Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55005 |
| ensemblid | ENSG00000155906.20 |
| hgncid | 21176 |
| symbol | RMND1 |
| name | required for meiotic nuclear division 1 homolog |
| refseq_nuc | NM_017909.4 |
| refseq_prot | NP_060379.2 |
| ensembl_nuc | ENST00000444024.3 |
| ensembl_prot | ENSP00000412708.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 151404762 |
| end | 151452126 |
| strand | - |
| ver | v1.2 |
| region | chr6:151404762-151452126 |
| region5000 | chr6:151399762-151457126 |
| regionname0 | RMND1_chr6_151404762_151452126 |
| regionname5000 | RMND1_chr6_151399762_151457126 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 449 | 265 | 70 | 48 | 114 | 11 | 21 | 92 | RMND1_chr6_151399762_151457126 | RMND1 | MPATL others(444): Show |
chr6 | 151399762 | 151457126 |
| a0002 | 0/0 | 449 | 90 | 10 | 10 | 64 | 0 | 6 | 52 | RMND1_chr6_151399762_151457126 | RMND1 | MPATL others(444): Show |
chr6 | 151399762 | 151457126 |
| a0003 | 0/1 | 449 | 28 | 4 | 8 | 4 | 3 | 8 | 2 | RMND1_chr6_151399762_151457126 | RMND1 | MPATL others(444): Show |
chr6 | 151399762 | 151457126 |
| a0004 | 0/0 | 449 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | MPATL others(444): Show |
chr6 | 151399762 | 151457126 |
| a0005 | 0/0 | 449 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | MPATL others(444): Show |
chr6 | 151399762 | 151457126 |
| a0006 | 0/0 | 449 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | MPATL others(444): Show |
chr6 | 151399762 | 151457126 |
| a0007 | 0/0 | 449 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | MPATL others(444): Show |
chr6 | 151399762 | 151457126 |
| a0008 | 0/0 | 449 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | MPATL others(444): Show |
chr6 | 151399762 | 151457126 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1347 | 240 | 47 | 47 | 114 | 11 | 20 | RMND1_chr6_151399762_151457126 | RMND1 | ATGCC others(1342): Show |
chr6 | 151399762 | 151457126 | ||
| a0001c0004 | 0/0 | 1347 | 22 | 20 | 1 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | ATGCC others(1342): Show |
chr6 | 151399762 | 151457126 | ||
| a0001c0006 | 0/0 | 1347 | 3 | 3 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | ATGCC others(1342): Show |
chr6 | 151399762 | 151457126 | ||
| a0002c0002 | 0/0 | 1347 | 88 | 10 | 10 | 62 | 0 | 6 | RMND1_chr6_151399762_151457126 | RMND1 | ATGCC others(1342): Show |
chr6 | 151399762 | 151457126 | ||
| a0002c0007 | 0/0 | 1347 | 2 | 0 | 0 | 2 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | ATGCC others(1342): Show |
chr6 | 151399762 | 151457126 | ||
| a0003c0003 | 0/1 | 1347 | 27 | 3 | 8 | 4 | 3 | 8 | RMND1_chr6_151399762_151457126 | RMND1 | ATGCC others(1342): Show |
chr6 | 151399762 | 151457126 | ||
| a0003c0013 | 0/0 | 1347 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | ATGCC others(1342): Show |
chr6 | 151399762 | 151457126 | ||
| a0004c0005 | 0/0 | 1347 | 4 | 4 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | ATGCC others(1342): Show |
chr6 | 151399762 | 151457126 | ||
| a0004c0009 | 0/0 | 1347 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | ATGCC others(1342): Show |
chr6 | 151399762 | 151457126 | ||
| a0005c0011 | 0/0 | 1347 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | ATGCC others(1342): Show |
chr6 | 151399762 | 151457126 | ||
| a0006c0010 | 0/0 | 1347 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | ATGCC others(1342): Show |
chr6 | 151399762 | 151457126 | ||
| a0007c0008 | 0/0 | 1347 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | ATGCC others(1342): Show |
chr6 | 151399762 | 151457126 | ||
| a0008c0012 | 0/0 | 1347 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | ATGCC others(1342): Show |
chr6 | 151399762 | 151457126 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1952 | 60 | 17 | 4 | 31 | 2 | 6 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1947): Show |
chr6 | 151399762 | 151457126 |
| a0001c0001t0002 | 1/0 | 1948 | 127 | 23 | 30 | 54 | 7 | 12 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1943): Show |
chr6 | 151399762 | 151457126 |
| a0001c0001t0003 | 0/0 | 1952 | 42 | 1 | 12 | 26 | 1 | 2 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1947): Show |
chr6 | 151399762 | 151457126 |
| a0001c0001t0005 | 0/0 | 1952 | 6 | 6 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1947): Show |
chr6 | 151399762 | 151457126 |
| a0001c0001t0007 | 0/0 | 1948 | 3 | 0 | 1 | 1 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1943): Show |
chr6 | 151399762 | 151457126 |
| a0001c0001t0013 | 0/0 | 1952 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1947): Show |
chr6 | 151399762 | 151457126 |
| a0001c0001t0014 | 0/0 | 1952 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1947): Show |
chr6 | 151399762 | 151457126 |
| a0001c0004t0001 | 0/0 | 1952 | 16 | 15 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1947): Show |
chr6 | 151399762 | 151457126 |
| a0001c0004t0002 | 0/0 | 1948 | 2 | 2 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1943): Show |
chr6 | 151399762 | 151457126 |
| a0001c0004t0006 | 0/0 | 1952 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1947): Show |
chr6 | 151399762 | 151457126 |
| a0001c0004t0008 | 0/0 | 1952 | 2 | 2 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1947): Show |
chr6 | 151399762 | 151457126 |
| a0001c0004t0011 | 0/0 | 1952 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1947): Show |
chr6 | 151399762 | 151457126 |
| a0001c0006t0001 | 0/0 | 1952 | 2 | 2 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1947): Show |
chr6 | 151399762 | 151457126 |
| a0001c0006t0002 | 0/0 | 1948 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1943): Show |
chr6 | 151399762 | 151457126 |
| a0002c0002t0001 | 0/0 | 1952 | 68 | 7 | 8 | 48 | 0 | 5 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1947): Show |
chr6 | 151399762 | 151457126 |
| a0002c0002t0002 | 0/0 | 1948 | 19 | 3 | 2 | 13 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1943): Show |
chr6 | 151399762 | 151457126 |
| a0002c0002t0010 | 0/0 | 1952 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1947): Show |
chr6 | 151399762 | 151457126 |
| a0002c0007t0001 | 0/0 | 1952 | 2 | 0 | 0 | 2 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1947): Show |
chr6 | 151399762 | 151457126 |
| a0003c0003t0001 | 0/0 | 1952 | 2 | 2 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1947): Show |
chr6 | 151399762 | 151457126 |
| a0003c0003t0004 | 0/1 | 1948 | 20 | 0 | 6 | 2 | 3 | 8 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1943): Show |
chr6 | 151399762 | 151457126 |
| a0003c0003t0006 | 0/0 | 1952 | 4 | 0 | 2 | 2 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1947): Show |
chr6 | 151399762 | 151457126 |
| a0003c0003t0012 | 0/0 | 1952 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1947): Show |
chr6 | 151399762 | 151457126 |
| a0003c0013t0001 | 0/0 | 1952 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1947): Show |
chr6 | 151399762 | 151457126 |
| a0004c0005t0001 | 0/0 | 1952 | 3 | 3 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1947): Show |
chr6 | 151399762 | 151457126 |
| a0004c0005t0002 | 0/0 | 1948 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1943): Show |
chr6 | 151399762 | 151457126 |
| a0004c0009t0015 | 0/0 | 1952 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1947): Show |
chr6 | 151399762 | 151457126 |
| a0005c0011t0002 | 0/0 | 1948 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1943): Show |
chr6 | 151399762 | 151457126 |
| a0006c0010t0009 | 0/0 | 1948 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1943): Show |
chr6 | 151399762 | 151457126 |
| a0007c0008t0002 | 0/0 | 1948 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1943): Show |
chr6 | 151399762 | 151457126 |
| a0008c0012t0001 | 0/0 | 1952 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | AGGAG others(1947): Show |
chr6 | 151399762 | 151457126 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0003 | 1/0 | 3 | 0 | 2 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0003g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0005g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0007g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0007g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0007g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0013g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0001t0014g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0004t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0004t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0004t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0004t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0004t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0004t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0004t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0004t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0004t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0004t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0004t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0004t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0004t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0004t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0004t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0004t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0004t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0004t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0004t0006g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0004t0008g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0004t0008g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0004t0011g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0006t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0006t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0001c0006t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0002t0010g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0007t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0002c0007t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0003c0003t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0003c0003t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0003c0003t0004g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0003c0003t0004g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0003c0003t0004g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0003c0003t0004g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0003c0003t0004g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0003c0003t0004g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0003c0003t0004g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0003c0003t0004g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0003c0003t0004g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0003c0003t0004g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0003c0003t0004g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0003c0003t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0003c0003t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0003c0003t0004g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0003c0003t0004g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0003c0003t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0003c0003t0004g0042 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0003c0003t0004g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0003c0003t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0003c0003t0006g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0003c0003t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0003c0003t0006g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0003c0003t0006g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0003c0003t0012g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0003c0013t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0004c0005t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0004c0005t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0004c0005t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0004c0005t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0004c0009t0015g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0005c0011t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0006c0010t0009g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0007c0008t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| a0008c0012t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0168 | EUR | GBR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG00099 | hp2 | a0001 | c0001 | t0007 | g0330 | EUR | GBR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG00140 | hp1 | a0003 | c0003 | t0004 | g0031 | EUR | GBR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0291 | EUR | GBR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0278 | EUR | FIN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0323 | EUR | FIN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0078 | EAS | CHS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG00408 | hp2 | a0001 | c0001 | t0014 | g0339 | EAS | CHS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG00423 | hp1 | a0001 | c0001 | t0007 | g0347 | EAS | CHS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | CHS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0337 | EAS | CHS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0356 | EAS | CHS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0362 | EAS | CHS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | CHS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | CHS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | CHS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | CHS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0358 | EAS | CHS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0328 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0283 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0311 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0335 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0294 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01069 | hp2 | a0003 | c0003 | t0006 | g0039 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0272 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01071 | hp1 | a0003 | c0003 | t0006 | g0038 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0270 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0297 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0079 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0329 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01168 | hp2 | a0003 | c0003 | t0004 | g0004 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01169 | hp2 | a0003 | c0003 | t0004 | g0004 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01175 | hp1 | a0001 | c0004 | t0001 | g0182 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0324 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0287 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0123 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01255 | hp2 | a0003 | c0003 | t0004 | g0028 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0327 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01261 | hp1 | a0003 | c0003 | t0004 | g0034 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0331 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0068 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0280 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0325 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01433 | hp1 | a0003 | c0003 | t0004 | g0044 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0124 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01496 | hp1 | a0003 | c0003 | t0004 | g0030 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0326 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0020 | EUR | IBS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01515 | hp2 | a0003 | c0003 | t0004 | g0033 | EUR | IBS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | IBS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0018 | EUR | IBS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0281 | EUR | IBS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01517 | hp2 | a0003 | c0003 | t0004 | g0032 | EUR | IBS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01884 | hp1 | a0001 | c0004 | t0011 | g0181 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01884 | hp2 | a0003 | c0013 | t0001 | g0319 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01891 | hp2 | a0001 | c0004 | t0001 | g0315 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0341 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0296 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0271 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0130 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0293 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0228 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0131 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0067 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0359 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0086 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0052 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02040 | hp2 | a0003 | c0003 | t0006 | g0035 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02055 | hp1 | a0001 | c0004 | t0001 | g0250 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02055 | hp2 | a0001 | c0006 | t0001 | g0245 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0364 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0355 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0056 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02135 | hp2 | a0002 | c0002 | t0010 | g0057 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0354 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CDX | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | CDX | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02165 | hp1 | a0003 | c0003 | t0004 | g0041 | EAS | CDX | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CDX | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02257 | hp1 | a0001 | c0004 | t0001 | g0246 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02257 | hp2 | a0001 | c0004 | t0001 | g0183 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02258 | hp1 | a0004 | c0009 | t0015 | g0367 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0111 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0360 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0132 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0110 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0109 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0200 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02615 | hp1 | a0001 | c0004 | t0001 | g0187 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02647 | hp1 | a0001 | c0004 | t0001 | g0241 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02647 | hp2 | a0001 | c0006 | t0002 | g0244 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0064 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0224 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0066 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0259 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02735 | hp1 | a0003 | c0003 | t0004 | g0043 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0199 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0134 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0194 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02809 | hp1 | a0001 | c0004 | t0001 | g0240 