011g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0012g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0001t0014g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0011t0009g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0013t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0001c0015t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0010 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0010g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0002t0010g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0002c0019t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0003c0003t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0004c0004t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0004c0004t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0004c0004t0005g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0004c0004t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0004c0004t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0004c0004t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0004c0004t0005g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0004c0004t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0004c0004t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0004c0004t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0004c0004t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0004c0004t0005g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0004c0004t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0004c0004t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0004c0004t0008g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0004c0004t0008g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0004c0004t0008g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0004c0004t0013g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0005c0005t0002g0005 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0005c0005t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0005c0005t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0005c0005t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0005c0005t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0005c0005t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0005c0005t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0006c0006t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0006c0006t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0006c0006t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0006c0006t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0007c0007t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0007c0007t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0007c0007t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0007c0007t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0008c0008t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0008c0008t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0008c0008t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0009c0009t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0009c0009t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0010c0017t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0011c0012t0003g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0012c0010t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0013c0018t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0014c0016t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| a0015c0014t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0303 | EUR | GBR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00099 | hp2 | a0005 | c0005 | t0002 | g0005 | EUR | GBR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00280 | hp1 | a0002 | c0019 | t0002 | g0072 | EUR | FIN | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00280 | hp2 | a0003 | c0003 | t0001 | g0150 | EUR | FIN | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0232 | EUR | FIN | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0320 | EUR | FIN | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0309 | EAS | CHS | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | CHS | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00423 | hp1 | a0004 | c0004 | t0005 | g0063 | EAS | CHS | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0091 | EAS | CHS | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0308 | EAS | CHS | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | CHS | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0338 | EAS | CHS | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0068 | EAS | CHS | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | CHS | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00597 | hp2 | a0003 | c0003 | t0001 | g0163 | EAS | CHS | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0082 | EAS | CHS | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0066 | EAS | CHS | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0104 | EAS | CHS | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00639 | hp1 | a0010 | c0017 | t0001 | g0221 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00639 | hp2 | a0011 | c0012 | t0003 | g0346 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0323 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0094 | EAS | CHS | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0296 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0317 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0301 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0300 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01069 | hp1 | a0005 | c0005 | t0002 | g0113 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0305 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0050 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0299 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0324 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01081 | hp2 | a0001 | c0001 | t0009 | g0347 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0307 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01106 | hp1 | a0003 | c0003 | t0001 | g0177 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0318 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01167 | hp2 | a0005 | c0005 | t0002 | g0115 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01169 | hp2 | a0005 | c0005 | t0002 | g0114 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01175 | hp2 | a0001 | c0001 | t0006 | g0294 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0344 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0020 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01243 | hp2 | a0006 | c0006 | t0002 | g0119 | AMR | PUR | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | CLM | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0326 | AMR | CLM | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | CLM | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0321 | AMR | CLM | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01346 | hp2 | a0005 | c0005 | t0002 | g0005 | AMR | CLM | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01358 | hp1 | a0003 | c0003 | t0001 | g0151 | AMR | CLM | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01361 | hp1 | a0001 | c0001 | t0006 | g0293 | AMR | CLM | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0312 | AMR | CLM | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | CLM | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0295 | EUR | IBS | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0310 | EUR | IBS | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0245 | EUR | IBS | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | ACB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0042 | AFR | ACB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01891 | hp2 | a0012 | c0010 | t0002 | g0125 | AFR | ACB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01934 | hp1 | a0004 | c0004 | t0005 | g0062 | AMR | PEL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01934 | hp2 | a0003 | c0003 | t0001 | g0176 | AMR | PEL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01943 | hp1 | a0001 | c0015 | t0001 | g0220 | AMR | PEL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01943 | hp2 | a0003 | c0003 | t0001 | g0143 | AMR | PEL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01978 | hp1 | a0004 | c0004 | t0005 | g0056 | AMR | PEL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01981 | hp1 | a0004 | c0004 | t0004 | g0034 | AMR | PEL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01993 | hp1 | a0003 | c0003 | t0001 | g0171 | AMR | PEL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01993 | hp2 | a0005 | c0005 | t0002 | g0005 | AMR | PEL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0335 | EAS | KHV | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0109 | EAS | KHV | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0343 | EAS | KHV | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02040 | hp1 | a0004 | c0004 | t0013 | g0065 | EAS | KHV | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | KHV | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | ACB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0033 | AFR | ACB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02056 | hp1 | a0005 | c0005 | t0002 | g0116 | EAS | KHV | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02056 | hp2 | a0003 | c0003 | t0001 | g0147 | EAS | KHV | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0093 | EAS | KHV | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | KHV | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02080 | hp2 | a0001 | c0001 | t0005 | g0061 | EAS | KHV | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0330 | EAS | KHV | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0337 | EAS | KHV | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0069 | EAS | KHV | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02132 | hp1 | a0004 | c0004 | t0005 | g0059 | EAS | KHV | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0333 | EAS | KHV | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02145 | hp1 | a0001 | c0001 | t0014 | g0285 | AFR | ACB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0051 | AFR | ACB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02155 | hp1 | a0003 | c0003 | t0001 | g0144 | EAS | CDX | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0098 | EAS | CDX | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | CDX | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | CDX | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0297 | AFR | ACB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0043 | AFR | ACB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | ACB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02273 | hp2 | a0003 | c0003 | t0001 | g0162 | AMR | PEL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0041 | AFR | ACB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02280 | hp2 | a0006 | c0006 | t0002 | g0117 | AFR | ACB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02293 | hp2 | a0003 | c0003 | t0001 | g0169 | AMR | PEL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02300 | hp2 | a0003 | c0003 | t0001 | g0165 | AMR | PEL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | ACB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02451 | hp2 | a0002 | c0002 | t0002 | g0106 | AFR | ACB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | KHV | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02523 | hp2 | a0003 | c0003 | t0001 | g0149 | EAS | KHV | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02602 | hp1 | a0013 | c0018 | t0001 | g0226 | SAS | PJL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0311 | SAS | PJL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02615 | hp1 | a0007 | c0007 | t0004 | g0035 | AFR | GWD | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | GWD | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02622 | hp2 | a0005 | c0005 | t0002 | g0121 | AFR | GWD | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02683 | hp1 | a0004 | c0004 | t0008 | g0044 | SAS | PJL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0107 | SAS | PJL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02735 | hp2 | a0004 | c0004 | t0005 | g0047 | SAS | PJL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0314 | SAS | PJL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0071 | AFR | GWD | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02886 | hp1 | a0014 | c0016 | t0001 | g0231 | AFR | GWD | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0032 | AFR | GWD | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02895 | hp1 | a0007 | c0007 | t0004 | g0037 | AFR | GWD | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02895 | hp2 | a0008 | c0008 | t0001 | g0139 | AFR | GWD | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | GWD | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02896 | hp2 | a0003 | c0003 | t0001 | g0145 | AFR | GWD | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02897 | hp1 | a0008 | c0008 | t0001 | g0142 | AFR | GWD | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | GWD | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ESN | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | ESN | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02965 | hp2 | a0007 | c0007 | t0004 | g0018 | AFR | ESN | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02970 | hp1 | a0003 | c0003 | t0001 | g0182 | AFR | ESN | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | ESN | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02976 | hp1 | a0006 | c0006 | t0002 | g0120 | AFR | ESN | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02976 | hp2 | a0008 | c0008 | t0001 | g0141 | AFR | ESN | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03017 | hp1 | a0003 | c0003 | t0001 | g0156 | SAS | PJL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03017 | hp2 | a0004 | c0004 | t0001 | g0278 | SAS | PJL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0038 | AFR | ESN | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | ESN | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | ESN | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03139 | hp2 | a0009 | c0009 | t0002 | g0123 | AFR | ESN | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ESN | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | ESN | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0288 | AFR | MSL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03239 | hp1 | a0003 | c0003 | t0001 | g0179 | SAS | PJL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03453 | hp1 | a0007 | c0007 | t0004 | g0036 | AFR | MSL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | MSL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0040 | AFR | MSL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03486 | hp2 | a0003 | c0003 | t0001 | g0184 | AFR | MSL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03516 | hp1 | a0006 | c0006 | t0002 | g0118 | AFR | ESN | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0049 | AFR | ESN | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | GWD | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03579 | hp1 | a0001 | c0001 | t0012 | g0017 | AFR | MSL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | MSL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03654 | hp1 | a0003 | c0003 | t0001 | g0160 | SAS | PJL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03669 | hp1 | a0015 | c0014 | t0001 | g0273 | SAS | PJL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03669 | hp2 | a0003 | c0003 | t0001 | g0161 | SAS | PJL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03831 | hp1 | a0002 | c0002 | t0010 | g0111 | SAS | BEB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | BEB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | BEB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03834 | hp2 | a0003 | c0003 | t0001 | g0157 | SAS | BEB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03927 | hp1 | a0003 | c0003 | t0001 | g0180 | SAS | BEB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | BEB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | BEB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03942 | hp2 | a0002 | c0002 | t0010 | g0102 | SAS | BEB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | STU | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0298 | SAS | STU | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | STU | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | STU | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0088 | SAS | STU | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG04204 | hp2 | a0003 | c0003 | t0001 | g0166 | SAS | STU | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0090 | SAS | STU | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0313 | SAS | STU | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | YRI | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | YRI | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18942 | hp1 | a0004 | c0004 | t0005 | g0057 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0339 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18943 | hp2 | a0001 | c0001 | t0006 | g0291 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18945 | hp2 | a0001 | c0001 | t0005 | g0052 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18946 | hp1 | a0004 | c0004 | t0005 | g0060 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18948 | hp2 | a0001 | c0001 | t0005 | g0048 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18949 | hp2 | a0003 | c0003 | t0001 | g0175 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18952 | hp1 | a0001 | c0001 | t0006 | g0289 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0334 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18956 | hp2 | a0004 | c0004 | t0005 | g0054 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18957 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18957 | hp2 | a0003 | c0003 | t0001 | g0146 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18959 | hp1 | a0003 | c0003 | t0001 | g0174 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18962 | hp1 | a0003 | c0003 | t0001 | g0153 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0327 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18967 | hp1 | a0001 | c0001 | t0006 | g0292 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0302 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18969 | hp1 | a0001 | c0001 | t0009 | g0348 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18969 | hp2 | a0003 | c0003 | t0001 | g0181 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18971 | hp1 | a0003 | c0003 | t0001 | g0158 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0342 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18974 | hp2 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0092 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0332 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18980 | hp1 | a0003 | c0003 | t0001 | g0155 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18982 | hp2 | a0003 | c0003 | t0001 | g0140 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18984 | hp2 | a0001 | c0001 | t0006 | g0290 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18985 | hp2 | a0004 | c0004 | t0005 | g0064 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18989 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18992 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18993 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18994 | hp2 | a0003 | c0003 | t0001 | g0183 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18998 | hp1 | a0003 | c0003 | t0001 | g0173 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18999 | hp1 | a0003 | c0003 | t0001 | g0167 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0345 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19005 | hp1 | a0004 | c0004 | t0005 | g0055 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0331 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19009 | hp1 | a0004 | c0004 | t0005 | g0058 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0341 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19012 | hp1 | a0003 | c0003 | t0001 | g0178 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | LWK | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | LWK | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19043 | hp1 | a0003 | c0003 | t0001 | g0164 | AFR | LWK | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | LWK | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0336 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19054 | hp2 | a0004 | c0004 | t0005 | g0053 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19055 | hp2 | a0003 | c0003 | t0001 | g0159 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0340 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19060 | hp2 | a0003 | c0003 | t0001 | g0154 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0304 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0329 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19067 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19067 | hp2 | a0003 | c0003 | t0001 | g0185 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0328 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19075 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19075 | hp2 | a0003 | c0003 | t0001 | g0172 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19077 | hp1 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19077 | hp2 | a0003 | c0003 | t0001 | g0168 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19084 | hp2 | a0004 | c0004 | t0008 | g0046 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19085 | hp1 | a0001 | c0011 | t0009 | g0349 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19086 | hp1 | a0003 | c0003 | t0001 | g0152 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19086 | hp2 | a0004 | c0004 | t0008 | g0045 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0319 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19091 | hp2 | a0002 | c0002 | t0003 | g0325 | EAS | JPT | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | YRI | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | YRI | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA20129 | hp1 | a0005 | c0005 | t0002 | g0122 | AFR | ASW | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0067 | AFR | ASW | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | TSI | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0306 | EUR | TSI | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA20905 | hp1 | a0001 | c0013 | t0001 | g0274 | SAS | GIH | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | GIH | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01123 | hp1 | a0003 | c0003 | t0001 | g0186 | AMR | CLM | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | ACB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02109 | hp2 | a0003 | c0003 | t0001 | g0170 | AFR | ACB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0322 | AFR | ACB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02486 | hp2 | a0003 | c0003 | t0001 | g0148 | AFR | ACB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | ACB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG02559 | hp2 | a0001 | c0001 | t0011 | g0287 | AFR | ACB | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | MSL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG06807 | hp1 | a0001 | c0001 | t0011 | g0286 | AFR | USA | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0039 | AFR | USA | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0021 | AFR | USA | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | USA | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0010 | AFR | LWK | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| NA21309 | hp2 | a0009 | c0009 | t0002 | g0124 | AFR | LWK | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0199 | REF | REF | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0196 | REF | REF | ASCC2_chr22_29783611_29843274 | ASCC2 | chr22 | 29783611 | 29843274 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:29793603 | C | T | 1 | a0007 | 4 | HG02615.hp1 HG02895.hp1 HG02965.hp2 others(1): Show |
missense_variant | MODERATE | c.1762G>A | p.Glu588Lys | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 16/20 | 1876/2790 | 1762/2274 | 588/757 | chr22 | 29793603 | |||
| chr22:29793653 | C | T | 1 | a0004 | 18 | HG00423.hp1 HG01934.hp1 HG01978.hp1 others(15): Show |
missense_variant | MODERATE | c.1712G>A | p.Arg571Gln | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 16/20 | 1826/2790 | 1712/2274 | 571/757 | chr22 | 29793653 | |||
| chr22:29802003 | T | C | 1 | a0015 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.1559A>G | p.Asn520Ser | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 14/20 | 1673/2790 | 1559/2274 | 520/757 | chr22 | 29802003 | |||
| chr22:29802036 | C | T | 2 | a0003 a0008 |
48 | HG00280.hp2 HG00597.hp2 HG01106.hp1 others(45): Show |
missense_variant | MODERATE | c.1526G>A | p.Arg509Gln | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 14/20 | 1640/2790 | 1526/2274 | 509/757 | chr22 | 29802036 | |||
| chr22:29804654 | T | A | 1 | a0011 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.1337A>T | p.Asn446Ile | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/20 | 1451/2790 | 1337/2274 | 446/757 | chr22 | 29804654 | |||
| chr22:29804724 | G | A | 1 | a0005 | 9 | HG00099.hp2 HG01069.hp1 HG01167.hp2 others(6): Show |
missense_variant | MODERATE | c.1267C>T | p.Pro423Ser | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/20 | 1381/2790 | 1267/2274 | 423/757 | chr22 | 29804724 | |||
| chr22:29804772 | C | G | 3 | a0005 a0006 a0009 |
15 | HG00099.hp2 HG01069.hp1 HG01167.hp2 others(12): Show |
missense_variant | MODERATE | c.1219G>C | p.Asp407His | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/20 | 1333/2790 | 1219/2274 | 407/757 | chr22 | 29804772 | |||
| chr22:29813445 | T | C | 1 | a0014 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.818A>G | p.His273Arg | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/20 | 932/2790 | 818/2274 | 273/757 | chr22 | 29813445 | |||
| chr22:29813500 | T | C | 1 | a0010 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.763A>G | p.Thr255Ala | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/20 | 877/2790 | 763/2274 | 255/757 | chr22 | 29813500 | |||
| chr22:29825131 | C | T | 2 | a0005 a0006 |
13 | HG00099.hp2 HG01069.hp1 HG01167.hp2 others(10): Show |
missense_variant | MODERATE | c.367G>A | p.Val123Ile | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/20 | 481/2790 | 367/2274 | 123/757 | chr22 | 29825131 | |||
| chr22:29825155 | T | C | 1 | a0013 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.343A>G | p.Met115Val | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/20 | 457/2790 | 343/2274 | 115/757 | chr22 | 29825155 | |||
| chr22:29825188 | C | T | 1 | a0012 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.310G>A | p.Glu104Lys | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/20 | 424/2790 | 310/2274 | 104/757 | chr22 | 29825188 | |||
| chr22:29825212 | G | A | 1 | a0002 | 62 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(59): Show |
missense_variant | MODERATE | c.286C>T | p.Arg96Cys | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/20 | 400/2790 | 286/2274 | 96/757 | chr22 | 29825212 | |||
| chr22:29832279 | G | A | 1 | a0008 | 3 | HG02895.hp2 HG02897.hp1 HG02976.hp2 |
missense_variant | MODERATE | c.47C>T | p.Pro16Leu | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/20 | 161/2790 | 47/2274 | 16/757 | chr22 | 29832279 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:29802116 | A | G | 1 | a0001c0011 | 1 | NA19085.hp1 | synonymous_variant | LOW | c.1446T>C | p.Leu482Leu | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 14/20 | 1560/2790 | 1446/2274 | 482/757 | chr22 | 29802116 | |||
| chr22:29802194 | G | A | 1 | a0002c0019 | 1 | HG00280.hp1 | synonymous_variant | LOW | c.1368C>T | p.Ala456Ala | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 14/20 | 1482/2790 | 1368/2274 | 456/757 | chr22 | 29802194 | |||
| chr22:29804812 | G | C | 2 | a0001c0013 a0015c0014 |
2 | HG03669.hp1 NA20905.hp1 |
synonymous_variant | LOW | c.1179C>G | p.Ala393Ala | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/20 | 1293/2790 | 1179/2274 | 393/757 | chr22 | 29804812 | |||
| chr22:29804827 | G | A | 1 | a0001c0015 | 1 | HG01943.hp1 | synonymous_variant | LOW | c.1164C>T | p.Asp388Asp | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/20 | 1278/2790 | 1164/2274 | 388/757 | chr22 | 29804827 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:29788627 | A | T | 1 | a0002c0002t0010 | 2 | HG03831.hp1 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*386T>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 20/20 | 386 | chr22 | 29788627 | ||||||
| chr22:29788656 | G | C | 1 | a0001c0001t0014 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*357C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 20/20 | 357 | chr22 | 29788656 | ||||||
| chr22:29788961 | A | G | 24 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(21): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*52T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 20/20 | 52 | chr22 | 29788961 | ||||||
| chr22:29838203 | T | TGCC | 3 | a0001c0001t0006 a0001c0001t0011 a0001c0001t0014 |
10 | HG01175.hp2 HG01361.hp1 HG02145.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-46_-44dupGGC | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/20 | 5879 | chr22 | 29838203 | ||||||
| chr22:29838203 | T | TGCCGCC | 6 | a0001c0001t0003 a0001c0001t0004 a0002c0002t0003 others(3): Show |
88 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
5_prime_UTR_variant | MODIFIER | c.-49_-44dupGGCGGC | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/20 | 5879 | chr22 | 29838203 | ||||||
| chr22:29838203 | T | TGCCGCCG others(2): Show |
3 | a0001c0001t0007 a0001c0001t0009 a0001c0011t0009 |
9 | HG01081.hp2 HG01891.hp1 HG02257.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-52_-44dupGGCGGCGG others(1): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/20 | 5879 | chr22 | 29838203 | ||||||
| chr22:29838203 | T | TGCCGCCG others(5): Show |
1 | a0004c0004t0008 | 3 | HG02683.hp1 NA19084.hp2 NA19086.hp2 |
5_prime_UTR_variant | MODIFIER | c.-55_-44dupGGCGGCGG others(4): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/20 | 5879 | chr22 | 29838203 | ||||||
| chr22:29838203 | T | TGCCGCCG others(8): Show |
2 | a0001c0001t0005 a0004c0004t0005 |
18 | HG00423.hp1 HG01070.hp1 HG01934.hp1 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-58_-44dupGGCGGCGG others(7): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/20 | 5879 | chr22 | 29838203 | ||||||
| chr22:29838203 | T | TGCCGCCG others(11): Show |
1 | a0004c0004t0013 | 1 | HG02040.hp1 | 5_prime_UTR_variant | MODIFIER | c.-61_-44dupGGCGGCGG others(10): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/20 | 5879 | chr22 | 29838203 | ||||||
| chr22:29838203 | TGCC | T | 8 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0010 others(5): Show |
92 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(89): Show |
5_prime_UTR_variant | MODIFIER | c.-46_-44delGGC | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/20 | 5879 | chr22 | 29838203 | ||||||
| chr22:29838206 | C | A | 1 | a0001c0001t0001 | 1 | HG00741.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-46G>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/20 | chr22 | 29838206 | |||||||
| chr22:29838229 | A | T | 9 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0007 others(6): Show |
54 | HG00423.hp1 HG01070.hp1 HG01243.hp1 others(51): Show |
5_prime_UTR_variant | MODIFIER | c.-69T>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/20 | 5904 | chr22 | 29838229 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:29789312 | C | A | 1 | a0001c0001t0002g0127 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2103-128G>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 19/19 | chr22 | 29789312 | |||||||
| chr22:29789362 | CTGACCAG others(7): Show |
C | 112 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0015 others(109): Show |
127 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.2103-192_2103-179d others(16): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 19/19 | chr22 | 29789362 | |||||||
| chr22:29789374 | G | A | 58 | a0001c0001t0002g0012 a0001c0001t0002g0133 a0001c0001t0002g0134 others(55): Show |
62 | HG00423.hp1 HG01070.hp1 HG01192.hp2 others(59): Show |
intron_variant | MODIFIER | c.2103-190C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 19/19 | chr22 | 29789374 | |||||||
| chr22:29789450 | G | A | 5 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0130 others(2): Show |
5 | HG01496.hp1 HG01891.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.2103-266C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 19/19 | chr22 | 29789450 | |||||||
| chr22:29789474 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2103-290C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 19/19 | chr22 | 29789474 | |||||||
| chr22:29789515 | G | A | 1 | a0003c0003t0001g0179 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2103-331C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 19/19 | chr22 | 29789515 | |||||||
| chr22:29789556 | T | C | 4 | a0007c0007t0004g0018 a0007c0007t0004g0035 a0007c0007t0004g0036 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2103-372A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 19/19 | chr22 | 29789556 | |||||||
| chr22:29789624 | C | T | 112 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0015 others(109): Show |
127 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.2103-440G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 19/19 | chr22 | 29789624 | |||||||
| chr22:29789635 | C | T | 1 | a0001c0001t0014g0285 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2103-451G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 19/19 | chr22 | 29789635 | |||||||
| chr22:29789730 | C | G | 116 | a0001c0001t0002g0012 a0001c0001t0002g0133 a0001c0001t0002g0134 others(113): Show |
132 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.2103-546G>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 19/19 | chr22 | 29789730 | |||||||
| chr22:29789818 | T | G | 1 | a0002c0002t0002g0067 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2103-634A>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 19/19 | chr22 | 29789818 | |||||||
| chr22:29789821 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2103-637C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 19/19 | chr22 | 29789821 | |||||||
| chr22:29789900 | A | T | 134 | a0001c0001t0002g0012 a0001c0001t0002g0126 a0001c0001t0002g0127 others(131): Show |
152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.2102+569T>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 19/19 | chr22 | 29789900 | |||||||
| chr22:29790108 | T | A | 1 | a0001c0001t0011g0286 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2102+361A>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 19/19 | chr22 | 29790108 | |||||||
| chr22:29790150 | C | T | 293 | a0001c0001t0001g0014 a0001c0001t0001g0187 a0001c0001t0001g0188 others(290): Show |
315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.2102+319G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 19/19 | chr22 | 29790150 | |||||||
| chr22:29790350 | G | A | 3 | a0001c0001t0003g0305 a0001c0001t0003g0306 a0001c0001t0003g0307 |
3 | HG01069.hp2 HG01099.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2102+119C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 19/19 | chr22 | 29790350 | |||||||
| chr22:29790643 | C | T | 4 | a0007c0007t0004g0018 a0007c0007t0004g0035 a0007c0007t0004g0036 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2023-95G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 18/19 | chr22 | 29790643 | |||||||
| chr22:29790770 | C | G | 3 | a0002c0002t0002g0066 a0002c0002t0002g0082 a0002c0002t0002g0083 |
3 | HG00609.hp1 HG00621.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.2023-222G>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 18/19 | chr22 | 29790770 | |||||||
| chr22:29790791 | G | A | 1 | a0003c0003t0001g0148 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2023-243C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 18/19 | chr22 | 29790791 | |||||||
| chr22:29790903 | C | T | 4 | a0007c0007t0004g0018 a0007c0007t0004g0035 a0007c0007t0004g0036 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2023-355G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 18/19 | chr22 | 29790903 | |||||||
| chr22:29791155 | C | T | 3 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 |
3 | HG02622.hp1 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2023-607G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 18/19 | chr22 | 29791155 | |||||||
| chr22:29791237 | C | T | 9 | a0001c0001t0003g0015 a0001c0001t0003g0302 a0001c0001t0003g0315 others(6): Show |
10 | NA18968.hp1 NA18969.hp1 NA18974.hp2 others(7): Show |
intron_variant | MODIFIER | c.2023-689G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 18/19 | chr22 | 29791237 | |||||||
| chr22:29791276 | C | T | 17 | a0004c0004t0004g0034 a0004c0004t0005g0047 a0004c0004t0005g0053 others(14): Show |
17 | HG00423.hp1 HG01934.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.2023-728G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 18/19 | chr22 | 29791276 | |||||||
| chr22:29791713 | C | T | 129 | a0001c0001t0002g0012 a0001c0001t0002g0126 a0001c0001t0002g0127 others(126): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.2022+720G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 18/19 | chr22 | 29791713 | |||||||
| chr22:29791734 | T | A | 1 | a0002c0002t0002g0071 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2022+699A>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 18/19 | chr22 | 29791734 | |||||||
| chr22:29791820 | CCT | C | 4 | a0007c0007t0004g0018 a0007c0007t0004g0035 a0007c0007t0004g0036 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2022+611_2022+612d others(4): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 18/19 | chr22 | 29791820 | |||||||
| chr22:29791976 | C | T | 1 | a0002c0002t0002g0098 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2022+457G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 18/19 | chr22 | 29791976 | |||||||
| chr22:29791994 | G | A | 1 | a0005c0005t0002g0116 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2022+439C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 18/19 | chr22 | 29791994 | |||||||
| chr22:29792095 | C | T | 130 | a0001c0001t0002g0012 a0001c0001t0002g0126 a0001c0001t0002g0127 others(127): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.2022+338G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 18/19 | chr22 | 29792095 | |||||||
| chr22:29792201 | C | T | 5 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0130 others(2): Show |
5 | HG01496.hp1 HG01891.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.2022+232G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 18/19 | chr22 | 29792201 | |||||||
| chr22:29792256 | T | G | 194 | a0001c0001t0002g0012 a0001c0001t0002g0126 a0001c0001t0002g0127 others(191): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.2022+177A>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 18/19 | chr22 | 29792256 | |||||||
| chr22:29792405 | C | A | 1 | a0003c0003t0001g0164 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2022+28G>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 18/19 | chr22 | 29792405 | |||||||
| chr22:29792622 | T | C | 15 | a0001c0001t0003g0016 a0001c0001t0003g0303 a0001c0001t0003g0305 others(12): Show |
16 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.1920-87A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 17/19 | chr22 | 29792622 | |||||||
| chr22:29792683 | C | T | 30 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(27): Show |
30 | HG00423.hp1 HG01070.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.1920-148G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 17/19 | chr22 | 29792683 | |||||||
| chr22:29792742 | G | A | 1 | a0001c0001t0011g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1920-207C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 17/19 | chr22 | 29792742 | |||||||
| chr22:29792752 | C | T | 58 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(55): Show |
61 | HG00423.hp1 HG01070.hp1 HG01243.hp1 others(58): Show |
intron_variant | MODIFIER | c.1920-217G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 17/19 | chr22 | 29792752 | |||||||
| chr22:29792810 | G | GA | 11 | a0001c0001t0003g0016 a0001c0001t0003g0303 a0001c0001t0003g0305 others(8): Show |
12 | HG00099.hp1 HG00735.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1920-276dupT | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 17/19 | chr22 | 29792810 | |||||||
| chr22:29792939 | A | T | 9 | a0005c0005t0002g0005 a0005c0005t0002g0113 a0005c0005t0002g0114 others(6): Show |
11 | HG00099.hp2 HG01069.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.1920-404T>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 17/19 | chr22 | 29792939 | |||||||
| chr22:29793354 | C | T | 3 | a0002c0002t0002g0009 a0002c0002t0002g0078 a0002c0019t0002g0072 |
4 | HG00280.hp1 HG02080.hp1 NA18966.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1919+6G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 17/19 | chr22 | 29793354 | |||||||
| chr22:29793357 | C | T | 1 | a0001c0013t0001g0274 | 1 | NA20905.hp1 | splice_region_variant&intron_variant | LOW | c.1919+3G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 17/19 | chr22 | 29793357 | |||||||
