Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 64795 |
| ensemblid | ENSG00000153561.13 |
| hgncid | 25850 |
| symbol | RMND5A |
| name | required for meiotic nuclear division 5 homolog A |
| refseq_nuc | NM_022780.4 |
| refseq_prot | NP_073617.1 |
| ensembl_nuc | ENST00000283632.5 |
| ensembl_prot | ENSP00000283632.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 86720291 |
| end | 86778041 |
| strand | + |
| ver | v1.2 |
| region | chr2:86720291-86778041 |
| region5000 | chr2:86715291-86783041 |
| regionname0 | RMND5A_chr2_86720291_86778041 |
| regionname5000 | RMND5A_chr2_86715291_86783041 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1173 | 178 | 51 | 35 | 58 | 9 | 24 | RMND5A_chr2_86715291_86783041 | RMND5A | ATGGA others(1168): Show |
chr2 | 86715291 | 86783041 | ||
| a0001c0002 | 1/0 | 1173 | 75 | 23 | 20 | 18 | 5 | 8 | RMND5A_chr2_86715291_86783041 | RMND5A | ATGGA others(1168): Show |
chr2 | 86715291 | 86783041 | ||
| a0001c0003 | 0/0 | 1173 | 34 | 1 | 5 | 24 | 0 | 4 | RMND5A_chr2_86715291_86783041 | RMND5A | ATGGA others(1168): Show |
chr2 | 86715291 | 86783041 | ||
| a0001c0004 | 0/0 | 1173 | 12 | 10 | 2 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | ATGGA others(1168): Show |
chr2 | 86715291 | 86783041 | ||
| a0001c0005 | 0/0 | 1173 | 5 | 1 | 4 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | ATGGA others(1168): Show |
chr2 | 86715291 | 86783041 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 6180 | 116 | 20 | 29 | 43 | 7 | 16 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6175): Show |
chr2 | 86715291 | 86783041 |
| a0001c0001t0003 | 0/0 | 6183 | 30 | 8 | 2 | 14 | 0 | 6 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6178): Show |
chr2 | 86715291 | 86783041 |
| a0001c0001t0005 | 0/0 | 6179 | 6 | 3 | 2 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6174): Show |
chr2 | 86715291 | 86783041 |
| a0001c0001t0007 | 0/0 | 6180 | 4 | 4 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6175): Show |
chr2 | 86715291 | 86783041 |
| a0001c0001t0009 | 0/0 | 6183 | 3 | 3 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6178): Show |
chr2 | 86715291 | 86783041 |
| a0001c0001t0012 | 0/0 | 6180 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6175): Show |
chr2 | 86715291 | 86783041 |
| a0001c0001t0014 | 0/0 | 6183 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6178): Show |
chr2 | 86715291 | 86783041 |
| a0001c0001t0015 | 0/0 | 6183 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6178): Show |
chr2 | 86715291 | 86783041 |
| a0001c0001t0017 | 0/0 | 6180 | 2 | 1 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6175): Show |
chr2 | 86715291 | 86783041 |
| a0001c0001t0018 | 0/0 | 6180 | 2 | 0 | 0 | 0 | 2 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6175): Show |
chr2 | 86715291 | 86783041 |
| a0001c0001t0019 | 0/0 | 6180 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6175): Show |
chr2 | 86715291 | 86783041 |
| a0001c0001t0022 | 0/0 | 6179 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6174): Show |
chr2 | 86715291 | 86783041 |
| a0001c0001t0024 | 0/0 | 6180 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6175): Show |
chr2 | 86715291 | 86783041 |
| a0001c0001t0025 | 0/0 | 6180 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6175): Show |
chr2 | 86715291 | 86783041 |
| a0001c0001t0031 | 0/0 | 6183 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6178): Show |
chr2 | 86715291 | 86783041 |
| a0001c0001t0032 | 0/0 | 6183 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6178): Show |
chr2 | 86715291 | 86783041 |
| a0001c0001t0033 | 0/0 | 6180 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6175): Show |
chr2 | 86715291 | 86783041 |
| a0001c0001t0036 | 0/0 | 6183 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6178): Show |
chr2 | 86715291 | 86783041 |
| a0001c0001t0037 | 0/0 | 6180 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6175): Show |
chr2 | 86715291 | 86783041 |
| a0001c0002t0001 | 0/0 | 6180 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6175): Show |
chr2 | 86715291 | 86783041 |
| a0001c0002t0002 | 1/0 | 6183 | 42 | 9 | 16 | 6 | 3 | 7 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6178): Show |
chr2 | 86715291 | 86783041 |
| a0001c0002t0004 | 0/0 | 6177 | 25 | 11 | 2 | 11 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6172): Show |
chr2 | 86715291 | 86783041 |
| a0001c0002t0013 | 0/0 | 6183 | 2 | 0 | 1 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6178): Show |
chr2 | 86715291 | 86783041 |
| a0001c0002t0028 | 0/0 | 6183 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6178): Show |
chr2 | 86715291 | 86783041 |
| a0001c0002t0029 | 0/0 | 6183 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6178): Show |
chr2 | 86715291 | 86783041 |
| a0001c0002t0030 | 0/0 | 6183 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6178): Show |
chr2 | 86715291 | 86783041 |
| a0001c0002t0034 | 0/0 | 6177 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6172): Show |
chr2 | 86715291 | 86783041 |
| a0001c0002t0035 | 0/0 | 6177 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6172): Show |
chr2 | 86715291 | 86783041 |
| a0001c0003t0001 | 0/0 | 6180 | 32 | 1 | 4 | 23 | 0 | 4 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6175): Show |
chr2 | 86715291 | 86783041 |
| a0001c0003t0005 | 0/0 | 6179 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6174): Show |
chr2 | 86715291 | 86783041 |
| a0001c0003t0027 | 0/0 | 6180 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6175): Show |
chr2 | 86715291 | 86783041 |
| a0001c0004t0006 | 0/0 | 6183 | 4 | 3 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6178): Show |
chr2 | 86715291 | 86783041 |
| a0001c0004t0011 | 0/0 | 6177 | 2 | 1 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6172): Show |
chr2 | 86715291 | 86783041 |
| a0001c0004t0016 | 0/0 | 6183 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6178): Show |
chr2 | 86715291 | 86783041 |
| a0001c0004t0020 | 0/0 | 6183 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6178): Show |
chr2 | 86715291 | 86783041 |
| a0001c0004t0021 | 0/0 | 6183 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6178): Show |
chr2 | 86715291 | 86783041 |
| a0001c0004t0023 | 0/0 | 6180 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6175): Show |
chr2 | 86715291 | 86783041 |
| a0001c0004t0026 | 0/0 | 6177 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6172): Show |
chr2 | 86715291 | 86783041 |
| a0001c0005t0008 | 0/0 | 6180 | 3 | 0 | 3 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6175): Show |
chr2 | 86715291 | 86783041 |
| a0001c0005t0010 | 0/0 | 6179 | 2 | 1 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | CTCCC others(6174): Show |
chr2 | 86715291 | 86783041 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 1 | 1 | 4 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0163 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0003g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0003g0009 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0005g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0005g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0005g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0007g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0007g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0007g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0007g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0009g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0009g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0009g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0012g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0012g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0014g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0014g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0015g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0015g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0017g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0018g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0018g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0019g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0022g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0024g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0025g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0031g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0032g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0033g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0036g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0001t0037g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0224 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0004g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0004g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0004g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0013g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0013g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0028g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0029g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0030g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0034g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0002t0035g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0003t0001g0002 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0003t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0003t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0003t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0003t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0003t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0003t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0003t0005g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0003t0027g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0004t0006g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0004t0006g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0004t0006g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0004t0011g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0004t0011g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0004t0016g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0004t0020g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0004t0021g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0004t0023g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0004t0026g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0005t0008g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0005t0008g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0005t0010g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| a0001c0005t0010g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | GBR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG00099 | hp2 | a0001 | c0002 | t0035 | g0066 | EUR | GBR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0227 | EUR | GBR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | GBR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | FIN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG00280 | hp2 | a0001 | c0001 | t0018 | g0135 | EUR | FIN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG00323 | hp1 | a0001 | c0001 | t0018 | g0004 | EUR | FIN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG00323 | hp2 | a0001 | c0002 | t0028 | g0233 | EUR | FIN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | CHS | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG00423 | hp2 | a0001 | c0002 | t0004 | g0017 | EAS | CHS | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG00544 | hp1 | a0001 | c0002 | t0004 | g0081 | EAS | CHS | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG00609 | hp2 | a0001 | c0002 | t0004 | g0068 | EAS | CHS | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0238 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0028 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0231 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0083 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0129 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0229 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01074 | hp2 | a0001 | c0002 | t0004 | g0077 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0218 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01099 | hp2 | a0001 | c0003 | t0001 | g0035 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0118 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01109 | hp2 | a0001 | c0001 | t0017 | g0018 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01167 | hp1 | a0001 | c0004 | t0006 | g0249 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01167 | hp2 | a0001 | c0005 | t0010 | g0008 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01168 | hp1 | a0001 | c0001 | t0036 | g0021 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0220 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0222 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01169 | hp2 | a0001 | c0005 | t0008 | g0008 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0028 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0235 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0221 | AMR | CLM | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01261 | hp2 | a0001 | c0002 | t0004 | g0015 | AMR | CLM | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0251 | AMR | CLM | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01358 | hp2 | a0001 | c0004 | t0011 | g0055 | AMR | CLM | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01433 | hp2 | a0001 | c0002 | t0013 | g0106 | AMR | CLM | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0198 | EUR | IBS | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0172 | EUR | IBS | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0244 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01884 | hp2 | a0001 | c0004 | t0026 | g0054 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01891 | hp2 | a0001 | c0001 | t0015 | g0101 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0214 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0242 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0212 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0215 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01943 | hp2 | a0001 | c0003 | t0005 | g0036 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01978 | hp2 | a0001 | c0003 | t0001 | g0038 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01993 | hp1 | a0001 | c0001 | t0005 | g0131 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0225 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02055 | hp1 | a0001 | c0002 | t0004 | g0065 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02074 | hp1 | a0001 | c0003 | t0001 | g0040 | EAS | KHV | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02129 | hp2 | a0001 | c0003 | t0001 | g0012 | EAS | KHV | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | KHV | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0104 | EAS | KHV | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0230 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02145 | hp2 | a0001 | c0005 | t0010 | g0053 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0232 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02148 | hp2 | a0001 | c0005 | t0008 | g0052 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0240 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0025 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02273 | hp1 | a0001 | c0005 | t0008 | g0008 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02280 | hp1 | a0001 | c0002 | t0004 | g0075 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02280 | hp2 | a0001 | c0001 | t0022 | g0113 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02300 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02451 | hp1 | a0001 | c0001 | t0024 | g0204 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0020 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02572 | hp2 | a0001 | c0002 | t0004 | g0016 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02602 | hp2 | a0001 | c0002 | t0004 | g0071 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0181 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02615 | hp2 | a0001 | c0002 | t0004 | g0073 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02622 | hp1 | a0001 | c0001 | t0014 | g0180 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02622 | hp2 | a0001 | c0002 | t0004 | g0072 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02630 | hp2 | a0001 | c0004 | t0016 | g0014 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0241 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0120 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02698 | hp1 | a0001 | c0001 | t0033 | g0143 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0146 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0243 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02735 | hp1 | a0001 | c0001 | t0005 | g0193 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02735 | hp2 | a0001 | c0003 | t0001 | g0030 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02809 | hp1 | a0001 | c0002 | t0004 | g0074 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02809 | hp2 | a0001 | c0004 | t0006 | g0248 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02818 | hp1 | a0001 | c0001 | t0032 | g0184 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02818 | hp2 | a0001 | c0001 | t0009 | g0100 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0091 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02895 | hp2 | a0001 | c0004 | t0006 | g0029 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0026 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02897 | hp2 | a0001 | c0004 | t0006 | g0029 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02922 | hp1 | a0001 | c0001 | t0009 | g0098 | AFR | ESN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ESN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02965 | hp1 | a0001 | c0002 | t0004 | g0064 | AFR | ESN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0089 | AFR | ESN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02970 | hp1 | a0001 | c0004 | t0021 | g0060 | AFR | ESN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02976 | hp1 | a0001 | c0004 | t0023 | g0061 | AFR | ESN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02976 | hp2 | a0001 | c0001 | t0015 | g0099 | AFR | ESN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0250 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03098 | hp2 | a0001 | c0002 | t0004 | g0062 | AFR | MSL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0092 | AFR | ESN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03139 | hp2 | a0001 | c0001 | t0014 | g0115 | AFR | ESN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ESN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | ESN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03209 | hp1 | a0001 | c0002 | t0004 | g0016 | AFR | MSL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0021 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0057 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0097 | AFR | MSL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0216 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03540 | hp1 | a0001 | c0004 | t0016 | g0014 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03579 | hp2 | a0001 | c0002 | t0004 | g0067 | AFR | MSL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0213 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0123 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0219 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | STU | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | STU | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0031 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0122 | SAS | BEB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0228 | SAS | BEB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03942 | hp1 | a0001 | c0003 | t0001 | g0050 | SAS | BEB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0234 | SAS | STU | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | STU | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | STU | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0226 | SAS | STU | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18522 | hp1 | a0001 | c0002 | t0029 | g0103 | AFR | YRI | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18522 | hp2 | a0001 | c0001 | t0012 | g0205 | AFR | YRI | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18747 | hp1 | a0001 | c0002 | t0004 | g0015 | EAS | CHB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18906 | hp1 | a0001 | c0001 | t0012 | g0203 | AFR | YRI | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18906 | hp2 | a0001 | c0001 | t0017 | g0018 | AFR | YRI | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0109 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18940 | hp2 | a0001 | c0001 | t0031 | g0087 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18943 | hp1 | a0001 | c0002 | t0004 | g0080 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18943 | hp2 | a0001 | c0003 | t0001 | g0043 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18944 | hp1 | a0001 | c0003 | t0027 | g0002 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18950 | hp1 | a0001 | c0003 | t0001 | g0049 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0111 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18967 | hp1 | a0001 | c0003 | t0001 | g0047 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18968 | hp1 | a0001 | c0003 | t0001 | g0042 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18971 | hp1 | a0001 | c0002 | t0004 | g0079 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18975 | hp1 | a0001 | c0003 | t0001 | g0051 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18975 | hp2 | a0001 | c0002 | t0013 | g0107 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18978 | hp1 | a0001 | c0002 | t0004 | g0082 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18983 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18986 | hp1 | a0001 | c0002 | t0004 | g0069 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18987 | hp2 | a0001 | c0003 | t0001 | g0034 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18988 | hp2 | a0001 | c0003 | t0001 | g0037 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19001 | hp2 | a0001 | c0002 | t0004 | g0017 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19002 | hp1 | a0001 | c0003 | t0001 | g0048 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19003 | hp2 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19005 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19010 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0105 | AFR | LWK | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0237 | AFR | LWK | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | LWK | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19043 | hp2 | a0001 | c0004 | t0020 | g0247 | AFR | LWK | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19055 | hp1 | a0001 | c0003 | t0001 | g0041 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19056 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19060 | hp1 | a0001 | c0003 | t0001 | g0044 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19065 | hp1 | a0001 | c0003 | t0001 | g0039 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19075 | hp1 | a0001 | c0002 | t0004 | g0078 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19080 | hp1 | a0001 | c0003 | t0001 | g0033 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19082 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0108 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19087 | hp2 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19088 | hp2 | a0001 | c0003 | t0001 | g0046 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA19091 | hp2 | a0001 | c0002 | t0004 | g0076 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA20129 | hp1 | a0001 | c0002 | t0034 | g0063 | AFR | ASW | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0102 | AFR | ASW | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | TSI | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0217 | EUR | TSI | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0236 | EUR | TSI | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | TSI | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA20905 | hp1 | a0001 | c0003 | t0001 | g0032 | SAS | GIH | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | GIH | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02109 | hp1 | a0001 | c0002 | t0030 | g0112 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02109 | hp2 | a0001 | c0001 | t0037 | g0001 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02559 | hp1 | a0001 | c0001 | t0025 | g0202 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG03471 | hp2 | a0001 | c0003 | t0001 | g0245 | AFR | MSL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG06807 | hp1 | a0001 | c0001 | t0019 | g0006 | AFR | USA | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | USA | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA18955 | hp2 | a0001 | c0003 | t0001 | g0045 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA20300 | hp1 | a0001 | c0002 | t0004 | g0070 | AFR | USA | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA20300 | hp2 | a0001 | c0004 | t0011 | g0056 | AFR | USA | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | LWK | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| NA21309 | hp2 | a0001 | c0001 | t0007 | g0169 | AFR | LWK | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0163 | REF | REF | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0224 | REF | REF | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
| 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 |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:86720724 | A | G | 2 | a0001c0004 a0001c0005 |
17 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
synonymous_variant | LOW | c.57A>G | p.Ser19Ser | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | 434/6183 | 57/1176 | 19/391 | chr2 | 86720724 | |||
| chr2:86720781 | C | T | 1 | a0001c0005 | 5 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(2): Show |
synonymous_variant | LOW | c.114C>T | p.Gly38Gly | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | 491/6183 | 114/1176 | 38/391 | chr2 | 86720781 | |||
| chr2:86741015 | C | T | 1 | a0001c0003 | 34 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(31): Show |
synonymous_variant | LOW | c.231C>T | p.Ser77Ser | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/9 | 608/6183 | 231/1176 | 77/391 | chr2 | 86741015 | |||
| chr2:86751970 | G | A | 3 | a0001c0001 a0001c0003 a0001c0005 |
216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
synonymous_variant | LOW | c.360G>A | p.Glu120Glu | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 3/9 | 737/6183 | 360/1176 | 120/391 | chr2 | 86751970 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:86720309 | G | A | 2 | a0001c0005t0008 a0001c0005t0010 |
5 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-359G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | 359 | chr2 | 86720309 | ||||||
| chr2:86720382 | C | T | 1 | a0001c0001t0037 | 1 | HG02109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-286C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | 286 | chr2 | 86720382 | ||||||
| chr2:86720421 | A | G | 2 | a0001c0005t0008 a0001c0005t0010 |
5 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-247A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | 247 | chr2 | 86720421 | ||||||
| chr2:86720462 | G | A | 2 | a0001c0005t0008 a0001c0005t0010 |
5 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-206G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | 206 | chr2 | 86720462 | ||||||
| chr2:86720462 | G | T | 1 | a0001c0001t0018 | 2 | HG00280.hp2 HG00323.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-206G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | chr2 | 86720462 | |||||||
| chr2:86720467 | G | T | 1 | a0001c0001t0036 | 1 | HG01168.hp1 | 5_prime_UTR_variant | MODIFIER | c.-201G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | 201 | chr2 | 86720467 | ||||||
| chr2:86720517 | C | A | 1 | a0001c0001t0019 | 1 | HG06807.hp1 | 5_prime_UTR_variant | MODIFIER | c.-151C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | 151 | chr2 | 86720517 | ||||||
| chr2:86720523 | G | T | 1 | a0001c0001t0017 | 2 | HG01109.hp2 NA18906.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-145G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | chr2 | 86720523 | |||||||
| chr2:86720560 | C | T | 1 | a0001c0002t0035 | 1 | HG00099.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-108C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | chr2 | 86720560 | |||||||
| chr2:86720577 | G | T | 1 | a0001c0004t0016 | 2 | HG02630.hp2 HG03540.hp1 |
5_prime_UTR_variant | MODIFIER | c.-91G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | 91 | chr2 | 86720577 | ||||||
| chr2:86720603 | T | C | 13 | a0001c0001t0012 a0001c0001t0022 a0001c0001t0024 others(10): Show |
22 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-65T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | 65 | chr2 | 86720603 | ||||||
| chr2:86720624 | G | A | 1 | a0001c0003t0027 | 1 | NA18944.hp1 | 5_prime_UTR_variant | MODIFIER | c.-44G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | 44 | chr2 | 86720624 | ||||||
| chr2:86720641 | G | A | 2 | a0001c0004t0006 a0001c0004t0020 |
5 | HG01167.hp1 HG02809.hp2 HG02895.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-27G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | 27 | chr2 | 86720641 | ||||||
| chr2:86720660 | C | T | 35 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(32): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
5_prime_UTR_variant | MODIFIER | c.-8C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | 8 | chr2 | 86720660 | ||||||
| chr2:86773715 | C | T | 1 | a0001c0001t0007 | 4 | HG01884.hp1 HG02257.hp1 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*304C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 304 | chr2 | 86773715 | ||||||
| chr2:86773799 | T | C | 1 | a0001c0002t0028 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*388T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 388 | chr2 | 86773799 | ||||||
| chr2:86774404 | A | G | 1 | a0001c0002t0034 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*993A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 993 | chr2 | 86774404 | ||||||
| chr2:86774418 | C | T | 1 | a0001c0001t0015 | 2 | HG01891.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1007C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 1007 | chr2 | 86774418 | ||||||
| chr2:86774940 | C | G | 1 | a0001c0004t0026 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1529C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 1529 | chr2 | 86774940 | ||||||
| chr2:86775106 | C | T | 26 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(23): Show |
218 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*1695C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 1695 | chr2 | 86775106 | ||||||
| chr2:86775221 | A | G | 2 | a0001c0001t0009 a0001c0001t0015 |
5 | HG01891.hp2 HG02818.hp2 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1810A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 1810 | chr2 | 86775221 | ||||||
| chr2:86775316 | TTTTC | T | 4 | a0001c0001t0005 a0001c0001t0022 a0001c0003t0005 others(1): Show |
10 | HG01070.hp2 HG01167.hp2 HG01943.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1917_*1920delCTTT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 1917 | INFO_REALIGN_3_PRIME | chr2 | 86775316 | |||||
| chr2:86775325 | TTTC | T | 15 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0012 others(12): Show |
168 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*1917_*1919delCTT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 1917 | INFO_REALIGN_3_PRIME | chr2 | 86775325 | |||||
| chr2:86775326 | TTC | T | 5 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0014 others(2): Show |
25 | HG00423.hp1 HG02135.hp1 HG02602.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1917_*1918delCT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 1917 | INFO_REALIGN_3_PRIME | chr2 | 86775326 | |||||
| chr2:86775327 | TC | T | 3 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0015 |
5 | HG01891.hp2 HG02818.hp2 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1917delC | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 1917 | chr2 | 86775327 | ||||||
| chr2:86775328 | C | CT | 3 | a0001c0002t0002 a0001c0002t0004 a0001c0004t0011 |
9 | HG01891.hp1 HG02451.hp2 HG02717.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1938dupT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 1939 | INFO_REALIGN_3_PRIME | chr2 | 86775328 | |||||
| chr2:86775328 | C | T | 2 | a0001c0004t0016 a0001c0004t0021 |
3 | HG02630.hp2 HG02970.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1917C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 1917 | chr2 | 86775328 | ||||||
| chr2:86775328 | CT | C | 3 | a0001c0002t0002 a0001c0002t0030 a0001c0004t0006 |
6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1938delT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 1938 | INFO_REALIGN_3_PRIME | chr2 | 86775328 | |||||
| chr2:86775328 | CTTT | C | 2 | a0001c0001t0003 a0001c0001t0036 |
10 | HG01106.hp2 HG01168.hp1 HG01934.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1936_*1938delTTT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 1936 | INFO_REALIGN_3_PRIME | chr2 | 86775328 | |||||
| chr2:86775349 | T | A | 2 | a0001c0004t0006 a0001c0004t0020 |
5 | HG01167.hp1 HG02809.hp2 HG02895.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1938T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 1938 | chr2 | 86775349 | ||||||
| chr2:86775502 | C | T | 2 | a0001c0001t0014 a0001c0001t0032 |
3 | HG02622.hp1 HG02818.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2091C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 2091 | chr2 | 86775502 | ||||||
| chr2:86775583 | G | A | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(19): Show |
213 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*2172G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 2172 | chr2 | 86775583 | ||||||
| chr2:86775763 | G | A | 1 | a0001c0002t0013 | 2 | HG01433.hp2 NA18975.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2352G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 2352 | chr2 | 86775763 | ||||||
| chr2:86775905 | C | T | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(19): Show |
213 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*2494C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 2494 | chr2 | 86775905 | ||||||
| chr2:86775995 | C | T | 1 | a0001c0001t0024 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2584C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 2584 | chr2 | 86775995 | ||||||
| chr2:86776074 | C | G | 26 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(23): Show |
218 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*2663C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 2663 | chr2 | 86776074 | ||||||
| chr2:86776228 | C | A | 1 | a0001c0002t0029 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2817C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 2817 | chr2 | 86776228 | ||||||
| chr2:86776421 | C | G | 2 | a0001c0004t0011 a0001c0004t0026 |
3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3010C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 3010 | chr2 | 86776421 | ||||||
| chr2:86776723 | C | A | 9 | a0001c0002t0004 a0001c0002t0030 a0001c0002t0034 others(6): Show |
37 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*3312C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 3312 | chr2 | 86776723 | ||||||
| chr2:86776819 | C | T | 1 | a0001c0001t0031 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3408C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 3408 | chr2 | 86776819 | ||||||
| chr2:86776849 | TTATCTC | T | 5 | a0001c0002t0004 a0001c0002t0034 a0001c0002t0035 others(2): Show |
30 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3440_*3445delATCT others(2): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 3440 | INFO_REALIGN_3_PRIME | chr2 | 86776849 | |||||
| chr2:86776855 | C | G | 1 | a0001c0002t0002 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3444C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 3444 | chr2 | 86776855 | ||||||
| chr2:86777361 | G | A | 1 | a0001c0004t0020 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3950G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 3950 | chr2 | 86777361 | ||||||
| chr2:86777631 | T | C | 1 | a0001c0004t0026 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4220T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 4220 | chr2 | 86777631 | ||||||
| chr2:86777802 | A | G | 1 | a0001c0001t0033 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4391A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 4391 | chr2 | 86777802 | ||||||
| chr2:86778003 | A | G | 1 | a0001c0001t0032 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4592A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 4592 | chr2 | 86778003 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:86720827 | G | C | 27 | a0001c0003t0001g0002 a0001c0003t0001g0011 a0001c0003t0001g0012 others(24): Show |
33 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.142+18G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86720827 | |||||||
| chr2:86720840 | T | G | 4 | a0001c0005t0008g0008 a0001c0005t0008g0052 a0001c0005t0010g0008 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+31T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86720840 | |||||||
| chr2:86720972 | T | A | 3 | a0001c0004t0011g0055 a0001c0004t0011g0056 a0001c0004t0026g0054 |
3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.142+163T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86720972 | |||||||
| chr2:86720972 | T | C | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0002t0002g0057 |
3 | HG01192.hp2 HG03239.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.142+163T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86720972 | |||||||
| chr2:86721041 | A | G | 30 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0003t0001g0002 others(27): Show |
37 | HG01099.hp2 HG01109.hp1 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.142+232A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721041 | |||||||
| chr2:86721045 | G | T | 4 | a0001c0004t0006g0029 a0001c0004t0006g0248 a0001c0004t0006g0249 others(1): Show |
5 | HG01167.hp1 HG02809.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+236G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721045 | |||||||
| chr2:86721109 | G | A | 4 | a0001c0004t0006g0029 a0001c0004t0006g0248 a0001c0004t0006g0249 others(1): Show |
5 | HG01167.hp1 HG02809.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+300G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721109 | |||||||
| chr2:86721143 | T | C | 4 | a0001c0005t0008g0008 a0001c0005t0008g0052 a0001c0005t0010g0008 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+334T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721143 | |||||||
| chr2:86721163 | C | T | 4 | a0001c0005t0008g0008 a0001c0005t0008g0052 a0001c0005t0010g0008 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+354C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721163 | |||||||
| chr2:86721191 | T | C | 39 | a0001c0002t0001g0083 a0001c0002t0004g0015 a0001c0002t0004g0016 others(36): Show |
45 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.142+382T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721191 | |||||||
| chr2:86721281 | C | A | 7 | a0001c0004t0016g0014 a0001c0004t0021g0060 a0001c0004t0023g0061 others(4): Show |
9 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.142+472C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721281 | |||||||
| chr2:86721355 | G | T | 29 | a0001c0001t0001g0246 a0001c0003t0001g0002 a0001c0003t0001g0011 others(26): Show |
35 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(32): Show |
intron_variant | MODIFIER | c.142+546G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721355 | |||||||
| chr2:86721408 | C | T | 6 | a0001c0001t0001g0239 a0001c0001t0003g0241 a0001c0001t0003g0242 others(3): Show |
6 | HG01884.hp1 HG01934.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+599C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721408 | |||||||
| chr2:86721477 | C | T | 4 | a0001c0005t0008g0008 a0001c0005t0008g0052 a0001c0005t0010g0008 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+668C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721477 | |||||||
| chr2:86721521 | T | G | 4 | a0001c0005t0008g0008 a0001c0005t0008g0052 a0001c0005t0010g0008 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+712T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721521 | |||||||
| chr2:86721566 | C | A | 1 | a0001c0003t0001g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.142+757C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721566 | |||||||
| chr2:86721593 | G | A | 3 | a0001c0005t0008g0008 a0001c0005t0008g0052 a0001c0005t0010g0008 |
4 | HG01167.hp2 HG01169.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+784G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721593 | |||||||
| chr2:86721594 | T | C | 10 | a0001c0001t0003g0009 a0001c0001t0003g0084 a0001c0001t0003g0085 others(7): Show |
13 | HG00423.hp1 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.142+785T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721594 | |||||||
| chr2:86721609 | G | A | 3 | a0001c0004t0011g0055 a0001c0004t0011g0056 a0001c0004t0026g0054 |