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0317 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0077 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0104 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02896 | hp2 | a0002 | c0002 | t0002 | g0070 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0080 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02922 | hp2 | a0001 | c0004 | t0001 | g0249 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02965 | hp1 | a0001 | c0004 | t0008 | g0366 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0017 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0318 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0261 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0333 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03041 | hp1 | a0004 | c0005 | t0001 | g0256 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0103 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03098 | hp1 | a0001 | c0004 | t0002 | g0238 | AFR | MSL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03130 | hp1 | a0005 | c0011 | t0002 | g0251 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0236 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0017 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03195 | hp1 | a0001 | c0004 | t0008 | g0365 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0096 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0303 | AFR | MSL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03225 | hp2 | a0004 | c0005 | t0001 | g0255 | AFR | MSL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0188 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0180 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | MSL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03486 | hp1 | a0003 | c0003 | t0001 | g0308 | AFR | MSL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03490 | hp2 | a0003 | c0003 | t0004 | g0037 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03491 | hp1 | a0003 | c0003 | t0004 | g0024 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03491 | hp2 | a0003 | c0003 | t0004 | g0040 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03516 | hp1 | a0006 | c0010 | t0009 | g0306 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03579 | hp1 | a0001 | c0006 | t0001 | g0243 | AFR | MSL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0138 | AFR | MSL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03654 | hp1 | a0003 | c0003 | t0004 | g0029 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0295 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03704 | hp1 | a0003 | c0003 | t0004 | g0022 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0346 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0120 | SAS | BEB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0282 | SAS | BEB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03834 | hp1 | a0003 | c0003 | t0004 | g0026 | SAS | BEB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03834 | hp2 | a0007 | c0008 | t0002 | g0191 | SAS | BEB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03927 | hp1 | a0001 | c0004 | t0006 | g0023 | SAS | BEB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0121 | SAS | BEB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03942 | hp1 | a0003 | c0003 | t0004 | g0025 | SAS | BEB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0063 | SAS | BEB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0332 | SAS | STU | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | STU | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | BEB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0189 | SAS | BEB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0119 | SAS | STU | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0220 | SAS | STU | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18522 | hp1 | a0001 | c0004 | t0001 | g0184 | AFR | YRI | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18522 | hp2 | a0008 | c0012 | t0001 | g0239 | AFR | YRI | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | CHB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18906 | hp1 | a0004 | c0005 | t0001 | g0257 | AFR | YRI | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | YRI | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18941 | hp2 | a0003 | c0003 | t0006 | g0027 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0351 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0349 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0048 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0129 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18977 | hp2 | a0003 | c0003 | t0004 | g0036 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0353 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0050 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0357 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0334 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0350 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0322 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0344 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19006 | hp1 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19007 | hp2 | a0002 | c0007 | t0001 | g0113 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0363 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19030 | hp1 | a0001 | c0004 | t0001 | g0316 | AFR | LWK | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19030 | hp2 | a0001 | c0004 | t0001 | g0248 | AFR | LWK | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0054 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19063 | hp1 | a0002 | c0007 | t0001 | g0061 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19067 | hp1 | a0001 | c0001 | t0013 | g0338 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0352 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0343 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0345 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0361 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0336 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0342 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0348 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0321 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | YRI | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | YRI | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0288 | AFR | ASW | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA20129 | hp2 | a0001 | c0004 | t0002 | g0186 | AFR | ASW | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0211 | EUR | TSI | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0206 | EUR | TSI | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01123 | hp1 | a0001 | c0001 | t0007 | g0340 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02109 | hp1 | a0001 | c0004 | t0001 | g0314 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0258 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02486 | hp1 | a0001 | c0004 | t0001 | g0242 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02486 | hp2 | a0003 | c0003 | t0012 | g0262 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG02559 | hp2 | a0001 | c0004 | t0001 | g0247 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0260 | AFR | USA | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| HG06807 | hp2 | a0001 | c0004 | t0001 | g0185 | AFR | USA | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0298 | AFR | USA | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA20300 | hp2 | a0004 | c0005 | t0002 | g0305 | AFR | USA | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0098 | AFR | LWK | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| NA21309 | hp2 | a0003 | c0003 | t0001 | g0309 | AFR | LWK | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| homoSapiens | chm13v2 | a0003 | c0003 | t0004 | g0042 | REF | REF | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0003 | REF | REF | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:151405236 | C | T | 1 | a0001 | 6 | HG02717.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
stop_retained_variant | LOW | c.1349G>A | p.Ter450Ter | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 12/12 | 1474/1948 | 1349/1350 | 450/449 | chr6 | 151405236 | |||
| chr6:151422601 | T | G | 1 | a0005 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.942A>C | p.Lys314Asn | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 8/12 | 1067/1948 | 942/1350 | 314/449 | chr6 | 151422601 | |||
| chr6:151423604 | T | A | 1 | a0008 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.858A>T | p.Glu286Asp | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 7/12 | 983/1948 | 858/1350 | 286/449 | chr6 | 151423604 | |||
| chr6:151427517 | G | C | 1 | a0006 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.795C>G | p.His265Gln | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/12 | 920/1948 | 795/1350 | 265/449 | chr6 | 151427517 | |||
| chr6:151445417 | G | A | 1 | a0002 | 90 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(87): Show |
missense_variant | MODERATE | c.395C>T | p.Thr132Met | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/12 | 520/1948 | 395/1350 | 132/449 | chr6 | 151445417 | |||
| chr6:151445672 | C | T | 2 | a0004 a0006 |
6 | HG02258.hp1 HG03041.hp1 HG03225.hp2 others(3): Show |
missense_variant | MODERATE | c.140G>A | p.Arg47His | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/12 | 265/1948 | 140/1350 | 47/449 | chr6 | 151445672 | |||
| chr6:151445687 | C | A | 1 | a0003 | 27 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(24): Show |
missense_variant | MODERATE | c.125G>T | p.Ser42Ile | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/12 | 250/1948 | 125/1350 | 42/449 | chr6 | 151445687 | |||
| chr6:151445736 | C | T | 1 | a0007 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.76G>A | p.Gly26Ser | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/12 | 201/1948 | 76/1350 | 26/449 | chr6 | 151445736 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:151417312 | C | T | 2 | a0003c0013 a0004c0009 |
2 | HG01884.hp2 HG02258.hp1 |
synonymous_variant | LOW | c.1167G>A | p.Thr389Thr | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/12 | 1292/1948 | 1167/1350 | 389/449 | chr6 | 151417312 | |||
| chr6:151423607 | C | G | 1 | a0007c0008 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.855G>C | p.Gly285Gly | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 7/12 | 980/1948 | 855/1350 | 285/449 | chr6 | 151423607 | |||
| chr6:151427529 | G | A | 1 | a0001c0006 | 3 | HG02055.hp2 HG02647.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.783C>T | p.Ile261Ile | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/12 | 908/1948 | 783/1350 | 261/449 | chr6 | 151427529 | |||
| chr6:151445353 | G | A | 1 | a0002c0007 | 2 | NA19007.hp2 NA19063.hp1 |
synonymous_variant | LOW | c.459C>T | p.Thr153Thr | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/12 | 584/1948 | 459/1350 | 153/449 | chr6 | 151445353 | |||
| chr6:151445365 | T | C | 3 | a0001c0004 a0001c0006 a0008c0012 |
26 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
synonymous_variant | LOW | c.447A>G | p.Lys149Lys | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/12 | 572/1948 | 447/1350 | 149/449 | chr6 | 151445365 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:151404857 | A | G | 1 | a0006c0010t0009 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*378T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 12/12 | 378 | chr6 | 151404857 | ||||||
| chr6:151404858 | C | CATTT | 20 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(17): Show |
216 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*373_*376dupAAAT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 12/12 | 376 | chr6 | 151404858 | ||||||
| chr6:151404890 | A | G | 1 | a0002c0002t0010 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*345T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 12/12 | 345 | chr6 | 151404890 | ||||||
| chr6:151405010 | G | A | 1 | a0003c0003t0012 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*225C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 12/12 | 225 | chr6 | 151405010 | ||||||
| chr6:151405040 | G | T | 20 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(17): Show |
216 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*195C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 12/12 | 195 | chr6 | 151405040 | ||||||
| chr6:151405055 | G | A | 1 | a0001c0001t0014 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*180C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 12/12 | 180 | chr6 | 151405055 | ||||||
| chr6:151405165 | G | C | 19 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(16): Show |
215 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*70C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 12/12 | 70 | chr6 | 151405165 | ||||||
| chr6:151405167 | G | T | 1 | a0001c0001t0013 | 1 | NA19067.hp1 | 3_prime_UTR_variant | MODIFIER | c.*68C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 12/12 | 68 | chr6 | 151405167 | ||||||
| chr6:151405180 | T | G | 2 | a0001c0004t0011 a0003c0003t0012 |
2 | HG01884.hp1 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*55A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 12/12 | 55 | chr6 | 151405180 | ||||||
| chr6:151452029 | G | A | 4 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0013 others(1): Show |
47 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(44): Show |
5_prime_UTR_variant | MODIFIER | c.-28C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/12 | 6218 | chr6 | 151452029 | ||||||
| chr6:151452071 | C | G | 3 | a0001c0004t0006 a0003c0003t0004 a0003c0003t0006 |
24 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-70G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/12 | 6260 | chr6 | 151452071 | ||||||
| chr6:151452084 | G | A | 1 | a0001c0004t0008 | 2 | HG02965.hp1 HG03195.hp1 |
5_prime_UTR_variant | MODIFIER | c.-83C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/12 | 6273 | chr6 | 151452084 | ||||||
| chr6:151452121 | T | A | 1 | a0004c0009t0015 | 1 | HG02258.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-120A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/12 | chr6 | 151452121 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:151405315 | A | G | 1 | a0003c0013t0001g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1318-48T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 11/11 | chr6 | 151405315 | |||||||
| chr6:151405424 | T | G | 1 | a0001c0001t0002g0297 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1318-157A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 11/11 | chr6 | 151405424 | |||||||
| chr6:151405512 | T | C | 1 | a0002c0002t0002g0046 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1317+208A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 11/11 | chr6 | 151405512 | |||||||
| chr6:151405621 | T | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(198): Show |
214 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.1317+99A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 11/11 | chr6 | 151405621 | |||||||
| chr6:151405624 | G | C | 2 | a0001c0001t0002g0258 a0001c0001t0002g0303 |
2 | HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1317+96C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 11/11 | chr6 | 151405624 | |||||||
| chr6:151405694 | C | T | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(201): Show |
217 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.1317+26G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 11/11 | chr6 | 151405694 | |||||||
| chr6:151405951 | C | T | 10 | a0001c0001t0003g0021 a0001c0001t0003g0341 a0001c0001t0003g0349 others(7): Show |
11 | HG00408.hp2 HG00609.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.1201-115G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151405951 | |||||||
| chr6:151405995 | T | C | 1 | a0001c0004t0001g0242 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1201-159A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151405995 | |||||||
| chr6:151406073 | A | G | 2 | a0001c0004t0008g0365 a0001c0004t0008g0366 |
2 | HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1201-237T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406073 | |||||||
| chr6:151406119 | T | C | 2 | a0001c0004t0001g0187 a0001c0004t0001g0316 |
2 | HG02615.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1201-283A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406119 | |||||||
| chr6:151406188 | C | A | 1 | a0002c0002t0001g0132 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1201-352G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406188 | |||||||
| chr6:151406351 | CTTT | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(193): Show |
208 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.1201-518_1201-516d others(5): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406351 | |||||||
| chr6:151406356 | T | TTTG | 6 | a0001c0001t0005g0017 a0001c0001t0005g0138 a0001c0001t0005g0259 others(3): Show |
7 | HG02717.hp2 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1201-521_1201-520i others(5): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406356 | |||||||
| chr6:151406359 | T | G | 9 | a0001c0001t0005g0017 a0001c0001t0005g0138 a0001c0001t0005g0259 others(6): Show |
10 | HG02717.hp2 HG02965.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.1201-523A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406359 | |||||||
| chr6:151406364 | T | C | 2 | a0001c0001t0001g0149 a0001c0001t0001g0156 |
2 | HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1201-528A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406364 | |||||||
| chr6:151406382 | G | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(201): Show |
217 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.1201-546C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406382 | |||||||
| chr6:151406410 | C | T | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(237): Show |
257 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.1201-574G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406410 | |||||||
| chr6:151406423 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1201-587G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406423 | |||||||
| chr6:151406447 | T | C | 143 | a0001c0001t0001g0002 a0001c0001t0001g0092 a0001c0001t0001g0143 others(140): Show |
148 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.1201-611A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406447 | |||||||
| chr6:151406458 | A | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(199): Show |
215 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.1201-622T>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406458 | |||||||
| chr6:151406522 | C | T | 1 | a0003c0003t0001g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1201-686G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406522 | |||||||
| chr6:151406523 | G | A | 5 | a0001c0001t0002g0016 a0001c0001t0002g0236 a0001c0001t0002g0237 others(2): Show |
6 | HG02572.hp1 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1201-687C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406523 | |||||||
| chr6:151406561 | A | G | 1 | a0001c0001t0002g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1201-725T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406561 | |||||||
| chr6:151406937 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1201-1101G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406937 | |||||||
