Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 225 |
| ensemblid | ENSG00000173208.4 |
| hgncid | 66 |
| symbol | ABCD2 |
| name | ATP binding cassette subfamily D member 2 |
| refseq_nuc | NM_005164.4 |
| refseq_prot | NP_005155.1 |
| ensembl_nuc | ENST00000308666.4 |
| ensembl_prot | ENSP00000310688.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 39550033 |
| end | 39619803 |
| strand | - |
| ver | v1.2 |
| region | chr12:39550033-39619803 |
| region5000 | chr12:39545033-39624803 |
| regionname0 | ABCD2_chr12_39550033_39619803 |
| regionname5000 | ABCD2_chr12_39545033_39624803 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 740 | 324 | 81 | 52 | 145 | 6 | 38 | 114 | ABCD2_chr12_39545033_39624803 | ABCD2 | MTHML others(735): Show |
chr12 | 39545033 | 39624803 |
| a0002 | 0/0 | 740 | 11 | 0 | 6 | 5 | 0 | 0 | 4 | ABCD2_chr12_39545033_39624803 | ABCD2 | MTHML others(735): Show |
chr12 | 39545033 | 39624803 |
| a0003 | 0/0 | 740 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | MTHML others(735): Show |
chr12 | 39545033 | 39624803 |
| a0004 | 0/0 | 740 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ABCD2_chr12_39545033_39624803 | ABCD2 | MTHML others(735): Show |
chr12 | 39545033 | 39624803 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2220 | 318 | 78 | 50 | 145 | 6 | 37 | ABCD2_chr12_39545033_39624803 | ABCD2 | ATGAC others(2215): Show |
chr12 | 39545033 | 39624803 | ||
| a0001c0003 | 0/0 | 2220 | 3 | 0 | 2 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | ATGAC others(2215): Show |
chr12 | 39545033 | 39624803 | ||
| a0001c0006 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | ATGAC others(2215): Show |
chr12 | 39545033 | 39624803 | ||
| a0001c0007 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | ATGAC others(2215): Show |
chr12 | 39545033 | 39624803 | ||
| a0001c0008 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | ATGAC others(2215): Show |
chr12 | 39545033 | 39624803 | ||
| a0002c0002 | 0/0 | 2220 | 11 | 0 | 6 | 5 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | ATGAC others(2215): Show |
chr12 | 39545033 | 39624803 | ||
| a0003c0005 | 0/0 | 2220 | 2 | 0 | 2 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | ATGAC others(2215): Show |
chr12 | 39545033 | 39624803 | ||
| a0003c0009 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | ATGAC others(2215): Show |
chr12 | 39545033 | 39624803 | ||
| a0004c0004 | 0/0 | 2220 | 2 | 0 | 0 | 2 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | ATGAC others(2215): Show |
chr12 | 39545033 | 39624803 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 6290 | 158 | 32 | 26 | 80 | 2 | 16 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0001t0002 | 0/0 | 6290 | 56 | 0 | 8 | 35 | 1 | 12 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0001t0003 | 0/0 | 6290 | 24 | 0 | 3 | 20 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0001t0004 | 0/0 | 6290 | 7 | 5 | 0 | 1 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0001t0005 | 0/0 | 6290 | 17 | 17 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0001t0006 | 0/0 | 6290 | 14 | 2 | 4 | 3 | 1 | 4 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0001t0007 | 0/0 | 6290 | 6 | 6 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0001t0008 | 0/0 | 6290 | 6 | 0 | 6 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0001t0009 | 0/0 | 6290 | 5 | 3 | 0 | 1 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0001t0010 | 0/0 | 6290 | 4 | 4 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0001t0011 | 0/0 | 6290 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0001t0012 | 0/0 | 6285 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6280): Show |
chr12 | 39545033 | 39624803 |
| a0001c0001t0013 | 0/0 | 6290 | 2 | 0 | 0 | 0 | 2 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0001t0014 | 0/0 | 6290 | 2 | 2 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0001t0015 | 0/0 | 6290 | 2 | 2 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0001t0016 | 0/0 | 6290 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0001t0017 | 0/0 | 6290 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0001t0018 | 0/0 | 6290 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0001t0019 | 0/0 | 6285 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6280): Show |
chr12 | 39545033 | 39624803 |
| a0001c0001t0020 | 0/0 | 6290 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0001t0021 | 0/0 | 6290 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0001t0022 | 0/0 | 6290 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0001t0023 | 0/0 | 6290 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0001t0025 | 0/0 | 6290 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0001t0027 | 0/0 | 6290 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0001t0028 | 0/0 | 6290 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0001t0029 | 0/0 | 6290 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0001t0030 | 0/0 | 6290 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0003t0001 | 0/0 | 6290 | 2 | 0 | 1 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0003t0026 | 0/0 | 6290 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0006t0024 | 0/0 | 6290 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0007t0007 | 0/0 | 6290 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0001c0008t0006 | 0/0 | 6290 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0002c0002t0004 | 0/0 | 6290 | 11 | 0 | 6 | 5 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0003c0005t0011 | 0/0 | 6290 | 2 | 0 | 2 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0003c0009t0011 | 0/0 | 6290 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6285): Show |
chr12 | 39545033 | 39624803 |
| a0004c0004t0012 | 0/0 | 6285 | 2 | 0 | 0 | 2 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | AGATG others(6280): Show |
chr12 | 39545033 | 39624803 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0010 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0173 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0003 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0004g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0005g0002 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0005g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0006g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0006g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0006g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0006g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0006g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0006g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0006g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0006g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0006g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0006g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0007g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0007g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0007g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0007g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0008g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0008g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0008g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0008g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0008g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0009g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0009g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0009g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0009g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0010g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0010g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0010g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0011g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0012g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0013g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0013g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0014g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0014g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0015g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0015g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0016g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0017g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0018g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0019g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0020g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0021g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0022g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0023g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0025g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0027g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0028g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0029g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0001t0030g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0003t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0003t0026g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0006t0024g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0007t0007g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0001c0008t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0002c0002t0004g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0002c0002t0004g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0002c0002t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0002c0002t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0002c0002t0004g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0002c0002t0004g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0002c0002t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0003c0005t0011g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0003c0009t0011g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| a0004c0004t0012g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0006 | g0013 | EUR | FIN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0118 | EUR | FIN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | CHS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | CHS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | CHS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | CHS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | CHS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00639 | hp1 | a0002 | c0002 | t0004 | g0276 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0040 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00733 | hp2 | a0001 | c0001 | t0023 | g0084 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0025 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01070 | hp1 | a0002 | c0002 | t0004 | g0005 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01071 | hp1 | a0002 | c0002 | t0004 | g0005 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01074 | hp1 | a0002 | c0002 | t0004 | g0005 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01106 | hp1 | a0001 | c0003 | t0026 | g0212 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01106 | hp2 | a0001 | c0001 | t0008 | g0114 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01109 | hp2 | a0001 | c0001 | t0008 | g0245 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01167 | hp1 | a0003 | c0005 | t0011 | g0031 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01168 | hp1 | a0002 | c0002 | t0004 | g0277 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01169 | hp1 | a0003 | c0005 | t0011 | g0031 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01169 | hp2 | a0002 | c0002 | t0004 | g0005 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01175 | hp2 | a0001 | c0001 | t0006 | g0056 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01192 | hp2 | a0001 | c0001 | t0018 | g0077 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0057 | AMR | CLM | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01361 | hp2 | a0001 | c0001 | t0006 | g0064 | AMR | CLM | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | IBS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01515 | hp2 | a0001 | c0001 | t0013 | g0036 | EUR | IBS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | IBS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01517 | hp2 | a0001 | c0001 | t0013 | g0035 | EUR | IBS | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0002 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01891 | hp2 | a0001 | c0006 | t0024 | g0034 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01934 | hp1 | a0001 | c0001 | t0030 | g0279 | AMR | PEL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01934 | hp2 | a0001 | c0001 | t0008 | g0244 | AMR | PEL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01952 | hp2 | a0001 | c0001 | t0008 | g0028 | AMR | PEL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01975 | hp2 | a0001 | c0001 | t0008 | g0220 | AMR | PEL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01981 | hp1 | a0001 | c0001 | t0006 | g0013 | AMR | PEL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01981 | hp2 | a0001 | c0001 | t0008 | g0028 | AMR | PEL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | KHV | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0091 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02055 | hp2 | a0001 | c0001 | t0007 | g0074 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02056 | hp1 | a0002 | c0002 | t0004 | g0275 | EAS | KHV | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | KHV | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02129 | hp1 | a0001 | c0001 | t0009 | g0016 | EAS | KHV | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02129 | hp2 | a0001 | c0001 | t0006 | g0066 | EAS | KHV | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | KHV | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0086 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02155 | hp1 | a0001 | c0001 | t0017 | g0218 | EAS | CDX | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | CDX | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0076 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02280 | hp1 | a0001 | c0001 | t0015 | g0098 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02451 | hp2 | a0001 | c0001 | t0010 | g0080 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0088 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0061 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0162 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02717 | hp1 | a0001 | c0001 | t0014 | g0211 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0089 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0092 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0081 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02809 | hp2 | a0001 | c0001 | t0014 | g0210 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0075 | AFR | ESN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0094 | AFR | ESN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0059 | AFR | ESN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02976 | hp2 | a0001 | c0001 | t0009 | g0037 | AFR | ESN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0178 | AFR | MSL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0093 | AFR | MSL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03130 | hp2 | a0001 | c0001 | t0010 | g0014 | AFR | ESN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03139 | hp1 | a0001 | c0001 | t0011 | g0085 | AFR | ESN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0096 | AFR | ESN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0002 | AFR | ESN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03195 | hp2 | a0001 | c0001 | t0009 | g0042 | AFR | ESN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0090 | AFR | MSL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03239 | hp1 | a0001 | c0001 | t0028 | g0039 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0120 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03453 | hp1 | a0001 | c0001 | t0022 | g0079 | AFR | MSL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03453 | hp2 | a0001 | c0001 | t0025 | g0191 | AFR | MSL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0095 | AFR | MSL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03492 | hp1 | a0001 | c0001 | t0006 | g0058 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03516 | hp1 | a0001 | c0001 | t0015 | g0097 | AFR | ESN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03516 | hp2 | a0003 | c0009 | t0011 | g0273 | AFR | ESN | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03579 | hp1 | a0001 | c0007 | t0007 | g0087 | AFR | MSL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0154 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | STU | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03688 | hp2 | a0001 | c0001 | t0006 | g0060 | SAS | STU | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03710 | hp1 | a0001 | c0001 | t0009 | g0016 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03834 | hp2 | a0001 | c0001 | t0006 | g0054 | SAS | BEB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0012 | SAS | STU | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0140 | SAS | STU | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0131 | SAS | BEB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0065 | SAS | BEB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | STU | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0025 | SAS | STU | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG04204 | hp1 | a0001 | c0001 | t0029 | g0215 | SAS | STU | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | STU | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0192 | SAS | STU | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0002 | AFR | YRI | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0082 | AFR | YRI | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | CHB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | CHB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0002 | AFR | YRI | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | YRI | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18939 | hp2 | a0004 | c0004 | t0012 | g0023 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18950 | hp2 | a0001 | c0001 | t0012 | g0190 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18957 | hp1 | a0004 | c0004 | t0012 | g0023 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18960 | hp1 | a0001 | c0001 | t0019 | g0184 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18969 | hp1 | a0001 | c0001 | t0016 | g0033 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18971 | hp1 | a0002 | c0002 | t0004 | g0032 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18979 | hp2 | a0001 | c0001 | t0020 | g0231 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18986 | hp1 | a0001 | c0001 | t0006 | g0067 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18988 | hp2 | a0002 | c0002 | t0004 | g0278 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19002 | hp2 | a0002 | c0002 | t0004 | g0274 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19030 | hp1 | a0001 | c0001 | t0010 | g0014 | AFR | LWK | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | LWK | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | LWK | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19043 | hp2 | a0001 | c0001 | t0027 | g0063 | AFR | LWK | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19067 | hp2 | a0001 | c0001 | t0006 | g0068 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19085 | hp1 | a0002 | c0002 | t0004 | g0032 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0002 | AFR | ASW | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0083 | AFR | ASW | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0038 | SAS | GIH | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | GIH | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02109 | hp1 | a0001 | c0001 | t0010 | g0078 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02109 | hp2 | a0001 | c0008 | t0006 | g0062 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02486 | hp2 | a0001 | c0001 | t0009 | g0043 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0002 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG03471 | hp2 | a0001 | c0001 | t0021 | g0202 | AFR | MSL | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | USA | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0002 | AFR | USA | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | USA | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0152 | AFR | USA | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0112 | REF | REF | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0173 | REF | REF | ABCD2_chr12_39545033_39624803 | ABCD2 | chr12 | 39545033 | 39624803 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:39554040 | C | G | 1 | a0004 | 2 | NA18939.hp2 NA18957.hp1 |
