Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5905 |
| ensemblid | ENSG00000100401.21 |
| hgncid | 9854 |
| symbol | RANGAP1 |
| name | Ran GTPase activating protein 1 |
| refseq_nuc | NM_002883.4 |
| refseq_prot | NP_002874.1 |
| ensembl_nuc | ENST00000356244.8 |
| ensembl_prot | ENSP00000348577.3 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 41244779 |
| end | 41286187 |
| strand | - |
| ver | v1.2 |
| region | chr22:41244779-41286187 |
| region5000 | chr22:41239779-41291187 |
| regionname0 | RANGAP1_chr22_41244779_41286187 |
| regionname5000 | RANGAP1_chr22_41239779_41291187 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 587 | 340 | 78 | 56 | 152 | 14 | 38 | 112 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | MASED others(582): Show |
chr22 | 41239779 | 41291187 |
| a0002 | 0/0 | 587 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | MASED others(582): Show |
chr22 | 41239779 | 41291187 |
| a0003 | 0/0 | 587 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | MASED others(582): Show |
chr22 | 41239779 | 41291187 |
| a0004 | 0/0 | 587 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | MASED others(582): Show |
chr22 | 41239779 | 41291187 |
| a0005 | 0/0 | 587 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | MASED others(582): Show |
chr22 | 41239779 | 41291187 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1761 | 185 | 28 | 35 | 95 | 6 | 20 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | ATGGC others(1756): Show |
chr22 | 41239779 | 41291187 | ||
| a0001c0002 | 1/0 | 1761 | 107 | 29 | 9 | 54 | 3 | 11 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | ATGGC others(1756): Show |
chr22 | 41239779 | 41291187 | ||
| a0001c0003 | 0/0 | 1761 | 44 | 20 | 12 | 1 | 4 | 7 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | ATGGC others(1756): Show |
chr22 | 41239779 | 41291187 | ||
| a0001c0008 | 0/0 | 1761 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | ATGGC others(1756): Show |
chr22 | 41239779 | 41291187 | ||
| a0001c0009 | 0/0 | 1761 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | ATGGC others(1756): Show |
chr22 | 41239779 | 41291187 | ||
| a0001c0010 | 0/0 | 1761 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | ATGGC others(1756): Show |
chr22 | 41239779 | 41291187 | ||
| a0001c0011 | 0/0 | 1761 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | ATGGC others(1756): Show |
chr22 | 41239779 | 41291187 | ||
| a0002c0004 | 0/0 | 1761 | 7 | 6 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | ATGGC others(1756): Show |
chr22 | 41239779 | 41291187 | ||
| a0003c0005 | 0/0 | 1761 | 3 | 2 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | ATGGC others(1756): Show |
chr22 | 41239779 | 41291187 | ||
| a0004c0007 | 0/0 | 1761 | 2 | 2 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | ATGGC others(1756): Show |
chr22 | 41239779 | 41291187 | ||
| a0005c0006 | 0/0 | 1761 | 2 | 0 | 0 | 0 | 0 | 2 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | ATGGC others(1756): Show |
chr22 | 41239779 | 41291187 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3828 | 60 | 12 | 2 | 45 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0001t0002 | 0/1 | 3828 | 43 | 3 | 21 | 5 | 3 | 10 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0001t0003 | 0/0 | 3828 | 37 | 1 | 2 | 28 | 2 | 4 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0001t0005 | 0/0 | 3828 | 12 | 0 | 1 | 11 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0001t0006 | 0/0 | 3828 | 11 | 0 | 8 | 3 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0001t0009 | 0/0 | 3828 | 4 | 0 | 1 | 0 | 0 | 3 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0001t0010 | 0/0 | 3828 | 5 | 5 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0001t0011 | 0/0 | 3828 | 3 | 3 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0001t0012 | 0/0 | 3828 | 2 | 0 | 0 | 1 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0001t0014 | 0/0 | 3828 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0001t0015 | 0/0 | 3828 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0001t0017 | 0/0 | 3828 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0001t0018 | 0/0 | 3828 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0001t0019 | 0/0 | 3828 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0001t0020 | 0/0 | 3828 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0001t0021 | 0/0 | 3828 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0001t0025 | 0/0 | 3828 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0002t0001 | 1/0 | 3828 | 85 | 24 | 7 | 47 | 1 | 5 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0002t0005 | 0/0 | 3828 | 16 | 4 | 2 | 3 | 2 | 5 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0002t0016 | 0/0 | 3828 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0002t0022 | 0/0 | 3828 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0002t0023 | 0/0 | 3828 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0002t0024 | 0/0 | 3828 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0002t0026 | 0/0 | 3828 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0002t0027 | 0/0 | 3828 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0003t0001 | 0/0 | 3828 | 2 | 2 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0003t0004 | 0/0 | 3828 | 36 | 18 | 10 | 1 | 2 | 5 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0003t0008 | 0/0 | 3828 | 6 | 0 | 2 | 0 | 2 | 2 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0008t0009 | 0/0 | 3828 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0009t0003 | 0/0 | 3828 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0010t0001 | 0/0 | 3828 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0001c0011t0001 | 0/0 | 3828 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0002c0004t0007 | 0/0 | 3828 | 7 | 6 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0003c0005t0006 | 0/0 | 3828 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0003c0005t0011 | 0/0 | 3828 | 2 | 1 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0004c0007t0001 | 0/0 | 3828 | 2 | 2 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| a0005c0006t0013 | 0/0 | 3828 | 2 | 0 | 0 | 0 | 0 | 2 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | GCCGC others(3823): Show |
chr22 | 41239779 | 41291187 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0006 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0032 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0274 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0005g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0005g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0005g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0005g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0005g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0006g0007 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0006g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0006g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0006g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0006g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0006g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0006g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0006g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0006g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0009g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0009g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0009g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0009g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0010g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0010g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0010g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0010g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0011g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0011g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0012g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0012g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0014g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0015g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0017g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0018g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0019g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0020g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0021g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0001t0025g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0001 | 0/0 | 8 | 1 | 0 | 6 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0224 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0005g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0005g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0005g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0005g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0005g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0005g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0005g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0005g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0005g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0005g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0016g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0022g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0023g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0024g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0026g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0002t0027g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0002 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0008g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0008g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0008g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0008g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0008g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0003t0008g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0008t0009g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0009t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0010t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0001c0011t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0002c0004t0007g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0002c0004t0007g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0002c0004t0007g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0002c0004t0007g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0002c0004t0007g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0002c0004t0007g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0002c0004t0007g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0003c0005t0006g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0003c0005t0011g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0003c0005t0011g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0004c0007t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0004c0007t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| a0005c0006t0013g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0071 | EUR | GBR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00099 | hp2 | a0001 | c0001 | t0012 | g0242 | EUR | GBR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00140 | hp1 | a0001 | c0003 | t0004 | g0002 | EUR | GBR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00140 | hp2 | a0001 | c0002 | t0005 | g0165 | EUR | GBR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00280 | hp1 | a0001 | c0003 | t0004 | g0101 | EUR | FIN | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0034 | EUR | FIN | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0273 | EUR | FIN | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00323 | hp2 | a0001 | c0008 | t0009 | g0065 | EUR | FIN | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00423 | hp2 | a0001 | c0001 | t0012 | g0263 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00621 | hp1 | a0001 | c0001 | t0019 | g0253 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00621 | hp2 | a0001 | c0002 | t0005 | g0021 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00639 | hp1 | a0002 | c0004 | t0007 | g0080 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0022 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00673 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00733 | hp2 | a0001 | c0003 | t0008 | g0119 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00735 | hp1 | a0001 | c0003 | t0004 | g0012 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00738 | hp2 | a0001 | c0003 | t0004 | g0102 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00741 | hp1 | a0001 | c0003 | t0004 | g0118 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG00741 | hp2 | a0001 | c0001 | t0006 | g0306 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01069 | hp1 | a0001 | c0003 | t0004 | g0114 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0284 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01070 | hp1 | a0001 | c0003 | t0004 | g0002 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01081 | hp1 | a0001 | c0003 | t0004 | g0015 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0178 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01099 | hp2 | a0001 | c0001 | t0006 | g0299 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0060 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01109 | hp2 | a0003 | c0005 | t0011 | g0303 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0257 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01167 | hp2 | a0001 | c0003 | t0004 | g0123 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01169 | hp1 | a0001 | c0003 | t0004 | g0015 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0177 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0267 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01175 | hp2 | a0001 | c0002 | t0005 | g0137 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01243 | hp1 | a0001 | c0003 | t0004 | g0099 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0189 | AMR | CLM | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | CLM | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01261 | hp1 | a0001 | c0001 | t0009 | g0059 | AMR | CLM | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0036 | AMR | CLM | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0296 | AMR | CLM | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01361 | hp1 | a0001 | c0001 | t0006 | g0278 | AMR | CLM | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0277 | AMR | CLM | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0290 | AMR | CLM | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0275 | AMR | CLM | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01496 | hp1 | a0001 | c0003 | t0004 | g0094 | AMR | CLM | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | CLM | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01517 | hp1 | a0001 | c0003 | t0008 | g0113 | EUR | IBS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0056 | EUR | IBS | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01884 | hp1 | a0002 | c0004 | t0007 | g0083 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0238 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0235 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0131 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01934 | hp2 | a0001 | c0001 | t0006 | g0283 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01943 | hp1 | a0001 | c0003 | t0008 | g0110 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01943 | hp2 | a0001 | c0001 | t0006 | g0282 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01952 | hp2 | a0001 | c0001 | t0006 | g0007 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01981 | hp1 | a0001 | c0002 | t0005 | g0127 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02004 | hp1 | a0001 | c0001 | t0006 | g0281 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0262 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02055 | hp1 | a0002 | c0004 | t0007 | g0081 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02055 | hp2 | a0001 | c0003 | t0004 | g0105 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02135 | hp2 | a0001 | c0011 | t0001 | g0226 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0232 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0240 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0069 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02258 | hp1 | a0001 | c0001 | t0018 | g0300 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02258 | hp2 | a0002 | c0004 | t0007 | g0087 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02280 | hp1 | a0001 | c0003 | t0004 | g0013 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0092 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0181 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02300 | hp2 | a0001 | c0001 | t0006 | g0007 | AMR | PEL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02451 | hp2 | a0001 | c0002 | t0005 | g0132 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02523 | hp2 | a0001 | c0001 | t0014 | g0055 | EAS | KHV | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02572 | hp1 | a0001 | c0003 | t0004 | g0121 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02572 | hp2 | a0001 | c0003 | t0004 | g0095 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0270 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02615 | hp1 | a0001 | c0003 | t0004 | g0098 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02622 | hp2 | a0001 | c0003 | t0004 | g0097 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02630 | hp1 | a0001 | c0003 | t0004 | g0103 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0134 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02647 | hp1 | a0004 | c0007 | t0001 | g0234 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02647 | hp2 | a0001 | c0003 | t0004 | g0109 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0072 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02698 | hp1 | a0001 | c0003 | t0004 | g0126 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0259 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0239 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02717 | hp2 | a0001 | c0003 | t0004 | g0108 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0171 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02723 | hp2 | a0004 | c0007 | t0001 | g0237 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02735 | hp2 | a0001 | c0001 | t0015 | g0063 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02818 | hp1 | a0001 | c0001 | t0020 | g0088 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02818 | hp2 | a0002 | c0004 | t0007 | g0082 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0183 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0291 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0169 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02965 | hp1 | a0001 | c0003 | t0004 | g0122 | AFR | ESN | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02965 | hp2 | a0001 | c0001 | t0011 | g0035 | AFR | ESN | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0230 | AFR | ESN | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02970 | hp2 | a0001 | c0002 | t0005 | g0305 | AFR | ESN | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03017 | hp1 | a0001 | c0002 | t0005 | g0143 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0272 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0093 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0236 | AFR | MSL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03130 | hp1 | a0001 | c0001 | t0010 | g0010 | AFR | ESN | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03130 | hp2 | a0001 | c0003 | t0004 | g0013 | AFR | ESN | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03139 | hp1 | a0002 | c0004 | t0007 | g0086 | AFR | ESN | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03139 | hp2 | a0001 | c0001 | t0010 | g0096 | AFR | ESN | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | ESN | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03195 | hp2 | a0001 | c0003 | t0004 | g0112 | AFR | ESN | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0233 | AFR | MSL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03209 | hp2 | a0001 | c0001 | t0025 | g0085 | AFR | MSL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03225 | hp2 | a0001 | c0010 | t0001 | g0227 | AFR | MSL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0070 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03453 | hp1 | a0003 | c0005 | t0011 | g0301 | AFR | MSL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03453 | hp2 | a0001 | c0002 | t0016 | g0078 | AFR | MSL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03486 | hp1 | a0001 | c0003 | t0004 | g0106 | AFR | MSL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03486 | hp2 | a0001 | c0002 | t0005 | g0188 | AFR | MSL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03490 | hp1 | a0001 | c0003 | t0004 | g0002 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03490 | hp2 | a0005 | c0006 | t0013 | g0031 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0265 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03491 | hp2 | a0001 | c0003 | t0008 | g0115 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03492 | hp1 | a0001 | c0003 | t0008 | g0120 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03492 | hp2 | a0005 | c0006 | t0013 | g0031 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0231 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0222 | AFR | GWD | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0135 | AFR | MSL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03579 | hp2 | a0001 | c0003 | t0004 | g0289 | AFR | MSL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03669 | hp1 | a0001 | c0002 | t0005 | g0225 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03669 | hp2 | a0001 | c0003 | t0004 | g0124 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0297 | SAS | STU | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03688 | hp2 | a0001 | c0001 | t0009 | g0068 | SAS | STU | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0221 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03704 | hp2 | a0001 | c0001 | t0009 | g0064 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03710 | hp1 | a0001 | c0002 | t0023 | g0144 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0258 | SAS | PJL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03831 | hp1 | a0001 | c0003 | t0004 | g0012 | SAS | BEB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0066 | SAS | BEB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0053 | SAS | BEB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03834 | hp2 | a0001 | c0003 | t0004 | g0100 | SAS | BEB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0266 | SAS | BEB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03942 | hp2 | a0001 | c0002 | t0005 | g0142 | SAS | BEB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0018 | SAS | STU | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG04115 | hp2 | a0001 | c0001 | t0021 | g0298 | SAS | STU | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0256 | SAS | BEB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG04204 | hp1 | a0001 | c0001 | t0009 | g0073 | SAS | STU | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0228 | SAS | STU | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG04228 | hp1 | a0001 | c0002 | t0005 | g0140 | SAS | STU | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG04228 | hp2 | a0001 | c0002 | t0005 | g0229 | SAS | STU | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18522 | hp1 | a0003 | c0005 | t0006 | g0302 | AFR | YRI | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18522 | hp2 | a0002 | c0004 | t0007 | g0089 | AFR | YRI | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18612 | hp1 | a0001 | c0001 | t0005 | g0174 | EAS | CHB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18747 | hp1 | a0001 | c0002 | t0005 | g0175 | EAS | CHB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | CHB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18906 | hp1 | a0001 | c0001 | t0011 | g0243 | AFR | YRI | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0217 | AFR | YRI | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18944 | hp1 | a0001 | c0002 | t0027 | g0307 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18947 | hp2 | a0001 | c0009 | t0003 | g0050 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18956 | hp2 | a0001 | c0002 | t0005 | g0021 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18969 | hp2 | a0001 | c0001 | t0005 | g0249 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18973 | hp2 | a0001 | c0002 | t0022 | g0241 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0248 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18982 | hp2 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18984 | hp2 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18985 | hp2 | a0001 | c0001 | t0005 | g0163 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18992 | hp1 | a0001 | c0003 | t0004 | g0125 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18992 | hp2 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19000 | hp1 | a0001 | c0001 | t0006 | g0279 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19000 | hp2 | a0001 | c0001 | t0005 | g0247 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | LWK | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19030 | hp2 | a0001 | c0003 | t0004 | g0117 | AFR | LWK | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0292 | AFR | LWK | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19043 | hp2 | a0001 | c0003 | t0004 | g0111 | AFR | LWK | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0288 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19062 | hp2 | a0001 | c0002 | t0024 | g0145 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19083 | hp1 | a0001 | c0001 | t0005 | g0252 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19087 | hp2 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19088 | hp1 | a0001 | c0001 | t0006 | g0280 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19088 | hp2 | a0001 | c0002 | t0026 | g0185 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0294 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19240 | hp1 | a0001 | c0001 | t0011 | g0035 | AFR | YRI | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA19240 | hp2 | a0001 | c0001 | t0010 | g0077 | AFR | YRI | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ASW | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA20129 | hp2 | a0001 | c0001 | t0010 | g0010 | AFR | ASW | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0022 | EUR | TSI | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA20752 | hp2 | a0001 | c0002 | t0005 | g0190 | EUR | TSI | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0032 | EUR | TSI | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA20805 | hp2 | a0001 | c0003 | t0008 | g0104 | EUR | TSI | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02109 | hp1 | a0001 | c0003 | t0004 | g0116 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02486 | hp1 | a0001 | c0002 | t0005 | g0133 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0130 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02559 | hp1 | a0001 | c0001 | t0017 | g0276 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0176 | AFR | MSL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG03471 | hp2 | a0001 | c0003 | t0004 | g0107 | AFR | MSL | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0271 | AFR | USA | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| HG06807 | hp2 | a0001 | c0001 | t0010 | g0084 | AFR | USA | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18955 | hp1 | a0001 | c0001 | t0005 | g0196 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | USA | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0293 | AFR | USA | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0274 | REF | REF | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0224 | REF | REF | RANGAP1_chr22_41239779_41291187 | RANGAP1 | chr22 | 41239779 | 41291187 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:41249805 | T | C | 1 | a0005 | 2 | HG03490.hp2 HG03492.hp2 |
missense_variant | MODERATE | c.1496A>G | p.Gln499Arg | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 14/16 | 1736/3828 | 1496/1764 | 499/587 | chr22 | 41249805 | |||
| chr22:41254367 | G | C | 1 | a0002 | 7 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(4): Show |
missense_variant | MODERATE | c.1201C>G | p.Arg401Gly | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 11/16 | 1441/3828 | 1201/1764 | 401/587 | chr22 | 41254367 | |||
| chr22:41256253 | G | C | 1 | a0004 | 2 | HG02647.hp1 HG02723.hp2 |
missense_variant | MODERATE | c.926C>G | p.Ala309Gly | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 9/16 | 1166/3828 | 926/1764 | 309/587 | chr22 | 41256253 | |||
| chr22:41264747 | C | G | 1 | a0003 | 3 | HG01109.hp2 HG03453.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.397G>C | p.Glu133Gln | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/16 | 637/3828 | 397/1764 | 133/587 | chr22 | 41264747 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:41249753 | C | G | 8 | a0001c0001 a0001c0003 a0001c0008 others(5): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
synonymous_variant | LOW | c.1548G>C | p.Leu516Leu | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 14/16 | 1788/3828 | 1548/1764 | 516/587 | chr22 | 41249753 | |||
| chr22:41256729 | G | A | 1 | a0001c0003 | 44 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(41): Show |
synonymous_variant | LOW | c.870C>T | p.Gly290Gly | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 8/16 | 1110/3828 | 870/1764 | 290/587 | chr22 | 41256729 | |||
| chr22:41258026 | G | A | 1 | a0001c0008 | 1 | HG00323.hp2 | synonymous_variant | LOW | c.696C>T | p.Phe232Phe | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 7/16 | 936/3828 | 696/1764 | 232/587 | chr22 | 41258026 | |||
| chr22:41261473 | G | A | 1 | a0001c0009 | 1 | NA18947.hp2 | synonymous_variant | LOW | c.588C>T | p.Gly196Gly | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/16 | 828/3828 | 588/1764 | 196/587 | chr22 | 41261473 | |||
| chr22:41264736 | G | C | 1 | a0001c0010 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.408C>G | p.Leu136Leu | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/16 | 648/3828 | 408/1764 | 136/587 | chr22 | 41264736 | |||
| chr22:41280964 | G | C | 1 | a0001c0011 | 1 | HG02135.hp2 | synonymous_variant | LOW | c.81C>G | p.Gly27Gly | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/16 | 321/3828 | 81/1764 | 27/587 | chr22 | 41280964 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:41244846 | T | C | 14 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(11): Show |
131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1757A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 1757 | chr22 | 41244846 | ||||||
| chr22:41245265 | A | G | 1 | a0001c0002t0023 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1338T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 1338 | chr22 | 41245265 | ||||||
| chr22:41245314 | T | C | 1 | a0001c0001t0021 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1289A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 1289 | chr22 | 41245314 | ||||||
| chr22:41245520 | C | G | 1 | a0001c0002t0022 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1083G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 1083 | chr22 | 41245520 | ||||||