| chr6:151406958 | G | C | 2 | a0002c0002t0001g0056 a0002c0002t0010g0057 |
2 | HG02132.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.1201-1122C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406958 | |||||||
| chr6:151407049 | A | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(204): Show |
220 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.1201-1213T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407049 | |||||||
| chr6:151407163 | A | C | 6 | a0001c0001t0005g0017 a0001c0001t0005g0138 a0001c0001t0005g0259 others(3): Show |
7 | HG02717.hp2 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1201-1327T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407163 | |||||||
| chr6:151407164 | CTG | C | 3 | a0001c0001t0002g0009 a0001c0001t0002g0150 a0001c0001t0002g0318 |
4 | HG02280.hp2 HG02723.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1201-1330_1201-132 others(6): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407164 | |||||||
| chr6:151407183 | A | G | 2 | a0001c0001t0002g0147 a0001c0001t0002g0235 |
2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1201-1347T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407183 | |||||||
| chr6:151407268 | A | G | 1 | a0003c0003t0001g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1201-1432T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407268 | |||||||
| chr6:151407337 | T | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(198): Show |
214 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.1201-1501A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407337 | |||||||
| chr6:151407531 | C | T | 1 | a0004c0009t0015g0367 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1201-1695G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407531 | |||||||
| chr6:151407579 | T | C | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(244): Show |
265 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.1201-1743A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407579 | |||||||
| chr6:151407615 | A | G | 7 | a0001c0001t0005g0017 a0001c0001t0005g0138 a0001c0001t0005g0259 others(4): Show |
8 | HG00423.hp1 HG02717.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1201-1779T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407615 | |||||||
| chr6:151407689 | C | T | 2 | a0001c0001t0001g0232 a0002c0002t0001g0045 |
2 | NA18982.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1201-1853G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407689 | |||||||
| chr6:151407732 | C | A | 1 | a0001c0001t0007g0347 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1201-1896G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407732 | |||||||
| chr6:151407764 | C | T | 1 | a0001c0001t0002g0266 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1201-1928G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407764 | |||||||
| chr6:151407765 | G | A | 1 | a0003c0003t0001g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1201-1929C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407765 | |||||||
| chr6:151407835 | C | T | 3 | a0002c0002t0001g0085 a0002c0002t0001g0098 a0002c0002t0002g0079 |
3 | HG00609.hp2 HG01109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1201-1999G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407835 | |||||||
| chr6:151407866 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1201-2030C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407866 | |||||||
| chr6:151407868 | G | A | 1 | a0002c0002t0001g0062 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1201-2032C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407868 | |||||||
| chr6:151407918 | A | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(216): Show |
234 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.1201-2082T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407918 | |||||||
| chr6:151407920 | A | C | 43 | a0001c0001t0001g0008 a0001c0001t0001g0142 a0001c0001t0001g0299 others(40): Show |
46 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.1201-2084T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407920 | |||||||
| chr6:151407949 | CTATT | C | 3 | a0001c0001t0002g0205 a0001c0001t0002g0300 a0001c0001t0002g0307 |
3 | NA18954.hp1 NA18965.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1201-2117_1201-211 others(8): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407949 | |||||||
| chr6:151407978 | C | T | 1 | a0001c0001t0002g0265 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1201-2142G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407978 | |||||||
| chr6:151408102 | T | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(228): Show |
248 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.1201-2266A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151408102 | |||||||
| chr6:151408104 | G | A | 1 | a0006c0010t0009g0306 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1201-2268C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151408104 | |||||||
| chr6:151408161 | T | C | 1 | a0002c0002t0001g0058 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1201-2325A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151408161 | |||||||
| chr6:151408220 | G | A | 2 | a0003c0003t0012g0262 a0004c0009t0015g0367 |
2 | HG02258.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1201-2384C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151408220 | |||||||
| chr6:151408221 | G | A | 1 | a0004c0009t0015g0367 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1201-2385C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151408221 | |||||||
| chr6:151408265 | C | A | 7 | a0001c0001t0001g0157 a0001c0001t0005g0138 a0001c0001t0005g0259 others(4): Show |
7 | HG02717.hp2 HG03041.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1201-2429G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151408265 | |||||||
| chr6:151408270 | G | A | 1 | a0001c0004t0002g0238 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1201-2434C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151408270 | |||||||
| chr6:151408321 | G | A | 3 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0210 |
3 | HG02809.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1201-2485C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151408321 | |||||||
| chr6:151408424 | G | A | 1 | a0003c0003t0004g0004 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1201-2588C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151408424 | |||||||
| chr6:151408446 | C | G | 152 | a0001c0001t0001g0002 a0001c0001t0001g0092 a0001c0001t0001g0143 others(149): Show |
158 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1201-2610G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151408446 | |||||||
| chr6:151408492 | T | A | 3 | a0001c0001t0002g0270 a0001c0001t0002g0272 a0001c0001t0002g0311 |
3 | HG00735.hp2 HG01070.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.1201-2656A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151408492 | |||||||
| chr6:151408682 | A | G | 1 | a0003c0003t0012g0262 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1201-2846T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151408682 | |||||||
| chr6:151408716 | G | A | 1 | a0001c0001t0007g0340 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1201-2880C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151408716 | |||||||
| chr6:151408910 | A | G | 6 | a0001c0001t0002g0226 a0001c0001t0002g0270 a0001c0001t0002g0272 others(3): Show |
6 | HG00735.hp2 HG01070.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.1201-3074T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151408910 | |||||||
| chr6:151409031 | C | A | 2 | a0003c0003t0004g0022 a0003c0003t0004g0043 |
2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1201-3195G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151409031 | |||||||
| chr6:151409097 | C | G | 30 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(27): Show |
36 | HG00099.hp1 HG01074.hp1 HG01516.hp1 others(33): Show |
intron_variant | MODIFIER | c.1201-3261G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151409097 | |||||||
| chr6:151409231 | G | A | 1 | a0002c0002t0001g0128 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1201-3395C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151409231 | |||||||
| chr6:151409307 | T | G | 3 | a0002c0002t0001g0080 a0002c0002t0001g0103 a0002c0002t0001g0104 |
3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1201-3471A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151409307 | |||||||
| chr6:151409480 | G | T | 1 | a0001c0001t0002g0276 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1201-3644C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151409480 | |||||||
| chr6:151409481 | T | G | 1 | a0001c0001t0002g0276 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1201-3645A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151409481 | |||||||
| chr6:151409606 | C | T | 1 | a0004c0009t0015g0367 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1201-3770G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151409606 | |||||||
| chr6:151409649 | A | G | 124 | a0001c0001t0001g0092 a0001c0001t0001g0143 a0001c0001t0001g0148 others(121): Show |
126 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.1201-3813T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151409649 | |||||||
| chr6:151409667 | C | T | 162 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(159): Show |
173 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.1201-3831G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151409667 | |||||||
| chr6:151409719 | C | G | 1 | a0002c0002t0001g0071 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1201-3883G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151409719 | |||||||
| chr6:151409768 | A | G | 27 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(24): Show |
33 | HG00099.hp1 HG00609.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.1201-3932T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151409768 | |||||||
| chr6:151409796 | A | G | 1 | a0002c0002t0001g0085 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1201-3960T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151409796 | |||||||
| chr6:151409812 | C | T | 1 | a0002c0002t0001g0119 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1201-3976G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151409812 | |||||||
| chr6:151410041 | C | T | 1 | a0002c0002t0001g0058 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1201-4205G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410041 | |||||||
| chr6:151410057 | A | AT | 159 | a0001c0001t0001g0092 a0001c0001t0001g0143 a0001c0001t0001g0149 others(156): Show |
165 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1201-4222dupA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410057 | |||||||
| chr6:151410057 | A | ATT | 12 | a0001c0001t0002g0258 a0001c0001t0002g0303 a0001c0001t0003g0321 others(9): Show |
12 | HG01433.hp2 HG01884.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1201-4223_1201-422 others(6): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410057 | |||||||
| chr6:151410057 | AT | A | 6 | a0001c0001t0002g0268 a0001c0001t0002g0273 a0001c0001t0002g0275 others(3): Show |
6 | HG03834.hp1 NA18955.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1201-4222delA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410057 | |||||||
| chr6:151410076 | G | A | 1 | a0001c0001t0002g0222 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1201-4240C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410076 | |||||||
| chr6:151410085 | T | C | 6 | a0001c0001t0002g0204 a0001c0001t0002g0265 a0001c0001t0002g0267 others(3): Show |
6 | NA18956.hp2 NA18963.hp1 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.1201-4249A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410085 | |||||||
| chr6:151410093 | C | G | 46 | a0001c0001t0001g0304 a0001c0001t0002g0179 a0001c0001t0002g0198 others(43): Show |
47 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.1201-4257G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410093 | |||||||
| chr6:151410094 | A | G | 7 | a0001c0001t0002g0019 a0001c0001t0002g0205 a0001c0001t0002g0222 others(4): Show |
8 | HG02074.hp1 NA18747.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1201-4258T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410094 | |||||||
| chr6:151410106 | C | G | 46 | a0001c0001t0001g0168 a0001c0001t0001g0174 a0001c0001t0002g0201 others(43): Show |
48 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.1201-4270G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410106 | |||||||
| chr6:151410124 | C | G | 1 | a0001c0001t0002g0196 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1201-4288G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410124 | |||||||
| chr6:151410155 | C | T | 2 | a0001c0001t0001g0142 a0002c0002t0001g0098 |
2 | HG02886.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1201-4319G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410155 | |||||||
| chr6:151410198 | A | G | 8 | a0001c0001t0001g0302 a0001c0001t0002g0236 a0001c0001t0002g0237 others(5): Show |
8 | HG02257.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1201-4362T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410198 | |||||||
| chr6:151410199 | C | T | 1 | a0003c0003t0004g0034 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1201-4363G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410199 | |||||||
| chr6:151410211 | C | T | 1 | a0001c0004t0001g0250 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1201-4375G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410211 | |||||||
| chr6:151410212 | G | A | 1 | a0002c0002t0001g0106 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1201-4376C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410212 | |||||||
| chr6:151410246 | G | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(143): Show |
154 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.1201-4410C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410246 | |||||||
| chr6:151410251 | C | T | 2 | a0002c0002t0001g0127 a0002c0002t0002g0107 |
2 | HG02129.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.1201-4415G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410251 | |||||||
| chr6:151410257 | A | G | 1 | a0002c0002t0001g0127 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1201-4421T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410257 | |||||||
| chr6:151410262 | A | G | 14 | a0001c0006t0001g0243 a0001c0006t0001g0245 a0001c0006t0002g0244 others(11): Show |
15 | HG02040.hp1 HG02055.hp2 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.1201-4426T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410262 | |||||||
| chr6:151410276 | G | C | 6 | a0001c0001t0002g0019 a0001c0001t0002g0274 a0001c0001t0002g0285 others(3): Show |
7 | HG02074.hp1 NA18946.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1201-4440C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410276 | |||||||
| chr6:151410284 | T | C | 1 | a0003c0003t0004g0026 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1201-4448A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410284 | |||||||
| chr6:151410290 | T | C | 25 | a0001c0001t0002g0009 a0001c0001t0002g0150 a0001c0001t0002g0172 others(22): Show |
27 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1201-4454A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410290 | |||||||
| chr6:151410297 | C | T | 3 | a0001c0001t0002g0016 a0001c0001t0002g0236 a0001c0001t0002g0237 |
4 | HG02572.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1201-4461G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410297 | |||||||
| chr6:151410298 | G | A | 1 | a0002c0002t0002g0107 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1201-4462C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410298 | |||||||
| chr6:151410302 | T | G | 2 | a0001c0001t0002g0267 a0001c0004t0002g0186 |
2 | NA18994.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1201-4466A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410302 | |||||||
| chr6:151410306 | T | C | 1 | a0001c0001t0002g0267 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1201-4470A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410306 | |||||||
| chr6:151410318 | A | G | 1 | a0007c0008t0002g0191 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1201-4482T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410318 | |||||||
| chr6:151410335 | A | G | 13 | a0001c0001t0001g0162 a0001c0001t0002g0010 a0001c0001t0002g0151 others(10): Show |
14 | HG01109.hp1 HG01884.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.1201-4499T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410335 | |||||||
| chr6:151410344 | C | T | 70 | a0001c0001t0001g0148 a0001c0001t0002g0212 a0001c0001t0002g0296 others(67): Show |
73 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.1201-4508G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410344 | |||||||
| chr6:151410346 | C | T | 1 | a0002c0002t0001g0120 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1201-4510G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410346 | |||||||
| chr6:151410347 | A | G | 1 | a0002c0002t0001g0120 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1201-4511T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410347 | |||||||
| chr6:151410347 | ACCCGGC | A | 4 | a0001c0001t0002g0193 a0001c0001t0002g0218 a0001c0001t0002g0223 others(1): Show |
4 | NA18961.hp1 NA18975.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1201-4517_1201-451 others(10): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410347 | |||||||
| chr6:151410440 | C | T | 1 | a0003c0003t0001g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1201-4604G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410440 | |||||||
| chr6:151410580 | T | C | 1 | a0001c0001t0002g0180 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1201-4744A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410580 | |||||||
| chr6:151410814 | C | T | 2 | a0001c0001t0001g0092 a0002c0002t0001g0085 |
2 | HG00609.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1201-4978G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410814 | |||||||
| chr6:151410838 | C | T | 39 | a0001c0001t0001g0304 a0001c0001t0002g0009 a0001c0001t0002g0150 others(36): Show |
41 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1201-5002G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410838 | |||||||
| chr6:151410882 | C | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(247): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1201-5046G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410882 | |||||||
| chr6:151410982 | A | G | 60 | a0001c0001t0001g0304 a0001c0001t0002g0009 a0001c0001t0002g0150 others(57): Show |
63 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.1201-5146T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410982 | |||||||
| chr6:151411100 | C | A | 4 | a0001c0001t0001g0304 a0004c0005t0001g0255 a0004c0005t0001g0256 others(1): Show |
4 | HG03041.hp1 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1201-5264G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151411100 | |||||||
| chr6:151411250 | T | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(248): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1201-5414A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151411250 | |||||||
| chr6:151411765 | A | G | 43 | a0001c0001t0001g0304 a0001c0001t0002g0009 a0001c0001t0002g0010 others(40): Show |
46 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.1200+5514T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151411765 | |||||||