missense_variant | MODERATE | c.2095G>C | p.Glu699Gln | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 2283/6290 | 2095/2223 | 699/740 | chr12 | 39554040 | |||
| chr12:39619428 | G | C | 1 | a0003 | 3 | HG01167.hp1 HG01169.hp1 HG03516.hp2 |
missense_variant | MODERATE | c.188C>G | p.Thr63Arg | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/10 | 376/6290 | 188/2223 | 63/740 | chr12 | 39619428 | |||
| chr12:39619590 | G | C | 1 | a0002 | 11 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(8): Show |
missense_variant | MODERATE | c.26C>G | p.Ala9Gly | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/10 | 214/6290 | 26/2223 | 9/740 | chr12 | 39619590 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:39553936 | A | G | 1 | a0001c0007 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.2199T>C | p.Ile733Ile | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 2387/6290 | 2199/2223 | 733/740 | chr12 | 39553936 | |||
| chr12:39554083 | G | A | 1 | a0001c0008 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.2052C>T | p.Arg684Arg | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 2240/6290 | 2052/2223 | 684/740 | chr12 | 39554083 | |||
| chr12:39586261 | G | T | 1 | a0001c0006 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.1683C>A | p.Val561Val | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/10 | 1871/6290 | 1683/2223 | 561/740 | chr12 | 39586261 | |||
| chr12:39617061 | C | T | 1 | a0001c0003 | 3 | HG00738.hp2 HG01106.hp1 HG04199.hp2 |
synonymous_variant | LOW | c.1047G>A | p.Lys349Lys | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/10 | 1235/6290 | 1047/2223 | 349/740 | chr12 | 39617061 | |||
| chr12:39619351 | G | A | 1 | a0003c0009 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.265C>T | p.Leu89Leu | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/10 | 453/6290 | 265/2223 | 89/740 | chr12 | 39619351 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:39550042 | G | C | 3 | a0001c0001t0011 a0003c0005t0011 a0003c0009t0011 |
4 | HG01167.hp1 HG01169.hp1 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3870C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 3870 | chr12 | 39550042 | ||||||
| chr12:39550117 | A | G | 1 | a0001c0001t0020 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3795T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 3795 | chr12 | 39550117 | ||||||
| chr12:39550488 | C | A | 1 | a0001c0001t0021 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3424G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 3424 | chr12 | 39550488 | ||||||
| chr12:39550501 | A | G | 2 | a0001c0001t0002 a0001c0001t0029 |
57 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*3411T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 3411 | chr12 | 39550501 | ||||||
| chr12:39550892 | T | C | 1 | a0001c0001t0014 | 2 | HG02717.hp1 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3020A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 3020 | chr12 | 39550892 | ||||||
| chr12:39551200 | A | G | 1 | a0001c0001t0027 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2712T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 2712 | chr12 | 39551200 | ||||||
| chr12:39551251 | T | G | 3 | a0001c0001t0010 a0001c0001t0018 a0001c0001t0022 |
6 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2661A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 2661 | chr12 | 39551251 | ||||||
| chr12:39551442 | A | G | 1 | a0001c0001t0019 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2470T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 2470 | chr12 | 39551442 | ||||||
| chr12:39551451 | G | A | 7 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0011 others(4): Show |
40 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2461C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 2461 | chr12 | 39551451 | ||||||
| chr12:39551930 | GTTAAC | G | 3 | a0001c0001t0012 a0001c0001t0019 a0004c0004t0012 |
4 | NA18939.hp2 NA18950.hp2 NA18957.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1977_*1981delGTTA others(1): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 1977 | chr12 | 39551930 | ||||||
| chr12:39552139 | G | T | 1 | a0001c0003t0026 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1773C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 1773 | chr12 | 39552139 | ||||||
| chr12:39552326 | A | G | 1 | a0001c0001t0028 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1586T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 1586 | chr12 | 39552326 | ||||||
| chr12:39552552 | C | A | 24 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(21): Show |
162 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*1360G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 1360 | chr12 | 39552552 | ||||||
| chr12:39552671 | C | T | 1 | a0001c0001t0005 | 17 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1241G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 1241 | chr12 | 39552671 | ||||||
| chr12:39552672 | G | A | 1 | a0001c0001t0023 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1240C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 1240 | chr12 | 39552672 | ||||||
| chr12:39552779 | G | A | 1 | a0001c0001t0008 | 6 | HG01106.hp2 HG01109.hp2 HG01934.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1133C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 1133 | chr12 | 39552779 | ||||||
| chr12:39552851 | T | G | 2 | a0001c0001t0003 a0001c0001t0028 |
25 | HG00642.hp2 HG00741.hp2 HG01243.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1061A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 1061 | chr12 | 39552851 | ||||||
| chr12:39552894 | G | A | 1 | a0001c0001t0029 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1018C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 1018 | chr12 | 39552894 | ||||||
| chr12:39552908 | C | T | 1 | a0001c0001t0018 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1004G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 1004 | chr12 | 39552908 | ||||||
| chr12:39553225 | C | T | 1 | a0001c0001t0017 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*687G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 687 | chr12 | 39553225 | ||||||
| chr12:39553338 | T | C | 1 | a0001c0006t0024 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*574A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 574 | chr12 | 39553338 | ||||||
| chr12:39553437 | T | C | 1 | a0001c0001t0025 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*475A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 475 | chr12 | 39553437 | ||||||
| chr12:39553506 | G | A | 7 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0013 others(4): Show |
44 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*406C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 406 | chr12 | 39553506 | ||||||
| chr12:39553523 | T | C | 2 | a0001c0001t0002 a0001c0001t0029 |
57 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*389A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 389 | chr12 | 39553523 | ||||||
| chr12:39553557 | A | C | 1 | a0001c0001t0013 | 2 | HG01515.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*355T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 355 | chr12 | 39553557 | ||||||
| chr12:39553603 | A | G | 2 | a0001c0001t0007 a0001c0007t0007 |
7 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*309T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 309 | chr12 | 39553603 | ||||||
| chr12:39553892 | T | G | 1 | a0001c0001t0015 | 2 | HG02280.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*20A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 10/10 | 20 | chr12 | 39553892 | ||||||
| chr12:39619626 | A | G | 1 | a0001c0001t0030 | 1 | HG01934.hp1 | 5_prime_UTR_variant | MODIFIER | c.-11T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/10 | 11 | chr12 | 39619626 | ||||||
| chr12:39619627 | C | A | 1 | a0001c0001t0030 | 1 | HG01934.hp1 | 5_prime_UTR_variant | MODIFIER | c.-12G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/10 | 12 | chr12 | 39619627 | ||||||
| chr12:39619753 | A | G | 1 | a0001c0001t0016 | 1 | NA18969.hp1 | 5_prime_UTR_variant | MODIFIER | c.-138T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/10 | 138 | chr12 | 39619753 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:39554162 | G | T | 1 | a0001c0001t0001g0099 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2004-31C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39554162 | |||||||
| chr12:39554239 | C | T | 1 | a0001c0001t0011g0085 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2004-108G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39554239 | |||||||
| chr12:39554275 | G | C | 1 | a0001c0001t0009g0042 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2004-144C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39554275 | |||||||
| chr12:39554327 | G | C | 41 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0012 others(38): Show |
50 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.2004-196C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39554327 | |||||||
| chr12:39554464 | G | T | 1 | a0001c0001t0001g0239 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2004-333C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39554464 | |||||||
| chr12:39554653 | G | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0026 others(38): Show |
58 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.2004-522C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39554653 | |||||||
| chr12:39554791 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2004-660A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39554791 | |||||||
| chr12:39554806 | G | C | 1 | a0001c0001t0001g0145 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2004-675C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39554806 | |||||||
| chr12:39554809 | G | A | 2 | a0001c0001t0010g0014 a0001c0001t0010g0078 |
3 | HG02109.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2004-678C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39554809 | |||||||
| chr12:39554820 | G | A | 1 | a0001c0001t0025g0191 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2004-689C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39554820 | |||||||
| chr12:39554852 | G | C | 1 | a0001c0001t0001g0026 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2004-721C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39554852 | |||||||
| chr12:39555004 | C | G | 18 | a0001c0001t0006g0013 a0001c0001t0006g0054 a0001c0001t0006g0056 others(15): Show |
19 | HG00280.hp1 HG01106.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.2004-873G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39555004 | |||||||
| chr12:39555081 | G | A | 5 | a0001c0001t0010g0014 a0001c0001t0010g0078 a0001c0001t0010g0080 others(2): Show |
6 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2004-950C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39555081 | |||||||
| chr12:39555242 | C | A | 1 | a0001c0001t0001g0267 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2004-1111G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39555242 | |||||||
| chr12:39555244 | A | G | 2 | a0001c0001t0009g0016 a0001c0001t0023g0084 |
3 | HG00733.hp2 HG02129.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2004-1113T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39555244 | |||||||
| chr12:39555345 | A | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(273): Show |
337 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(334): Show |
intron_variant | MODIFIER | c.2004-1214T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39555345 | |||||||
| chr12:39555491 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0262 |
3 | HG02257.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2004-1360T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39555491 | |||||||
| chr12:39555593 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2004-1462G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39555593 | |||||||
| chr12:39555656 | C | T | 1 | a0001c0001t0006g0081 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2004-1525G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39555656 | |||||||
| chr12:39555798 | A | G | 1 | a0001c0001t0009g0042 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2004-1667T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39555798 | |||||||
| chr12:39555805 | C | T | 1 | a0001c0001t0023g0084 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2004-1674G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39555805 | |||||||
| chr12:39555852 | G | C | 7 | a0001c0001t0007g0074 a0001c0001t0007g0075 a0001c0001t0007g0076 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2004-1721C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39555852 | |||||||
| chr12:39555853 | C | A | 7 | a0001c0001t0007g0074 a0001c0001t0007g0075 a0001c0001t0007g0076 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2004-1722G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39555853 | |||||||
| chr12:39555921 | A | G | 2 | a0002c0002t0004g0275 a0002c0002t0004g0278 |
2 | HG02056.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.2004-1790T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39555921 | |||||||
| chr12:39555943 | T | C | 2 | a0001c0001t0003g0047 a0001c0001t0003g0052 |
2 | NA18947.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.2004-1812A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39555943 | |||||||
| chr12:39556207 | C | T | 1 | a0001c0001t0011g0085 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2004-2076G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39556207 | |||||||
| chr12:39556250 | A | G | 3 | a0001c0001t0001g0116 a0001c0001t0001g0219 a0001c0001t0001g0240 |
3 | HG01975.hp1 HG02738.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2004-2119T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39556250 | |||||||
| chr12:39556368 | G | A | 1 | a0001c0003t0001g0025 | 2 | HG00738.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2004-2237C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39556368 | |||||||
| chr12:39556605 | A | G | 1 | a0003c0009t0011g0273 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2004-2474T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39556605 | |||||||
| chr12:39556615 | C | T | 7 | a0001c0001t0007g0074 a0001c0001t0007g0075 a0001c0001t0007g0076 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2004-2484G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39556615 | |||||||
| chr12:39556639 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2004-2508C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39556639 | |||||||
| chr12:39556649 | C | T | 1 | a0001c0001t0002g0154 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2004-2518G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39556649 | |||||||
| chr12:39556680 | T | C | 1 | a0001c0001t0009g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2004-2549A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39556680 | |||||||
| chr12:39556758 | A | T | 2 | a0001c0001t0009g0016 a0001c0001t0023g0084 |
3 | HG00733.hp2 HG02129.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2004-2627T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39556758 | |||||||
| chr12:39556982 | C | CA | 114 | a0001c0001t0001g0105 a0001c0001t0001g0142 a0001c0001t0002g0003 others(111): Show |
145 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.2004-2852dupT | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39556982 | |||||||
| chr12:39557034 | T | C | 7 | a0001c0001t0007g0074 a0001c0001t0007g0075 a0001c0001t0007g0076 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2004-2903A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39557034 | |||||||
| chr12:39557114 | T | C | 1 | a0001c0001t0009g0042 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2004-2983A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39557114 | |||||||
| chr12:39557189 | G | A | 36 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0012 others(33): Show |
44 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.2004-3058C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39557189 | |||||||
| chr12:39557251 | C | T | 48 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0021 others(45): Show |
57 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.2004-3120G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39557251 | |||||||
| chr12:39557332 | A | G | 14 | a0001c0001t0004g0020 a0001c0001t0004g0055 a0001c0001t0004g0065 others(11): Show |
20 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2004-3201T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39557332 | |||||||
| chr12:39557529 | A | C | 5 | a0001c0001t0009g0037 a0001c0001t0009g0042 a0001c0001t0009g0043 others(2): Show |
5 | HG02280.hp1 HG02486.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2004-3398T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39557529 | |||||||
| chr12:39557675 | T | C | 26 | a0001c0001t0004g0020 a0001c0001t0004g0055 a0001c0001t0004g0065 others(23): Show |
39 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.2004-3544A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39557675 | |||||||
| chr12:39557717 | C | T | 3 | a0001c0001t0006g0066 a0001c0001t0006g0067 a0001c0001t0006g0068 |
3 | HG02129.hp2 NA18986.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.2004-3586G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39557717 | |||||||
| chr12:39557718 | C | G | 36 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0012 others(33): Show |
44 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.2004-3587G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39557718 | |||||||
| chr12:39557749 | G | T | 1 | a0001c0001t0003g0189 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2004-3618C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39557749 | |||||||
| chr12:39557761 | G | A | 123 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0021 others(120): Show |
154 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.2004-3630C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39557761 | |||||||
| chr12:39558127 | C | T | 1 | a0001c0001t0002g0192 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2004-3996G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39558127 | |||||||
| chr12:39558216 | G | A | 1 | a0001c0001t0009g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2004-4085C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39558216 | |||||||
| chr12:39558263 | G | C | 5 | a0001c0001t0010g0014 a0001c0001t0010g0078 a0001c0001t0010g0080 others(2): Show |
6 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2004-4132C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39558263 | |||||||
| chr12:39558507 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2004-4376C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39558507 | |||||||
| chr12:39558585 | A | C | 1 | a0001c0001t0006g0067 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2004-4454T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39558585 | |||||||
| chr12:39558610 | T | C | 123 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0021 others(120): Show |
154 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.2004-4479A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39558610 | |||||||
| chr12:39558611 | G | A | 1 | a0001c0001t0006g0060 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2004-4480C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39558611 | |||||||
| chr12:39558615 | T | C | 89 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0021 others(86): Show |
107 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.2004-4484A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39558615 | |||||||
| chr12:39558684 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2004-4553G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39558684 | |||||||
| chr12:39558754 | A | G | 2 | a0001c0001t0004g0082 a0001c0001t0004g0083 |
2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2004-4623T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39558754 | |||||||
| chr12:39558907 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0149 a0001c0001t0001g0262 |