| chr22:41245535 | A | C | 1 | a0001c0001t0015 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1068T>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 1068 | chr22 | 41245535 | ||||||
| chr22:41245566 | C | T | 7 | a0001c0001t0006 a0001c0001t0011 a0001c0001t0017 others(4): Show |
20 | HG00673.hp1 HG00741.hp2 HG01099.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1037G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 1037 | chr22 | 41245566 | ||||||
| chr22:41245800 | T | C | 1 | a0001c0002t0024 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*803A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 803 | chr22 | 41245800 | ||||||
| chr22:41245919 | C | T | 1 | a0001c0001t0020 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*684G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 684 | chr22 | 41245919 | ||||||
| chr22:41245920 | G | A | 3 | a0001c0001t0010 a0001c0001t0025 a0002c0004t0007 |
13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*683C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 683 | chr22 | 41245920 | ||||||
| chr22:41245980 | C | T | 2 | a0001c0003t0004 a0001c0003t0008 |
42 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*623G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 623 | chr22 | 41245980 | ||||||
| chr22:41245988 | G | A | 1 | a0005c0006t0013 | 2 | HG03490.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*615C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 615 | chr22 | 41245988 | ||||||
| chr22:41246020 | G | A | 1 | a0001c0002t0026 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*583C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 583 | chr22 | 41246020 | ||||||
| chr22:41246208 | C | T | 13 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(10): Show |
69 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*395G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 395 | chr22 | 41246208 | ||||||
| chr22:41246277 | C | T | 2 | a0001c0001t0010 a0002c0004t0007 |
12 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*326G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 326 | chr22 | 41246277 | ||||||
| chr22:41246320 | C | T | 1 | a0001c0001t0019 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*283G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 283 | chr22 | 41246320 | ||||||
| chr22:41246434 | C | T | 1 | a0001c0001t0018 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*169G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 169 | chr22 | 41246434 | ||||||
| chr22:41246441 | C | G | 1 | a0001c0001t0017 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*162G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 162 | chr22 | 41246441 | ||||||
| chr22:41246488 | C | T | 1 | a0001c0002t0016 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*115G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 16/16 | 115 | chr22 | 41246488 | ||||||
| chr22:41286010 | G | T | 6 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0014 others(3): Show |
45 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(42): Show |
5_prime_UTR_variant | MODIFIER | c.-63C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/16 | 4966 | chr22 | 41286010 | ||||||
| chr22:41286129 | G | A | 1 | a0001c0002t0027 | 1 | NA18944.hp1 | 5_prime_UTR_variant | MODIFIER | c.-182C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/16 | 5085 | chr22 | 41286129 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:41246777 | G | T | 1 | a0001c0002t0005g0175 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1695-105C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41246777 | |||||||
| chr22:41246825 | G | A | 1 | a0001c0001t0003g0036 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1695-153C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41246825 | |||||||
| chr22:41246845 | G | A | 4 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(1): Show |
5 | HG03130.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1695-173C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41246845 | |||||||
| chr22:41246903 | C | A | 12 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(9): Show |
13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1695-231G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41246903 | |||||||
| chr22:41246992 | A | G | 12 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(9): Show |
13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1695-320T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41246992 | |||||||
| chr22:41247141 | C | T | 12 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(9): Show |
13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1695-469G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247141 | |||||||
| chr22:41247207 | C | A | 1 | a0004c0007t0001g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1695-535G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247207 | |||||||
| chr22:41247344 | C | T | 1 | a0001c0003t0004g0111 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1695-672G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247344 | |||||||
| chr22:41247347 | G | A | 1 | a0001c0002t0001g0290 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1695-675C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247347 | |||||||
| chr22:41247393 | C | T | 43 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(40): Show |
48 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.1695-721G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247393 | |||||||
| chr22:41247435 | T | C | 12 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(9): Show |
13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1695-763A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247435 | |||||||
| chr22:41247591 | A | G | 1 | a0001c0001t0003g0008 | 2 | HG00558.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1695-919T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247591 | |||||||
| chr22:41247664 | C | A | 1 | a0001c0002t0001g0173 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1695-992G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247664 | |||||||
| chr22:41247728 | A | G | 5 | a0001c0001t0002g0006 a0001c0001t0002g0244 a0001c0001t0002g0264 others(2): Show |
7 | HG00323.hp1 HG00733.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.1695-1056T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247728 | |||||||
| chr22:41247732 | C | T | 1 | a0001c0003t0001g0092 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1695-1060G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247732 | |||||||
| chr22:41247734 | G | T | 11 | a0001c0002t0001g0230 a0001c0002t0001g0231 a0001c0002t0001g0232 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1695-1062C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247734 | |||||||
| chr22:41247738 | G | A | 3 | a0001c0002t0001g0290 a0001c0002t0001g0292 a0001c0002t0001g0293 |
3 | HG01433.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1695-1066C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247738 | |||||||
| chr22:41247758 | C | G | 1 | a0001c0002t0027g0307 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1695-1086G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247758 | |||||||
| chr22:41247779 | A | G | 12 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(9): Show |
13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1695-1107T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247779 | |||||||
| chr22:41247780 | G | A | 12 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(9): Show |
13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1695-1108C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41247780 | |||||||
| chr22:41248011 | C | G | 12 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(9): Show |
13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1694+1319G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41248011 | |||||||
| chr22:41248070 | C | T | 77 | a0001c0001t0001g0251 a0001c0001t0002g0005 a0001c0001t0002g0006 others(74): Show |
92 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1694+1260G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41248070 | |||||||
| chr22:41248128 | G | A | 1 | a0001c0001t0006g0282 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1694+1202C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41248128 | |||||||
| chr22:41248131 | A | T | 7 | a0001c0002t0001g0014 a0001c0002t0001g0171 a0001c0002t0001g0176 others(4): Show |
8 | HG01243.hp2 HG01433.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1694+1199T>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41248131 | |||||||
| chr22:41248191 | G | C | 1 | a0001c0003t0004g0111 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1694+1139C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41248191 | |||||||
| chr22:41248230 | G | C | 96 | a0001c0001t0001g0079 a0001c0001t0003g0008 a0001c0001t0003g0009 others(93): Show |
104 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1694+1100C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41248230 | |||||||
| chr22:41248358 | G | GGCCT | 4 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(1): Show |
5 | HG03130.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1694+968_1694+971d others(6): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41248358 | |||||||
| chr22:41248424 | G | A | 70 | a0001c0001t0001g0251 a0001c0001t0002g0005 a0001c0001t0002g0006 others(67): Show |
84 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1694+906C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41248424 | |||||||
| chr22:41248708 | G | GCCT | 3 | a0001c0003t0004g0013 a0001c0003t0004g0106 a0001c0003t0004g0107 |
4 | HG02280.hp1 HG03130.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1694+619_1694+621d others(5): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41248708 | |||||||
| chr22:41248816 | C | CACACATT others(12): Show |
1 | a0001c0001t0003g0076 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1694+495_1694+513d others(21): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41248816 | |||||||
| chr22:41248864 | G | A | 3 | a0001c0001t0001g0136 a0001c0001t0001g0153 a0001c0001t0001g0204 |
3 | HG00544.hp2 HG02056.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1694+466C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41248864 | |||||||
| chr22:41249081 | A | G | 171 | a0001c0001t0001g0079 a0001c0001t0001g0251 a0001c0001t0002g0005 others(168): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1694+249T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41249081 | |||||||
| chr22:41249253 | C | T | 2 | a0001c0001t0002g0284 a0001c0001t0002g0295 |
2 | HG01069.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1694+77G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41249253 | |||||||
| chr22:41249299 | G | T | 11 | a0001c0002t0001g0230 a0001c0002t0001g0231 a0001c0002t0001g0232 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1694+31C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41249299 | |||||||
| chr22:41249305 | G | A | 1 | a0001c0002t0001g0186 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1694+25C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 15/15 | chr22 | 41249305 | |||||||
| chr22:41249496 | TG | T | 245 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(242): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.1573-46delC | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 14/15 | chr22 | 41249496 | |||||||
| chr22:41249520 | T | A | 8 | a0001c0003t0004g0013 a0001c0003t0004g0103 a0001c0003t0004g0106 others(5): Show |
9 | HG02280.hp1 HG02572.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1573-69A>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 14/15 | chr22 | 41249520 | |||||||
| chr22:41249585 | G | A | 12 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(9): Show |
13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1573-134C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 14/15 | chr22 | 41249585 | |||||||
| chr22:41249605 | C | T | 2 | a0004c0007t0001g0234 a0004c0007t0001g0237 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1572+124G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 14/15 | chr22 | 41249605 | |||||||
| chr22:41249867 | G | A | 12 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(9): Show |
13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1484-50C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 13/15 | chr22 | 41249867 | |||||||
| chr22:41249903 | G | C | 3 | a0001c0002t0001g0147 a0001c0002t0001g0172 a0001c0002t0001g0187 |
3 | HG02080.hp2 NA18948.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.1484-86C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 13/15 | chr22 | 41249903 | |||||||
| chr22:41250039 | C | T | 2 | a0001c0003t0004g0116 a0001c0003t0004g0117 |
2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1484-222G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 13/15 | chr22 | 41250039 | |||||||
| chr22:41250266 | G | A | 1 | a0001c0001t0003g0038 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1484-449C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 13/15 | chr22 | 41250266 | |||||||
| chr22:41250333 | C | A | 1 | a0001c0002t0001g0168 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1484-516G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 13/15 | chr22 | 41250333 | |||||||
| chr22:41250450 | G | A | 1 | a0001c0001t0011g0035 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1483+557C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 13/15 | chr22 | 41250450 | |||||||
| chr22:41250488 | G | A | 1 | a0001c0002t0005g0188 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1483+519C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 13/15 | chr22 | 41250488 | |||||||
| chr22:41250565 | G | T | 1 | a0002c0004t0007g0082 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1483+442C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 13/15 | chr22 | 41250565 | |||||||
| chr22:41250566 | C | A | 1 | a0002c0004t0007g0082 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1483+441G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 13/15 | chr22 | 41250566 | |||||||
| chr22:41250571 | G | A | 11 | a0001c0002t0001g0230 a0001c0002t0001g0231 a0001c0002t0001g0232 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1483+436C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 13/15 | chr22 | 41250571 | |||||||
| chr22:41250583 | C | G | 4 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(1): Show |
5 | HG03130.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1483+424G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 13/15 | chr22 | 41250583 | |||||||
| chr22:41250734 | A | G | 84 | a0001c0001t0001g0079 a0001c0001t0003g0008 a0001c0001t0003g0009 others(81): Show |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1483+273T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 13/15 | chr22 | 41250734 | |||||||
| chr22:41250799 | G | A | 1 | a0001c0002t0001g0214 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1483+208C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 13/15 | chr22 | 41250799 | |||||||
| chr22:41250829 | G | A | 1 | a0001c0001t0025g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1483+178C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 13/15 | chr22 | 41250829 | |||||||
| chr22:41251121 | A | C | 1 | a0001c0002t0005g0143 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1381-12T>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41251121 | |||||||
| chr22:41251213 | G | A | 12 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(9): Show |
13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1381-104C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41251213 | |||||||
| chr22:41251232 | C | T | 12 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(9): Show |