3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.142+800G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721609 | |||||||
| chr2:86721609 | G | GT | 37 | a0001c0002t0002g0236 a0001c0002t0002g0237 a0001c0002t0002g0238 others(34): Show |
44 | HG00639.hp2 HG01099.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.142+811dupT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86721609 | ||||||
| chr2:86721672 | C | G | 4 | a0001c0005t0008g0008 a0001c0005t0008g0052 a0001c0005t0010g0008 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+863C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721672 | |||||||
| chr2:86721688 | G | C | 1 | a0001c0004t0016g0014 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.142+879G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721688 | |||||||
| chr2:86721699 | T | C | 4 | a0001c0004t0006g0029 a0001c0004t0006g0248 a0001c0004t0006g0249 others(1): Show |
5 | HG01167.hp1 HG02809.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+890T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721699 | |||||||
| chr2:86721712 | G | A | 235 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(232): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.142+903G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721712 | |||||||
| chr2:86721722 | T | C | 2 | a0001c0001t0003g0084 a0001c0001t0003g0085 |
2 | NA18999.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.142+913T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721722 | |||||||
| chr2:86721726 | A | G | 3 | a0001c0005t0008g0008 a0001c0005t0008g0052 a0001c0005t0010g0008 |
4 | HG01167.hp2 HG01169.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+917A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721726 | |||||||
| chr2:86721751 | G | A | 23 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0090 others(20): Show |
28 | HG00642.hp1 HG01109.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.142+942G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721751 | |||||||
| chr2:86721946 | A | G | 1 | a0001c0004t0023g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.142+1137A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721946 | |||||||
| chr2:86722021 | A | G | 7 | a0001c0004t0006g0029 a0001c0004t0006g0248 a0001c0004t0006g0249 others(4): Show |
9 | HG01167.hp1 HG02630.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.142+1212A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86722021 | |||||||
| chr2:86722063 | T | C | 1 | a0001c0002t0029g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.142+1254T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86722063 | |||||||
| chr2:86722149 | A | G | 1 | a0001c0004t0021g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.142+1340A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86722149 | |||||||
| chr2:86722514 | C | T | 1 | a0001c0003t0001g0013 | 2 | NA18983.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.142+1705C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86722514 | |||||||
| chr2:86722594 | A | C | 32 | a0001c0001t0001g0027 a0001c0001t0001g0211 a0001c0002t0001g0083 others(29): Show |
37 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.142+1785A>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86722594 | |||||||
| chr2:86722763 | C | A | 1 | a0001c0001t0001g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.142+1954C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86722763 | |||||||
| chr2:86722809 | A | T | 1 | a0001c0004t0021g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.142+2000A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86722809 | |||||||
| chr2:86722959 | CCA | C | 4 | a0001c0003t0001g0013 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
5 | HG03942.hp1 NA18950.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.142+2155_142+2156d others(4): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86722959 | ||||||
| chr2:86723015 | C | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.142+2206C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86723015 | |||||||
| chr2:86723148 | A | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.142+2339A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86723148 | |||||||
| chr2:86723159 | G | A | 11 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(8): Show |
13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.142+2350G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86723159 | |||||||
| chr2:86723218 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.142+2409A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86723218 | |||||||
| chr2:86723324 | A | AT | 4 | a0001c0002t0002g0028 a0001c0002t0002g0234 a0001c0002t0002g0235 others(1): Show |
5 | HG00323.hp2 HG00733.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.142+2516dupT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86723324 | ||||||
| chr2:86723491 | C | T | 1 | a0001c0002t0030g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.142+2682C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86723491 | |||||||
| chr2:86723560 | G | C | 1 | a0001c0004t0021g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.142+2751G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86723560 | |||||||
| chr2:86723721 | G | A | 1 | a0001c0002t0029g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.142+2912G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86723721 | |||||||
| chr2:86723758 | G | A | 2 | a0001c0003t0001g0033 a0001c0003t0001g0049 |
2 | NA18950.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.142+2949G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86723758 | |||||||
| chr2:86723776 | C | T | 1 | a0001c0001t0005g0102 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.142+2967C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86723776 | |||||||
| chr2:86723830 | C | T | 5 | a0001c0001t0009g0097 a0001c0001t0009g0098 a0001c0001t0009g0100 others(2): Show |
5 | HG01891.hp2 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.142+3021C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86723830 | |||||||
| chr2:86723960 | C | G | 1 | a0001c0003t0001g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.142+3151C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86723960 | |||||||
| chr2:86724064 | G | A | 14 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0090 others(11): Show |
18 | HG00642.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.142+3255G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86724064 | |||||||
| chr2:86724249 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.142+3440C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86724249 | |||||||
| chr2:86724352 | G | T | 10 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(7): Show |
12 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.142+3543G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86724352 | |||||||
| chr2:86724369 | G | T | 1 | a0001c0001t0001g0019 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.142+3560G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86724369 | |||||||
| chr2:86724552 | C | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.142+3743C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86724552 | |||||||
| chr2:86724555 | C | G | 1 | a0001c0002t0001g0083 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.142+3746C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86724555 | |||||||
| chr2:86724680 | G | T | 1 | a0001c0002t0002g0235 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.142+3871G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86724680 | |||||||
| chr2:86725012 | A | C | 28 | a0001c0003t0001g0002 a0001c0003t0001g0011 a0001c0003t0001g0012 others(25): Show |
34 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(31): Show |
intron_variant | MODIFIER | c.142+4203A>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86725012 | |||||||
| chr2:86725499 | T | G | 3 | a0001c0004t0011g0055 a0001c0004t0011g0056 a0001c0004t0026g0054 |
3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.142+4690T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86725499 | |||||||
| chr2:86725547 | T | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
221 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.142+4738T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86725547 | |||||||
| chr2:86725636 | G | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.142+4827G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86725636 | |||||||
| chr2:86725637 | C | T | 1 | a0001c0003t0001g0048 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.142+4828C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86725637 | |||||||
| chr2:86725643 | G | A | 2 | a0001c0001t0003g0114 a0001c0002t0030g0112 |
2 | HG02109.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.142+4834G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86725643 | |||||||
| chr2:86725648 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.142+4839T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86725648 | |||||||
| chr2:86725651 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.142+4842A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86725651 | |||||||
| chr2:86725683 | G | A | 1 | a0001c0004t0006g0029 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.142+4874G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86725683 | |||||||
| chr2:86725708 | A | G | 1 | a0001c0002t0004g0082 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.142+4899A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86725708 | |||||||
| chr2:86725733 | T | C | 5 | a0001c0001t0009g0097 a0001c0001t0009g0098 a0001c0001t0009g0100 others(2): Show |
5 | HG01891.hp2 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.142+4924T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86725733 | |||||||
| chr2:86725761 | A | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(182): Show |
219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.142+4952A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86725761 | |||||||
| chr2:86725951 | T | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(182): Show |
219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.142+5142T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86725951 | |||||||
| chr2:86725976 | CTT | C | 5 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(2): Show |
6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+5169_142+5170d others(4): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86725976 | ||||||
| chr2:86726002 | T | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(182): Show |
219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.142+5193T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726002 | |||||||
| chr2:86726066 | A | G | 1 | a0001c0004t0016g0014 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.142+5257A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726066 | |||||||
| chr2:86726090 | A | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(182): Show |
219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.142+5281A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726090 | |||||||
| chr2:86726106 | T | C | 1 | a0001c0001t0014g0115 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.142+5297T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726106 | |||||||
| chr2:86726121 | C | T | 5 | a0001c0002t0004g0017 a0001c0002t0004g0078 a0001c0002t0004g0079 others(2): Show |
6 | HG00423.hp2 HG00544.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+5312C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726121 | |||||||
| chr2:86726133 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.142+5324A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726133 | |||||||
| chr2:86726203 | C | T | 5 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(2): Show |
6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+5394C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726203 | |||||||
| chr2:86726250 | C | A | 8 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(5): Show |
10 | HG01167.hp1 HG02109.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+5441C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726250 | |||||||
| chr2:86726376 | C | T | 5 | a0001c0001t0012g0203 a0001c0001t0012g0205 a0001c0001t0022g0113 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.142+5567C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726376 | |||||||
| chr2:86726377 | C | T | 8 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(5): Show |
10 | HG01167.hp1 HG02109.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+5568C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726377 | |||||||
| chr2:86726536 | A | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.142+5727A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726536 | |||||||
| chr2:86726568 | A | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(182): Show |
219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.142+5759A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726568 | |||||||
| chr2:86726638 | GT | G | 4 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0119 others(1): Show |
4 | HG00140.hp2 HG01106.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+5831delT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86726638 | ||||||
| chr2:86726710 | T | G | 1 | a0001c0004t0023g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.142+5901T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726710 | |||||||
| chr2:86726725 | G | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.142+5916G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726725 | |||||||
| chr2:86726758 | G | T | 185 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(182): Show |
219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.142+5949G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726758 | |||||||
| chr2:86726877 | T | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
223 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.142+6068T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726877 | |||||||
| chr2:86726957 | A | G | 5 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(2): Show |
6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+6148A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726957 | |||||||
| chr2:86726965 | C | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(180): Show |
218 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.142+6156C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726965 | |||||||
| chr2:86726991 | T | C | 25 | a0001c0002t0001g0083 a0001c0002t0004g0015 a0001c0002t0004g0016 others(22): Show |
28 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.142+6182T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726991 | |||||||
| chr2:86727176 | T | G | 5 | a0001c0001t0012g0203 a0001c0001t0012g0205 a0001c0001t0022g0113 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.142+6367T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86727176 | |||||||
| chr2:86727225 | G | A | 10 | a0001c0001t0003g0021 a0001c0001t0003g0120 a0001c0001t0003g0122 others(7): Show |
11 | HG01167.hp1 HG01168.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.142+6416G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86727225 | |||||||
| chr2:86727267 | A | G | 1 | a0001c0002t0030g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.142+6458A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86727267 | |||||||
| chr2:86727295 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.142+6486A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86727295 | |||||||
| chr2:86727486 | C | T | 1 | a0001c0002t0002g0231 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.142+6677C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86727486 | |||||||
| chr2:86727635 | A | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
214 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.142+6826A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86727635 | |||||||
| chr2:86727677 | G | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
213 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.142+6868G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86727677 | |||||||
| chr2:86727789 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.142+6980T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86727789 | |||||||
| chr2:86727940 | G | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.142+7131G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86727940 | |||||||
| chr2:86728008 | A | C | 1 | a0001c0001t0001g0210 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.142+7199A>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728008 | |||||||
| chr2:86728140 | A | T | 11 | a0001c0001t0001g0121 a0001c0001t0005g0102 a0001c0001t0009g0097 others(8): Show |
11 | HG00609.hp1 HG01358.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.142+7331A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728140 | |||||||
| chr2:86728164 | AAC | A | 185 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(182): Show |
219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.142+7357_142+7358d others(4): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86728164 | ||||||
| chr2:86728169 | T | C | 9 | a0001c0003t0001g0002 a0001c0003t0001g0011 a0001c0003t0001g0034 others(6): Show |
13 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.142+7360T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728169 | |||||||
| chr2:86728183 | G | T | 8 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(5): Show |
10 | HG01167.hp1 HG02109.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+7374G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728183 | |||||||
| chr2:86728215 | A | T | 3 | a0001c0004t0011g0055 a0001c0004t0011g0056 a0001c0004t0026g0054 |
3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.142+7406A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728215 | |||||||
| chr2:86728313 | CTT | C | 9 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0002t0030g0112 others(6): Show |
10 | HG01167.hp1 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.142+7518_142+7519d others(4): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86728313 | ||||||
| chr2:86728313 | CTTT | C | 183 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(180): Show |
217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.142+7517_142+7519d others(5): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86728313 | ||||||
| chr2:86728323 | T | C | 3 | a0001c0001t0001g0090 a0001c0001t0003g0089 a0001c0001t0017g0018 |
4 | HG01109.hp2 HG02647.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+7514T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728323 | |||||||
| chr2:86728437 | G | A | 185 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(182): Show |
219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.142+7628G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728437 | |||||||
| chr2:86728450 | G | C | 3 | a0001c0004t0011g0055 a0001c0004t0011g0056 a0001c0004t0026g0054 |
3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.142+7641G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728450 | |||||||
| chr2:86728491 | A | G | 1 | a0001c0004t0016g0014 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.142+7682A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728491 | |||||||
| chr2:86728516 | C | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(182): Show |
219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.142+7707C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728516 | |||||||
| chr2:86728745 | T | C | 1 | a0001c0002t0002g0104 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.142+7936T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728745 | |||||||
| chr2:86728872 | G | GC | 192 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(189): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.142+8068dupC | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86728872 | ||||||
| chr2:86728897 | C | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.142+8088C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728897 | |||||||
| chr2:86728900 | A | G | 2 | a0001c0001t0005g0102 a0001c0002t0034g0063 |
2 | NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.142+8091A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728900 | |||||||
| chr2:86728918 | A | T | 3 | a0001c0004t0011g0055 a0001c0004t0011g0056 a0001c0004t0026g0054 |
3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.142+8109A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728918 | |||||||
| chr2:86728929 | G | T | 3 | a0001c0004t0011g0055 a0001c0004t0011g0056 a0001c0004t0026g0054 |
3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.142+8120G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728929 | |||||||
| chr2:86728931 | A | T | 3 | a0001c0004t0011g0055 a0001c0004t0011g0056 a0001c0004t0026g0054 |
