Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51455 |
| ensemblid | ENSG00000135945.10 |
| hgncid | 14060 |
| symbol | REV1 |
| name | REV1 DNA directed polymerase |
| refseq_nuc | NM_016316.4 |
| refseq_prot | NP_057400.1 |
| ensembl_nuc | ENST00000258428.8 |
| ensembl_prot | ENSP00000258428.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 99400477 |
| end | 99490017 |
| strand | - |
| ver | v1.2 |
| region | chr2:99400477-99490017 |
| region5000 | chr2:99395477-99495017 |
| regionname0 | REV1_chr2_99400477_99490017 |
| regionname5000 | REV1_chr2_99395477_99495017 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1251 | 98 | 18 | 29 | 44 | 2 | 5 | 37 | REV1_chr2_99395477_99495017 | REV1 | MRRGG others(1246): Show |
chr2 | 99395477 | 99495017 |
| a0002 | 1/1 | 1251 | 97 | 20 | 17 | 47 | 1 | 10 | 35 | REV1_chr2_99395477_99495017 | REV1 | MRRGG others(1246): Show |
chr2 | 99395477 | 99495017 |
| a0003 | 0/0 | 1251 | 68 | 27 | 16 | 13 | 4 | 8 | 10 | REV1_chr2_99395477_99495017 | REV1 | MRRGG others(1246): Show |
chr2 | 99395477 | 99495017 |
| a0004 | 0/0 | 1251 | 42 | 22 | 2 | 7 | 2 | 9 | 5 | REV1_chr2_99395477_99495017 | REV1 | MRRGG others(1246): Show |
chr2 | 99395477 | 99495017 |
| a0005 | 0/0 | 1251 | 10 | 0 | 10 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | MRRGG others(1246): Show |
chr2 | 99395477 | 99495017 |
| a0006 | 0/0 | 1251 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | REV1_chr2_99395477_99495017 | REV1 | MRRGG others(1246): Show |
chr2 | 99395477 | 99495017 |
| a0007 | 0/0 | 1251 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | MRRGG others(1246): Show |
chr2 | 99395477 | 99495017 |
| a0008 | 0/0 | 1251 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | MRRGG others(1246): Show |
chr2 | 99395477 | 99495017 |
| a0009 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | MRRGG others(1246): Show |
chr2 | 99395477 | 99495017 |
| a0010 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | MRRGG others(1246): Show |
chr2 | 99395477 | 99495017 |
| a0011 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | MRRGG others(1246): Show |
chr2 | 99395477 | 99495017 |
| a0012 | 0/0 | 1245 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | MRRGG others(1240): Show |
chr2 | 99395477 | 99495017 |
| a0013 | 0/0 | 1251 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | MRRGG others(1246): Show |
chr2 | 99395477 | 99495017 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3753 | 97 | 17 | 29 | 44 | 2 | 5 | REV1_chr2_99395477_99495017 | REV1 | ATGAG others(3748): Show |
chr2 | 99395477 | 99495017 | ||
| a0001c0015 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | ATGAG others(3748): Show |
chr2 | 99395477 | 99495017 | ||
| a0002c0002 | 1/1 | 3753 | 94 | 20 | 17 | 44 | 1 | 10 | REV1_chr2_99395477_99495017 | REV1 | ATGAG others(3748): Show |
chr2 | 99395477 | 99495017 | ||
| a0002c0007 | 0/0 | 3753 | 3 | 0 | 0 | 3 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | ATGAG others(3748): Show |
chr2 | 99395477 | 99495017 | ||
| a0003c0003 | 0/0 | 3753 | 62 | 23 | 15 | 12 | 4 | 8 | REV1_chr2_99395477_99495017 | REV1 | ATGAG others(3748): Show |
chr2 | 99395477 | 99495017 | ||
| a0003c0006 | 0/0 | 3753 | 3 | 3 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | ATGAG others(3748): Show |
chr2 | 99395477 | 99495017 | ||
| a0003c0010 | 0/0 | 3753 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | ATGAG others(3748): Show |
chr2 | 99395477 | 99495017 | ||
| a0003c0012 | 0/0 | 3753 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | ATGAG others(3748): Show |
chr2 | 99395477 | 99495017 | ||
| a0003c0013 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | ATGAG others(3748): Show |
chr2 | 99395477 | 99495017 | ||
| a0004c0004 | 0/0 | 3753 | 39 | 21 | 2 | 5 | 2 | 9 | REV1_chr2_99395477_99495017 | REV1 | ATGAG others(3748): Show |
chr2 | 99395477 | 99495017 | ||
| a0004c0008 | 0/0 | 3753 | 2 | 0 | 0 | 2 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | ATGAG others(3748): Show |
chr2 | 99395477 | 99495017 | ||
| a0004c0017 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | ATGAG others(3748): Show |
chr2 | 99395477 | 99495017 | ||
| a0005c0005 | 0/0 | 3753 | 10 | 0 | 10 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | ATGAG others(3748): Show |
chr2 | 99395477 | 99495017 | ||
| a0006c0009 | 0/0 | 3753 | 2 | 0 | 0 | 2 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | ATGAG others(3748): Show |
chr2 | 99395477 | 99495017 | ||
| a0007c0020 | 0/0 | 3753 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | ATGAG others(3748): Show |
chr2 | 99395477 | 99495017 | ||
| a0008c0014 | 0/0 | 3753 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | ATGAG others(3748): Show |
chr2 | 99395477 | 99495017 | ||
| a0009c0016 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | ATGAG others(3748): Show |
chr2 | 99395477 | 99495017 | ||
| a0010c0011 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | ATGAG others(3748): Show |
chr2 | 99395477 | 99495017 | ||
| a0011c0021 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | ATGAG others(3748): Show |
chr2 | 99395477 | 99495017 | ||
| a0012c0019 | 0/0 | 3735 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | ATGAG others(3730): Show |
chr2 | 99395477 | 99495017 | ||
| a0013c0018 | 0/0 | 3753 | 1 | 0 | 0 | 0 | 1 | 0 | REV1_chr2_99395477_99495017 | REV1 | ATGAG others(3748): Show |
chr2 | 99395477 | 99495017 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4731 | 50 | 11 | 12 | 22 | 1 | 4 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4726): Show |
chr2 | 99395477 | 99495017 |
| a0001c0001t0002 | 0/0 | 4727 | 43 | 5 | 17 | 19 | 1 | 1 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4722): Show |
chr2 | 99395477 | 99495017 |
| a0001c0001t0004 | 0/0 | 4727 | 3 | 0 | 0 | 3 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4722): Show |
chr2 | 99395477 | 99495017 |
| a0001c0001t0009 | 0/0 | 4727 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4722): Show |
chr2 | 99395477 | 99495017 |
| a0001c0015t0002 | 0/0 | 4727 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4722): Show |
chr2 | 99395477 | 99495017 |
| a0002c0002t0001 | 1/1 | 4731 | 63 | 18 | 11 | 24 | 1 | 7 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4726): Show |
chr2 | 99395477 | 99495017 |
| a0002c0002t0003 | 0/0 | 4731 | 28 | 1 | 6 | 19 | 0 | 2 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4726): Show |
chr2 | 99395477 | 99495017 |
| a0002c0002t0007 | 0/0 | 4731 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4726): Show |
chr2 | 99395477 | 99495017 |
| a0002c0002t0008 | 0/0 | 4731 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4726): Show |
chr2 | 99395477 | 99495017 |
| a0002c0002t0010 | 0/0 | 4731 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4726): Show |
chr2 | 99395477 | 99495017 |
| a0002c0007t0001 | 0/0 | 4731 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4726): Show |
chr2 | 99395477 | 99495017 |
| a0002c0007t0002 | 0/0 | 4727 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4722): Show |
chr2 | 99395477 | 99495017 |
| a0002c0007t0004 | 0/0 | 4727 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4722): Show |
chr2 | 99395477 | 99495017 |
| a0003c0003t0001 | 0/0 | 4731 | 57 | 23 | 15 | 7 | 4 | 8 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4726): Show |
chr2 | 99395477 | 99495017 |
| a0003c0003t0003 | 0/0 | 4731 | 5 | 0 | 0 | 5 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4726): Show |
chr2 | 99395477 | 99495017 |
| a0003c0006t0001 | 0/0 | 4731 | 3 | 3 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4726): Show |
chr2 | 99395477 | 99495017 |
| a0003c0010t0001 | 0/0 | 4731 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4726): Show |
chr2 | 99395477 | 99495017 |
| a0003c0012t0001 | 0/0 | 4731 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4726): Show |
chr2 | 99395477 | 99495017 |
| a0003c0013t0006 | 0/0 | 4731 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4726): Show |
chr2 | 99395477 | 99495017 |
| a0004c0004t0001 | 0/0 | 4731 | 38 | 21 | 2 | 5 | 2 | 8 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4726): Show |
chr2 | 99395477 | 99495017 |
| a0004c0004t0005 | 0/0 | 4731 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4726): Show |
chr2 | 99395477 | 99495017 |
| a0004c0008t0001 | 0/0 | 4731 | 2 | 0 | 0 | 2 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4726): Show |
chr2 | 99395477 | 99495017 |
| a0004c0017t0001 | 0/0 | 4731 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4726): Show |
chr2 | 99395477 | 99495017 |
| a0005c0005t0001 | 0/0 | 4731 | 10 | 0 | 10 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4726): Show |
chr2 | 99395477 | 99495017 |
| a0006c0009t0001 | 0/0 | 4731 | 2 | 0 | 0 | 2 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4726): Show |
chr2 | 99395477 | 99495017 |
| a0007c0020t0001 | 0/0 | 4731 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4726): Show |
chr2 | 99395477 | 99495017 |
| a0008c0014t0001 | 0/0 | 4731 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4726): Show |
chr2 | 99395477 | 99495017 |
| a0009c0016t0001 | 0/0 | 4731 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4726): Show |
chr2 | 99395477 | 99495017 |
| a0010c0011t0001 | 0/0 | 4731 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4726): Show |
chr2 | 99395477 | 99495017 |
| a0011c0021t0001 | 0/0 | 4731 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4726): Show |
chr2 | 99395477 | 99495017 |
| a0012c0019t0001 | 0/0 | 4713 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4708): Show |
chr2 | 99395477 | 99495017 |
| a0013c0018t0001 | 0/0 | 4731 | 1 | 0 | 0 | 0 | 1 | 0 | REV1_chr2_99395477_99495017 | REV1 | GAGCC others(4726): Show |
chr2 | 99395477 | 99495017 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0001t0009g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0001c0015t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0052 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0221 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0003g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0007g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0008g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0002t0010g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0007t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0007t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0002c0007t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0003t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0006t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0006t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0006t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0010t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0012t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0003c0013t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0004t0005g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0008t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0008t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0004c0017t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0005c0005t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0005c0005t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0005c0005t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0005c0005t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0005c0005t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0005c0005t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0005c0005t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0005c0005t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0005c0005t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0005c0005t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0006c0009t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0006c0009t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0007c0020t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0008c0014t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0009c0016t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0010c0011t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0011c0021t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0012c0019t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| a0013c0018t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0003 | c0003 | t0001 | g0102 | EUR | GBR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0135 | EUR | GBR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG00280 | hp1 | a0003 | c0003 | t0001 | g0076 | EUR | FIN | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG00280 | hp2 | a0004 | c0004 | t0001 | g0046 | EUR | FIN | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0246 | EAS | CHS | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | CHS | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG00544 | hp1 | a0003 | c0003 | t0001 | g0056 | EAS | CHS | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG00544 | hp2 | a0002 | c0002 | t0003 | g0225 | EAS | CHS | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG00558 | hp1 | a0002 | c0002 | t0003 | g0284 | EAS | CHS | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0262 | EAS | CHS | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG00609 | hp1 | a0003 | c0003 | t0001 | g0087 | EAS | CHS | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0256 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG00642 | hp2 | a0003 | c0003 | t0001 | g0119 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG00733 | hp2 | a0003 | c0003 | t0001 | g0101 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG00735 | hp2 | a0003 | c0003 | t0001 | g0081 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0240 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG00741 | hp2 | a0003 | c0003 | t0001 | g0065 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01070 | hp1 | a0005 | c0005 | t0001 | g0073 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01071 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01074 | hp1 | a0002 | c0002 | t0003 | g0230 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01074 | hp2 | a0007 | c0020 | t0001 | g0239 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0265 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01099 | hp2 | a0003 | c0003 | t0001 | g0055 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01106 | hp2 | a0003 | c0003 | t0001 | g0068 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01109 | hp1 | a0003 | c0003 | t0001 | g0211 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01168 | hp1 | a0004 | c0004 | t0001 | g0027 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01168 | hp2 | a0003 | c0003 | t0001 | g0054 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01175 | hp1 | a0003 | c0003 | t0001 | g0069 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0258 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01192 | hp1 | a0002 | c0002 | t0003 | g0254 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01243 | hp1 | a0003 | c0010 | t0001 | g0107 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PUR | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0311 | AMR | CLM | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01256 | hp1 | a0003 | c0003 | t0001 | g0064 | AMR | CLM | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01256 | hp2 | a0002 | c0002 | t0003 | g0274 | AMR | CLM | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01258 | hp1 | a0003 | c0003 | t0001 | g0070 | AMR | CLM | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01258 | hp2 | a0002 | c0002 | t0003 | g0275 | AMR | CLM | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0227 | AMR | CLM | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01261 | hp2 | a0003 | c0003 | t0001 | g0061 | AMR | CLM | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0234 | AMR | CLM | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01358 | hp1 | a0004 | c0004 | t0001 | g0036 | AMR | CLM | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | CLM | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01361 | hp2 | a0003 | c0003 | t0001 | g0122 | AMR | CLM | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | CLM | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | CLM | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01516 | hp1 | a0004 | c0004 | t0001 | g0014 | EUR | IBS | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0297 | EUR | IBS | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01884 | hp1 | a0009 | c0016 | t0001 | g0053 | AFR | ACB | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01884 | hp2 | a0002 | c0002 | t0010 | g0318 | AFR | ACB | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01891 | hp1 | a0004 | c0004 | t0001 | g0037 | AFR | ACB | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01891 | hp2 | a0003 | c0003 | t0001 | g0127 | AFR | ACB | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0304 | AMR | PEL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01934 | hp2 | a0005 | c0005 | t0001 | g0080 | AMR | PEL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01943 | hp1 | a0005 | c0005 | t0001 | g0071 | AMR | PEL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0138 | AMR | PEL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | PEL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01952 | hp2 | a0005 | c0005 | t0001 | g0078 | AMR | PEL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0224 | AMR | PEL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PEL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0238 | AMR | PEL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01978 | hp2 | a0005 | c0005 | t0001 | g0072 | AMR | PEL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01981 | hp1 | a0002 | c0002 | t0003 | g0242 | AMR | PEL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0185 | AMR | PEL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | PEL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01993 | hp2 | a0005 | c0005 | t0001 | g0074 | AMR | PEL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | PEL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02004 | hp2 | a0005 | c0005 | t0001 | g0075 | AMR | PEL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02027 | hp1 | a0004 | c0004 | t0001 | g0040 | EAS | KHV | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02027 | hp2 | a0002 | c0002 | t0003 | g0300 | EAS | KHV | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02040 | hp2 | a0002 | c0002 | t0003 | g0282 | EAS | KHV | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02055 | hp1 | a0003 | c0003 | t0001 | g0114 | AFR | ACB | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02055 | hp2 | a0010 | c0011 | t0001 | g0113 | AFR | ACB | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02083 | hp2 | a0002 | c0002 | t0003 | g0293 | EAS | KHV | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0302 | EAS | KHV | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02135 | hp2 | a0004 | c0004 | t0001 | g0010 | EAS | KHV | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0295 | AFR | ACB | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02145 | hp2 | a0004 | c0004 | t0001 | g0018 | AFR | ACB | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02148 | hp1 | a0003 | c0003 | t0001 | g0104 | AMR | PEL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02148 | hp2 | a0005 | c0005 | t0001 | g0097 | AMR | PEL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02155 | hp1 | a0003 | c0012 | t0001 | g0095 | EAS | CDX | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0270 | EAS | CDX | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | CDX | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CDX | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02257 | hp1 | a0004 | c0004 | t0001 | g0043 | AFR | ACB | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02257 | hp2 | a0003 | c0003 | t0001 | g0123 | AFR | ACB | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0308 | AFR | ACB | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02258 | hp2 | a0003 | c0003 | t0001 | g0060 | AFR | ACB | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0248 | AMR | PEL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02280 | hp1 | a0011 | c0021 | t0001 | g0309 | AFR | ACB | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02280 | hp2 | a0003 | c0003 | t0001 | g0002 | AFR | ACB | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | PEL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02293 | hp2 | a0005 | c0005 | t0001 | g0057 | AMR | PEL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02300 | hp2 | a0005 | c0005 | t0001 | g0086 | AMR | PEL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02451 | hp1 | a0004 | c0004 | t0001 | g0012 | AFR | ACB | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0305 | AFR | ACB | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0259 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02615 | hp1 | a0004 | c0004 | t0001 | g0024 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02615 | hp2 | a0003 | c0003 | t0001 | g0116 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02622 | hp1 | a0004 | c0004 | t0001 | g0017 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02622 | hp2 | a0004 | c0004 | t0001 | g0021 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02630 | hp1 | a0004 | c0004 | t0001 | g0011 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0219 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02647 | hp2 | a0004 | c0004 | t0001 | g0042 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02683 | hp1 | a0004 | c0004 | t0005 | g0007 | SAS | PJL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02683 | hp2 | a0003 | c0003 | t0001 | g0059 | SAS | PJL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02698 | hp1 | a0003 | c0003 | t0001 | g0067 | SAS | PJL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0243 | SAS | PJL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0241 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02723 | hp1 | a0004 | c0004 | t0001 | g0050 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02723 | hp2 | a0003 | c0003 | t0001 | g0118 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02735 | hp1 | a0003 | c0003 | t0001 | g0058 | SAS | PJL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0310 | SAS | PJL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0233 | SAS | PJL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02809 | hp1 | a0003 | c0006 | t0001 | g0209 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02818 | hp2 | a0004 | c0004 | t0001 | g0022 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0278 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02886 | hp2 | a0004 | c0004 | t0001 | g0019 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02895 | hp1 | a0003 | c0006 | t0001 | g0208 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02895 | hp2 | a0003 | c0003 | t0001 | g0099 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02897 | hp2 | a0003 | c0003 | t0001 | g0100 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02922 | hp1 | a0004 | c0004 | t0001 | g0023 | AFR | ESN | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02922 | hp2 | a0003 | c0003 | t0001 | g0002 | AFR | ESN | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0276 | AFR | ESN | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | ESN | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0214 | AFR | ESN | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0294 | AFR | ESN | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02976 | hp1 | a0003 | c0006 | t0001 | g0210 | AFR | ESN | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0226 | AFR | ESN | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03017 | hp1 | a0004 | c0004 | t0001 | g0030 | SAS | PJL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03017 | hp2 | a0002 | c0002 | t0007 | g0249 | SAS | PJL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03041 | hp1 | a0003 | c0003 | t0001 | g0198 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03098 | hp1 | a0003 | c0003 | t0001 | g0103 | AFR | MSL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03098 | hp2 | a0003 | c0003 | t0001 | g0120 | AFR | MSL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03130 | hp1 | a0004 | c0004 | t0001 | g0013 | AFR | ESN | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03130 | hp2 | a0003 | c0003 | t0001 | g0084 | AFR | ESN | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03209 | hp1 | a0003 | c0003 | t0001 | g0121 | AFR | MSL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0218 | AFR | MSL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03225 | hp1 | a0004 | c0004 | t0001 | g0048 | AFR | MSL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03225 | hp2 | a0004 | c0004 | t0001 | g0044 | AFR | MSL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03239 | hp1 | a0004 | c0004 | t0001 | g0015 | SAS | PJL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03239 | hp2 | a0003 | c0003 | t0001 | g0096 | SAS | PJL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | MSL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03453 | hp2 | a0004 | c0004 | t0001 | g0020 | AFR | MSL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03486 | hp1 | a0003 | c0003 | t0001 | g0124 | AFR | MSL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0213 | AFR | MSL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03490 | hp1 | a0004 | c0004 | t0001 | g0029 | SAS | PJL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03490 | hp2 | a0002 | c0002 | t0003 | g0223 | SAS | PJL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03491 | hp1 | a0004 | c0004 | t0001 | g0033 | SAS | PJL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0267 | SAS | PJL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03516 | hp1 | a0003 | c0013 | t0006 | g0128 | AFR | ESN | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0273 | AFR | ESN | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03540 | hp1 | a0004 | c0004 | t0001 | g0025 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0217 | AFR | GWD | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | MSL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03579 | hp2 | a0004 | c0004 | t0001 | g0016 | AFR | MSL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03669 | hp1 | a0004 | c0004 | t0001 | g0047 | SAS | PJL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03669 | hp2 | a0003 | c0003 | t0001 | g0094 | SAS | PJL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03688 | hp1 | a0003 | c0003 | t0001 | g0001 | SAS | STU | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0279 | SAS | STU | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03710 | hp1 | a0003 | c0003 | t0001 | g0079 | SAS | PJL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0232 | SAS | PJL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03834 | hp2 | a0003 | c0003 | t0001 | g0062 | SAS | BEB | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0220 | SAS | BEB | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0147 | SAS | BEB | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG04184 | hp2 | a0004 | c0004 | t0001 | g0031 | SAS | BEB | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG04199 | hp1 | a0002 | c0002 | t0003 | g0222 | SAS | STU | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG04199 | hp2 | a0004 | c0004 | t0001 | g0032 | SAS | STU | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18522 | hp1 | a0003 | c0003 | t0001 | g0082 | AFR | YRI | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | YRI | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0269 | EAS | CHB | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | CHB | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18906 | hp1 | a0003 | c0003 | t0001 | g0115 | AFR | YRI | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | YRI | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18939 | hp1 | a0002 | c0002 | t0003 | g0303 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18939 | hp2 | a0003 | c0003 | t0003 | g0090 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18941 | hp1 | a0003 | c0003 | t0003 | g0089 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0149 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0237 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18945 | hp2 | a0003 | c0003 | t0003 | g0088 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18947 | hp2 | a0002 | c0002 | t0003 | g0288 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18948 | hp1 | a0002 | c0002 | t0003 | g0228 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18950 | hp2 | a0002 | c0002 | t0003 | g0229 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0251 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18952 | hp1 | a0002 | c0002 | t0003 | g0260 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18954 | hp1 | a0003 | c0003 | t0003 | g0092 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18960 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18962 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18962 | hp2 | a0006 | c0009 | t0001 | g0255 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18964 | hp2 | a0006 | c0009 | t0001 | g0250 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0244 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0283 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18971 | hp2 | a0004 | c0004 | t0001 | g0009 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18972 | hp1 | a0002 | c0002 | t0003 | g0280 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18979 | hp1 | a0012 | c0019 | t0001 | g0272 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18979 | hp2 | a0004 | c0004 | t0001 | g0028 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18988 | hp2 | a0002 | c0002 | t0003 | g0307 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18989 | hp1 | a0004 | c0004 | t0001 | g0035 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18989 | hp2 | a0003 | c0003 | t0001 | g0091 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18990 | hp1 | a0002 | c0002 | t0003 | g0285 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18991 | hp2 | a0002 | c0002 | t0003 | g0298 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18998 | hp1 | a0004 | c0008 | t0001 | g0041 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19002 | hp1 | a0002 | c0002 | t0003 | g0292 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19002 | hp2 | a0002 | c0007 | t0002 | g0247 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19005 | hp1 | a0002 | c0002 | t0003 | g0291 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19006 | hp1 | a0003 | c0003 | t0001 | g0077 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0137 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19030 | hp1 | a0004 | c0004 | t0001 | g0026 | AFR | LWK | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19030 | hp2 | a0001 | c0001 | t0009 | g0199 | AFR | LWK | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19043 | hp1 | a0003 | c0003 | t0001 | g0117 | AFR | LWK | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19043 | hp2 | a0003 | c0003 | t0001 | g0083 | AFR | LWK | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19060 | hp1 | a0002 | c0002 | t0003 | g0268 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19081 | hp2 | a0002 | c0002 | t0003 | g0287 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19084 | hp2 | a0003 | c0003 | t0001 | g0098 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19086 | hp1 | a0003 | c0003 | t0003 | g0093 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19086 | hp2 | a0002 | c0007 | t0001 | g0245 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0146 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19088 | hp2 | a0002 | c0002 | t0003 | g0289 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19090 | hp1 | a0002 | c0007 | t0004 | g0286 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19091 | hp1 | a0004 | c0008 | t0001 | g0038 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19091 | hp2 | a0002 | c0002 | t0008 | g0290 | EAS | JPT | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0216 | AFR | YRI | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA19240 | hp2 | a0001 | c0015 | t0002 | g0201 | AFR | YRI | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA20129 | hp1 | a0003 | c0003 | t0001 | g0085 | AFR | ASW | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA20129 | hp2 | a0004 | c0017 | t0001 | g0039 | AFR | ASW | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | TSI | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA20752 | hp2 | a0003 | c0003 | t0001 | g0063 | EUR | TSI | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA20805 | hp1 | a0003 | c0003 | t0001 | g0066 | EUR | TSI | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA20805 | hp2 | a0013 | c0018 | t0001 | g0045 | EUR | TSI | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | GIH | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| NA20905 | hp2 | a0004 | c0004 | t0001 | g0034 | SAS | GIH | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01123 | hp1 | a0002 | c0002 | t0003 | g0281 | AMR | CLM | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG01123 | hp2 | a0008 | c0014 | t0001 | g0125 | AMR | CLM | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02109 | hp1 | a0003 | c0003 | t0001 | g0126 | AFR | ACB | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0215 | AFR | ACB | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02486 | hp1 | a0002 | c0002 | t0003 | g0299 | AFR | ACB | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG02486 | hp2 | a0004 | c0004 | t0001 | g0049 | AFR | ACB | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03471 | hp1 | a0003 | c0003 | t0001 | g0207 | AFR | MSL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | MSL | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0296 | AFR | USA | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | USA | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0052 | REF | REF | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0221 | REF | REF | REV1_chr2_99395477_99495017 | REV1 | chr2 | 99395477 | 99495017 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:99402793 | A | T | 1 | a0007 | 1 | HG01074.hp2 | missense_variant | MODERATE | c.3392T>A | p.Leu1131His | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 21/23 | 3603/4731 | 3392/3756 | 1131/1251 | chr2 | 99402793 | |||
| chr2:99402968 | A | G | 1 | a0010 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.3305T>C | p.Leu1102Pro | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 20/23 | 3516/4731 | 3305/3756 | 1102/1251 | chr2 | 99402968 | |||
| chr2:99404482 | C | T | 1 | a0005 | 10 | HG01070.hp1 HG01934.hp2 HG01943.hp1 others(7): Show |
missense_variant | MODERATE | c.3007G>A | p.Ala1003Thr | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 18/23 | 3218/4731 | 3007/3756 | 1003/1251 | chr2 | 99404482 | |||
| chr2:99405959 | C | A | 1 | a0008 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.2762G>T | p.Ser921Ile | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 17/23 | 2973/4731 | 2762/3756 | 921/1251 | chr2 | 99405959 | |||
| chr2:99406016 | G | T | 1 | a0009 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.2705C>A | p.Pro902His | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 17/23 | 2916/4731 | 2705/3756 | 902/1251 | chr2 | 99406016 | |||
| chr2:99406017 | G | A | 1 | a0009 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.2704C>T | p.Pro902Ser | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 17/23 | 2915/4731 | 2704/3756 | 902/1251 | chr2 | 99406017 | |||
| chr2:99412792 | C | T | 1 | a0006 | 2 | NA18962.hp2 NA18964.hp2 |
missense_variant | MODERATE | c.2111G>A | p.Arg704Gln | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/23 | 2322/4731 | 2111/3756 | 704/1251 | chr2 | 99412792 | |||
| chr2:99438696 | T | C | 2 | a0004 a0013 |
43 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(40): Show |
missense_variant | MODERATE | c.1118A>G | p.Asn373Ser | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/23 | 1329/4731 | 1118/3756 | 373/1251 | chr2 | 99438696 | |||
| chr2:99438946 | G | A | 1 | a0013 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.868C>T | p.Arg290Trp | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/23 | 1079/4731 | 868/3756 | 290/1251 | chr2 | 99438946 | |||
| chr2:99438988 | GAGTGCAG others(11): Show |
G | 1 | a0012 | 1 | NA18979.hp1 | conservative_inframe_deletion | MODERATE | c.808_825delGATTTCAG others(10): Show |
p.Asp270_Thr275del | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/23 | 1036/4731 | 808/3756 | 270/1251 | chr2 | 99438988 | |||
| chr2:99439044 | A | G | 8 | a0001 a0003 a0004 others(5): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
missense_variant | MODERATE | c.770T>C | p.Phe257Ser | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/23 | 981/4731 | 770/3756 | 257/1251 | chr2 | 99439044 | |||
| chr2:99442408 | C | T | 4 | a0003 a0005 a0008 others(1): Show |
80 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(77): Show |
missense_variant | MODERATE | c.412G>A | p.Val138Met | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/23 | 623/4731 | 412/3756 | 138/1251 | chr2 | 99442408 | |||
| chr2:99464953 | T | C | 1 | a0011 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.23A>G | p.Lys8Arg | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 2/23 | 234/4731 | 23/3756 | 8/1251 | chr2 | 99464953 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:99402928 | C | A | 2 | a0003c0006 a0003c0010 |
4 | HG01243.hp1 HG02809.hp1 HG02895.hp1 others(1): Show |
synonymous_variant | LOW | c.3345G>T | p.Gly1115Gly | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 20/23 | 3556/4731 | 3345/3756 | 1115/1251 | chr2 | 99402928 | |||
| chr2:99403033 | A | G | 15 | a0001c0001 a0001c0015 a0002c0007 others(12): Show |
224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
synonymous_variant | LOW | c.3240T>C | p.Ile1080Ile | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 20/23 | 3451/4731 | 3240/3756 | 1080/1251 | chr2 | 99403033 | |||
| chr2:99404456 | T | C | 1 | a0003c0013 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.3033A>G | p.Pro1011Pro | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 18/23 | 3244/4731 | 3033/3756 | 1011/1251 | chr2 | 99404456 | |||
| chr2:99404492 | C | T | 1 | a0004c0008 | 2 | NA18998.hp1 NA19091.hp1 |
synonymous_variant | LOW | c.2997G>A | p.Ser999Ser | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 18/23 | 3208/4731 | 2997/3756 | 999/1251 | chr2 | 99404492 | |||
| chr2:99421614 | C | T | 2 | a0003c0006 a0003c0010 |
4 | HG01243.hp1 HG02809.hp1 HG02895.hp1 others(1): Show |
synonymous_variant | LOW | c.1716G>A | p.Ala572Ala | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/23 | 1927/4731 | 1716/3756 | 572/1251 | chr2 | 99421614 | |||
| chr2:99429863 | A | G | 1 | a0003c0006 | 3 | HG02809.hp1 HG02895.hp1 HG02976.hp1 |
synonymous_variant | LOW | c.1524T>C | p.Ile508Ile | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/23 | 1735/4731 | 1524/3756 | 508/1251 | chr2 | 99429863 | |||
| chr2:99429905 | C | T | 1 | a0001c0015 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.1482G>A | p.Ala494Ala | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/23 | 1693/4731 | 1482/3756 | 494/1251 | chr2 | 99429905 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:99400611 | A | C | 3 | a0002c0002t0003 a0002c0002t0008 a0003c0003t0003 |
34 | HG00544.hp2 HG00558.hp1 HG01074.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*630T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 23/23 | 630 | chr2 | 99400611 | ||||||
| chr2:99400718 | T | A | 1 | a0002c0002t0007 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*523A>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 23/23 | 523 | chr2 | 99400718 | ||||||
| chr2:99400812 | C | T | 1 | a0003c0013t0006 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*429G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 23/23 | 429 | chr2 | 99400812 | ||||||
| chr2:99400820 | G | A | 1 | a0002c0002t0008 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*421C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 23/23 | 421 | chr2 | 99400820 | ||||||
| chr2:99401051 | ATAAT | A | 6 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0009 others(3): Show |
50 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*186_*189delATTA | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 23/23 | 186 | chr2 | 99401051 | ||||||
| chr2:99401082 | G | A | 2 | a0001c0001t0004 a0002c0007t0004 |
4 | NA18941.hp2 NA19010.hp2 NA19088.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*159C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 23/23 | 159 | chr2 | 99401082 | ||||||
| chr2:99401210 | T | C | 1 | a0001c0001t0009 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*31A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 23/23 | 31 | chr2 | 99401210 | ||||||
| chr2:99489943 | A | G | 1 | a0004c0004t0005 | 1 | HG02683.hp1 | 5_prime_UTR_variant | MODIFIER | c.-137T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/23 | 24968 | chr2 | 99489943 | ||||||
| chr2:99489962 | G | A | 1 | a0002c0002t0010 | 1 | HG01884.hp2 | 5_prime_UTR_variant | MODIFIER | c.-156C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/23 | 24987 | chr2 | 99489962 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:99401405 | A | G | 13 | a0001c0001t0001g0174 a0003c0003t0001g0114 a0003c0003t0001g0115 others(10): Show |
13 | HG00642.hp2 HG01123.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.3645-53T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 22/22 | chr2 | 99401405 | |||||||
| chr2:99401443 | C | CAA | 46 | a0003c0003t0001g0120 a0003c0003t0001g0126 a0003c0003t0001g0127 others(43): Show |
46 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(43): Show |
intron_variant | MODIFIER | c.3645-93_3645-92dup others(2): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 22/22 | chr2 | 99401443 | |||||||
| chr2:99401575 | C | T | 12 | a0003c0003t0001g0114 a0003c0003t0001g0115 a0003c0003t0001g0116 others(9): Show |
12 | HG00642.hp2 HG01123.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.3645-223G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 22/22 | chr2 | 99401575 | |||||||
| chr2:99401576 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3645-224C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 22/22 | chr2 | 99401576 | |||||||
| chr2:99401613 | G | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.3645-261C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 22/22 | chr2 | 99401613 | |||||||
| chr2:99401632 | A | G | 1 | a0002c0002t0001g0265 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3645-280T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 22/22 | chr2 | 99401632 | |||||||
| chr2:99401725 | C | T | 1 | a0010c0011t0001g0113 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3645-373G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 22/22 | chr2 | 99401725 | |||||||
| chr2:99401808 | G | A | 53 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(50): Show |
53 | HG00280.hp2 HG01168.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.3644+436C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 22/22 | chr2 | 99401808 | |||||||
| chr2:99401808 | G | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.3644+436C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 22/22 | chr2 | 99401808 | |||||||
| chr2:99401841 | G | A | 69 | a0001c0001t0001g0196 a0003c0003t0001g0001 a0003c0003t0001g0002 others(66): Show |
72 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.3644+403C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 22/22 | chr2 | 99401841 | |||||||
| chr2:99401895 | A | AC | 214 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(211): Show |
220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.3644+348dupG | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 22/22 | chr2 | 99401895 | |||||||
| chr2:99401974 | T | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.3644+270A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 22/22 | chr2 | 99401974 | |||||||
| chr2:99402076 | T | C | 1 | a0001c0001t0001g0176 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3644+168A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 22/22 | chr2 | 99402076 | |||||||
| chr2:99402173 | A | C | 1 | a0001c0001t0001g0109 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.3644+71T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 22/22 | chr2 | 99402173 | |||||||
| chr2:99402447 | A | G | 2 | a0002c0002t0001g0251 a0002c0002t0001g0257 |
2 | NA18951.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.3542-101T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 21/22 | chr2 | 99402447 | |||||||
| chr2:99402596 | AGAC | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.3541+45_3541+47del others(3): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 21/22 | chr2 | 99402596 | |||||||
| chr2:99402820 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3385-20A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 20/22 | chr2 | 99402820 | |||||||
| chr2:99403149 | TG | T | 162 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(159): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.3167-44delC | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 19/22 | chr2 | 99403149 | |||||||
| chr2:99403282 | T | C | 3 | a0003c0006t0001g0208 a0003c0006t0001g0209 a0003c0006t0001g0210 |
3 | HG02809.hp1 HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3167-176A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 19/22 | chr2 | 99403282 | |||||||
| chr2:99403361 | G | T | 1 | a0001c0001t0001g0152 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3167-255C>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 19/22 | chr2 | 99403361 | |||||||
| chr2:99403426 | A | G | 1 | a0002c0002t0001g0238 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.3166+269T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 19/22 | chr2 | 99403426 | |||||||
| chr2:99403530 | TATG | T | 4 | a0001c0001t0002g0006 a0001c0001t0002g0144 a0001c0001t0002g0145 others(1): Show |
5 | NA18952.hp2 NA18964.hp1 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.3166+162_3166+164d others(5): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 19/22 | chr2 | 99403530 | |||||||
| chr2:99403574 | A | G | 1 | a0007c0020t0001g0239 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3166+121T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 19/22 | chr2 | 99403574 | |||||||
| chr2:99403979 | TAGAGCAA others(13): Show |
T | 3 | a0002c0002t0001g0215 a0002c0002t0001g0216 a0010c0011t0001g0113 |
3 | HG02055.hp2 HG02109.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3046-184_3046-165d others(22): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 18/22 | chr2 | 99403979 | |||||||
| chr2:99404004 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3046-189G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 18/22 | chr2 | 99404004 | |||||||
| chr2:99404015 | A | T | 2 | a0004c0008t0001g0038 a0004c0008t0001g0041 |
2 | NA18998.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.3046-200T>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 18/22 | chr2 | 99404015 | |||||||
| chr2:99404077 | T | C | 1 | a0004c0004t0001g0044 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3046-262A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 18/22 | chr2 | 99404077 | |||||||
| chr2:99404171 | G | T | 19 | a0001c0001t0001g0051 a0001c0001t0001g0129 a0001c0001t0001g0130 others(16): Show |
19 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.3045+273C>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 18/22 | chr2 | 99404171 | |||||||
| chr2:99404279 | G | A | 162 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(159): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.3045+165C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 18/22 | chr2 | 99404279 | |||||||
| chr2:99404721 | A | G | 162 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(159): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.2812-44T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 17/22 | chr2 | 99404721 | |||||||
| chr2:99404787 | T | C | 1 | a0002c0002t0001g0234 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2812-110A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 17/22 | chr2 | 99404787 | |||||||
| chr2:99404935 | G | T | 1 | a0010c0011t0001g0113 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2812-258C>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 17/22 | chr2 | 99404935 | |||||||
| chr2:99405044 | G | A | 1 | a0004c0004t0001g0034 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2812-367C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 17/22 | chr2 | 99405044 | |||||||
| chr2:99405390 | C | T | 1 | a0002c0002t0001g0297 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2811+520G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 17/22 | chr2 | 99405390 | |||||||
| chr2:99405521 | A | T | 1 | a0002c0002t0001g0244 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2811+389T>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 17/22 | chr2 | 99405521 | |||||||
| chr2:99405628 | T | C | 1 | a0004c0017t0001g0039 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2811+282A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 17/22 | chr2 | 99405628 | |||||||
| chr2:99405807 | C | A | 1 | a0002c0007t0001g0245 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2811+103G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 17/22 | chr2 | 99405807 | |||||||
| chr2:99405808 | G | A | 162 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(159): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.2811+102C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 17/22 | chr2 | 99405808 | |||||||
| chr2:99406155 | G | A | 55 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(52): Show |
56 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(53): Show |
intron_variant | MODIFIER | c.2615-49C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 16/22 | chr2 | 99406155 | |||||||
| chr2:99406203 | C | T | 1 | a0003c0013t0006g0128 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2615-97G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 16/22 | chr2 | 99406203 | |||||||
| chr2:99406310 | T | C | 162 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(159): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.2614+15A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 16/22 | chr2 | 99406310 | |||||||
| chr2:99406517 | T | G | 1 | a0001c0001t0002g0183 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2449-27A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99406517 | |||||||
| chr2:99406780 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2449-290G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99406780 | |||||||
| chr2:99406796 | C | G | 1 | a0002c0002t0001g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2449-306G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99406796 | |||||||
| chr2:99406939 | A | T | 1 | a0003c0003t0001g0058 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2449-449T>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99406939 | |||||||
| chr2:99407080 | C | CT | 88 | a0001c0001t0001g0129 a0001c0001t0001g0188 a0001c0001t0001g0206 others(85): Show |
88 | HG00423.hp2 HG00558.hp1 HG00738.hp1 others(85): Show |
intron_variant | MODIFIER | c.2449-591dupA | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99407080 | |||||||
| chr2:99407080 | C | CTT | 82 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0131 others(79): Show |
84 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.2449-592_2449-591d others(4): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99407080 | |||||||
| chr2:99407080 | C | CTTT | 38 | a0001c0001t0001g0130 a0001c0001t0001g0150 a0001c0001t0001g0153 others(35): Show |
38 | HG00140.hp2 HG01192.hp2 HG01361.hp1 others(35): Show |
intron_variant | MODIFIER | c.2449-593_2449-591d others(5): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99407080 | |||||||
| chr2:99407080 | C | CTTTT | 13 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0162 others(10): Show |
13 | HG01981.hp2 HG02280.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.2449-594_2449-591d others(6): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99407080 | |||||||
| chr2:99407080 | C | CTTTTTTT others(3): Show |
6 | a0003c0003t0001g0001 a0003c0003t0001g0062 a0003c0003t0001g0066 others(3): Show |
6 | HG01071.hp2 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2449-600_2449-591d others(12): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99407080 | |||||||
| chr2:99407080 | C | CTTTTTTT others(4): Show |
12 | a0001c0001t0001g0196 a0003c0003t0001g0058 a0003c0003t0001g0059 others(9): Show |
12 | HG01175.hp1 HG01258.hp1 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.2449-601_2449-591d others(13): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99407080 | |||||||
| chr2:99407080 | C | CTTTTTTT others(5): Show |
13 | a0003c0003t0001g0054 a0003c0003t0001g0055 a0003c0003t0001g0060 others(10): Show |
13 | HG00140.hp1 HG00280.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.2449-602_2449-591d others(14): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99407080 | |||||||
| chr2:99407080 | C | CTTTTTTT others(6): Show |
11 | a0003c0003t0001g0001 a0003c0003t0001g0003 a0003c0003t0001g0061 others(8): Show |
11 | HG00733.hp2 HG00735.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.2449-603_2449-591d others(15): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99407080 | |||||||
| chr2:99407080 | C | CTTTTTTT others(7): Show |
7 | a0003c0003t0001g0003 a0003c0003t0001g0056 a0003c0003t0001g0065 others(4): Show |
7 | HG00544.hp1 HG00741.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.2449-604_2449-591d others(16): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99407080 | |||||||
| chr2:99407080 | C | CTTTTTTT others(8): Show |
2 | a0003c0003t0001g0087 a0003c0003t0001g0091 |
2 | HG00609.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.2449-605_2449-591d others(17): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99407080 | |||||||
| chr2:99407080 | C | CTTTTTTT others(10): Show |
2 | a0003c0003t0001g0083 a0003c0003t0001g0094 |
2 | HG03669.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2449-607_2449-591d others(19): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99407080 | |||||||
| chr2:99407080 | C | CTTTTTTT others(11): Show |
3 | a0003c0003t0001g0068 a0003c0003t0001g0085 a0005c0005t0001g0057 |
3 | HG01106.hp2 HG02293.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2449-608_2449-591d others(20): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99407080 | |||||||
| chr2:99407080 | C | CTTTTTTT others(12): Show |
1 | a0003c0003t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2449-609_2449-591d others(21): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99407080 | |||||||
| chr2:99407080 | C | CTTTTTTT others(13): Show |
1 | a0003c0003t0001g0082 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2449-610_2449-591d others(22): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99407080 | |||||||
| chr2:99407080 | C | T | 1 | a0001c0001t0001g0317 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2449-590G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99407080 | |||||||
| chr2:99407080 | CTTTTTTT others(4): Show |
C | 2 | a0002c0002t0001g0253 a0002c0002t0001g0264 |
2 | NA18956.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.2449-601_2449-591d others(13): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99407080 | |||||||
| chr2:99407080 | CTTTTTTT others(7): Show |
C | 2 | a0003c0003t0001g0002 a0003c0003t0001g0103 |
2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2449-604_2449-591d others(16): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99407080 | |||||||
| chr2:99407145 | G | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.2449-655C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99407145 | |||||||
| chr2:99407250 | C | T | 2 | a0001c0001t0001g0317 a0002c0002t0001g0214 |
2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2449-760G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99407250 | |||||||
| chr2:99407396 | C | CA | 43 | a0003c0003t0001g0120 a0004c0004t0001g0009 a0004c0004t0001g0010 others(40): Show |
43 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.2448+632dupT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99407396 | |||||||
| chr2:99407508 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.2448+521G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99407508 | |||||||
| chr2:99407509 | G | A | 1 | a0010c0011t0001g0113 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2448+520C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99407509 | |||||||