4 | HG02257.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2004-4776C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39558907 | |||||||
| chr12:39558935 | G | T | 10 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(7): Show |
10 | NA18944.hp2 NA18959.hp1 NA19000.hp2 others(7): Show |
intron_variant | MODIFIER | c.2004-4804C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39558935 | |||||||
| chr12:39558936 | C | T | 26 | a0001c0001t0004g0020 a0001c0001t0004g0055 a0001c0001t0004g0065 others(23): Show |
39 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.2004-4805G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39558936 | |||||||
| chr12:39559145 | G | A | 1 | a0001c0006t0024g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2004-5014C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39559145 | |||||||
| chr12:39559149 | G | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0072 |
4 | HG01884.hp1 HG02622.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2004-5018C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39559149 | |||||||
| chr12:39559183 | A | G | 2 | a0002c0002t0004g0275 a0002c0002t0004g0278 |
2 | HG02056.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.2004-5052T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39559183 | |||||||
| chr12:39559261 | A | G | 2 | a0001c0001t0015g0097 a0001c0001t0015g0098 |
2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2004-5130T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39559261 | |||||||
| chr12:39559308 | C | T | 1 | a0001c0008t0006g0062 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2004-5177G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39559308 | |||||||
| chr12:39559309 | G | A | 48 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0021 others(45): Show |
57 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.2004-5178C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39559309 | |||||||
| chr12:39559331 | C | T | 36 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0012 others(33): Show |
44 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.2004-5200G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39559331 | |||||||
| chr12:39559378 | C | CA | 66 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0111 others(63): Show |
78 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.2004-5248dupT | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39559378 | |||||||
| chr12:39559378 | C | CAA | 7 | a0001c0001t0001g0204 a0001c0001t0002g0046 a0001c0001t0002g0119 others(4): Show |
7 | HG00423.hp2 HG00741.hp2 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.2004-5249_2004-524 others(6): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39559378 | |||||||
| chr12:39559378 | CA | C | 11 | a0001c0001t0001g0150 a0001c0001t0001g0207 a0001c0001t0001g0232 others(8): Show |
12 | HG01167.hp2 HG01192.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.2004-5248delT | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39559378 | |||||||
| chr12:39559378 | CAAAAAAA others(5): Show |
C | 26 | a0001c0001t0004g0020 a0001c0001t0004g0055 a0001c0001t0004g0065 others(23): Show |
39 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.2004-5259_2004-524 others(16): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39559378 | |||||||
| chr12:39559400 | A | G | 26 | a0001c0001t0004g0020 a0001c0001t0004g0055 a0001c0001t0004g0065 others(23): Show |
39 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.2004-5269T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39559400 | |||||||
| chr12:39559571 | C | T | 2 | a0001c0001t0002g0003 a0001c0001t0002g0167 |
7 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.2004-5440G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39559571 | |||||||
| chr12:39559727 | C | G | 1 | a0001c0001t0001g0107 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2004-5596G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39559727 | |||||||
| chr12:39560072 | A | G | 1 | a0001c0001t0003g0051 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2004-5941T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39560072 | |||||||
| chr12:39560147 | C | T | 1 | a0001c0006t0024g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2004-6016G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39560147 | |||||||
| chr12:39560162 | G | T | 1 | a0001c0001t0014g0210 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2004-6031C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39560162 | |||||||
| chr12:39560191 | T | A | 1 | a0001c0001t0022g0079 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2004-6060A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39560191 | |||||||
| chr12:39560289 | C | T | 3 | a0001c0001t0002g0131 a0001c0001t0002g0158 a0001c0001t0002g0160 |
3 | HG03491.hp2 HG04184.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2004-6158G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39560289 | |||||||
| chr12:39560471 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2004-6340T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39560471 | |||||||
| chr12:39560508 | C | G | 1 | a0001c0001t0002g0140 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2004-6377G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39560508 | |||||||
| chr12:39560905 | G | A | 5 | a0001c0001t0007g0074 a0001c0001t0007g0075 a0001c0001t0007g0076 others(2): Show |
5 | HG02055.hp2 HG02257.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2004-6774C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39560905 | |||||||
| chr12:39560938 | A | G | 1 | a0001c0001t0003g0006 | 3 | NA18939.hp1 NA18997.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.2004-6807T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39560938 | |||||||
| chr12:39561115 | G | A | 1 | a0001c0001t0005g0178 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2004-6984C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39561115 | |||||||
| chr12:39561233 | T | TAA | 18 | a0001c0001t0006g0013 a0001c0001t0006g0054 a0001c0001t0006g0056 others(15): Show |
19 | HG00280.hp1 HG01106.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.2004-7104_2004-710 others(6): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39561233 | |||||||
| chr12:39561233 | T | TAAA | 95 | a0001c0001t0001g0250 a0001c0001t0001g0252 a0001c0001t0002g0003 others(92): Show |
118 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.2004-7105_2004-710 others(7): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39561233 | |||||||
| chr12:39561283 | C | G | 1 | a0001c0001t0001g0129 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2004-7152G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39561283 | |||||||
| chr12:39561391 | C | CA | 33 | a0001c0001t0001g0073 a0001c0001t0001g0106 a0001c0001t0001g0177 others(30): Show |
43 | HG00741.hp1 HG01192.hp2 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.2004-7261dupT | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39561391 | |||||||
| chr12:39561391 | CA | C | 6 | a0001c0001t0001g0103 a0001c0001t0001g0150 a0001c0001t0001g0254 others(3): Show |
6 | HG01168.hp1 HG01943.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.2004-7261delT | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39561391 | |||||||
| chr12:39561428 | A | C | 1 | a0001c0001t0001g0221 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2004-7297T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39561428 | |||||||
| chr12:39561446 | C | T | 41 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0012 others(38): Show |
50 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.2004-7315G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39561446 | |||||||
| chr12:39561480 | A | T | 1 | a0001c0001t0023g0084 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2004-7349T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39561480 | |||||||
| chr12:39561624 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2004-7493T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39561624 | |||||||
| chr12:39561653 | T | G | 10 | a0001c0001t0007g0074 a0001c0001t0007g0075 a0001c0001t0007g0076 others(7): Show |
10 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.2004-7522A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39561653 | |||||||
| chr12:39561707 | A | G | 2 | a0001c0001t0001g0219 a0001c0001t0001g0240 |
2 | HG01975.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.2004-7576T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39561707 | |||||||
| chr12:39561937 | T | C | 48 | a0001c0001t0001g0193 a0001c0001t0002g0003 a0001c0001t0002g0011 others(45): Show |
57 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.2004-7806A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39561937 | |||||||
| chr12:39562000 | T | C | 128 | a0001c0001t0001g0193 a0001c0001t0002g0003 a0001c0001t0002g0011 others(125): Show |
160 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.2004-7869A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39562000 | |||||||
| chr12:39562084 | GT | G | 11 | a0001c0001t0005g0002 a0001c0001t0005g0017 a0001c0001t0005g0090 others(8): Show |
18 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.2004-7954delA | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39562084 | |||||||
| chr12:39562089 | C | A | 1 | a0001c0001t0027g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2004-7958G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39562089 | |||||||
| chr12:39562132 | T | A | 1 | a0001c0001t0025g0191 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2004-8001A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39562132 | |||||||
| chr12:39562306 | C | G | 1 | a0001c0001t0001g0171 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2004-8175G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39562306 | |||||||
| chr12:39562374 | A | C | 1 | a0001c0001t0028g0039 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2004-8243T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39562374 | |||||||
| chr12:39562458 | A | G | 1 | a0001c0001t0017g0218 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2004-8327T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39562458 | |||||||
| chr12:39562541 | G | T | 2 | a0001c0001t0002g0192 a0001c0001t0002g0194 |
2 | HG01168.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.2004-8410C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39562541 | |||||||
| chr12:39562587 | A | G | 1 | a0001c0006t0024g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2004-8456T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39562587 | |||||||
| chr12:39562607 | C | T | 1 | a0001c0006t0024g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2004-8476G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39562607 | |||||||
| chr12:39562732 | A | T | 1 | a0001c0001t0001g0102 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2004-8601T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39562732 | |||||||
| chr12:39563141 | A | C | 1 | a0001c0001t0001g0246 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2004-9010T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39563141 | |||||||
| chr12:39563146 | T | C | 2 | a0001c0001t0004g0082 a0001c0001t0004g0083 |
2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2004-9015A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39563146 | |||||||
| chr12:39563180 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2004-9049T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39563180 | |||||||
| chr12:39563582 | T | C | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | HG03540.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2004-9451A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39563582 | |||||||
| chr12:39563645 | C | CT | 35 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0012 others(32): Show |
43 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.2004-9515dupA | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39563645 | |||||||
| chr12:39563709 | T | C | 1 | a0001c0006t0024g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2004-9578A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39563709 | |||||||
| chr12:39563782 | T | A | 35 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0012 others(32): Show |
43 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.2004-9651A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39563782 | |||||||
| chr12:39563947 | A | G | 128 | a0001c0001t0001g0193 a0001c0001t0002g0003 a0001c0001t0002g0011 others(125): Show |
160 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.2003+9769T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39563947 | |||||||
| chr12:39564202 | C | A | 1 | a0001c0006t0024g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2003+9514G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39564202 | |||||||
| chr12:39564257 | G | A | 3 | a0001c0001t0003g0006 a0001c0001t0003g0044 a0001c0001t0003g0045 |
5 | NA18939.hp1 NA18941.hp2 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.2003+9459C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39564257 | |||||||
| chr12:39564273 | A | G | 15 | a0001c0001t0004g0020 a0001c0001t0004g0055 a0001c0001t0004g0065 others(12): Show |
20 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2003+9443T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39564273 | |||||||
| chr12:39564286 | C | T | 128 | a0001c0001t0001g0193 a0001c0001t0002g0003 a0001c0001t0002g0011 others(125): Show |
160 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.2003+9430G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39564286 | |||||||
| chr12:39564310 | A | G | 3 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 |
3 | NA19062.hp1 NA19080.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.2003+9406T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39564310 | |||||||
| chr12:39564324 | C | T | 1 | a0001c0001t0002g0162 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2003+9392G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39564324 | |||||||
| chr12:39564348 | T | C | 7 | a0001c0001t0007g0074 a0001c0001t0007g0075 a0001c0001t0007g0076 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2003+9368A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39564348 | |||||||
| chr12:39564379 | A | G | 4 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(1): Show |
4 | HG00609.hp2 NA18747.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.2003+9337T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39564379 | |||||||
| chr12:39564464 | T | G | 1 | a0001c0001t0005g0092 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2003+9252A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39564464 | |||||||
| chr12:39564582 | C | T | 2 | a0001c0001t0015g0097 a0001c0001t0015g0098 |
2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2003+9134G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39564582 | |||||||
| chr12:39564593 | A | G | 1 | a0001c0006t0024g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2003+9123T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39564593 | |||||||
| chr12:39564713 | G | T | 1 | a0001c0001t0001g0224 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2003+9003C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39564713 | |||||||
| chr12:39564797 | A | G | 4 | a0001c0001t0001g0019 a0001c0001t0001g0133 a0001c0001t0001g0207 others(1): Show |
5 | HG01167.hp2 HG02723.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2003+8919T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39564797 | |||||||
| chr12:39565031 | G | C | 5 | a0001c0001t0010g0014 a0001c0001t0010g0078 a0001c0001t0010g0080 others(2): Show |
6 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2003+8685C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39565031 | |||||||
| chr12:39565036 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2003+8680C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39565036 | |||||||
| chr12:39565362 | T | C | 2 | a0001c0001t0011g0085 a0003c0009t0011g0273 |
2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2003+8354A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39565362 | |||||||
| chr12:39565482 | A | G | 48 | a0001c0001t0001g0193 a0001c0001t0002g0003 a0001c0001t0002g0011 others(45): Show |
57 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.2003+8234T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39565482 | |||||||
| chr12:39565556 | T | A | 112 | a0001c0001t0001g0193 a0001c0001t0002g0003 a0001c0001t0002g0011 others(109): Show |
136 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.2003+8160A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39565556 | |||||||
| chr12:39565679 | G | A | 1 | a0001c0006t0024g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2003+8037C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39565679 | |||||||
| chr12:39565686 | A | G | 1 | a0001c0001t0002g0264 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2003+8030T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39565686 | |||||||
| chr12:39565726 | C | T | 2 | a0001c0001t0006g0013 a0001c0001t0006g0057 |
3 | HG00280.hp1 HG01346.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.2003+7990G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39565726 | |||||||
| chr12:39565840 | G | C | 1 | a0001c0001t0001g0122 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2003+7876C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39565840 | |||||||
| chr12:39566164 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2003+7552G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566164 | |||||||
| chr12:39566207 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2003+7509G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566207 | |||||||
| chr12:39566211 | T | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0153 a0001c0001t0001g0170 |
4 | HG02922.hp1 HG03486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2003+7505A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566211 | |||||||
| chr12:39566317 | G | T | 4 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(1): Show |
4 | HG00609.hp2 NA18747.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.2003+7399C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566317 | |||||||
| chr12:39566349 | T | G | 1 | a0003c0005t0011g0031 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2003+7367A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566349 | |||||||
| chr12:39566370 | G | T | 16 | a0001c0001t0005g0002 a0001c0001t0005g0017 a0001c0001t0005g0090 others(13): Show |
24 | HG00733.hp2 HG01884.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.2003+7346C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566370 | |||||||
| chr12:39566373 | G | A | 2 | a0001c0001t0009g0016 a0001c0001t0023g0084 |
3 | HG00733.hp2 HG02129.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2003+7343C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566373 | |||||||
| chr12:39566435 | T | C | 112 | a0001c0001t0001g0193 a0001c0001t0002g0003 a0001c0001t0002g0011 others(109): Show |
136 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.2003+7281A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566435 | |||||||
| chr12:39566490 | T | C | 1 | a0001c0001t0017g0218 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2003+7226A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566490 | |||||||
| chr12:39566511 | C | A | 7 | a0001c0001t0007g0074 a0001c0001t0007g0075 a0001c0001t0007g0076 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2003+7205G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566511 | |||||||
| chr12:39566545 | G | A | 1 | a0001c0001t0002g0200 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2003+7171C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566545 | |||||||
| chr12:39566581 | C | T | 2 | a0001c0001t0006g0056 a0001c0001t0006g0059 |
2 | HG01175.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2003+7135G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566581 | |||||||
| chr12:39566606 | A | G | 5 | a0001c0001t0001g0019 a0001c0001t0001g0133 a0001c0001t0001g0134 others(2): Show |
6 | HG01167.hp2 HG02723.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2003+7110T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566606 | |||||||
| chr12:39566736 | T | G | 13 | a0001c0001t0004g0020 a0001c0001t0004g0055 a0001c0001t0004g0065 others(10): Show |
18 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.2003+6980A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566736 | |||||||
| chr12:39566741 | C | A | 21 | a0001c0001t0001g0142 a0001c0001t0001g0144 a0001c0001t0001g0145 others(18): Show |