| chr22:29793508 | T | A | 6 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(3): Show |
6 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1789-18A>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 16/19 | chr22 | 29793508 | |||||||
| chr22:29793515 | G | A | 1 | a0002c0002t0002g0098 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1789-25C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 16/19 | chr22 | 29793515 | |||||||
| chr22:29793778 | C | A | 1 | a0003c0003t0001g0148 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1689-102G>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29793778 | |||||||
| chr22:29793821 | G | A | 4 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0131 others(1): Show |
4 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1689-145C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29793821 | |||||||
| chr22:29793856 | A | G | 1 | a0004c0004t0005g0063 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1689-180T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29793856 | |||||||
| chr22:29793901 | G | GT | 13 | a0001c0001t0001g0230 a0001c0001t0001g0236 a0001c0001t0001g0270 others(10): Show |
13 | HG01074.hp2 HG01891.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.1689-226dupA | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29793901 | |||||||
| chr22:29793948 | C | T | 4 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0131 others(1): Show |
4 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1689-272G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29793948 | |||||||
| chr22:29794067 | T | C | 1 | a0003c0003t0001g0174 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1689-391A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29794067 | |||||||
| chr22:29794068 | A | G | 30 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(27): Show |
30 | HG00423.hp1 HG01070.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.1689-392T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29794068 | |||||||
| chr22:29794153 | G | T | 6 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0261 others(3): Show |
6 | HG00673.hp1 HG02074.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.1689-477C>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29794153 | |||||||
| chr22:29794246 | C | G | 1 | a0001c0001t0011g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1689-570G>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29794246 | |||||||
| chr22:29794260 | G | T | 1 | a0003c0003t0001g0148 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1689-584C>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29794260 | |||||||
| chr22:29794261 | A | T | 1 | a0003c0003t0001g0148 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1689-585T>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29794261 | |||||||
| chr22:29794396 | C | G | 333 | a0001c0001t0001g0014 a0001c0001t0001g0187 a0001c0001t0001g0188 others(330): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.1689-720G>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29794396 | |||||||
| chr22:29794440 | C | T | 58 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(55): Show |
61 | HG00423.hp1 HG01070.hp1 HG01243.hp1 others(58): Show |
intron_variant | MODIFIER | c.1689-764G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29794440 | |||||||
| chr22:29794522 | T | C | 2 | a0001c0001t0011g0286 a0001c0001t0011g0287 |
2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1689-846A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29794522 | |||||||
| chr22:29794710 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG00609.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1689-1034C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29794710 | |||||||
| chr22:29794954 | C | CT | 7 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(4): Show |
7 | HG01884.hp2 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1689-1279dupA | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29794954 | |||||||
| chr22:29794954 | CT | C | 7 | a0001c0001t0001g0225 a0001c0001t0001g0235 a0001c0001t0001g0247 others(4): Show |
7 | HG00280.hp2 HG01069.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1689-1279delA | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29794954 | |||||||
| chr22:29795021 | C | T | 1 | a0003c0003t0001g0166 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1689-1345G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29795021 | |||||||
| chr22:29795316 | C | A | 4 | a0007c0007t0004g0018 a0007c0007t0004g0035 a0007c0007t0004g0036 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1689-1640G>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29795316 | |||||||
| chr22:29795355 | C | G | 1 | a0004c0004t0008g0044 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1689-1679G>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29795355 | |||||||
| chr22:29795501 | G | A | 3 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 |
3 | HG02622.hp1 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1689-1825C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29795501 | |||||||
| chr22:29795927 | A | G | 1 | a0001c0015t0001g0220 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1689-2251T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29795927 | |||||||
| chr22:29795932 | A | G | 8 | a0001c0001t0001g0262 a0005c0005t0002g0005 a0005c0005t0002g0113 others(5): Show |
10 | HG00099.hp2 HG01069.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1689-2256T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29795932 | |||||||
| chr22:29795960 | G | A | 1 | a0001c0001t0014g0285 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1689-2284C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29795960 | |||||||
| chr22:29796003 | G | C | 2 | a0009c0009t0002g0123 a0009c0009t0002g0124 |
2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1689-2327C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29796003 | |||||||
| chr22:29796012 | G | A | 4 | a0001c0001t0002g0012 a0001c0001t0002g0133 a0001c0001t0002g0134 others(1): Show |
5 | HG01192.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1689-2336C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29796012 | |||||||
| chr22:29796235 | A | G | 1 | a0001c0001t0004g0025 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1689-2559T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29796235 | |||||||
| chr22:29796299 | T | C | 1 | a0001c0001t0001g0253 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1689-2623A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29796299 | |||||||
| chr22:29796300 | C | T | 6 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 others(3): Show |
6 | HG03834.hp1 NA18956.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.1689-2624G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29796300 | |||||||
| chr22:29796494 | T | C | 5 | a0001c0001t0001g0218 a0001c0001t0001g0222 a0001c0001t0001g0224 others(2): Show |
5 | HG01175.hp1 HG02258.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.1689-2818A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29796494 | |||||||
| chr22:29796600 | A | T | 1 | a0003c0003t0001g0157 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1689-2924T>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29796600 | |||||||
| chr22:29796703 | G | C | 14 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0130 others(11): Show |
16 | HG00099.hp2 HG01069.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.1689-3027C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29796703 | |||||||
| chr22:29797004 | G | A | 4 | a0001c0001t0003g0303 a0001c0001t0003g0310 a0001c0001t0003g0318 others(1): Show |
4 | HG00099.hp1 HG01106.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1689-3328C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29797004 | |||||||
| chr22:29797270 | C | T | 1 | a0003c0003t0001g0156 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1689-3594G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29797270 | |||||||
| chr22:29797350 | G | C | 1 | a0002c0002t0002g0088 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1688+3641C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29797350 | |||||||
| chr22:29797559 | A | T | 286 | a0001c0001t0001g0014 a0001c0001t0001g0244 a0001c0001t0001g0245 others(283): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.1688+3432T>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29797559 | |||||||
| chr22:29797563 | C | T | 18 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0019 others(15): Show |
21 | HG01243.hp1 HG01496.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1688+3428G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29797563 | |||||||
| chr22:29797565 | C | G | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG02257.hp2 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1688+3426G>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29797565 | |||||||
| chr22:29797609 | T | C | 5 | a0001c0001t0001g0201 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
5 | HG00323.hp1 HG00738.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.1688+3382A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29797609 | |||||||
| chr22:29797804 | T | A | 1 | a0001c0001t0011g0286 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1688+3187A>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29797804 | |||||||
| chr22:29797825 | G | A | 1 | a0003c0003t0001g0170 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1688+3166C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29797825 | |||||||
| chr22:29797913 | C | T | 1 | a0001c0001t0009g0347 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1688+3078G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29797913 | |||||||
| chr22:29797916 | C | A | 1 | a0001c0001t0011g0286 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1688+3075G>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29797916 | |||||||
| chr22:29798051 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG00609.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1688+2940G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29798051 | |||||||
| chr22:29798060 | G | A | 9 | a0003c0003t0001g0150 a0003c0003t0001g0151 a0003c0003t0001g0162 others(6): Show |
9 | HG00280.hp2 HG01106.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.1688+2931C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29798060 | |||||||
| chr22:29798443 | C | G | 1 | a0001c0001t0003g0313 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1688+2548G>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29798443 | |||||||
| chr22:29798790 | C | T | 1 | a0003c0003t0001g0177 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1688+2201G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29798790 | |||||||
| chr22:29798824 | A | G | 2 | a0009c0009t0002g0123 a0009c0009t0002g0124 |
2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1688+2167T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29798824 | |||||||
| chr22:29799353 | G | T | 1 | a0003c0003t0001g0145 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1688+1638C>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29799353 | |||||||
| chr22:29799536 | C | G | 26 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(23): Show |
26 | HG00423.hp1 HG01070.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.1688+1455G>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29799536 | |||||||
| chr22:29799581 | T | C | 3 | a0001c0001t0004g0019 a0001c0001t0004g0031 a0001c0001t0004g0033 |
3 | HG02055.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1688+1410A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29799581 | |||||||
| chr22:29799776 | G | A | 7 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(4): Show |
7 | HG01070.hp1 HG02080.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1688+1215C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29799776 | |||||||
| chr22:29799850 | C | A | 1 | a0001c0001t0001g0265 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1688+1141G>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29799850 | |||||||
| chr22:29799935 | G | T | 54 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(51): Show |
57 | HG00423.hp1 HG01070.hp1 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.1688+1056C>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29799935 | |||||||
| chr22:29799960 | G | C | 18 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0130 others(15): Show |
20 | HG00099.hp2 HG01069.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.1688+1031C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29799960 | |||||||
| chr22:29800072 | C | T | 1 | a0001c0001t0003g0330 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1688+919G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29800072 | |||||||
| chr22:29800132 | G | A | 1 | a0006c0006t0002g0119 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1688+859C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29800132 | |||||||
| chr22:29800158 | T | G | 1 | a0001c0001t0001g0251 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1688+833A>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29800158 | |||||||
| chr22:29800160 | G | A | 2 | a0001c0001t0011g0286 a0001c0001t0011g0287 |
2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1688+831C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29800160 | |||||||
| chr22:29800275 | T | C | 56 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(53): Show |
59 | HG00423.hp1 HG01070.hp1 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.1688+716A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29800275 | |||||||
| chr22:29800848 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1688+143C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29800848 | |||||||
| chr22:29800867 | G | C | 1 | a0001c0001t0003g0303 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1688+124C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29800867 | |||||||
| chr22:29800907 | C | T | 2 | a0001c0001t0002g0136 a0001c0001t0002g0137 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1688+84G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29800907 | |||||||
| chr22:29800908 | G | A | 28 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0131 others(25): Show |
31 | HG01099.hp1 HG01243.hp1 HG01496.hp2 others(28): Show |
intron_variant | MODIFIER | c.1688+83C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29800908 | |||||||
| chr22:29800942 | T | C | 3 | a0001c0001t0003g0322 a0001c0001t0003g0323 a0001c0001t0003g0324 |
3 | HG00642.hp2 HG01074.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1688+49A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 15/19 | chr22 | 29800942 | |||||||
| chr22:29801244 | C | T | 1 | a0007c0007t0004g0037 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1569-134G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 14/19 | chr22 | 29801244 | |||||||
| chr22:29801436 | A | ACCTCATT others(12): Show |
56 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(53): Show |
59 | HG00423.hp1 HG01070.hp1 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.1569-327_1569-326i others(21): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 14/19 | chr22 | 29801436 | |||||||
| chr22:29801614 | T | C | 6 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(3): Show |
6 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1568+380A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 14/19 | chr22 | 29801614 | |||||||
| chr22:29801625 | C | T | 1 | a0003c0003t0001g0179 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1568+369G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 14/19 | chr22 | 29801625 | |||||||
| chr22:29801808 | G | C | 4 | a0007c0007t0004g0018 a0007c0007t0004g0035 a0007c0007t0004g0036 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1568+186C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 14/19 | chr22 | 29801808 | |||||||
| chr22:29801964 | C | T | 1 | a0001c0001t0011g0286 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1568+30G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 14/19 | chr22 | 29801964 | |||||||
| chr22:29802236 | G | T | 1 | a0001c0001t0002g0012 | 2 | HG01192.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1354-28C>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29802236 | |||||||
| chr22:29802492 | CA | C | 159 | a0001c0001t0002g0012 a0001c0001t0002g0128 a0001c0001t0002g0129 others(156): Show |
174 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.1354-285delT | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29802492 | |||||||
| chr22:29802492 | CAAAAA | C | 14 | a0001c0001t0003g0001 a0001c0001t0003g0015 a0001c0001t0003g0302 others(11): Show |
18 | HG00438.hp1 HG00741.hp2 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.1354-289_1354-285d others(7): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29802492 | |||||||
| chr22:29802498 | A | T | 5 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0130 others(2): Show |
5 | HG01496.hp1 HG01891.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1354-290T>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29802498 | |||||||
| chr22:29802499 | A | T | 7 | a0001c0001t0001g0270 a0001c0001t0002g0012 a0001c0001t0002g0133 others(4): Show |
8 | HG01074.hp2 HG01192.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1354-291T>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29802499 | |||||||
| chr22:29802501 | A | T | 100 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(97): Show |
111 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.1354-293T>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29802501 | |||||||
| chr22:29802600 | A | G | 23 | a0001c0001t0001g0248 a0001c0001t0001g0256 a0001c0001t0001g0257 others(20): Show |
23 | HG00673.hp1 HG01074.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.1354-392T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29802600 | |||||||
| chr22:29803020 | G | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG00609.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1354-812C>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29803020 | |||||||
| chr22:29803095 | C | T | 116 | a0001c0001t0002g0012 a0001c0001t0002g0133 a0001c0001t0002g0134 others(113): Show |
132 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1354-887G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29803095 | |||||||
| chr22:29803174 | C | T | 2 | a0001c0001t0011g0286 a0001c0001t0011g0287 |
2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1354-966G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29803174 | |||||||
| chr22:29803206 | G | A | 6 | a0003c0003t0001g0162 a0003c0003t0001g0165 a0003c0003t0001g0169 others(3): Show |
6 | HG01123.hp1 HG01934.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-998C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29803206 | |||||||
| chr22:29803215 | C | T | 4 | a0001c0001t0002g0012 a0001c0001t0002g0133 a0001c0001t0002g0134 others(1): Show |
5 | HG01192.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1354-1007G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29803215 | |||||||
| chr22:29803252 | C | CA | 234 | a0001c0001t0001g0014 a0001c0001t0001g0187 a0001c0001t0001g0188 others(231): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1354-1045dupT | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29803252 | |||||||
| chr22:29803252 | C | CAA | 59 | a0001c0001t0001g0272 a0001c0001t0004g0002 a0001c0001t0004g0007 others(56): Show |
62 | HG00423.hp1 HG01070.hp1 HG01123.hp1 others(59): Show |
intron_variant | MODIFIER | c.1354-1046_1354-104 others(6): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29803252 | |||||||
| chr22:29803263 | C | A | 1 | a0004c0004t0005g0064 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1354-1055G>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29803263 | |||||||
| chr22:29803349 | T | C | 11 | a0005c0005t0002g0005 a0005c0005t0002g0113 a0005c0005t0002g0114 others(8): Show |
13 | HG00099.hp2 HG01069.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1354-1141A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29803349 | |||||||
| chr22:29803358 | G | A | 6 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(3): Show |
6 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-1150C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29803358 | |||||||
| chr22:29803403 | T | C | 8 | a0003c0003t0001g0145 a0003c0003t0001g0148 a0003c0003t0001g0170 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1354-1195A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29803403 | |||||||
| chr22:29803642 | C | T | 23 | a0001c0001t0005g0048 a0001c0001t0005g0049 a0001c0001t0005g0050 others(20): Show |
23 | HG00423.hp1 HG01070.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.1353+996G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29803642 | |||||||