13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1381-123G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41251232 | |||||||
| chr22:41251299 | G | A | 10 | a0001c0001t0001g0148 a0001c0001t0001g0157 a0001c0001t0001g0164 others(7): Show |
10 | HG02083.hp1 HG02135.hp1 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.1381-190C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41251299 | |||||||
| chr22:41251443 | T | C | 1 | a0005c0006t0013g0031 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1381-334A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41251443 | |||||||
| chr22:41251487 | T | A | 239 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(236): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1381-378A>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41251487 | |||||||
| chr22:41251627 | G | GA | 25 | a0001c0001t0001g0194 a0001c0001t0001g0201 a0001c0001t0001g0304 others(22): Show |
28 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.1381-519dupT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41251627 | |||||||
| chr22:41251684 | C | A | 1 | a0001c0002t0023g0144 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1381-575G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41251684 | |||||||
| chr22:41251868 | C | T | 1 | a0001c0003t0004g0126 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1381-759G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41251868 | |||||||
| chr22:41251991 | G | A | 8 | a0001c0001t0025g0085 a0002c0004t0007g0080 a0002c0004t0007g0081 others(5): Show |
8 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1380+881C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41251991 | |||||||
| chr22:41251991 | G | GA | 4 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(1): Show |
5 | HG03130.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1380+880_1380+881i others(3): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41251991 | |||||||
| chr22:41252016 | C | T | 5 | a0001c0001t0001g0152 a0001c0001t0001g0156 a0001c0001t0001g0191 others(2): Show |
5 | NA18948.hp2 NA18949.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.1380+856G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41252016 | |||||||
| chr22:41252054 | C | T | 2 | a0001c0001t0006g0299 a0001c0001t0011g0035 |
3 | HG01099.hp2 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1380+818G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41252054 | |||||||
| chr22:41252087 | C | T | 83 | a0001c0001t0001g0079 a0001c0001t0003g0008 a0001c0001t0003g0009 others(80): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.1380+785G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41252087 | |||||||
| chr22:41252309 | T | A | 2 | a0004c0007t0001g0234 a0004c0007t0001g0237 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1380+563A>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41252309 | |||||||
| chr22:41252427 | G | A | 1 | a0001c0002t0005g0133 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1380+445C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41252427 | |||||||
| chr22:41252498 | T | C | 121 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(118): Show |
141 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1380+374A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41252498 | |||||||
| chr22:41252583 | G | C | 12 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(9): Show |
13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1380+289C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41252583 | |||||||
| chr22:41252586 | G | C | 2 | a0001c0003t0004g0116 a0001c0003t0004g0117 |
2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1380+286C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41252586 | |||||||
| chr22:41252644 | C | T | 3 | a0001c0003t0004g0094 a0001c0003t0004g0095 a0001c0003t0004g0097 |
3 | HG01496.hp1 HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1380+228G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41252644 | |||||||
| chr22:41252695 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1380+177G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41252695 | |||||||
| chr22:41252726 | C | T | 1 | a0001c0001t0020g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1380+146G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41252726 | |||||||
| chr22:41252779 | G | A | 1 | a0001c0001t0011g0243 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1380+93C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41252779 | |||||||
| chr22:41252804 | G | A | 1 | a0001c0001t0001g0025 | 2 | HG00609.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1380+68C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 12/15 | chr22 | 41252804 | |||||||
| chr22:41253043 | C | A | 1 | a0001c0002t0005g0140 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1261-52G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 11/15 | chr22 | 41253043 | |||||||
| chr22:41253256 | G | A | 1 | a0001c0003t0004g0102 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1261-265C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 11/15 | chr22 | 41253256 | |||||||
| chr22:41253305 | C | T | 7 | a0001c0001t0006g0299 a0001c0001t0011g0035 a0001c0001t0017g0276 others(4): Show |
8 | HG01099.hp2 HG01109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1261-314G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 11/15 | chr22 | 41253305 | |||||||
| chr22:41253321 | G | C | 1 | a0001c0001t0002g0258 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1261-330C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 11/15 | chr22 | 41253321 | |||||||
| chr22:41253322 | G | C | 1 | a0001c0001t0002g0244 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1261-331C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 11/15 | chr22 | 41253322 | |||||||
| chr22:41253498 | G | A | 1 | a0001c0001t0019g0253 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1261-507C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 11/15 | chr22 | 41253498 | |||||||
| chr22:41253746 | T | C | 3 | a0001c0002t0005g0021 a0001c0002t0005g0175 a0001c0002t0024g0145 |
4 | HG00621.hp2 NA18747.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260+562A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 11/15 | chr22 | 41253746 | |||||||
| chr22:41253831 | G | A | 1 | a0001c0001t0020g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1260+477C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 11/15 | chr22 | 41253831 | |||||||
| chr22:41253928 | C | T | 3 | a0001c0001t0001g0203 a0001c0001t0001g0209 a0001c0001t0001g0210 |
3 | HG00423.hp1 NA19068.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1260+380G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 11/15 | chr22 | 41253928 | |||||||
| chr22:41253937 | G | A | 84 | a0001c0001t0001g0079 a0001c0001t0003g0008 a0001c0001t0003g0009 others(81): Show |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1260+371C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 11/15 | chr22 | 41253937 | |||||||
| chr22:41254186 | C | A | 56 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0030 others(53): Show |
68 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1260+122G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 11/15 | chr22 | 41254186 | |||||||
| chr22:41254237 | T | A | 1 | a0001c0001t0011g0035 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1260+71A>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 11/15 | chr22 | 41254237 | |||||||
| chr22:41254579 | C | G | 12 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(9): Show |
13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1074-85G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41254579 | |||||||
| chr22:41254695 | C | G | 171 | a0001c0001t0001g0079 a0001c0001t0001g0251 a0001c0001t0002g0005 others(168): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1074-201G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41254695 | |||||||
| chr22:41254739 | G | A | 1 | a0001c0010t0001g0227 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1074-245C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41254739 | |||||||
| chr22:41254826 | G | T | 1 | a0001c0002t0027g0307 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1074-332C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41254826 | |||||||
| chr22:41254844 | C | T | 5 | a0001c0001t0002g0006 a0001c0001t0002g0244 a0001c0001t0002g0264 others(2): Show |
7 | HG00323.hp1 HG00733.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.1074-350G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41254844 | |||||||
| chr22:41254879 | G | A | 3 | a0003c0005t0006g0302 a0003c0005t0011g0301 a0003c0005t0011g0303 |
3 | HG01109.hp2 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1074-385C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41254879 | |||||||
| chr22:41254959 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1074-465C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41254959 | |||||||
| chr22:41254964 | T | C | 2 | a0004c0007t0001g0234 a0004c0007t0001g0237 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1074-470A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41254964 | |||||||
| chr22:41254983 | C | CA | 69 | a0001c0001t0001g0197 a0001c0001t0001g0251 a0001c0001t0002g0005 others(66): Show |
83 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1074-490dupT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41254983 | |||||||
| chr22:41254996 | C | A | 1 | a0001c0001t0005g0252 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1074-502G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41254996 | |||||||
| chr22:41254997 | A | C | 1 | a0001c0001t0003g0076 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1074-503T>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41254997 | |||||||
| chr22:41255022 | T | C | 39 | a0001c0003t0001g0092 a0001c0003t0001g0093 a0001c0003t0004g0002 others(36): Show |
44 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.1074-528A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41255022 | |||||||
| chr22:41255030 | G | A | 83 | a0001c0001t0001g0079 a0001c0001t0003g0008 a0001c0001t0003g0009 others(80): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.1074-536C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41255030 | |||||||
| chr22:41255207 | T | C | 12 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(9): Show |
13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1074-713A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41255207 | |||||||
| chr22:41255343 | G | A | 11 | a0001c0002t0001g0230 a0001c0002t0001g0231 a0001c0002t0001g0232 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1073+678C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41255343 | |||||||
| chr22:41255356 | G | A | 1 | a0002c0004t0007g0089 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1073+665C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41255356 | |||||||
| chr22:41255436 | A | G | 97 | a0001c0001t0001g0079 a0001c0001t0003g0008 a0001c0001t0003g0009 others(94): Show |
105 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1073+585T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41255436 | |||||||
| chr22:41255463 | T | C | 76 | a0001c0001t0001g0079 a0001c0001t0003g0008 a0001c0001t0003g0009 others(73): Show |
82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1073+558A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41255463 | |||||||
| chr22:41255589 | C | T | 1 | a0001c0001t0017g0276 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1073+432G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41255589 | |||||||
| chr22:41255700 | G | A | 160 | a0001c0001t0001g0079 a0001c0001t0001g0251 a0001c0001t0002g0005 others(157): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.1073+321C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41255700 | |||||||
| chr22:41255774 | T | A | 1 | a0001c0002t0001g0291 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1073+247A>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41255774 | |||||||
| chr22:41255816 | T | A | 1 | a0001c0001t0001g0204 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1073+205A>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41255816 | |||||||
| chr22:41255818 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1073+203C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 10/15 | chr22 | 41255818 | |||||||
| chr22:41256328 | C | T | 12 | a0001c0001t0002g0005 a0001c0001t0002g0030 a0001c0001t0002g0033 others(9): Show |
16 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.889-38G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 8/15 | chr22 | 41256328 | |||||||
| chr22:41256341 | C | G | 84 | a0001c0001t0001g0079 a0001c0001t0003g0008 a0001c0001t0003g0009 others(81): Show |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.889-51G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 8/15 | chr22 | 41256341 | |||||||
| chr22:41256373 | G | A | 1 | a0001c0002t0005g0137 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.889-83C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 8/15 | chr22 | 41256373 | |||||||
| chr22:41256425 | A | G | 1 | a0001c0001t0020g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.889-135T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 8/15 | chr22 | 41256425 | |||||||
| chr22:41256475 | C | T | 1 | a0001c0001t0002g0245 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.889-185G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 8/15 | chr22 | 41256475 | |||||||
| chr22:41256517 | C | G | 7 | a0001c0002t0001g0014 a0001c0002t0001g0171 a0001c0002t0001g0176 others(4): Show |
8 | HG01243.hp2 HG01433.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.888+194G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 8/15 | chr22 | 41256517 | |||||||
| chr22:41256615 | A | G | 12 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(9): Show |
13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.888+96T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 8/15 | chr22 | 41256615 | |||||||
| chr22:41256842 | G | T | 49 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0030 others(46): Show |
60 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.775-18C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 7/15 | chr22 | 41256842 | |||||||
| chr22:41256856 | G | A | 1 | a0002c0004t0007g0086 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.775-32C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 7/15 | chr22 | 41256856 | |||||||
| chr22:41257013 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.775-189G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 7/15 | chr22 | 41257013 | |||||||
| chr22:41257464 | G | A | 7 | a0001c0002t0001g0014 a0001c0002t0001g0171 a0001c0002t0001g0176 others(4): Show |
8 | HG01243.hp2 HG01433.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.774+484C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 7/15 | chr22 | 41257464 | |||||||
| chr22:41257536 | T | G | 133 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(130): Show |
154 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.774+412A>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 7/15 | chr22 | 41257536 | |||||||
| chr22:41257744 | A | G | 61 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(58): Show |
67 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.774+204T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 7/15 | chr22 | 41257744 | |||||||
| chr22:41257868 | C | T | 11 | a0001c0002t0001g0230 a0001c0002t0001g0231 a0001c0002t0001g0232 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.774+80G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 7/15 | chr22 | 41257868 | |||||||
| chr22:41258119 | G | A | 1 | a0001c0002t0005g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.616-13C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41258119 | |||||||