| chr6:151411820 | G | A | 2 | a0001c0001t0001g0233 a0001c0001t0001g0254 |
2 | HG02683.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1200+5459C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151411820 | |||||||
| chr6:151411884 | C | T | 1 | a0001c0001t0003g0321 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1200+5395G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151411884 | |||||||
| chr6:151411914 | T | C | 1 | a0001c0004t0008g0365 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1200+5365A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151411914 | |||||||
| chr6:151411951 | C | T | 1 | a0001c0001t0002g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1200+5328G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151411951 | |||||||
| chr6:151412078 | C | T | 40 | a0001c0001t0001g0304 a0001c0001t0002g0009 a0001c0001t0002g0150 others(37): Show |
42 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.1200+5201G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412078 | |||||||
| chr6:151412091 | C | A | 1 | a0001c0001t0002g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1200+5188G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412091 | |||||||
| chr6:151412141 | A | G | 9 | a0001c0001t0002g0059 a0001c0001t0002g0076 a0001c0001t0002g0088 others(6): Show |
9 | HG02155.hp2 NA18942.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.1200+5138T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412141 | |||||||
| chr6:151412209 | C | T | 1 | a0001c0001t0002g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1200+5070G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412209 | |||||||
| chr6:151412254 | G | A | 1 | a0001c0001t0003g0359 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1200+5025C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412254 | |||||||
| chr6:151412317 | AT | A | 55 | a0001c0001t0002g0163 a0001c0001t0002g0166 a0001c0001t0002g0231 others(52): Show |
56 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.1200+4961delA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412317 | |||||||
| chr6:151412317 | ATT | A | 24 | a0001c0001t0001g0148 a0001c0001t0002g0258 a0001c0001t0002g0303 others(21): Show |
25 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1200+4960_1200+496 others(6): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412317 | |||||||
| chr6:151412448 | T | C | 115 | a0001c0001t0001g0148 a0001c0001t0001g0304 a0001c0001t0002g0009 others(112): Show |
119 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1200+4831A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412448 | |||||||
| chr6:151412514 | A | G | 3 | a0002c0002t0001g0080 a0002c0002t0001g0103 a0002c0002t0001g0104 |
3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1200+4765T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412514 | |||||||
| chr6:151412598 | A | G | 3 | a0002c0002t0001g0080 a0002c0002t0001g0103 a0002c0002t0001g0104 |
3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1200+4681T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412598 | |||||||
| chr6:151412674 | A | G | 7 | a0001c0001t0002g0180 a0001c0001t0002g0194 a0001c0001t0002g0196 others(4): Show |
7 | HG00639.hp1 HG02602.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1200+4605T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412674 | |||||||
| chr6:151412695 | T | C | 1 | a0001c0001t0001g0161 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1200+4584A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412695 | |||||||
| chr6:151412784 | C | T | 1 | a0004c0009t0015g0367 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1200+4495G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412784 | |||||||
| chr6:151412830 | G | T | 28 | a0001c0001t0001g0148 a0001c0001t0002g0258 a0001c0001t0002g0303 others(25): Show |
29 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1200+4449C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412830 | |||||||
| chr6:151412875 | C | T | 2 | a0002c0002t0001g0093 a0002c0002t0001g0137 |
2 | NA18985.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1200+4404G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412875 | |||||||
| chr6:151412916 | C | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(133): Show |
148 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.1200+4363G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412916 | |||||||
| chr6:151412916 | C | G | 1 | a0001c0001t0002g0278 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1200+4363G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412916 | |||||||
| chr6:151412926 | C | T | 35 | a0001c0001t0001g0304 a0001c0001t0002g0009 a0001c0001t0002g0150 others(32): Show |
37 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1200+4353G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412926 | |||||||
| chr6:151412999 | T | TA | 96 | a0001c0001t0001g0092 a0001c0001t0001g0143 a0001c0001t0001g0149 others(93): Show |
99 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.1200+4279dupT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412999 | |||||||
| chr6:151413062 | C | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(133): Show |
148 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.1200+4217G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151413062 | |||||||
| chr6:151413064 | T | A | 115 | a0001c0001t0001g0148 a0001c0001t0001g0304 a0001c0001t0002g0009 others(112): Show |
119 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1200+4215A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151413064 | |||||||
| chr6:151413296 | G | A | 2 | a0001c0004t0001g0247 a0003c0003t0012g0262 |
2 | HG02486.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1200+3983C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151413296 | |||||||
| chr6:151413428 | T | C | 115 | a0001c0001t0001g0148 a0001c0001t0001g0304 a0001c0001t0002g0009 others(112): Show |
119 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1200+3851A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151413428 | |||||||
| chr6:151413593 | A | C | 1 | a0001c0004t0002g0186 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1200+3686T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151413593 | |||||||
| chr6:151413728 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1200+3551A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151413728 | |||||||
| chr6:151413760 | C | T | 115 | a0001c0001t0001g0148 a0001c0001t0001g0304 a0001c0001t0002g0009 others(112): Show |
119 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1200+3519G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151413760 | |||||||
| chr6:151413863 | T | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(44): Show |
56 | HG00099.hp1 HG01074.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.1200+3416A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151413863 | |||||||
| chr6:151413866 | C | T | 1 | a0001c0001t0002g0291 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1200+3413G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151413866 | |||||||
| chr6:151413877 | G | C | 7 | a0001c0001t0001g0277 a0001c0001t0002g0226 a0001c0001t0002g0270 others(4): Show |
7 | HG00735.hp2 HG01070.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.1200+3402C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151413877 | |||||||
| chr6:151414244 | T | A | 2 | a0001c0001t0002g0264 a0001c0001t0002g0287 |
2 | HG01243.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1200+3035A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151414244 | |||||||
| chr6:151414483 | C | G | 1 | a0002c0002t0001g0094 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1200+2796G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151414483 | |||||||
| chr6:151414492 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1200+2787C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151414492 | |||||||
| chr6:151414643 | T | C | 115 | a0001c0001t0001g0148 a0001c0001t0001g0304 a0001c0001t0002g0009 others(112): Show |
119 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1200+2636A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151414643 | |||||||
| chr6:151414747 | A | G | 52 | a0001c0001t0003g0021 a0001c0001t0003g0320 a0001c0001t0003g0321 others(49): Show |
53 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.1200+2532T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151414747 | |||||||
| chr6:151414929 | T | C | 7 | a0001c0004t0001g0240 a0001c0004t0001g0241 a0001c0004t0001g0242 others(4): Show |
7 | HG02055.hp1 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1200+2350A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151414929 | |||||||
| chr6:151414949 | G | T | 251 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(248): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1200+2330C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151414949 | |||||||
| chr6:151415049 | GA | G | 74 | a0001c0001t0001g0148 a0001c0001t0002g0258 a0001c0001t0002g0303 others(71): Show |
76 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.1200+2229delT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415049 | |||||||
| chr6:151415185 | A | G | 2 | a0001c0001t0005g0017 a0001c0001t0005g0261 |
3 | HG02965.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1200+2094T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415185 | |||||||
| chr6:151415234 | A | T | 1 | a0001c0001t0002g0211 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1200+2045T>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415234 | |||||||
| chr6:151415281 | C | CT | 28 | a0001c0001t0001g0148 a0001c0001t0002g0258 a0001c0001t0002g0303 others(25): Show |
29 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1200+1997dupA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415281 | |||||||
| chr6:151415302 | A | G | 1 | a0001c0001t0007g0330 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1200+1977T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415302 | |||||||
| chr6:151415782 | G | C | 2 | a0002c0002t0001g0133 a0002c0002t0002g0129 |
2 | NA18950.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1200+1497C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415782 | |||||||
| chr6:151415792 | C | CA | 17 | a0001c0001t0001g0227 a0001c0001t0002g0020 a0001c0001t0002g0189 others(14): Show |
18 | HG00423.hp2 HG00621.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.1200+1486dupT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415792 | |||||||
| chr6:151415792 | CA | C | 6 | a0001c0001t0001g0161 a0001c0001t0001g0207 a0001c0001t0001g0208 others(3): Show |
6 | HG02735.hp2 HG02809.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1200+1486delT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415792 | |||||||
| chr6:151415792 | CAA | C | 9 | a0001c0001t0001g0164 a0001c0001t0003g0331 a0001c0001t0003g0332 others(6): Show |
9 | HG00609.hp1 HG01261.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1200+1485_1200+148 others(6): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415792 | |||||||
| chr6:151415792 | CAAA | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(143): Show |
159 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.1200+1484_1200+148 others(7): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415792 | |||||||
| chr6:151415792 | CAAAA | C | 93 | a0001c0001t0001g0174 a0001c0001t0001g0304 a0001c0001t0002g0009 others(90): Show |
96 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.1200+1483_1200+148 others(8): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415792 | |||||||
| chr6:151415874 | G | A | 1 | a0003c0003t0004g0025 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1200+1405C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415874 | |||||||
| chr6:151415888 | C | G | 35 | a0001c0001t0001g0304 a0001c0001t0002g0009 a0001c0001t0002g0150 others(32): Show |
37 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1200+1391G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415888 | |||||||
| chr6:151415963 | A | G | 1 | a0002c0002t0001g0108 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1200+1316T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415963 | |||||||
| chr6:151415988 | G | GT | 43 | a0001c0001t0001g0304 a0001c0001t0002g0009 a0001c0001t0002g0150 others(40): Show |
45 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.1200+1290dupA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415988 | |||||||
| chr6:151416042 | G | T | 30 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(27): Show |
36 | HG00099.hp1 HG01074.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.1200+1237C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151416042 | |||||||
| chr6:151416171 | G | C | 1 | a0002c0002t0001g0072 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1200+1108C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151416171 | |||||||
| chr6:151416270 | G | A | 2 | a0001c0001t0001g0227 a0002c0002t0001g0075 |
2 | NA18952.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1200+1009C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151416270 | |||||||
| chr6:151416420 | C | CT | 12 | a0001c0001t0001g0141 a0001c0001t0001g0161 a0001c0001t0001g0253 others(9): Show |
12 | HG01433.hp2 HG02132.hp1 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.1200+858dupA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151416420 | |||||||
| chr6:151416420 | CT | C | 113 | a0001c0001t0001g0002 a0001c0001t0001g0207 a0001c0001t0001g0208 others(110): Show |
120 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.1200+858delA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151416420 | |||||||
| chr6:151416420 | CTT | C | 69 | a0001c0001t0001g0148 a0001c0001t0001g0304 a0001c0001t0002g0009 others(66): Show |
72 | HG00140.hp1 HG01069.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.1200+857_1200+858d others(4): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151416420 | |||||||
| chr6:151416446 | C | T | 5 | a0001c0001t0001g0148 a0001c0004t0001g0185 a0001c0004t0001g0314 others(2): Show |
5 | HG01891.hp2 HG02109.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1200+833G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151416446 | |||||||
| chr6:151416487 | G | A | 1 | a0001c0001t0003g0362 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1200+792C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151416487 | |||||||
| chr6:151416754 | A | G | 2 | a0001c0004t0001g0182 a0001c0004t0001g0183 |
2 | HG01175.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1200+525T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151416754 | |||||||
| chr6:151416755 | C | T | 1 | a0003c0003t0001g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1200+524G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151416755 | |||||||
| chr6:151416865 | C | T | 1 | a0001c0001t0002g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1200+414G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151416865 | |||||||
| chr6:151416870 | C | G | 8 | a0001c0004t0008g0365 a0001c0004t0008g0366 a0002c0002t0001g0080 others(5): Show |
8 | HG01884.hp2 HG02258.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1200+409G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151416870 | |||||||
| chr6:151416911 | G | A | 1 | a0006c0010t0009g0306 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1200+368C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151416911 | |||||||
| chr6:151416996 | A | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(248): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1200+283T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151416996 | |||||||
| chr6:151417235 | C | T | 1 | a0001c0001t0002g0211 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1200+44G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151417235 | |||||||
| chr6:151417241 | C | T | 21 | a0001c0001t0001g0148 a0001c0004t0001g0182 a0001c0004t0001g0183 others(18): Show |
21 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1200+38G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151417241 | |||||||
| chr6:151417431 | A | G | 35 | a0001c0001t0001g0304 a0001c0001t0002g0009 a0001c0001t0002g0150 others(32): Show |
37 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1080-32T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151417431 | |||||||
| chr6:151417492 | CT | C | 35 | a0001c0001t0001g0304 a0001c0001t0002g0009 a0001c0001t0002g0150 others(32): Show |
37 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1080-94delA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151417492 | |||||||
| chr6:151417719 | A | G | 43 | a0001c0001t0001g0304 a0001c0001t0002g0009 a0001c0001t0002g0150 others(40): Show |
45 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.1080-320T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151417719 | |||||||
| chr6:151417816 | T | A | 180 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(177): Show |
193 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1080-417A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151417816 | |||||||
| chr6:151417816 | T | TA | 43 | a0001c0001t0001g0304 a0001c0001t0002g0009 a0001c0001t0002g0150 others(40): Show |
45 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.1080-418_1080-417i others(3): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151417816 | |||||||
| chr6:151417817 | T | A | 28 | a0001c0001t0001g0148 a0001c0001t0002g0258 a0001c0001t0002g0303 others(25): Show |
29 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1080-418A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151417817 | |||||||
| chr6:151417895 | G | A | 28 | a0001c0001t0001g0148 a0001c0001t0002g0258 a0001c0001t0002g0303 others(25): Show |
29 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1080-496C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151417895 | |||||||
| chr6:151418021 | G | A | 8 | a0001c0004t0008g0365 a0001c0004t0008g0366 a0002c0002t0001g0080 others(5): Show |
8 | HG01884.hp2 HG02258.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1080-622C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418021 | |||||||
| chr6:151418026 | G | A | 25 | a0001c0001t0002g0009 a0001c0001t0002g0150 a0001c0001t0002g0172 others(22): Show |
27 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1080-627C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418026 | |||||||
| chr6:151418048 | T | C | 5 | a0001c0004t0008g0365 a0001c0004t0008g0366 a0003c0003t0001g0309 others(2): Show |
5 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1080-649A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418048 | |||||||
| chr6:151418052 | T | C | 71 | a0001c0001t0001g0148 a0001c0001t0001g0304 a0001c0001t0002g0009 others(68): Show |
74 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(71): Show |
intron_variant | MODIFIER | c.1080-653A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418052 | |||||||
| chr6:151418109 | A | G | 71 | a0001c0001t0001g0148 a0001c0001t0001g0304 a0001c0001t0002g0009 others(68): Show |
74 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(71): Show |
intron_variant | MODIFIER | c.1080-710T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418109 | |||||||
| chr6:151418171 | T | C | 2 | a0003c0013t0001g0319 a0004c0009t0015g0367 |
2 | HG01884.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1080-772A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418171 | |||||||
| chr6:151418178 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(88): Show |