| chr22:29803754 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1353+884C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29803754 | |||||||
| chr22:29803756 | C | G | 5 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0130 others(2): Show |
5 | HG01496.hp1 HG01891.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1353+882G>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29803756 | |||||||
| chr22:29803906 | A | G | 1 | a0001c0001t0011g0286 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1353+732T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29803906 | |||||||
| chr22:29803913 | G | A | 1 | a0002c0002t0002g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1353+725C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29803913 | |||||||
| chr22:29803937 | C | T | 44 | a0001c0001t0001g0014 a0001c0001t0001g0244 a0001c0001t0001g0245 others(41): Show |
45 | HG00558.hp2 HG00673.hp1 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.1353+701G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29803937 | |||||||
| chr22:29804090 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1353+548G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29804090 | |||||||
| chr22:29804104 | C | T | 4 | a0001c0001t0001g0255 a0001c0001t0001g0260 a0001c0001t0001g0262 others(1): Show |
4 | HG00558.hp2 NA18962.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.1353+534G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29804104 | |||||||
| chr22:29804110 | A | G | 115 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(112): Show |
130 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1353+528T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29804110 | |||||||
| chr22:29804119 | G | C | 7 | a0002c0002t0002g0004 a0002c0002t0002g0070 a0002c0002t0002g0073 others(4): Show |
9 | HG02027.hp1 HG02165.hp2 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.1353+519C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29804119 | |||||||
| chr22:29804222 | C | T | 8 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(5): Show |
8 | HG00609.hp2 HG03098.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1353+416G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29804222 | |||||||
| chr22:29804271 | T | G | 5 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0130 others(2): Show |
5 | HG01496.hp1 HG01891.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1353+367A>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29804271 | |||||||
| chr22:29804357 | C | T | 1 | a0003c0003t0001g0152 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1353+281G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29804357 | |||||||
| chr22:29804373 | C | G | 137 | a0001c0001t0002g0012 a0001c0001t0002g0126 a0001c0001t0002g0127 others(134): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1353+265G>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29804373 | |||||||
| chr22:29804410 | A | G | 51 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0019 others(48): Show |
54 | HG00423.hp1 HG01070.hp1 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.1353+228T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29804410 | |||||||
| chr22:29804479 | C | T | 6 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(3): Show |
6 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1353+159G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29804479 | |||||||
| chr22:29804627 | C | G | 1 | a0001c0001t0001g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1353+11G>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29804627 | |||||||
| chr22:29804632 | A | G | 2 | a0002c0002t0002g0099 a0002c0002t0002g0100 |
2 | NA18945.hp1 NA18998.hp2 |
splice_region_variant&intron_variant | LOW | c.1353+6T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 13/19 | chr22 | 29804632 | |||||||
| chr22:29804904 | G | C | 115 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 others(112): Show |
130 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1161-74C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 12/19 | chr22 | 29804904 | |||||||
| chr22:29804931 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1161-101C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 12/19 | chr22 | 29804931 | |||||||
| chr22:29804947 | T | C | 194 | a0001c0001t0002g0012 a0001c0001t0002g0126 a0001c0001t0002g0127 others(191): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1161-117A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 12/19 | chr22 | 29804947 | |||||||
| chr22:29804992 | G | C | 1 | a0001c0001t0003g0339 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1161-162C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 12/19 | chr22 | 29804992 | |||||||
| chr22:29805013 | G | T | 1 | a0001c0001t0001g0275 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1161-183C>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 12/19 | chr22 | 29805013 | |||||||
| chr22:29805077 | G | A | 1 | a0001c0001t0003g0016 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1161-247C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 12/19 | chr22 | 29805077 | |||||||
| chr22:29805169 | C | T | 2 | a0001c0001t0011g0286 a0001c0001t0011g0287 |
2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1161-339G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 12/19 | chr22 | 29805169 | |||||||
| chr22:29805196 | G | T | 1 | a0003c0003t0001g0152 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1161-366C>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 12/19 | chr22 | 29805196 | |||||||
| chr22:29805392 | C | T | 47 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0019 others(44): Show |
50 | HG00423.hp1 HG01070.hp1 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.1161-562G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 12/19 | chr22 | 29805392 | |||||||
| chr22:29805511 | T | C | 23 | a0001c0001t0005g0048 a0001c0001t0005g0049 a0001c0001t0005g0050 others(20): Show |
23 | HG00423.hp1 HG01070.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.1161-681A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 12/19 | chr22 | 29805511 | |||||||
| chr22:29805591 | A | C | 4 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0131 others(1): Show |
4 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160+625T>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 12/19 | chr22 | 29805591 | |||||||
| chr22:29805618 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG00609.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1160+598G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 12/19 | chr22 | 29805618 | |||||||
| chr22:29805629 | C | T | 3 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 |
3 | HG02622.hp1 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1160+587G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 12/19 | chr22 | 29805629 | |||||||
| chr22:29805634 | C | T | 4 | a0001c0001t0002g0012 a0001c0001t0002g0133 a0001c0001t0002g0134 others(1): Show |
5 | HG01192.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1160+582G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 12/19 | chr22 | 29805634 | |||||||
| chr22:29805691 | T | C | 1 | a0007c0007t0004g0018 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1160+525A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 12/19 | chr22 | 29805691 | |||||||
| chr22:29805845 | G | A | 4 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0131 others(1): Show |
4 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160+371C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 12/19 | chr22 | 29805845 | |||||||
| chr22:29805854 | G | A | 2 | a0001c0001t0011g0286 a0001c0001t0011g0287 |
2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1160+362C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 12/19 | chr22 | 29805854 | |||||||
| chr22:29805868 | C | T | 1 | a0001c0001t0003g0317 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1160+348G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 12/19 | chr22 | 29805868 | |||||||
| chr22:29806090 | G | A | 51 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0019 others(48): Show |
54 | HG00423.hp1 HG01070.hp1 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.1160+126C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 12/19 | chr22 | 29806090 | |||||||
| chr22:29806361 | C | T | 1 | a0014c0016t0001g0231 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1086-71G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 11/19 | chr22 | 29806361 | |||||||
| chr22:29806379 | C | T | 2 | a0002c0002t0002g0107 a0002c0002t0002g0108 |
2 | HG02735.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1086-89G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 11/19 | chr22 | 29806379 | |||||||
| chr22:29806410 | C | T | 1 | a0002c0002t0002g0090 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1085+75G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 11/19 | chr22 | 29806410 | |||||||
| chr22:29806567 | C | T | 1 | a0001c0001t0003g0308 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1017-14G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 10/19 | chr22 | 29806567 | |||||||
| chr22:29806617 | C | G | 1 | a0003c0003t0001g0152 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1017-64G>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 10/19 | chr22 | 29806617 | |||||||
| chr22:29806618 | A | C | 1 | a0003c0003t0001g0152 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1017-65T>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 10/19 | chr22 | 29806618 | |||||||
| chr22:29806619 | C | T | 1 | a0003c0003t0001g0152 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1017-66G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 10/19 | chr22 | 29806619 | |||||||
| chr22:29806620 | C | G | 1 | a0003c0003t0001g0152 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1017-67G>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 10/19 | chr22 | 29806620 | |||||||
| chr22:29806622 | G | A | 1 | a0003c0003t0001g0152 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1017-69C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 10/19 | chr22 | 29806622 | |||||||
| chr22:29806624 | T | C | 1 | a0003c0003t0001g0152 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1017-71A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 10/19 | chr22 | 29806624 | |||||||
| chr22:29806627 | C | T | 1 | a0003c0003t0001g0152 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1017-74G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 10/19 | chr22 | 29806627 | |||||||
| chr22:29806698 | C | A | 1 | a0001c0001t0003g0344 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1016+99G>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 10/19 | chr22 | 29806698 | |||||||
| chr22:29806747 | G | C | 6 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(3): Show |
6 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1016+50C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 10/19 | chr22 | 29806747 | |||||||
| chr22:29806785 | G | C | 176 | a0001c0001t0002g0012 a0001c0001t0002g0128 a0001c0001t0002g0129 others(173): Show |
195 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.1016+12C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 10/19 | chr22 | 29806785 | |||||||
| chr22:29806909 | G | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG00609.hp2 NA19012.hp2 |
splice_region_variant&intron_variant | LOW | c.909-5C>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 9/19 | chr22 | 29806909 | |||||||
| chr22:29806995 | T | C | 47 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0019 others(44): Show |
50 | HG00423.hp1 HG01070.hp1 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.909-91A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 9/19 | chr22 | 29806995 | |||||||
| chr22:29807147 | A | G | 1 | a0004c0004t0005g0055 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.909-243T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 9/19 | chr22 | 29807147 | |||||||
| chr22:29807235 | C | CA | 44 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(41): Show |
46 | HG00597.hp2 HG00609.hp2 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.909-332dupT | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 9/19 | chr22 | 29807235 | |||||||
| chr22:29807235 | C | CAA | 7 | a0001c0001t0001g0195 a0001c0001t0007g0041 a0001c0001t0007g0043 others(4): Show |
7 | HG02257.hp2 HG02280.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.909-333_909-332dup others(2): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 9/19 | chr22 | 29807235 | |||||||
| chr22:29807235 | C | CAAA | 22 | a0001c0001t0005g0048 a0001c0001t0005g0049 a0001c0001t0005g0050 others(19): Show |
22 | HG00423.hp1 HG01070.hp1 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.909-334_909-332dup others(3): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 9/19 | chr22 | 29807235 | |||||||
| chr22:29807235 | CA | C | 25 | a0001c0001t0001g0188 a0001c0001t0001g0208 a0001c0001t0001g0245 others(22): Show |
27 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.909-332delT | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 9/19 | chr22 | 29807235 | |||||||
| chr22:29807235 | CAA | C | 9 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0001g0190 others(6): Show |
9 | HG01167.hp2 HG01496.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.909-333_909-332del others(2): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 9/19 | chr22 | 29807235 | |||||||
| chr22:29807251 | A | C | 1 | a0001c0001t0003g0320 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.909-347T>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 9/19 | chr22 | 29807251 | |||||||
| chr22:29807478 | C | G | 4 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0131 others(1): Show |
4 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.909-574G>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 9/19 | chr22 | 29807478 | |||||||
| chr22:29807578 | G | A | 53 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0019 others(50): Show |
56 | HG00423.hp1 HG01070.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.908+533C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 9/19 | chr22 | 29807578 | |||||||
| chr22:29807610 | C | G | 119 | a0001c0001t0002g0012 a0001c0001t0002g0133 a0001c0001t0002g0134 others(116): Show |
135 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.908+501G>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 9/19 | chr22 | 29807610 | |||||||
| chr22:29807690 | A | T | 4 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(1): Show |
4 | HG03098.hp1 HG03209.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.908+421T>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 9/19 | chr22 | 29807690 | |||||||
| chr22:29807726 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.908+385G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 9/19 | chr22 | 29807726 | |||||||
| chr22:29807748 | A | C | 1 | a0002c0002t0002g0096 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.908+363T>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 9/19 | chr22 | 29807748 | |||||||
| chr22:29807844 | G | A | 39 | a0003c0003t0001g0140 a0003c0003t0001g0143 a0003c0003t0001g0144 others(36): Show |
39 | HG00280.hp2 HG00597.hp2 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.908+267C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 9/19 | chr22 | 29807844 | |||||||
| chr22:29807853 | G | A | 114 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(111): Show |
129 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.908+258C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 9/19 | chr22 | 29807853 | |||||||
| chr22:29807927 | C | A | 12 | a0001c0001t0001g0255 a0001c0001t0001g0260 a0001c0001t0001g0262 others(9): Show |
12 | HG00558.hp2 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.908+184G>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 9/19 | chr22 | 29807927 | |||||||
| chr22:29807930 | A | C | 51 | a0001c0001t0001g0014 a0001c0001t0001g0191 a0001c0001t0001g0192 others(48): Show |
53 | HG00423.hp1 HG00733.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.908+181T>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 9/19 | chr22 | 29807930 | |||||||
| chr22:29808498 | G | A | 4 | a0001c0001t0002g0012 a0001c0001t0002g0133 a0001c0001t0002g0134 others(1): Show |
5 | HG01192.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.834-313C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29808498 | |||||||
| chr22:29808540 | G | C | 5 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0130 others(2): Show |
5 | HG01496.hp1 HG01891.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.834-355C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29808540 | |||||||
| chr22:29808659 | C | T | 1 | a0002c0002t0002g0081 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.834-474G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29808659 | |||||||
| chr22:29808801 | C | A | 44 | a0001c0001t0001g0014 a0001c0001t0001g0244 a0001c0001t0001g0245 others(41): Show |
45 | HG00558.hp2 HG00673.hp1 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.834-616G>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29808801 | |||||||
| chr22:29808809 | C | CA | 83 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0190 others(80): Show |
91 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.834-625dupT | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29808809 | |||||||
| chr22:29808809 | CA | C | 32 | a0001c0001t0001g0228 a0001c0001t0001g0253 a0001c0001t0003g0299 others(29): Show |
35 | HG00639.hp2 HG01070.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.834-625delT | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29808809 | |||||||
| chr22:29808991 | A | T | 137 | a0001c0001t0002g0012 a0001c0001t0002g0126 a0001c0001t0002g0127 others(134): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.834-806T>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29808991 | |||||||
| chr22:29809113 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0284 |
2 | HG03942.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.834-928G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29809113 | |||||||
| chr22:29809141 | A | AAAT | 12 | a0001c0001t0002g0130 a0001c0001t0003g0315 a0001c0001t0003g0317 others(9): Show |
12 | HG00408.hp2 HG00621.hp1 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.834-957_834-956ins others(3): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29809141 | |||||||
| chr22:29809141 | A | AAT | 117 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0136 others(114): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.834-957_834-956ins others(2): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29809141 | |||||||
| chr22:29809141 | A | AT | 14 | a0001c0001t0002g0012 a0001c0001t0002g0133 a0001c0001t0002g0134 others(11): Show |
15 | HG00558.hp1 HG01069.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.834-957dupA | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29809141 | |||||||
| chr22:29809141 | A | T | 155 | a0001c0001t0001g0014 a0001c0001t0001g0187 a0001c0001t0001g0188 others(152): Show |
159 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.834-956T>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29809141 | |||||||
| chr22:29809165 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.834-980T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29809165 | |||||||
| chr22:29809184 | A | C | 4 | a0007c0007t0004g0018 a0007c0007t0004g0035 a0007c0007t0004g0036 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.834-999T>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29809184 | |||||||
| chr22:29809238 | AT | A | 39 | a0003c0003t0001g0140 a0003c0003t0001g0143 a0003c0003t0001g0144 others(36): Show |
39 | HG00280.hp2 HG00597.hp2 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.834-1054delA | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29809238 | |||||||
| chr22:29809288 | G | A | 4 | a0003c0003t0001g0152 a0003c0003t0001g0159 a0003c0003t0001g0174 others(1): Show |
4 | NA18949.hp2 NA18959.hp1 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.834-1103C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29809288 | |||||||
| chr22:29809362 | A | C | 1 | a0001c0001t0001g0228 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.834-1177T>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29809362 | |||||||
| chr22:29809428 | G | A | 1 | a0004c0004t0005g0056 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.834-1243C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29809428 | |||||||
| chr22:29809583 | C | T | 18 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0130 others(15): Show |
20 | HG00099.hp2 HG01069.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.834-1398G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29809583 | |||||||