| chr22:41258197 | A | G | 12 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(9): Show |
13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.616-91T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41258197 | |||||||
| chr22:41258452 | T | C | 12 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(9): Show |
13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.616-346A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41258452 | |||||||
| chr22:41258564 | G | A | 84 | a0001c0001t0001g0079 a0001c0001t0003g0008 a0001c0001t0003g0009 others(81): Show |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.616-458C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41258564 | |||||||
| chr22:41258565 | A | G | 84 | a0001c0001t0001g0079 a0001c0001t0003g0008 a0001c0001t0003g0009 others(81): Show |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.616-459T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41258565 | |||||||
| chr22:41258666 | CTTT | C | 3 | a0001c0002t0001g0236 a0001c0002t0001g0238 a0001c0002t0001g0239 |
3 | HG01884.hp2 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.616-563_616-561del others(3): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41258666 | |||||||
| chr22:41258710 | G | C | 1 | a0001c0001t0014g0055 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.616-604C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41258710 | |||||||
| chr22:41258892 | C | T | 2 | a0001c0002t0005g0140 a0001c0002t0005g0142 |
2 | HG03942.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.616-786G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41258892 | |||||||
| chr22:41258950 | C | T | 12 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(9): Show |
13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.616-844G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41258950 | |||||||
| chr22:41258951 | A | G | 224 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(221): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.616-845T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41258951 | |||||||
| chr22:41259053 | G | A | 1 | a0001c0001t0006g0278 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.616-947C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259053 | |||||||
| chr22:41259054 | A | G | 217 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(214): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.616-948T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259054 | |||||||
| chr22:41259080 | C | T | 1 | a0001c0001t0017g0276 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.616-974G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259080 | |||||||
| chr22:41259146 | G | A | 1 | a0001c0002t0001g0147 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.616-1040C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259146 | |||||||
| chr22:41259327 | C | A | 3 | a0002c0004t0007g0080 a0002c0004t0007g0081 a0002c0004t0007g0089 |
3 | HG00639.hp1 HG02055.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.616-1221G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259327 | |||||||
| chr22:41259336 | G | A | 9 | a0001c0001t0011g0035 a0001c0001t0017g0276 a0001c0002t0001g0177 others(6): Show |
10 | HG00639.hp1 HG01169.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.616-1230C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259336 | |||||||
| chr22:41259428 | T | G | 1 | a0001c0002t0001g0236 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.616-1322A>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259428 | |||||||
| chr22:41259435 | A | T | 2 | a0001c0001t0009g0068 a0001c0001t0009g0073 |
2 | HG03688.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.616-1329T>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259435 | |||||||
| chr22:41259436 | A | G | 1 | a0001c0001t0002g0268 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.616-1330T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259436 | |||||||
| chr22:41259560 | C | A | 1 | a0001c0001t0001g0304 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.616-1454G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259560 | |||||||
| chr22:41259627 | A | G | 1 | a0001c0001t0002g0257 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.616-1521T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259627 | |||||||
| chr22:41259673 | C | T | 12 | a0001c0002t0001g0011 a0001c0002t0001g0020 a0001c0002t0001g0090 others(9): Show |
14 | NA18956.hp1 NA18982.hp1 NA18986.hp2 others(11): Show |
intron_variant | MODIFIER | c.616-1567G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259673 | |||||||
| chr22:41259747 | A | T | 1 | a0001c0001t0001g0304 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.616-1641T>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259747 | |||||||
| chr22:41259754 | G | A | 1 | a0001c0002t0005g0188 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.616-1648C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259754 | |||||||
| chr22:41259966 | G | A | 11 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(8): Show |
12 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.615+1480C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259966 | |||||||
| chr22:41259993 | G | A | 1 | a0002c0004t0007g0089 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.615+1453C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41259993 | |||||||
| chr22:41260012 | A | AT | 97 | a0001c0001t0001g0079 a0001c0001t0003g0008 a0001c0001t0003g0009 others(94): Show |
105 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.615+1433dupA | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41260012 | |||||||
| chr22:41260129 | A | G | 96 | a0001c0001t0001g0079 a0001c0001t0003g0008 a0001c0001t0003g0009 others(93): Show |
104 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.615+1317T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41260129 | |||||||
| chr22:41260290 | T | C | 1 | a0001c0002t0027g0307 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.615+1156A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41260290 | |||||||
| chr22:41260328 | G | A | 118 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(115): Show |
138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.615+1118C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41260328 | |||||||
| chr22:41260370 | G | A | 7 | a0001c0002t0001g0130 a0001c0002t0001g0131 a0001c0002t0001g0134 others(4): Show |
7 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.615+1076C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41260370 | |||||||
| chr22:41260474 | G | A | 1 | a0001c0011t0001g0226 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.615+972C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41260474 | |||||||
| chr22:41260505 | G | A | 119 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(116): Show |
139 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.615+941C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41260505 | |||||||
| chr22:41260566 | G | A | 2 | a0001c0002t0001g0236 a0001c0002t0001g0239 |
2 | HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.615+880C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41260566 | |||||||
| chr22:41260567 | G | A | 2 | a0001c0002t0001g0236 a0001c0002t0001g0239 |
2 | HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.615+879C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41260567 | |||||||
| chr22:41260574 | G | A | 1 | a0001c0001t0020g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.615+872C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41260574 | |||||||
| chr22:41260674 | C | T | 1 | a0001c0002t0005g0229 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.615+772G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41260674 | |||||||
| chr22:41261071 | T | C | 1 | a0001c0002t0001g0177 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.615+375A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41261071 | |||||||
| chr22:41261168 | C | T | 1 | a0001c0003t0004g0124 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.615+278G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 6/15 | chr22 | 41261168 | |||||||
| chr22:41261604 | T | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0194 |
3 | NA19010.hp1 NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.481-24A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41261604 | |||||||
| chr22:41261622 | C | T | 119 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(116): Show |
139 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.481-42G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41261622 | |||||||
| chr22:41261634 | G | A | 11 | a0001c0002t0001g0230 a0001c0002t0001g0231 a0001c0002t0001g0232 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.481-54C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41261634 | |||||||
| chr22:41261694 | A | G | 1 | a0001c0001t0002g0254 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.481-114T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41261694 | |||||||
| chr22:41261701 | G | A | 85 | a0001c0001t0001g0079 a0001c0001t0003g0008 a0001c0001t0003g0009 others(82): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.481-121C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41261701 | |||||||
| chr22:41261774 | T | TG | 3 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 |
4 | HG03130.hp1 HG06807.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-195_481-194ins others(1): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41261774 | |||||||
| chr22:41261776 | A | T | 3 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 |
4 | HG03130.hp1 HG06807.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-196T>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41261776 | |||||||
| chr22:41261840 | T | G | 1 | a0001c0001t0003g0066 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.481-260A>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41261840 | |||||||
| chr22:41261996 | G | A | 1 | a0001c0010t0001g0227 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.481-416C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41261996 | |||||||
| chr22:41262071 | T | C | 11 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(8): Show |
12 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.481-491A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262071 | |||||||
| chr22:41262166 | G | A | 1 | a0001c0001t0001g0304 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.481-586C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262166 | |||||||
| chr22:41262167 | A | G | 1 | a0001c0001t0001g0304 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.481-587T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262167 | |||||||
| chr22:41262217 | G | A | 4 | a0001c0003t0004g0013 a0001c0003t0004g0106 a0001c0003t0004g0107 others(1): Show |
5 | HG02280.hp1 HG02965.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.481-637C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262217 | |||||||
| chr22:41262242 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.481-662G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262242 | |||||||
| chr22:41262277 | G | A | 4 | a0001c0002t0001g0003 a0001c0002t0001g0146 a0001c0002t0001g0294 others(1): Show |
6 | HG00558.hp2 HG02056.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.481-697C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262277 | |||||||
| chr22:41262316 | G | A | 4 | a0001c0003t0001g0092 a0001c0003t0001g0093 a0001c0003t0004g0098 others(1): Show |
4 | HG02280.hp2 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-736C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262316 | |||||||
| chr22:41262333 | A | C | 2 | a0001c0001t0006g0279 a0001c0001t0006g0280 |
2 | NA19000.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.481-753T>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262333 | |||||||
| chr22:41262370 | C | G | 3 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 |
4 | HG03130.hp1 HG06807.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-790G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262370 | |||||||
| chr22:41262597 | A | G | 215 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(212): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.481-1017T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262597 | |||||||
| chr22:41262600 | C | CT | 55 | a0001c0001t0001g0251 a0001c0001t0002g0005 a0001c0001t0002g0006 others(52): Show |
68 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.481-1021dupA | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262600 | |||||||
| chr22:41262628 | C | T | 119 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(116): Show |
139 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.481-1048G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262628 | |||||||
| chr22:41262650 | GGATCACG others(7): Show |
G | 6 | a0001c0002t0001g0014 a0001c0002t0001g0171 a0001c0002t0001g0290 others(3): Show |
7 | HG01243.hp2 HG01433.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.481-1084_481-1071d others(16): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262650 | |||||||
| chr22:41262655 | A | T | 11 | a0001c0002t0001g0230 a0001c0002t0001g0231 a0001c0002t0001g0232 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.481-1075T>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262655 | |||||||
| chr22:41262685 | T | C | 11 | a0001c0002t0001g0230 a0001c0002t0001g0231 a0001c0002t0001g0232 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.481-1105A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262685 | |||||||
| chr22:41262705 | C | T | 1 | a0001c0002t0001g0022 | 2 | HG00639.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.481-1125G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41262705 | |||||||
| chr22:41263010 | C | T | 1 | a0001c0002t0005g0137 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.481-1430G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41263010 | |||||||
| chr22:41263094 | T | C | 1 | a0001c0001t0003g0045 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.481-1514A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41263094 | |||||||
| chr22:41263322 | G | T | 11 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(8): Show |
12 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.480+1342C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41263322 | |||||||
| chr22:41263372 | CTGTT | C | 4 | a0001c0001t0001g0149 a0001c0001t0001g0210 a0001c0001t0020g0088 others(1): Show |
4 | HG02818.hp1 HG04184.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+1288_480+1291d others(6): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41263372 | |||||||
| chr22:41263576 | G | A | 119 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(116): Show |
139 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.480+1088C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41263576 | |||||||
| chr22:41263646 | A | C | 3 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 |
4 | HG03130.hp1 HG06807.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+1018T>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41263646 | |||||||
| chr22:41263962 | G | A | 11 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(8): Show |
12 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.480+702C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41263962 | |||||||
| chr22:41264141 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.480+523G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41264141 | |||||||
| chr22:41264285 | G | A | 1 | a0001c0001t0002g0266 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.480+379C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41264285 | |||||||