22 | HG00597.hp2 HG00621.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.2003+6975G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566741 | |||||||
| chr12:39566755 | G | C | 1 | a0001c0001t0003g0040 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2003+6961C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566755 | |||||||
| chr12:39566933 | T | G | 7 | a0001c0001t0007g0074 a0001c0001t0007g0075 a0001c0001t0007g0076 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2003+6783A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39566933 | |||||||
| chr12:39567220 | C | T | 1 | a0003c0005t0011g0031 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2003+6496G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567220 | |||||||
| chr12:39567221 | G | A | 15 | a0001c0001t0004g0020 a0001c0001t0004g0055 a0001c0001t0004g0065 others(12): Show |
20 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2003+6495C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567221 | |||||||
| chr12:39567260 | G | A | 1 | a0001c0001t0009g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2003+6456C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567260 | |||||||
| chr12:39567322 | G | T | 4 | a0001c0001t0004g0020 a0001c0001t0004g0055 a0001c0001t0004g0065 others(1): Show |
5 | HG02809.hp1 HG03041.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.2003+6394C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567322 | |||||||
| chr12:39567341 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2003+6375T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567341 | |||||||
| chr12:39567342 | T | G | 1 | a0001c0001t0001g0142 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2003+6374A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567342 | |||||||
| chr12:39567422 | A | C | 2 | a0001c0001t0001g0225 a0001c0001t0001g0228 |
2 | NA18956.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2003+6294T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567422 | |||||||
| chr12:39567492 | C | T | 2 | a0001c0001t0004g0020 a0001c0001t0004g0152 |
3 | HG02809.hp1 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2003+6224G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567492 | |||||||
| chr12:39567511 | A | T | 1 | a0001c0001t0001g0208 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2003+6205T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567511 | |||||||
| chr12:39567516 | A | G | 15 | a0001c0001t0004g0020 a0001c0001t0004g0055 a0001c0001t0004g0065 others(12): Show |
20 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2003+6200T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567516 | |||||||
| chr12:39567532 | A | G | 128 | a0001c0001t0001g0193 a0001c0001t0002g0003 a0001c0001t0002g0011 others(125): Show |
160 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.2003+6184T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567532 | |||||||
| chr12:39567561 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2003+6155A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567561 | |||||||
| chr12:39567562 | G | T | 1 | a0001c0001t0001g0175 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2003+6154C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567562 | |||||||
| chr12:39567644 | T | TTGTTA | 227 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(224): Show |
281 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(278): Show |
intron_variant | MODIFIER | c.2003+6071_2003+607 others(9): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567644 | |||||||
| chr12:39567654 | T | A | 1 | a0001c0001t0002g0168 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2003+6062A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567654 | |||||||
| chr12:39567786 | G | C | 2 | a0001c0001t0009g0016 a0001c0001t0023g0084 |
3 | HG00733.hp2 HG02129.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2003+5930C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567786 | |||||||
| chr12:39567957 | A | C | 11 | a0001c0001t0004g0020 a0001c0001t0004g0055 a0001c0001t0004g0065 others(8): Show |
16 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.2003+5759T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567957 | |||||||
| chr12:39567988 | T | G | 128 | a0001c0001t0001g0193 a0001c0001t0002g0003 a0001c0001t0002g0011 others(125): Show |
160 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.2003+5728A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39567988 | |||||||
| chr12:39568010 | G | C | 1 | a0001c0001t0002g0139 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2003+5706C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568010 | |||||||
| chr12:39568011 | G | C | 1 | a0001c0001t0001g0180 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2003+5705C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568011 | |||||||
| chr12:39568032 | C | G | 128 | a0001c0001t0001g0193 a0001c0001t0002g0003 a0001c0001t0002g0011 others(125): Show |
160 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.2003+5684G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568032 | |||||||
| chr12:39568302 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2003+5414A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568302 | |||||||
| chr12:39568442 | C | A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0133 a0001c0001t0001g0207 others(1): Show |
5 | HG01167.hp2 HG02723.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2003+5274G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568442 | |||||||
| chr12:39568450 | A | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(222): Show |
279 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.2003+5266T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568450 | |||||||
| chr12:39568455 | C | T | 30 | a0001c0001t0001g0018 a0001c0001t0001g0117 a0001c0001t0001g0121 others(27): Show |
31 | HG01175.hp2 HG01255.hp1 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.2003+5261G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568455 | |||||||
| chr12:39568526 | G | A | 48 | a0001c0001t0001g0193 a0001c0001t0002g0003 a0001c0001t0002g0011 others(45): Show |
57 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.2003+5190C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568526 | |||||||
| chr12:39568569 | C | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0071 a0001c0001t0001g0072 others(1): Show |
6 | HG00741.hp1 HG01884.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2003+5147G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568569 | |||||||
| chr12:39568589 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2003+5127C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568589 | |||||||
| chr12:39568627 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2003+5089G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568627 | |||||||
| chr12:39568649 | G | A | 12 | a0001c0001t0002g0011 a0001c0001t0002g0132 a0001c0001t0002g0157 others(9): Show |
14 | HG00438.hp2 HG02040.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.2003+5067C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568649 | |||||||
| chr12:39568678 | G | A | 38 | a0001c0001t0002g0131 a0001c0001t0002g0158 a0001c0001t0002g0160 others(35): Show |
46 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.2003+5038C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568678 | |||||||
| chr12:39568760 | A | G | 4 | a0001c0001t0001g0225 a0001c0001t0001g0228 a0001c0001t0001g0229 others(1): Show |
4 | HG02071.hp1 NA18956.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.2003+4956T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568760 | |||||||
| chr12:39568919 | G | T | 14 | a0001c0001t0005g0002 a0001c0001t0005g0017 a0001c0001t0005g0090 others(11): Show |
21 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.2003+4797C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568919 | |||||||
| chr12:39568961 | T | C | 1 | a0003c0005t0011g0031 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2003+4755A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39568961 | |||||||
| chr12:39569040 | T | G | 97 | a0001c0001t0001g0193 a0001c0001t0002g0003 a0001c0001t0002g0011 others(94): Show |
116 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.2003+4676A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569040 | |||||||
| chr12:39569055 | G | C | 1 | a0001c0001t0008g0244 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2003+4661C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569055 | |||||||
| chr12:39569131 | A | G | 1 | a0001c0006t0024g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2003+4585T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569131 | |||||||
| chr12:39569150 | A | G | 18 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0012 others(15): Show |
25 | HG00642.hp2 HG00741.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.2003+4566T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569150 | |||||||
| chr12:39569294 | C | T | 13 | a0001c0001t0004g0020 a0001c0001t0004g0055 a0001c0001t0004g0065 others(10): Show |
18 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.2003+4422G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569294 | |||||||
| chr12:39569295 | G | A | 2 | a0001c0001t0009g0016 a0001c0001t0023g0084 |
3 | HG00733.hp2 HG02129.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2003+4421C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569295 | |||||||
| chr12:39569332 | A | G | 128 | a0001c0001t0001g0193 a0001c0001t0002g0003 a0001c0001t0002g0011 others(125): Show |
160 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.2003+4384T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569332 | |||||||
| chr12:39569338 | C | A | 40 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0012 others(37): Show |
49 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.2003+4378G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569338 | |||||||
| chr12:39569411 | A | C | 3 | a0001c0001t0001g0115 a0001c0001t0001g0127 a0001c0001t0008g0114 |
3 | HG01106.hp2 HG01433.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.2003+4305T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569411 | |||||||
| chr12:39569421 | G | A | 1 | a0001c0001t0001g0027 | 2 | HG00423.hp1 HG00544.hp1 |
intron_variant | MODIFIER | c.2003+4295C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569421 | |||||||
| chr12:39569459 | G | C | 1 | a0001c0001t0002g0159 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2003+4257C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569459 | |||||||
| chr12:39569460 | C | G | 1 | a0001c0001t0001g0101 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2003+4256G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569460 | |||||||
| chr12:39569559 | A | T | 13 | a0001c0001t0005g0002 a0001c0001t0005g0017 a0001c0001t0005g0090 others(10): Show |
20 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.2003+4157T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569559 | |||||||
| chr12:39569608 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2003+4108G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569608 | |||||||
| chr12:39569612 | C | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | NA19005.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.2003+4104G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569612 | |||||||
| chr12:39569641 | G | A | 3 | a0001c0001t0002g0197 a0001c0001t0009g0016 a0002c0002t0004g0274 |
4 | HG02129.hp1 HG03710.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.2003+4075C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569641 | |||||||
| chr12:39569672 | G | A | 6 | a0001c0001t0001g0117 a0001c0001t0010g0014 a0001c0001t0010g0078 others(3): Show |
7 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2003+4044C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569672 | |||||||
| chr12:39569863 | T | G | 1 | a0001c0001t0003g0189 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2003+3853A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569863 | |||||||
| chr12:39569885 | A | G | 1 | a0001c0006t0024g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2003+3831T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569885 | |||||||
| chr12:39569917 | A | T | 1 | a0001c0001t0009g0016 | 2 | HG02129.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2003+3799T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39569917 | |||||||
| chr12:39570204 | A | G | 90 | a0001c0001t0001g0193 a0001c0001t0002g0003 a0001c0001t0002g0011 others(87): Show |
109 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.2003+3512T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39570204 | |||||||
| chr12:39570310 | C | T | 1 | a0001c0001t0018g0077 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2003+3406G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39570310 | |||||||
| chr12:39570573 | A | C | 49 | a0001c0001t0001g0193 a0001c0001t0002g0003 a0001c0001t0002g0011 others(46): Show |
59 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.2003+3143T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39570573 | |||||||
| chr12:39570661 | G | C | 2 | a0001c0001t0009g0016 a0001c0001t0023g0084 |
3 | HG00733.hp2 HG02129.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2003+3055C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39570661 | |||||||
| chr12:39570697 | C | A | 14 | a0001c0001t0005g0002 a0001c0001t0005g0017 a0001c0001t0005g0090 others(11): Show |
21 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.2003+3019G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39570697 | |||||||
| chr12:39570728 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2003+2988G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39570728 | |||||||
| chr12:39570878 | A | T | 1 | a0001c0001t0001g0270 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2003+2838T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39570878 | |||||||
| chr12:39571010 | AATC | A | 13 | a0001c0001t0004g0020 a0001c0001t0004g0055 a0001c0001t0004g0065 others(10): Show |
18 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.2003+2703_2003+270 others(7): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39571010 | |||||||
| chr12:39571069 | A | T | 1 | a0001c0001t0001g0247 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2003+2647T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39571069 | |||||||
| chr12:39571130 | A | AATTAGTA others(5): Show |
1 | a0001c0001t0001g0147 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2003+2574_2003+258 others(16): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39571130 | |||||||
| chr12:39571135 | G | A | 1 | a0001c0001t0023g0084 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2003+2581C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39571135 | |||||||
| chr12:39571406 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2003+2310C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39571406 | |||||||
| chr12:39571471 | A | T | 1 | a0001c0006t0024g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2003+2245T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39571471 | |||||||
| chr12:39571476 | A | G | 1 | a0003c0005t0011g0031 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2003+2240T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39571476 | |||||||
| chr12:39571516 | T | C | 1 | a0001c0001t0006g0057 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2003+2200A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39571516 | |||||||
| chr12:39571580 | A | G | 23 | a0001c0001t0005g0002 a0001c0001t0005g0017 a0001c0001t0005g0090 others(20): Show |
30 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.2003+2136T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39571580 | |||||||
| chr12:39571639 | C | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(273): Show |
337 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(334): Show |
intron_variant | MODIFIER | c.2003+2077G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39571639 | |||||||
| chr12:39571812 | A | C | 1 | a0001c0001t0001g0260 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2003+1904T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39571812 | |||||||
| chr12:39571835 | T | A | 18 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0012 others(15): Show |
25 | HG00642.hp2 HG00741.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.2003+1881A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39571835 | |||||||
| chr12:39572113 | T | G | 1 | a0001c0001t0001g0129 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2003+1603A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39572113 | |||||||
| chr12:39572120 | G | A | 5 | a0001c0001t0010g0014 a0001c0001t0010g0078 a0001c0001t0010g0080 others(2): Show |
6 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2003+1596C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39572120 | |||||||
| chr12:39572140 | G | C | 1 | a0001c0001t0010g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2003+1576C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39572140 | |||||||
| chr12:39572197 | T | C | 18 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0012 others(15): Show |
25 | HG00642.hp2 HG00741.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.2003+1519A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39572197 | |||||||
| chr12:39572514 | T | A | 13 | a0001c0001t0004g0020 a0001c0001t0004g0055 a0001c0001t0004g0065 others(10): Show |
18 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.2003+1202A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39572514 | |||||||
| chr12:39572522 | T | C | 1 | a0001c0001t0001g0257 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2003+1194A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39572522 | |||||||
| chr12:39572527 | A | G | 1 | a0001c0001t0002g0160 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2003+1189T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39572527 | |||||||
| chr12:39572608 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2003+1108T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39572608 | |||||||
| chr12:39572924 | A | G | 1 | a0001c0001t0005g0095 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2003+792T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39572924 | |||||||
| chr12:39573141 | T | A | 1 | a0001c0001t0001g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2003+575A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39573141 | |||||||
| chr12:39573211 | T | C | 1 | a0001c0001t0003g0053 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2003+505A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39573211 | |||||||
| chr12:39573332 | G | A | 125 | a0001c0001t0001g0193 a0001c0001t0002g0003 a0001c0001t0002g0011 others(122): Show |
156 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.2003+384C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39573332 | |||||||
| chr12:39573621 | T | A | 1 | a0001c0001t0003g0048 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2003+95A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39573621 | |||||||
| chr12:39573677 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2003+39T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39573677 | |||||||
| chr12:39573708 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG02698.hp1 | splice_region_variant&intron_variant | LOW | c.2003+8T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 9/9 | chr12 | 39573708 | |||||||
| chr12:39573859 | C | G | 2 | a0001c0001t0009g0016 a0001c0001t0023g0084 |
3 | HG00733.hp2 HG02129.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1878-18G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39573859 | |||||||
| chr12:39573954 | G | T | 1 | a0001c0001t0001g0169 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1878-113C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39573954 | |||||||
| chr12:39573998 | C | A | 1 | a0001c0001t0001g0128 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1878-157G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39573998 | |||||||
| chr12:39574052 | C | T | 60 | a0001c0001t0001g0193 a0001c0001t0002g0003 a0001c0001t0002g0011 others(57): Show |
74 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.1878-211G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39574052 | |||||||
| chr12:39574096 | G | T | 9 | a0001c0001t0005g0002 a0001c0001t0005g0017 a0001c0001t0005g0090 others(6): Show |
16 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1878-255C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39574096 | |||||||