3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.142+8122A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728931 | |||||||
| chr2:86728934 | T | TTG | 3 | a0001c0004t0011g0055 a0001c0004t0011g0056 a0001c0004t0026g0054 |
3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.142+8126_142+8127i others(4): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86728934 | ||||||
| chr2:86729000 | C | T | 7 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0005g0025 others(4): Show |
7 | HG01358.hp2 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.142+8191C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729000 | |||||||
| chr2:86729018 | T | A | 1 | a0001c0001t0001g0125 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.142+8209T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729018 | |||||||
| chr2:86729022 | A | G | 5 | a0001c0001t0001g0201 a0001c0002t0002g0238 a0001c0004t0011g0055 others(2): Show |
5 | HG00639.hp2 HG01358.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+8213A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729022 | |||||||
| chr2:86729174 | TAAGA | T | 3 | a0001c0004t0011g0055 a0001c0004t0011g0056 a0001c0004t0026g0054 |
3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.142+8370_142+8373d others(6): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86729174 | ||||||
| chr2:86729204 | T | A | 1 | a0001c0004t0021g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.142+8395T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729204 | |||||||
| chr2:86729225 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.142+8416T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729225 | |||||||
| chr2:86729253 | C | T | 4 | a0001c0001t0001g0201 a0001c0004t0011g0055 a0001c0004t0011g0056 others(1): Show |
4 | HG01358.hp2 HG01884.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+8444C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729253 | |||||||
| chr2:86729266 | A | G | 4 | a0001c0001t0001g0201 a0001c0004t0011g0055 a0001c0004t0011g0056 others(1): Show |
4 | HG01358.hp2 HG01884.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+8457A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729266 | |||||||
| chr2:86729283 | G | T | 13 | a0001c0001t0001g0201 a0001c0001t0001g0246 a0001c0002t0030g0112 others(10): Show |
15 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.142+8474G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729283 | |||||||
| chr2:86729443 | A | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.142+8634A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729443 | |||||||
| chr2:86729501 | C | T | 1 | a0001c0004t0021g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.142+8692C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729501 | |||||||
| chr2:86729536 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.142+8727C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729536 | |||||||
| chr2:86729537 | G | A | 1 | a0001c0001t0009g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.142+8728G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729537 | |||||||
| chr2:86729547 | C | T | 1 | a0001c0002t0030g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.142+8738C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729547 | |||||||
| chr2:86729588 | G | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.142+8779G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729588 | |||||||
| chr2:86729642 | G | A | 8 | a0001c0001t0009g0097 a0001c0002t0002g0010 a0001c0002t0002g0020 others(5): Show |
11 | HG01358.hp2 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.142+8833G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729642 | |||||||
| chr2:86729667 | C | CT | 137 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.142+8858_142+8859i others(3): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729667 | |||||||
| chr2:86729669 | G | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.142+8860G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729669 | |||||||
| chr2:86729797 | G | T | 1 | a0001c0005t0010g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.142+8988G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729797 | |||||||
| chr2:86729958 | C | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.142+9149C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729958 | |||||||
| chr2:86730276 | G | A | 30 | a0001c0001t0001g0128 a0001c0002t0002g0105 a0001c0002t0002g0212 others(27): Show |
35 | HG01099.hp2 HG01109.hp1 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.142+9467G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86730276 | |||||||
| chr2:86730367 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.142+9558A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86730367 | |||||||
| chr2:86730435 | G | C | 4 | a0001c0002t0002g0236 a0001c0002t0002g0238 a0001c0002t0002g0250 others(1): Show |
4 | HG00639.hp2 HG01346.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+9626G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86730435 | |||||||
| chr2:86730933 | G | A | 1 | a0001c0002t0002g0218 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.143-9994G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86730933 | |||||||
| chr2:86731075 | T | C | 22 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0022 others(19): Show |
31 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.143-9852T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86731075 | |||||||
| chr2:86731084 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.143-9843A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86731084 | |||||||
| chr2:86731206 | G | A | 1 | a0001c0004t0023g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.143-9721G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86731206 | |||||||
| chr2:86731246 | T | G | 25 | a0001c0003t0001g0002 a0001c0003t0001g0011 a0001c0003t0001g0012 others(22): Show |
30 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(27): Show |
intron_variant | MODIFIER | c.143-9681T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86731246 | |||||||
| chr2:86731496 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(224): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.143-9431T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86731496 | |||||||
| chr2:86731521 | T | C | 2 | a0001c0004t0011g0055 a0001c0004t0026g0054 |
2 | HG01358.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.143-9406T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86731521 | |||||||
| chr2:86731592 | T | G | 1 | a0001c0004t0026g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.143-9335T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86731592 | |||||||
| chr2:86731635 | G | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
213 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.143-9292G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86731635 | |||||||
| chr2:86731895 | A | G | 1 | a0001c0004t0011g0056 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.143-9032A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86731895 | |||||||
| chr2:86732119 | G | A | 12 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0090 others(9): Show |
16 | HG00642.hp1 HG01109.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.143-8808G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86732119 | |||||||
| chr2:86732289 | C | T | 1 | a0001c0001t0007g0244 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.143-8638C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86732289 | |||||||
| chr2:86732302 | C | CAG | 12 | a0001c0001t0001g0121 a0001c0002t0030g0112 a0001c0004t0006g0029 others(9): Show |
14 | HG00609.hp1 HG01167.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.143-8624_143-8623d others(4): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86732302 | ||||||
| chr2:86732346 | G | A | 11 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(8): Show |
13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.143-8581G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86732346 | |||||||
| chr2:86732408 | T | C | 1 | a0001c0001t0001g0140 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.143-8519T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86732408 | |||||||
| chr2:86732420 | T | C | 5 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(2): Show |
6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.143-8507T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86732420 | |||||||
| chr2:86732524 | A | G | 3 | a0001c0004t0011g0055 a0001c0004t0011g0056 a0001c0004t0026g0054 |
3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.143-8403A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86732524 | |||||||
| chr2:86732527 | G | A | 2 | a0001c0001t0005g0102 a0001c0005t0010g0053 |
2 | HG02145.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.143-8400G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86732527 | |||||||
| chr2:86732650 | AT | A | 11 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(8): Show |
13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.143-8275delT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86732650 | ||||||
| chr2:86732754 | C | G | 10 | a0001c0004t0006g0029 a0001c0004t0006g0248 a0001c0004t0006g0249 others(7): Show |
12 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.143-8173C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86732754 | |||||||
| chr2:86732756 | A | G | 25 | a0001c0002t0001g0083 a0001c0002t0004g0015 a0001c0002t0004g0016 others(22): Show |
28 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.143-8171A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86732756 | |||||||
| chr2:86732792 | C | T | 1 | a0001c0001t0005g0102 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.143-8135C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86732792 | |||||||
| chr2:86732916 | G | T | 1 | a0001c0004t0023g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.143-8011G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86732916 | |||||||
| chr2:86733090 | A | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
224 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.143-7837A>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86733090 | |||||||
| chr2:86733095 | G | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.143-7832G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86733095 | |||||||
| chr2:86733129 | G | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.143-7798G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86733129 | |||||||
| chr2:86733305 | G | A | 1 | a0001c0002t0035g0066 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.143-7622G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86733305 | |||||||
| chr2:86733428 | T | C | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0033g0143 |
3 | HG00099.hp1 HG00280.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.143-7499T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86733428 | |||||||
| chr2:86733512 | A | G | 28 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0090 others(25): Show |
34 | HG00642.hp1 HG01109.hp2 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.143-7415A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86733512 | |||||||
| chr2:86733514 | C | T | 22 | a0001c0003t0001g0002 a0001c0003t0001g0011 a0001c0003t0001g0012 others(19): Show |
27 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(24): Show |
intron_variant | MODIFIER | c.143-7413C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86733514 | |||||||
| chr2:86733707 | A | G | 8 | a0001c0002t0004g0016 a0001c0002t0004g0064 a0001c0002t0004g0065 others(5): Show |
9 | HG02055.hp1 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.143-7220A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86733707 | |||||||
| chr2:86733750 | G | C | 2 | a0001c0001t0001g0025 a0001c0001t0005g0025 |
2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.143-7177G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86733750 | |||||||
| chr2:86733949 | C | A | 1 | a0001c0002t0029g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.143-6978C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86733949 | |||||||
| chr2:86733967 | A | G | 12 | a0001c0002t0004g0076 a0001c0002t0030g0112 a0001c0004t0006g0029 others(9): Show |
14 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.143-6960A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86733967 | |||||||
| chr2:86734004 | T | A | 1 | a0001c0002t0004g0064 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.143-6923T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86734004 | |||||||
| chr2:86734071 | G | A | 206 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(203): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.143-6856G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86734071 | |||||||
| chr2:86734336 | C | G | 2 | a0001c0002t0004g0015 a0001c0002t0004g0077 |
3 | HG01074.hp2 HG01261.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.143-6591C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86734336 | |||||||
| chr2:86734370 | G | T | 16 | a0001c0001t0001g0019 a0001c0001t0001g0094 a0001c0001t0001g0095 others(13): Show |
19 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.143-6557G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86734370 | |||||||
| chr2:86734478 | C | T | 6 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(3): Show |
8 | HG01167.hp1 HG02109.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-6449C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86734478 | |||||||
| chr2:86734519 | A | G | 2 | a0001c0002t0002g0110 a0001c0002t0002g0111 |
2 | NA18960.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.143-6408A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86734519 | |||||||
| chr2:86734555 | A | G | 5 | a0001c0001t0009g0097 a0001c0001t0009g0098 a0001c0001t0009g0100 others(2): Show |
5 | HG01891.hp2 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-6372A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86734555 | |||||||
| chr2:86734659 | T | C | 1 | a0001c0001t0003g0144 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.143-6268T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86734659 | |||||||
| chr2:86734682 | T | A | 2 | a0001c0002t0002g0237 a0001c0002t0029g0103 |
2 | NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.143-6245T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86734682 | |||||||
| chr2:86734707 | G | A | 1 | a0001c0004t0016g0014 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.143-6220G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86734707 | |||||||
| chr2:86734772 | A | G | 21 | a0001c0001t0001g0019 a0001c0001t0001g0094 a0001c0001t0001g0095 others(18): Show |
24 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.143-6155A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86734772 | |||||||
| chr2:86734779 | C | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(167): Show |
203 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.143-6148C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86734779 | |||||||
| chr2:86734961 | TTGTCTAT others(13): Show |
T | 1 | a0001c0004t0011g0055 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.143-5963_143-5944d others(22): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86734961 | ||||||
| chr2:86735013 | T | C | 1 | a0001c0001t0005g0129 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.143-5914T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86735013 | |||||||
| chr2:86735029 | A | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(168): Show |
200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.143-5898A>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86735029 | |||||||
| chr2:86735061 | G | A | 24 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0090 others(21): Show |
30 | HG00642.hp1 HG01109.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.143-5866G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86735061 | |||||||
| chr2:86735318 | G | A | 2 | a0001c0001t0001g0194 a0001c0001t0005g0193 |
2 | HG02735.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.143-5609G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86735318 | |||||||
| chr2:86735326 | C | A | 1 | a0001c0001t0001g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.143-5601C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86735326 | |||||||
| chr2:86735361 | A | G | 1 | a0001c0002t0004g0081 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.143-5566A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86735361 | |||||||
| chr2:86735419 | G | A | 1 | a0001c0002t0004g0067 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.143-5508G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86735419 | |||||||
| chr2:86735522 | T | C | 1 | a0001c0002t0004g0062 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.143-5405T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86735522 | |||||||
| chr2:86735550 | C | CT | 5 | a0001c0001t0001g0027 a0001c0001t0001g0189 a0001c0001t0003g0085 others(2): Show |
7 | NA18975.hp1 NA18983.hp1 NA18999.hp1 others(4): Show |
intron_variant | MODIFIER | c.143-5367dupT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86735550 | ||||||
| chr2:86735675 | A | C | 1 | a0001c0004t0011g0056 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.143-5252A>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86735675 | |||||||
| chr2:86735832 | G | C | 25 | a0001c0003t0001g0002 a0001c0003t0001g0011 a0001c0003t0001g0012 others(22): Show |
30 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(27): Show |
intron_variant | MODIFIER | c.143-5095G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86735832 | |||||||
| chr2:86736190 | C | T | 218 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(215): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.143-4737C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86736190 | |||||||
| chr2:86736253 | A | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(140): Show |
170 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.143-4674A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86736253 | |||||||
| chr2:86736341 | C | A | 1 | a0001c0002t0004g0076 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.143-4586C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86736341 | |||||||
| chr2:86736468 | A | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.143-4459A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86736468 | |||||||
| chr2:86736484 | CATT | C | 53 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0090 others(50): Show |
63 | HG00642.hp1 HG01099.hp2 HG01109.hp1 others(60): Show |
intron_variant | MODIFIER | c.143-4442_143-4440d others(5): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86736484 | |||||||
| chr2:86736631 | T | C | 10 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(7): Show |
12 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.143-4296T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86736631 | |||||||
| chr2:86736640 | C | T | 1 | a0001c0004t0016g0014 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.143-4287C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86736640 | |||||||
| chr2:86736732 | G | T | 1 | a0001c0002t0002g0105 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.143-4195G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86736732 | |||||||
| chr2:86736739 | G | GTA | 1 | a0001c0002t0002g0010 | 3 | HG02717.hp2 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.143-4178_143-4177d others(4): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86736739 | ||||||
| chr2:86736748 | T | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(215): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.143-4179T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86736748 | |||||||
| chr2:86736962 | C | A | 1 | a0001c0004t0011g0055 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.143-3965C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86736962 | |||||||
| chr2:86736964 | G | C | 1 | a0001c0004t0011g0055 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.143-3963G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86736964 | |||||||
| chr2:86737123 | T | C | 11 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(8): Show |
13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.143-3804T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86737123 | |||||||
| chr2:86737278 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.143-3649A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86737278 | |||||||
| chr2:86737290 | A | G | 11 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(8): Show |
13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.143-3637A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86737290 | |||||||
| chr2:86737315 | C | T | 11 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(8): Show |
13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.143-3612C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86737315 | |||||||