| chr22:41264288 | GC | G | 235 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(232): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.480+375delG | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41264288 | |||||||
| chr22:41264297 | G | A | 119 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(116): Show |
139 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.480+367C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41264297 | |||||||
| chr22:41264360 | G | A | 11 | a0001c0002t0001g0230 a0001c0002t0001g0231 a0001c0002t0001g0232 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.480+304C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41264360 | |||||||
| chr22:41264406 | C | G | 85 | a0001c0001t0001g0079 a0001c0001t0003g0008 a0001c0001t0003g0009 others(82): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.480+258G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41264406 | |||||||
| chr22:41264431 | T | C | 11 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(8): Show |
12 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.480+233A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41264431 | |||||||
| chr22:41264586 | G | C | 1 | a0001c0010t0001g0227 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.480+78C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41264586 | |||||||
| chr22:41264641 | G | A | 45 | a0001c0001t0001g0079 a0001c0001t0003g0008 a0001c0001t0003g0009 others(42): Show |
47 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.480+23C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 5/15 | chr22 | 41264641 | |||||||
| chr22:41264875 | T | C | 1 | a0001c0001t0010g0096 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.301-32A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41264875 | |||||||
| chr22:41264960 | A | G | 215 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(212): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.301-117T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41264960 | |||||||
| chr22:41265040 | G | T | 1 | a0001c0002t0001g0022 | 2 | HG00639.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.301-197C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41265040 | |||||||
| chr22:41265150 | G | T | 119 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(116): Show |
139 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.301-307C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41265150 | |||||||
| chr22:41265225 | C | T | 4 | a0001c0001t0001g0155 a0001c0001t0001g0192 a0001c0001t0001g0304 others(1): Show |
4 | HG02027.hp2 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.301-382G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41265225 | |||||||
| chr22:41265764 | G | A | 1 | a0001c0001t0020g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.301-921C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41265764 | |||||||
| chr22:41265854 | A | G | 11 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(8): Show |
12 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.301-1011T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41265854 | |||||||
| chr22:41265887 | C | T | 2 | a0004c0007t0001g0234 a0004c0007t0001g0237 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.301-1044G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41265887 | |||||||
| chr22:41265973 | T | C | 225 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(222): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.301-1130A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41265973 | |||||||
| chr22:41265980 | A | G | 9 | a0001c0002t0001g0011 a0001c0002t0001g0020 a0001c0002t0001g0090 others(6): Show |
11 | NA18956.hp1 NA18982.hp1 NA18986.hp2 others(8): Show |
intron_variant | MODIFIER | c.301-1137T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41265980 | |||||||
| chr22:41265998 | C | T | 1 | a0001c0002t0001g0221 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.301-1155G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41265998 | |||||||
| chr22:41266022 | G | A | 8 | a0001c0001t0006g0007 a0001c0001t0006g0278 a0001c0001t0006g0279 others(5): Show |
10 | HG00673.hp1 HG00741.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.301-1179C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41266022 | |||||||
| chr22:41266074 | C | T | 1 | a0001c0001t0011g0035 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.301-1231G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41266074 | |||||||
| chr22:41266134 | G | A | 8 | a0001c0001t0001g0148 a0001c0001t0001g0164 a0001c0001t0001g0195 others(5): Show |
8 | HG02083.hp1 HG02135.hp1 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.301-1291C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41266134 | |||||||
| chr22:41266201 | CA | C | 117 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(114): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.301-1359delT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41266201 | |||||||
| chr22:41266252 | T | TAGCCCTG others(10): Show |
226 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(223): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.301-1410_301-1409i others(19): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41266252 | |||||||
| chr22:41266396 | A | G | 1 | a0001c0002t0005g0165 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.301-1553T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41266396 | |||||||
| chr22:41266692 | G | A | 1 | a0001c0001t0002g0272 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.300+1405C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41266692 | |||||||
| chr22:41266792 | C | A | 1 | a0001c0002t0005g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.300+1305G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41266792 | |||||||
| chr22:41266792 | C | T | 1 | a0001c0002t0001g0183 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.300+1305G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41266792 | |||||||
| chr22:41266888 | C | CTTTTTTT others(1): Show |
214 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(211): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.300+1201_300+1208d others(10): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41266888 | |||||||
| chr22:41266888 | C | CTTTTTTT others(3): Show |
2 | a0001c0002t0001g0230 a0001c0002t0001g0231 |
2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.300+1199_300+1208d others(12): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41266888 | |||||||
| chr22:41267095 | A | T | 226 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(223): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.300+1002T>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41267095 | |||||||
| chr22:41267161 | G | A | 44 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(41): Show |
49 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.300+936C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41267161 | |||||||
| chr22:41267589 | G | A | 7 | a0001c0002t0001g0130 a0001c0002t0001g0131 a0001c0002t0001g0134 others(4): Show |
7 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.300+508C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41267589 | |||||||
| chr22:41267742 | G | C | 11 | a0001c0002t0001g0230 a0001c0002t0001g0231 a0001c0002t0001g0232 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.300+355C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41267742 | |||||||
| chr22:41267763 | G | A | 3 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 |
4 | HG03130.hp1 HG06807.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.300+334C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41267763 | |||||||
| chr22:41268067 | G | A | 5 | a0001c0003t0004g0015 a0001c0003t0004g0101 a0001c0003t0004g0102 others(2): Show |
6 | HG00280.hp1 HG00738.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+30C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 4/15 | chr22 | 41268067 | |||||||
| chr22:41268181 | T | C | 1 | a0001c0001t0002g0258 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.241-25A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41268181 | |||||||
| chr22:41268406 | C | T | 44 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(41): Show |
49 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.241-250G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41268406 | |||||||
| chr22:41268509 | T | C | 227 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(224): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.241-353A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41268509 | |||||||
| chr22:41268535 | A | G | 143 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(140): Show |
164 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.241-379T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41268535 | |||||||
| chr22:41268739 | G | C | 2 | a0001c0001t0003g0038 a0001c0001t0003g0045 |
2 | HG00408.hp2 HG00544.hp1 |
intron_variant | MODIFIER | c.241-583C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41268739 | |||||||
| chr22:41268826 | G | A | 1 | a0001c0001t0025g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.241-670C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41268826 | |||||||
| chr22:41268874 | G | C | 11 | a0001c0002t0001g0230 a0001c0002t0001g0231 a0001c0002t0001g0232 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.241-718C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41268874 | |||||||
| chr22:41268874 | G | T | 12 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(9): Show |
13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.241-718C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41268874 | |||||||
| chr22:41268934 | A | C | 8 | a0001c0001t0010g0096 a0001c0003t0004g0094 a0001c0003t0004g0095 others(5): Show |
8 | HG01243.hp1 HG01496.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.241-778T>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41268934 | |||||||
| chr22:41268938 | G | A | 85 | a0001c0001t0001g0079 a0001c0001t0003g0008 a0001c0001t0003g0009 others(82): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.241-782C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41268938 | |||||||
| chr22:41269086 | C | T | 1 | a0001c0001t0011g0243 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.241-930G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41269086 | |||||||
| chr22:41269329 | T | C | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.241-1173A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41269329 | |||||||
| chr22:41269428 | T | A | 1 | a0001c0001t0002g0268 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.241-1272A>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41269428 | |||||||
| chr22:41269718 | G | A | 118 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(115): Show |
138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.241-1562C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41269718 | |||||||
| chr22:41269739 | C | CA | 48 | a0001c0001t0001g0079 a0001c0001t0001g0138 a0001c0001t0001g0203 others(45): Show |
50 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.241-1584dupT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41269739 | |||||||
| chr22:41269739 | CA | C | 10 | a0001c0001t0001g0191 a0001c0001t0002g0272 a0001c0001t0005g0249 others(7): Show |
10 | HG01943.hp1 HG02293.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.241-1584delT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41269739 | |||||||
| chr22:41269961 | G | T | 1 | a0002c0004t0007g0089 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.241-1805C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41269961 | |||||||
| chr22:41269991 | G | A | 3 | a0001c0002t0001g0178 a0001c0002t0001g0189 a0001c0002t0005g0190 |
3 | HG01081.hp2 HG01258.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.241-1835C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41269991 | |||||||
| chr22:41270025 | G | C | 8 | a0001c0003t0004g0013 a0001c0003t0004g0103 a0001c0003t0004g0106 others(5): Show |
9 | HG02280.hp1 HG02572.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.241-1869C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41270025 | |||||||
| chr22:41270165 | G | A | 1 | a0001c0010t0001g0227 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.241-2009C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41270165 | |||||||
| chr22:41270181 | C | A | 2 | a0001c0001t0002g0284 a0001c0001t0002g0295 |
2 | HG01069.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.241-2025G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41270181 | |||||||
| chr22:41270273 | T | C | 1 | a0001c0001t0002g0259 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.241-2117A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41270273 | |||||||
| chr22:41270298 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.241-2142C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41270298 | |||||||
| chr22:41270591 | G | A | 1 | a0001c0001t0020g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.241-2435C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41270591 | |||||||
| chr22:41270757 | A | G | 1 | a0001c0001t0003g0070 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.241-2601T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41270757 | |||||||
| chr22:41270939 | TG | T | 54 | a0001c0001t0001g0251 a0001c0001t0002g0005 a0001c0001t0002g0006 others(51): Show |
67 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.241-2784delC | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41270939 | |||||||
| chr22:41270971 | G | A | 1 | a0001c0002t0005g0305 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.241-2815C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41270971 | |||||||
| chr22:41270983 | A | G | 5 | a0001c0002t0001g0017 a0001c0002t0001g0129 a0001c0002t0001g0179 others(2): Show |
6 | NA18943.hp2 NA18967.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-2827T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41270983 | |||||||
| chr22:41271224 | TA | T | 7 | a0001c0001t0001g0208 a0001c0001t0001g0219 a0001c0001t0005g0249 others(4): Show |
7 | HG01433.hp1 HG02109.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.241-3069delT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271224 | |||||||
| chr22:41271386 | T | TA | 100 | a0001c0001t0001g0026 a0001c0001t0001g0148 a0001c0001t0001g0155 others(97): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.240+3213dupT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271386 | |||||||
| chr22:41271386 | T | TAA | 18 | a0001c0001t0001g0079 a0001c0001t0003g0042 a0001c0001t0003g0046 others(15): Show |
19 | HG00423.hp2 HG00735.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.240+3212_240+3213d others(4): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271386 | |||||||
| chr22:41271395 | AC | A | 3 | a0001c0001t0001g0149 a0001c0001t0001g0204 a0001c0002t0001g0214 |
3 | HG04184.hp1 NA19074.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.240+3204delG | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271395 | |||||||
| chr22:41271396 | C | A | 213 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(210): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.240+3204G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271396 | |||||||
| chr22:41271402 | A | C | 12 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(9): Show |
13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.240+3198T>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271402 | |||||||
| chr22:41271409 | C | A | 1 | a0001c0010t0001g0227 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.240+3191G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271409 | |||||||
| chr22:41271489 | G | C | 117 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(114): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.240+3111C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271489 | |||||||