| chr22:29809647 | C | T | 5 | a0002c0002t0002g0008 a0002c0002t0002g0068 a0002c0002t0002g0075 others(2): Show |
6 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(3): Show |
intron_variant | MODIFIER | c.834-1462G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29809647 | |||||||
| chr22:29809948 | G | A | 57 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0131 others(54): Show |
60 | HG00423.hp1 HG01070.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.834-1763C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29809948 | |||||||
| chr22:29810226 | T | C | 1 | a0001c0001t0003g0343 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.834-2041A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29810226 | |||||||
| chr22:29810302 | C | A | 136 | a0001c0001t0002g0012 a0001c0001t0002g0126 a0001c0001t0002g0127 others(133): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.834-2117G>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29810302 | |||||||
| chr22:29810482 | C | G | 1 | a0005c0005t0002g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.834-2297G>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29810482 | |||||||
| chr22:29810602 | G | T | 1 | a0001c0001t0003g0316 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.834-2417C>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29810602 | |||||||
| chr22:29810735 | A | AT | 21 | a0001c0001t0001g0262 a0001c0001t0001g0277 a0001c0001t0002g0132 others(18): Show |
25 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.834-2551dupA | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29810735 | |||||||
| chr22:29810735 | AT | A | 8 | a0001c0001t0001g0230 a0001c0001t0001g0236 a0001c0001t0003g0332 others(5): Show |
8 | HG02300.hp2 HG02615.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.834-2551delA | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29810735 | |||||||
| chr22:29810875 | T | C | 4 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0131 others(1): Show |
4 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.833+2555A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29810875 | |||||||
| chr22:29810878 | G | A | 2 | a0009c0009t0002g0123 a0009c0009t0002g0124 |
2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.833+2552C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29810878 | |||||||
| chr22:29810919 | TG | T | 15 | a0001c0001t0003g0006 a0001c0001t0003g0304 a0001c0001t0003g0327 others(12): Show |
17 | HG00544.hp2 HG02083.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.833+2510delC | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29810919 | |||||||
| chr22:29810945 | G | C | 1 | a0003c0003t0001g0171 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.833+2485C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29810945 | |||||||
| chr22:29810946 | G | T | 2 | a0002c0002t0002g0107 a0002c0002t0002g0108 |
2 | HG02735.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.833+2484C>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29810946 | |||||||
| chr22:29811050 | T | C | 53 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0019 others(50): Show |
56 | HG00423.hp1 HG01070.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.833+2380A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29811050 | |||||||
| chr22:29811624 | C | T | 1 | a0002c0002t0002g0110 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.833+1806G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29811624 | |||||||
| chr22:29811826 | T | A | 1 | a0001c0001t0005g0050 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.833+1604A>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29811826 | |||||||
| chr22:29811917 | C | T | 1 | a0001c0001t0003g0327 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.833+1513G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29811917 | |||||||
| chr22:29812366 | C | A | 1 | a0001c0001t0001g0284 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.833+1064G>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29812366 | |||||||
| chr22:29812403 | C | T | 1 | a0001c0011t0009g0349 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.833+1027G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29812403 | |||||||
| chr22:29812408 | T | G | 1 | a0001c0001t0001g0259 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.833+1022A>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29812408 | |||||||
| chr22:29812504 | A | G | 2 | a0001c0001t0003g0016 a0001c0001t0003g0326 |
3 | HG01256.hp1 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.833+926T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29812504 | |||||||
| chr22:29812619 | G | A | 115 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(112): Show |
130 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.833+811C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29812619 | |||||||
| chr22:29812671 | T | C | 4 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0131 others(1): Show |
4 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.833+759A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29812671 | |||||||
| chr22:29812773 | C | G | 1 | a0001c0001t0004g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.833+657G>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29812773 | |||||||
| chr22:29812886 | G | GT | 122 | a0001c0001t0001g0191 a0001c0001t0001g0259 a0001c0001t0002g0012 others(119): Show |
138 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.833+543dupA | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29812886 | |||||||
| chr22:29813227 | T | C | 5 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0228 others(2): Show |
5 | HG01081.hp1 HG01167.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.833+203A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29813227 | |||||||
| chr22:29813320 | G | A | 24 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0019 others(21): Show |
27 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.833+110C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29813320 | |||||||
| chr22:29813380 | T | C | 18 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0130 others(15): Show |
20 | HG00099.hp2 HG01069.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.833+50A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29813380 | |||||||
| chr22:29813385 | C | T | 1 | a0001c0001t0011g0286 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.833+45G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29813385 | |||||||
| chr22:29813386 | A | G | 1 | a0008c0008t0001g0141 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.833+44T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 8/19 | chr22 | 29813386 | |||||||
| chr22:29813757 | T | C | 1 | a0001c0001t0011g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.721-215A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 7/19 | chr22 | 29813757 | |||||||
| chr22:29813827 | C | T | 24 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0019 others(21): Show |
27 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.721-285G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 7/19 | chr22 | 29813827 | |||||||
| chr22:29813956 | T | G | 4 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0131 others(1): Show |
4 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-414A>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 7/19 | chr22 | 29813956 | |||||||
| chr22:29814049 | G | A | 1 | a0002c0002t0002g0091 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.721-507C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 7/19 | chr22 | 29814049 | |||||||
| chr22:29814093 | C | T | 4 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0131 others(1): Show |
4 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-551G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 7/19 | chr22 | 29814093 | |||||||
| chr22:29814173 | G | A | 1 | a0004c0004t0005g0047 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.720+484C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 7/19 | chr22 | 29814173 | |||||||
| chr22:29814366 | C | T | 3 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 |
3 | HG02622.hp1 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.720+291G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 7/19 | chr22 | 29814366 | |||||||
| chr22:29814367 | G | A | 114 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(111): Show |
129 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.720+290C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 7/19 | chr22 | 29814367 | |||||||
| chr22:29814380 | T | G | 1 | a0001c0001t0004g0033 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.720+277A>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 7/19 | chr22 | 29814380 | |||||||
| chr22:29814584 | C | T | 2 | a0003c0003t0001g0154 a0003c0003t0001g0155 |
2 | NA18980.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.720+73G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 7/19 | chr22 | 29814584 | |||||||
| chr22:29814866 | T | C | 1 | a0002c0002t0002g0098 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.610-99A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 6/19 | chr22 | 29814866 | |||||||
| chr22:29814949 | T | C | 3 | a0007c0007t0004g0035 a0007c0007t0004g0036 a0007c0007t0004g0037 |
3 | HG02615.hp1 HG02895.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.610-182A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 6/19 | chr22 | 29814949 | |||||||
| chr22:29815213 | A | G | 1 | a0001c0001t0004g0033 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.610-446T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 6/19 | chr22 | 29815213 | |||||||
| chr22:29815385 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.610-618A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 6/19 | chr22 | 29815385 | |||||||
| chr22:29815523 | A | G | 286 | a0001c0001t0001g0014 a0001c0001t0001g0244 a0001c0001t0001g0245 others(283): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.609+483T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 6/19 | chr22 | 29815523 | |||||||
| chr22:29815655 | T | A | 1 | a0003c0003t0001g0177 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.609+351A>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 6/19 | chr22 | 29815655 | |||||||
| chr22:29815814 | T | C | 1 | a0001c0001t0003g0335 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.609+192A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 6/19 | chr22 | 29815814 | |||||||
| chr22:29815887 | A | G | 125 | a0001c0001t0002g0012 a0001c0001t0002g0128 a0001c0001t0002g0129 others(122): Show |
141 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.609+119T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 6/19 | chr22 | 29815887 | |||||||
| chr22:29816205 | C | G | 115 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(112): Show |
130 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.542-132G>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29816205 | |||||||
| chr22:29816209 | G | C | 1 | a0001c0001t0006g0288 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.542-136C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29816209 | |||||||
| chr22:29816251 | C | T | 1 | a0001c0001t0002g0012 | 2 | HG01192.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.542-178G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29816251 | |||||||
| chr22:29816357 | A | G | 1 | a0001c0001t0004g0026 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.542-284T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29816357 | |||||||
| chr22:29816377 | C | T | 123 | a0001c0001t0002g0012 a0001c0001t0002g0128 a0001c0001t0002g0129 others(120): Show |
139 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.542-304G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29816377 | |||||||
| chr22:29816655 | G | C | 1 | a0002c0002t0002g0104 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.542-582C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29816655 | |||||||
| chr22:29816701 | C | T | 1 | a0001c0001t0003g0308 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.542-628G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29816701 | |||||||
| chr22:29816784 | C | CGAGAGAG others(1): Show |
7 | a0001c0001t0001g0212 a0001c0001t0003g0303 a0001c0001t0003g0318 others(4): Show |
7 | HG00099.hp1 HG00741.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.542-719_542-712dup others(8): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29816784 | |||||||
| chr22:29816812 | A | AGAGG | 6 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(3): Show |
6 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.542-743_542-740dup others(4): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29816812 | |||||||
| chr22:29816873 | C | T | 17 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0019 others(14): Show |
20 | HG01243.hp1 HG01496.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.542-800G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29816873 | |||||||
| chr22:29816924 | A | G | 4 | a0001c0001t0002g0012 a0001c0001t0002g0133 a0001c0001t0002g0134 others(1): Show |
5 | HG01192.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.542-851T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29816924 | |||||||
| chr22:29816997 | C | T | 115 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(112): Show |
130 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.542-924G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29816997 | |||||||
| chr22:29817227 | A | C | 1 | a0001c0001t0004g0024 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.542-1154T>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29817227 | |||||||
| chr22:29817257 | C | T | 4 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0131 others(1): Show |
4 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.542-1184G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29817257 | |||||||
| chr22:29817518 | G | C | 11 | a0003c0003t0001g0146 a0003c0003t0001g0149 a0003c0003t0001g0153 others(8): Show |
11 | HG02523.hp2 NA18957.hp2 NA18962.hp1 others(8): Show |
intron_variant | MODIFIER | c.542-1445C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29817518 | |||||||
| chr22:29817545 | C | T | 2 | a0009c0009t0002g0123 a0009c0009t0002g0124 |
2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.542-1472G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29817545 | |||||||
| chr22:29817945 | T | C | 3 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0131 |
3 | HG01884.hp1 HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.542-1872A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29817945 | |||||||
| chr22:29817977 | C | T | 4 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0131 others(1): Show |
4 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.542-1904G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29817977 | |||||||
| chr22:29817983 | T | G | 194 | a0001c0001t0002g0012 a0001c0001t0002g0126 a0001c0001t0002g0127 others(191): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.542-1910A>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29817983 | |||||||
| chr22:29818047 | A | G | 194 | a0001c0001t0002g0012 a0001c0001t0002g0126 a0001c0001t0002g0127 others(191): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.542-1974T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818047 | |||||||
| chr22:29818102 | GA | G | 18 | a0001c0001t0002g0012 a0001c0001t0002g0133 a0001c0001t0002g0134 others(15): Show |
21 | HG00099.hp2 HG01069.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.542-2030delT | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818102 | |||||||
| chr22:29818181 | C | T | 1 | a0001c0001t0003g0344 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.542-2108G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818181 | |||||||
| chr22:29818344 | T | C | 18 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0019 others(15): Show |
21 | HG01243.hp1 HG01496.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.542-2271A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818344 | |||||||
| chr22:29818403 | T | TAC | 10 | a0001c0001t0001g0227 a0003c0003t0001g0155 a0003c0003t0001g0163 others(7): Show |
10 | HG00597.hp2 HG01928.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.542-2332_542-2331d others(4): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818403 | |||||||
| chr22:29818403 | T | TACAC | 4 | a0001c0001t0001g0223 a0001c0001t0002g0131 a0003c0003t0001g0179 others(1): Show |
4 | HG02148.hp1 HG02897.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.542-2334_542-2331d others(6): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818403 | |||||||
| chr22:29818403 | T | TACACAC | 4 | a0001c0001t0006g0291 a0001c0001t0011g0287 a0003c0003t0001g0154 others(1): Show |
4 | HG02559.hp2 NA18943.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.542-2336_542-2331d others(8): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818403 | |||||||
| chr22:29818403 | T | TACACACA others(5): Show |
1 | a0001c0001t0006g0290 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.542-2342_542-2331d others(14): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818403 | |||||||
| chr22:29818403 | TAC | T | 13 | a0001c0001t0001g0222 a0001c0001t0001g0237 a0001c0001t0001g0241 others(10): Show |
13 | HG00280.hp2 HG00438.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.542-2332_542-2331d others(4): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818403 | |||||||
| chr22:29818403 | TACAC | T | 21 | a0001c0001t0001g0014 a0001c0001t0001g0188 a0001c0001t0001g0214 others(18): Show |
22 | HG01074.hp2 HG01168.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.542-2334_542-2331d others(6): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818403 | |||||||
| chr22:29818403 | TACACAC | T | 21 | a0001c0001t0001g0013 a0001c0001t0001g0207 a0001c0001t0001g0208 others(18): Show |
22 | HG00639.hp1 HG01261.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.542-2336_542-2331d others(8): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818403 | |||||||
| chr22:29818403 | TACACACA others(1): Show |
T | 28 | a0001c0001t0001g0200 a0001c0001t0001g0203 a0001c0001t0001g0211 others(25): Show |
29 | HG01070.hp1 HG01168.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.542-2338_542-2331d others(10): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818403 | |||||||
| chr22:29818403 | TACACACA others(3): Show |
T | 19 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0001g0206 others(16): Show |
19 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.542-2340_542-2331d others(12): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818403 | |||||||
| chr22:29818403 | TACACACA others(5): Show |
T | 12 | a0001c0001t0001g0195 a0001c0001t0001g0201 a0001c0001t0001g0230 others(9): Show |
12 | HG01106.hp1 HG01123.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.542-2342_542-2331d others(14): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818403 | |||||||
| chr22:29818403 | TACACACA others(7): Show |
T | 14 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0224 others(11): Show |
14 | HG01081.hp1 HG01167.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.542-2344_542-2331d others(16): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818403 | |||||||
| chr22:29818403 | TACACACA others(9): Show |
T | 8 | a0001c0001t0001g0202 a0001c0001t0001g0204 a0001c0001t0001g0229 others(5): Show |
8 | HG00673.hp1 HG02735.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.542-2346_542-2331d others(18): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818403 | |||||||
| chr22:29818403 | TACACACA others(11): Show |
T | 5 | a0001c0001t0001g0228 a0001c0001t0001g0234 a0001c0001t0001g0244 others(2): Show |
5 | HG00558.hp2 HG00733.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.542-2348_542-2331d others(20): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818403 | |||||||
| chr22:29818403 | TACACACA others(13): Show |
T | 3 | a0001c0001t0001g0192 a0001c0001t0001g0197 a0001c0001t0001g0212 |
3 | HG00741.hp1 HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.542-2350_542-2331d others(22): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818403 | |||||||
| chr22:29818403 | TACACACA others(15): Show |
T | 5 | a0001c0001t0004g0020 a0001c0001t0004g0022 a0001c0001t0004g0028 others(2): Show |
5 | HG01243.hp1 NA18522.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.542-2352_542-2331d others(24): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818403 | |||||||
| chr22:29818403 | TACACACA others(17): Show |
T | 14 | a0001c0001t0001g0191 a0001c0001t0001g0193 a0001c0001t0004g0002 others(11): Show |
16 | HG00609.hp2 HG01496.hp2 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.542-2354_542-2331d others(26): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818403 | |||||||
| chr22:29818403 | TACACACA others(19): Show |
T | 2 | a0001c0001t0001g0194 a0007c0007t0004g0036 |