| chr2:86737342 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.143-3585C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86737342 | |||||||
| chr2:86737444 | G | A | 1 | a0001c0002t0002g0217 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.143-3483G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86737444 | |||||||
| chr2:86737462 | A | G | 1 | a0001c0004t0021g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.143-3465A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86737462 | |||||||
| chr2:86737574 | C | CATATATA others(7): Show |
1 | a0001c0001t0003g0092 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.143-3346_143-3333d others(16): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737574 | ||||||
| chr2:86737574 | C | CATATATA others(11): Show |
6 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0094 others(3): Show |
9 | HG00642.hp1 HG02055.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.143-3350_143-3333d others(20): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737574 | ||||||
| chr2:86737574 | C | CATATATA others(13): Show |
2 | a0001c0001t0001g0090 a0001c0001t0017g0018 |
3 | HG01109.hp2 HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.143-3352_143-3333d others(22): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737574 | ||||||
| chr2:86737574 | C | CATATATA others(15): Show |
2 | a0001c0001t0001g0093 a0001c0001t0003g0089 |
2 | HG02630.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.143-3333_143-3332i others(24): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737574 | ||||||
| chr2:86737574 | C | CATATATA others(19): Show |
1 | a0001c0001t0001g0096 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.143-3333_143-3332i others(28): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737574 | ||||||
| chr2:86737574 | C | CATATATA others(21): Show |
1 | a0001c0001t0001g0125 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.143-3333_143-3332i others(30): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737574 | ||||||
| chr2:86737574 | C | CATATATA others(25): Show |
1 | a0001c0001t0005g0102 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.143-3333_143-3332i others(34): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737574 | ||||||
| chr2:86737574 | C | CATATATA others(27): Show |
1 | a0001c0005t0010g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.143-3333_143-3332i others(36): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737574 | ||||||
| chr2:86737574 | C | CATATATA others(29): Show |
1 | a0001c0001t0009g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.143-3333_143-3332i others(38): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737574 | ||||||
| chr2:86737574 | C | CATATATA others(31): Show |
1 | a0001c0001t0015g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.143-3333_143-3332i others(40): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737574 | ||||||
| chr2:86737574 | C | CATATATA others(33): Show |
2 | a0001c0001t0009g0100 a0001c0001t0015g0099 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.143-3333_143-3332i others(42): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737574 | ||||||
| chr2:86737574 | C | CATATATA others(37): Show |
1 | a0001c0001t0009g0098 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.143-3333_143-3332i others(46): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737574 | ||||||
| chr2:86737574 | CAT | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(70): Show |
88 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.143-3334_143-3333d others(4): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737574 | ||||||
| chr2:86737574 | CATAT | C | 74 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0022 others(71): Show |
89 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.143-3336_143-3333d others(6): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737574 | ||||||
| chr2:86737592 | T | TATATATA | 13 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0145 others(10): Show |
13 | HG00099.hp1 HG00280.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.143-3333_143-3332i others(9): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737592 | ||||||
| chr2:86737592 | T | TATATATA others(2): Show |
3 | a0001c0001t0003g0150 a0001c0003t0001g0032 a0001c0004t0021g0060 |
3 | HG02970.hp1 NA19068.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.143-3333_143-3332i others(11): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737592 | ||||||
| chr2:86737592 | T | TATATATA others(4): Show |
1 | a0001c0004t0016g0014 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.143-3333_143-3332i others(13): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737592 | ||||||
| chr2:86737592 | T | TATATATA others(7): Show |
1 | a0001c0004t0011g0055 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.143-3333_143-3332i others(16): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737592 | ||||||
| chr2:86737592 | T | TATATATA others(8): Show |
2 | a0001c0002t0030g0112 a0001c0004t0011g0056 |
2 | HG02109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.143-3333_143-3332i others(17): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737592 | ||||||
| chr2:86737592 | T | TATATATA others(10): Show |
1 | a0001c0004t0026g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.143-3333_143-3332i others(19): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737592 | ||||||
| chr2:86737592 | T | TATATATA others(14): Show |
1 | a0001c0004t0020g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.143-3333_143-3332i others(23): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737592 | ||||||
| chr2:86737592 | T | TATATATA others(16): Show |
1 | a0001c0004t0006g0248 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.143-3333_143-3332i others(25): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737592 | ||||||
| chr2:86737592 | T | TATATATA others(18): Show |
1 | a0001c0004t0006g0249 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.143-3333_143-3332i others(27): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737592 | ||||||
| chr2:86737592 | T | TATATATA others(24): Show |
1 | a0001c0004t0006g0029 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.143-3333_143-3332i others(33): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737592 | ||||||
| chr2:86737686 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.143-3241T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86737686 | |||||||
| chr2:86737725 | C | G | 1 | a0001c0001t0001g0178 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.143-3202C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86737725 | |||||||
| chr2:86737745 | C | T | 1 | a0001c0001t0003g0088 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.143-3182C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86737745 | |||||||
| chr2:86737820 | T | G | 1 | a0001c0004t0021g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.143-3107T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86737820 | |||||||
| chr2:86737959 | G | A | 32 | a0001c0001t0001g0246 a0001c0001t0012g0203 a0001c0001t0012g0205 others(29): Show |
38 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(35): Show |
intron_variant | MODIFIER | c.143-2968G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86737959 | |||||||
| chr2:86738029 | A | C | 1 | a0001c0002t0001g0083 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.143-2898A>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86738029 | |||||||
| chr2:86738047 | T | C | 1 | a0001c0001t0001g0145 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.143-2880T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86738047 | |||||||
| chr2:86738058 | A | C | 1 | a0001c0002t0034g0063 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.143-2869A>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86738058 | |||||||
| chr2:86738282 | G | A | 50 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0090 others(47): Show |
60 | HG00642.hp1 HG01099.hp2 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.143-2645G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86738282 | |||||||
| chr2:86738292 | C | T | 34 | a0001c0002t0001g0083 a0001c0002t0004g0015 a0001c0002t0004g0016 others(31): Show |
39 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.143-2635C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86738292 | |||||||
| chr2:86738309 | C | T | 1 | a0001c0002t0004g0062 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.143-2618C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86738309 | |||||||
| chr2:86738416 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0005g0026 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.143-2511G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86738416 | |||||||
| chr2:86738467 | C | T | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0022 others(24): Show |
36 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.143-2460C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86738467 | |||||||
| chr2:86738514 | G | C | 1 | a0001c0001t0025g0202 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.143-2413G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86738514 | |||||||
| chr2:86738542 | CA | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(181): Show |
219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.143-2373delA | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86738542 | ||||||
| chr2:86738588 | C | CA | 11 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(8): Show |
13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.143-2338dupA | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86738588 | ||||||
| chr2:86738703 | T | C | 1 | a0001c0003t0001g0040 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.143-2224T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86738703 | |||||||
| chr2:86738823 | A | G | 11 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(8): Show |
13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.143-2104A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86738823 | |||||||
| chr2:86738955 | G | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.143-1972G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86738955 | |||||||
| chr2:86738968 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.143-1959T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86738968 | |||||||
| chr2:86739008 | A | C | 1 | a0001c0001t0025g0202 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.143-1919A>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86739008 | |||||||
| chr2:86739108 | G | T | 1 | a0001c0004t0011g0055 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.143-1819G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86739108 | |||||||
| chr2:86739351 | G | A | 9 | a0001c0004t0006g0029 a0001c0004t0006g0248 a0001c0004t0006g0249 others(6): Show |
11 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-1576G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86739351 | |||||||
| chr2:86739404 | G | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(189): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.143-1523G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86739404 | |||||||
| chr2:86739485 | G | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
213 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.143-1442G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86739485 | |||||||
| chr2:86739518 | G | A | 4 | a0001c0002t0002g0028 a0001c0002t0002g0234 a0001c0002t0002g0235 others(1): Show |
5 | HG00323.hp2 HG00733.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-1409G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86739518 | |||||||
| chr2:86739894 | G | A | 1 | a0001c0004t0021g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.143-1033G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86739894 | |||||||
| chr2:86739905 | C | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(189): Show |
227 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.143-1022C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86739905 | |||||||
| chr2:86739923 | G | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.143-1004G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86739923 | |||||||
| chr2:86740082 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.143-845G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86740082 | |||||||
| chr2:86740122 | A | G | 6 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(3): Show |
7 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.143-805A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86740122 | |||||||
| chr2:86740276 | C | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(97): Show |
115 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.143-651C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86740276 | |||||||
| chr2:86740278 | G | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
213 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.143-649G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86740278 | |||||||
| chr2:86740307 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.143-620C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86740307 | |||||||
| chr2:86740336 | G | A | 34 | a0001c0002t0001g0083 a0001c0002t0002g0010 a0001c0002t0002g0020 others(31): Show |
40 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.143-591G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86740336 | |||||||
| chr2:86740344 | G | T | 5 | a0001c0001t0012g0203 a0001c0001t0012g0205 a0001c0001t0022g0113 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-583G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86740344 | |||||||
| chr2:86740445 | G | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.143-482G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86740445 | |||||||
| chr2:86740731 | C | CA | 4 | a0001c0001t0001g0175 a0001c0002t0002g0212 a0001c0004t0016g0014 others(1): Show |
5 | HG01934.hp2 HG02630.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-191dupA | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86740731 | ||||||
| chr2:86741235 | C | G | 1 | a0001c0002t0004g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.285+166C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86741235 | |||||||
| chr2:86741305 | C | T | 2 | a0001c0003t0001g0033 a0001c0003t0001g0049 |
2 | NA18950.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.285+236C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86741305 | |||||||
| chr2:86741518 | C | T | 1 | a0001c0002t0002g0228 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.285+449C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86741518 | |||||||
| chr2:86741565 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.285+496A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86741565 | |||||||
| chr2:86741662 | A | C | 1 | a0001c0003t0001g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.285+593A>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86741662 | |||||||
| chr2:86741774 | G | A | 1 | a0001c0002t0004g0062 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.285+705G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86741774 | |||||||
| chr2:86741849 | T | C | 5 | a0001c0001t0012g0203 a0001c0001t0012g0205 a0001c0001t0022g0113 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+780T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86741849 | |||||||
| chr2:86741850 | T | G | 5 | a0001c0001t0012g0203 a0001c0001t0012g0205 a0001c0001t0022g0113 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+781T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86741850 | |||||||
| chr2:86742069 | A | G | 3 | a0001c0001t0001g0024 a0001c0001t0001g0172 a0001c0001t0001g0173 |
4 | HG01071.hp1 HG01106.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.285+1000A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86742069 | |||||||
| chr2:86742174 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.285+1105A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86742174 | |||||||
| chr2:86742198 | T | A | 1 | a0001c0004t0011g0055 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.285+1129T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86742198 | |||||||
| chr2:86742647 | A | G | 4 | a0001c0002t0030g0112 a0001c0003t0001g0030 a0001c0003t0001g0031 others(1): Show |
4 | HG02109.hp1 HG02735.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+1578A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86742647 | |||||||
| chr2:86742648 | G | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
213 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.285+1579G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86742648 | |||||||
| chr2:86742656 | T | C | 3 | a0001c0003t0001g0030 a0001c0003t0001g0031 a0001c0003t0001g0032 |
3 | HG02735.hp2 HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.285+1587T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86742656 | |||||||
| chr2:86742670 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.285+1601A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86742670 | |||||||
| chr2:86742740 | G | A | 5 | a0001c0002t0002g0219 a0001c0002t0002g0220 a0001c0002t0002g0221 others(2): Show |
5 | HG01074.hp1 HG01168.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+1671G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86742740 | |||||||
| chr2:86742770 | T | C | 1 | a0001c0001t0009g0098 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.285+1701T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86742770 | |||||||
| chr2:86742998 | C | G | 3 | a0001c0004t0011g0055 a0001c0004t0011g0056 a0001c0004t0026g0054 |
3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.285+1929C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86742998 | |||||||
| chr2:86743251 | G | C | 11 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(8): Show |
13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.285+2182G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86743251 | |||||||
| chr2:86743283 | T | A | 5 | a0001c0001t0012g0203 a0001c0001t0012g0205 a0001c0001t0022g0113 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+2214T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86743283 | |||||||
| chr2:86743364 | C | CT | 28 | a0001c0002t0034g0063 a0001c0003t0001g0002 a0001c0003t0001g0011 others(25): Show |
34 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(31): Show |
intron_variant | MODIFIER | c.285+2308dupT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 86743364 | ||||||
| chr2:86743364 | CT | C | 11 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(8): Show |
13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.285+2308delT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 86743364 | ||||||
| chr2:86743498 | CT | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.285+2434delT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 86743498 | ||||||
| chr2:86743531 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.285+2462C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86743531 | |||||||
| chr2:86743567 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.285+2498C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86743567 | |||||||
| chr2:86743707 | T | G | 1 | a0001c0002t0004g0071 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.285+2638T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86743707 | |||||||
| chr2:86743710 | G | A | 5 | a0001c0002t0002g0104 a0001c0002t0002g0108 a0001c0002t0002g0109 others(2): Show |
5 | HG01433.hp2 HG02135.hp2 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+2641G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86743710 | |||||||
| chr2:86743748 | G | A | 1 | a0001c0004t0021g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.285+2679G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86743748 | |||||||
| chr2:86743760 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.285+2691C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86743760 | |||||||
| chr2:86743884 | AG | A | 3 | a0001c0004t0011g0055 a0001c0004t0011g0056 a0001c0004t0026g0054 |
3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.285+2817delG | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 86743884 | ||||||
| chr2:86743964 | C | T | 5 | a0001c0001t0001g0134 a0001c0001t0001g0138 a0001c0005t0008g0008 others(2): Show |
6 | HG01167.hp2 HG01169.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.285+2895C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86743964 | |||||||
| chr2:86743977 | C | CA | 10 | a0001c0001t0001g0141 a0001c0001t0001g0206 a0001c0001t0001g0210 others(7): Show |
11 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.285+2924dupA | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 86743977 | ||||||
| chr2:86743977 | CA | C | 35 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0239 others(32): Show |