| chr22:41271610 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.240+2990G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271610 | |||||||
| chr22:41271625 | C | T | 1 | a0001c0001t0017g0276 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.240+2975G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271625 | |||||||
| chr22:41271687 | C | T | 1 | a0001c0010t0001g0227 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.240+2913G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271687 | |||||||
| chr22:41271692 | C | CA | 16 | a0001c0001t0001g0206 a0001c0001t0002g0262 a0001c0001t0002g0267 others(13): Show |
17 | HG00639.hp1 HG01175.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.240+2907dupT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271692 | |||||||
| chr22:41271692 | CA | C | 10 | a0001c0002t0001g0230 a0001c0002t0001g0231 a0001c0002t0001g0232 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.240+2907delT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271692 | |||||||
| chr22:41271723 | A | G | 85 | a0001c0001t0001g0079 a0001c0001t0003g0008 a0001c0001t0003g0009 others(82): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.240+2877T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271723 | |||||||
| chr22:41271993 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.240+2607T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41271993 | |||||||
| chr22:41272004 | C | T | 1 | a0001c0002t0005g0140 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.240+2596G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41272004 | |||||||
| chr22:41272110 | G | T | 2 | a0001c0001t0003g0054 a0001c0001t0003g0057 |
2 | NA18986.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.240+2490C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41272110 | |||||||
| chr22:41272245 | G | C | 1 | a0001c0001t0018g0300 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.240+2355C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41272245 | |||||||
| chr22:41272521 | A | C | 2 | a0004c0007t0001g0234 a0004c0007t0001g0237 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.240+2079T>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41272521 | |||||||
| chr22:41272715 | C | T | 2 | a0001c0002t0001g0168 a0001c0002t0022g0241 |
2 | NA18969.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.240+1885G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41272715 | |||||||
| chr22:41272798 | C | G | 1 | a0001c0010t0001g0227 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.240+1802G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41272798 | |||||||
| chr22:41273214 | C | T | 1 | a0001c0001t0020g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.240+1386G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273214 | |||||||
| chr22:41273338 | T | C | 1 | a0001c0010t0001g0227 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.240+1262A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273338 | |||||||
| chr22:41273406 | C | T | 1 | a0001c0001t0006g0299 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.240+1194G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273406 | |||||||
| chr22:41273467 | A | C | 1 | a0001c0001t0011g0243 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.240+1133T>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273467 | |||||||
| chr22:41273494 | G | A | 13 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(10): Show |
16 | HG00609.hp1 HG00673.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.240+1106C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273494 | |||||||
| chr22:41273766 | C | CA | 106 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(103): Show |
129 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.240+833dupT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273766 | |||||||
| chr22:41273766 | C | CAA | 43 | a0001c0001t0001g0026 a0001c0001t0001g0136 a0001c0001t0001g0161 others(40): Show |
45 | HG00423.hp1 HG00423.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.240+832_240+833dup others(2): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273766 | |||||||
| chr22:41273766 | C | CAAAA | 7 | a0001c0001t0003g0053 a0001c0001t0010g0010 a0001c0001t0010g0077 others(4): Show |
8 | HG00639.hp1 HG01884.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+830_240+833dup others(4): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273766 | |||||||
| chr22:41273766 | C | CAAAAAAA others(1): Show |
5 | a0001c0003t0004g0013 a0001c0003t0004g0106 a0001c0003t0004g0109 others(2): Show |
6 | HG01167.hp2 HG02280.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.240+826_240+833dup others(8): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273766 | |||||||
| chr22:41273766 | C | CAAAAAAA others(2): Show |
18 | a0001c0001t0010g0096 a0001c0003t0004g0002 a0001c0003t0004g0015 others(15): Show |
21 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.240+825_240+833dup others(9): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273766 | |||||||
| chr22:41273766 | C | CAAAAAAA others(3): Show |
11 | a0001c0003t0004g0012 a0001c0003t0004g0095 a0001c0003t0004g0097 others(8): Show |
12 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.240+824_240+833dup others(10): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273766 | |||||||
| chr22:41273766 | C | CAAAAAAA others(4): Show |
6 | a0001c0001t0003g0009 a0001c0001t0003g0039 a0001c0001t0003g0040 others(3): Show |
7 | HG00733.hp2 HG03492.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.240+823_240+833dup others(11): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273766 | |||||||
| chr22:41273766 | C | CAAAAAAA others(5): Show |
12 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0003g0043 others(9): Show |
12 | HG00408.hp2 HG00544.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.240+822_240+833dup others(12): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273766 | |||||||
| chr22:41273766 | C | CAAAAAAA others(6): Show |
9 | a0001c0001t0003g0057 a0001c0001t0003g0058 a0001c0001t0003g0069 others(6): Show |
9 | HG00099.hp1 HG02055.hp2 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.240+821_240+833dup others(13): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273766 | |||||||
| chr22:41273766 | C | CAAAAAAA others(7): Show |
4 | a0001c0001t0003g0060 a0001c0001t0003g0072 a0001c0001t0005g0275 others(1): Show |
4 | HG01106.hp2 HG01261.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.240+820_240+833dup others(14): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273766 | |||||||
| chr22:41273766 | C | CAAAAAAA others(8): Show |
3 | a0001c0001t0001g0079 a0001c0001t0003g0008 a0001c0001t0003g0047 |
4 | HG00558.hp1 NA18949.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.240+819_240+833dup others(15): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273766 | |||||||
| chr22:41273766 | C | CAAAAAAA others(9): Show |
3 | a0001c0001t0003g0037 a0001c0001t0003g0061 a0001c0001t0003g0076 |
3 | NA18946.hp2 NA19077.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.240+818_240+833dup others(16): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273766 | |||||||
| chr22:41273766 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0003g0062 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.240+817_240+833dup others(17): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273766 | |||||||
| chr22:41273766 | CA | C | 7 | a0001c0001t0003g0041 a0001c0001t0003g0042 a0001c0001t0003g0048 others(4): Show |
7 | NA18947.hp2 NA18964.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.240+833delT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273766 | |||||||
| chr22:41273824 | C | T | 3 | a0001c0001t0001g0128 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG00673.hp2 HG02015.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.240+776G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41273824 | |||||||
| chr22:41274265 | C | T | 1 | a0001c0001t0017g0276 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.240+335G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41274265 | |||||||
| chr22:41274366 | G | A | 1 | a0001c0003t0004g0121 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.240+234C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 3/15 | chr22 | 41274366 | |||||||
| chr22:41275048 | C | G | 1 | a0002c0004t0007g0087 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.113-321G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41275048 | |||||||
| chr22:41275395 | G | A | 3 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 |
4 | HG03130.hp1 HG06807.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.113-668C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41275395 | |||||||
| chr22:41275405 | T | C | 1 | a0001c0002t0001g0221 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.113-678A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41275405 | |||||||
| chr22:41275447 | A | G | 304 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(301): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.113-720T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41275447 | |||||||
| chr22:41275728 | G | A | 84 | a0001c0001t0001g0079 a0001c0001t0003g0008 a0001c0001t0003g0009 others(81): Show |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.113-1001C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41275728 | |||||||
| chr22:41275758 | G | A | 4 | a0001c0003t0004g0013 a0001c0003t0004g0106 a0001c0003t0004g0107 others(1): Show |
5 | HG02280.hp1 HG02965.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-1031C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41275758 | |||||||
| chr22:41275781 | G | GA | 56 | a0001c0001t0001g0215 a0001c0001t0001g0251 a0001c0001t0002g0005 others(53): Show |
69 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.113-1055dupT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41275781 | |||||||
| chr22:41275804 | G | A | 8 | a0001c0001t0006g0007 a0001c0001t0006g0278 a0001c0001t0006g0279 others(5): Show |
10 | HG00673.hp1 HG00741.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.113-1077C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41275804 | |||||||
| chr22:41275904 | C | T | 1 | a0001c0001t0009g0073 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.113-1177G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41275904 | |||||||
| chr22:41276236 | C | T | 1 | a0002c0004t0007g0082 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.113-1509G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41276236 | |||||||
| chr22:41276267 | A | C | 161 | a0001c0001t0001g0079 a0001c0001t0001g0251 a0001c0001t0002g0005 others(158): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.113-1540T>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41276267 | |||||||
| chr22:41276510 | A | G | 162 | a0001c0001t0001g0079 a0001c0001t0001g0251 a0001c0001t0002g0005 others(159): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.113-1783T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41276510 | |||||||
| chr22:41276626 | C | T | 1 | a0001c0001t0011g0243 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.113-1899G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41276626 | |||||||
| chr22:41276812 | G | A | 2 | a0001c0003t0004g0015 a0001c0003t0004g0123 |
3 | HG01081.hp1 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.113-2085C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41276812 | |||||||
| chr22:41276913 | G | C | 1 | a0001c0001t0003g0074 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.113-2186C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41276913 | |||||||
| chr22:41276922 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.113-2195C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41276922 | |||||||
| chr22:41276986 | G | GA | 10 | a0001c0001t0002g0269 a0001c0001t0003g0040 a0001c0002t0001g0130 others(7): Show |
10 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.113-2260dupT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41276986 | |||||||
| chr22:41277071 | A | AT | 109 | a0001c0001t0001g0019 a0001c0001t0001g0079 a0001c0001t0001g0136 others(106): Show |
120 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.113-2345dupA | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277071 | |||||||
| chr22:41277071 | A | ATT | 12 | a0001c0001t0003g0008 a0001c0001t0003g0041 a0001c0001t0003g0042 others(9): Show |
13 | HG00544.hp1 HG00558.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.113-2346_113-2345d others(4): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277071 | |||||||
| chr22:41277071 | AT | A | 11 | a0001c0001t0001g0027 a0001c0001t0001g0138 a0001c0001t0001g0218 others(8): Show |
12 | HG01884.hp2 HG01934.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.113-2345delA | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277071 | |||||||
| chr22:41277170 | C | T | 1 | a0002c0004t0007g0080 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.113-2443G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277170 | |||||||
| chr22:41277227 | G | T | 13 | a0001c0001t0001g0251 a0001c0001t0002g0245 a0001c0001t0002g0246 others(10): Show |
15 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.113-2500C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277227 | |||||||
| chr22:41277300 | G | A | 1 | a0001c0010t0001g0227 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.113-2573C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277300 | |||||||
| chr22:41277321 | G | A | 8 | a0001c0001t0006g0007 a0001c0001t0006g0278 a0001c0001t0006g0279 others(5): Show |
10 | HG00673.hp1 HG00741.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.113-2594C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277321 | |||||||
| chr22:41277324 | C | T | 1 | a0001c0001t0002g0244 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.113-2597G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277324 | |||||||
| chr22:41277325 | G | A | 1 | a0001c0002t0001g0221 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.113-2598C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277325 | |||||||
| chr22:41277348 | G | A | 1 | a0001c0002t0001g0222 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.113-2621C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277348 | |||||||
| chr22:41277399 | C | G | 1 | a0001c0002t0001g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.113-2672G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277399 | |||||||
| chr22:41277413 | T | A | 1 | a0001c0003t0004g0124 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.113-2686A>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277413 | |||||||
| chr22:41277588 | A | T | 46 | a0001c0001t0001g0079 a0001c0001t0003g0008 a0001c0001t0003g0009 others(43): Show |
48 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.113-2861T>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277588 | |||||||
| chr22:41277611 | A | G | 1 | a0001c0001t0020g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.113-2884T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277611 | |||||||
| chr22:41277983 | G | C | 1 | a0001c0003t0004g0097 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.112+2950C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41277983 | |||||||
| chr22:41278038 | G | GT | 72 | a0001c0001t0001g0138 a0001c0001t0001g0223 a0001c0001t0001g0251 others(69): Show |
86 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.112+2894dupA | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41278038 | |||||||
| chr22:41278160 | C | T | 4 | a0001c0001t0010g0096 a0001c0003t0004g0094 a0001c0003t0004g0095 others(1): Show |
4 | HG01496.hp1 HG02572.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+2773G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41278160 | |||||||