2 | HG03453.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.542-2356_542-2331d others(28): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818403 | |||||||
| chr22:29818403 | TACACACA others(21): Show |
T | 2 | a0007c0007t0004g0035 a0007c0007t0004g0037 |
2 | HG02615.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.542-2358_542-2331d others(30): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818403 | |||||||
| chr22:29818403 | TACACACA others(23): Show |
T | 2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | NA19003.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.542-2360_542-2331d others(32): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818403 | |||||||
| chr22:29818403 | TACACACA others(31): Show |
T | 1 | a0001c0001t0001g0272 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.542-2368_542-2331d others(40): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818403 | |||||||
| chr22:29818403 | TACACACA others(39): Show |
T | 1 | a0002c0002t0002g0071 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.542-2376_542-2331d others(48): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818403 | |||||||
| chr22:29818403 | TACACACA others(47): Show |
T | 1 | a0001c0001t0003g0310 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.542-2384_542-2331d others(56): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818403 | |||||||
| chr22:29818403 | TACACACA others(49): Show |
T | 135 | a0001c0001t0002g0012 a0001c0001t0002g0126 a0001c0001t0002g0127 others(132): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.542-2386_542-2331d others(58): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818403 | |||||||
| chr22:29818477 | C | CAG | 4 | a0001c0001t0001g0280 a0001c0001t0001g0282 a0001c0001t0001g0283 others(1): Show |
4 | HG02809.hp1 HG03579.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.542-2406_542-2405d others(4): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818477 | |||||||
| chr22:29818477 | C | G | 33 | a0001c0001t0001g0244 a0001c0001t0001g0248 a0001c0001t0001g0249 others(30): Show |
33 | HG00558.hp2 HG01074.hp2 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.542-2404G>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818477 | |||||||
| chr22:29818715 | G | C | 137 | a0001c0001t0001g0260 a0001c0001t0002g0012 a0001c0001t0002g0126 others(134): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.542-2642C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818715 | |||||||
| chr22:29818716 | C | T | 2 | a0001c0001t0001g0203 a0001c0001t0001g0211 |
2 | HG01346.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.542-2643G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818716 | |||||||
| chr22:29818922 | C | G | 1 | a0003c0003t0001g0179 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.542-2849G>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29818922 | |||||||
| chr22:29819125 | C | T | 4 | a0007c0007t0004g0018 a0007c0007t0004g0035 a0007c0007t0004g0036 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.542-3052G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29819125 | |||||||
| chr22:29819188 | T | C | 58 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0019 others(55): Show |
63 | HG00099.hp2 HG00423.hp1 HG01069.hp1 others(60): Show |
intron_variant | MODIFIER | c.542-3115A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29819188 | |||||||
| chr22:29819229 | C | T | 2 | a0001c0001t0011g0286 a0001c0001t0011g0287 |
2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.541+3106G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29819229 | |||||||
| chr22:29819398 | G | C | 1 | a0001c0001t0001g0259 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.541+2937C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29819398 | |||||||
| chr22:29819489 | C | G | 2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | NA19003.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.541+2846G>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29819489 | |||||||
| chr22:29819559 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.541+2776T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29819559 | |||||||
| chr22:29819603 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.541+2732C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29819603 | |||||||
| chr22:29819618 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.541+2717G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29819618 | |||||||
| chr22:29819682 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.541+2653A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29819682 | |||||||
| chr22:29819705 | C | G | 1 | a0006c0006t0002g0117 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.541+2630G>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29819705 | |||||||
| chr22:29819729 | G | A | 48 | a0001c0001t0001g0014 a0001c0001t0001g0244 a0001c0001t0001g0245 others(45): Show |
49 | HG00558.hp2 HG00673.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.541+2606C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29819729 | |||||||
| chr22:29819736 | G | C | 1 | a0002c0002t0002g0067 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.541+2599C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29819736 | |||||||
| chr22:29819750 | G | A | 1 | a0001c0001t0001g0272 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.541+2585C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29819750 | |||||||
| chr22:29819914 | T | C | 295 | a0001c0001t0001g0014 a0001c0001t0001g0187 a0001c0001t0001g0188 others(292): Show |
317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.541+2421A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29819914 | |||||||
| chr22:29819954 | G | C | 3 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 |
3 | HG02622.hp1 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.541+2381C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29819954 | |||||||
| chr22:29820109 | A | C | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.541+2226T>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29820109 | |||||||
| chr22:29820116 | T | G | 1 | a0003c0003t0001g0164 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.541+2219A>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29820116 | |||||||
| chr22:29820179 | C | T | 181 | a0001c0001t0002g0012 a0001c0001t0002g0128 a0001c0001t0002g0129 others(178): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.541+2156G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29820179 | |||||||
| chr22:29820185 | C | T | 60 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0019 others(57): Show |
65 | HG00099.hp2 HG00423.hp1 HG01069.hp1 others(62): Show |
intron_variant | MODIFIER | c.541+2150G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29820185 | |||||||
| chr22:29820329 | A | G | 1 | a0001c0001t0005g0049 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.541+2006T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29820329 | |||||||
| chr22:29820369 | G | A | 4 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0131 others(1): Show |
4 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.541+1966C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29820369 | |||||||
| chr22:29820413 | C | T | 1 | a0003c0003t0001g0169 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.541+1922G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29820413 | |||||||
| chr22:29820901 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.541+1434G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29820901 | |||||||
| chr22:29820909 | T | TAA | 8 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 others(5): Show |
8 | HG00099.hp1 HG01106.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.541+1425_541+1426i others(4): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29820909 | |||||||
| chr22:29820911 | C | A | 163 | a0001c0001t0002g0012 a0001c0001t0002g0136 a0001c0001t0002g0137 others(160): Show |
182 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.541+1424G>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29820911 | |||||||
| chr22:29820913 | C | A | 8 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 others(5): Show |
8 | HG00099.hp1 HG01106.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.541+1422G>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29820913 | |||||||
| chr22:29820913 | C | CA | 22 | a0001c0001t0001g0207 a0001c0001t0001g0213 a0001c0001t0001g0224 others(19): Show |
24 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.541+1421dupT | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29820913 | |||||||
| chr22:29820913 | CAA | C | 51 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0019 others(48): Show |
54 | HG00423.hp1 HG01243.hp1 HG01496.hp2 others(51): Show |
intron_variant | MODIFIER | c.541+1420_541+1421d others(4): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29820913 | |||||||
| chr22:29820993 | C | A | 175 | a0001c0001t0002g0012 a0001c0001t0002g0128 a0001c0001t0002g0129 others(172): Show |
194 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.541+1342G>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29820993 | |||||||
| chr22:29821165 | T | G | 17 | a0004c0004t0004g0034 a0004c0004t0005g0047 a0004c0004t0005g0053 others(14): Show |
17 | HG00423.hp1 HG01934.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.541+1170A>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29821165 | |||||||
| chr22:29821167 | G | T | 1 | a0002c0002t0002g0077 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.541+1168C>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29821167 | |||||||
| chr22:29821179 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.541+1156C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29821179 | |||||||
| chr22:29821417 | C | T | 4 | a0007c0007t0004g0018 a0007c0007t0004g0035 a0007c0007t0004g0036 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.541+918G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29821417 | |||||||
| chr22:29821593 | G | A | 8 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(5): Show |
8 | HG00609.hp2 HG03098.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.541+742C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29821593 | |||||||
| chr22:29821601 | C | A | 1 | a0001c0001t0003g0343 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.541+734G>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29821601 | |||||||
| chr22:29821652 | A | G | 4 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0131 others(1): Show |
4 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.541+683T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29821652 | |||||||
| chr22:29821837 | A | T | 1 | a0001c0001t0003g0339 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.541+498T>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29821837 | |||||||
| chr22:29821838 | A | T | 118 | a0001c0001t0002g0012 a0001c0001t0002g0133 a0001c0001t0002g0134 others(115): Show |
134 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.541+497T>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29821838 | |||||||
| chr22:29821839 | T | A | 1 | a0003c0003t0001g0166 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.541+496A>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29821839 | |||||||
| chr22:29821842 | T | G | 1 | a0003c0003t0001g0183 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.541+493A>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29821842 | |||||||
| chr22:29821903 | T | C | 2 | a0001c0001t0011g0286 a0001c0001t0011g0287 |
2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.541+432A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29821903 | |||||||
| chr22:29821908 | G | C | 1 | a0001c0001t0005g0052 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.541+427C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29821908 | |||||||
| chr22:29821996 | C | CT | 5 | a0001c0001t0002g0130 a0002c0002t0002g0097 a0002c0002t0002g0105 others(2): Show |
5 | HG02055.hp1 HG02056.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.541+338dupA | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29821996 | |||||||
| chr22:29822002 | TC | T | 4 | a0001c0001t0011g0286 a0001c0001t0011g0287 a0009c0009t0002g0123 others(1): Show |
4 | HG02559.hp2 HG03139.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.541+332delG | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29822002 | |||||||
| chr22:29822003 | C | T | 189 | a0001c0001t0002g0012 a0001c0001t0002g0126 a0001c0001t0002g0127 others(186): Show |
210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.541+332G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29822003 | |||||||
| chr22:29822224 | C | A | 53 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0019 others(50): Show |
56 | HG00423.hp1 HG01070.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.541+111G>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29822224 | |||||||
| chr22:29822232 | G | A | 4 | a0001c0001t0002g0012 a0001c0001t0002g0133 a0001c0001t0002g0134 others(1): Show |
5 | HG01192.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.541+103C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29822232 | |||||||
| chr22:29822281 | T | C | 23 | a0001c0001t0005g0048 a0001c0001t0005g0049 a0001c0001t0005g0050 others(20): Show |
23 | HG00423.hp1 HG01070.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.541+54A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 5/19 | chr22 | 29822281 | |||||||
| chr22:29822585 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.412-121A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29822585 | |||||||
| chr22:29822619 | G | A | 4 | a0003c0003t0001g0167 a0003c0003t0001g0168 a0003c0003t0001g0183 others(1): Show |
4 | NA18994.hp2 NA18999.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.412-155C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29822619 | |||||||
| chr22:29822623 | T | C | 1 | a0005c0005t0002g0116 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.412-159A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29822623 | |||||||
| chr22:29822716 | C | CT | 51 | a0001c0001t0001g0187 a0001c0001t0001g0192 a0001c0001t0001g0213 others(48): Show |
53 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.412-253dupA | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29822716 | |||||||
| chr22:29822716 | CT | C | 14 | a0001c0001t0001g0208 a0001c0001t0001g0225 a0001c0001t0002g0132 others(11): Show |
14 | HG01099.hp1 HG01168.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.412-253delA | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29822716 | |||||||
| chr22:29822812 | G | A | 1 | a0001c0001t0001g0272 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.412-348C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29822812 | |||||||
| chr22:29823135 | T | G | 1 | a0001c0001t0014g0285 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.412-671A>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29823135 | |||||||
| chr22:29823337 | C | T | 111 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0015 others(108): Show |
126 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.412-873G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29823337 | |||||||
| chr22:29823426 | G | A | 44 | a0001c0001t0001g0014 a0001c0001t0001g0244 a0001c0001t0001g0245 others(41): Show |
45 | HG00558.hp2 HG00673.hp1 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.412-962C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29823426 | |||||||
| chr22:29823461 | A | T | 1 | a0004c0004t0001g0278 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.412-997T>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29823461 | |||||||
| chr22:29823556 | T | C | 11 | a0005c0005t0002g0005 a0005c0005t0002g0113 a0005c0005t0002g0114 others(8): Show |
13 | HG00099.hp2 HG01069.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.412-1092A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29823556 | |||||||
| chr22:29823613 | C | T | 26 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(23): Show |
26 | HG00423.hp1 HG01070.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.412-1149G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29823613 | |||||||
| chr22:29823617 | G | A | 3 | a0001c0001t0003g0322 a0001c0001t0003g0323 a0001c0001t0003g0324 |
3 | HG00642.hp2 HG01074.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.412-1153C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29823617 | |||||||
| chr22:29823621 | A | G | 3 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 |
3 | HG02622.hp1 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.412-1157T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29823621 | |||||||
| chr22:29823622 | C | T | 4 | a0007c0007t0004g0018 a0007c0007t0004g0035 a0007c0007t0004g0036 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.412-1158G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29823622 | |||||||
| chr22:29823715 | G | T | 4 | a0001c0001t0002g0012 a0001c0001t0002g0133 a0001c0001t0002g0134 others(1): Show |
5 | HG01192.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.412-1251C>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29823715 | |||||||
| chr22:29823766 | G | C | 2 | a0001c0013t0001g0274 a0015c0014t0001g0273 |
2 | HG03669.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.412-1302C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29823766 | |||||||
| chr22:29823899 | T | C | 2 | a0009c0009t0002g0123 a0009c0009t0002g0124 |
2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.411+1188A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29823899 | |||||||
| chr22:29824193 | A | G | 54 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(51): Show |
57 | HG00423.hp1 HG01070.hp1 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.411+894T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29824193 | |||||||
| chr22:29824201 | G | A | 175 | a0001c0001t0002g0012 a0001c0001t0002g0128 a0001c0001t0002g0129 others(172): Show |
194 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.411+886C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29824201 | |||||||
| chr22:29824207 | A | G | 6 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(3): Show |
6 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.411+880T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29824207 | |||||||
| chr22:29824251 | T | TAC | 21 | a0001c0001t0001g0203 a0001c0001t0001g0211 a0001c0001t0001g0225 others(18): Show |
22 | HG01168.hp1 HG01346.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.411+834_411+835dup others(2): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29824251 | |||||||
| chr22:29824251 | T | TACAC | 15 | a0001c0001t0001g0201 a0001c0001t0001g0209 a0001c0001t0001g0210 others(12): Show |
17 | HG00733.hp2 HG00738.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.411+832_411+835dup others(4): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29824251 | |||||||
| chr22:29824251 | TAC | T | 70 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0202 others(67): Show |
71 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.411+834_411+835del others(2): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29824251 | |||||||
| chr22:29824251 | TACAC | T | 74 | a0001c0001t0001g0014 a0001c0001t0001g0187 a0001c0001t0001g0188 others(71): Show |
75 | HG00558.hp2 HG00609.hp2 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.411+832_411+835del others(4): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29824251 | |||||||
| chr22:29824251 | TACACAC | T | 92 | a0001c0001t0002g0132 a0001c0001t0003g0001 a0001c0001t0003g0006 others(89): Show |
103 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.411+830_411+835del others(6): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29824251 | |||||||
| chr22:29824251 | TACACACA others(1): Show |
T | 27 | a0002c0002t0002g0008 a0002c0002t0002g0009 a0002c0002t0002g0010 others(24): Show |
33 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.411+828_411+835del others(8): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29824251 | |||||||
| chr22:29824251 | TACACACA others(3): Show |
T | 6 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 others(3): Show |
6 | HG02622.hp1 HG03130.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.411+826_411+835del others(10): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29824251 | |||||||
| chr22:29824251 | TACACACA others(11): Show |
T | 1 | a0001c0001t0003g0311 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.411+818_411+835del others(18): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29824251 | |||||||
| chr22:29824342 | T | C | 2 | a0002c0002t0002g0094 a0002c0002t0002g0096 |
2 | HG00673.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.411+745A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29824342 | |||||||