| chr12:39574181 | G | C | 1 | a0001c0001t0023g0084 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1878-340C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39574181 | |||||||
| chr12:39574184 | T | G | 1 | a0001c0001t0001g0171 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1878-343A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39574184 | |||||||
| chr12:39574330 | C | T | 1 | a0001c0001t0003g0050 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1878-489G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39574330 | |||||||
| chr12:39574485 | C | T | 1 | a0001c0001t0023g0084 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1878-644G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39574485 | |||||||
| chr12:39575144 | A | G | 13 | a0001c0001t0004g0020 a0001c0001t0004g0055 a0001c0001t0004g0065 others(10): Show |
18 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1878-1303T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39575144 | |||||||
| chr12:39575305 | T | G | 48 | a0001c0001t0001g0193 a0001c0001t0002g0003 a0001c0001t0002g0011 others(45): Show |
58 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1878-1464A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39575305 | |||||||
| chr12:39575567 | T | C | 7 | a0001c0001t0007g0074 a0001c0001t0007g0075 a0001c0001t0007g0076 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1878-1726A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39575567 | |||||||
| chr12:39575910 | T | C | 1 | a0001c0001t0008g0245 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1878-2069A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39575910 | |||||||
| chr12:39576198 | T | C | 3 | a0001c0001t0001g0030 a0001c0001t0001g0226 a0001c0001t0002g0233 |
4 | HG00438.hp1 NA19011.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.1878-2357A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39576198 | |||||||
| chr12:39576268 | C | T | 1 | a0003c0009t0011g0273 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1878-2427G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39576268 | |||||||
| chr12:39576269 | G | C | 1 | a0003c0009t0011g0273 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1878-2428C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39576269 | |||||||
| chr12:39576471 | G | A | 3 | a0001c0001t0001g0206 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG00408.hp1 NA18962.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1878-2630C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39576471 | |||||||
| chr12:39576514 | C | A | 7 | a0002c0002t0004g0005 a0002c0002t0004g0032 a0002c0002t0004g0274 others(4): Show |
11 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1878-2673G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39576514 | |||||||
| chr12:39576552 | T | C | 1 | a0001c0006t0024g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1878-2711A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39576552 | |||||||
| chr12:39576917 | C | T | 1 | a0001c0001t0015g0098 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1877+2618G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39576917 | |||||||
| chr12:39577026 | A | G | 2 | a0001c0001t0004g0020 a0001c0001t0004g0152 |
3 | HG02809.hp1 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1877+2509T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39577026 | |||||||
| chr12:39577412 | C | G | 2 | a0001c0001t0011g0085 a0003c0009t0011g0273 |
2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1877+2123G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39577412 | |||||||
| chr12:39577438 | T | C | 40 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0012 others(37): Show |
49 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.1877+2097A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39577438 | |||||||
| chr12:39577475 | T | A | 48 | a0001c0001t0001g0193 a0001c0001t0002g0003 a0001c0001t0002g0011 others(45): Show |
58 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1877+2060A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39577475 | |||||||
| chr12:39577557 | T | A | 47 | a0001c0001t0001g0193 a0001c0001t0002g0003 a0001c0001t0002g0011 others(44): Show |
56 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.1877+1978A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39577557 | |||||||
| chr12:39577708 | G | T | 2 | a0001c0001t0011g0085 a0003c0009t0011g0273 |
2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1877+1827C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39577708 | |||||||
| chr12:39577779 | T | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0205 a0001c0001t0001g0234 others(2): Show |
7 | NA18951.hp2 NA18957.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.1877+1756A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39577779 | |||||||
| chr12:39577840 | C | G | 2 | a0001c0001t0011g0085 a0003c0009t0011g0273 |
2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1877+1695G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39577840 | |||||||
| chr12:39577990 | A | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0071 a0001c0001t0001g0072 others(1): Show |
6 | HG00741.hp1 HG01884.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1877+1545T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39577990 | |||||||
| chr12:39578019 | C | G | 128 | a0001c0001t0001g0193 a0001c0001t0002g0003 a0001c0001t0002g0011 others(125): Show |
160 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.1877+1516G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39578019 | |||||||
| chr12:39578078 | T | C | 1 | a0001c0008t0006g0062 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1877+1457A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39578078 | |||||||
| chr12:39578196 | C | T | 2 | a0001c0001t0011g0085 a0003c0009t0011g0273 |
2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1877+1339G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39578196 | |||||||
| chr12:39578212 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1877+1323G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39578212 | |||||||
| chr12:39578240 | C | T | 1 | a0001c0001t0009g0042 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1877+1295G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39578240 | |||||||
| chr12:39578290 | C | T | 2 | a0001c0001t0013g0035 a0001c0001t0013g0036 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1877+1245G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39578290 | |||||||
| chr12:39578473 | C | CA | 21 | a0001c0001t0001g0015 a0001c0001t0001g0071 a0001c0001t0001g0107 others(18): Show |
29 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(26): Show |
intron_variant | MODIFIER | c.1877+1061dupT | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39578473 | |||||||
| chr12:39578473 | CA | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0026 others(91): Show |
120 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.1877+1061delT | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39578473 | |||||||
| chr12:39578517 | C | T | 1 | a0001c0001t0009g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1877+1018G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39578517 | |||||||
| chr12:39578748 | A | T | 1 | a0001c0001t0023g0084 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1877+787T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39578748 | |||||||
| chr12:39579137 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1877+398C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39579137 | |||||||
| chr12:39579137 | G | T | 1 | a0001c0001t0009g0043 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1877+398C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39579137 | |||||||
| chr12:39579154 | G | A | 1 | a0001c0001t0027g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1877+381C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39579154 | |||||||
| chr12:39579402 | A | G | 2 | a0001c0001t0011g0085 a0003c0009t0011g0273 |
2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1877+133T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 8/9 | chr12 | 39579402 | |||||||
| chr12:39579636 | A | T | 1 | a0001c0001t0009g0042 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1793-17T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39579636 | |||||||
| chr12:39579733 | T | C | 1 | a0001c0001t0002g0120 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1793-114A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39579733 | |||||||
| chr12:39580017 | C | G | 1 | a0001c0006t0024g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1793-398G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39580017 | |||||||
| chr12:39580231 | A | G | 236 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(233): Show |
292 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(289): Show |
intron_variant | MODIFIER | c.1793-612T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39580231 | |||||||
| chr12:39580359 | T | G | 2 | a0001c0001t0004g0082 a0001c0001t0004g0083 |
2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1793-740A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39580359 | |||||||
| chr12:39580540 | A | T | 1 | a0001c0001t0001g0113 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1793-921T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39580540 | |||||||
| chr12:39580579 | C | A | 9 | a0001c0001t0005g0002 a0001c0001t0005g0017 a0001c0001t0005g0090 others(6): Show |
16 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1793-960G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39580579 | |||||||
| chr12:39580658 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1793-1039G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39580658 | |||||||
| chr12:39580776 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1793-1157A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39580776 | |||||||
| chr12:39580800 | C | A | 33 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0040 others(30): Show |
40 | HG00280.hp1 HG00642.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.1793-1181G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39580800 | |||||||
| chr12:39580804 | G | C | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | NA19064.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1793-1185C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39580804 | |||||||
| chr12:39581084 | C | G | 7 | a0001c0001t0007g0074 a0001c0001t0007g0075 a0001c0001t0007g0076 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1793-1465G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39581084 | |||||||
| chr12:39581432 | A | G | 2 | a0001c0001t0004g0020 a0001c0001t0004g0152 |
3 | HG02809.hp1 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1793-1813T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39581432 | |||||||
| chr12:39581435 | T | A | 9 | a0001c0001t0005g0002 a0001c0001t0005g0017 a0001c0001t0005g0090 others(6): Show |
16 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1793-1816A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39581435 | |||||||
| chr12:39581517 | A | T | 1 | a0001c0001t0002g0223 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1793-1898T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39581517 | |||||||
| chr12:39581594 | T | C | 1 | a0001c0001t0005g0093 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1793-1975A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39581594 | |||||||
| chr12:39581694 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1793-2075C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39581694 | |||||||
| chr12:39581700 | A | C | 9 | a0001c0001t0005g0002 a0001c0001t0005g0017 a0001c0001t0005g0090 others(6): Show |
16 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1793-2081T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39581700 | |||||||
| chr12:39581846 | C | T | 1 | a0001c0001t0002g0140 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1793-2227G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39581846 | |||||||
| chr12:39581900 | T | C | 49 | a0001c0001t0001g0193 a0001c0001t0002g0003 a0001c0001t0002g0011 others(46): Show |
59 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.1793-2281A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39581900 | |||||||
| chr12:39581929 | G | A | 1 | a0001c0006t0024g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1793-2310C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39581929 | |||||||
| chr12:39582084 | G | C | 1 | a0001c0001t0002g0140 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1793-2465C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39582084 | |||||||
| chr12:39582174 | T | C | 48 | a0001c0001t0001g0193 a0001c0001t0002g0003 a0001c0001t0002g0011 others(45): Show |
57 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.1793-2555A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39582174 | |||||||
| chr12:39582188 | AG | A | 1 | a0001c0001t0003g0006 | 3 | NA18939.hp1 NA18997.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1793-2570delC | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39582188 | |||||||
| chr12:39582389 | A | G | 1 | a0001c0001t0002g0139 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1793-2770T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39582389 | |||||||
| chr12:39582648 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1793-3029T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39582648 | |||||||
| chr12:39582663 | T | G | 1 | a0001c0001t0001g0236 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1793-3044A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39582663 | |||||||
| chr12:39582880 | A | G | 1 | a0003c0005t0011g0031 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1793-3261T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39582880 | |||||||
| chr12:39583020 | C | G | 1 | a0003c0005t0011g0031 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1792+3132G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39583020 | |||||||
| chr12:39583136 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1792+3016T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39583136 | |||||||
| chr12:39583207 | A | C | 3 | a0001c0001t0002g0046 a0001c0001t0002g0197 a0001c0001t0002g0269 |
3 | HG00423.hp2 NA18952.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1792+2945T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39583207 | |||||||
| chr12:39583224 | C | T | 1 | a0003c0005t0011g0031 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1792+2928G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39583224 | |||||||
| chr12:39583410 | A | T | 1 | a0001c0001t0001g0121 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1792+2742T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39583410 | |||||||
| chr12:39583821 | C | A | 1 | a0001c0001t0001g0177 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1792+2331G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39583821 | |||||||
| chr12:39583848 | T | G | 1 | a0001c0001t0006g0054 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1792+2304A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39583848 | |||||||
| chr12:39583972 | T | G | 1 | a0001c0001t0001g0267 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1792+2180A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39583972 | |||||||
| chr12:39583990 | T | C | 1 | a0001c0001t0009g0042 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1792+2162A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39583990 | |||||||
| chr12:39584081 | A | G | 2 | a0001c0001t0004g0082 a0001c0001t0004g0083 |
2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1792+2071T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39584081 | |||||||
| chr12:39584098 | C | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0026 others(39): Show |
59 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.1792+2054G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39584098 | |||||||
| chr12:39584111 | G | T | 2 | a0001c0001t0015g0097 a0001c0001t0015g0098 |
2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1792+2041C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39584111 | |||||||
| chr12:39584237 | G | A | 2 | a0001c0001t0002g0132 a0001c0001t0002g0237 |
2 | HG02056.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1792+1915C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39584237 | |||||||
| chr12:39584258 | C | G | 1 | a0003c0005t0011g0031 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1792+1894G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39584258 | |||||||
| chr12:39584430 | T | C | 40 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0012 others(37): Show |
49 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.1792+1722A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39584430 | |||||||
| chr12:39584434 | T | G | 1 | a0001c0001t0025g0191 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1792+1718A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39584434 | |||||||
| chr12:39584477 | C | G | 1 | a0001c0001t0006g0066 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1792+1675G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39584477 | |||||||
| chr12:39584541 | T | G | 1 | a0001c0001t0001g0185 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1792+1611A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39584541 | |||||||
| chr12:39584602 | T | C | 5 | a0001c0001t0010g0014 a0001c0001t0010g0078 a0001c0001t0010g0080 others(2): Show |
6 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1792+1550A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39584602 | |||||||
| chr12:39584785 | C | T | 2 | a0001c0001t0006g0058 a0001c0001t0006g0081 |
2 | HG02735.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1792+1367G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39584785 | |||||||
| chr12:39584927 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1792+1225T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39584927 | |||||||
| chr12:39585018 | A | G | 13 | a0001c0001t0004g0020 a0001c0001t0004g0055 a0001c0001t0004g0065 others(10): Show |
18 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1792+1134T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39585018 | |||||||
| chr12:39585034 | G | T | 3 | a0001c0001t0001g0151 a0001c0001t0001g0181 a0001c0001t0001g0195 |
3 | HG01070.hp2 HG01433.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.1792+1118C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39585034 | |||||||
| chr12:39585060 | G | A | 1 | a0001c0001t0009g0042 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1792+1092C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39585060 | |||||||
| chr12:39585167 | C | T | 1 | a0001c0001t0002g0159 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1792+985G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39585167 | |||||||
| chr12:39585265 | T | C | 1 | a0001c0001t0006g0081 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1792+887A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39585265 | |||||||
| chr12:39585270 | T | C | 2 | a0001c0001t0013g0035 a0001c0001t0013g0036 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1792+882A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39585270 | |||||||
| chr12:39585294 | C | G | 1 | a0001c0001t0003g0041 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1792+858G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39585294 | |||||||
| chr12:39585314 | G | A | 40 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0012 others(37): Show |
49 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.1792+838C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39585314 | |||||||
| chr12:39585590 | A | G | 1 | a0001c0001t0001g0261 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1792+562T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39585590 | |||||||
| chr12:39585615 | A | G | 1 | a0001c0001t0011g0085 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1792+537T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39585615 | |||||||
| chr12:39585642 | C | T | 13 | a0001c0001t0004g0020 a0001c0001t0004g0055 a0001c0001t0004g0065 others(10): Show |
18 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1792+510G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39585642 | |||||||
| chr12:39585732 | C | T | 1 | a0001c0006t0024g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1792+420G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39585732 | |||||||