41 | HG01099.hp2 HG01109.hp1 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.285+2924delA | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 86743977 | ||||||
| chr2:86743994 | T | A | 2 | a0001c0004t0011g0055 a0001c0004t0026g0054 |
2 | HG01358.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.285+2925T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86743994 | |||||||
| chr2:86744209 | A | G | 2 | a0001c0002t0004g0074 a0001c0002t0004g0075 |
2 | HG02280.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.285+3140A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86744209 | |||||||
| chr2:86744224 | C | T | 12 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0090 others(9): Show |
16 | HG00642.hp1 HG01109.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.285+3155C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86744224 | |||||||
| chr2:86744246 | A | C | 1 | a0001c0001t0025g0202 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.285+3177A>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86744246 | |||||||
| chr2:86744729 | T | TG | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.285+3662dupG | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 86744729 | ||||||
| chr2:86744854 | A | G | 1 | a0001c0001t0025g0202 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.285+3785A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86744854 | |||||||
| chr2:86744859 | A | T | 1 | a0001c0004t0011g0055 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.285+3790A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86744859 | |||||||
| chr2:86744991 | A | T | 1 | a0001c0004t0011g0055 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.285+3922A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86744991 | |||||||
| chr2:86744993 | ATTTG | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(146): Show |
177 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.285+3927_285+3930d others(6): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 86744993 | ||||||
| chr2:86744994 | T | A | 1 | a0001c0004t0011g0055 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.285+3925T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86744994 | |||||||
| chr2:86745005 | A | G | 1 | a0001c0001t0031g0087 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.285+3936A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86745005 | |||||||
| chr2:86745008 | A | AT | 11 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(8): Show |
13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.285+3952dupT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 86745008 | ||||||
| chr2:86745008 | AT | A | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
214 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.285+3952delT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 86745008 | ||||||
| chr2:86745014 | T | A | 1 | a0001c0001t0001g0191 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.285+3945T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86745014 | |||||||
| chr2:86745038 | T | G | 4 | a0001c0002t0002g0236 a0001c0002t0002g0238 a0001c0002t0002g0250 others(1): Show |
4 | HG00639.hp2 HG01346.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.285+3969T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86745038 | |||||||
| chr2:86745099 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.285+4030G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86745099 | |||||||
| chr2:86745293 | T | C | 11 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(8): Show |
13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.285+4224T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86745293 | |||||||
| chr2:86745307 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.285+4238A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86745307 | |||||||
| chr2:86745959 | T | C | 4 | a0001c0004t0006g0029 a0001c0004t0006g0248 a0001c0004t0006g0249 others(1): Show |
5 | HG01167.hp1 HG02809.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+4890T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86745959 | |||||||
| chr2:86745973 | T | C | 11 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(8): Show |
13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.285+4904T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86745973 | |||||||
| chr2:86746004 | C | T | 5 | a0001c0001t0012g0203 a0001c0001t0012g0205 a0001c0001t0022g0113 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+4935C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86746004 | |||||||
| chr2:86746070 | T | A | 1 | a0001c0004t0011g0055 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.285+5001T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86746070 | |||||||
| chr2:86746138 | A | G | 1 | a0001c0002t0002g0228 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.285+5069A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86746138 | |||||||
| chr2:86746499 | G | A | 3 | a0001c0003t0001g0030 a0001c0003t0001g0031 a0001c0003t0001g0032 |
3 | HG02735.hp2 HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.286-5397G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86746499 | |||||||
| chr2:86746499 | G | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0152 a0001c0001t0001g0164 others(5): Show |
12 | HG02015.hp1 HG02074.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.286-5397G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86746499 | |||||||
| chr2:86746661 | C | G | 1 | a0001c0001t0001g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.286-5235C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86746661 | |||||||
| chr2:86746711 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.286-5185A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86746711 | |||||||
| chr2:86746785 | G | A | 1 | a0001c0002t0002g0237 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.286-5111G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86746785 | |||||||
| chr2:86746828 | C | A | 1 | a0001c0001t0001g0121 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.286-5068C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86746828 | |||||||
| chr2:86746926 | A | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(126): Show |
153 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.286-4970A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86746926 | |||||||
| chr2:86747195 | A | G | 23 | a0001c0002t0001g0083 a0001c0002t0004g0015 a0001c0002t0004g0016 others(20): Show |
26 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.286-4701A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86747195 | |||||||
| chr2:86747218 | G | A | 1 | a0001c0004t0016g0014 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.286-4678G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86747218 | |||||||
| chr2:86747343 | TGTTAA | T | 1 | a0001c0002t0002g0010 | 3 | HG02717.hp2 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.286-4548_286-4544d others(7): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 86747343 | ||||||
| chr2:86747566 | A | G | 5 | a0001c0001t0012g0205 a0001c0002t0002g0028 a0001c0002t0002g0234 others(2): Show |
6 | HG00323.hp2 HG00733.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.286-4330A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86747566 | |||||||
| chr2:86747682 | T | C | 1 | a0001c0004t0021g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.286-4214T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86747682 | |||||||
| chr2:86747711 | A | C | 25 | a0001c0002t0001g0083 a0001c0002t0004g0015 a0001c0002t0004g0016 others(22): Show |
28 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.286-4185A>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86747711 | |||||||
| chr2:86747748 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.286-4148G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86747748 | |||||||
| chr2:86747756 | C | T | 3 | a0001c0004t0011g0055 a0001c0004t0011g0056 a0001c0004t0026g0054 |
3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.286-4140C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86747756 | |||||||
| chr2:86747828 | G | A | 1 | a0001c0001t0003g0085 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.286-4068G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86747828 | |||||||
| chr2:86747936 | G | A | 1 | a0001c0002t0002g0020 | 2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.286-3960G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86747936 | |||||||
| chr2:86748042 | A | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.286-3854A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86748042 | |||||||
| chr2:86748097 | T | C | 3 | a0001c0004t0011g0055 a0001c0004t0011g0056 a0001c0004t0026g0054 |
3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.286-3799T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86748097 | |||||||
| chr2:86748585 | T | G | 11 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(8): Show |
13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.286-3311T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86748585 | |||||||
| chr2:86748847 | G | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.286-3049G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86748847 | |||||||
| chr2:86749064 | C | T | 5 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(2): Show |
6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.286-2832C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86749064 | |||||||
| chr2:86749116 | G | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.286-2780G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86749116 | |||||||
| chr2:86749170 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0005g0026 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.286-2726G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86749170 | |||||||
| chr2:86749170 | G | C | 1 | a0001c0005t0008g0052 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.286-2726G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86749170 | |||||||
| chr2:86749176 | G | A | 4 | a0001c0001t0001g0024 a0001c0001t0001g0128 a0001c0001t0001g0172 others(1): Show |
5 | HG01071.hp1 HG01106.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.286-2720G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86749176 | |||||||
| chr2:86749183 | T | C | 1 | a0001c0001t0009g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.286-2713T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86749183 | |||||||
| chr2:86749225 | G | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.286-2671G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86749225 | |||||||
| chr2:86749344 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.286-2552A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86749344 | |||||||
| chr2:86749396 | CT | C | 23 | a0001c0002t0001g0083 a0001c0002t0004g0015 a0001c0002t0004g0016 others(20): Show |
26 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.286-2489delT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 86749396 | ||||||
| chr2:86749505 | C | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0162 a0001c0001t0003g0023 |
3 | NA18978.hp2 NA18998.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.286-2391C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86749505 | |||||||
| chr2:86749538 | C | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.286-2358C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86749538 | |||||||
| chr2:86749578 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.286-2318C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86749578 | |||||||
| chr2:86749869 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.286-2027T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86749869 | |||||||
| chr2:86750104 | T | G | 1 | a0001c0001t0001g0141 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.286-1792T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86750104 | |||||||
| chr2:86750442 | C | A | 11 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(8): Show |
13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.286-1454C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86750442 | |||||||
| chr2:86750502 | CAT | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.286-1393_286-1392d others(4): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86750502 | |||||||
| chr2:86750718 | G | A | 1 | a0001c0002t0030g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.286-1178G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86750718 | |||||||
| chr2:86750729 | C | T | 2 | a0001c0001t0009g0097 a0001c0002t0002g0227 |
2 | HG00140.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.286-1167C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86750729 | |||||||
| chr2:86750771 | GT | G | 206 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(203): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.286-1109delT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 86750771 | ||||||
| chr2:86750812 | T | C | 1 | a0001c0002t0030g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.286-1084T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86750812 | |||||||
| chr2:86751010 | T | C | 5 | a0001c0001t0012g0203 a0001c0001t0012g0205 a0001c0001t0022g0113 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.286-886T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86751010 | |||||||
| chr2:86751072 | G | A | 1 | a0001c0001t0003g0114 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.286-824G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86751072 | |||||||
| chr2:86751741 | A | G | 1 | a0001c0002t0002g0238 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.286-155A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86751741 | |||||||
| chr2:86751772 | G | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.286-124G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86751772 | |||||||
| chr2:86751773 | A | G | 1 | a0001c0001t0001g0189 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.286-123A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86751773 | |||||||
| chr2:86751774 | C | T | 3 | a0001c0001t0005g0102 a0001c0003t0001g0245 a0001c0005t0010g0053 |
3 | HG02145.hp2 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.286-122C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86751774 | |||||||
| chr2:86752294 | G | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.420+264G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 3/8 | chr2 | 86752294 | |||||||
| chr2:86752297 | G | A | 5 | a0001c0001t0001g0134 a0001c0001t0001g0138 a0001c0005t0008g0008 others(2): Show |
6 | HG01167.hp2 HG01169.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.420+267G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 3/8 | chr2 | 86752297 | |||||||
| chr2:86752370 | A | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(189): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.420+340A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 3/8 | chr2 | 86752370 | |||||||
| chr2:86752560 | C | A | 1 | a0001c0002t0002g0237 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.420+530C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 3/8 | chr2 | 86752560 | |||||||
| chr2:86752599 | A | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.420+569A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 3/8 | chr2 | 86752599 | |||||||
| chr2:86752778 | C | T | 11 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(8): Show |
13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.421-680C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 3/8 | chr2 | 86752778 | |||||||
| chr2:86752882 | C | T | 5 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(2): Show |
6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.421-576C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 3/8 | chr2 | 86752882 | |||||||
| chr2:86752987 | T | C | 11 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(8): Show |
13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.421-471T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 3/8 | chr2 | 86752987 | |||||||
| chr2:86753115 | G | A | 11 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(8): Show |
13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.421-343G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 3/8 | chr2 | 86753115 | |||||||
| chr2:86753137 | A | G | 3 | a0001c0003t0001g0045 a0001c0003t0001g0046 a0001c0003t0001g0047 |
3 | NA18955.hp2 NA18967.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.421-321A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 3/8 | chr2 | 86753137 | |||||||
| chr2:86753387 | A | G | 1 | a0001c0001t0009g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-71A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 3/8 | chr2 | 86753387 | |||||||
| chr2:86753663 | G | A | 1 | a0001c0004t0006g0029 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.521+105G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86753663 | |||||||
| chr2:86753711 | A | T | 1 | a0001c0004t0016g0014 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.521+153A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86753711 | |||||||
| chr2:86753744 | A | G | 1 | a0001c0004t0021g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.521+186A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86753744 | |||||||
| chr2:86753963 | G | A | 1 | a0001c0002t0002g0057 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.521+405G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86753963 | |||||||
| chr2:86754000 | T | C | 12 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0090 others(9): Show |
16 | HG00642.hp1 HG01109.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.521+442T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86754000 | |||||||
| chr2:86754534 | C | G | 5 | a0001c0001t0009g0097 a0001c0001t0009g0098 a0001c0001t0009g0100 others(2): Show |
5 | HG01891.hp2 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.521+976C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86754534 | |||||||
| chr2:86754595 | G | T | 1 | a0001c0001t0003g0085 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.521+1037G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86754595 | |||||||
| chr2:86754620 | G | A | 5 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(2): Show |
6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.521+1062G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86754620 | |||||||
| chr2:86754654 | C | T | 1 | a0001c0002t0004g0073 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.521+1096C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86754654 | |||||||
| chr2:86754668 | G | A | 14 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0090 others(11): Show |
18 | HG00642.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.521+1110G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86754668 | |||||||
| chr2:86754705 | G | A | 11 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(8): Show |
13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.521+1147G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86754705 | |||||||
| chr2:86754732 | A | T | 2 | a0001c0001t0001g0201 a0001c0001t0003g0118 |
2 | HG01106.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.521+1174A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86754732 | |||||||
| chr2:86755076 | C | T | 29 | a0001c0001t0001g0246 a0001c0003t0001g0002 a0001c0003t0001g0011 others(26): Show |
35 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(32): Show |
intron_variant | MODIFIER | c.521+1518C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86755076 | |||||||
| chr2:86755097 | A | G | 3 | a0001c0004t0011g0055 a0001c0004t0011g0056 a0001c0004t0026g0054 |
3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.521+1539A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86755097 | |||||||
| chr2:86755112 | C | CT | 28 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0090 others(25): Show |
34 | HG00642.hp1 HG01109.hp2 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.521+1570dupT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86755112 | ||||||
| chr2:86755158 | C | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
4 | HG03942.hp2 NA18978.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.521+1600C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86755158 | |||||||
| chr2:86755170 | G | A | 5 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(2): Show |
6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.521+1612G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86755170 | |||||||
| chr2:86755319 | A | G | 1 | a0001c0002t0004g0080 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.521+1761A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86755319 | |||||||
| chr2:86755381 | C | G | 25 | a0001c0002t0001g0083 a0001c0002t0004g0015 a0001c0002t0004g0016 others(22): Show |