| chr22:41278183 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.112+2750A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41278183 | |||||||
| chr22:41278199 | C | T | 61 | a0001c0001t0001g0251 a0001c0001t0002g0005 a0001c0001t0002g0006 others(58): Show |
75 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.112+2734G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41278199 | |||||||
| chr22:41278259 | G | C | 1 | a0001c0001t0003g0074 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.112+2674C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41278259 | |||||||
| chr22:41278444 | A | G | 1 | a0001c0001t0011g0243 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.112+2489T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41278444 | |||||||
| chr22:41278517 | G | A | 155 | a0001c0001t0001g0079 a0001c0001t0002g0005 a0001c0001t0002g0006 others(152): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.112+2416C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41278517 | |||||||
| chr22:41278521 | T | A | 1 | a0001c0002t0001g0091 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.112+2412A>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41278521 | |||||||
| chr22:41278523 | C | A | 1 | a0001c0002t0001g0091 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.112+2410G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41278523 | |||||||
| chr22:41278653 | C | G | 1 | a0001c0010t0001g0227 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.112+2280G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41278653 | |||||||
| chr22:41278776 | G | T | 1 | a0001c0001t0020g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.112+2157C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41278776 | |||||||
| chr22:41278832 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.112+2101G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41278832 | |||||||
| chr22:41278956 | C | G | 2 | a0001c0002t0001g0230 a0001c0002t0001g0231 |
2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.112+1977G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41278956 | |||||||
| chr22:41278979 | A | T | 1 | a0001c0001t0003g0038 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.112+1954T>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41278979 | |||||||
| chr22:41279011 | C | T | 143 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(140): Show |
167 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.112+1922G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41279011 | |||||||
| chr22:41279035 | C | T | 1 | a0001c0001t0003g0037 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.112+1898G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41279035 | |||||||
| chr22:41279104 | G | A | 162 | a0001c0001t0001g0079 a0001c0001t0001g0251 a0001c0001t0002g0005 others(159): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.112+1829C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41279104 | |||||||
| chr22:41279122 | A | G | 74 | a0001c0001t0001g0251 a0001c0001t0002g0005 a0001c0001t0002g0006 others(71): Show |
89 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.112+1811T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41279122 | |||||||
| chr22:41279325 | C | T | 1 | a0001c0001t0017g0276 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.112+1608G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41279325 | |||||||
| chr22:41279373 | G | A | 1 | a0001c0002t0005g0225 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.112+1560C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41279373 | |||||||
| chr22:41279558 | T | C | 3 | a0001c0002t0001g0134 a0001c0002t0001g0135 a0001c0002t0005g0133 |
3 | HG02486.hp1 HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.112+1375A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41279558 | |||||||
| chr22:41279698 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.112+1235T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41279698 | |||||||
| chr22:41279699 | G | T | 1 | a0001c0001t0001g0079 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.112+1234C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41279699 | |||||||
| chr22:41279800 | CA | C | 164 | a0001c0001t0001g0251 a0001c0001t0002g0005 a0001c0001t0002g0006 others(161): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.112+1132delT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41279800 | |||||||
| chr22:41279954 | C | T | 1 | a0001c0010t0001g0227 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.112+979G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41279954 | |||||||
| chr22:41279990 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.112+943G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41279990 | |||||||
| chr22:41280172 | A | G | 41 | a0001c0001t0010g0096 a0001c0002t0001g0014 a0001c0003t0001g0092 others(38): Show |
47 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.112+761T>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41280172 | |||||||
| chr22:41280484 | C | G | 1 | a0001c0011t0001g0226 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.112+449G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41280484 | |||||||
| chr22:41280555 | C | CAGCT | 86 | a0001c0001t0001g0079 a0001c0001t0003g0008 a0001c0001t0003g0009 others(83): Show |
94 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.112+374_112+377dup others(4): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41280555 | |||||||
| chr22:41280595 | GCAAGGGT others(5): Show |
G | 1 | a0001c0001t0017g0276 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.112+326_112+337del others(12): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 2/15 | chr22 | 41280595 | |||||||
| chr22:41281149 | G | C | 3 | a0003c0005t0006g0302 a0003c0005t0011g0301 a0003c0005t0011g0303 |
3 | HG01109.hp2 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-38-67C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41281149 | |||||||
| chr22:41281210 | T | C | 161 | a0001c0001t0001g0079 a0001c0001t0001g0251 a0001c0001t0002g0005 others(158): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.-38-128A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41281210 | |||||||
| chr22:41281237 | GA | G | 85 | a0001c0001t0001g0079 a0001c0001t0003g0008 a0001c0001t0003g0009 others(82): Show |
93 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.-38-156delT | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41281237 | |||||||
| chr22:41281313 | C | T | 56 | a0001c0001t0001g0251 a0001c0001t0002g0005 a0001c0001t0002g0006 others(53): Show |
69 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-38-231G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41281313 | |||||||
| chr22:41281735 | T | C | 1 | a0002c0004t0007g0087 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-38-653A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41281735 | |||||||
| chr22:41282347 | T | C | 97 | a0001c0001t0001g0079 a0001c0001t0003g0008 a0001c0001t0003g0009 others(94): Show |
106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.-38-1265A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41282347 | |||||||
| chr22:41282634 | T | A | 1 | a0001c0010t0001g0227 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-38-1552A>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41282634 | |||||||
| chr22:41282691 | T | C | 1 | a0001c0002t0001g0228 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-38-1609A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41282691 | |||||||
| chr22:41282812 | G | A | 1 | a0001c0002t0005g0229 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-38-1730C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41282812 | |||||||
| chr22:41282892 | G | A | 12 | a0001c0002t0001g0230 a0001c0002t0001g0231 a0001c0002t0001g0232 others(9): Show |
12 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-38-1810C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41282892 | |||||||
| chr22:41283222 | GTT | G | 41 | a0001c0001t0010g0096 a0001c0002t0001g0014 a0001c0003t0001g0092 others(38): Show |
47 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.-38-2142_-38-2141d others(4): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283222 | |||||||
| chr22:41283224 | TGGG | T | 43 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0036 others(40): Show |
45 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.-38-2145_-38-2143d others(5): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283224 | |||||||
| chr22:41283226 | G | T | 41 | a0001c0001t0010g0096 a0001c0002t0001g0014 a0001c0003t0001g0092 others(38): Show |
47 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.-38-2144C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283226 | |||||||
| chr22:41283227 | G | T | 41 | a0001c0001t0010g0096 a0001c0002t0001g0014 a0001c0003t0001g0092 others(38): Show |
47 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.-38-2145C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283227 | |||||||
| chr22:41283230 | G | C | 1 | a0001c0001t0001g0079 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-38-2148C>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283230 | |||||||
| chr22:41283232 | C | G | 1 | a0001c0001t0001g0079 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-38-2150G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283232 | |||||||
| chr22:41283279 | G | A | 1 | a0001c0002t0022g0241 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-38-2197C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283279 | |||||||
| chr22:41283381 | C | T | 2 | a0001c0003t0001g0092 a0001c0003t0001g0093 |
2 | HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-38-2299G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283381 | |||||||
| chr22:41283408 | T | A | 1 | a0001c0001t0020g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-38-2326A>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283408 | |||||||
| chr22:41283516 | C | T | 1 | a0001c0001t0012g0242 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-38-2434G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283516 | |||||||
| chr22:41283520 | T | C | 2 | a0001c0001t0002g0284 a0001c0001t0002g0295 |
2 | HG01069.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-38-2438A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283520 | |||||||
| chr22:41283520 | T | TAAC | 9 | a0001c0001t0002g0277 a0001c0001t0006g0007 a0001c0001t0006g0278 others(6): Show |
11 | HG00673.hp1 HG00741.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38-2441_-38-2439d others(5): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283520 | |||||||
| chr22:41283832 | G | T | 3 | a0001c0002t0001g0011 a0001c0002t0001g0090 a0001c0002t0001g0091 |
4 | NA18956.hp1 NA18982.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39+2154C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283832 | |||||||
| chr22:41283896 | CAT | C | 63 | a0001c0001t0001g0251 a0001c0001t0002g0005 a0001c0001t0002g0006 others(60): Show |
77 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.-39+2088_-39+2089d others(4): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283896 | |||||||
| chr22:41283923 | C | CAAGAAAC others(22): Show |
1 | a0001c0001t0001g0304 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-39+2034_-39+2062d others(31): Show |
RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283923 | |||||||
| chr22:41283975 | G | A | 2 | a0001c0001t0002g0284 a0001c0001t0002g0295 |
2 | HG01069.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-39+2011C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41283975 | |||||||
| chr22:41284044 | C | G | 1 | a0001c0001t0003g0036 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-39+1942G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41284044 | |||||||
| chr22:41284045 | G | A | 4 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 others(1): Show |
4 | NA19054.hp2 NA19070.hp1 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39+1941C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41284045 | |||||||
| chr22:41284125 | T | C | 1 | a0001c0003t0004g0289 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-39+1861A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41284125 | |||||||
| chr22:41284290 | G | A | 12 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(9): Show |
13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-39+1696C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41284290 | |||||||
| chr22:41284296 | G | A | 4 | a0001c0002t0001g0290 a0001c0002t0001g0291 a0001c0002t0001g0292 others(1): Show |
4 | HG01433.hp1 HG02895.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39+1690C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41284296 | |||||||
| chr22:41284634 | G | A | 1 | a0001c0002t0001g0294 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-39+1352C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41284634 | |||||||
| chr22:41284647 | G | A | 1 | a0002c0004t0007g0089 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-39+1339C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41284647 | |||||||
| chr22:41284651 | C | G | 12 | a0001c0001t0010g0010 a0001c0001t0010g0077 a0001c0001t0010g0084 others(9): Show |
13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-39+1335G>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41284651 | |||||||
| chr22:41284894 | C | T | 44 | a0001c0001t0001g0079 a0001c0001t0003g0008 a0001c0001t0003g0009 others(41): Show |
46 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.-39+1092G>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41284894 | |||||||
| chr22:41284975 | A | T | 1 | a0001c0001t0001g0304 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-39+1011T>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41284975 | |||||||
| chr22:41285003 | T | G | 1 | a0001c0001t0001g0304 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-39+983A>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41285003 | |||||||
| chr22:41285043 | T | A | 1 | a0001c0001t0002g0295 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-39+943A>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41285043 | |||||||
| chr22:41285105 | G | A | 3 | a0001c0001t0002g0296 a0001c0001t0002g0297 a0001c0001t0021g0298 |
3 | HG01346.hp2 HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-39+881C>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41285105 | |||||||
| chr22:41285367 | T | G | 6 | a0001c0001t0006g0299 a0001c0001t0011g0035 a0001c0001t0018g0300 others(3): Show |
7 | HG01099.hp2 HG01109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-39+619A>C | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41285367 | |||||||
| chr22:41285368 | A | T | 1 | a0001c0001t0001g0304 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-39+618T>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41285368 | |||||||
| chr22:41285371 | C | A | 1 | a0001c0001t0001g0304 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-39+615G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41285371 | |||||||
| chr22:41285443 | C | A | 1 | a0001c0002t0005g0305 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-39+543G>T | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41285443 | |||||||
| chr22:41285479 | G | T | 1 | a0001c0002t0016g0078 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-39+507C>A | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41285479 | |||||||
| chr22:41285617 | A | C | 1 | a0001c0001t0010g0077 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-39+369T>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41285617 | |||||||
| chr22:41285699 | T | C | 1 | a0001c0001t0006g0306 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-39+287A>G | RANGAP1 | ENSG00000100401.21 | transcript | ENST00000356244.8 | protein_coding | 1/15 | chr22 | 41285699 |