| chr12:39585756 | C | T | 7 | a0001c0001t0007g0074 a0001c0001t0007g0075 a0001c0001t0007g0076 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1792+396G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39585756 | |||||||
| chr12:39585889 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1792+263G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39585889 | |||||||
| chr12:39586014 | A | T | 13 | a0001c0001t0004g0020 a0001c0001t0004g0055 a0001c0001t0004g0065 others(10): Show |
18 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1792+138T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39586014 | |||||||
| chr12:39586037 | T | C | 40 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0012 others(37): Show |
49 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.1792+115A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39586037 | |||||||
| chr12:39586050 | G | A | 11 | a0001c0001t0004g0020 a0001c0001t0004g0055 a0001c0001t0004g0065 others(8): Show |
16 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1792+102C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39586050 | |||||||
| chr12:39586098 | G | C | 2 | a0001c0001t0004g0082 a0001c0001t0004g0083 |
2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1792+54C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39586098 | |||||||
| chr12:39586109 | A | T | 7 | a0002c0002t0004g0005 a0002c0002t0004g0032 a0002c0002t0004g0274 others(4): Show |
11 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1792+43T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 7/9 | chr12 | 39586109 | |||||||
| chr12:39586332 | A | G | 1 | a0001c0001t0006g0066 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1647-35T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39586332 | |||||||
| chr12:39586422 | T | C | 2 | a0001c0001t0002g0003 a0001c0001t0002g0167 |
7 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1647-125A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39586422 | |||||||
| chr12:39586446 | C | A | 1 | a0001c0001t0001g0248 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1647-149G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39586446 | |||||||
| chr12:39586456 | G | A | 1 | a0001c0001t0002g0168 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1647-159C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39586456 | |||||||
| chr12:39586554 | A | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG01069.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.1647-257T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39586554 | |||||||
| chr12:39586684 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1647-387A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39586684 | |||||||
| chr12:39586721 | T | C | 48 | a0001c0001t0001g0193 a0001c0001t0002g0003 a0001c0001t0002g0011 others(45): Show |
57 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.1647-424A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39586721 | |||||||
| chr12:39586735 | T | A | 1 | a0001c0001t0009g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1647-438A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39586735 | |||||||
| chr12:39586815 | G | A | 35 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0012 others(32): Show |
43 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.1647-518C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39586815 | |||||||
| chr12:39586904 | A | G | 1 | a0001c0001t0009g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1647-607T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39586904 | |||||||
| chr12:39587169 | C | A | 1 | a0001c0001t0001g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1647-872G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39587169 | |||||||
| chr12:39587202 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1647-905A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39587202 | |||||||
| chr12:39587741 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1647-1444A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39587741 | |||||||
| chr12:39587928 | A | G | 1 | a0001c0001t0002g0158 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1647-1631T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39587928 | |||||||
| chr12:39587932 | T | C | 2 | a0001c0001t0015g0097 a0001c0001t0015g0098 |
2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1647-1635A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39587932 | |||||||
| chr12:39587937 | C | T | 9 | a0001c0001t0001g0238 a0001c0001t0001g0249 a0001c0001t0007g0074 others(6): Show |
9 | HG00639.hp2 HG01081.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1647-1640G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39587937 | |||||||
| chr12:39588031 | C | T | 13 | a0001c0001t0004g0020 a0001c0001t0004g0055 a0001c0001t0004g0065 others(10): Show |
18 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1647-1734G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39588031 | |||||||
| chr12:39588118 | G | A | 1 | a0001c0001t0005g0094 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1647-1821C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39588118 | |||||||
| chr12:39588176 | T | A | 2 | a0001c0001t0004g0082 a0001c0001t0004g0083 |
2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1647-1879A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39588176 | |||||||
| chr12:39588494 | C | T | 17 | a0001c0001t0006g0013 a0001c0001t0006g0054 a0001c0001t0006g0056 others(14): Show |
18 | HG00280.hp1 HG01175.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.1647-2197G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39588494 | |||||||
| chr12:39588528 | A | C | 2 | a0001c0001t0009g0016 a0001c0001t0023g0084 |
3 | HG00733.hp2 HG02129.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1647-2231T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39588528 | |||||||
| chr12:39588611 | A | G | 48 | a0001c0001t0001g0193 a0001c0001t0002g0003 a0001c0001t0002g0011 others(45): Show |
57 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.1647-2314T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39588611 | |||||||
| chr12:39588751 | G | T | 1 | a0001c0001t0001g0072 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1647-2454C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39588751 | |||||||
| chr12:39589080 | G | A | 80 | a0001c0001t0003g0004 a0001c0001t0003g0006 a0001c0001t0003g0012 others(77): Show |
103 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.1647-2783C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589080 | |||||||
| chr12:39589149 | A | G | 5 | a0001c0001t0010g0014 a0001c0001t0010g0078 a0001c0001t0010g0080 others(2): Show |
6 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1647-2852T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589149 | |||||||
| chr12:39589200 | A | T | 1 | a0001c0001t0001g0267 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1647-2903T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589200 | |||||||
| chr12:39589202 | C | T | 1 | a0003c0005t0011g0031 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1647-2905G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589202 | |||||||
| chr12:39589209 | T | G | 11 | a0001c0001t0004g0020 a0001c0001t0004g0055 a0001c0001t0004g0065 others(8): Show |
16 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1647-2912A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589209 | |||||||
| chr12:39589350 | A | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | HG03540.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1647-3053T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589350 | |||||||
| chr12:39589384 | G | GT | 33 | a0001c0001t0001g0109 a0001c0001t0001g0115 a0001c0001t0001g0116 others(30): Show |
34 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.1647-3088dupA | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589384 | |||||||
| chr12:39589384 | GT | G | 51 | a0001c0001t0001g0145 a0001c0001t0001g0271 a0001c0001t0003g0004 others(48): Show |
64 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.1647-3088delA | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589384 | |||||||
| chr12:39589417 | C | T | 1 | a0001c0001t0009g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1647-3120G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589417 | |||||||
| chr12:39589509 | T | C | 4 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0214 others(1): Show |
4 | HG02071.hp2 NA18942.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.1647-3212A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589509 | |||||||
| chr12:39589600 | G | A | 17 | a0001c0001t0006g0013 a0001c0001t0006g0054 a0001c0001t0006g0056 others(14): Show |
18 | HG00280.hp1 HG01175.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.1647-3303C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589600 | |||||||
| chr12:39589623 | G | A | 11 | a0001c0001t0004g0020 a0001c0001t0004g0055 a0001c0001t0004g0065 others(8): Show |
16 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1647-3326C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589623 | |||||||
| chr12:39589629 | C | T | 16 | a0001c0001t0005g0002 a0001c0001t0005g0017 a0001c0001t0005g0090 others(13): Show |
24 | HG00733.hp2 HG01884.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1647-3332G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589629 | |||||||
| chr12:39589630 | G | A | 1 | a0003c0005t0011g0031 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1647-3333C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589630 | |||||||
| chr12:39589660 | T | C | 9 | a0001c0001t0005g0002 a0001c0001t0005g0017 a0001c0001t0005g0090 others(6): Show |
16 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1647-3363A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589660 | |||||||
| chr12:39589676 | C | T | 2 | a0001c0001t0009g0016 a0001c0001t0023g0084 |
3 | HG00733.hp2 HG02129.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1647-3379G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589676 | |||||||
| chr12:39589681 | C | A | 1 | a0001c0001t0001g0146 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1647-3384G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589681 | |||||||
| chr12:39589896 | T | C | 1 | a0003c0005t0011g0031 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1647-3599A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589896 | |||||||
| chr12:39589960 | T | A | 2 | a0001c0001t0004g0082 a0001c0001t0004g0083 |
2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1647-3663A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39589960 | |||||||
| chr12:39590222 | C | T | 14 | a0001c0001t0005g0002 a0001c0001t0005g0017 a0001c0001t0005g0090 others(11): Show |
21 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.1647-3925G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39590222 | |||||||
| chr12:39590590 | T | G | 1 | a0001c0001t0001g0138 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1647-4293A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39590590 | |||||||
| chr12:39590756 | A | AT | 10 | a0001c0001t0001g0148 a0001c0001t0001g0193 a0001c0001t0005g0096 others(7): Show |
10 | HG01175.hp1 HG01255.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1647-4460dupA | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39590756 | |||||||
| chr12:39590889 | A | G | 4 | a0001c0001t0001g0142 a0001c0001t0001g0179 a0001c0001t0001g0180 others(1): Show |
4 | HG00738.hp1 HG02145.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1647-4592T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39590889 | |||||||
| chr12:39590967 | A | G | 1 | a0001c0001t0002g0155 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1647-4670T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39590967 | |||||||
| chr12:39591026 | CAA | C | 2 | a0001c0001t0009g0016 a0001c0001t0023g0084 |
3 | HG00733.hp2 HG02129.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1647-4731_1647-473 others(6): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39591026 | |||||||
| chr12:39591110 | A | G | 1 | a0001c0007t0007g0087 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1647-4813T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39591110 | |||||||
| chr12:39591183 | A | G | 2 | a0001c0001t0009g0016 a0001c0001t0023g0084 |
3 | HG00733.hp2 HG02129.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1647-4886T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39591183 | |||||||
| chr12:39591255 | T | C | 1 | a0001c0001t0002g0046 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1647-4958A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39591255 | |||||||
| chr12:39591404 | A | G | 43 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0026 others(40): Show |
60 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1647-5107T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39591404 | |||||||
| chr12:39591570 | G | T | 2 | a0001c0001t0011g0085 a0003c0009t0011g0273 |
2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1647-5273C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39591570 | |||||||
| chr12:39591987 | A | G | 1 | a0001c0001t0023g0084 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1647-5690T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39591987 | |||||||
| chr12:39592124 | C | T | 7 | a0001c0001t0007g0074 a0001c0001t0007g0075 a0001c0001t0007g0076 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1647-5827G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39592124 | |||||||
| chr12:39592191 | C | T | 1 | a0001c0001t0003g0044 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1647-5894G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39592191 | |||||||
| chr12:39592290 | C | A | 1 | a0001c0001t0018g0077 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1647-5993G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39592290 | |||||||
| chr12:39592302 | G | C | 1 | a0001c0001t0001g0187 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1647-6005C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39592302 | |||||||
| chr12:39592457 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1647-6160T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39592457 | |||||||
| chr12:39592576 | A | G | 1 | a0001c0001t0002g0266 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1647-6279T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39592576 | |||||||
| chr12:39592646 | C | T | 3 | a0001c0001t0006g0066 a0001c0001t0006g0067 a0001c0001t0006g0068 |
3 | HG02129.hp2 NA18986.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1647-6349G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39592646 | |||||||
| chr12:39592664 | G | A | 1 | a0001c0001t0002g0141 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1647-6367C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39592664 | |||||||
| chr12:39592880 | A | G | 1 | a0001c0001t0004g0065 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1647-6583T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39592880 | |||||||
| chr12:39593105 | C | T | 1 | a0001c0001t0002g0154 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1647-6808G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39593105 | |||||||
| chr12:39593126 | G | A | 5 | a0001c0001t0010g0014 a0001c0001t0010g0078 a0001c0001t0010g0080 others(2): Show |
6 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1647-6829C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39593126 | |||||||
| chr12:39593238 | A | G | 1 | a0001c0001t0002g0192 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1647-6941T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39593238 | |||||||
| chr12:39593562 | T | C | 1 | a0001c0001t0002g0176 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1646+7009A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39593562 | |||||||
| chr12:39593825 | C | A | 1 | a0003c0005t0011g0031 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1646+6746G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39593825 | |||||||
| chr12:39593853 | A | G | 9 | a0001c0001t0007g0074 a0001c0001t0007g0075 a0001c0001t0007g0076 others(6): Show |
9 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1646+6718T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39593853 | |||||||
| chr12:39593896 | A | T | 84 | a0001c0001t0001g0007 a0001c0001t0001g0071 a0001c0001t0001g0072 others(81): Show |
109 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(106): Show |
intron_variant | MODIFIER | c.1646+6675T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39593896 | |||||||
| chr12:39593968 | C | T | 13 | a0001c0001t0005g0002 a0001c0001t0005g0017 a0001c0001t0005g0090 others(10): Show |
20 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.1646+6603G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39593968 | |||||||
| chr12:39594042 | T | C | 1 | a0001c0001t0002g0201 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1646+6529A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39594042 | |||||||
| chr12:39594105 | C | G | 1 | a0001c0001t0001g0177 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1646+6466G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39594105 | |||||||
| chr12:39594260 | T | G | 7 | a0001c0001t0007g0074 a0001c0001t0007g0075 a0001c0001t0007g0076 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1646+6311A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39594260 | |||||||
| chr12:39594348 | T | TATA | 2 | a0001c0001t0004g0020 a0001c0001t0004g0152 |
3 | HG02809.hp1 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1646+6220_1646+622 others(7): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39594348 | |||||||
| chr12:39594348 | T | TATATA | 80 | a0001c0001t0001g0007 a0001c0001t0001g0071 a0001c0001t0001g0072 others(77): Show |
103 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.1646+6218_1646+622 others(9): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39594348 | |||||||
| chr12:39594381 | T | G | 1 | a0001c0006t0024g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1646+6190A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39594381 | |||||||
| chr12:39594426 | A | G | 11 | a0001c0001t0005g0002 a0001c0001t0005g0017 a0001c0001t0005g0090 others(8): Show |
18 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.1646+6145T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39594426 | |||||||
| chr12:39594434 | T | C | 1 | a0003c0005t0011g0031 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1646+6137A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39594434 | |||||||
| chr12:39594713 | T | C | 84 | a0001c0001t0001g0007 a0001c0001t0001g0071 a0001c0001t0001g0072 others(81): Show |
108 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.1646+5858A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39594713 | |||||||
| chr12:39594761 | G | T | 1 | a0003c0009t0011g0273 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1646+5810C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39594761 | |||||||
| chr12:39594837 | C | G | 84 | a0001c0001t0001g0007 a0001c0001t0001g0071 a0001c0001t0001g0072 others(81): Show |
108 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.1646+5734G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39594837 | |||||||
| chr12:39594847 | G | A | 3 | a0001c0001t0009g0037 a0001c0001t0009g0042 a0001c0001t0009g0043 |
3 | HG02486.hp2 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1646+5724C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39594847 | |||||||
| chr12:39595169 | G | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(57): Show |
82 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.1646+5402C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39595169 | |||||||
| chr12:39595225 | G | C | 1 | a0003c0005t0011g0031 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1646+5346C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39595225 | |||||||
| chr12:39595370 | A | C | 78 | a0001c0001t0001g0007 a0001c0001t0001g0071 a0001c0001t0001g0072 others(75): Show |
101 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.1646+5201T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39595370 | |||||||
| chr12:39595685 | T | C | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG01069.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.1646+4886A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39595685 | |||||||
| chr12:39595818 | T | G | 1 | a0001c0006t0024g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1646+4753A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39595818 | |||||||
| chr12:39596274 | T | A | 1 | a0003c0005t0011g0031 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1646+4297A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39596274 | |||||||