101 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1080-779G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418178 | |||||||
| chr6:151418272 | G | A | 3 | a0002c0002t0001g0080 a0002c0002t0001g0103 a0002c0002t0001g0104 |
3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1080-873C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418272 | |||||||
| chr6:151418369 | G | A | 3 | a0002c0002t0001g0080 a0002c0002t0001g0103 a0002c0002t0001g0104 |
3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1080-970C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418369 | |||||||
| chr6:151418417 | T | TA | 38 | a0001c0001t0001g0148 a0001c0001t0002g0258 a0001c0001t0002g0303 others(35): Show |
39 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.1080-1019dupT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418417 | |||||||
| chr6:151418417 | T | TAA | 32 | a0001c0001t0001g0304 a0001c0001t0002g0009 a0001c0001t0002g0150 others(29): Show |
34 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1080-1020_1080-101 others(6): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418417 | |||||||
| chr6:151418460 | T | A | 71 | a0001c0001t0001g0148 a0001c0001t0001g0304 a0001c0001t0002g0009 others(68): Show |
74 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(71): Show |
intron_variant | MODIFIER | c.1080-1061A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418460 | |||||||
| chr6:151418466 | A | T | 3 | a0002c0002t0001g0080 a0002c0002t0001g0103 a0002c0002t0001g0104 |
3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1080-1067T>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418466 | |||||||
| chr6:151418507 | G | A | 251 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(248): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1080-1108C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418507 | |||||||
| chr6:151418675 | G | T | 251 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(248): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1080-1276C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418675 | |||||||
| chr6:151418825 | T | C | 71 | a0001c0001t0001g0148 a0001c0001t0001g0304 a0001c0001t0002g0009 others(68): Show |
74 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(71): Show |
intron_variant | MODIFIER | c.1080-1426A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418825 | |||||||
| chr6:151418833 | C | T | 1 | a0001c0004t0001g0187 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1080-1434G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418833 | |||||||
| chr6:151418858 | C | A | 1 | a0001c0001t0002g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1080-1459G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418858 | |||||||
| chr6:151418871 | A | G | 1 | a0001c0001t0002g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1080-1472T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418871 | |||||||
| chr6:151418928 | G | A | 1 | a0001c0004t0008g0366 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1080-1529C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418928 | |||||||
| chr6:151418946 | T | C | 6 | a0001c0001t0002g0258 a0001c0001t0005g0017 a0001c0001t0005g0138 others(3): Show |
7 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1080-1547A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418946 | |||||||
| chr6:151418987 | C | T | 1 | a0001c0001t0003g0361 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1080-1588G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418987 | |||||||
| chr6:151419301 | G | A | 1 | a0002c0002t0002g0068 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1080-1902C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151419301 | |||||||
| chr6:151419354 | C | T | 1 | a0008c0012t0001g0239 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1079+1891G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151419354 | |||||||
| chr6:151419368 | C | A | 1 | a0001c0001t0001g0165 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1079+1877G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151419368 | |||||||
| chr6:151419509 | C | A | 1 | a0001c0001t0001g0140 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1079+1736G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151419509 | |||||||
| chr6:151419671 | T | TA | 38 | a0001c0001t0001g0148 a0001c0001t0002g0258 a0001c0001t0002g0303 others(35): Show |
39 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.1079+1573dupT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151419671 | |||||||
| chr6:151419671 | TA | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(142): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.1079+1573delT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151419671 | |||||||
| chr6:151419717 | T | A | 71 | a0001c0001t0001g0148 a0001c0001t0001g0304 a0001c0001t0002g0009 others(68): Show |
74 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(71): Show |
intron_variant | MODIFIER | c.1079+1528A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151419717 | |||||||
| chr6:151419832 | T | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(177): Show |
193 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1079+1413A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151419832 | |||||||
| chr6:151419978 | G | GT | 71 | a0001c0001t0001g0148 a0001c0001t0001g0304 a0001c0001t0002g0009 others(68): Show |
74 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(71): Show |
intron_variant | MODIFIER | c.1079+1266dupA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151419978 | |||||||
| chr6:151419991 | A | G | 35 | a0001c0001t0001g0304 a0001c0001t0002g0009 a0001c0001t0002g0150 others(32): Show |
37 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1079+1254T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151419991 | |||||||
| chr6:151420042 | C | T | 1 | a0001c0001t0003g0350 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1079+1203G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151420042 | |||||||
| chr6:151420121 | G | A | 1 | a0004c0009t0015g0367 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1079+1124C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151420121 | |||||||
| chr6:151420152 | A | G | 5 | a0001c0004t0008g0365 a0001c0004t0008g0366 a0003c0003t0001g0309 others(2): Show |
5 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1079+1093T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151420152 | |||||||
| chr6:151420292 | G | A | 2 | a0001c0004t0008g0365 a0001c0004t0008g0366 |
2 | HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1079+953C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151420292 | |||||||
| chr6:151420655 | C | T | 2 | a0002c0002t0001g0006 a0002c0002t0001g0067 |
3 | HG02004.hp1 HG02148.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1079+590G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151420655 | |||||||
| chr6:151420840 | C | T | 1 | a0001c0001t0002g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1079+405G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151420840 | |||||||
| chr6:151420880 | T | A | 3 | a0002c0002t0001g0080 a0002c0002t0001g0103 a0002c0002t0001g0104 |
3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1079+365A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151420880 | |||||||
| chr6:151420990 | T | C | 1 | a0001c0004t0001g0185 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1079+255A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151420990 | |||||||
| chr6:151421032 | CTT | C | 3 | a0002c0002t0001g0080 a0002c0002t0001g0103 a0002c0002t0001g0104 |
3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1079+211_1079+212d others(4): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151421032 | |||||||
| chr6:151421096 | A | G | 1 | a0001c0001t0003g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1079+149T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151421096 | |||||||
| chr6:151421151 | G | A | 1 | a0002c0002t0002g0047 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1079+94C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151421151 | |||||||
| chr6:151421406 | T | C | 365 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(362): Show |
388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.1003-85A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 8/11 | chr6 | 151421406 | |||||||
| chr6:151421407 | G | A | 28 | a0001c0001t0001g0148 a0001c0001t0002g0258 a0001c0001t0002g0303 others(25): Show |
29 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1003-86C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 8/11 | chr6 | 151421407 | |||||||
| chr6:151421782 | G | T | 35 | a0001c0001t0001g0304 a0001c0001t0002g0009 a0001c0001t0002g0150 others(32): Show |
37 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1003-461C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 8/11 | chr6 | 151421782 | |||||||
| chr6:151421836 | G | A | 2 | a0001c0001t0003g0336 a0002c0002t0001g0128 |
2 | NA18995.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1003-515C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 8/11 | chr6 | 151421836 | |||||||
| chr6:151421888 | G | T | 1 | a0002c0002t0002g0068 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1003-567C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 8/11 | chr6 | 151421888 | |||||||
| chr6:151421949 | A | C | 1 | a0003c0003t0001g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1002+592T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 8/11 | chr6 | 151421949 | |||||||
| chr6:151422205 | G | A | 1 | a0001c0001t0002g0200 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1002+336C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 8/11 | chr6 | 151422205 | |||||||
| chr6:151422205 | G | GC | 3 | a0002c0002t0001g0080 a0002c0002t0001g0103 a0002c0002t0001g0104 |
3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1002+335dupG | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 8/11 | chr6 | 151422205 | |||||||
| chr6:151422234 | TTTTCTTG others(3): Show |
T | 2 | a0001c0001t0002g0059 a0001c0001t0002g0089 |
2 | NA18982.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1002+297_1002+306d others(12): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 8/11 | chr6 | 151422234 | |||||||
| chr6:151422273 | CTATT | C | 28 | a0001c0001t0001g0148 a0001c0001t0002g0258 a0001c0001t0002g0303 others(25): Show |
29 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1002+264_1002+267d others(6): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 8/11 | chr6 | 151422273 | |||||||
| chr6:151422280 | C | T | 1 | a0002c0002t0002g0111 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1002+261G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 8/11 | chr6 | 151422280 | |||||||
| chr6:151422494 | A | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(248): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1002+47T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 8/11 | chr6 | 151422494 | |||||||
| chr6:151422661 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.938-56T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 7/11 | chr6 | 151422661 | |||||||
| chr6:151422803 | T | C | 2 | a0002c0002t0001g0093 a0002c0002t0001g0137 |
2 | NA18985.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.938-198A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 7/11 | chr6 | 151422803 | |||||||
| chr6:151422813 | A | G | 28 | a0001c0001t0001g0148 a0001c0001t0002g0258 a0001c0001t0002g0303 others(25): Show |
29 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.938-208T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 7/11 | chr6 | 151422813 | |||||||
| chr6:151422927 | C | T | 44 | a0001c0001t0003g0021 a0001c0001t0003g0320 a0001c0001t0003g0321 others(41): Show |
45 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.938-322G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 7/11 | chr6 | 151422927 | |||||||
| chr6:151422950 | C | T | 1 | a0001c0001t0002g0271 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.938-345G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 7/11 | chr6 | 151422950 | |||||||
| chr6:151423014 | C | T | 1 | a0001c0006t0001g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.938-409G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 7/11 | chr6 | 151423014 | |||||||
| chr6:151423019 | C | T | 21 | a0001c0001t0001g0148 a0001c0004t0001g0182 a0001c0004t0001g0183 others(18): Show |
21 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.938-414G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 7/11 | chr6 | 151423019 | |||||||
| chr6:151423148 | G | A | 254 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(251): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.937+377C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 7/11 | chr6 | 151423148 | |||||||
| chr6:151423173 | C | G | 28 | a0001c0001t0001g0148 a0001c0001t0002g0258 a0001c0001t0002g0303 others(25): Show |
29 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.937+352G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 7/11 | chr6 | 151423173 | |||||||
| chr6:151423268 | A | C | 3 | a0002c0002t0001g0080 a0002c0002t0001g0103 a0002c0002t0001g0104 |
3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.937+257T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 7/11 | chr6 | 151423268 | |||||||
| chr6:151423401 | A | C | 1 | a0003c0003t0001g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.937+124T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 7/11 | chr6 | 151423401 | |||||||
| chr6:151423455 | G | T | 3 | a0002c0002t0001g0080 a0002c0002t0001g0103 a0002c0002t0001g0104 |
3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.937+70C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 7/11 | chr6 | 151423455 | |||||||
| chr6:151423676 | C | A | 6 | a0002c0002t0001g0078 a0002c0002t0001g0094 a0002c0002t0001g0095 others(3): Show |
6 | HG00408.hp1 NA18943.hp2 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.831-45G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151423676 | |||||||
| chr6:151423764 | T | C | 1 | a0001c0004t0002g0238 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.831-133A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151423764 | |||||||
| chr6:151423802 | T | TC | 6 | a0001c0001t0002g0258 a0001c0001t0005g0017 a0001c0001t0005g0138 others(3): Show |
7 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.831-172dupG | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151423802 | |||||||
| chr6:151423851 | C | CT | 43 | a0001c0001t0002g0009 a0001c0001t0002g0150 a0001c0001t0002g0172 others(40): Show |
45 | HG00140.hp1 HG00140.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.831-221dupA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151423851 | |||||||
| chr6:151423851 | CT | C | 34 | a0001c0001t0001g0148 a0001c0001t0002g0166 a0001c0001t0002g0196 others(31): Show |
35 | HG00323.hp1 HG01167.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.831-221delA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151423851 | |||||||
| chr6:151423887 | G | A | 5 | a0001c0004t0008g0365 a0001c0004t0008g0366 a0003c0003t0001g0309 others(2): Show |
5 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831-256C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151423887 | |||||||
| chr6:151423909 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.831-278C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151423909 | |||||||
| chr6:151424024 | T | G | 1 | a0004c0005t0001g0256 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.831-393A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424024 | |||||||
| chr6:151424198 | C | T | 3 | a0002c0002t0001g0080 a0002c0002t0001g0103 a0002c0002t0001g0104 |
3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.831-567G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424198 | |||||||
| chr6:151424210 | C | T | 1 | a0003c0003t0012g0262 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.831-579G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424210 | |||||||
| chr6:151424255 | T | G | 1 | a0001c0004t0002g0186 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.831-624A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424255 | |||||||
| chr6:151424322 | G | T | 1 | a0001c0001t0002g0197 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.831-691C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424322 | |||||||
| chr6:151424335 | C | T | 2 | a0001c0004t0001g0182 a0001c0004t0001g0183 |
2 | HG01175.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.831-704G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424335 | |||||||
| chr6:151424387 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(123): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.831-756G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424387 | |||||||
| chr6:151424407 | A | G | 10 | a0001c0001t0002g0258 a0001c0001t0005g0017 a0001c0001t0005g0138 others(7): Show |
11 | HG02109.hp2 HG02717.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.831-776T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424407 | |||||||
| chr6:151424414 | A | G | 3 | a0002c0002t0001g0080 a0002c0002t0001g0103 a0002c0002t0001g0104 |
3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.831-783T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424414 | |||||||
| chr6:151424417 | C | T | 3 | a0002c0002t0001g0080 a0002c0002t0001g0103 a0002c0002t0001g0104 |
3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.831-786G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424417 | |||||||
| chr6:151424418 | A | G | 3 | a0002c0002t0001g0080 a0002c0002t0001g0103 a0002c0002t0001g0104 |
3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.831-787T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424418 | |||||||
| chr6:151424419 | C | T | 1 | a0001c0001t0002g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.831-788G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424419 | |||||||
| chr6:151424463 | C | CA | 93 | a0001c0001t0001g0092 a0001c0001t0001g0143 a0001c0001t0001g0174 others(90): Show |
96 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.831-833dupT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424463 | |||||||
| chr6:151424463 | CA | C | 8 | a0001c0001t0001g0144 a0001c0001t0001g0167 a0001c0001t0001g0168 others(5): Show |
8 | HG00099.hp1 HG01074.hp1 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.831-833delT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424463 | |||||||
| chr6:151424550 | T | G | 1 | a0001c0001t0002g0216 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.831-919A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424550 | |||||||
| chr6:151424596 | A | G | 3 | a0002c0002t0001g0064 a0002c0002t0001g0134 a0002c0002t0002g0063 |
3 | HG02683.hp1 HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.831-965T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424596 | |||||||
| chr6:151424759 | CA | C | 35 | a0001c0001t0001g0304 a0001c0001t0002g0009 a0001c0001t0002g0150 others(32): Show |
37 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.831-1129delT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424759 | |||||||
| chr6:151424852 | C | T | 6 | a0001c0001t0002g0258 a0001c0001t0005g0017 a0001c0001t0005g0138 others(3): Show |
7 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.831-1221G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424852 | |||||||
| chr6:151424853 | G | A | 1 | a0001c0001t0002g0236 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.831-1222C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424853 | |||||||