| chr22:29824435 | C | T | 4 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0131 others(1): Show |
4 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.411+652G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29824435 | |||||||
| chr22:29824571 | C | G | 26 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(23): Show |
26 | HG00423.hp1 HG01070.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.411+516G>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29824571 | |||||||
| chr22:29824576 | C | T | 1 | a0001c0001t0003g0329 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.411+511G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29824576 | |||||||
| chr22:29824606 | C | G | 1 | a0001c0001t0001g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.411+481G>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29824606 | |||||||
| chr22:29824689 | T | C | 2 | a0001c0001t0011g0286 a0001c0001t0011g0287 |
2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.411+398A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29824689 | |||||||
| chr22:29824743 | G | GA | 50 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(47): Show |
53 | HG00423.hp1 HG01070.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.411+343dupT | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29824743 | |||||||
| chr22:29824829 | A | C | 2 | a0001c0001t0001g0203 a0001c0001t0001g0211 |
2 | HG01346.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.411+258T>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29824829 | |||||||
| chr22:29824845 | C | T | 27 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(24): Show |
27 | HG00423.hp1 HG01070.hp1 HG01934.hp1 others(24): Show |
intron_variant | MODIFIER | c.411+242G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29824845 | |||||||
| chr22:29824867 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.411+220C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29824867 | |||||||
| chr22:29824936 | C | T | 26 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(23): Show |
26 | HG00423.hp1 HG01070.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.411+151G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 4/19 | chr22 | 29824936 | |||||||
| chr22:29825339 | C | T | 1 | a0004c0004t0005g0053 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.241-82G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 3/19 | chr22 | 29825339 | |||||||
| chr22:29825483 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.240+139G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 3/19 | chr22 | 29825483 | |||||||
| chr22:29825837 | T | A | 112 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0015 others(109): Show |
127 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.82-57A>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29825837 | |||||||
| chr22:29825940 | T | C | 1 | a0003c0003t0001g0177 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.82-160A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29825940 | |||||||
| chr22:29826270 | C | T | 5 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0130 others(2): Show |
5 | HG01496.hp1 HG01891.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-490G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29826270 | |||||||
| chr22:29826275 | T | A | 2 | a0008c0008t0001g0139 a0008c0008t0001g0142 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.82-495A>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29826275 | |||||||
| chr22:29826275 | TA | T | 6 | a0001c0001t0001g0235 a0001c0001t0002g0012 a0001c0001t0002g0128 others(3): Show |
7 | HG01099.hp1 HG01192.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-496delT | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29826275 | |||||||
| chr22:29826427 | C | T | 1 | a0002c0002t0002g0071 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.82-647G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29826427 | |||||||
| chr22:29826527 | T | A | 26 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(23): Show |
26 | HG00423.hp1 HG01070.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.82-747A>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29826527 | |||||||
| chr22:29826590 | T | G | 3 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 |
3 | HG02135.hp2 NA18979.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.82-810A>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29826590 | |||||||
| chr22:29826596 | C | T | 56 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(53): Show |
59 | HG00423.hp1 HG01070.hp1 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.82-816G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29826596 | |||||||
| chr22:29826689 | C | T | 54 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(51): Show |
57 | HG00423.hp1 HG01070.hp1 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.82-909G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29826689 | |||||||
| chr22:29826877 | C | T | 7 | a0003c0003t0001g0146 a0003c0003t0001g0149 a0003c0003t0001g0153 others(4): Show |
7 | HG02523.hp2 NA18957.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-1097G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29826877 | |||||||
| chr22:29826880 | G | A | 10 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0130 others(7): Show |
10 | HG00673.hp2 HG01496.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.82-1100C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29826880 | |||||||
| chr22:29826893 | C | T | 26 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(23): Show |
26 | HG00423.hp1 HG01070.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.82-1113G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29826893 | |||||||
| chr22:29827097 | C | CA | 121 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(118): Show |
132 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.82-1318dupT | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827097 | |||||||
| chr22:29827097 | C | CAA | 19 | a0001c0001t0001g0187 a0001c0001t0002g0126 a0001c0001t0002g0127 others(16): Show |
19 | HG01243.hp2 HG01358.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.82-1319_82-1318dup others(2): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827097 | |||||||
| chr22:29827097 | C | CAAA | 6 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(3): Show |
6 | HG01099.hp1 HG01884.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-1320_82-1318dup others(3): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827097 | |||||||
| chr22:29827097 | CA | C | 19 | a0001c0001t0001g0202 a0001c0001t0001g0254 a0001c0001t0001g0266 others(16): Show |
22 | HG00323.hp2 HG01169.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.82-1318delT | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827097 | |||||||
| chr22:29827147 | G | C | 1 | a0001c0001t0001g0237 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.82-1367C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827147 | |||||||
| chr22:29827150 | T | C | 1 | a0008c0008t0001g0141 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.82-1370A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827150 | |||||||
| chr22:29827158 | CCTT | C | 4 | a0007c0007t0004g0018 a0007c0007t0004g0035 a0007c0007t0004g0036 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-1381_82-1379del others(3): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827158 | |||||||
| chr22:29827595 | A | G | 7 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(4): Show |
7 | HG01070.hp1 HG02080.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-1815T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827595 | |||||||
| chr22:29827756 | C | CAACACAC others(5): Show |
1 | a0001c0001t0002g0129 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.82-1977_82-1976ins others(12): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827756 | |||||||
| chr22:29827756 | C | CAACACAC others(7): Show |
1 | a0001c0001t0002g0128 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.82-1977_82-1976ins others(14): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827756 | |||||||
| chr22:29827756 | C | CAACACAC others(9): Show |
2 | a0001c0001t0002g0131 a0001c0001t0002g0132 |
2 | HG01099.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.82-1977_82-1976ins others(16): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827756 | |||||||
| chr22:29827757 | G | C | 4 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0131 others(1): Show |
4 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-1977C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827757 | |||||||
| chr22:29827757 | G | GAC | 40 | a0001c0001t0001g0195 a0001c0001t0001g0228 a0001c0001t0001g0229 others(37): Show |
43 | HG01496.hp2 HG01515.hp2 HG01517.hp1 others(40): Show |
intron_variant | MODIFIER | c.82-1979_82-1978dup others(2): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827757 | |||||||
| chr22:29827757 | G | GACAC | 22 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(19): Show |
22 | HG00280.hp1 HG00609.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.82-1981_82-1978dup others(4): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827757 | |||||||
| chr22:29827757 | G | GACACAC | 115 | a0001c0001t0001g0014 a0001c0001t0001g0187 a0001c0001t0001g0245 others(112): Show |
134 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.82-1983_82-1978dup others(6): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827757 | |||||||
| chr22:29827757 | G | GACACACA others(1): Show |
31 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(28): Show |
31 | HG00323.hp2 HG00621.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.82-1985_82-1978dup others(8): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827757 | |||||||
| chr22:29827757 | G | GACACACA others(3): Show |
5 | a0001c0001t0002g0134 a0002c0002t0002g0098 a0002c0002t0002g0105 others(2): Show |
5 | HG02155.hp2 HG02976.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.82-1987_82-1978dup others(10): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827757 | |||||||
| chr22:29827757 | G | GACACACA others(5): Show |
3 | a0001c0001t0011g0287 a0002c0002t0002g0099 a0002c0002t0002g0100 |
3 | HG02559.hp2 NA18945.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.82-1989_82-1978dup others(12): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827757 | |||||||
| chr22:29827757 | G | GACACACA others(7): Show |
1 | a0001c0001t0002g0135 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.82-1991_82-1978dup others(14): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827757 | |||||||
| chr22:29827757 | GAC | G | 69 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(66): Show |
69 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.82-1979_82-1978del others(2): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827757 | |||||||
| chr22:29827807 | T | TCTC | 194 | a0001c0001t0002g0012 a0001c0001t0002g0126 a0001c0001t0002g0127 others(191): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.82-2028_82-2027ins others(3): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827807 | |||||||
| chr22:29827824 | C | T | 194 | a0001c0001t0002g0012 a0001c0001t0002g0126 a0001c0001t0002g0127 others(191): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.82-2044G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827824 | |||||||
| chr22:29827856 | G | GAC | 156 | a0001c0001t0001g0195 a0001c0001t0002g0133 a0001c0001t0002g0134 others(153): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.82-2078_82-2077dup others(2): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827856 | |||||||
| chr22:29827856 | GACAC | G | 4 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0009c0009t0002g0123 others(1): Show |
4 | HG02717.hp1 HG03139.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-2080_82-2077del others(4): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827856 | |||||||
| chr22:29827872 | C | A | 24 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0019 others(21): Show |
27 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.82-2092G>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827872 | |||||||
| chr22:29827899 | G | GAC | 103 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(100): Show |
108 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.82-2121_82-2120dup others(2): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827899 | |||||||
| chr22:29827899 | G | GACAC | 16 | a0001c0001t0002g0012 a0001c0001t0002g0126 a0001c0001t0002g0127 others(13): Show |
17 | HG01192.hp2 HG01496.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.82-2123_82-2120dup others(4): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827899 | |||||||
| chr22:29827899 | G | GACACACA others(3): Show |
1 | a0001c0001t0011g0286 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.82-2129_82-2120dup others(10): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827899 | |||||||
| chr22:29827899 | G | GACACACA others(13): Show |
1 | a0001c0001t0011g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.82-2139_82-2120dup others(20): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827899 | |||||||
| chr22:29827899 | GAC | G | 109 | a0001c0001t0001g0014 a0001c0001t0001g0195 a0001c0001t0001g0201 others(106): Show |
117 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.82-2121_82-2120del others(2): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827899 | |||||||
| chr22:29827899 | GACAC | G | 5 | a0001c0001t0001g0234 a0001c0001t0001g0249 a0001c0001t0001g0250 others(2): Show |
5 | HG00733.hp2 NA18956.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.82-2123_82-2120del others(4): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827899 | |||||||
| chr22:29827933 | G | A | 1 | a0002c0002t0002g0106 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.82-2153C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827933 | |||||||
| chr22:29827948 | G | GAC | 3 | a0003c0003t0001g0146 a0003c0003t0001g0181 a0003c0003t0001g0182 |
3 | HG02970.hp1 NA18957.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.82-2170_82-2169dup others(2): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827948 | |||||||
| chr22:29827948 | GAC | G | 81 | a0001c0001t0001g0014 a0001c0001t0001g0187 a0001c0001t0001g0188 others(78): Show |
82 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.82-2170_82-2169del others(2): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827948 | |||||||
| chr22:29827948 | GACACAC | G | 166 | a0001c0001t0001g0195 a0001c0001t0001g0198 a0001c0001t0002g0012 others(163): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.82-2174_82-2169del others(6): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827948 | |||||||
| chr22:29827948 | GACACACA others(1): Show |
G | 26 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0019 others(23): Show |
29 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.82-2176_82-2169del others(8): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827948 | |||||||
| chr22:29827948 | GACACACA others(3): Show |
G | 3 | a0001c0001t0003g0327 a0001c0001t0003g0328 a0001c0001t0003g0345 |
3 | NA18966.hp2 NA19003.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.82-2178_82-2169del others(10): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827948 | |||||||
| chr22:29827979 | A | C | 1 | a0001c0001t0011g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.82-2199T>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29827979 | |||||||
| chr22:29828002 | A | G | 298 | a0001c0001t0001g0014 a0001c0001t0001g0187 a0001c0001t0001g0188 others(295): Show |
320 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.82-2222T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29828002 | |||||||
| chr22:29828152 | G | A | 33 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(30): Show |
35 | HG00099.hp2 HG00423.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.82-2372C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29828152 | |||||||
| chr22:29828620 | T | A | 1 | a0002c0002t0002g0067 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.82-2840A>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29828620 | |||||||
| chr22:29828862 | G | C | 4 | a0007c0007t0004g0018 a0007c0007t0004g0035 a0007c0007t0004g0036 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-3082C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29828862 | |||||||
| chr22:29829138 | T | C | 44 | a0001c0001t0001g0014 a0001c0001t0001g0244 a0001c0001t0001g0245 others(41): Show |
45 | HG00558.hp2 HG00673.hp1 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.81+3107A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29829138 | |||||||
| chr22:29829385 | A | G | 26 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(23): Show |
26 | HG00423.hp1 HG01070.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.81+2860T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29829385 | |||||||
| chr22:29829518 | C | T | 4 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0131 others(1): Show |
4 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+2727G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29829518 | |||||||
| chr22:29829631 | G | A | 115 | a0001c0001t0002g0012 a0001c0001t0002g0133 a0001c0001t0002g0134 others(112): Show |
131 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.81+2614C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29829631 | |||||||
| chr22:29829700 | GA | G | 19 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0130 others(16): Show |
21 | HG00099.hp2 HG01069.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.81+2544delT | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29829700 | |||||||
| chr22:29829732 | G | A | 4 | a0001c0001t0002g0012 a0001c0001t0002g0133 a0001c0001t0002g0134 others(1): Show |
5 | HG01192.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+2513C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29829732 | |||||||
| chr22:29829849 | A | G | 6 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(3): Show |
6 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+2396T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29829849 | |||||||
| chr22:29829984 | A | G | 55 | a0001c0001t0002g0012 a0001c0001t0002g0136 a0001c0001t0002g0137 others(52): Show |
59 | HG00423.hp1 HG01070.hp1 HG01192.hp2 others(56): Show |
intron_variant | MODIFIER | c.81+2261T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29829984 | |||||||
| chr22:29830026 | A | G | 1 | a0001c0001t0011g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.81+2219T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29830026 | |||||||
| chr22:29830101 | A | C | 2 | a0001c0001t0011g0286 a0001c0001t0014g0285 |
2 | HG02145.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.81+2144T>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29830101 | |||||||
| chr22:29830269 | T | A | 1 | a0002c0002t0002g0067 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.81+1976A>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29830269 | |||||||
| chr22:29830275 | G | T | 1 | a0002c0002t0002g0067 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.81+1970C>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29830275 | |||||||
| chr22:29830393 | T | C | 1 | a0001c0001t0003g0326 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.81+1852A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29830393 | |||||||
| chr22:29830664 | C | T | 1 | a0003c0003t0001g0148 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.81+1581G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29830664 | |||||||
| chr22:29830858 | G | T | 1 | a0001c0001t0003g0308 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.81+1387C>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29830858 | |||||||
| chr22:29831047 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.81+1198C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29831047 | |||||||
| chr22:29831052 | T | C | 1 | a0007c0007t0004g0037 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.81+1193A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29831052 | |||||||
| chr22:29831150 | G | A | 4 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0131 others(1): Show |
4 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+1095C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29831150 | |||||||
| chr22:29831203 | T | C | 4 | a0001c0001t0002g0012 a0001c0001t0002g0133 a0001c0001t0002g0134 others(1): Show |
5 | HG01192.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+1042A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29831203 | |||||||
| chr22:29831295 | G | A | 4 | a0001c0001t0002g0012 a0001c0001t0002g0133 a0001c0001t0002g0134 others(1): Show |
5 | HG01192.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+950C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29831295 | |||||||
| chr22:29831457 | G | A | 14 | a0001c0001t0003g0006 a0001c0001t0003g0304 a0001c0001t0003g0327 others(11): Show |