28 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.521+1823C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86755381 | |||||||
| chr2:86755400 | G | T | 1 | a0001c0001t0001g0019 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.521+1842G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86755400 | |||||||
| chr2:86755417 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.521+1859C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86755417 | |||||||
| chr2:86755521 | T | C | 1 | a0001c0002t0029g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.521+1963T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86755521 | |||||||
| chr2:86755528 | G | A | 23 | a0001c0002t0001g0083 a0001c0002t0004g0015 a0001c0002t0004g0016 others(20): Show |
26 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.521+1970G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86755528 | |||||||
| chr2:86755659 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.521+2101A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86755659 | |||||||
| chr2:86755753 | T | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.521+2195T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86755753 | |||||||
| chr2:86755832 | G | A | 2 | a0001c0001t0001g0194 a0001c0001t0003g0153 |
2 | NA18949.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.521+2274G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86755832 | |||||||
| chr2:86755955 | T | C | 1 | a0001c0002t0004g0062 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.521+2397T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86755955 | |||||||
| chr2:86756263 | T | C | 5 | a0001c0001t0012g0203 a0001c0001t0012g0205 a0001c0001t0022g0113 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.521+2705T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86756263 | |||||||
| chr2:86756265 | C | T | 1 | a0001c0002t0029g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.521+2707C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86756265 | |||||||
| chr2:86756538 | A | G | 2 | a0001c0001t0001g0151 a0001c0001t0001g0197 |
2 | HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.521+2980A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86756538 | |||||||
| chr2:86756563 | C | T | 1 | a0001c0003t0001g0040 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.521+3005C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86756563 | |||||||
| chr2:86756808 | A | G | 11 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(8): Show |
13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.521+3250A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86756808 | |||||||
| chr2:86756856 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.521+3298A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86756856 | |||||||
| chr2:86757030 | A | G | 12 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0090 others(9): Show |
16 | HG00642.hp1 HG01109.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.521+3472A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86757030 | |||||||
| chr2:86757042 | G | A | 1 | a0001c0004t0023g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.521+3484G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86757042 | |||||||
| chr2:86757059 | G | T | 1 | a0001c0001t0001g0187 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.521+3501G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86757059 | |||||||
| chr2:86757106 | G | A | 1 | a0001c0001t0015g0099 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.521+3548G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86757106 | |||||||
| chr2:86757174 | C | CAAA | 7 | a0001c0002t0001g0083 a0001c0002t0004g0064 a0001c0002t0004g0071 others(4): Show |
7 | HG00544.hp1 HG00738.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.521+3647_521+3649d others(5): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86757174 | ||||||
| chr2:86757174 | C | CAAAA | 9 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0069 others(6): Show |
11 | HG00099.hp2 HG00423.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.521+3646_521+3649d others(6): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86757174 | ||||||
| chr2:86757174 | C | CAAAAAA | 5 | a0001c0002t0004g0067 a0001c0002t0004g0068 a0001c0002t0004g0072 others(2): Show |
6 | HG00609.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.521+3644_521+3649d others(8): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86757174 | ||||||
| chr2:86757174 | CA | C | 29 | a0001c0002t0002g0010 a0001c0002t0002g0028 a0001c0002t0002g0057 others(26): Show |
32 | HG00140.hp1 HG00733.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.521+3649delA | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86757174 | ||||||
| chr2:86757174 | CAA | C | 7 | a0001c0002t0002g0020 a0001c0002t0002g0105 a0001c0002t0002g0111 others(4): Show |
8 | HG00639.hp2 HG01074.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.521+3648_521+3649d others(4): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86757174 | ||||||
| chr2:86757174 | CAAAAAAA others(4): Show |
C | 1 | a0001c0004t0021g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.521+3639_521+3649d others(13): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86757174 | ||||||
| chr2:86757174 | CAAAAAAA others(7): Show |
C | 20 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0154 others(17): Show |
21 | HG00733.hp2 HG01891.hp2 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.521+3636_521+3649d others(16): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86757174 | ||||||
| chr2:86757174 | CAAAAAAA others(8): Show |
C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
188 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.521+3635_521+3649d others(17): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86757174 | ||||||
| chr2:86757174 | CAAAAAAA others(9): Show |
C | 7 | a0001c0001t0001g0026 a0001c0001t0001g0151 a0001c0001t0001g0162 others(4): Show |
7 | HG01243.hp2 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.521+3634_521+3649d others(18): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86757174 | ||||||
| chr2:86757174 | CAAAAAAA others(10): Show |
C | 1 | a0001c0002t0004g0062 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.521+3633_521+3649d others(19): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86757174 | ||||||
| chr2:86757269 | C | T | 3 | a0001c0004t0016g0014 a0001c0004t0021g0060 a0001c0004t0023g0061 |
4 | HG02630.hp2 HG02970.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.521+3711C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86757269 | |||||||
| chr2:86757274 | C | T | 1 | a0001c0004t0023g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.521+3716C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86757274 | |||||||
| chr2:86757403 | T | C | 1 | a0001c0002t0013g0106 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.521+3845T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86757403 | |||||||
| chr2:86757419 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.521+3861C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86757419 | |||||||
| chr2:86757424 | C | T | 3 | a0001c0004t0016g0014 a0001c0004t0021g0060 a0001c0004t0023g0061 |
4 | HG02630.hp2 HG02970.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.521+3866C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86757424 | |||||||
| chr2:86757425 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.521+3867G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86757425 | |||||||
| chr2:86757964 | A | G | 1 | a0001c0004t0021g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.521+4406A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86757964 | |||||||
| chr2:86758161 | CACA | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
213 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.521+4608_521+4610d others(5): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86758161 | ||||||
| chr2:86758360 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.521+4802A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86758360 | |||||||
| chr2:86758364 | A | AT | 12 | a0001c0001t0001g0132 a0001c0001t0001g0139 a0001c0001t0001g0145 others(9): Show |
13 | HG01978.hp1 HG02055.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.521+4818dupT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86758364 | ||||||
| chr2:86758420 | TA | T | 3 | a0001c0004t0011g0055 a0001c0004t0011g0056 a0001c0004t0026g0054 |
3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.521+4863delA | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86758420 | |||||||
| chr2:86758598 | G | A | 11 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(8): Show |
13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.521+5040G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86758598 | |||||||
| chr2:86758612 | G | A | 1 | a0001c0004t0021g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.521+5054G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86758612 | |||||||
| chr2:86758971 | T | A | 1 | a0001c0002t0002g0010 | 3 | HG02717.hp2 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.521+5413T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86758971 | |||||||
| chr2:86759079 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.521+5521A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86759079 | |||||||
| chr2:86759109 | A | T | 1 | a0001c0001t0001g0132 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.521+5551A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86759109 | |||||||
| chr2:86759210 | G | A | 20 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0022 others(17): Show |
29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.521+5652G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86759210 | |||||||
| chr2:86759351 | C | G | 1 | a0001c0003t0001g0040 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.522-5676C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86759351 | |||||||
| chr2:86759565 | TA | T | 5 | a0001c0002t0004g0071 a0001c0004t0006g0029 a0001c0004t0006g0248 others(2): Show |
6 | HG01167.hp1 HG02602.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.522-5455delA | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86759565 | ||||||
| chr2:86759566 | A | T | 16 | a0001c0001t0001g0201 a0001c0001t0001g0246 a0001c0001t0007g0169 others(13): Show |
16 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.522-5461A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86759566 | |||||||
| chr2:86759612 | G | GC | 84 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0023 others(81): Show |
99 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.522-5408dupC | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86759612 | ||||||
| chr2:86759620 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(127): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.522-5407G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86759620 | |||||||
| chr2:86759686 | G | C | 4 | a0001c0002t0004g0070 a0001c0004t0006g0029 a0001c0004t0006g0248 others(1): Show |
5 | HG01167.hp1 HG02809.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.522-5341G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86759686 | |||||||
| chr2:86759721 | A | G | 1 | a0001c0005t0010g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.522-5306A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86759721 | |||||||
| chr2:86759724 | C | T | 1 | a0001c0001t0003g0122 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.522-5303C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86759724 | |||||||
| chr2:86759761 | C | T | 1 | a0001c0003t0001g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.522-5266C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86759761 | |||||||
| chr2:86759879 | C | T | 2 | a0001c0004t0023g0061 a0001c0005t0010g0053 |
2 | HG02145.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.522-5148C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86759879 | |||||||
| chr2:86760002 | T | G | 1 | a0001c0002t0002g0212 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.522-5025T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86760002 | |||||||
| chr2:86760194 | G | A | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0003g0146 |
3 | HG00099.hp1 HG00280.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.522-4833G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86760194 | |||||||
| chr2:86760295 | C | T | 2 | a0001c0002t0004g0068 a0001c0002t0004g0069 |
2 | HG00609.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.522-4732C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86760295 | |||||||
| chr2:86760355 | T | C | 1 | a0001c0002t0004g0067 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.522-4672T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86760355 | |||||||
| chr2:86760648 | T | C | 191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
227 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.522-4379T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86760648 | |||||||
| chr2:86760762 | GA | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
227 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.522-4260delA | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86760762 | ||||||
| chr2:86760860 | G | C | 191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
227 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.522-4167G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86760860 | |||||||
| chr2:86760864 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(127): Show |
154 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.522-4163G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86760864 | |||||||
| chr2:86760965 | A | AGT | 47 | a0001c0001t0001g0025 a0001c0001t0001g0090 a0001c0001t0001g0093 others(44): Show |
50 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.522-4024_522-4023d others(4): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86760965 | ||||||
| chr2:86760965 | A | AGTGT | 32 | a0001c0001t0001g0004 a0001c0001t0001g0095 a0001c0001t0001g0117 others(29): Show |
36 | HG00323.hp1 HG00735.hp1 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.522-4026_522-4023d others(6): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86760965 | ||||||
| chr2:86760965 | A | AGTGTGT | 24 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0130 others(21): Show |
35 | HG00642.hp2 HG00741.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.522-4028_522-4023d others(8): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86760965 | ||||||
| chr2:86760965 | A | AGTGTGTG others(1): Show |
5 | a0001c0001t0005g0131 a0001c0002t0034g0063 a0001c0003t0001g0039 others(2): Show |
5 | HG01993.hp1 HG02976.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.522-4030_522-4023d others(10): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86760965 | ||||||
| chr2:86760965 | AGT | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(88): Show |
104 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.522-4024_522-4023d others(4): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86760965 | ||||||
| chr2:86760965 | AGTGT | A | 11 | a0001c0001t0001g0121 a0001c0001t0001g0154 a0001c0001t0003g0009 others(8): Show |
13 | HG00423.hp1 HG00609.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.522-4026_522-4023d others(6): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86760965 | ||||||
| chr2:86761208 | G | T | 1 | a0001c0001t0001g0138 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.522-3819G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86761208 | |||||||
| chr2:86761232 | A | G | 1 | a0001c0001t0001g0194 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.522-3795A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86761232 | |||||||
| chr2:86761655 | A | G | 1 | a0001c0002t0002g0109 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.522-3372A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86761655 | |||||||
| chr2:86761672 | T | A | 1 | a0001c0001t0003g0114 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.522-3355T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86761672 | |||||||
| chr2:86761739 | C | T | 1 | a0001c0004t0016g0014 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.522-3288C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86761739 | |||||||
| chr2:86761849 | G | A | 1 | a0001c0001t0003g0089 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.522-3178G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86761849 | |||||||
| chr2:86761945 | G | A | 5 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(2): Show |
6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.522-3082G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86761945 | |||||||
| chr2:86762149 | A | G | 4 | a0001c0004t0006g0029 a0001c0004t0006g0248 a0001c0004t0006g0249 others(1): Show |
5 | HG01167.hp1 HG02809.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.522-2878A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86762149 | |||||||
| chr2:86762343 | A | T | 191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
227 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.522-2684A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86762343 | |||||||
| chr2:86762644 | C | CA | 32 | a0001c0002t0002g0217 a0001c0002t0002g0237 a0001c0002t0004g0015 others(29): Show |
36 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.522-2371dupA | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86762644 | ||||||
| chr2:86762644 | CAAAA | C | 183 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(180): Show |
217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.522-2374_522-2371d others(6): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86762644 | ||||||
| chr2:86762655 | A | T | 1 | a0001c0005t0010g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.522-2372A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86762655 | |||||||
| chr2:86762658 | A | T | 1 | a0001c0005t0010g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.522-2369A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86762658 | |||||||
| chr2:86762664 | T | A | 12 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0090 others(9): Show |
16 | HG00642.hp1 HG01109.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.522-2363T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86762664 | |||||||
| chr2:86762671 | T | TATATATA others(22): Show |
12 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0090 others(9): Show |
16 | HG00642.hp1 HG01109.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.522-2337_522-2336i others(31): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86762671 | ||||||
| chr2:86762671 | TATATATA others(31): Show |
T | 1 | a0001c0003t0001g0038 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.522-2338_522-2301d others(40): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86762671 | ||||||
| chr2:86762682 | TATATATA others(2): Show |
T | 37 | a0001c0002t0002g0010 a0001c0002t0002g0028 a0001c0002t0002g0057 others(34): Show |
40 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.522-2291_522-2283d others(11): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86762682 | ||||||
| chr2:86762682 | TATATATA others(11): Show |
T | 35 | a0001c0001t0012g0203 a0001c0001t0012g0205 a0001c0001t0022g0113 others(32): Show |
37 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.522-2300_522-2283d others(20): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86762682 | ||||||
| chr2:86762682 | TATATATA others(20): Show |
T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
173 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.522-2309_522-2283d others(29): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86762682 | ||||||
| chr2:86762682 | TATATATA others(29): Show |
T | 10 | a0001c0001t0001g0157 a0001c0001t0001g0199 a0001c0001t0009g0097 others(7): Show |
10 | HG01891.hp2 HG02145.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.522-2318_522-2283d others(38): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86762682 | ||||||
| chr2:86762682 | TATATATA others(38): Show |
T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0152 a0001c0001t0001g0164 others(7): Show |
14 | HG00544.hp2 HG02015.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.522-2327_522-2283d others(47): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86762682 | ||||||
| chr2:86762684 | TATATATC others(18): Show |
T | 5 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(2): Show |
6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.522-2336_522-2312d others(27): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86762684 | ||||||
| chr2:86762693 | TATATATC others(9): Show |
T | 12 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0090 others(9): Show |
16 | HG00642.hp1 HG01109.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.522-2327_522-2312d others(18): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86762693 | ||||||
| chr2:86762709 | C | CATATATA others(6): Show |