| chr6:151424886 | G | GGGCTGAG others(1): Show |
46 | a0001c0001t0001g0304 a0001c0001t0002g0009 a0001c0001t0002g0150 others(43): Show |
49 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.831-1256_831-1255i others(10): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424886 | |||||||
| chr6:151425189 | C | T | 4 | a0001c0001t0002g0268 a0001c0001t0002g0273 a0001c0001t0002g0289 others(1): Show |
4 | NA18970.hp1 NA18983.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.831-1558G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425189 | |||||||
| chr6:151425413 | A | G | 1 | a0002c0007t0001g0113 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.831-1782T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425413 | |||||||
| chr6:151425416 | G | A | 3 | a0001c0001t0001g0302 a0001c0001t0002g0016 a0001c0001t0002g0237 |
4 | HG02572.hp1 HG02622.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.831-1785C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425416 | |||||||
| chr6:151425425 | CGT | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(86): Show |
99 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.831-1796_831-1795d others(4): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425425 | |||||||
| chr6:151425451 | T | C | 89 | a0001c0001t0001g0092 a0001c0001t0001g0143 a0001c0001t0001g0174 others(86): Show |
92 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.831-1820A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425451 | |||||||
| chr6:151425451 | T | TAC | 18 | a0001c0001t0002g0204 a0001c0001t0003g0021 a0001c0001t0003g0320 others(15): Show |
19 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.831-1822_831-1821d others(4): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425451 | |||||||
| chr6:151425589 | A | G | 1 | a0001c0004t0002g0238 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.830+1893T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425589 | |||||||
| chr6:151425597 | G | A | 1 | a0003c0003t0001g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.830+1885C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425597 | |||||||
| chr6:151425650 | T | C | 2 | a0002c0007t0001g0061 a0002c0007t0001g0113 |
2 | NA19007.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.830+1832A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425650 | |||||||
| chr6:151425665 | C | T | 2 | a0001c0004t0001g0247 a0003c0003t0012g0262 |
2 | HG02486.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.830+1817G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425665 | |||||||
| chr6:151425832 | G | C | 1 | a0002c0002t0001g0108 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.830+1650C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425832 | |||||||
| chr6:151425907 | G | A | 5 | a0001c0004t0008g0365 a0001c0004t0008g0366 a0003c0003t0001g0309 others(2): Show |
5 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.830+1575C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425907 | |||||||
| chr6:151425946 | C | CT | 123 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(120): Show |
135 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.830+1535dupA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425946 | |||||||
| chr6:151425946 | C | CTT | 77 | a0001c0001t0001g0092 a0001c0001t0001g0143 a0001c0001t0001g0170 others(74): Show |
78 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.830+1534_830+1535d others(4): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425946 | |||||||
| chr6:151425946 | C | CTTT | 13 | a0001c0004t0001g0240 a0001c0004t0001g0241 a0001c0004t0001g0242 others(10): Show |
13 | HG01884.hp2 HG02055.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.830+1533_830+1535d others(5): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425946 | |||||||
| chr6:151425974 | C | T | 1 | a0002c0002t0010g0057 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.830+1508G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425974 | |||||||
| chr6:151426017 | C | T | 89 | a0001c0001t0001g0092 a0001c0001t0001g0143 a0001c0001t0001g0174 others(86): Show |
92 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.830+1465G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151426017 | |||||||
| chr6:151426054 | T | TGCCTCC | 8 | a0001c0001t0002g0180 a0001c0001t0002g0194 a0001c0001t0002g0196 others(5): Show |
8 | HG00639.hp1 HG00639.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.830+1422_830+1427d others(8): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151426054 | |||||||
| chr6:151426065 | C | T | 6 | a0001c0001t0002g0303 a0001c0004t0008g0365 a0001c0004t0008g0366 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.830+1417G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151426065 | |||||||
| chr6:151426097 | C | T | 6 | a0001c0001t0002g0303 a0001c0004t0008g0365 a0001c0004t0008g0366 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.830+1385G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151426097 | |||||||
| chr6:151426111 | G | T | 32 | a0001c0001t0001g0304 a0001c0001t0002g0009 a0001c0001t0002g0150 others(29): Show |
34 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.830+1371C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151426111 | |||||||
| chr6:151426503 | C | T | 1 | a0003c0013t0001g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.830+979G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151426503 | |||||||
| chr6:151426617 | T | C | 1 | a0001c0001t0002g0217 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.830+865A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151426617 | |||||||
| chr6:151426749 | T | A | 1 | a0003c0003t0004g0037 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.830+733A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151426749 | |||||||
| chr6:151426839 | G | C | 1 | a0002c0002t0001g0083 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.830+643C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151426839 | |||||||
| chr6:151426849 | A | G | 3 | a0002c0002t0001g0110 a0002c0002t0002g0111 a0004c0005t0002g0305 |
3 | HG02258.hp2 HG02451.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.830+633T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151426849 | |||||||
| chr6:151426854 | C | T | 6 | a0001c0001t0002g0303 a0001c0004t0008g0365 a0001c0004t0008g0366 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.830+628G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151426854 | |||||||
| chr6:151426855 | C | T | 5 | a0001c0004t0008g0365 a0001c0004t0008g0366 a0003c0003t0001g0309 others(2): Show |
5 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.830+627G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151426855 | |||||||
| chr6:151426871 | G | A | 32 | a0001c0001t0001g0304 a0001c0001t0002g0009 a0001c0001t0002g0150 others(29): Show |
34 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.830+611C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151426871 | |||||||
| chr6:151426944 | A | AT | 23 | a0001c0001t0001g0148 a0001c0004t0001g0182 a0001c0004t0001g0183 others(20): Show |
23 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.830+537dupA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151426944 | |||||||
| chr6:151427073 | T | A | 1 | a0001c0001t0002g0214 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.830+409A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151427073 | |||||||
| chr6:151427116 | C | T | 1 | a0001c0001t0002g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.830+366G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151427116 | |||||||
| chr6:151427185 | G | A | 3 | a0001c0001t0001g0144 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | HG00099.hp1 HG01074.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.830+297C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151427185 | |||||||
| chr6:151427199 | A | G | 6 | a0001c0001t0002g0303 a0001c0004t0008g0365 a0001c0004t0008g0366 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.830+283T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151427199 | |||||||
| chr6:151427224 | A | G | 1 | a0001c0001t0002g0307 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.830+258T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151427224 | |||||||
| chr6:151427237 | G | A | 2 | a0003c0003t0004g0028 a0003c0003t0004g0031 |
2 | HG00140.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.830+245C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151427237 | |||||||
| chr6:151427348 | C | A | 1 | a0002c0002t0001g0096 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.830+134G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151427348 | |||||||
| chr6:151427375 | C | CA | 57 | a0001c0001t0002g0278 a0001c0001t0003g0356 a0002c0002t0001g0045 others(54): Show |
58 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.830+106dupT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151427375 | |||||||
| chr6:151427375 | CA | C | 10 | a0001c0001t0001g0144 a0001c0001t0002g0203 a0001c0001t0002g0258 others(7): Show |
11 | HG01074.hp1 HG01975.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.830+106delT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151427375 | |||||||
| chr6:151427407 | T | C | 1 | a0002c0002t0001g0121 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.830+75A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151427407 | |||||||
| chr6:151427673 | C | A | 1 | a0001c0001t0002g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.730-91G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151427673 | |||||||
| chr6:151427734 | A | G | 3 | a0001c0001t0003g0324 a0001c0001t0003g0326 a0001c0001t0003g0327 |
3 | HG01175.hp2 HG01256.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.730-152T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151427734 | |||||||
| chr6:151427820 | T | A | 2 | a0001c0001t0002g0224 a0001c0001t0002g0283 |
2 | HG00735.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.730-238A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151427820 | |||||||
| chr6:151427860 | T | C | 88 | a0001c0001t0001g0092 a0001c0001t0001g0143 a0001c0001t0002g0317 others(85): Show |
91 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.730-278A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151427860 | |||||||
| chr6:151427946 | C | T | 4 | a0001c0001t0001g0302 a0001c0001t0002g0016 a0001c0001t0002g0236 others(1): Show |
5 | HG02572.hp1 HG02622.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.730-364G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151427946 | |||||||
| chr6:151427991 | A | C | 6 | a0001c0001t0002g0303 a0001c0004t0008g0365 a0001c0004t0008g0366 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.730-409T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151427991 | |||||||
| chr6:151428087 | G | T | 6 | a0001c0001t0002g0303 a0001c0004t0008g0365 a0001c0004t0008g0366 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.730-505C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151428087 | |||||||
| chr6:151428398 | G | T | 1 | a0002c0002t0001g0105 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.730-816C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151428398 | |||||||
| chr6:151428425 | A | G | 1 | a0004c0005t0002g0305 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.730-843T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151428425 | |||||||
| chr6:151428584 | T | G | 1 | a0004c0005t0002g0305 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.730-1002A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151428584 | |||||||
| chr6:151428634 | C | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(86): Show |
99 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.730-1052G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151428634 | |||||||
| chr6:151428635 | G | A | 1 | a0001c0001t0002g0221 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.730-1053C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151428635 | |||||||
| chr6:151428680 | C | T | 5 | a0001c0004t0008g0365 a0001c0004t0008g0366 a0003c0003t0001g0309 others(2): Show |
5 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.730-1098G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151428680 | |||||||
| chr6:151428796 | A | C | 1 | a0001c0001t0002g0234 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.730-1214T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151428796 | |||||||
| chr6:151428848 | T | C | 12 | a0002c0002t0001g0075 a0002c0002t0001g0093 a0002c0002t0001g0108 others(9): Show |
12 | HG01975.hp2 HG01993.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.730-1266A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151428848 | |||||||
| chr6:151428994 | A | G | 1 | a0001c0001t0002g0194 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.729+1144T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151428994 | |||||||
| chr6:151429009 | T | C | 6 | a0001c0001t0002g0303 a0001c0004t0008g0365 a0001c0004t0008g0366 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.729+1129A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429009 | |||||||
| chr6:151429064 | T | C | 5 | a0001c0004t0008g0365 a0001c0004t0008g0366 a0003c0003t0001g0309 others(2): Show |
5 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.729+1074A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429064 | |||||||
| chr6:151429073 | C | A | 1 | a0001c0001t0002g0194 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.729+1065G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429073 | |||||||
| chr6:151429123 | C | CT | 8 | a0001c0001t0001g0254 a0001c0001t0002g0288 a0002c0002t0001g0080 others(5): Show |
8 | HG02683.hp2 HG02717.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.729+1014dupA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429123 | |||||||
| chr6:151429141 | G | A | 1 | a0001c0001t0003g0361 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.729+997C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429141 | |||||||
| chr6:151429162 | C | T | 1 | a0002c0002t0001g0085 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.729+976G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429162 | |||||||
| chr6:151429187 | C | T | 6 | a0001c0001t0002g0303 a0001c0004t0008g0365 a0001c0004t0008g0366 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.729+951G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429187 | |||||||
| chr6:151429230 | T | G | 11 | a0002c0002t0001g0062 a0002c0002t0001g0064 a0002c0002t0001g0065 others(8): Show |
11 | HG00621.hp1 HG01346.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.729+908A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429230 | |||||||
| chr6:151429363 | T | C | 6 | a0001c0001t0001g0002 a0001c0001t0002g0178 a0001c0001t0002g0214 others(3): Show |
8 | HG00741.hp1 HG01928.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.729+775A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429363 | |||||||
| chr6:151429465 | A | G | 1 | a0002c0002t0001g0124 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.729+673T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429465 | |||||||
| chr6:151429479 | G | C | 2 | a0001c0004t0001g0247 a0003c0003t0012g0262 |
2 | HG02486.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.729+659C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429479 | |||||||
| chr6:151429491 | C | T | 1 | a0001c0001t0002g0196 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.729+647G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429491 | |||||||
| chr6:151429535 | G | GT | 39 | a0001c0001t0001g0304 a0001c0001t0002g0009 a0001c0001t0002g0150 others(36): Show |
41 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.729+602_729+603ins others(1): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429535 | |||||||
| chr6:151429543 | A | C | 1 | a0001c0001t0002g0194 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.729+595T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429543 | |||||||
| chr6:151429563 | G | T | 2 | a0001c0004t0001g0247 a0003c0003t0012g0262 |
2 | HG02486.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.729+575C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429563 | |||||||
| chr6:151429628 | C | T | 39 | a0001c0001t0001g0304 a0001c0001t0002g0009 a0001c0001t0002g0150 others(36): Show |
41 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.729+510G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429628 | |||||||
| chr6:151429803 | T | C | 6 | a0001c0001t0002g0303 a0001c0004t0008g0365 a0001c0004t0008g0366 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.729+335A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429803 | |||||||
| chr6:151429825 | C | T | 4 | a0001c0001t0002g0073 a0001c0001t0002g0074 a0001c0001t0002g0195 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.729+313G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429825 | |||||||
| chr6:151429902 | G | A | 1 | a0001c0001t0002g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.729+236C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429902 | |||||||
| chr6:151430277 | C | T | 2 | a0001c0004t0001g0247 a0003c0003t0012g0262 |
2 | HG02486.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.690-100G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151430277 | |||||||
| chr6:151430505 | G | C | 2 | a0003c0003t0004g0032 a0003c0003t0004g0033 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.690-328C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151430505 | |||||||
| chr6:151430556 | T | C | 1 | a0002c0002t0001g0096 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.690-379A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151430556 | |||||||
| chr6:151430750 | C | T | 1 | a0002c0002t0001g0124 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.690-573G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151430750 | |||||||
| chr6:151430773 | C | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(248): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.690-596G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151430773 | |||||||
| chr6:151430881 | T | TATTAATG others(307): Show |
1 | a0003c0003t0001g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.690-705_690-704ins others(314): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151430881 | |||||||
| chr6:151430881 | T | TATTAATG others(308): Show |
2 | a0003c0013t0001g0319 a0004c0009t0015g0367 |
2 | HG01884.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.690-705_690-704ins others(315): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151430881 | |||||||
| chr6:151430914 | C | CTTAAG | 4 | a0001c0001t0002g0303 a0003c0003t0001g0309 a0003c0013t0001g0319 others(1): Show |
4 | HG01884.hp2 HG02258.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.690-738_690-737ins others(5): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151430914 | |||||||
| chr6:151431059 | A | G | 3 | a0003c0003t0001g0309 a0003c0013t0001g0319 a0004c0009t0015g0367 |
3 | HG01884.hp2 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.690-882T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151431059 | |||||||
| chr6:151431124 | A | T | 3 | a0003c0003t0001g0309 a0003c0013t0001g0319 a0004c0009t0015g0367 |
3 | HG01884.hp2 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.690-947T>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151431124 | |||||||
| chr6:151431192 | C | G | 1 | a0001c0001t0002g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.690-1015G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151431192 | |||||||