| chr2:99407550 | C | CA | 25 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0109 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.2448+478dupT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99407550 | |||||||
| chr2:99407608 | T | C | 1 | a0004c0004t0001g0029 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2448+421A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99407608 | |||||||
| chr2:99407996 | A | C | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2448+33T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 15/22 | chr2 | 99407996 | |||||||
| chr2:99408309 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.2346-178G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99408309 | |||||||
| chr2:99408357 | G | T | 217 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(214): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.2346-226C>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99408357 | |||||||
| chr2:99408707 | C | T | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG02896.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2346-576G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99408707 | |||||||
| chr2:99408892 | A | T | 218 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(215): Show |
224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.2346-761T>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99408892 | |||||||
| chr2:99408998 | A | G | 49 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(46): Show |
50 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.2346-867T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99408998 | |||||||
| chr2:99409021 | G | A | 162 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(159): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.2346-890C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99409021 | |||||||
| chr2:99409367 | G | A | 1 | a0004c0004t0001g0036 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2346-1236C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99409367 | |||||||
| chr2:99409566 | G | A | 1 | a0010c0011t0001g0113 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2345+1129C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99409566 | |||||||
| chr2:99409702 | G | C | 2 | a0002c0002t0001g0226 a0002c0002t0001g0227 |
2 | HG01261.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2345+993C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99409702 | |||||||
| chr2:99409760 | T | C | 3 | a0004c0004t0001g0015 a0004c0004t0001g0030 a0004c0004t0001g0031 |
3 | HG03017.hp1 HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2345+935A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99409760 | |||||||
| chr2:99409798 | G | A | 2 | a0003c0003t0001g0099 a0003c0003t0001g0100 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2345+897C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99409798 | |||||||
| chr2:99409853 | A | AC | 20 | a0002c0002t0001g0212 a0002c0002t0001g0214 a0002c0002t0001g0224 others(17): Show |
20 | HG01074.hp1 HG01074.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.2345+841dupG | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99409853 | |||||||
| chr2:99409853 | A | ACC | 23 | a0002c0002t0001g0220 a0002c0002t0001g0236 a0002c0002t0001g0237 others(20): Show |
23 | HG00423.hp2 HG01099.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.2345+840_2345+841d others(4): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99409853 | |||||||
| chr2:99409853 | AC | A | 80 | a0001c0001t0001g0109 a0001c0001t0001g0133 a0001c0001t0001g0134 others(77): Show |
82 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.2345+841delG | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99409853 | |||||||
| chr2:99409853 | ACC | A | 65 | a0001c0001t0001g0004 a0001c0001t0001g0110 a0001c0001t0001g0112 others(62): Show |
69 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.2345+840_2345+841d others(4): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99409853 | |||||||
| chr2:99409859 | C | A | 2 | a0002c0002t0003g0274 a0002c0002t0003g0275 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2345+836G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99409859 | |||||||
| chr2:99409864 | C | G | 3 | a0002c0002t0001g0269 a0002c0002t0001g0270 a0004c0004t0001g0036 |
3 | HG01358.hp1 HG02155.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.2345+831G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99409864 | |||||||
| chr2:99409866 | C | A | 4 | a0001c0001t0002g0169 a0003c0003t0001g0103 a0004c0004t0001g0031 others(1): Show |
4 | HG03098.hp1 HG04184.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.2345+829G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99409866 | |||||||
| chr2:99409866 | C | G | 12 | a0003c0003t0001g0114 a0003c0003t0001g0115 a0003c0003t0001g0116 others(9): Show |
12 | HG00642.hp2 HG01123.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.2345+829G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99409866 | |||||||
| chr2:99409867 | C | A | 156 | a0001c0001t0001g0004 a0001c0001t0001g0112 a0001c0001t0001g0133 others(153): Show |
162 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.2345+828G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99409867 | |||||||
| chr2:99409867 | C | CA | 23 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(20): Show |
23 | HG00408.hp2 HG00642.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.2345+827dupT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99409867 | |||||||
| chr2:99409867 | C | CCA | 14 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0143 others(11): Show |
14 | HG00609.hp2 HG00738.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.2345+827_2345+828i others(4): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99409867 | |||||||
| chr2:99410011 | T | C | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2345+684A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99410011 | |||||||
| chr2:99410071 | C | T | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2345+624G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99410071 | |||||||
| chr2:99410080 | A | G | 217 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(214): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.2345+615T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99410080 | |||||||
| chr2:99410166 | A | G | 1 | a0002c0002t0001g0263 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2345+529T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99410166 | |||||||
| chr2:99410478 | A | G | 162 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(159): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.2345+217T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99410478 | |||||||
| chr2:99410528 | T | A | 1 | a0004c0004t0001g0048 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2345+167A>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99410528 | |||||||
| chr2:99410642 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2345+53G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99410642 | |||||||
| chr2:99410689 | G | C | 1 | a0003c0003t0001g0065 | 1 | HG00741.hp2 | splice_region_variant&intron_variant | LOW | c.2345+6C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 14/22 | chr2 | 99410689 | |||||||
| chr2:99411014 | C | T | 1 | a0002c0002t0001g0276 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2173-147G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99411014 | |||||||
| chr2:99411149 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2173-282C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99411149 | |||||||
| chr2:99411152 | G | T | 1 | a0010c0011t0001g0113 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2173-285C>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99411152 | |||||||
| chr2:99411283 | G | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.2173-416C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99411283 | |||||||
| chr2:99411327 | C | T | 48 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(45): Show |
49 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.2173-460G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99411327 | |||||||
| chr2:99411405 | TCTTTC | T | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2173-543_2173-539d others(7): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99411405 | |||||||
| chr2:99411411 | C | CT | 84 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(81): Show |
86 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.2173-545dupA | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99411411 | |||||||
| chr2:99411650 | C | T | 85 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(82): Show |
87 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.2173-783G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99411650 | |||||||
| chr2:99411666 | CCCAAAGT others(383): Show |
C | 1 | a0010c0011t0001g0113 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2172+675_2173-800d others(2): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99411666 | |||||||
| chr2:99411827 | A | G | 48 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(45): Show |
49 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.2172+904T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99411827 | |||||||
| chr2:99411910 | A | G | 4 | a0002c0002t0001g0217 a0002c0002t0001g0218 a0002c0002t0001g0262 others(1): Show |
4 | HG00558.hp2 HG03209.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2172+821T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99411910 | |||||||
| chr2:99412013 | C | T | 43 | a0003c0003t0001g0120 a0004c0004t0001g0009 a0004c0004t0001g0010 others(40): Show |
43 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.2172+718G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99412013 | |||||||
| chr2:99412049 | C | T | 1 | a0003c0003t0001g0085 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2172+682G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99412049 | |||||||
| chr2:99412091 | G | A | 161 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(158): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.2172+640C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99412091 | |||||||
| chr2:99412093 | C | T | 43 | a0003c0003t0001g0120 a0004c0004t0001g0009 a0004c0004t0001g0010 others(40): Show |
43 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.2172+638G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99412093 | |||||||
| chr2:99412094 | G | A | 1 | a0002c0002t0003g0287 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2172+637C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99412094 | |||||||
| chr2:99412147 | C | T | 2 | a0002c0002t0001g0310 a0002c0002t0001g0311 |
2 | HG01255.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.2172+584G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99412147 | |||||||
| chr2:99412162 | A | G | 1 | a0004c0004t0001g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2172+569T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99412162 | |||||||
| chr2:99412164 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2172+567G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99412164 | |||||||
| chr2:99412181 | C | A | 1 | a0009c0016t0001g0053 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2172+550G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99412181 | |||||||
| chr2:99412190 | G | A | 2 | a0003c0003t0001g0099 a0003c0003t0001g0100 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2172+541C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99412190 | |||||||
| chr2:99412197 | CACTCCAC others(18): Show |
C | 7 | a0003c0003t0001g0091 a0003c0003t0001g0098 a0003c0003t0003g0088 others(4): Show |
7 | NA18939.hp2 NA18941.hp1 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.2172+509_2172+533d others(27): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99412197 | |||||||
| chr2:99412257 | C | CA | 53 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(50): Show |
53 | HG00408.hp2 HG00609.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.2172+473dupT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99412257 | |||||||
| chr2:99412257 | C | CAA | 6 | a0001c0001t0001g0150 a0001c0001t0001g0161 a0001c0001t0001g0174 others(3): Show |
6 | HG01106.hp1 HG01192.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.2172+472_2172+473d others(4): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99412257 | |||||||
| chr2:99412257 | CA | C | 94 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(91): Show |
98 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.2172+473delT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99412257 | |||||||
| chr2:99412257 | CAA | C | 17 | a0002c0002t0001g0308 a0003c0003t0003g0092 a0004c0004t0001g0015 others(14): Show |
17 | HG00280.hp2 HG02027.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.2172+472_2172+473d others(4): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99412257 | |||||||
| chr2:99412257 | CAAA | C | 27 | a0003c0003t0001g0120 a0004c0004t0001g0009 a0004c0004t0001g0010 others(24): Show |
27 | HG01168.hp1 HG01358.hp1 HG01516.hp1 others(24): Show |
intron_variant | MODIFIER | c.2172+471_2172+473d others(5): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99412257 | |||||||
| chr2:99412282 | A | C | 3 | a0004c0004t0001g0046 a0004c0004t0001g0047 a0013c0018t0001g0045 |
3 | HG00280.hp2 HG03669.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2172+449T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99412282 | |||||||
| chr2:99412356 | C | A | 1 | a0004c0004t0001g0047 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2172+375G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99412356 | |||||||
| chr2:99412428 | C | G | 86 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(83): Show |
88 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.2172+303G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99412428 | |||||||
| chr2:99412644 | T | C | 217 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(214): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.2172+87A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99412644 | |||||||
| chr2:99412671 | G | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.2172+60C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 13/22 | chr2 | 99412671 | |||||||
| chr2:99413137 | T | C | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1952-186A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99413137 | |||||||
| chr2:99413224 | T | C | 1 | a0004c0004t0001g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1952-273A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99413224 | |||||||
| chr2:99414302 | A | T | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1952-1351T>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99414302 | |||||||
| chr2:99414380 | G | A | 1 | a0003c0003t0001g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1952-1429C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99414380 | |||||||
| chr2:99414444 | G | A | 1 | a0002c0002t0001g0241 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1952-1493C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99414444 | |||||||
| chr2:99414456 | TA | T | 10 | a0001c0001t0001g0155 a0001c0001t0001g0313 a0001c0001t0002g0200 others(7): Show |
10 | HG01168.hp2 HG01943.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1952-1506delT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99414456 | |||||||
| chr2:99414564 | A | G | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1952-1613T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99414564 | |||||||
| chr2:99414648 | CTT | C | 42 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(39): Show |
42 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(39): Show |
intron_variant | MODIFIER | c.1952-1699_1952-169 others(6): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99414648 | |||||||
| chr2:99415065 | G | A | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1952-2114C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99415065 | |||||||
| chr2:99415089 | A | G | 217 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(214): Show |
223 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.1952-2138T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99415089 | |||||||
| chr2:99415206 | T | G | 1 | a0007c0020t0001g0239 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1952-2255A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99415206 | |||||||
| chr2:99415350 | G | A | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1952-2399C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99415350 | |||||||
| chr2:99415389 | A | G | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1952-2438T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99415389 | |||||||
| chr2:99415610 | C | A | 217 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(214): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1952-2659G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99415610 | |||||||
| chr2:99415783 | A | G | 7 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(4): Show |
7 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1952-2832T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99415783 | |||||||
| chr2:99415890 | G | A | 3 | a0003c0006t0001g0208 a0003c0006t0001g0209 a0003c0006t0001g0210 |
3 | HG02809.hp1 HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1951+2938C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99415890 | |||||||
| chr2:99415987 | T | C | 47 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(44): Show |
48 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.1951+2841A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99415987 | |||||||
| chr2:99416174 | C | G | 1 | a0001c0001t0001g0312 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1951+2654G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99416174 | |||||||
| chr2:99416329 | G | C | 1 | a0005c0005t0001g0071 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1951+2499C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99416329 | |||||||
| chr2:99416449 | A | G | 2 | a0001c0001t0001g0143 a0001c0001t0002g0135 |
2 | HG00140.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1951+2379T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99416449 | |||||||
| chr2:99416723 | G | A | 3 | a0003c0003t0001g0094 a0003c0003t0001g0126 a0003c0003t0001g0127 |
3 | HG01891.hp2 HG02109.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1951+2105C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99416723 | |||||||
| chr2:99416868 | G | A | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1951+1960C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99416868 | |||||||
| chr2:99416912 | C | CA | 16 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(13): Show |
16 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1951+1915dupT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99416912 | |||||||
| chr2:99416912 | C | CAA | 38 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(35): Show |
38 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(35): Show |
intron_variant | MODIFIER | c.1951+1914_1951+191 others(6): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99416912 | |||||||
| chr2:99416912 | C | CAAAAAAA | 83 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(80): Show |
85 | HG00423.hp1 HG00609.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.1951+1909_1951+191 others(11): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99416912 | |||||||
| chr2:99416912 | C | CAAAAAAA others(1): Show |
19 | a0001c0001t0001g0152 a0001c0001t0001g0162 a0001c0001t0001g0164 others(16): Show |
19 | HG00738.hp2 HG01109.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1951+1908_1951+191 others(12): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99416912 | |||||||
| chr2:99416912 | CAAAAAA | C | 55 | a0001c0001t0001g0196 a0003c0003t0001g0001 a0003c0003t0001g0002 others(52): Show |
58 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.1951+1910_1951+191 others(10): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99416912 | |||||||
| chr2:99416938 | T | G | 54 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(51): Show |
55 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.1951+1890A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99416938 | |||||||
| chr2:99417043 | G | C | 47 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(44): Show |
48 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.1951+1785C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99417043 | |||||||
| chr2:99417098 | G | T | 1 | a0002c0002t0001g0296 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1951+1730C>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99417098 | |||||||
| chr2:99417099 | C | A | 1 | a0002c0002t0001g0296 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1951+1729G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99417099 | |||||||
| chr2:99417332 | C | G | 69 | a0001c0001t0001g0196 a0003c0003t0001g0001 a0003c0003t0001g0002 others(66): Show |
72 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1951+1496G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99417332 | |||||||
| chr2:99417550 | A | G | 4 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(1): Show |
4 | HG02040.hp1 NA18612.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.1951+1278T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99417550 | |||||||
| chr2:99417869 | A | G | 163 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(160): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1951+959T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99417869 | |||||||
| chr2:99417979 | T | C | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1951+849A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99417979 | |||||||
| chr2:99418173 | A | C | 1 | a0002c0002t0001g0244 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1951+655T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99418173 | |||||||
| chr2:99418184 | TA | T | 69 | a0001c0001t0001g0196 a0003c0003t0001g0001 a0003c0003t0001g0002 others(66): Show |
72 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1951+643delT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99418184 | |||||||
| chr2:99418753 | A | C | 1 | a0001c0001t0002g0200 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1951+75T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99418753 | |||||||
| chr2:99418811 | A | T | 3 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 |
3 | HG02818.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1951+17T>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 12/22 | chr2 | 99418811 | |||||||
| chr2:99418979 | TCA | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.1832-34_1832-33del others(2): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/22 | chr2 | 99418979 | |||||||
| chr2:99419037 | T | G | 2 | a0002c0002t0003g0274 a0002c0002t0003g0275 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1832-90A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/22 | chr2 | 99419037 | |||||||
| chr2:99419205 | A | AT | 19 | a0001c0001t0001g0051 a0001c0001t0001g0109 a0001c0001t0009g0199 others(16): Show |
19 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1832-259dupA | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/22 | chr2 | 99419205 | |||||||
| chr2:99419205 | A | ATT | 134 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(131): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.1832-260_1832-259d others(4): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/22 | chr2 | 99419205 | |||||||
| chr2:99419205 | A | ATTT | 21 | a0001c0001t0001g0108 a0001c0001t0001g0134 a0001c0001t0001g0150 others(18): Show |
21 | HG00544.hp1 HG00741.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1832-261_1832-259d others(5): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/22 | chr2 | 99419205 | |||||||
| chr2:99419205 | AT | A | 44 | a0001c0001t0001g0004 a0001c0001t0001g0110 a0001c0001t0001g0111 others(41): Show |
45 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.1832-259delA | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/22 | chr2 | 99419205 | |||||||
| chr2:99419205 | ATTT | A | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1832-261_1832-259d others(5): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/22 | chr2 | 99419205 | |||||||
| chr2:99419225 | T | G | 2 | a0004c0008t0001g0038 a0004c0008t0001g0041 |
2 | NA18998.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1832-278A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/22 | chr2 | 99419225 | |||||||
| chr2:99419226 | T | G | 41 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(38): Show |
41 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(38): Show |
intron_variant | MODIFIER | c.1832-279A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/22 | chr2 | 99419226 | |||||||
| chr2:99419227 | T | G | 41 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(38): Show |
41 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(38): Show |
intron_variant | MODIFIER | c.1832-280A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/22 | chr2 | 99419227 | |||||||
| chr2:99419367 | C | T | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1832-420G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/22 | chr2 | 99419367 | |||||||
| chr2:99419375 | G | T | 1 | a0004c0004t0001g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1832-428C>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/22 | chr2 | 99419375 | |||||||
| chr2:99419400 | C | T | 2 | a0004c0004t0001g0049 a0004c0004t0001g0050 |
2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1832-453G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/22 | chr2 | 99419400 | |||||||
| chr2:99419401 | G | A | 1 | a0003c0003t0001g0063 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1832-454C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/22 | chr2 | 99419401 | |||||||
| chr2:99419550 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1832-603T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/22 | chr2 | 99419550 | |||||||
| chr2:99419589 | G | A | 1 | a0013c0018t0001g0045 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1832-642C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/22 | chr2 | 99419589 | |||||||
| chr2:99419602 | T | A | 1 | a0004c0004t0001g0049 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1832-655A>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/22 | chr2 | 99419602 | |||||||
| chr2:99419683 | G | C | 1 | a0001c0001t0002g0136 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1832-736C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/22 | chr2 | 99419683 | |||||||
| chr2:99419696 | A | G | 219 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(216): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1832-749T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/22 | chr2 | 99419696 | |||||||
| chr2:99420130 | G | T | 2 | a0002c0002t0001g0240 a0002c0002t0001g0243 |
2 | HG00738.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1832-1183C>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/22 | chr2 | 99420130 | |||||||
| chr2:99420281 | G | A | 2 | a0003c0003t0001g0126 a0003c0003t0001g0127 |
2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1831+1218C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/22 | chr2 | 99420281 | |||||||
| chr2:99420339 | C | T | 2 | a0003c0003t0001g0126 a0003c0003t0001g0127 |
2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1831+1160G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/22 | chr2 | 99420339 | |||||||
| chr2:99420554 | G | A | 1 | a0002c0002t0001g0240 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1831+945C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/22 | chr2 | 99420554 | |||||||
| chr2:99420590 | G | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.1831+909C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/22 | chr2 | 99420590 | |||||||
| chr2:99420673 | TCA | T | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1831+824_1831+825d others(4): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/22 | chr2 | 99420673 | |||||||
| chr2:99420756 | A | G | 1 | a0002c0002t0001g0302 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1831+743T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/22 | chr2 | 99420756 | |||||||