16 | HG00544.hp2 HG02083.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.81+788C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29831457 | |||||||
| chr22:29831493 | G | T | 1 | a0001c0001t0003g0340 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.81+752C>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29831493 | |||||||
| chr22:29831533 | G | A | 4 | a0001c0001t0002g0012 a0001c0001t0002g0133 a0001c0001t0002g0134 others(1): Show |
5 | HG01192.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+712C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29831533 | |||||||
| chr22:29831636 | C | T | 1 | a0005c0005t0002g0122 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.81+609G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29831636 | |||||||
| chr22:29831665 | T | G | 1 | a0003c0003t0001g0182 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.81+580A>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29831665 | |||||||
| chr22:29831745 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.81+500G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29831745 | |||||||
| chr22:29831761 | C | T | 1 | a0001c0001t0003g0339 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.81+484G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29831761 | |||||||
| chr22:29831837 | A | G | 4 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0130 others(1): Show |
4 | HG01496.hp1 HG01891.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+408T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29831837 | |||||||
| chr22:29831935 | G | C | 1 | a0014c0016t0001g0231 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.81+310C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29831935 | |||||||
| chr22:29831946 | G | A | 1 | a0001c0001t0002g0012 | 2 | HG01192.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.81+299C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29831946 | |||||||
| chr22:29831962 | G | C | 23 | a0001c0001t0005g0048 a0001c0001t0005g0049 a0001c0001t0005g0050 others(20): Show |
23 | HG00423.hp1 HG01070.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.81+283C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29831962 | |||||||
| chr22:29831993 | T | G | 3 | a0001c0001t0011g0286 a0001c0001t0011g0287 a0001c0001t0014g0285 |
3 | HG02145.hp1 HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.81+252A>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29831993 | |||||||
| chr22:29832015 | G | C | 2 | a0002c0002t0002g0107 a0002c0002t0002g0108 |
2 | HG02735.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.81+230C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29832015 | |||||||
| chr22:29832077 | G | A | 1 | a0001c0001t0003g0335 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.81+168C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29832077 | |||||||
| chr22:29832238 | G | A | 2 | a0009c0009t0002g0123 a0009c0009t0002g0124 |
2 | HG03139.hp2 NA21309.hp2 |
splice_region_variant&intron_variant | LOW | c.81+7C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 2/19 | chr22 | 29832238 | |||||||
| chr22:29832587 | C | CT | 8 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0002g0128 others(5): Show |
8 | HG01099.hp1 HG01175.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-246dupA | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29832587 | |||||||
| chr22:29832617 | C | T | 24 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0019 others(21): Show |
27 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.-17-275G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29832617 | |||||||
| chr22:29832642 | G | C | 1 | a0001c0001t0003g0336 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-17-300C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29832642 | |||||||
| chr22:29832728 | A | G | 296 | a0001c0001t0001g0014 a0001c0001t0001g0187 a0001c0001t0001g0188 others(293): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.-17-386T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29832728 | |||||||
| chr22:29832863 | C | G | 4 | a0001c0001t0002g0012 a0001c0001t0002g0133 a0001c0001t0002g0134 others(1): Show |
5 | HG01192.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-521G>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29832863 | |||||||
| chr22:29833046 | G | A | 1 | a0001c0001t0004g0032 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-17-704C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29833046 | |||||||
| chr22:29833047 | C | T | 4 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0131 others(1): Show |
4 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-705G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29833047 | |||||||
| chr22:29833095 | A | C | 1 | a0001c0001t0003g0337 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-17-753T>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29833095 | |||||||
| chr22:29833195 | C | T | 24 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0019 others(21): Show |
27 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.-17-853G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29833195 | |||||||
| chr22:29833226 | G | A | 13 | a0005c0005t0002g0005 a0005c0005t0002g0113 a0005c0005t0002g0114 others(10): Show |
15 | HG00099.hp2 HG01069.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-17-884C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29833226 | |||||||
| chr22:29833319 | T | C | 1 | a0004c0004t0005g0059 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-17-977A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29833319 | |||||||
| chr22:29833410 | C | G | 291 | a0001c0001t0001g0014 a0001c0001t0001g0187 a0001c0001t0001g0188 others(288): Show |
313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.-17-1068G>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29833410 | |||||||
| chr22:29833410 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-17-1068G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29833410 | |||||||
| chr22:29833415 | T | C | 1 | a0001c0001t0002g0012 | 2 | HG01192.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-17-1073A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29833415 | |||||||
| chr22:29833420 | A | G | 1 | a0001c0001t0006g0288 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-17-1078T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29833420 | |||||||
| chr22:29833652 | C | T | 11 | a0005c0005t0002g0005 a0005c0005t0002g0113 a0005c0005t0002g0114 others(8): Show |
13 | HG00099.hp2 HG01069.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.-17-1310G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29833652 | |||||||
| chr22:29833739 | G | C | 1 | a0004c0004t0005g0047 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-17-1397C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29833739 | |||||||
| chr22:29833825 | G | C | 4 | a0007c0007t0004g0018 a0007c0007t0004g0035 a0007c0007t0004g0036 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-1483C>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29833825 | |||||||
| chr22:29833849 | T | C | 1 | a0005c0005t0002g0122 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-17-1507A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29833849 | |||||||
| chr22:29833879 | C | CT | 112 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0015 others(109): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.-17-1538dupA | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29833879 | |||||||
| chr22:29833879 | CT | C | 52 | a0001c0001t0001g0014 a0001c0001t0001g0232 a0001c0001t0001g0277 others(49): Show |
53 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.-17-1538delA | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29833879 | |||||||
| chr22:29833895 | T | A | 1 | a0001c0001t0001g0233 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-17-1553A>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29833895 | |||||||
| chr22:29833965 | T | C | 112 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(109): Show |
127 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.-17-1623A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29833965 | |||||||
| chr22:29833978 | A | T | 48 | a0003c0003t0001g0140 a0003c0003t0001g0143 a0003c0003t0001g0144 others(45): Show |
48 | HG00280.hp2 HG00597.hp2 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.-17-1636T>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29833978 | |||||||
| chr22:29834013 | T | C | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG00609.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-17-1671A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29834013 | |||||||
| chr22:29834324 | AGG | A | 4 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0130 others(1): Show |
4 | HG01496.hp1 HG01891.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-1984_-17-1983d others(4): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29834324 | |||||||
| chr22:29834667 | G | A | 4 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(1): Show |
4 | HG01884.hp2 HG02809.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-2325C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29834667 | |||||||
| chr22:29834827 | AAT | A | 51 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0019 others(48): Show |
54 | HG00423.hp1 HG01070.hp1 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.-17-2487_-17-2486d others(4): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29834827 | |||||||
| chr22:29834848 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-17-2506T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29834848 | |||||||
| chr22:29835160 | G | A | 17 | a0004c0004t0004g0034 a0004c0004t0005g0047 a0004c0004t0005g0053 others(14): Show |
17 | HG00423.hp1 HG01934.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-2818C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29835160 | |||||||
| chr22:29835181 | G | A | 1 | a0001c0001t0006g0288 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-17-2839C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29835181 | |||||||
| chr22:29835399 | A | C | 1 | a0001c0001t0001g0239 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-18+2779T>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29835399 | |||||||
| chr22:29835404 | TA | T | 7 | a0001c0001t0002g0136 a0001c0001t0003g0303 a0001c0001t0003g0304 others(4): Show |
7 | HG00099.hp1 HG00558.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+2773delT | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29835404 | |||||||
| chr22:29835412 | A | T | 1 | a0001c0001t0001g0239 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-18+2766T>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29835412 | |||||||
| chr22:29835420 | A | T | 54 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0019 others(51): Show |
57 | HG00423.hp1 HG01070.hp1 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.-18+2758T>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29835420 | |||||||
| chr22:29835458 | T | C | 6 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(3): Show |
6 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+2720A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29835458 | |||||||
| chr22:29835597 | A | T | 1 | a0001c0001t0001g0239 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-18+2581T>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29835597 | |||||||
| chr22:29835637 | T | A | 1 | a0001c0001t0001g0239 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-18+2541A>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29835637 | |||||||
| chr22:29835694 | A | G | 1 | a0003c0003t0001g0143 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-18+2484T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29835694 | |||||||
| chr22:29835859 | C | A | 2 | a0009c0009t0002g0123 a0009c0009t0002g0124 |
2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-18+2319G>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29835859 | |||||||
| chr22:29835926 | C | G | 3 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 |
3 | HG02622.hp1 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-18+2252G>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29835926 | |||||||
| chr22:29836035 | G | A | 54 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0019 others(51): Show |
57 | HG00423.hp1 HG01070.hp1 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.-18+2143C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29836035 | |||||||
| chr22:29836222 | G | A | 11 | a0005c0005t0002g0005 a0005c0005t0002g0113 a0005c0005t0002g0114 others(8): Show |
13 | HG00099.hp2 HG01069.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.-18+1956C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29836222 | |||||||
| chr22:29836365 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-18+1813C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29836365 | |||||||
| chr22:29836366 | C | T | 1 | a0002c0002t0002g0067 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-18+1812G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29836366 | |||||||
| chr22:29836379 | C | CA | 27 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 others(24): Show |
27 | HG00733.hp2 HG00735.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18+1798dupT | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29836379 | |||||||
| chr22:29836379 | C | CAA | 24 | a0001c0001t0002g0131 a0001c0001t0005g0048 a0001c0001t0005g0049 others(21): Show |
24 | HG01070.hp1 HG01978.hp1 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.-18+1797_-18+1798d others(4): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29836379 | |||||||
| chr22:29836379 | C | CAAA | 8 | a0001c0001t0005g0061 a0001c0001t0007g0042 a0001c0001t0007g0043 others(5): Show |
8 | HG00423.hp1 HG01891.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18+1796_-18+1798d others(5): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29836379 | |||||||
| chr22:29836379 | CA | C | 20 | a0001c0001t0002g0012 a0001c0001t0003g0302 a0001c0001t0004g0033 others(17): Show |
23 | HG00099.hp2 HG01069.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18+1798delT | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29836379 | |||||||
| chr22:29836379 | CAA | C | 17 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0019 others(14): Show |
20 | HG01243.hp1 HG01496.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-18+1797_-18+1798d others(4): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29836379 | |||||||
| chr22:29836379 | CAAAAA | C | 6 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 others(3): Show |
6 | HG02615.hp1 HG02622.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+1794_-18+1798d others(7): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29836379 | |||||||
| chr22:29836397 | A | G | 2 | a0009c0009t0002g0123 a0009c0009t0002g0124 |
2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-18+1781T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29836397 | |||||||
| chr22:29836532 | G | A | 4 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(1): Show |
4 | HG00438.hp2 NA18975.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+1646C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29836532 | |||||||
| chr22:29836648 | T | C | 339 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0187 others(336): Show |
362 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.-18+1530A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29836648 | |||||||
| chr22:29836686 | G | A | 1 | a0011c0012t0003g0346 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-18+1492C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29836686 | |||||||
| chr22:29836706 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-18+1472T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29836706 | |||||||
| chr22:29836709 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0245 a0001c0001t0001g0246 others(1): Show |
5 | HG01256.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+1469G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29836709 | |||||||
| chr22:29836854 | C | T | 115 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(112): Show |
130 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.-18+1324G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29836854 | |||||||
| chr22:29836913 | G | A | 51 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0019 others(48): Show |
54 | HG00423.hp1 HG01070.hp1 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.-18+1265C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29836913 | |||||||
| chr22:29836970 | A | G | 3 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 |
3 | HG02896.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-18+1208T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29836970 | |||||||
| chr22:29837052 | T | C | 24 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0019 others(21): Show |
27 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.-18+1126A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29837052 | |||||||
| chr22:29837174 | T | TAATCCCA others(30): Show |
1 | a0002c0002t0002g0110 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-18+967_-18+1003du others(38): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29837174 | |||||||
| chr22:29837234 | T | C | 23 | a0001c0001t0005g0048 a0001c0001t0005g0049 a0001c0001t0005g0050 others(20): Show |
23 | HG00423.hp1 HG01070.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.-18+944A>G | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29837234 | |||||||
| chr22:29837266 | C | T | 54 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0019 others(51): Show |
57 | HG00423.hp1 HG01070.hp1 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.-18+912G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29837266 | |||||||
| chr22:29837267 | GA | G | 270 | a0001c0001t0001g0014 a0001c0001t0001g0245 a0001c0001t0001g0246 others(267): Show |
290 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.-18+910delT | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29837267 | |||||||
| chr22:29837267 | GAA | G | 12 | a0001c0001t0001g0244 a0005c0005t0002g0005 a0005c0005t0002g0113 others(9): Show |
14 | HG00099.hp2 HG01069.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.-18+909_-18+910del others(2): Show |
ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29837267 | |||||||
| chr22:29837337 | G | A | 1 | a0001c0001t0002g0012 | 2 | HG01192.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-18+841C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29837337 | |||||||
| chr22:29837349 | C | T | 4 | a0001c0001t0011g0286 a0001c0001t0011g0287 a0001c0001t0014g0285 others(1): Show |
4 | HG00621.hp1 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+829G>A | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29837349 | |||||||
| chr22:29837438 | GA | G | 115 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(112): Show |
130 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.-18+739delT | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29837438 | |||||||
| chr22:29837457 | A | G | 294 | a0001c0001t0001g0014 a0001c0001t0001g0187 a0001c0001t0001g0188 others(291): Show |
316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.-18+721T>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29837457 | |||||||
| chr22:29837619 | C | G | 54 | a0001c0001t0004g0002 a0001c0001t0004g0007 a0001c0001t0004g0019 others(51): Show |
57 | HG00423.hp1 HG01070.hp1 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.-18+559G>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29837619 | |||||||
| chr22:29837690 | G | A | 44 | a0001c0001t0001g0014 a0001c0001t0001g0244 a0001c0001t0001g0245 others(41): Show |
45 | HG00558.hp2 HG00673.hp1 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.-18+488C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29837690 | |||||||
| chr22:29837750 | T | A | 4 | a0001c0001t0002g0012 a0001c0001t0002g0133 a0001c0001t0002g0134 others(1): Show |
5 | HG01192.hp2 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+428A>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29837750 | |||||||
| chr22:29837982 | G | A | 3 | a0007c0007t0004g0035 a0007c0007t0004g0036 a0007c0007t0004g0037 |
3 | HG02615.hp1 HG02895.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-18+196C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29837982 | |||||||
| chr22:29838027 | T | G | 1 | a0004c0004t0013g0065 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-18+151A>C | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29838027 | |||||||
| chr22:29838056 | G | A | 62 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(59): Show |
69 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.-18+122C>T | ASCC2 | ENSG00000100325.15 | transcript | ENST00000307790.8 | protein_coding | 1/19 | chr22 | 29838056 |