| chr6:151431487 | C | T | 26 | a0001c0001t0001g0148 a0001c0004t0001g0182 a0001c0004t0001g0183 others(23): Show |
26 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.690-1310G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151431487 | |||||||
| chr6:151431720 | C | A | 36 | a0001c0001t0001g0304 a0001c0001t0002g0009 a0001c0001t0002g0150 others(33): Show |
38 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.689+1435G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151431720 | |||||||
| chr6:151431826 | G | T | 1 | a0001c0001t0002g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.689+1329C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151431826 | |||||||
| chr6:151431876 | A | G | 35 | a0001c0001t0001g0304 a0001c0001t0002g0009 a0001c0001t0002g0150 others(32): Show |
37 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.689+1279T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151431876 | |||||||
| chr6:151432039 | G | GA | 26 | a0001c0001t0001g0148 a0001c0004t0001g0182 a0001c0004t0001g0183 others(23): Show |
26 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.689+1115dupT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151432039 | |||||||
| chr6:151432085 | TCCA | T | 3 | a0003c0003t0001g0309 a0003c0013t0001g0319 a0004c0009t0015g0367 |
3 | HG01884.hp2 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.689+1067_689+1069d others(5): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151432085 | |||||||
| chr6:151432260 | A | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(248): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.689+895T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151432260 | |||||||
| chr6:151432286 | C | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(248): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.689+869G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151432286 | |||||||
| chr6:151432305 | C | T | 88 | a0001c0001t0001g0092 a0001c0001t0001g0143 a0001c0001t0002g0317 others(85): Show |
91 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.689+850G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151432305 | |||||||
| chr6:151432335 | G | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(236): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.689+820C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151432335 | |||||||
| chr6:151432499 | G | A | 5 | a0002c0002t0001g0006 a0002c0002t0001g0007 a0002c0002t0001g0067 others(2): Show |
7 | HG02004.hp1 HG02148.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.689+656C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151432499 | |||||||
| chr6:151432531 | C | CACTT | 120 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(117): Show |
130 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.689+623_689+624ins others(4): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151432531 | |||||||
| chr6:151432559 | G | C | 121 | a0001c0001t0001g0092 a0001c0001t0001g0143 a0001c0001t0001g0148 others(118): Show |
124 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(121): Show |
intron_variant | MODIFIER | c.689+596C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151432559 | |||||||
| chr6:151432567 | T | C | 7 | a0001c0001t0002g0180 a0001c0001t0002g0190 a0001c0001t0002g0193 others(4): Show |
7 | HG00639.hp1 HG01993.hp1 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.689+588A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151432567 | |||||||
| chr6:151432860 | G | A | 3 | a0003c0003t0001g0309 a0003c0013t0001g0319 a0004c0009t0015g0367 |
3 | HG01884.hp2 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.689+295C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151432860 | |||||||
| chr6:151432923 | G | A | 30 | a0001c0001t0001g0148 a0001c0004t0001g0182 a0001c0004t0001g0183 others(27): Show |
30 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.689+232C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151432923 | |||||||
| chr6:151433138 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(210): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.689+17A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151433138 | |||||||
| chr6:151433292 | C | T | 6 | a0001c0001t0001g0302 a0001c0001t0002g0016 a0001c0001t0002g0147 others(3): Show |
7 | HG01891.hp1 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.614-62G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151433292 | |||||||
| chr6:151433437 | A | C | 3 | a0003c0003t0001g0309 a0003c0013t0001g0319 a0004c0009t0015g0367 |
3 | HG01884.hp2 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.614-207T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151433437 | |||||||
| chr6:151433609 | G | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(209): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.614-379C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151433609 | |||||||
| chr6:151433825 | G | GT | 12 | a0001c0001t0003g0323 a0001c0001t0003g0324 a0001c0001t0003g0325 others(9): Show |
12 | HG00099.hp2 HG00323.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.614-596dupA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151433825 | |||||||
| chr6:151433827 | T | G | 3 | a0002c0002t0001g0080 a0002c0002t0001g0103 a0002c0002t0001g0104 |
3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.614-597A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151433827 | |||||||
| chr6:151433869 | CTG | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(123): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.614-641_614-640del others(2): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151433869 | |||||||
| chr6:151433939 | A | AC | 31 | a0001c0001t0001g0227 a0001c0001t0001g0233 a0001c0001t0001g0302 others(28): Show |
31 | HG00621.hp2 HG00741.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.614-710dupG | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151433939 | |||||||
| chr6:151433939 | AC | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(71): Show |
85 | HG00099.hp1 HG00140.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.614-710delG | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151433939 | |||||||
| chr6:151433947 | CCG | C | 27 | a0001c0001t0001g0148 a0001c0001t0002g0267 a0001c0001t0002g0310 others(24): Show |
27 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(24): Show |
intron_variant | MODIFIER | c.614-719_614-718del others(2): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151433947 | |||||||
| chr6:151433948 | CG | C | 78 | a0001c0001t0003g0021 a0001c0001t0003g0322 a0001c0001t0003g0324 others(75): Show |
79 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.614-719delC | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151433948 | |||||||
| chr6:151433949 | G | C | 61 | a0001c0001t0001g0143 a0001c0001t0003g0357 a0001c0004t0001g0184 others(58): Show |
61 | HG00408.hp1 HG00621.hp1 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.614-719C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151433949 | |||||||
| chr6:151433953 | C | A | 1 | a0001c0001t0007g0330 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.614-723G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151433953 | |||||||
| chr6:151434000 | C | T | 2 | a0001c0001t0002g0267 a0001c0001t0002g0310 |
2 | NA18994.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.614-770G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434000 | |||||||
| chr6:151434024 | T | C | 1 | a0001c0001t0002g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.614-794A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434024 | |||||||
| chr6:151434068 | T | A | 7 | a0001c0001t0001g0149 a0001c0001t0001g0154 a0001c0001t0001g0155 others(4): Show |
7 | HG02559.hp1 HG02615.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.614-838A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434068 | |||||||
| chr6:151434135 | G | A | 1 | a0001c0004t0001g0247 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.614-905C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434135 | |||||||
| chr6:151434232 | A | C | 1 | a0001c0001t0001g0176 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.614-1002T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434232 | |||||||
| chr6:151434276 | TA | T | 3 | a0002c0002t0001g0007 a0002c0002t0001g0069 a0002c0002t0001g0072 |
4 | NA18943.hp1 NA18944.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.614-1047delT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434276 | |||||||
| chr6:151434327 | CAT | C | 88 | a0001c0001t0002g0317 a0002c0002t0001g0006 a0002c0002t0001g0007 others(85): Show |
91 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.614-1099_614-1098d others(4): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434327 | |||||||
| chr6:151434328 | A | G | 2 | a0001c0004t0008g0365 a0001c0004t0008g0366 |
2 | HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.614-1098T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434328 | |||||||
| chr6:151434409 | A | AT | 115 | a0001c0001t0001g0148 a0001c0001t0002g0147 a0001c0001t0002g0235 others(112): Show |
118 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.614-1180dupA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434409 | |||||||
| chr6:151434409 | A | ATTTT | 6 | a0001c0001t0002g0258 a0001c0001t0005g0017 a0001c0001t0005g0138 others(3): Show |
7 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.614-1183_614-1180d others(6): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434409 | |||||||
| chr6:151434409 | AT | A | 26 | a0001c0001t0001g0173 a0001c0001t0002g0009 a0001c0001t0002g0150 others(23): Show |
28 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.614-1180delA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434409 | |||||||
| chr6:151434424 | C | G | 6 | a0001c0001t0002g0258 a0001c0001t0005g0017 a0001c0001t0005g0138 others(3): Show |
7 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.614-1194G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434424 | |||||||
| chr6:151434671 | G | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(244): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.614-1441C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434671 | |||||||
| chr6:151434814 | T | C | 1 | a0002c0002t0001g0118 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.614-1584A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434814 | |||||||
| chr6:151434845 | T | C | 3 | a0003c0003t0001g0309 a0003c0013t0001g0319 a0004c0009t0015g0367 |
3 | HG01884.hp2 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.613+1601A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434845 | |||||||
| chr6:151434894 | G | A | 1 | a0006c0010t0009g0306 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.613+1552C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434894 | |||||||
| chr6:151434898 | G | T | 1 | a0001c0001t0001g0143 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.613+1548C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434898 | |||||||
| chr6:151434918 | G | C | 3 | a0003c0003t0001g0309 a0003c0013t0001g0319 a0004c0009t0015g0367 |
3 | HG01884.hp2 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.613+1528C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434918 | |||||||
| chr6:151434935 | A | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(246): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.613+1511T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434935 | |||||||
| chr6:151435006 | G | A | 1 | a0001c0001t0005g0138 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.613+1440C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151435006 | |||||||
| chr6:151435030 | G | A | 6 | a0001c0001t0002g0258 a0001c0001t0005g0017 a0001c0001t0005g0138 others(3): Show |
7 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.613+1416C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151435030 | |||||||
| chr6:151435164 | A | G | 126 | a0001c0001t0001g0148 a0001c0001t0002g0258 a0001c0001t0002g0303 others(123): Show |
130 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(127): Show |
intron_variant | MODIFIER | c.613+1282T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151435164 | |||||||
| chr6:151435192 | T | C | 89 | a0001c0001t0002g0303 a0001c0001t0002g0317 a0002c0002t0001g0006 others(86): Show |
92 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.613+1254A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151435192 | |||||||
| chr6:151435202 | G | A | 49 | a0001c0001t0001g0008 a0001c0001t0001g0142 a0001c0001t0001g0143 others(46): Show |
51 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.613+1244C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151435202 | |||||||
| chr6:151435207 | A | G | 95 | a0001c0001t0002g0258 a0001c0001t0002g0303 a0001c0001t0002g0317 others(92): Show |
99 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.613+1239T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151435207 | |||||||
| chr6:151435254 | T | G | 2 | a0001c0001t0002g0179 a0001c0001t0002g0201 |
2 | HG02155.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.613+1192A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151435254 | |||||||
| chr6:151435432 | C | A | 1 | a0001c0001t0003g0321 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.613+1014G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151435432 | |||||||
| chr6:151435477 | A | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(215): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.613+969T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151435477 | |||||||
| chr6:151435530 | TTTAA | T | 3 | a0003c0003t0001g0309 a0003c0013t0001g0319 a0004c0009t0015g0367 |
3 | HG01884.hp2 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.613+912_613+915del others(4): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151435530 | |||||||
| chr6:151435589 | T | A | 1 | a0001c0001t0002g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.613+857A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151435589 | |||||||
| chr6:151435744 | T | C | 2 | a0001c0001t0002g0202 a0001c0001t0002g0280 |
2 | HG00639.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.613+702A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151435744 | |||||||
| chr6:151435804 | C | T | 31 | a0001c0001t0001g0148 a0001c0004t0001g0182 a0001c0004t0001g0183 others(28): Show |
31 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.613+642G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151435804 | |||||||
| chr6:151436060 | G | A | 1 | a0001c0001t0007g0347 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.613+386C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151436060 | |||||||
| chr6:151436105 | C | CA | 10 | a0001c0001t0002g0303 a0002c0002t0001g0084 a0002c0002t0001g0099 others(7): Show |
10 | HG02071.hp2 HG02451.hp1 HG03209.hp1 others(7): Show |
intron_variant | MODIFIER | c.613+340dupT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151436105 | |||||||
| chr6:151436110 | A | AAAC | 6 | a0002c0002t0001g0051 a0002c0002t0001g0056 a0002c0002t0001g0082 others(3): Show |
6 | HG02132.hp1 NA18978.hp2 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.613+335_613+336ins others(3): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151436110 | |||||||
| chr6:151436111 | A | AAC | 73 | a0001c0001t0002g0317 a0002c0002t0001g0006 a0002c0002t0001g0007 others(70): Show |
76 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.613+334_613+335ins others(2): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151436111 | |||||||
| chr6:151436112 | C | A | 79 | a0001c0001t0002g0317 a0002c0002t0001g0006 a0002c0002t0001g0007 others(76): Show |
82 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.613+334G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151436112 | |||||||
| chr6:151436112 | C | CA | 29 | a0001c0001t0001g0304 a0001c0001t0002g0009 a0001c0001t0002g0150 others(26): Show |
31 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.613+333dupT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151436112 | |||||||
| chr6:151436112 | CA | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(87): Show |
100 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.613+333delT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151436112 | |||||||
| chr6:151436116 | A | AC | 8 | a0002c0002t0001g0084 a0002c0002t0001g0099 a0002c0002t0001g0100 others(5): Show |
8 | HG02071.hp2 HG02451.hp1 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.613+329_613+330ins others(1): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151436116 | |||||||
| chr6:151436116 | A | C | 10 | a0001c0001t0001g0233 a0001c0001t0002g0258 a0001c0001t0003g0352 others(7): Show |
11 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(8): Show |
intron_variant | MODIFIER | c.613+330T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151436116 | |||||||
| chr6:151436117 | A | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(119): Show |
132 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.613+329T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151436117 | |||||||
| chr6:151436192 | T | C | 249 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(246): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.613+254A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151436192 | |||||||
| chr6:151436197 | T | C | 25 | a0001c0001t0001g0148 a0001c0004t0001g0182 a0001c0004t0001g0183 others(22): Show |
25 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.613+249A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151436197 | |||||||
| chr6:151436610 | C | T | 3 | a0003c0003t0001g0309 a0003c0013t0001g0319 a0004c0009t0015g0367 |
3 | HG01884.hp2 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.505-56G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151436610 | |||||||
| chr6:151436772 | C | T | 6 | a0001c0001t0002g0258 a0001c0001t0005g0017 a0001c0001t0005g0138 others(3): Show |
7 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.505-218G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151436772 | |||||||
| chr6:151436825 | G | A | 31 | a0001c0001t0001g0148 a0001c0004t0001g0182 a0001c0004t0001g0183 others(28): Show |
31 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.505-271C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151436825 | |||||||
| chr6:151436894 | A | AATG | 249 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(246): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.505-343_505-341dup others(3): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151436894 | |||||||
| chr6:151436907 | C | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(89): Show |
102 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.505-353G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151436907 | |||||||
| chr6:151436961 | C | T | 1 | a0002c0002t0002g0047 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.505-407G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151436961 | |||||||
| chr6:151437266 | A | G | 31 | a0001c0001t0001g0304 a0001c0001t0002g0009 a0001c0001t0002g0150 others(28): Show |
33 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.505-712T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151437266 | |||||||
| chr6:151437297 | T | C | 1 | a0002c0002t0001g0078 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.505-743A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151437297 | |||||||
| chr6:151437426 | A | G | 4 | a0003c0003t0001g0308 a0003c0003t0001g0309 a0003c0013t0001g0319 others(1): Show |