| chr2:99420857 | G | A | 3 | a0001c0001t0002g0136 a0001c0001t0002g0170 a0001c0001t0002g0173 |
3 | NA18995.hp1 NA19011.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1831+642C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/22 | chr2 | 99420857 | |||||||
| chr2:99421370 | T | C | 42 | a0001c0001t0001g0143 a0001c0001t0002g0005 a0001c0001t0002g0006 others(39): Show |
44 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.1831+129A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 11/22 | chr2 | 99421370 | |||||||
| chr2:99422045 | T | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.1677-392A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 10/22 | chr2 | 99422045 | |||||||
| chr2:99422171 | T | C | 1 | a0003c0003t0003g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1677-518A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 10/22 | chr2 | 99422171 | |||||||
| chr2:99422353 | C | T | 1 | a0004c0004t0001g0018 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1677-700G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 10/22 | chr2 | 99422353 | |||||||
| chr2:99422591 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1677-938C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 10/22 | chr2 | 99422591 | |||||||
| chr2:99422628 | A | G | 1 | a0002c0002t0003g0260 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1677-975T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 10/22 | chr2 | 99422628 | |||||||
| chr2:99422692 | C | T | 4 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0193 others(1): Show |
4 | HG02040.hp1 NA18612.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.1677-1039G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 10/22 | chr2 | 99422692 | |||||||
| chr2:99422817 | A | G | 4 | a0003c0006t0001g0208 a0003c0006t0001g0209 a0003c0006t0001g0210 others(1): Show |
4 | HG01243.hp1 HG02809.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1677-1164T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 10/22 | chr2 | 99422817 | |||||||
| chr2:99423100 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.1676+1052G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 10/22 | chr2 | 99423100 | |||||||
| chr2:99423119 | G | A | 1 | a0002c0002t0001g0220 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1676+1033C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 10/22 | chr2 | 99423119 | |||||||
| chr2:99423124 | G | A | 1 | a0001c0001t0002g0200 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1676+1028C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 10/22 | chr2 | 99423124 | |||||||
| chr2:99423202 | C | T | 312 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(309): Show |
318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.1676+950G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 10/22 | chr2 | 99423202 | |||||||
| chr2:99423437 | G | A | 82 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0131 others(79): Show |
84 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.1676+715C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 10/22 | chr2 | 99423437 | |||||||
| chr2:99423494 | C | T | 42 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(39): Show |
42 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(39): Show |
intron_variant | MODIFIER | c.1676+658G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 10/22 | chr2 | 99423494 | |||||||
| chr2:99423710 | A | G | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1676+442T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 10/22 | chr2 | 99423710 | |||||||
| chr2:99423818 | A | T | 216 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(213): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1676+334T>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 10/22 | chr2 | 99423818 | |||||||
| chr2:99423853 | G | T | 1 | a0001c0001t0001g0188 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1676+299C>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 10/22 | chr2 | 99423853 | |||||||
| chr2:99424366 | C | T | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1548-86G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99424366 | |||||||
| chr2:99424437 | T | C | 1 | a0002c0002t0001g0214 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1548-157A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99424437 | |||||||
| chr2:99424992 | G | C | 1 | a0001c0001t0001g0312 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1548-712C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99424992 | |||||||
| chr2:99425103 | T | C | 13 | a0003c0003t0001g0114 a0003c0003t0001g0115 a0003c0003t0001g0116 others(10): Show |
13 | HG00642.hp2 HG01123.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.1548-823A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99425103 | |||||||
| chr2:99425185 | A | C | 47 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(44): Show |
48 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.1548-905T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99425185 | |||||||
| chr2:99425196 | C | T | 1 | a0002c0002t0001g0311 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1548-916G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99425196 | |||||||
| chr2:99425387 | G | A | 69 | a0001c0001t0001g0196 a0003c0003t0001g0001 a0003c0003t0001g0002 others(66): Show |
72 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1548-1107C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99425387 | |||||||
| chr2:99425676 | T | G | 47 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(44): Show |
48 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.1548-1396A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99425676 | |||||||
| chr2:99425796 | G | C | 1 | a0001c0001t0001g0108 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1548-1516C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99425796 | |||||||
| chr2:99426263 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1548-1983G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99426263 | |||||||
| chr2:99426291 | G | A | 5 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0315 others(2): Show |
5 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1548-2011C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99426291 | |||||||
| chr2:99426347 | CA | C | 10 | a0001c0001t0001g0109 a0001c0001t0001g0166 a0002c0002t0001g0224 others(7): Show |
10 | HG01975.hp1 HG02083.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.1548-2068delT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99426347 | |||||||
| chr2:99426409 | T | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.1548-2129A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99426409 | |||||||
| chr2:99426424 | CATTAA | C | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1548-2149_1548-214 others(9): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99426424 | |||||||
| chr2:99426457 | T | A | 1 | a0001c0001t0002g0135 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1548-2177A>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99426457 | |||||||
| chr2:99426482 | C | G | 1 | a0010c0011t0001g0113 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1548-2202G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99426482 | |||||||
| chr2:99426737 | C | G | 1 | a0001c0001t0001g0111 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1548-2457G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99426737 | |||||||
| chr2:99426808 | A | C | 1 | a0004c0004t0001g0048 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1548-2528T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99426808 | |||||||
| chr2:99426897 | T | C | 1 | a0003c0013t0006g0128 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1548-2617A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99426897 | |||||||
| chr2:99427044 | G | A | 1 | a0001c0001t0001g0312 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1548-2764C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99427044 | |||||||
| chr2:99427095 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.1547+2745G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99427095 | |||||||
| chr2:99427153 | G | A | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1547+2687C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99427153 | |||||||
| chr2:99427261 | G | T | 1 | a0006c0009t0001g0255 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1547+2579C>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99427261 | |||||||
| chr2:99427283 | G | A | 1 | a0002c0002t0001g0283 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1547+2557C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99427283 | |||||||
| chr2:99427387 | TAA | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.1547+2451_1547+245 others(6): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99427387 | |||||||
| chr2:99427659 | G | A | 1 | a0002c0002t0001g0220 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1547+2181C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99427659 | |||||||
| chr2:99427916 | G | A | 1 | a0003c0003t0001g0116 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1547+1924C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99427916 | |||||||
| chr2:99428086 | C | A | 1 | a0002c0002t0001g0308 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1547+1754G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99428086 | |||||||
| chr2:99428463 | A | T | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1547+1377T>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99428463 | |||||||
| chr2:99428609 | A | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.1547+1231T>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99428609 | |||||||
| chr2:99428631 | C | T | 2 | a0002c0002t0001g0294 a0004c0017t0001g0039 |
2 | HG02970.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1547+1209G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99428631 | |||||||
| chr2:99428632 | G | A | 1 | a0009c0016t0001g0053 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1547+1208C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99428632 | |||||||
| chr2:99428646 | A | G | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1547+1194T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99428646 | |||||||
| chr2:99428659 | A | G | 4 | a0003c0006t0001g0208 a0003c0006t0001g0209 a0003c0006t0001g0210 others(1): Show |
4 | HG01243.hp1 HG02809.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1547+1181T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99428659 | |||||||
| chr2:99428722 | A | G | 219 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(216): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1547+1118T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99428722 | |||||||
| chr2:99428766 | C | T | 1 | a0003c0003t0001g0198 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1547+1074G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99428766 | |||||||
| chr2:99428785 | G | A | 85 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(82): Show |
87 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.1547+1055C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99428785 | |||||||
| chr2:99428805 | C | T | 1 | a0003c0003t0001g0058 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1547+1035G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99428805 | |||||||
| chr2:99428813 | T | C | 221 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(218): Show |
227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.1547+1027A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99428813 | |||||||
| chr2:99428852 | T | C | 1 | a0003c0003t0001g0123 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1547+988A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99428852 | |||||||
| chr2:99428923 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1547+917A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99428923 | |||||||
| chr2:99428968 | G | A | 1 | a0003c0003t0001g0198 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1547+872C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99428968 | |||||||
| chr2:99428984 | T | G | 1 | a0002c0002t0001g0231 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1547+856A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99428984 | |||||||
| chr2:99428991 | C | CA | 44 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(41): Show |
44 | HG00423.hp1 HG00609.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.1547+848dupT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99428991 | |||||||
| chr2:99428991 | CA | C | 27 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(24): Show |
28 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.1547+848delT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99428991 | |||||||
| chr2:99429049 | T | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.1547+791A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99429049 | |||||||
| chr2:99429314 | A | T | 1 | a0004c0004t0001g0048 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1547+526T>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99429314 | |||||||
| chr2:99429321 | C | T | 42 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(39): Show |
42 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(39): Show |
intron_variant | MODIFIER | c.1547+519G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99429321 | |||||||
| chr2:99429346 | C | T | 1 | a0002c0002t0001g0231 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1547+494G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99429346 | |||||||
| chr2:99429508 | G | A | 2 | a0003c0003t0001g0126 a0003c0003t0001g0127 |
2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1547+332C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99429508 | |||||||
| chr2:99429576 | C | T | 63 | a0002c0002t0010g0318 a0003c0003t0001g0002 a0003c0003t0001g0003 others(60): Show |
65 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.1547+264G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99429576 | |||||||
| chr2:99429641 | G | C | 1 | a0002c0002t0001g0234 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1547+199C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99429641 | |||||||
| chr2:99429699 | T | C | 1 | a0010c0011t0001g0113 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1547+141A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99429699 | |||||||
| chr2:99429747 | A | AAATCACT others(19): Show |
71 | a0001c0001t0001g0004 a0001c0001t0001g0112 a0001c0001t0001g0133 others(68): Show |
73 | HG00609.hp1 HG00738.hp1 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.1547+92_1547+93ins others(26): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99429747 | |||||||
| chr2:99429747 | A | AAATCCAC others(20): Show |
7 | a0002c0002t0001g0217 a0003c0003t0001g0002 a0003c0003t0001g0082 others(4): Show |
8 | HG02280.hp2 HG02922.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.1547+92_1547+93ins others(27): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 9/22 | chr2 | 99429747 | |||||||
| chr2:99430117 | G | A | 4 | a0003c0006t0001g0208 a0003c0006t0001g0209 a0003c0006t0001g0210 others(1): Show |
4 | HG01243.hp1 HG02809.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1439-169C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99430117 | |||||||
| chr2:99430122 | G | A | 2 | a0004c0004t0001g0010 a0004c0004t0001g0035 |
2 | HG02135.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1439-174C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99430122 | |||||||
| chr2:99430273 | C | T | 1 | a0003c0003t0003g0088 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1439-325G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99430273 | |||||||
| chr2:99430321 | C | T | 77 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(74): Show |
81 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1439-373G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99430321 | |||||||
| chr2:99430477 | C | G | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1439-529G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99430477 | |||||||
| chr2:99430481 | A | C | 210 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(207): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1439-533T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99430481 | |||||||
| chr2:99430873 | T | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.1439-925A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99430873 | |||||||
| chr2:99431138 | A | G | 218 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(215): Show |
224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1439-1190T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99431138 | |||||||
| chr2:99431180 | G | A | 1 | a0002c0002t0001g0305 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1439-1232C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99431180 | |||||||
| chr2:99431194 | C | T | 1 | a0002c0002t0003g0230 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1439-1246G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99431194 | |||||||
| chr2:99431200 | C | T | 42 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(39): Show |
42 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(39): Show |
intron_variant | MODIFIER | c.1439-1252G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99431200 | |||||||
| chr2:99431267 | A | C | 1 | a0002c0002t0001g0212 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1439-1319T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99431267 | |||||||
| chr2:99431285 | T | C | 3 | a0003c0006t0001g0208 a0003c0006t0001g0209 a0003c0006t0001g0210 |
3 | HG02809.hp1 HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1439-1337A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99431285 | |||||||
| chr2:99431318 | G | A | 1 | a0004c0004t0005g0007 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1439-1370C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99431318 | |||||||
| chr2:99431340 | A | AC | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.1439-1393_1439-139 others(5): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99431340 | |||||||
| chr2:99431489 | C | G | 1 | a0003c0003t0001g0104 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1439-1541G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99431489 | |||||||
| chr2:99431527 | CAACT | C | 14 | a0003c0003t0001g0114 a0003c0003t0001g0115 a0003c0003t0001g0116 others(11): Show |
14 | HG00642.hp2 HG01123.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1439-1583_1439-158 others(8): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99431527 | |||||||
| chr2:99431531 | T | C | 1 | a0003c0003t0001g0087 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1439-1583A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99431531 | |||||||
| chr2:99431561 | C | T | 1 | a0002c0002t0001g0234 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1439-1613G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99431561 | |||||||
| chr2:99431714 | G | A | 1 | a0003c0003t0001g0062 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1439-1766C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99431714 | |||||||
| chr2:99431721 | T | G | 1 | a0002c0002t0003g0230 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1439-1773A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99431721 | |||||||
| chr2:99431910 | G | C | 1 | a0003c0003t0001g0207 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1439-1962C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99431910 | |||||||
| chr2:99432053 | G | A | 1 | a0001c0001t0002g0136 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1439-2105C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99432053 | |||||||
| chr2:99432328 | C | CT | 8 | a0005c0005t0001g0057 a0005c0005t0001g0071 a0005c0005t0001g0072 others(5): Show |
8 | HG01070.hp1 HG01934.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.1438+2003dupA | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99432328 | |||||||
| chr2:99432563 | A | G | 1 | a0005c0005t0001g0078 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1438+1769T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99432563 | |||||||
| chr2:99433017 | G | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.1438+1315C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99433017 | |||||||
| chr2:99433120 | A | G | 2 | a0003c0003t0001g0126 a0003c0003t0001g0127 |
2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1438+1212T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99433120 | |||||||
| chr2:99433964 | TGTTA | T | 164 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(161): Show |
170 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.1438+364_1438+367d others(6): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99433964 | |||||||
| chr2:99434127 | T | C | 1 | a0002c0002t0001g0265 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1438+205A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99434127 | |||||||
| chr2:99434278 | A | C | 45 | a0003c0003t0001g0120 a0003c0003t0001g0121 a0004c0004t0001g0009 others(42): Show |
45 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(42): Show |
intron_variant | MODIFIER | c.1438+54T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 8/22 | chr2 | 99434278 | |||||||
| chr2:99434742 | T | C | 1 | a0004c0004t0001g0047 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1322-294A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 7/22 | chr2 | 99434742 | |||||||
| chr2:99434794 | A | G | 1 | a0002c0007t0002g0247 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1322-346T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 7/22 | chr2 | 99434794 | |||||||
| chr2:99434815 | A | G | 30 | a0002c0002t0001g0277 a0002c0002t0001g0283 a0002c0002t0003g0222 others(27): Show |
30 | HG00544.hp2 HG00558.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.1322-367T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 7/22 | chr2 | 99434815 | |||||||
| chr2:99434854 | C | CA | 218 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(215): Show |
224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1322-407_1322-406i others(3): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 7/22 | chr2 | 99434854 | |||||||
| chr2:99434859 | C | G | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1322-411G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 7/22 | chr2 | 99434859 | |||||||
| chr2:99434986 | T | C | 1 | a0002c0002t0001g0276 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1322-538A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 7/22 | chr2 | 99434986 | |||||||
| chr2:99435012 | T | C | 3 | a0002c0002t0001g0262 a0002c0002t0001g0263 a0002c0002t0001g0266 |
3 | HG00558.hp2 NA19010.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1322-564A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 7/22 | chr2 | 99435012 | |||||||
| chr2:99435060 | C | T | 217 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(214): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1322-612G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 7/22 | chr2 | 99435060 | |||||||
| chr2:99435200 | C | A | 2 | a0003c0003t0001g0126 a0003c0003t0001g0127 |
2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1321+634G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 7/22 | chr2 | 99435200 | |||||||
| chr2:99435246 | A | T | 1 | a0001c0001t0001g0312 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1321+588T>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 7/22 | chr2 | 99435246 | |||||||
| chr2:99435291 | A | G | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1321+543T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 7/22 | chr2 | 99435291 | |||||||
| chr2:99435426 | A | C | 1 | a0004c0004t0001g0028 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1321+408T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 7/22 | chr2 | 99435426 | |||||||
| chr2:99435731 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG00408.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.1321+103G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 7/22 | chr2 | 99435731 | |||||||
| chr2:99436096 | C | A | 1 | a0002c0002t0010g0318 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1214-155G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/22 | chr2 | 99436096 | |||||||
| chr2:99436132 | A | AGTTT | 210 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(207): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1214-192_1214-191i others(6): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/22 | chr2 | 99436132 | |||||||
| chr2:99436411 | C | G | 1 | a0002c0002t0001g0266 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1214-470G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/22 | chr2 | 99436411 | |||||||
| chr2:99436455 | T | C | 43 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(40): Show |
43 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.1214-514A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/22 | chr2 | 99436455 | |||||||
| chr2:99436459 | G | A | 1 | a0002c0002t0001g0265 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1214-518C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/22 | chr2 | 99436459 | |||||||
| chr2:99436833 | T | C | 80 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(77): Show |
82 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.1214-892A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/22 | chr2 | 99436833 | |||||||
| chr2:99436980 | C | CT | 7 | a0001c0001t0002g0132 a0001c0001t0002g0136 a0001c0001t0002g0147 others(4): Show |
7 | HG02148.hp1 HG04184.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.1214-1040dupA | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/22 | chr2 | 99436980 | |||||||
| chr2:99436990 | G | GT | 88 | a0001c0001t0001g0051 a0001c0001t0001g0129 a0001c0001t0001g0130 others(85): Show |
90 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.1214-1050dupA | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/22 | chr2 | 99436990 | |||||||
| chr2:99436990 | G | T | 13 | a0001c0001t0001g0196 a0001c0001t0002g0132 a0001c0001t0002g0136 others(10): Show |
13 | HG03579.hp1 HG04184.hp1 NA18612.hp1 others(10): Show |
intron_variant | MODIFIER | c.1214-1049C>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/22 | chr2 | 99436990 | |||||||
| chr2:99437007 | G | A | 1 | a0003c0003t0001g0076 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1214-1066C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/22 | chr2 | 99437007 | |||||||
| chr2:99437050 | G | A | 1 | a0003c0010t0001g0107 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1214-1109C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/22 | chr2 | 99437050 | |||||||
| chr2:99437061 | C | A | 43 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(40): Show |
43 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.1214-1120G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/22 | chr2 | 99437061 | |||||||
| chr2:99437076 | C | G | 1 | a0002c0002t0001g0219 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1214-1135G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/22 | chr2 | 99437076 | |||||||
| chr2:99437119 | G | A | 1 | a0004c0004t0001g0021 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1214-1178C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/22 | chr2 | 99437119 | |||||||
| chr2:99437229 | C | A | 1 | a0004c0004t0001g0047 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1214-1288G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/22 | chr2 | 99437229 | |||||||
| chr2:99437323 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1213+1278T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/22 | chr2 | 99437323 | |||||||
| chr2:99437404 | C | A | 217 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(214): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1213+1197G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/22 | chr2 | 99437404 | |||||||
| chr2:99437618 | C | T | 2 | a0003c0003t0001g0126 a0003c0003t0001g0127 |
2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1213+983G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/22 | chr2 | 99437618 | |||||||
| chr2:99437678 | T | A | 43 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(40): Show |
43 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.1213+923A>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/22 | chr2 | 99437678 | |||||||