| chr12:39596447 | G | T | 1 | a0002c0002t0004g0278 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1646+4124C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39596447 | |||||||
| chr12:39596463 | C | T | 3 | a0001c0001t0002g0038 a0001c0001t0009g0016 a0001c0001t0023g0084 |
4 | HG00733.hp2 HG02129.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1646+4108G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39596463 | |||||||
| chr12:39596476 | TCC | T | 2 | a0001c0001t0006g0013 a0001c0001t0006g0057 |
3 | HG00280.hp1 HG01346.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1646+4093_1646+409 others(6): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39596476 | |||||||
| chr12:39596477 | C | A | 1 | a0001c0001t0001g0001 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1646+4094G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39596477 | |||||||
| chr12:39596507 | A | T | 1 | a0003c0005t0011g0031 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1646+4064T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39596507 | |||||||
| chr12:39596775 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1646+3796G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39596775 | |||||||
| chr12:39596797 | T | G | 1 | a0001c0001t0001g0147 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1646+3774A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39596797 | |||||||
| chr12:39596802 | G | C | 1 | a0001c0001t0001g0213 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1646+3769C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39596802 | |||||||
| chr12:39597227 | C | T | 17 | a0001c0001t0002g0038 a0001c0001t0004g0082 a0001c0001t0004g0083 others(14): Show |
23 | HG00639.hp1 HG00733.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.1646+3344G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39597227 | |||||||
| chr12:39597234 | T | A | 17 | a0001c0001t0002g0038 a0001c0001t0004g0082 a0001c0001t0004g0083 others(14): Show |
23 | HG00639.hp1 HG00733.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.1646+3337A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39597234 | |||||||
| chr12:39597238 | T | A | 1 | a0001c0001t0007g0086 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1646+3333A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39597238 | |||||||
| chr12:39597695 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1646+2876T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39597695 | |||||||
| chr12:39597760 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1646+2811A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39597760 | |||||||
| chr12:39597800 | T | C | 3 | a0001c0001t0011g0085 a0001c0006t0024g0034 a0003c0009t0011g0273 |
3 | HG01891.hp2 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1646+2771A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39597800 | |||||||
| chr12:39598156 | A | G | 1 | a0001c0006t0024g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1646+2415T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39598156 | |||||||
| chr12:39598185 | T | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0071 a0001c0001t0001g0072 others(4): Show |
9 | HG00741.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1646+2386A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39598185 | |||||||
| chr12:39598307 | C | A | 2 | a0001c0001t0011g0085 a0003c0009t0011g0273 |
2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1646+2264G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39598307 | |||||||
| chr12:39598476 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1646+2095G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39598476 | |||||||
| chr12:39598479 | C | T | 1 | a0001c0001t0002g0024 | 2 | NA18956.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1646+2092G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39598479 | |||||||
| chr12:39598486 | T | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(198): Show |
251 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.1646+2085A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39598486 | |||||||
| chr12:39598487 | G | A | 2 | a0001c0001t0005g0017 a0001c0001t0005g0095 |
3 | HG02895.hp1 HG02897.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1646+2084C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39598487 | |||||||
| chr12:39598562 | G | A | 1 | a0003c0009t0011g0273 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1646+2009C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39598562 | |||||||
| chr12:39599071 | G | T | 1 | a0001c0001t0011g0085 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1646+1500C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39599071 | |||||||
| chr12:39599073 | T | G | 1 | a0003c0005t0011g0031 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1646+1498A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39599073 | |||||||
| chr12:39599135 | G | A | 1 | a0001c0001t0008g0114 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1646+1436C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39599135 | |||||||
| chr12:39599271 | T | C | 5 | a0001c0001t0010g0014 a0001c0001t0010g0078 a0001c0001t0010g0080 others(2): Show |
6 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1646+1300A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39599271 | |||||||
| chr12:39599307 | A | T | 1 | a0001c0001t0001g0208 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1646+1264T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39599307 | |||||||
| chr12:39599335 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1646+1236G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39599335 | |||||||
| chr12:39599456 | G | A | 1 | a0002c0002t0004g0278 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1646+1115C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39599456 | |||||||
| chr12:39599658 | C | T | 15 | a0001c0001t0001g0015 a0001c0001t0004g0082 a0001c0001t0004g0083 others(12): Show |
21 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.1646+913G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39599658 | |||||||
| chr12:39600192 | T | TA | 4 | a0001c0001t0007g0086 a0001c0001t0007g0088 a0001c0001t0007g0089 others(1): Show |
4 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1646+378_1646+379i others(3): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39600192 | |||||||
| chr12:39600229 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1646+342C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 6/9 | chr12 | 39600229 | |||||||
| chr12:39600872 | T | C | 21 | a0001c0001t0002g0046 a0001c0001t0003g0004 a0001c0001t0003g0006 others(18): Show |
28 | HG00423.hp2 HG00642.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.1501-156A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39600872 | |||||||
| chr12:39601160 | A | G | 1 | a0001c0001t0016g0033 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1501-444T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39601160 | |||||||
| chr12:39601388 | AAT | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0071 a0001c0001t0001g0072 others(4): Show |
9 | HG00741.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1501-674_1501-673d others(4): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39601388 | |||||||
| chr12:39601421 | GTTAT | G | 5 | a0001c0001t0008g0028 a0001c0001t0008g0220 a0001c0001t0008g0244 others(2): Show |
6 | HG00733.hp2 HG01109.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.1501-709_1501-706d others(6): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39601421 | |||||||
| chr12:39601544 | T | C | 3 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0201 |
3 | HG02132.hp1 NA18947.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1501-828A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39601544 | |||||||
| chr12:39601559 | G | A | 5 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
5 | HG00609.hp2 HG02080.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.1501-843C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39601559 | |||||||
| chr12:39601571 | C | A | 4 | a0001c0001t0007g0086 a0001c0001t0007g0088 a0001c0001t0007g0089 others(1): Show |
4 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1501-855G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39601571 | |||||||
| chr12:39601729 | G | T | 1 | a0001c0001t0001g0026 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1501-1013C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39601729 | |||||||
| chr12:39601757 | G | C | 1 | a0001c0001t0001g0246 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1501-1041C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39601757 | |||||||
| chr12:39601766 | T | C | 1 | a0001c0006t0024g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1501-1050A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39601766 | |||||||
| chr12:39602127 | T | TTTTA | 37 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0101 others(34): Show |
45 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.1501-1415_1501-141 others(8): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602127 | |||||||
| chr12:39602127 | T | TTTTATTT others(1): Show |
4 | a0001c0001t0001g0249 a0001c0001t0010g0078 a0001c0001t0018g0077 others(1): Show |
4 | HG00639.hp2 HG01192.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1501-1419_1501-141 others(12): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602127 | |||||||
| chr12:39602127 | T | TTTTATTT others(5): Show |
4 | a0001c0001t0001g0015 a0001c0001t0010g0014 a0001c0001t0010g0080 others(1): Show |
6 | HG01891.hp2 HG02451.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1501-1423_1501-141 others(16): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602127 | |||||||
| chr12:39602127 | TTTTA | T | 19 | a0001c0001t0001g0113 a0001c0001t0001g0149 a0001c0001t0001g0151 others(16): Show |
21 | HG00544.hp2 HG01106.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.1501-1415_1501-141 others(8): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602127 | |||||||
| chr12:39602127 | TTTTATTT others(1): Show |
T | 57 | a0001c0001t0001g0007 a0001c0001t0001g0071 a0001c0001t0001g0072 others(54): Show |
74 | HG00280.hp1 HG00423.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.1501-1419_1501-141 others(12): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602127 | |||||||
| chr12:39602127 | TTTTATTT others(5): Show |
T | 2 | a0001c0001t0001g0073 a0001c0001t0006g0056 |
2 | HG00741.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1501-1423_1501-141 others(16): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602127 | |||||||
| chr12:39602256 | G | T | 1 | a0001c0001t0009g0043 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1501-1540C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602256 | |||||||
| chr12:39602296 | G | T | 7 | a0002c0002t0004g0005 a0002c0002t0004g0032 a0002c0002t0004g0274 others(4): Show |
11 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1501-1580C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602296 | |||||||
| chr12:39602341 | A | G | 1 | a0001c0001t0001g0010 | 3 | HG01257.hp1 HG01361.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1500+1571T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602341 | |||||||
| chr12:39602345 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1500+1567C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602345 | |||||||
| chr12:39602445 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1500+1467G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602445 | |||||||
| chr12:39602643 | T | A | 1 | a0001c0001t0001g0142 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1500+1269A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602643 | |||||||
| chr12:39602671 | T | G | 1 | a0001c0001t0001g0142 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1500+1241A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602671 | |||||||
| chr12:39602684 | CTGAG | C | 4 | a0001c0001t0002g0038 a0001c0001t0009g0016 a0001c0001t0023g0084 others(1): Show |
5 | HG00733.hp2 HG01891.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.1500+1224_1500+122 others(8): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602684 | |||||||
| chr12:39602708 | T | A | 1 | a0001c0001t0025g0191 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1500+1204A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602708 | |||||||
| chr12:39602857 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1500+1055G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602857 | |||||||
| chr12:39602891 | A | T | 15 | a0001c0001t0001g0015 a0001c0001t0004g0082 a0001c0001t0004g0083 others(12): Show |
21 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.1500+1021T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602891 | |||||||
| chr12:39602931 | G | A | 4 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(1): Show |
4 | NA18988.hp1 NA18989.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1500+981C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39602931 | |||||||
| chr12:39603259 | G | A | 3 | a0001c0001t0001g0193 a0001c0001t0002g0192 a0001c0001t0002g0194 |
3 | HG01168.hp2 HG01255.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1500+653C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39603259 | |||||||
| chr12:39603353 | A | G | 18 | a0001c0001t0001g0015 a0001c0001t0004g0082 a0001c0001t0004g0083 others(15): Show |
24 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1500+559T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39603353 | |||||||
| chr12:39603381 | T | G | 1 | a0001c0001t0009g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1500+531A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39603381 | |||||||
| chr12:39603388 | A | T | 1 | a0001c0001t0009g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1500+524T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39603388 | |||||||
| chr12:39603645 | C | G | 84 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0071 others(81): Show |
109 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.1500+267G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39603645 | |||||||
| chr12:39603692 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1500+220A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39603692 | |||||||
| chr12:39603796 | C | T | 4 | a0001c0001t0001g0026 a0001c0001t0001g0221 a0001c0001t0001g0222 others(1): Show |
5 | HG02602.hp1 HG02735.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.1500+116G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39603796 | |||||||
| chr12:39603844 | C | T | 9 | a0001c0001t0005g0002 a0001c0001t0005g0017 a0001c0001t0005g0090 others(6): Show |
16 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1500+68G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 5/9 | chr12 | 39603844 | |||||||
| chr12:39604065 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1406-59C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 4/9 | chr12 | 39604065 | |||||||
| chr12:39604065 | G | T | 83 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0071 others(80): Show |
107 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(104): Show |
intron_variant | MODIFIER | c.1406-59C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 4/9 | chr12 | 39604065 | |||||||
| chr12:39604067 | A | T | 1 | a0001c0001t0003g0040 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1406-61T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 4/9 | chr12 | 39604067 | |||||||
| chr12:39604195 | A | T | 1 | a0001c0001t0001g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1406-189T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 4/9 | chr12 | 39604195 | |||||||
| chr12:39604296 | C | G | 3 | a0001c0001t0002g0038 a0001c0001t0009g0016 a0001c0001t0023g0084 |
4 | HG00733.hp2 HG02129.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1406-290G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 4/9 | chr12 | 39604296 | |||||||
| chr12:39604342 | T | C | 44 | a0001c0001t0001g0007 a0001c0001t0001g0071 a0001c0001t0001g0072 others(41): Show |
54 | HG00280.hp1 HG00423.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1406-336A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 4/9 | chr12 | 39604342 | |||||||
| chr12:39604371 | G | T | 1 | a0002c0002t0004g0276 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1406-365C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 4/9 | chr12 | 39604371 | |||||||
| chr12:39604468 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1405+294A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 4/9 | chr12 | 39604468 | |||||||
| chr12:39604965 | T | C | 9 | a0001c0001t0002g0024 a0001c0001t0002g0196 a0001c0001t0002g0197 others(6): Show |
10 | HG00621.hp1 HG02132.hp1 NA18747.hp1 others(7): Show |
intron_variant | MODIFIER | c.1237-35A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39604965 | |||||||
| chr12:39605006 | A | T | 2 | a0001c0001t0004g0082 a0001c0001t0004g0083 |
2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1237-76T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605006 | |||||||
| chr12:39605031 | T | C | 63 | a0001c0001t0001g0007 a0001c0001t0001g0071 a0001c0001t0001g0072 others(60): Show |
82 | HG00280.hp1 HG00423.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1237-101A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605031 | |||||||
| chr12:39605344 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1237-414G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605344 | |||||||
| chr12:39605523 | C | T | 1 | a0001c0001t0009g0042 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1237-593G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605523 | |||||||
| chr12:39605535 | T | A | 1 | a0001c0001t0001g0254 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1237-605A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605535 | |||||||
| chr12:39605550 | A | G | 1 | a0003c0009t0011g0273 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1237-620T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605550 | |||||||
| chr12:39605585 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1237-655T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605585 | |||||||
| chr12:39605613 | C | G | 4 | a0001c0001t0007g0086 a0001c0001t0007g0088 a0001c0001t0007g0089 others(1): Show |
4 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1237-683G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605613 | |||||||
| chr12:39605623 | C | T | 4 | a0001c0001t0007g0086 a0001c0001t0007g0088 a0001c0001t0007g0089 others(1): Show |
4 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1237-693G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605623 | |||||||
| chr12:39605761 | T | C | 1 | a0001c0001t0009g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1237-831A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605761 | |||||||
| chr12:39605796 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1237-866A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605796 | |||||||
| chr12:39605834 | TACA | T | 8 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(5): Show |
8 | HG00597.hp2 HG00621.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.1237-907_1237-905d others(5): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605834 | |||||||
| chr12:39605885 | A | G | 1 | a0001c0001t0009g0042 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1237-955T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605885 | |||||||
| chr12:39605933 | C | G | 1 | a0001c0001t0008g0220 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1237-1003G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605933 | |||||||
| chr12:39605983 | T | C | 1 | a0001c0001t0003g0070 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1237-1053A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39605983 | |||||||
| chr12:39606200 | G | A | 1 | a0001c0001t0023g0084 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1237-1270C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39606200 | |||||||
| chr12:39606282 | C | A | 4 | a0001c0001t0007g0086 a0001c0001t0007g0088 a0001c0001t0007g0089 others(1): Show |
4 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1236+1317G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39606282 | |||||||
| chr12:39606348 | T | C | 2 | a0001c0001t0001g0115 a0001c0001t0008g0114 |
2 | HG01106.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1236+1251A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39606348 | |||||||