1 | a0001c0001t0005g0102 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.522-2310_522-2309i others(15): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86762709 | ||||||
| chr2:86762808 | A | C | 1 | a0001c0002t0035g0066 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.522-2219A>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86762808 | |||||||
| chr2:86762811 | C | T | 2 | a0001c0002t0013g0106 a0001c0002t0013g0107 |
2 | HG01433.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.522-2216C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86762811 | |||||||
| chr2:86762839 | G | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(181): Show |
218 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.522-2188G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86762839 | |||||||
| chr2:86763124 | T | C | 1 | a0001c0004t0016g0014 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.522-1903T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86763124 | |||||||
| chr2:86763192 | GTAGT | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(127): Show |
154 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.522-1832_522-1829d others(6): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86763192 | ||||||
| chr2:86763295 | C | G | 1 | a0001c0003t0001g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.522-1732C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86763295 | |||||||
| chr2:86763499 | G | A | 1 | a0001c0004t0016g0014 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.522-1528G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86763499 | |||||||
| chr2:86763553 | G | A | 2 | a0001c0002t0004g0062 a0001c0002t0034g0063 |
2 | HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.522-1474G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86763553 | |||||||
| chr2:86763583 | C | T | 7 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(4): Show |
9 | HG01167.hp1 HG02109.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.522-1444C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86763583 | |||||||
| chr2:86763771 | G | A | 5 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(2): Show |
6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.522-1256G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86763771 | |||||||
| chr2:86763904 | A | T | 3 | a0001c0004t0011g0055 a0001c0004t0011g0056 a0001c0004t0026g0054 |
3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.522-1123A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86763904 | |||||||
| chr2:86764178 | G | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0132 others(2): Show |
9 | HG00642.hp2 HG00741.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.522-849G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86764178 | |||||||
| chr2:86764515 | T | G | 1 | a0001c0002t0002g0230 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.522-512T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86764515 | |||||||
| chr2:86764680 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.522-347G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86764680 | |||||||
| chr2:86764723 | C | T | 1 | a0001c0001t0031g0087 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.522-304C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86764723 | |||||||
| chr2:86764751 | C | A | 1 | a0001c0002t0004g0078 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.522-276C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86764751 | |||||||
| chr2:86764770 | A | C | 5 | a0001c0001t0012g0203 a0001c0001t0012g0205 a0001c0001t0022g0113 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.522-257A>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86764770 | |||||||
| chr2:86765214 | T | TAA | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(181): Show |
218 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.688+22_688+23insAA | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 86765214 | ||||||
| chr2:86765419 | A | G | 3 | a0001c0001t0001g0140 a0001c0001t0001g0168 a0001c0001t0001g0198 |
3 | HG01517.hp1 HG06807.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.688+226A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 5/8 | chr2 | 86765419 | |||||||
| chr2:86765489 | C | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0157 a0001c0001t0001g0199 |
3 | HG00609.hp1 NA18967.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.688+296C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 5/8 | chr2 | 86765489 | |||||||
| chr2:86765618 | C | G | 2 | a0001c0004t0016g0014 a0001c0004t0021g0060 |
3 | HG02630.hp2 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.689-241C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 5/8 | chr2 | 86765618 | |||||||
| chr2:86766183 | G | A | 1 | a0001c0001t0024g0204 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.854+159G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86766183 | |||||||
| chr2:86766194 | G | T | 4 | a0001c0002t0002g0214 a0001c0002t0002g0215 a0001c0002t0002g0225 others(1): Show |
4 | HG01928.hp2 HG01943.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.854+170G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86766194 | |||||||
| chr2:86766403 | C | T | 28 | a0001c0003t0001g0002 a0001c0003t0001g0011 a0001c0003t0001g0012 others(25): Show |
34 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(31): Show |
intron_variant | MODIFIER | c.854+379C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86766403 | |||||||
| chr2:86766405 | T | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(215): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.854+381T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86766405 | |||||||
| chr2:86766516 | T | C | 5 | a0001c0001t0012g0203 a0001c0001t0012g0205 a0001c0001t0022g0113 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.854+492T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86766516 | |||||||
| chr2:86766525 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.854+501G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86766525 | |||||||
| chr2:86766537 | A | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
227 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.854+513A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86766537 | |||||||
| chr2:86766597 | G | A | 34 | a0001c0001t0012g0203 a0001c0001t0012g0205 a0001c0001t0022g0113 others(31): Show |
40 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(37): Show |
intron_variant | MODIFIER | c.854+573G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86766597 | |||||||
| chr2:86766633 | C | T | 1 | a0001c0001t0033g0143 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.854+609C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86766633 | |||||||
| chr2:86766647 | A | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
227 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.854+623A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86766647 | |||||||
| chr2:86766651 | G | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(181): Show |
218 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.854+627G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86766651 | |||||||
| chr2:86766661 | C | CA | 42 | a0001c0001t0001g0170 a0001c0001t0001g0174 a0001c0001t0001g0211 others(39): Show |
47 | HG01074.hp1 HG01099.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.854+658dupA | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 86766661 | ||||||
| chr2:86766661 | C | CAA | 5 | a0001c0001t0001g0188 a0001c0003t0001g0013 a0001c0004t0011g0055 others(2): Show |
6 | HG01358.hp2 HG01884.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.854+657_854+658dup others(2): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 86766661 | ||||||
| chr2:86766661 | CA | C | 10 | a0001c0001t0001g0208 a0001c0001t0003g0242 a0001c0001t0009g0098 others(7): Show |
10 | HG01070.hp1 HG01891.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.854+658delA | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 86766661 | ||||||
| chr2:86766661 | CAAAAAAA | C | 29 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0022 others(26): Show |
38 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.854+652_854+658del others(7): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 86766661 | ||||||
| chr2:86766661 | CAAAAAAA others(5): Show |
C | 2 | a0001c0002t0002g0237 a0001c0002t0004g0070 |
2 | NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.854+647_854+658del others(12): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 86766661 | ||||||
| chr2:86766678 | A | G | 1 | a0001c0002t0004g0067 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.854+654A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86766678 | |||||||
| chr2:86766807 | A | G | 1 | a0001c0002t0002g0028 | 2 | HG00733.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.854+783A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86766807 | |||||||
| chr2:86767023 | G | A | 30 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0022 others(27): Show |
39 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.854+999G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86767023 | |||||||
| chr2:86767158 | G | A | 24 | a0001c0002t0004g0015 a0001c0002t0004g0016 a0001c0002t0004g0017 others(21): Show |
27 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.854+1134G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86767158 | |||||||
| chr2:86767167 | G | A | 27 | a0001c0003t0001g0002 a0001c0003t0001g0011 a0001c0003t0001g0012 others(24): Show |
33 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.854+1143G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86767167 | |||||||
| chr2:86767314 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.854+1290T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86767314 | |||||||
| chr2:86767424 | T | C | 1 | a0001c0002t0002g0237 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.854+1400T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86767424 | |||||||
| chr2:86767425 | C | CT | 6 | a0001c0002t0002g0028 a0001c0002t0002g0110 a0001c0002t0002g0234 others(3): Show |
7 | HG00323.hp2 HG00733.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.854+1422dupT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 86767425 | ||||||
| chr2:86767425 | CT | C | 8 | a0001c0002t0002g0111 a0001c0002t0002g0215 a0001c0002t0002g0221 others(5): Show |
9 | HG01257.hp2 HG01943.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.854+1422delT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 86767425 | ||||||
| chr2:86767425 | CTTTTTTT others(3): Show |
C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(181): Show |
218 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.854+1413_854+1422d others(12): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 86767425 | ||||||
| chr2:86767596 | C | T | 191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
227 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.854+1572C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86767596 | |||||||
| chr2:86768383 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.855-1640A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86768383 | |||||||
| chr2:86768428 | C | T | 1 | a0001c0003t0001g0051 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.855-1595C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86768428 | |||||||
| chr2:86768801 | G | T | 1 | a0001c0002t0004g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.855-1222G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86768801 | |||||||
| chr2:86768902 | A | G | 5 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(2): Show |
6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.855-1121A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86768902 | |||||||
| chr2:86768989 | A | G | 5 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(2): Show |
6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.855-1034A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86768989 | |||||||
| chr2:86769012 | C | T | 28 | a0001c0003t0001g0002 a0001c0003t0001g0011 a0001c0003t0001g0012 others(25): Show |
34 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(31): Show |
intron_variant | MODIFIER | c.855-1011C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86769012 | |||||||
| chr2:86769047 | C | T | 3 | a0001c0004t0011g0055 a0001c0004t0011g0056 a0001c0004t0026g0054 |
3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.855-976C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86769047 | |||||||
| chr2:86769305 | A | T | 5 | a0001c0001t0012g0203 a0001c0001t0012g0205 a0001c0001t0022g0113 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.855-718A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86769305 | |||||||
| chr2:86769678 | G | GT | 15 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0090 others(12): Show |
19 | HG00642.hp1 HG01109.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.855-333dupT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 86769678 | ||||||
| chr2:86769678 | GT | G | 6 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(3): Show |
8 | HG01167.hp1 HG02109.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.855-333delT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 86769678 | ||||||
| chr2:86769725 | A | G | 25 | a0001c0001t0009g0100 a0001c0002t0004g0015 a0001c0002t0004g0016 others(22): Show |
28 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.855-298A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86769725 | |||||||
| chr2:86770017 | T | C | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG00738.hp2 HG00741.hp2 |
splice_region_variant&intron_variant | LOW | c.855-6T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86770017 | |||||||
| chr2:86770193 | T | G | 3 | a0001c0003t0001g0030 a0001c0003t0001g0031 a0001c0003t0001g0032 |
3 | HG02735.hp2 HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.957+68T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86770193 | |||||||
| chr2:86770270 | T | C | 1 | a0001c0004t0021g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.957+145T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86770270 | |||||||
| chr2:86770425 | G | A | 218 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(215): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.957+300G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86770425 | |||||||
| chr2:86770510 | C | T | 1 | a0001c0001t0003g0085 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.957+385C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86770510 | |||||||
| chr2:86770532 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.957+407G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86770532 | |||||||
| chr2:86770614 | C | G | 1 | a0001c0001t0001g0191 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.957+489C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86770614 | |||||||
| chr2:86770648 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.957+523C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86770648 | |||||||
| chr2:86770860 | G | A | 1 | a0001c0004t0011g0055 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.958-698G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86770860 | |||||||
| chr2:86771010 | C | T | 14 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0090 others(11): Show |
18 | HG00642.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.958-548C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86771010 | |||||||
| chr2:86771090 | G | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(181): Show |
218 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.958-468G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86771090 | |||||||
| chr2:86771157 | G | A | 1 | a0001c0003t0001g0044 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.958-401G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86771157 | |||||||
| chr2:86771261 | C | G | 2 | a0001c0001t0001g0026 a0001c0001t0005g0026 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.958-297C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86771261 | |||||||
| chr2:86771444 | C | T | 3 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 |
3 | HG00738.hp2 HG00741.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.958-114C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86771444 | |||||||
| chr2:86771445 | A | T | 1 | a0001c0001t0001g0185 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.958-113A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86771445 | |||||||
| chr2:86771489 | A | G | 1 | a0001c0005t0010g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.958-69A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86771489 | |||||||
| chr2:86771536 | C | CT | 5 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(2): Show |
6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.958-6dupT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 86771536 | ||||||
| chr2:86771536 | CT | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(175): Show |
213 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
splice_region_variant&intron_variant | LOW | c.958-6delT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 86771536 | ||||||
| chr2:86771536 | CTT | C | 9 | a0001c0001t0001g0145 a0001c0001t0001g0168 a0001c0001t0003g0084 others(6): Show |
9 | HG01891.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.958-7_958-6delTT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 86771536 | ||||||
| chr2:86771749 | A | G | 4 | a0001c0004t0006g0029 a0001c0004t0006g0248 a0001c0004t0006g0249 others(1): Show |
5 | HG01167.hp1 HG02809.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1112+37A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | chr2 | 86771749 | |||||||
| chr2:86771759 | G | A | 1 | a0001c0004t0021g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1112+47G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | chr2 | 86771759 | |||||||
| chr2:86771818 | CTAAA | C | 27 | a0001c0003t0001g0002 a0001c0003t0001g0011 a0001c0003t0001g0012 others(24): Show |
33 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.1112+112_1112+115d others(6): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 86771818 | ||||||
| chr2:86772021 | G | A | 1 | a0001c0002t0002g0236 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1112+309G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | chr2 | 86772021 | |||||||
| chr2:86772048 | C | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(181): Show |
218 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1112+336C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | chr2 | 86772048 | |||||||
| chr2:86772168 | G | A | 1 | a0001c0004t0020g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1112+456G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | chr2 | 86772168 | |||||||
| chr2:86772224 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1112+512C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | chr2 | 86772224 | |||||||
| chr2:86772311 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1112+599C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | chr2 | 86772311 | |||||||
| chr2:86772323 | C | T | 1 | a0001c0002t0029g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1112+611C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | chr2 | 86772323 | |||||||
| chr2:86772379 | C | T | 5 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(2): Show |
6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1112+667C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | chr2 | 86772379 | |||||||
| chr2:86772695 | A | G | 2 | a0001c0002t0002g0110 a0001c0002t0002g0111 |
2 | NA18960.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1113-653A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | chr2 | 86772695 | |||||||
| chr2:86772739 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(98): Show |
116 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1113-609C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | chr2 | 86772739 | |||||||
| chr2:86772752 | A | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
227 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.1113-596A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | chr2 | 86772752 | |||||||
| chr2:86772877 | CA | C | 7 | a0001c0002t0030g0112 a0001c0004t0006g0029 a0001c0004t0006g0248 others(4): Show |
9 | HG01167.hp1 HG02109.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1113-467delA | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 86772877 | ||||||
| chr2:86772999 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1113-349C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | chr2 | 86772999 | |||||||
| chr2:86773264 | T | G | 24 | a0001c0002t0004g0015 a0001c0002t0004g0016 a0001c0002t0004g0017 others(21): Show |
27 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.1113-84T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | chr2 | 86773264 |