| chr2:99437719 | A | C | 1 | a0001c0001t0002g0181 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1213+882T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/22 | chr2 | 99437719 | |||||||
| chr2:99437761 | G | A | 11 | a0003c0003t0001g0003 a0003c0003t0001g0087 a0003c0003t0001g0091 others(8): Show |
12 | HG00609.hp1 HG02148.hp1 HG03669.hp2 others(9): Show |
intron_variant | MODIFIER | c.1213+840C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/22 | chr2 | 99437761 | |||||||
| chr2:99437879 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1213+722T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/22 | chr2 | 99437879 | |||||||
| chr2:99438065 | C | T | 1 | a0002c0002t0001g0251 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1213+536G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/22 | chr2 | 99438065 | |||||||
| chr2:99438196 | A | AAATT | 210 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(207): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1213+401_1213+404d others(6): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/22 | chr2 | 99438196 | |||||||
| chr2:99438216 | T | C | 1 | a0006c0009t0001g0250 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1213+385A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/22 | chr2 | 99438216 | |||||||
| chr2:99438450 | T | C | 1 | a0001c0001t0002g0197 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1213+151A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/22 | chr2 | 99438450 | |||||||
| chr2:99438456 | T | A | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1213+145A>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/22 | chr2 | 99438456 | |||||||
| chr2:99438571 | C | A | 43 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(40): Show |
43 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.1213+30G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 6/22 | chr2 | 99438571 | |||||||
| chr2:99439363 | C | G | 1 | a0003c0003t0001g0064 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.504-53G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99439363 | |||||||
| chr2:99439870 | C | T | 43 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(40): Show |
43 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.504-560G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99439870 | |||||||
| chr2:99440066 | C | A | 6 | a0002c0002t0001g0217 a0002c0002t0001g0218 a0002c0002t0001g0219 others(3): Show |
6 | HG02572.hp1 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.504-756G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99440066 | |||||||
| chr2:99440131 | T | G | 2 | a0003c0003t0001g0126 a0003c0003t0001g0127 |
2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.504-821A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99440131 | |||||||
| chr2:99440155 | C | T | 217 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(214): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.504-845G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99440155 | |||||||
| chr2:99440220 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.504-910G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99440220 | |||||||
| chr2:99440274 | T | C | 166 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(163): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.504-964A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99440274 | |||||||
| chr2:99440491 | T | C | 1 | a0002c0002t0010g0318 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.504-1181A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99440491 | |||||||
| chr2:99440558 | C | T | 55 | a0003c0003t0001g0001 a0003c0003t0001g0002 a0003c0003t0001g0003 others(52): Show |
58 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.504-1248G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99440558 | |||||||
| chr2:99440585 | G | A | 1 | a0004c0004t0001g0023 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.504-1275C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99440585 | |||||||
| chr2:99440719 | T | C | 1 | a0004c0004t0001g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.504-1409A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99440719 | |||||||
| chr2:99440746 | C | A | 165 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(162): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.504-1436G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99440746 | |||||||
| chr2:99440756 | C | G | 1 | a0002c0002t0003g0281 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.504-1446G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99440756 | |||||||
| chr2:99440772 | G | A | 4 | a0001c0001t0002g0006 a0001c0001t0002g0144 a0001c0001t0002g0145 others(1): Show |
5 | NA18952.hp2 NA18964.hp1 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.504-1462C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99440772 | |||||||
| chr2:99441027 | G | A | 90 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(87): Show |
93 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.503+1290C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99441027 | |||||||
| chr2:99441123 | CGTATTCT | C | 41 | a0003c0003t0001g0001 a0003c0003t0001g0002 a0003c0003t0001g0054 others(38): Show |
43 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.503+1187_503+1193d others(9): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99441123 | |||||||
| chr2:99441455 | A | G | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.503+862T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99441455 | |||||||
| chr2:99441468 | A | T | 1 | a0002c0002t0001g0305 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.503+849T>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99441468 | |||||||
| chr2:99441525 | G | C | 1 | a0004c0004t0001g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.503+792C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99441525 | |||||||
| chr2:99441727 | A | G | 217 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(214): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.503+590T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99441727 | |||||||
| chr2:99441794 | G | A | 1 | a0003c0003t0001g0102 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.503+523C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99441794 | |||||||
| chr2:99441798 | A | C | 2 | a0002c0002t0001g0235 a0002c0002t0001g0246 |
2 | HG00408.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.503+519T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99441798 | |||||||
| chr2:99441962 | C | T | 49 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(46): Show |
49 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(46): Show |
intron_variant | MODIFIER | c.503+355G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99441962 | |||||||
| chr2:99442112 | C | T | 5 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0174 others(2): Show |
5 | HG02630.hp2 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.503+205G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99442112 | |||||||
| chr2:99442125 | G | A | 1 | a0002c0002t0001g0302 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.503+192C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99442125 | |||||||
| chr2:99442145 | G | A | 1 | a0003c0013t0006g0128 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.503+172C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99442145 | |||||||
| chr2:99442227 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.503+90G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99442227 | |||||||
| chr2:99442252 | C | CA | 21 | a0002c0002t0001g0219 a0002c0002t0001g0224 a0002c0002t0001g0236 others(18): Show |
21 | HG00423.hp2 HG01168.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.503+64dupT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99442252 | |||||||
| chr2:99442252 | C | CAA | 117 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(114): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.503+63_503+64dupTT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99442252 | |||||||
| chr2:99442252 | C | CAAA | 36 | a0001c0001t0001g0004 a0001c0001t0001g0110 a0001c0001t0001g0111 others(33): Show |
37 | HG00609.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.503+62_503+64dupTT others(1): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99442252 | |||||||
| chr2:99442252 | C | CAAAA | 10 | a0001c0001t0001g0109 a0001c0001t0001g0112 a0003c0003t0001g0114 others(7): Show |
10 | HG01123.hp2 HG01358.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.503+61_503+64dupTT others(2): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99442252 | |||||||
| chr2:99442252 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0317 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.503+49_503+64dupTT others(14): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99442252 | |||||||
| chr2:99442252 | C | CAAAAAAA others(10): Show |
2 | a0001c0001t0001g0313 a0001c0001t0001g0315 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.503+48_503+64dupTT others(15): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99442252 | |||||||
| chr2:99442252 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.503+47_503+64dupTT others(16): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99442252 | |||||||
| chr2:99442264 | A | AAAAAAAA others(11): Show |
1 | a0001c0001t0001g0314 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.503+52_503+53insGT others(16): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 5/22 | chr2 | 99442264 | |||||||
| chr2:99442664 | G | A | 3 | a0003c0003t0001g0126 a0003c0003t0001g0127 a0010c0011t0001g0113 |
3 | HG01891.hp2 HG02055.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.351-195C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99442664 | |||||||
| chr2:99443105 | T | C | 3 | a0003c0006t0001g0208 a0003c0006t0001g0209 a0003c0006t0001g0210 |
3 | HG02809.hp1 HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.351-636A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99443105 | |||||||
| chr2:99443166 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.351-697G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99443166 | |||||||
| chr2:99443247 | A | C | 216 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(213): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.351-778T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99443247 | |||||||
| chr2:99443307 | A | G | 1 | a0004c0004t0001g0049 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.351-838T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99443307 | |||||||
| chr2:99443435 | A | T | 1 | a0003c0003t0003g0090 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.351-966T>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99443435 | |||||||
| chr2:99443555 | T | C | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.351-1086A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99443555 | |||||||
| chr2:99443842 | T | G | 43 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(40): Show |
43 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.351-1373A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99443842 | |||||||
| chr2:99443848 | C | CT | 44 | a0003c0003t0003g0090 a0004c0004t0001g0009 a0004c0004t0001g0010 others(41): Show |
44 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(41): Show |
intron_variant | MODIFIER | c.351-1380dupA | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99443848 | |||||||
| chr2:99443929 | C | T | 1 | a0010c0011t0001g0113 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.351-1460G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99443929 | |||||||
| chr2:99443979 | C | T | 173 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(170): Show |
179 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.351-1510G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99443979 | |||||||
| chr2:99443980 | G | A | 1 | a0003c0003t0001g0058 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.351-1511C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99443980 | |||||||
| chr2:99444021 | C | T | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.351-1552G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99444021 | |||||||
| chr2:99444051 | A | G | 1 | a0010c0011t0001g0113 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.351-1582T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99444051 | |||||||
| chr2:99444099 | T | C | 216 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(213): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.351-1630A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99444099 | |||||||
| chr2:99444111 | C | T | 1 | a0004c0004t0001g0019 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.351-1642G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99444111 | |||||||
| chr2:99444112 | G | A | 2 | a0001c0001t0002g0194 a0001c0001t0002g0195 |
2 | NA18947.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.351-1643C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99444112 | |||||||
| chr2:99444143 | C | T | 1 | a0002c0002t0001g0273 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.351-1674G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99444143 | |||||||
| chr2:99444152 | C | T | 1 | a0010c0011t0001g0113 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.351-1683G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99444152 | |||||||
| chr2:99444484 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.351-2015A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99444484 | |||||||
| chr2:99444537 | A | C | 41 | a0001c0001t0001g0143 a0001c0001t0001g0196 a0001c0001t0002g0005 others(38): Show |
43 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.351-2068T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99444537 | |||||||
| chr2:99444538 | T | G | 1 | a0003c0013t0006g0128 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.351-2069A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99444538 | |||||||
| chr2:99444732 | T | C | 1 | a0004c0004t0001g0032 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.351-2263A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99444732 | |||||||
| chr2:99444862 | C | T | 44 | a0002c0002t0001g0219 a0004c0004t0001g0009 a0004c0004t0001g0010 others(41): Show |
44 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(41): Show |
intron_variant | MODIFIER | c.351-2393G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99444862 | |||||||
| chr2:99445035 | A | C | 1 | a0001c0001t0002g0184 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.351-2566T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99445035 | |||||||
| chr2:99445090 | G | T | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.351-2621C>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99445090 | |||||||
| chr2:99445131 | C | CA | 7 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(4): Show |
7 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.351-2663dupT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99445131 | |||||||
| chr2:99445131 | CA | C | 205 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(202): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.351-2663delT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99445131 | |||||||
| chr2:99445169 | T | C | 2 | a0002c0002t0001g0217 a0002c0002t0001g0218 |
2 | HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.351-2700A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99445169 | |||||||
| chr2:99445243 | A | C | 2 | a0004c0008t0001g0038 a0004c0008t0001g0041 |
2 | NA18998.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.351-2774T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99445243 | |||||||
| chr2:99445286 | C | A | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.351-2817G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99445286 | |||||||
| chr2:99445311 | G | A | 85 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(82): Show |
87 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.351-2842C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99445311 | |||||||
| chr2:99445386 | T | C | 7 | a0001c0001t0002g0008 a0001c0001t0002g0200 a0001c0001t0002g0202 others(4): Show |
7 | HG02572.hp2 HG03041.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.351-2917A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99445386 | |||||||
| chr2:99445424 | G | A | 1 | a0004c0004t0001g0022 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.351-2955C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99445424 | |||||||
| chr2:99445591 | T | C | 1 | a0004c0004t0001g0016 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.351-3122A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99445591 | |||||||
| chr2:99445635 | T | C | 2 | a0003c0003t0001g0126 a0003c0003t0001g0127 |
2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.351-3166A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99445635 | |||||||
| chr2:99445701 | T | C | 90 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(87): Show |
93 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.351-3232A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99445701 | |||||||
| chr2:99445901 | T | C | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.351-3432A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99445901 | |||||||
| chr2:99445952 | C | T | 1 | a0004c0004t0001g0043 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.350+3384G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99445952 | |||||||
| chr2:99445960 | A | T | 1 | a0001c0001t0001g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.350+3376T>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99445960 | |||||||
| chr2:99445988 | A | G | 2 | a0004c0008t0001g0038 a0004c0008t0001g0041 |
2 | NA18998.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.350+3348T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99445988 | |||||||
| chr2:99446525 | C | T | 2 | a0003c0003t0001g0126 a0003c0003t0001g0127 |
2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.350+2811G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99446525 | |||||||
| chr2:99446577 | C | T | 1 | a0001c0001t0002g0008 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.350+2759G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99446577 | |||||||
| chr2:99446602 | C | T | 5 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0315 others(2): Show |
5 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.350+2734G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99446602 | |||||||
| chr2:99446649 | C | T | 31 | a0002c0002t0001g0276 a0002c0002t0001g0277 a0002c0002t0001g0278 others(28): Show |
31 | HG00544.hp2 HG00558.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.350+2687G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99446649 | |||||||
| chr2:99446788 | C | A | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.350+2548G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99446788 | |||||||
| chr2:99447098 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.350+2238C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99447098 | |||||||
| chr2:99447219 | T | C | 173 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(170): Show |
179 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.350+2117A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99447219 | |||||||
| chr2:99447246 | T | C | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.350+2090A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99447246 | |||||||
| chr2:99447382 | G | C | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.350+1954C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99447382 | |||||||
| chr2:99447461 | C | T | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.350+1875G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99447461 | |||||||
| chr2:99447492 | T | C | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.350+1844A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99447492 | |||||||
| chr2:99447494 | G | A | 1 | a0002c0002t0010g0318 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.350+1842C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99447494 | |||||||
| chr2:99447609 | C | T | 3 | a0003c0006t0001g0208 a0003c0006t0001g0209 a0003c0006t0001g0210 |
3 | HG02809.hp1 HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.350+1727G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99447609 | |||||||
| chr2:99447610 | A | G | 173 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(170): Show |
179 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.350+1726T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99447610 | |||||||
| chr2:99447718 | T | C | 43 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(40): Show |
43 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.350+1618A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99447718 | |||||||
| chr2:99447802 | C | T | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.350+1534G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99447802 | |||||||
| chr2:99447821 | C | A | 173 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(170): Show |
179 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.350+1515G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99447821 | |||||||
| chr2:99447863 | G | C | 1 | a0003c0003t0001g0085 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.350+1473C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99447863 | |||||||
| chr2:99447987 | T | C | 2 | a0003c0003t0001g0003 a0003c0003t0001g0087 |
3 | HG00609.hp1 NA18960.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.350+1349A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99447987 | |||||||
| chr2:99447991 | C | T | 2 | a0003c0003t0001g0003 a0003c0003t0001g0087 |
3 | HG00609.hp1 NA18960.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.350+1345G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99447991 | |||||||
| chr2:99448030 | T | G | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.350+1306A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99448030 | |||||||
| chr2:99448106 | C | T | 4 | a0001c0001t0002g0136 a0001c0001t0002g0169 a0001c0001t0002g0170 others(1): Show |
4 | NA18972.hp2 NA18995.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.350+1230G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99448106 | |||||||
| chr2:99448309 | A | AT | 43 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(40): Show |
43 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.350+1026dupA | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99448309 | |||||||
| chr2:99448594 | T | C | 1 | a0002c0002t0001g0302 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.350+742A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99448594 | |||||||
| chr2:99448759 | G | T | 19 | a0001c0001t0001g0051 a0001c0001t0001g0129 a0001c0001t0001g0130 others(16): Show |
19 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.350+577C>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99448759 | |||||||
| chr2:99448804 | A | G | 1 | a0002c0002t0010g0318 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.350+532T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99448804 | |||||||
| chr2:99448881 | A | G | 1 | a0003c0003t0001g0060 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.350+455T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99448881 | |||||||
| chr2:99448904 | T | G | 49 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(46): Show |
49 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(46): Show |
intron_variant | MODIFIER | c.350+432A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99448904 | |||||||
| chr2:99448907 | T | A | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.350+429A>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99448907 | |||||||
| chr2:99448944 | T | C | 1 | a0002c0002t0010g0318 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.350+392A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99448944 | |||||||
| chr2:99449179 | T | C | 1 | a0003c0003t0001g0056 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.350+157A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99449179 | |||||||
| chr2:99449285 | A | C | 1 | a0001c0001t0001g0004 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.350+51T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99449285 | |||||||
| chr2:99449291 | C | T | 1 | a0001c0001t0002g0184 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.350+45G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99449291 | |||||||
| chr2:99449304 | T | C | 1 | a0002c0002t0001g0277 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.350+32A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 4/22 | chr2 | 99449304 | |||||||
| chr2:99449678 | CT | C | 216 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(213): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.182-175delA | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99449678 | |||||||
| chr2:99449690 | C | A | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.182-186G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99449690 | |||||||
| chr2:99449758 | AG | A | 78 | a0001c0001t0001g0151 a0003c0003t0001g0001 a0003c0003t0001g0002 others(75): Show |
81 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.182-255delC | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99449758 | |||||||
| chr2:99449842 | TTG | T | 3 | a0002c0002t0003g0287 a0002c0002t0003g0288 a0002c0002t0003g0307 |
3 | NA18947.hp2 NA18988.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.182-340_182-339del others(2): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99449842 | |||||||
| chr2:99450105 | G | A | 1 | a0004c0004t0001g0023 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.182-601C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99450105 | |||||||
| chr2:99450230 | T | C | 1 | a0001c0001t0002g0200 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.182-726A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99450230 | |||||||
| chr2:99450318 | T | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.182-814A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99450318 | |||||||
| chr2:99450383 | T | C | 43 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(40): Show |
43 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.182-879A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99450383 | |||||||
| chr2:99450474 | T | C | 1 | a0002c0002t0003g0292 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.182-970A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99450474 | |||||||
| chr2:99450635 | A | C | 43 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(40): Show |
43 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.182-1131T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99450635 | |||||||
| chr2:99450761 | C | T | 15 | a0003c0003t0001g0003 a0003c0003t0001g0087 a0003c0003t0001g0091 others(12): Show |
16 | HG00609.hp1 HG02148.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.182-1257G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99450761 | |||||||
| chr2:99450880 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.182-1376A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99450880 | |||||||
| chr2:99450994 | A | G | 43 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(40): Show |
43 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.182-1490T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99450994 | |||||||
| chr2:99451092 | C | T | 217 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(214): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.182-1588G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99451092 | |||||||
| chr2:99451116 | G | A | 220 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(217): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.182-1612C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99451116 | |||||||
| chr2:99451607 | T | C | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.182-2103A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99451607 | |||||||
| chr2:99451724 | C | T | 1 | a0001c0001t0002g0139 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.182-2220G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99451724 | |||||||
| chr2:99451772 | C | T | 1 | a0002c0002t0001g0304 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.182-2268G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99451772 | |||||||