| chr12:39606651 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1236+948A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39606651 | |||||||
| chr12:39606989 | G | A | 1 | a0001c0001t0001g0260 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1236+610C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39606989 | |||||||
| chr12:39607200 | A | G | 1 | a0001c0001t0002g0264 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1236+399T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39607200 | |||||||
| chr12:39607282 | A | G | 4 | a0001c0001t0007g0086 a0001c0001t0007g0088 a0001c0001t0007g0089 others(1): Show |
4 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1236+317T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 3/9 | chr12 | 39607282 | |||||||
| chr12:39607745 | G | GT | 15 | a0001c0001t0001g0116 a0001c0001t0001g0135 a0001c0001t0001g0142 others(12): Show |
15 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.1121-32dupA | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39607745 | |||||||
| chr12:39607745 | GT | G | 59 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0071 others(56): Show |
80 | HG00280.hp1 HG00423.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.1121-32delA | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39607745 | |||||||
| chr12:39607745 | GTT | G | 6 | a0001c0001t0004g0055 a0001c0001t0004g0065 a0001c0001t0005g0096 others(3): Show |
6 | HG00733.hp2 HG01515.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1121-33_1121-32del others(2): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39607745 | |||||||
| chr12:39607812 | A | C | 1 | a0001c0001t0004g0055 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1121-98T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39607812 | |||||||
| chr12:39608023 | C | T | 1 | a0003c0009t0011g0273 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1121-309G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39608023 | |||||||
| chr12:39608180 | G | A | 4 | a0001c0001t0007g0086 a0001c0001t0007g0088 a0001c0001t0007g0089 others(1): Show |
4 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121-466C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39608180 | |||||||
| chr12:39608327 | A | G | 4 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(1): Show |
4 | HG00609.hp2 NA18747.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121-613T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39608327 | |||||||
| chr12:39608405 | G | A | 2 | a0001c0001t0003g0012 a0001c0001t0003g0041 |
3 | HG00741.hp2 HG01243.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1121-691C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39608405 | |||||||
| chr12:39608469 | T | G | 4 | a0001c0001t0007g0086 a0001c0001t0007g0088 a0001c0001t0007g0089 others(1): Show |
4 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121-755A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39608469 | |||||||
| chr12:39608533 | C | T | 1 | a0003c0005t0011g0031 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1121-819G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39608533 | |||||||
| chr12:39608551 | G | A | 1 | a0001c0001t0001g0010 | 3 | HG01257.hp1 HG01361.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1121-837C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39608551 | |||||||
| chr12:39608618 | G | A | 3 | a0001c0001t0009g0037 a0001c0001t0009g0042 a0001c0001t0009g0043 |
3 | HG02486.hp2 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1121-904C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39608618 | |||||||
| chr12:39608741 | C | A | 1 | a0001c0001t0004g0065 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1121-1027G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39608741 | |||||||
| chr12:39608853 | T | G | 1 | a0001c0006t0024g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1121-1139A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39608853 | |||||||
| chr12:39609089 | CTG | C | 3 | a0001c0001t0002g0038 a0001c0001t0009g0016 a0001c0001t0023g0084 |
4 | HG00733.hp2 HG02129.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1121-1377_1121-137 others(6): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39609089 | |||||||
| chr12:39609395 | G | A | 2 | a0001c0001t0007g0075 a0001c0001t0007g0076 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1121-1681C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39609395 | |||||||
| chr12:39609570 | T | A | 1 | a0002c0002t0004g0032 | 2 | NA18971.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1121-1856A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39609570 | |||||||
| chr12:39609633 | A | G | 19 | a0001c0001t0002g0046 a0001c0001t0003g0004 a0001c0001t0003g0006 others(16): Show |
26 | HG00423.hp2 HG00642.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.1121-1919T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39609633 | |||||||
| chr12:39609740 | C | T | 1 | a0001c0006t0024g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1121-2026G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39609740 | |||||||
| chr12:39609927 | C | T | 2 | a0001c0001t0010g0014 a0001c0001t0010g0078 |
3 | HG02109.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1121-2213G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39609927 | |||||||
| chr12:39610049 | G | A | 1 | a0001c0001t0009g0043 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1121-2335C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39610049 | |||||||
| chr12:39610150 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1121-2436G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39610150 | |||||||
| chr12:39610235 | C | A | 1 | a0001c0001t0002g0131 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1121-2521G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39610235 | |||||||
| chr12:39610773 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0008g0114 |
2 | HG01106.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1121-3059G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39610773 | |||||||
| chr12:39610932 | CCTAAAAT others(22): Show |
C | 1 | a0001c0001t0001g0207 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1121-3247_1121-321 others(33): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39610932 | |||||||
| chr12:39610986 | T | C | 62 | a0001c0001t0001g0007 a0001c0001t0001g0071 a0001c0001t0001g0072 others(59): Show |
81 | HG00280.hp1 HG00423.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.1121-3272A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39610986 | |||||||
| chr12:39610987 | G | A | 2 | a0001c0001t0015g0097 a0001c0001t0015g0098 |
2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1121-3273C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39610987 | |||||||
| chr12:39611048 | C | T | 1 | a0003c0005t0011g0031 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1121-3334G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39611048 | |||||||
| chr12:39611066 | A | C | 63 | a0001c0001t0001g0007 a0001c0001t0001g0071 a0001c0001t0001g0072 others(60): Show |
82 | HG00280.hp1 HG00423.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1121-3352T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39611066 | |||||||
| chr12:39611103 | T | C | 3 | a0001c0001t0006g0066 a0001c0001t0006g0067 a0001c0001t0006g0068 |
3 | HG02129.hp2 NA18986.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1121-3389A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39611103 | |||||||
| chr12:39611104 | T | C | 3 | a0001c0001t0001g0204 a0001c0001t0014g0210 a0001c0001t0014g0211 |
3 | HG02717.hp1 HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1121-3390A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39611104 | |||||||
| chr12:39611842 | G | C | 3 | a0001c0001t0001g0206 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG00408.hp1 NA18962.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1121-4128C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39611842 | |||||||
| chr12:39611929 | G | A | 1 | a0003c0005t0011g0031 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1121-4215C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39611929 | |||||||
| chr12:39611947 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1121-4233G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39611947 | |||||||
| chr12:39612335 | A | T | 1 | a0001c0001t0018g0077 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1121-4621T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39612335 | |||||||
| chr12:39612375 | G | A | 59 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(56): Show |
81 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.1120+4613C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39612375 | |||||||
| chr12:39612439 | A | G | 1 | a0001c0001t0001g0214 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1120+4549T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39612439 | |||||||
| chr12:39612599 | C | T | 5 | a0001c0001t0001g0019 a0001c0001t0001g0133 a0001c0001t0001g0134 others(2): Show |
6 | HG01167.hp2 HG02723.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1120+4389G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39612599 | |||||||
| chr12:39612664 | C | T | 1 | a0001c0001t0004g0082 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1120+4324G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39612664 | |||||||
| chr12:39612822 | T | C | 1 | a0003c0005t0011g0031 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1120+4166A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39612822 | |||||||
| chr12:39613041 | C | T | 1 | a0002c0002t0004g0274 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1120+3947G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39613041 | |||||||
| chr12:39613087 | TAAAGAAT others(320): Show |
T | 80 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0071 others(77): Show |
105 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.1120+3574_1120+390 others(4): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39613087 | |||||||
| chr12:39613164 | A | T | 2 | a0001c0001t0001g0227 a0001c0001t0001g0254 |
2 | HG00597.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1120+3824T>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39613164 | |||||||
| chr12:39613242 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1120+3746G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39613242 | |||||||
| chr12:39613385 | C | CA | 23 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0027 others(20): Show |
23 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1120+3602dupT | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39613385 | |||||||
| chr12:39613385 | CA | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
87 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.1120+3602delT | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39613385 | |||||||
| chr12:39613711 | C | T | 3 | a0001c0001t0002g0038 a0001c0001t0009g0016 a0001c0001t0023g0084 |
4 | HG00733.hp2 HG02129.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1120+3277G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39613711 | |||||||
| chr12:39613901 | T | A | 2 | a0001c0001t0002g0038 a0001c0001t0023g0084 |
2 | HG00733.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1120+3087A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39613901 | |||||||
| chr12:39614154 | G | T | 19 | a0001c0001t0002g0046 a0001c0001t0003g0004 a0001c0001t0003g0006 others(16): Show |
26 | HG00423.hp2 HG00642.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.1120+2834C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39614154 | |||||||
| chr12:39614422 | G | A | 1 | a0003c0009t0011g0273 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1120+2566C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39614422 | |||||||
| chr12:39614498 | C | G | 1 | a0001c0001t0002g0132 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1120+2490G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39614498 | |||||||
| chr12:39614552 | C | CT | 35 | a0001c0001t0002g0046 a0001c0001t0003g0004 a0001c0001t0003g0006 others(32): Show |
43 | HG00280.hp1 HG00423.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.1120+2435dupA | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39614552 | |||||||
| chr12:39614571 | A | G | 16 | a0001c0001t0005g0002 a0001c0001t0005g0017 a0001c0001t0005g0090 others(13): Show |
23 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.1120+2417T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39614571 | |||||||
| chr12:39615051 | GTGGGATT others(2): Show |
G | 44 | a0001c0001t0001g0007 a0001c0001t0001g0071 a0001c0001t0001g0072 others(41): Show |
54 | HG00280.hp1 HG00423.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1120+1928_1120+193 others(13): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615051 | |||||||
| chr12:39615074 | T | C | 60 | a0001c0001t0001g0007 a0001c0001t0001g0071 a0001c0001t0001g0072 others(57): Show |
77 | HG00280.hp1 HG00423.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.1120+1914A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615074 | |||||||
| chr12:39615198 | C | CCCCCCCC others(22): Show |
1 | a0001c0001t0001g0207 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1120+1789_1120+179 others(33): Show |
ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615198 | |||||||
| chr12:39615200 | A | C | 1 | a0001c0001t0001g0207 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1120+1788T>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615200 | |||||||
| chr12:39615201 | G | C | 1 | a0001c0001t0001g0207 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1120+1787C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615201 | |||||||
| chr12:39615202 | G | C | 1 | a0001c0001t0001g0207 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1120+1786C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615202 | |||||||
| chr12:39615203 | G | C | 1 | a0001c0001t0001g0207 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1120+1785C>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615203 | |||||||
| chr12:39615204 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1120+1784A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615204 | |||||||
| chr12:39615290 | T | C | 3 | a0001c0001t0002g0038 a0001c0001t0009g0016 a0001c0001t0023g0084 |
4 | HG00733.hp2 HG02129.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1120+1698A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615290 | |||||||
| chr12:39615293 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1120+1695T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615293 | |||||||
| chr12:39615392 | T | A | 1 | a0001c0001t0001g0208 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1120+1596A>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615392 | |||||||
| chr12:39615597 | C | T | 4 | a0001c0001t0003g0012 a0001c0001t0003g0040 a0001c0001t0003g0041 others(1): Show |
5 | HG00642.hp2 HG00741.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.1120+1391G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615597 | |||||||
| chr12:39615728 | A | G | 3 | a0001c0001t0002g0038 a0001c0001t0009g0016 a0001c0001t0023g0084 |
4 | HG00733.hp2 HG02129.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1120+1260T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615728 | |||||||
| chr12:39615809 | T | C | 1 | a0001c0006t0024g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1120+1179A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615809 | |||||||
| chr12:39615950 | C | G | 1 | a0001c0001t0009g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1120+1038G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615950 | |||||||
| chr12:39615954 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1120+1034T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39615954 | |||||||
| chr12:39616024 | C | T | 22 | a0001c0001t0001g0018 a0001c0001t0001g0113 a0001c0001t0001g0115 others(19): Show |
23 | HG00280.hp2 HG01106.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.1120+964G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39616024 | |||||||
| chr12:39616468 | G | A | 6 | a0001c0001t0001g0015 a0001c0001t0010g0014 a0001c0001t0010g0078 others(3): Show |
8 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1120+520C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39616468 | |||||||
| chr12:39616601 | G | T | 10 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(7): Show |
10 | NA18944.hp2 NA18959.hp1 NA19000.hp2 others(7): Show |
intron_variant | MODIFIER | c.1120+387C>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39616601 | |||||||
| chr12:39616619 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1120+369A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39616619 | |||||||
| chr12:39616623 | T | C | 2 | a0001c0006t0024g0034 a0003c0005t0011g0031 |
3 | HG01167.hp1 HG01169.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.1120+365A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39616623 | |||||||
| chr12:39616707 | A | G | 1 | a0001c0001t0001g0261 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1120+281T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39616707 | |||||||
| chr12:39616780 | T | G | 1 | a0001c0001t0006g0081 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1120+208A>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39616780 | |||||||
| chr12:39616794 | G | A | 9 | a0001c0001t0005g0002 a0001c0001t0005g0017 a0001c0001t0005g0090 others(6): Show |
16 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1120+194C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39616794 | |||||||
| chr12:39616893 | C | T | 1 | a0003c0005t0011g0031 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1120+95G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39616893 | |||||||
| chr12:39616914 | A | G | 3 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 |
3 | NA19062.hp1 NA19080.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1120+74T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39616914 | |||||||
| chr12:39616980 | G | A | 2 | a0001c0001t0014g0210 a0001c0001t0014g0211 |
2 | HG02717.hp1 HG02809.hp2 |
splice_region_variant&intron_variant | LOW | c.1120+8C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 2/9 | chr12 | 39616980 | |||||||
| chr12:39617223 | CT | C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(57): Show |
82 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.940-56delA | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/9 | chr12 | 39617223 | |||||||
| chr12:39617346 | G | A | 1 | a0001c0001t0001g0258 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.940-178C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/9 | chr12 | 39617346 | |||||||
| chr12:39617524 | T | C | 2 | a0001c0001t0001g0259 a0001c0001t0001g0260 |
2 | NA18944.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.940-356A>G | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/9 | chr12 | 39617524 | |||||||
| chr12:39617722 | G | A | 8 | a0001c0001t0004g0082 a0001c0001t0004g0083 a0002c0002t0004g0005 others(5): Show |
12 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.940-554C>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/9 | chr12 | 39617722 | |||||||
| chr12:39617931 | A | G | 2 | a0001c0001t0013g0035 a0001c0001t0013g0036 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.939+746T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/9 | chr12 | 39617931 | |||||||
| chr12:39618025 | CT | C | 31 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(28): Show |
41 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.939+651delA | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/9 | chr12 | 39618025 | |||||||
| chr12:39618234 | C | A | 2 | a0001c0001t0015g0097 a0001c0001t0015g0098 |
2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.939+443G>T | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/9 | chr12 | 39618234 | |||||||
| chr12:39618235 | C | G | 1 | a0003c0005t0011g0031 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.939+442G>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/9 | chr12 | 39618235 | |||||||
| chr12:39618323 | A | G | 1 | a0001c0006t0024g0034 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.939+354T>C | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/9 | chr12 | 39618323 | |||||||
| chr12:39618495 | C | T | 83 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0071 others(80): Show |
108 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.939+182G>A | ABCD2 | ENSG00000173208.4 | transcript | ENST00000308666.4 | protein_coding | 1/9 | chr12 | 39618495 |