| chr2:99451773 | G | GA | 90 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(87): Show |
93 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.182-2270dupT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99451773 | |||||||
| chr2:99451805 | G | A | 1 | a0002c0002t0010g0318 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.182-2301C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99451805 | |||||||
| chr2:99451844 | C | T | 1 | a0002c0002t0001g0243 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.182-2340G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99451844 | |||||||
| chr2:99451902 | T | G | 1 | a0004c0004t0005g0007 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.182-2398A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99451902 | |||||||
| chr2:99452421 | T | TA | 198 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(195): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.182-2918dupT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99452421 | |||||||
| chr2:99452421 | T | TAA | 17 | a0001c0001t0001g0162 a0001c0001t0001g0175 a0001c0001t0001g0312 others(14): Show |
17 | HG01070.hp1 HG01934.hp2 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.182-2919_182-2918d others(4): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99452421 | |||||||
| chr2:99452439 | A | G | 1 | a0002c0002t0001g0267 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.182-2935T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99452439 | |||||||
| chr2:99452533 | C | G | 1 | a0002c0002t0003g0223 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.182-3029G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99452533 | |||||||
| chr2:99452590 | CTGTT | C | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.182-3090_182-3087d others(6): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99452590 | |||||||
| chr2:99452923 | T | G | 217 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(214): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.182-3419A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99452923 | |||||||
| chr2:99453104 | T | C | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.182-3600A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99453104 | |||||||
| chr2:99453109 | C | T | 2 | a0003c0003t0001g0126 a0003c0003t0001g0127 |
2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.182-3605G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99453109 | |||||||
| chr2:99453127 | A | G | 217 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(214): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.182-3623T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99453127 | |||||||
| chr2:99453188 | G | A | 3 | a0001c0001t0002g0202 a0001c0001t0009g0199 a0001c0015t0002g0201 |
3 | HG03579.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.182-3684C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99453188 | |||||||
| chr2:99453355 | C | CA | 93 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(90): Show |
96 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.182-3852dupT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99453355 | |||||||
| chr2:99453406 | T | G | 1 | a0001c0001t0001g0164 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.182-3902A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99453406 | |||||||
| chr2:99453451 | C | A | 2 | a0002c0002t0001g0251 a0002c0002t0001g0257 |
2 | NA18951.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.182-3947G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99453451 | |||||||
| chr2:99453589 | A | C | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.182-4085T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99453589 | |||||||
| chr2:99453626 | G | A | 5 | a0001c0001t0001g0196 a0001c0001t0002g0191 a0001c0001t0002g0192 others(2): Show |
5 | HG02040.hp1 NA18612.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.182-4122C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99453626 | |||||||
| chr2:99453757 | G | T | 1 | a0002c0002t0003g0281 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.182-4253C>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99453757 | |||||||
| chr2:99453766 | G | A | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.182-4262C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99453766 | |||||||
| chr2:99453832 | A | G | 211 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(208): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.182-4328T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99453832 | |||||||
| chr2:99453850 | G | A | 1 | a0002c0002t0010g0318 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.182-4346C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99453850 | |||||||
| chr2:99453892 | C | CA | 55 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0131 others(52): Show |
55 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.182-4389dupT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99453892 | |||||||
| chr2:99453892 | C | CAA | 9 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0143 others(6): Show |
9 | HG00423.hp1 HG01255.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.182-4390_182-4389d others(4): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99453892 | |||||||
| chr2:99453892 | C | CAAA | 31 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0012 others(28): Show |
31 | HG00280.hp2 HG01168.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.182-4391_182-4389d others(5): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99453892 | |||||||
| chr2:99453892 | C | CAAAA | 11 | a0004c0004t0001g0011 a0004c0004t0001g0014 a0004c0004t0001g0015 others(8): Show |
11 | HG01516.hp1 HG02486.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.182-4392_182-4389d others(6): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99453892 | |||||||
| chr2:99453892 | CA | C | 8 | a0002c0002t0001g0215 a0002c0002t0001g0216 a0002c0002t0001g0295 others(5): Show |
8 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.182-4389delT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99453892 | |||||||
| chr2:99453913 | AAAATCAA others(3): Show |
A | 8 | a0003c0003t0001g0060 a0003c0003t0001g0061 a0003c0003t0001g0062 others(5): Show |
8 | HG00609.hp1 HG01261.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.182-4419_182-4410d others(12): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99453913 | |||||||
| chr2:99453918 | CAAAATAA others(4): Show |
C | 47 | a0003c0003t0001g0001 a0003c0003t0001g0002 a0003c0003t0001g0003 others(44): Show |
50 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.182-4425_182-4415d others(13): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99453918 | |||||||
| chr2:99453928 | C | T | 8 | a0003c0003t0001g0060 a0003c0003t0001g0061 a0003c0003t0001g0062 others(5): Show |
8 | HG00609.hp1 HG01261.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.182-4424G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99453928 | |||||||
| chr2:99453929 | A | C | 8 | a0003c0003t0001g0060 a0003c0003t0001g0061 a0003c0003t0001g0062 others(5): Show |
8 | HG00609.hp1 HG01261.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.182-4425T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99453929 | |||||||
| chr2:99453950 | C | G | 1 | a0003c0003t0001g0059 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.182-4446G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99453950 | |||||||
| chr2:99454028 | C | A | 43 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(40): Show |
43 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.182-4524G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454028 | |||||||
| chr2:99454113 | A | G | 210 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(207): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.182-4609T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454113 | |||||||
| chr2:99454370 | G | A | 1 | a0001c0001t0002g0169 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.182-4866C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454370 | |||||||
| chr2:99454376 | C | A | 3 | a0002c0002t0003g0284 a0002c0002t0003g0285 a0002c0002t0003g0289 |
3 | HG00558.hp1 NA18990.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.182-4872G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454376 | |||||||
| chr2:99454379 | C | T | 1 | a0010c0011t0001g0113 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.182-4875G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454379 | |||||||
| chr2:99454383 | A | G | 2 | a0003c0003t0001g0099 a0003c0003t0001g0100 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.182-4879T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454383 | |||||||
| chr2:99454422 | C | T | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.182-4918G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454422 | |||||||
| chr2:99454550 | C | CAAAAAAA others(4): Show |
2 | a0002c0002t0001g0215 a0002c0002t0001g0273 |
2 | HG02109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.182-5057_182-5047d others(13): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454550 | |||||||
| chr2:99454550 | C | CAAAAAAA others(17): Show |
1 | a0002c0002t0001g0259 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.182-5070_182-5047d others(26): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454550 | |||||||
| chr2:99454550 | CA | C | 24 | a0002c0002t0001g0217 a0002c0002t0001g0233 a0002c0002t0001g0238 others(21): Show |
24 | HG00408.hp1 HG01099.hp1 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.182-5047delT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454550 | |||||||
| chr2:99454550 | CAA | C | 24 | a0002c0002t0001g0212 a0002c0002t0001g0214 a0002c0002t0001g0219 others(21): Show |
24 | HG00558.hp1 HG01074.hp1 HG01516.hp2 others(21): Show |
intron_variant | MODIFIER | c.182-5048_182-5047d others(4): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454550 | |||||||
| chr2:99454550 | CAAA | C | 7 | a0002c0002t0001g0218 a0002c0002t0001g0283 a0002c0002t0001g0308 others(4): Show |
7 | HG01123.hp1 HG02040.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.182-5049_182-5047d others(5): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454550 | |||||||
| chr2:99454550 | CAAAAAA | C | 17 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(14): Show |
18 | HG00558.hp2 HG01070.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.182-5052_182-5047d others(8): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454550 | |||||||
| chr2:99454550 | CAAAAAAA | C | 203 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(200): Show |
208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.182-5053_182-5047d others(9): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454550 | |||||||
| chr2:99454550 | CAAAAAAA others(5): Show |
C | 4 | a0002c0002t0001g0269 a0002c0002t0001g0270 a0002c0002t0003g0242 others(1): Show |
4 | HG01981.hp1 HG02155.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.182-5058_182-5047d others(14): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454550 | |||||||
| chr2:99454550 | CAAAAAAA others(7): Show |
C | 2 | a0002c0002t0001g0227 a0002c0002t0001g0279 |
2 | HG01261.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.182-5060_182-5047d others(16): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454550 | |||||||
| chr2:99454550 | CAAAAAAA others(8): Show |
C | 3 | a0002c0002t0001g0226 a0002c0002t0001g0278 a0002c0002t0003g0275 |
3 | HG01258.hp2 HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.182-5061_182-5047d others(17): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454550 | |||||||
| chr2:99454550 | CAAAAAAA others(9): Show |
C | 1 | a0002c0002t0003g0274 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.182-5062_182-5047d others(18): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454550 | |||||||
| chr2:99454550 | CAAAAAAA others(11): Show |
C | 1 | a0002c0002t0003g0287 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.182-5064_182-5047d others(20): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454550 | |||||||
| chr2:99454550 | CAAAAAAA others(12): Show |
C | 1 | a0002c0002t0001g0241 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.182-5065_182-5047d others(21): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454550 | |||||||
| chr2:99454550 | CAAAAAAA others(16): Show |
C | 1 | a0002c0002t0001g0277 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.182-5069_182-5047d others(25): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454550 | |||||||
| chr2:99454567 | A | C | 32 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(29): Show |
32 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.182-5063T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454567 | |||||||
| chr2:99454570 | A | C | 1 | a0002c0002t0010g0318 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.182-5066T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454570 | |||||||
| chr2:99454573 | A | C | 1 | a0003c0013t0006g0128 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.182-5069T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454573 | |||||||
| chr2:99454574 | A | C | 194 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(191): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.182-5070T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454574 | |||||||
| chr2:99454580 | A | C | 1 | a0003c0013t0006g0128 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.182-5076T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454580 | |||||||
| chr2:99454581 | A | C | 217 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(214): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.182-5077T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454581 | |||||||
| chr2:99454591 | A | C | 208 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(205): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.182-5087T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454591 | |||||||
| chr2:99454603 | C | T | 1 | a0001c0001t0002g0193 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.182-5099G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454603 | |||||||
| chr2:99454878 | C | A | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.182-5374G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454878 | |||||||
| chr2:99454879 | C | A | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.182-5375G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99454879 | |||||||
| chr2:99455176 | A | C | 2 | a0001c0001t0002g0178 a0001c0001t0002g0179 |
2 | HG00741.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.182-5672T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99455176 | |||||||
| chr2:99455558 | G | T | 1 | a0002c0002t0001g0302 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.182-6054C>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99455558 | |||||||
| chr2:99455621 | T | C | 2 | a0004c0004t0001g0033 a0004c0004t0001g0034 |
2 | HG03491.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.182-6117A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99455621 | |||||||
| chr2:99455636 | T | A | 2 | a0002c0002t0001g0261 a0002c0002t0003g0260 |
2 | NA18952.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.182-6132A>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99455636 | |||||||
| chr2:99456323 | T | C | 1 | a0001c0001t0001g0143 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.181+6173A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99456323 | |||||||
| chr2:99456327 | A | G | 1 | a0003c0010t0001g0107 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.181+6169T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99456327 | |||||||
| chr2:99456335 | T | C | 3 | a0003c0006t0001g0208 a0003c0006t0001g0209 a0003c0006t0001g0210 |
3 | HG02809.hp1 HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.181+6161A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99456335 | |||||||
| chr2:99456436 | G | A | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.181+6060C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99456436 | |||||||
| chr2:99456453 | T | G | 1 | a0002c0002t0001g0240 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.181+6043A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99456453 | |||||||
| chr2:99456620 | C | T | 1 | a0002c0002t0001g0240 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.181+5876G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99456620 | |||||||
| chr2:99456668 | T | C | 218 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(215): Show |
224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.181+5828A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99456668 | |||||||
| chr2:99456876 | G | A | 1 | a0003c0003t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.181+5620C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99456876 | |||||||
| chr2:99456963 | A | T | 1 | a0001c0001t0002g0204 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.181+5533T>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99456963 | |||||||
| chr2:99457042 | T | C | 1 | a0003c0003t0001g0094 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.181+5454A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99457042 | |||||||
| chr2:99457050 | G | C | 43 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(40): Show |
43 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.181+5446C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99457050 | |||||||
| chr2:99457082 | T | G | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.181+5414A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99457082 | |||||||
| chr2:99457425 | T | C | 2 | a0003c0003t0001g0126 a0003c0003t0001g0127 |
2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.181+5071A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99457425 | |||||||
| chr2:99457479 | C | T | 2 | a0004c0004t0001g0010 a0004c0004t0001g0035 |
2 | HG02135.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.181+5017G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99457479 | |||||||
| chr2:99457503 | G | A | 4 | a0002c0002t0003g0228 a0002c0002t0003g0287 a0002c0002t0003g0288 others(1): Show |
4 | NA18947.hp2 NA18948.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.181+4993C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99457503 | |||||||
| chr2:99457509 | C | T | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.181+4987G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99457509 | |||||||
| chr2:99457608 | CA | C | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.181+4887delT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99457608 | |||||||
| chr2:99457687 | G | GA | 43 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(40): Show |
43 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.181+4808dupT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99457687 | |||||||
| chr2:99457700 | A | G | 1 | a0002c0002t0001g0276 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.181+4796T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99457700 | |||||||
| chr2:99457937 | TA | T | 85 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(82): Show |
87 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.181+4558delT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99457937 | |||||||
| chr2:99458025 | C | T | 168 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(165): Show |
174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.181+4471G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99458025 | |||||||
| chr2:99458134 | G | C | 43 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(40): Show |
43 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.181+4362C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99458134 | |||||||
| chr2:99458284 | T | C | 218 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(215): Show |
224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.181+4212A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99458284 | |||||||
| chr2:99458300 | A | C | 1 | a0010c0011t0001g0113 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.181+4196T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99458300 | |||||||
| chr2:99458364 | G | A | 1 | a0003c0012t0001g0095 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.181+4132C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99458364 | |||||||
| chr2:99458759 | C | T | 1 | a0007c0020t0001g0239 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.181+3737G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99458759 | |||||||
| chr2:99458895 | A | G | 1 | a0002c0002t0001g0220 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.181+3601T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99458895 | |||||||
| chr2:99458989 | A | G | 2 | a0003c0003t0001g0118 a0003c0003t0001g0119 |
2 | HG00642.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.181+3507T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99458989 | |||||||
| chr2:99459011 | A | G | 2 | a0002c0002t0003g0274 a0002c0002t0003g0275 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.181+3485T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99459011 | |||||||
| chr2:99459013 | A | C | 4 | a0001c0001t0001g0051 a0002c0002t0001g0226 a0002c0002t0001g0227 others(1): Show |
4 | HG01261.hp1 HG02280.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.181+3483T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99459013 | |||||||
| chr2:99459024 | C | T | 1 | a0001c0001t0002g0135 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.181+3472G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99459024 | |||||||
| chr2:99459025 | G | A | 1 | a0002c0002t0001g0212 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.181+3471C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99459025 | |||||||
| chr2:99459034 | C | T | 1 | a0001c0001t0002g0138 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.181+3462G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99459034 | |||||||
| chr2:99459067 | GCGTGGTG others(17): Show |
G | 1 | a0002c0002t0001g0238 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.181+3405_181+3428d others(26): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99459067 | |||||||
| chr2:99459101 | G | A | 7 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(4): Show |
7 | HG02165.hp1 HG02818.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.181+3395C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99459101 | |||||||
| chr2:99459156 | C | T | 1 | a0002c0002t0001g0237 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.181+3340G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99459156 | |||||||
| chr2:99459207 | CA | C | 214 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(211): Show |
220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.181+3288delT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99459207 | |||||||
| chr2:99459342 | C | T | 127 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(124): Show |
129 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.181+3154G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99459342 | |||||||
| chr2:99459380 | G | A | 1 | a0003c0003t0001g0117 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.181+3116C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99459380 | |||||||
| chr2:99459456 | C | T | 1 | a0002c0002t0001g0297 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.181+3040G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99459456 | |||||||
| chr2:99459568 | T | A | 90 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(87): Show |
93 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.181+2928A>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99459568 | |||||||
| chr2:99459655 | G | A | 2 | a0001c0001t0002g0203 a0001c0001t0002g0204 |
2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.181+2841C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99459655 | |||||||
| chr2:99459849 | G | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG01255.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.181+2647C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99459849 | |||||||
| chr2:99459961 | G | A | 1 | a0001c0001t0002g0148 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.181+2535C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99459961 | |||||||
| chr2:99460117 | G | A | 55 | a0003c0003t0001g0001 a0003c0003t0001g0002 a0003c0003t0001g0003 others(52): Show |
58 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.181+2379C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99460117 | |||||||
| chr2:99460140 | A | G | 211 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(208): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.181+2356T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99460140 | |||||||
| chr2:99460168 | C | G | 1 | a0002c0002t0010g0318 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.181+2328G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99460168 | |||||||
| chr2:99460170 | G | A | 3 | a0002c0002t0001g0262 a0002c0002t0001g0263 a0002c0002t0001g0266 |
3 | HG00558.hp2 NA19010.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.181+2326C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99460170 | |||||||
| chr2:99460171 | G | A | 1 | a0002c0002t0010g0318 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.181+2325C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99460171 | |||||||
| chr2:99460194 | A | T | 1 | a0001c0001t0001g0110 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.181+2302T>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99460194 | |||||||
| chr2:99460225 | C | T | 1 | a0002c0002t0001g0296 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.181+2271G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99460225 | |||||||
| chr2:99460226 | G | A | 68 | a0003c0003t0001g0001 a0003c0003t0001g0002 a0003c0003t0001g0003 others(65): Show |
71 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.181+2270C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99460226 | |||||||
| chr2:99460774 | T | C | 1 | a0002c0002t0001g0234 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.181+1722A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99460774 | |||||||
| chr2:99460801 | GAT | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.181+1693_181+1694d others(4): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99460801 | |||||||
| chr2:99460865 | G | C | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.181+1631C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99460865 | |||||||
| chr2:99460983 | C | T | 1 | a0003c0003t0001g0104 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.181+1513G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99460983 | |||||||
| chr2:99461021 | C | CCTAT | 216 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(213): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.181+1474_181+1475i others(6): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99461021 | |||||||
| chr2:99461043 | T | C | 7 | a0001c0001t0002g0005 a0001c0001t0002g0138 a0001c0001t0002g0139 others(4): Show |
8 | HG00639.hp1 HG01433.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.181+1453A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99461043 | |||||||
| chr2:99461504 | G | A | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.181+992C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99461504 | |||||||
| chr2:99461539 | C | A | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.181+957G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99461539 | |||||||
| chr2:99461864 | G | C | 217 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(214): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.181+632C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99461864 | |||||||
| chr2:99461878 | T | C | 1 | a0010c0011t0001g0113 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.181+618A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99461878 | |||||||
| chr2:99462013 | A | G | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.181+483T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99462013 | |||||||
| chr2:99462043 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.181+453G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99462043 | |||||||
| chr2:99462092 | G | C | 1 | a0003c0003t0001g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.181+404C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99462092 | |||||||
| chr2:99462145 | C | T | 1 | a0002c0002t0001g0236 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.181+351G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99462145 | |||||||
| chr2:99462298 | C | T | 42 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(39): Show |
42 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(39): Show |
intron_variant | MODIFIER | c.181+198G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 3/22 | chr2 | 99462298 | |||||||
| chr2:99462704 | A | G | 1 | a0002c0002t0001g0235 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.55-82T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 2/22 | chr2 | 99462704 | |||||||
| chr2:99462791 | A | G | 1 | a0009c0016t0001g0053 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.55-169T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 2/22 | chr2 | 99462791 | |||||||
| chr2:99462981 | G | A | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.55-359C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 2/22 | chr2 | 99462981 | |||||||
| chr2:99463225 | T | A | 1 | a0003c0003t0001g0070 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.55-603A>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 2/22 | chr2 | 99463225 | |||||||
| chr2:99463266 | T | A | 1 | a0002c0002t0001g0264 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.55-644A>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 2/22 | chr2 | 99463266 | |||||||
| chr2:99463391 | T | C | 1 | a0012c0019t0001g0272 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.55-769A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 2/22 | chr2 | 99463391 | |||||||
| chr2:99463475 | G | A | 1 | a0003c0013t0006g0128 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.55-853C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 2/22 | chr2 | 99463475 | |||||||
| chr2:99463710 | C | T | 1 | a0002c0002t0001g0295 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.55-1088G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 2/22 | chr2 | 99463710 | |||||||
| chr2:99464031 | C | A | 1 | a0002c0002t0010g0318 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.54+891G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 2/22 | chr2 | 99464031 | |||||||
| chr2:99464056 | A | G | 1 | a0002c0002t0001g0308 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.54+866T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 2/22 | chr2 | 99464056 | |||||||
| chr2:99464127 | T | C | 216 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(213): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.54+795A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 2/22 | chr2 | 99464127 | |||||||
| chr2:99464280 | T | A | 1 | a0008c0014t0001g0125 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.54+642A>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 2/22 | chr2 | 99464280 | |||||||
| chr2:99464420 | A | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG00733.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.54+502T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 2/22 | chr2 | 99464420 | |||||||
| chr2:99464433 | G | A | 69 | a0003c0003t0001g0001 a0003c0003t0001g0002 a0003c0003t0001g0003 others(66): Show |
72 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.54+489C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 2/22 | chr2 | 99464433 | |||||||
| chr2:99464466 | C | G | 41 | a0003c0003t0001g0001 a0003c0003t0001g0002 a0003c0003t0001g0054 others(38): Show |
43 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.54+456G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 2/22 | chr2 | 99464466 | |||||||
| chr2:99464536 | C | T | 5 | a0003c0003t0001g0002 a0003c0003t0001g0083 a0003c0003t0001g0084 others(2): Show |
6 | HG02280.hp2 HG02922.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.54+386G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 2/22 | chr2 | 99464536 | |||||||
| chr2:99464855 | T | C | 32 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(29): Show |
32 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.54+67A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 2/22 | chr2 | 99464855 | |||||||
| chr2:99464861 | C | T | 218 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(215): Show |
224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.54+61G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 2/22 | chr2 | 99464861 | |||||||
| chr2:99464991 | T | C | 1 | a0002c0002t0001g0265 | 1 | HG01099.hp1 | splice_region_variant&intron_variant | LOW | c.-10-6A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99464991 | |||||||
| chr2:99464999 | G | GA | 11 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(8): Show |
11 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.-10-15dupT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99464999 | |||||||
| chr2:99465099 | A | AAAGTC | 218 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(215): Show |
224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-10-115_-10-114ins others(5): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99465099 | |||||||
| chr2:99465187 | CAT | C | 43 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(40): Show |
43 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.-10-204_-10-203del others(2): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99465187 | |||||||
| chr2:99465448 | T | C | 1 | a0001c0001t0002g0008 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-10-463A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99465448 | |||||||
| chr2:99465519 | T | C | 10 | a0005c0005t0001g0057 a0005c0005t0001g0071 a0005c0005t0001g0072 others(7): Show |
10 | HG01070.hp1 HG01934.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10-534A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99465519 | |||||||
| chr2:99465580 | C | T | 1 | a0004c0004t0001g0048 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-10-595G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99465580 | |||||||
| chr2:99465683 | A | T | 42 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(39): Show |
42 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(39): Show |
intron_variant | MODIFIER | c.-10-698T>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99465683 | |||||||
| chr2:99465829 | C | T | 1 | a0002c0002t0001g0234 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-10-844G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99465829 | |||||||
| chr2:99465832 | C | T | 2 | a0002c0002t0001g0267 a0011c0021t0001g0309 |
2 | HG02280.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.-10-847G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99465832 | |||||||
| chr2:99465964 | C | T | 85 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(82): Show |
87 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.-10-979G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99465964 | |||||||
| chr2:99465990 | G | A | 4 | a0003c0006t0001g0208 a0003c0006t0001g0209 a0003c0006t0001g0210 others(1): Show |
4 | HG01243.hp1 HG02809.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-1005C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99465990 | |||||||
| chr2:99466141 | C | T | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-10-1156G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99466141 | |||||||
| chr2:99466142 | G | A | 2 | a0004c0004t0001g0010 a0004c0004t0001g0035 |
2 | HG02135.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.-10-1157C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99466142 | |||||||
| chr2:99466197 | G | A | 2 | a0002c0002t0001g0308 a0003c0003t0001g0076 |
2 | HG00280.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-10-1212C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99466197 | |||||||
| chr2:99466217 | C | T | 41 | a0003c0003t0001g0001 a0003c0003t0001g0002 a0003c0003t0001g0054 others(38): Show |
43 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.-10-1232G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99466217 | |||||||
| chr2:99466324 | C | T | 1 | a0003c0003t0001g0104 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-10-1339G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99466324 | |||||||
| chr2:99466420 | T | C | 7 | a0001c0001t0002g0008 a0001c0001t0002g0200 a0001c0001t0002g0202 others(4): Show |
7 | HG02572.hp2 HG03041.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10-1435A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99466420 | |||||||
| chr2:99466543 | G | A | 1 | a0003c0003t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-10-1558C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99466543 | |||||||
| chr2:99466716 | C | T | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-10-1731G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99466716 | |||||||
| chr2:99466717 | G | A | 1 | a0003c0003t0001g0207 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-10-1732C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99466717 | |||||||
| chr2:99466753 | T | C | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-1768A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99466753 | |||||||
| chr2:99467263 | A | T | 1 | a0004c0004t0001g0023 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-10-2278T>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99467263 | |||||||
| chr2:99467546 | T | C | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-10-2561A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99467546 | |||||||
| chr2:99467614 | A | T | 1 | a0001c0001t0001g0133 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-10-2629T>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99467614 | |||||||
| chr2:99467615 | A | T | 1 | a0001c0001t0001g0133 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-10-2630T>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99467615 | |||||||
| chr2:99467651 | C | T | 1 | a0002c0002t0003g0303 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-10-2666G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99467651 | |||||||
| chr2:99467873 | C | G | 1 | a0002c0002t0001g0308 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-10-2888G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99467873 | |||||||
| chr2:99468145 | AC | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0112 |
3 | HG01070.hp2 HG01071.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.-10-3161delG | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99468145 | |||||||
| chr2:99468177 | T | A | 1 | a0002c0002t0001g0266 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-10-3192A>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99468177 | |||||||
| chr2:99468180 | CA | C | 203 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(200): Show |
208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.-10-3196delT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99468180 | |||||||
| chr2:99468180 | CAA | C | 15 | a0001c0001t0002g0008 a0003c0003t0001g0003 a0003c0003t0001g0087 others(12): Show |
16 | HG00609.hp1 HG02148.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.-10-3197_-10-3196d others(4): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99468180 | |||||||
| chr2:99468208 | A | C | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-10-3223T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99468208 | |||||||
| chr2:99468227 | T | C | 3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0186 |
3 | NA18950.hp1 NA18966.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-10-3242A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99468227 | |||||||
| chr2:99468297 | A | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-3312T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99468297 | |||||||
| chr2:99468637 | C | G | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-3652G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99468637 | |||||||
| chr2:99468712 | C | G | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-10-3727G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99468712 | |||||||
| chr2:99468795 | T | G | 4 | a0001c0001t0002g0006 a0001c0001t0002g0144 a0001c0001t0002g0145 others(1): Show |
5 | NA18952.hp2 NA18964.hp1 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-3810A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99468795 | |||||||
| chr2:99468966 | G | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-3981C>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99468966 | |||||||
| chr2:99468990 | C | T | 1 | a0004c0004t0001g0027 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-10-4005G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99468990 | |||||||
| chr2:99469096 | G | T | 1 | a0010c0011t0001g0113 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-10-4111C>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99469096 | |||||||
| chr2:99469119 | T | C | 21 | a0001c0001t0001g0166 a0004c0004t0001g0009 a0004c0004t0001g0010 others(18): Show |
21 | HG01168.hp1 HG02083.hp1 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.-10-4134A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99469119 | |||||||
| chr2:99469342 | T | C | 46 | a0001c0001t0001g0166 a0001c0001t0001g0317 a0002c0002t0001g0267 others(43): Show |
46 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(43): Show |
intron_variant | MODIFIER | c.-10-4357A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99469342 | |||||||
| chr2:99469499 | C | A | 1 | a0001c0001t0001g0167 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-10-4514G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99469499 | |||||||
| chr2:99469638 | C | G | 1 | a0002c0002t0003g0268 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-10-4653G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99469638 | |||||||
| chr2:99469853 | T | C | 2 | a0004c0004t0001g0036 a0004c0004t0001g0037 |
2 | HG01358.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.-10-4868A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99469853 | |||||||
| chr2:99469949 | G | A | 2 | a0004c0008t0001g0038 a0004c0008t0001g0041 |
2 | NA18998.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-10-4964C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99469949 | |||||||
| chr2:99469972 | T | G | 3 | a0003c0006t0001g0208 a0003c0006t0001g0209 a0003c0006t0001g0210 |
3 | HG02809.hp1 HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-10-4987A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99469972 | |||||||
| chr2:99469978 | G | A | 1 | a0002c0002t0003g0268 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-10-4993C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99469978 | |||||||
| chr2:99470038 | G | A | 1 | a0004c0017t0001g0039 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-10-5053C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99470038 | |||||||
| chr2:99470120 | C | CA | 9 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(6): Show |
10 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-5136dupT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99470120 | |||||||
| chr2:99470142 | C | T | 4 | a0003c0003t0001g0126 a0003c0003t0001g0127 a0003c0003t0001g0207 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-5157G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99470142 | |||||||
| chr2:99470276 | A | G | 1 | a0003c0003t0001g0058 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-10-5291T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99470276 | |||||||
| chr2:99470404 | C | T | 1 | a0002c0002t0001g0233 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-10-5419G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99470404 | |||||||
| chr2:99470405 | G | A | 3 | a0003c0003t0001g0126 a0003c0003t0001g0127 a0003c0003t0001g0207 |
3 | HG01891.hp2 HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-10-5420C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99470405 | |||||||
| chr2:99470456 | G | C | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-10-5471C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99470456 | |||||||
| chr2:99470511 | T | C | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-5526A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99470511 | |||||||
| chr2:99470553 | C | G | 1 | a0003c0003t0001g0207 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-10-5568G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99470553 | |||||||
| chr2:99470581 | G | A | 1 | a0004c0004t0001g0043 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-10-5596C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99470581 | |||||||
| chr2:99470627 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-5642G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99470627 | |||||||
| chr2:99470738 | T | A | 4 | a0003c0006t0001g0208 a0003c0006t0001g0209 a0003c0006t0001g0210 others(1): Show |
4 | HG01243.hp1 HG02809.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-5753A>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99470738 | |||||||
| chr2:99470807 | C | G | 1 | a0004c0004t0001g0044 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-10-5822G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99470807 | |||||||
| chr2:99470850 | G | A | 1 | a0002c0002t0001g0218 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-10-5865C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99470850 | |||||||
| chr2:99470911 | C | T | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-10-5926G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99470911 | |||||||
| chr2:99471006 | T | C | 49 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(46): Show |
49 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(46): Show |
intron_variant | MODIFIER | c.-10-6021A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99471006 | |||||||
| chr2:99471016 | T | C | 41 | a0001c0001t0001g0143 a0001c0001t0001g0196 a0001c0001t0002g0005 others(38): Show |
43 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.-10-6031A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99471016 | |||||||
| chr2:99471138 | AAC | A | 162 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(159): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.-10-6155_-10-6154d others(4): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99471138 | |||||||
| chr2:99471141 | A | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-6156T>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99471141 | |||||||
| chr2:99471176 | C | T | 1 | a0002c0002t0001g0310 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-10-6191G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99471176 | |||||||
| chr2:99471234 | G | C | 1 | a0004c0004t0005g0007 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-10-6249C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99471234 | |||||||
| chr2:99471429 | T | TA | 77 | a0003c0003t0001g0001 a0003c0003t0001g0002 a0003c0003t0001g0003 others(74): Show |
80 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.-10-6445dupT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99471429 | |||||||
| chr2:99471535 | T | C | 4 | a0002c0002t0001g0269 a0002c0002t0001g0270 a0002c0002t0001g0271 others(1): Show |
4 | HG02155.hp2 NA18612.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-6550A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99471535 | |||||||
| chr2:99471850 | A | C | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-10-6865T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99471850 | |||||||
| chr2:99471870 | C | G | 42 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(39): Show |
42 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(39): Show |
intron_variant | MODIFIER | c.-10-6885G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99471870 | |||||||
| chr2:99471877 | G | A | 1 | a0002c0002t0003g0289 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-10-6892C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99471877 | |||||||
| chr2:99471889 | T | TA | 17 | a0001c0001t0001g0168 a0001c0001t0001g0172 a0001c0001t0002g0147 others(14): Show |
17 | HG01243.hp1 HG02027.hp2 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.-10-6905dupT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99471889 | |||||||
| chr2:99471889 | TA | T | 11 | a0001c0001t0001g0130 a0001c0001t0002g0008 a0001c0001t0002g0191 others(8): Show |
11 | HG02615.hp2 HG03041.hp2 HG03486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-10-6905delT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99471889 | |||||||
| chr2:99471902 | A | C | 1 | a0003c0013t0006g0128 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-10-6917T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99471902 | |||||||
| chr2:99472160 | T | C | 1 | a0004c0004t0001g0016 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-10-7175A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99472160 | |||||||
| chr2:99472231 | G | A | 1 | a0001c0001t0004g0149 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-10-7246C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99472231 | |||||||
| chr2:99472616 | G | A | 41 | a0003c0003t0001g0001 a0003c0003t0001g0002 a0003c0003t0001g0054 others(38): Show |
43 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.-10-7631C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99472616 | |||||||
| chr2:99472624 | G | C | 3 | a0003c0003t0001g0115 a0003c0003t0001g0116 a0003c0003t0001g0117 |
3 | HG02615.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-10-7639C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99472624 | |||||||
| chr2:99472750 | G | A | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-10-7765C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99472750 | |||||||
| chr2:99473063 | G | A | 31 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(28): Show |
31 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.-10-8078C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99473063 | |||||||
| chr2:99473365 | C | CAAA | 160 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0109 others(157): Show |
165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-10-8383_-10-8381d others(5): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99473365 | |||||||
| chr2:99473365 | C | CAAAA | 5 | a0001c0001t0001g0004 a0001c0001t0001g0205 a0001c0001t0002g0169 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-8384_-10-8381d others(6): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99473365 | |||||||
| chr2:99473409 | A | C | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-10-8424T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99473409 | |||||||
| chr2:99473636 | A | G | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-10-8651T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99473636 | |||||||
| chr2:99473764 | T | G | 80 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(77): Show |
82 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.-10-8779A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99473764 | |||||||
| chr2:99473915 | T | C | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-10-8930A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99473915 | |||||||
| chr2:99473963 | T | C | 2 | a0002c0002t0001g0226 a0002c0002t0001g0227 |
2 | HG01261.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-10-8978A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99473963 | |||||||
| chr2:99474020 | A | C | 1 | a0003c0003t0001g0118 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-10-9035T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99474020 | |||||||
| chr2:99474178 | C | A | 1 | a0002c0002t0010g0318 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-10-9193G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99474178 | |||||||
| chr2:99474502 | G | T | 1 | a0004c0004t0001g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-10-9517C>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99474502 | |||||||
| chr2:99474704 | C | T | 1 | a0009c0016t0001g0053 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-10-9719G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99474704 | |||||||
| chr2:99474824 | C | G | 1 | a0001c0001t0009g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10-9839G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99474824 | |||||||
| chr2:99474851 | G | A | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-10-9866C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99474851 | |||||||
| chr2:99474883 | C | A | 8 | a0003c0003t0001g0118 a0003c0003t0001g0119 a0003c0003t0001g0120 others(5): Show |
8 | HG00642.hp2 HG01123.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10-9898G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99474883 | |||||||
| chr2:99474908 | GA | G | 85 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(82): Show |
87 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.-10-9924delT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99474908 | |||||||
| chr2:99474989 | T | G | 1 | a0005c0005t0001g0078 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-10-10004A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99474989 | |||||||
| chr2:99475163 | G | C | 210 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(207): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.-10-10178C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99475163 | |||||||
| chr2:99475537 | T | C | 5 | a0002c0002t0003g0225 a0002c0002t0003g0291 a0002c0002t0003g0292 others(2): Show |
5 | HG00544.hp2 HG02083.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-10552A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99475537 | |||||||
| chr2:99475660 | T | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-10675A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99475660 | |||||||
| chr2:99475677 | ACT | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-10694_-10-1069 others(6): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99475677 | |||||||
| chr2:99475686 | C | CA | 41 | a0003c0003t0001g0001 a0003c0003t0001g0002 a0003c0003t0001g0054 others(38): Show |
43 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.-10-10702dupT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99475686 | |||||||
| chr2:99475715 | T | G | 1 | a0003c0003t0001g0079 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-10-10730A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99475715 | |||||||
| chr2:99475887 | G | C | 31 | a0002c0002t0001g0276 a0002c0002t0001g0277 a0002c0002t0001g0278 others(28): Show |
31 | HG00544.hp2 HG00558.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.-10-10902C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99475887 | |||||||
| chr2:99476012 | T | C | 1 | a0001c0001t0002g0132 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-10-11027A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99476012 | |||||||
| chr2:99476053 | C | T | 1 | a0004c0004t0001g0016 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-10-11068G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99476053 | |||||||
| chr2:99476174 | C | A | 43 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(40): Show |
43 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.-10-11189G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99476174 | |||||||
| chr2:99476211 | T | C | 13 | a0003c0003t0001g0114 a0003c0003t0001g0115 a0003c0003t0001g0116 others(10): Show |
13 | HG00642.hp2 HG01123.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.-10-11226A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99476211 | |||||||
| chr2:99476217 | C | T | 1 | a0001c0001t0002g0177 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-10-11232G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99476217 | |||||||
| chr2:99476326 | G | A | 3 | a0004c0004t0001g0046 a0004c0004t0001g0047 a0013c0018t0001g0045 |
3 | HG00280.hp2 HG03669.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-10-11341C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99476326 | |||||||
| chr2:99476509 | T | C | 1 | a0004c0004t0001g0040 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-10-11524A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99476509 | |||||||
| chr2:99476513 | G | A | 1 | a0002c0002t0003g0229 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-10-11528C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99476513 | |||||||
| chr2:99476553 | CAAT | C | 217 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(214): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.-10-11571_-10-1156 others(7): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99476553 | |||||||
| chr2:99476616 | C | T | 90 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(87): Show |
93 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.-10-11631G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99476616 | |||||||
| chr2:99476630 | A | T | 1 | a0003c0003t0001g0114 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-10-11645T>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99476630 | |||||||
| chr2:99476683 | A | G | 1 | a0001c0001t0002g0132 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-10-11698T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99476683 | |||||||
| chr2:99476698 | G | A | 1 | a0002c0002t0001g0294 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-10-11713C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99476698 | |||||||
| chr2:99477145 | G | A | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-12160C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99477145 | |||||||
| chr2:99477211 | C | A | 2 | a0001c0001t0002g0170 a0001c0001t0002g0173 |
2 | NA18995.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-10-12226G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99477211 | |||||||
| chr2:99477229 | G | A | 1 | a0002c0002t0010g0318 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-10-12244C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99477229 | |||||||
| chr2:99477586 | T | C | 1 | a0002c0002t0010g0318 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-11+12231A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99477586 | |||||||
| chr2:99477608 | T | C | 1 | a0010c0011t0001g0113 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-11+12209A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99477608 | |||||||
| chr2:99478337 | C | T | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-11+11480G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99478337 | |||||||
| chr2:99478358 | C | G | 1 | a0013c0018t0001g0045 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-11+11459G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99478358 | |||||||
| chr2:99478473 | G | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+11344C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99478473 | |||||||
| chr2:99478713 | C | G | 7 | a0002c0002t0001g0214 a0002c0002t0001g0215 a0002c0002t0001g0216 others(4): Show |
7 | HG01261.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+11104G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99478713 | |||||||
| chr2:99478757 | C | T | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-11+11060G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99478757 | |||||||
| chr2:99478854 | G | C | 7 | a0002c0002t0001g0214 a0002c0002t0001g0215 a0002c0002t0001g0216 others(4): Show |
7 | HG01261.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+10963C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99478854 | |||||||
| chr2:99479110 | A | G | 1 | a0002c0002t0010g0318 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-11+10707T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99479110 | |||||||
| chr2:99479286 | T | C | 218 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(215): Show |
224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-11+10531A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99479286 | |||||||
| chr2:99479299 | C | G | 1 | a0002c0002t0003g0230 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-11+10518G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99479299 | |||||||
| chr2:99479314 | G | A | 5 | a0003c0003t0001g0002 a0003c0003t0001g0083 a0003c0003t0001g0084 others(2): Show |
6 | HG02280.hp2 HG02922.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+10503C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99479314 | |||||||
| chr2:99479326 | C | CA | 51 | a0001c0001t0001g0312 a0002c0002t0001g0297 a0002c0002t0001g0302 others(48): Show |
51 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(48): Show |
intron_variant | MODIFIER | c.-11+10490dupT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99479326 | |||||||
| chr2:99479326 | CA | C | 162 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0109 others(159): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.-11+10490delT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99479326 | |||||||
| chr2:99479345 | C | A | 1 | a0001c0001t0001g0312 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-11+10472G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99479345 | |||||||
| chr2:99479687 | C | T | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+10130G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99479687 | |||||||
| chr2:99479779 | AAATAAT | A | 217 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(214): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.-11+10032_-11+1003 others(10): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99479779 | |||||||
| chr2:99479909 | T | C | 43 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(40): Show |
43 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.-11+9908A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99479909 | |||||||
| chr2:99479973 | G | A | 3 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 |
3 | HG02809.hp2 HG02896.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-11+9844C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99479973 | |||||||
| chr2:99480086 | C | T | 1 | a0002c0002t0001g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-11+9731G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99480086 | |||||||
| chr2:99480116 | C | T | 2 | a0002c0002t0001g0226 a0002c0002t0001g0227 |
2 | HG01261.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-11+9701G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99480116 | |||||||
| chr2:99480217 | G | A | 1 | a0003c0003t0001g0081 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-11+9600C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99480217 | |||||||
| chr2:99480222 | G | A | 9 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(6): Show |
9 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11+9595C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99480222 | |||||||
| chr2:99480245 | C | T | 1 | a0002c0002t0003g0222 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-11+9572G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99480245 | |||||||
| chr2:99480577 | A | G | 1 | a0002c0002t0003g0225 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-11+9240T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99480577 | |||||||
| chr2:99480721 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-11+9096G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99480721 | |||||||
| chr2:99480859 | T | A | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-11+8958A>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99480859 | |||||||
| chr2:99480893 | T | C | 1 | a0003c0003t0001g0098 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-11+8924A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99480893 | |||||||
| chr2:99481151 | T | C | 218 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(215): Show |
224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-11+8666A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99481151 | |||||||
| chr2:99481168 | T | C | 2 | a0002c0002t0001g0301 a0002c0002t0001g0302 |
2 | HG02135.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-11+8649A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99481168 | |||||||
| chr2:99481211 | A | C | 1 | a0009c0016t0001g0053 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-11+8606T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99481211 | |||||||
| chr2:99481251 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-11+8566G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99481251 | |||||||
| chr2:99481414 | C | A | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+8403G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99481414 | |||||||
| chr2:99481503 | T | G | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-11+8314A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99481503 | |||||||
| chr2:99481580 | G | A | 6 | a0003c0003t0001g0002 a0003c0003t0001g0082 a0003c0003t0001g0083 others(3): Show |
7 | HG02280.hp2 HG02922.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+8237C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99481580 | |||||||
| chr2:99481692 | T | TAC | 163 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(160): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.-11+8123_-11+8124d others(4): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99481692 | |||||||
| chr2:99481692 | T | TACAC | 5 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+8121_-11+8124d others(6): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99481692 | |||||||
| chr2:99481692 | T | TACACAC | 5 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0315 others(2): Show |
5 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11+8119_-11+8124d others(8): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99481692 | |||||||
| chr2:99481710 | A | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0109 a0001c0001t0001g0110 others(3): Show |
7 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11+8107T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99481710 | |||||||
| chr2:99481731 | C | T | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0206 |
3 | NA18945.hp1 NA18968.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.-11+8086G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99481731 | |||||||
| chr2:99481954 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-11+7863T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99481954 | |||||||
| chr2:99482079 | G | A | 13 | a0003c0003t0001g0114 a0003c0003t0001g0115 a0003c0003t0001g0116 others(10): Show |
13 | HG00642.hp2 HG01123.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11+7738C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99482079 | |||||||
| chr2:99482115 | T | C | 1 | a0002c0002t0001g0305 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-11+7702A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99482115 | |||||||
| chr2:99482291 | T | G | 85 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(82): Show |
87 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.-11+7526A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99482291 | |||||||
| chr2:99482448 | T | C | 3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0186 |
3 | NA18950.hp1 NA18966.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-11+7369A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99482448 | |||||||
| chr2:99482463 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-11+7354G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99482463 | |||||||
| chr2:99482534 | G | A | 1 | a0005c0005t0001g0086 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-11+7283C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99482534 | |||||||
| chr2:99482680 | G | A | 2 | a0003c0003t0001g0126 a0003c0003t0001g0127 |
2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-11+7137C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99482680 | |||||||
| chr2:99482887 | G | C | 4 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(1): Show |
4 | HG00423.hp1 HG00609.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+6930C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99482887 | |||||||
| chr2:99482951 | A | G | 1 | a0004c0004t0001g0013 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-11+6866T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99482951 | |||||||
| chr2:99483017 | C | CA | 46 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(43): Show |
46 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(43): Show |
intron_variant | MODIFIER | c.-11+6799dupT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99483017 | |||||||
| chr2:99483017 | CA | C | 39 | a0002c0002t0003g0223 a0003c0003t0001g0001 a0003c0003t0001g0002 others(36): Show |
41 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.-11+6799delT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99483017 | |||||||
| chr2:99483035 | T | A | 43 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(40): Show |
43 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.-11+6782A>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99483035 | |||||||
| chr2:99483146 | G | C | 1 | a0004c0004t0001g0042 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-11+6671C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99483146 | |||||||
| chr2:99483207 | A | G | 1 | a0002c0002t0003g0222 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-11+6610T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99483207 | |||||||
| chr2:99483230 | G | A | 1 | a0004c0004t0001g0043 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-11+6587C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99483230 | |||||||
| chr2:99483314 | G | A | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+6503C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99483314 | |||||||
| chr2:99483388 | G | A | 7 | a0001c0001t0001g0196 a0001c0001t0002g0191 a0001c0001t0002g0192 others(4): Show |
7 | HG02040.hp1 NA18612.hp2 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+6429C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99483388 | |||||||
| chr2:99483859 | T | C | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-11+5958A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99483859 | |||||||
| chr2:99484035 | AC | A | 85 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0129 others(82): Show |
87 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.-11+5781delG | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99484035 | |||||||
| chr2:99484043 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-11+5774G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99484043 | |||||||
| chr2:99484053 | C | T | 2 | a0004c0004t0001g0011 a0004c0004t0001g0012 |
2 | HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-11+5764G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99484053 | |||||||
| chr2:99484153 | T | C | 1 | a0004c0004t0001g0044 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-11+5664A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99484153 | |||||||
| chr2:99484184 | T | C | 43 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(40): Show |
43 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.-11+5633A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99484184 | |||||||
| chr2:99484262 | T | G | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+5555A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99484262 | |||||||
| chr2:99484318 | C | A | 1 | a0002c0002t0003g0303 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-11+5499G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99484318 | |||||||
| chr2:99484386 | A | C | 43 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(40): Show |
43 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.-11+5431T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99484386 | |||||||
| chr2:99484597 | T | TATA | 315 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(312): Show |
321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.-11+5219_-11+5220i others(5): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99484597 | |||||||
| chr2:99484692 | T | TA | 7 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(4): Show |
7 | HG01934.hp1 HG02818.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+5124dupT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99484692 | |||||||
| chr2:99484702 | A | C | 2 | a0003c0010t0001g0107 a0011c0021t0001g0309 |
2 | HG01243.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-11+5115T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99484702 | |||||||
| chr2:99484832 | C | T | 1 | a0002c0002t0001g0214 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-11+4985G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99484832 | |||||||
| chr2:99485014 | T | G | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+4803A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99485014 | |||||||
| chr2:99485054 | C | G | 1 | a0002c0002t0001g0220 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-11+4763G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99485054 | |||||||
| chr2:99485102 | C | T | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+4715G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99485102 | |||||||
| chr2:99485300 | C | A | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-11+4517G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99485300 | |||||||
| chr2:99485351 | A | G | 1 | a0004c0004t0001g0010 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-11+4466T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99485351 | |||||||
| chr2:99485389 | T | C | 49 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(46): Show |
49 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(46): Show |
intron_variant | MODIFIER | c.-11+4428A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99485389 | |||||||
| chr2:99485759 | T | C | 1 | a0003c0003t0001g0198 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-11+4058A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99485759 | |||||||
| chr2:99485874 | GGGAGGAT others(6): Show |
G | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-11+3930_-11+3942d others(15): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99485874 | |||||||
| chr2:99485907 | T | G | 2 | a0003c0003t0001g0099 a0003c0003t0001g0100 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-11+3910A>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99485907 | |||||||
| chr2:99486018 | G | A | 1 | a0002c0002t0001g0305 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-11+3799C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99486018 | |||||||
| chr2:99486087 | TGCATTCC others(16): Show |
T | 1 | a0003c0003t0001g0055 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-11+3707_-11+3729d others(25): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99486087 | |||||||
| chr2:99486306 | G | A | 1 | a0004c0004t0001g0050 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-11+3511C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99486306 | |||||||
| chr2:99486328 | C | G | 217 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(214): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.-11+3489G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99486328 | |||||||
| chr2:99486386 | G | A | 1 | a0002c0002t0001g0306 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-11+3431C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99486386 | |||||||
| chr2:99486480 | G | A | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-11+3337C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99486480 | |||||||
| chr2:99486515 | C | A | 2 | a0003c0003t0001g0101 a0003c0003t0001g0102 |
2 | HG00140.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.-11+3302G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99486515 | |||||||
| chr2:99486520 | C | T | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+3297G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99486520 | |||||||
| chr2:99486528 | C | CA | 154 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(151): Show |
160 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.-11+3288dupT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99486528 | |||||||
| chr2:99486528 | C | CAA | 9 | a0001c0001t0001g0205 a0001c0001t0002g0008 a0001c0001t0002g0200 others(6): Show |
9 | HG02572.hp2 HG02738.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11+3287_-11+3288d others(4): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99486528 | |||||||
| chr2:99486528 | CAAAA | C | 43 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(40): Show |
43 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.-11+3285_-11+3288d others(6): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99486528 | |||||||
| chr2:99486608 | G | T | 1 | a0004c0004t0001g0009 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-11+3209C>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99486608 | |||||||
| chr2:99486917 | GA | G | 166 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(163): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.-11+2899delT | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99486917 | |||||||
| chr2:99486953 | T | C | 1 | a0003c0003t0001g0207 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-11+2864A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99486953 | |||||||
| chr2:99487051 | C | G | 3 | a0002c0002t0001g0217 a0002c0002t0001g0218 a0002c0002t0001g0219 |
3 | HG02647.hp1 HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-11+2766G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99487051 | |||||||
| chr2:99487251 | GCTATGCC others(1300): Show |
G | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-11+1259_-11+2565d others(2): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99487251 | |||||||
| chr2:99487635 | T | C | 2 | a0004c0004t0001g0049 a0004c0004t0001g0050 |
2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-11+2182A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99487635 | |||||||
| chr2:99487638 | T | TAA | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+2177_-11+2178d others(4): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99487638 | |||||||
| chr2:99487647 | A | C | 1 | a0002c0002t0010g0318 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-11+2170T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99487647 | |||||||
| chr2:99487908 | C | T | 4 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(1): Show |
4 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+1909G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99487908 | |||||||
| chr2:99488151 | T | C | 1 | a0002c0002t0003g0242 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-11+1666A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99488151 | |||||||
| chr2:99488232 | T | C | 5 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0315 others(2): Show |
5 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11+1585A>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99488232 | |||||||
| chr2:99488275 | G | A | 2 | a0004c0004t0001g0009 a0004c0004t0001g0028 |
2 | NA18971.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.-11+1542C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99488275 | |||||||
| chr2:99488560 | T | A | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-11+1257A>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99488560 | |||||||
| chr2:99488561 | A | T | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-11+1256T>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99488561 | |||||||
| chr2:99488563 | A | C | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-11+1254T>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99488563 | |||||||
| chr2:99488568 | A | AAT | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-11+1248_-11+1249i others(4): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99488568 | |||||||
| chr2:99488569 | G | C | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-11+1248C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99488569 | |||||||
| chr2:99488651 | C | T | 1 | a0001c0001t0001g0004 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-11+1166G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99488651 | |||||||
| chr2:99488704 | G | T | 2 | a0001c0001t0002g0105 a0001c0001t0002g0106 |
2 | NA18966.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-11+1113C>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99488704 | |||||||
| chr2:99488754 | G | A | 1 | a0002c0002t0003g0307 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-11+1063C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99488754 | |||||||
| chr2:99488800 | G | A | 1 | a0002c0002t0001g0216 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-11+1017C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99488800 | |||||||
| chr2:99488850 | A | G | 217 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(214): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.-11+967T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99488850 | |||||||
| chr2:99489007 | T | A | 1 | a0002c0002t0001g0308 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-11+810A>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99489007 | |||||||
| chr2:99489014 | G | A | 3 | a0004c0004t0001g0046 a0004c0004t0001g0047 a0013c0018t0001g0045 |
3 | HG00280.hp2 HG03669.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-11+803C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99489014 | |||||||
| chr2:99489100 | G | C | 1 | a0011c0021t0001g0309 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-11+717C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99489100 | |||||||
| chr2:99489113 | C | G | 3 | a0002c0002t0001g0214 a0002c0002t0001g0215 a0002c0002t0001g0216 |
3 | HG02109.hp2 HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-11+704G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99489113 | |||||||
| chr2:99489141 | G | A | 1 | a0003c0003t0001g0104 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-11+676C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99489141 | |||||||
| chr2:99489212 | A | G | 1 | a0002c0002t0001g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-11+605T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99489212 | |||||||
| chr2:99489267 | G | A | 3 | a0003c0006t0001g0208 a0003c0006t0001g0209 a0003c0006t0001g0210 |
3 | HG02809.hp1 HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-11+550C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99489267 | |||||||
| chr2:99489284 | G | A | 2 | a0002c0002t0001g0310 a0002c0002t0001g0311 |
2 | HG01255.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-11+533C>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99489284 | |||||||
| chr2:99489313 | G | T | 55 | a0003c0003t0001g0001 a0003c0003t0001g0002 a0003c0003t0001g0003 others(52): Show |
58 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.-11+504C>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99489313 | |||||||
| chr2:99489334 | C | A | 1 | a0003c0003t0001g0211 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-11+483G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99489334 | |||||||
| chr2:99489410 | C | A | 3 | a0004c0004t0001g0048 a0004c0004t0001g0049 a0004c0004t0001g0050 |
3 | HG02486.hp2 HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-11+407G>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99489410 | |||||||
| chr2:99489423 | C | G | 1 | a0002c0002t0001g0212 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-11+394G>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99489423 | |||||||
| chr2:99489446 | G | C | 6 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+371C>G | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99489446 | |||||||
| chr2:99489455 | T | A | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-11+362A>T | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99489455 | |||||||
| chr2:99489467 | CGGGATGC others(13): Show |
C | 1 | a0009c0016t0001g0053 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-11+330_-11+349del others(20): Show |
REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99489467 | |||||||
| chr2:99489506 | A | G | 167 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0108 others(164): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-11+311T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99489506 | |||||||
| chr2:99489562 | A | G | 1 | a0001c0001t0001g0051 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-11+255T>C | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99489562 | |||||||
| chr2:99489734 | C | CG | 43 | a0004c0004t0001g0009 a0004c0004t0001g0010 a0004c0004t0001g0011 others(40): Show |
43 | HG00280.hp2 HG01168.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.-11+82dupC | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99489734 | |||||||
| chr2:99489781 | C | T | 1 | a0001c0001t0002g0008 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-11+36G>A | REV1 | ENSG00000135945.10 | transcript | ENST00000258428.8 | protein_coding | 1/22 | chr2 | 99489781 |