4 | HG01884.hp2 HG02258.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.505-872T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151437426 | |||||||
| chr6:151437771 | C | A | 2 | a0001c0001t0002g0147 a0001c0001t0002g0235 |
2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.505-1217G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151437771 | |||||||
| chr6:151437900 | G | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(242): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.505-1346C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151437900 | |||||||
| chr6:151438057 | T | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(191): Show |
208 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.505-1503A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438057 | |||||||
| chr6:151438107 | A | G | 3 | a0001c0001t0001g0304 a0001c0001t0002g0303 a0003c0003t0012g0262 |
3 | HG02486.hp2 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.505-1553T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438107 | |||||||
| chr6:151438359 | T | C | 1 | a0001c0001t0001g0169 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.505-1805A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438359 | |||||||
| chr6:151438495 | T | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(133): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.505-1941A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438495 | |||||||
| chr6:151438504 | C | T | 1 | a0002c0002t0001g0045 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.505-1950G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438504 | |||||||
| chr6:151438723 | C | T | 6 | a0004c0005t0001g0255 a0004c0005t0001g0256 a0004c0005t0001g0257 others(3): Show |
6 | HG02258.hp1 HG03041.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.505-2169G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438723 | |||||||
| chr6:151438763 | G | A | 1 | a0002c0002t0001g0123 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.505-2209C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438763 | |||||||
| chr6:151438764 | C | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(88): Show |
101 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.505-2210G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438764 | |||||||
| chr6:151438795 | C | CT | 16 | a0001c0001t0001g0304 a0001c0001t0002g0204 a0001c0001t0002g0265 others(13): Show |
16 | HG01175.hp1 HG02258.hp1 HG03041.hp1 others(13): Show |
intron_variant | MODIFIER | c.505-2242dupA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438795 | |||||||
| chr6:151438809 | T | C | 1 | a0001c0001t0005g0259 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.505-2255A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438809 | |||||||
| chr6:151438809 | T | TTTC | 26 | a0003c0003t0001g0308 a0003c0003t0001g0309 a0003c0003t0004g0004 others(23): Show |
27 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.505-2256_505-2255i others(5): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438809 | |||||||
| chr6:151438810 | C | T | 2 | a0001c0001t0001g0304 a0001c0001t0002g0303 |
2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.505-2256G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438810 | |||||||
| chr6:151438811 | C | A | 26 | a0003c0003t0001g0308 a0003c0003t0001g0309 a0003c0003t0004g0004 others(23): Show |
27 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.505-2257G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438811 | |||||||
| chr6:151438812 | A | C | 2 | a0001c0001t0001g0304 a0001c0001t0002g0303 |
2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.505-2258T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438812 | |||||||
| chr6:151438819 | A | C | 4 | a0002c0002t0001g0062 a0002c0002t0001g0065 a0002c0002t0002g0046 others(1): Show |
4 | HG00621.hp1 HG02040.hp1 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.505-2265T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438819 | |||||||
| chr6:151438820 | C | A | 31 | a0001c0001t0003g0021 a0001c0001t0003g0320 a0001c0001t0003g0321 others(28): Show |
32 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.505-2266G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438820 | |||||||
| chr6:151438851 | C | T | 32 | a0001c0001t0002g0258 a0001c0001t0005g0017 a0001c0001t0005g0138 others(29): Show |
34 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.505-2297G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438851 | |||||||
| chr6:151438870 | T | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(93): Show |
107 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.505-2316A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438870 | |||||||
| chr6:151438984 | C | A | 6 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(3): Show |
6 | HG02615.hp2 HG03098.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-2430G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438984 | |||||||
| chr6:151439007 | G | A | 1 | a0002c0002t0001g0109 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.505-2453C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151439007 | |||||||
| chr6:151439009 | G | A | 1 | a0002c0002t0001g0124 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.505-2455C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151439009 | |||||||
| chr6:151439072 | C | T | 26 | a0003c0003t0001g0308 a0003c0003t0001g0309 a0003c0003t0004g0004 others(23): Show |
27 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.505-2518G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151439072 | |||||||
| chr6:151439117 | A | T | 26 | a0003c0003t0001g0308 a0003c0003t0001g0309 a0003c0003t0004g0004 others(23): Show |
27 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.505-2563T>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151439117 | |||||||
| chr6:151439183 | T | C | 6 | a0001c0001t0002g0258 a0001c0001t0005g0017 a0001c0001t0005g0138 others(3): Show |
7 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.505-2629A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151439183 | |||||||
| chr6:151439242 | T | C | 26 | a0003c0003t0001g0308 a0003c0003t0001g0309 a0003c0003t0004g0004 others(23): Show |
27 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.505-2688A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151439242 | |||||||
| chr6:151439247 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(133): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.505-2693G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151439247 | |||||||
| chr6:151439335 | A | G | 3 | a0001c0001t0001g0232 a0001c0001t0002g0146 a0001c0001t0002g0215 |
3 | HG00423.hp2 NA18951.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.505-2781T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151439335 | |||||||
| chr6:151439362 | T | C | 26 | a0003c0003t0001g0308 a0003c0003t0001g0309 a0003c0003t0004g0004 others(23): Show |
27 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.505-2808A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151439362 | |||||||
| chr6:151439649 | TG | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0170 |
3 | NA18957.hp1 NA19001.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.505-3096delC | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151439649 | |||||||
| chr6:151439651 | T | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0170 |
3 | NA18957.hp1 NA19001.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.505-3097A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151439651 | |||||||
| chr6:151439803 | G | A | 17 | a0002c0002t0001g0056 a0002c0002t0001g0075 a0002c0002t0001g0093 others(14): Show |
17 | HG01975.hp2 HG01993.hp2 HG02132.hp1 others(14): Show |
intron_variant | MODIFIER | c.505-3249C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151439803 | |||||||
| chr6:151439887 | C | G | 1 | a0001c0004t0001g0187 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.505-3333G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151439887 | |||||||
| chr6:151439996 | G | T | 1 | a0001c0001t0002g0285 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.505-3442C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151439996 | |||||||
| chr6:151440209 | G | A | 26 | a0003c0003t0001g0308 a0003c0003t0001g0309 a0003c0003t0004g0004 others(23): Show |
27 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.505-3655C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151440209 | |||||||
| chr6:151440394 | G | A | 26 | a0003c0003t0001g0308 a0003c0003t0001g0309 a0003c0003t0004g0004 others(23): Show |
27 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.505-3840C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151440394 | |||||||
| chr6:151440411 | T | C | 5 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0002g0009 others(2): Show |
6 | HG02280.hp2 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-3857A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151440411 | |||||||
| chr6:151440416 | T | C | 1 | a0003c0003t0001g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.505-3862A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151440416 | |||||||
| chr6:151440486 | A | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(132): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.505-3932T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151440486 | |||||||
| chr6:151440548 | T | C | 1 | a0002c0002t0002g0068 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.505-3994A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151440548 | |||||||
| chr6:151440728 | T | C | 1 | a0001c0001t0002g0264 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.505-4174A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151440728 | |||||||
| chr6:151440837 | T | C | 1 | a0001c0001t0002g0278 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.505-4283A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151440837 | |||||||
| chr6:151440953 | T | C | 3 | a0002c0002t0001g0096 a0002c0002t0001g0110 a0002c0002t0002g0111 |
3 | HG02258.hp2 HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.504+4355A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151440953 | |||||||
| chr6:151441034 | T | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(46): Show |
59 | HG00099.hp1 HG01074.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.504+4274A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151441034 | |||||||
| chr6:151441155 | G | C | 1 | a0001c0001t0003g0336 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.504+4153C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151441155 | |||||||
| chr6:151441157 | T | C | 1 | a0002c0002t0001g0098 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.504+4151A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151441157 | |||||||
| chr6:151441170 | A | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(46): Show |
59 | HG00099.hp1 HG01074.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.504+4138T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151441170 | |||||||
| chr6:151441202 | A | T | 26 | a0001c0004t0001g0182 a0001c0004t0001g0183 a0001c0004t0001g0184 others(23): Show |
26 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.504+4106T>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151441202 | |||||||
| chr6:151441209 | A | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(86): Show |
101 | HG00099.hp1 HG00140.hp1 HG01069.hp2 others(98): Show |
intron_variant | MODIFIER | c.504+4099T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151441209 | |||||||
| chr6:151441369 | TG | T | 6 | a0001c0001t0002g0258 a0001c0001t0005g0017 a0001c0001t0005g0138 others(3): Show |
7 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+3938delC | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151441369 | |||||||
| chr6:151441419 | C | T | 26 | a0003c0003t0001g0308 a0003c0003t0001g0309 a0003c0003t0004g0004 others(23): Show |
27 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.504+3889G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151441419 | |||||||
| chr6:151441474 | A | G | 26 | a0003c0003t0001g0308 a0003c0003t0001g0309 a0003c0003t0004g0004 others(23): Show |
27 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.504+3834T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151441474 | |||||||
| chr6:151441475 | G | C | 44 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(41): Show |
53 | HG00099.hp1 HG01074.hp1 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.504+3833C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151441475 | |||||||
| chr6:151441727 | A | G | 1 | a0003c0003t0001g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.504+3581T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151441727 | |||||||
| chr6:151441740 | A | C | 24 | a0001c0004t0001g0182 a0001c0004t0001g0183 a0001c0004t0001g0184 others(21): Show |
24 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.504+3568T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151441740 | |||||||
| chr6:151441806 | T | C | 26 | a0003c0003t0001g0308 a0003c0003t0001g0309 a0003c0003t0004g0004 others(23): Show |
27 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.504+3502A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151441806 | |||||||
| chr6:151442055 | G | A | 3 | a0002c0002t0001g0081 a0002c0002t0001g0112 a0002c0002t0001g0127 |
3 | HG02080.hp2 HG02129.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.504+3253C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442055 | |||||||
| chr6:151442091 | C | T | 3 | a0001c0001t0001g0304 a0001c0001t0002g0303 a0001c0001t0002g0317 |
3 | HG02886.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.504+3217G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442091 | |||||||
| chr6:151442148 | A | G | 29 | a0001c0001t0001g0304 a0001c0001t0002g0303 a0001c0001t0002g0317 others(26): Show |
30 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.504+3160T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442148 | |||||||
| chr6:151442265 | A | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(46): Show |
59 | HG00099.hp1 HG01074.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.504+3043T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442265 | |||||||
| chr6:151442285 | C | CAAT | 90 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(87): Show |
102 | HG00099.hp1 HG00140.hp1 HG01069.hp2 others(99): Show |
intron_variant | MODIFIER | c.504+3020_504+3022d others(5): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442285 | |||||||
| chr6:151442353 | A | G | 6 | a0001c0001t0002g0258 a0001c0001t0005g0017 a0001c0001t0005g0138 others(3): Show |
7 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+2955T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442353 | |||||||
| chr6:151442462 | A | T | 26 | a0003c0003t0001g0308 a0003c0003t0001g0309 a0003c0003t0004g0004 others(23): Show |
27 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.504+2846T>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442462 | |||||||
| chr6:151442528 | T | C | 2 | a0001c0001t0002g0203 a0001c0001t0002g0209 |
2 | NA18978.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.504+2780A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442528 | |||||||
| chr6:151442586 | G | A | 26 | a0003c0003t0001g0308 a0003c0003t0001g0309 a0003c0003t0004g0004 others(23): Show |
27 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.504+2722C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442586 | |||||||
| chr6:151442598 | C | T | 6 | a0001c0001t0002g0258 a0001c0001t0005g0017 a0001c0001t0005g0138 others(3): Show |
7 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+2710G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442598 | |||||||
| chr6:151442677 | G | A | 6 | a0004c0005t0001g0255 a0004c0005t0001g0256 a0004c0005t0001g0257 others(3): Show |
6 | HG02258.hp1 HG03041.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.504+2631C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442677 | |||||||
| chr6:151442693 | C | CT | 90 | a0001c0001t0002g0147 a0001c0001t0002g0193 a0001c0001t0002g0194 others(87): Show |
93 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.504+2614dupA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442693 | |||||||
| chr6:151442693 | CT | C | 51 | a0001c0001t0003g0021 a0001c0001t0003g0321 a0001c0001t0003g0323 others(48): Show |
52 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.504+2614delA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442693 | |||||||
| chr6:151442711 | TC | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(74): Show |
89 | HG00099.hp1 HG00140.hp1 HG01069.hp2 others(86): Show |
intron_variant | MODIFIER | c.504+2596delG | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442711 | |||||||
| chr6:151442712 | C | T | 7 | a0001c0001t0001g0171 a0001c0001t0001g0173 a0001c0001t0001g0253 others(4): Show |
7 | HG01884.hp2 HG02886.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.504+2596G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442712 | |||||||
| chr6:151442763 | C | A | 6 | a0001c0001t0002g0258 a0001c0001t0005g0017 a0001c0001t0005g0138 others(3): Show |
7 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+2545G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442763 | |||||||
| chr6:151442904 | A | G | 6 | a0001c0001t0002g0258 a0001c0001t0005g0017 a0001c0001t0005g0138 others(3): Show |
7 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+2404T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442904 | |||||||
| chr6:151442945 | T | C | 1 | a0001c0001t0002g0295 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.504+2363A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442945 | |||||||
| chr6:151443104 | T | C | 64 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(61): Show |
75 | HG00099.hp1 HG01074.hp1 HG01081.hp2 others(72): Show |
intron_variant | MODIFIER | c.504+2204A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443104 | |||||||
| chr6:151443115 | A | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0092 a0001c0001t0001g0192 others(52): Show |
58 | HG00423.hp2 HG00621.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.504+2193T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443115 | |||||||
| chr6:151443129 | G | A | 3 | a0001c0001t0001g0304 a0001c0001t0002g0303 a0001c0001t0002g0317 |
3 | HG02886.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.504+2179C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443129 | |||||||
| chr6:151443404 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(61): Show |
75 | HG00099.hp1 HG01074.hp1 HG01081.hp2 others(72): Show |
intron_variant | MODIFIER | c.504+1904G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443404 | |||||||
| chr6:151443465 | C | G | 1 | a0003c0003t0004g0028 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.504+1843G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443465 | |||||||
| chr6:151443472 | T | G | 1 | a0001c0004t0002g0186 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.504+1836A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443472 | |||||||
| chr6:151443513 | A | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(87): Show |
102 | HG00099.hp1 HG00140.hp1 HG01069.hp2 others(99): Show |
intron_variant | MODIFIER | c.504+1795T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443513 | |||||||
| chr6:151443530 | C | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(46): Show |
59 | HG00099.hp1 HG01074.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.504+1778G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443530 | |||||||
| chr6:151443553 | G | A | 3 | a0003c0003t0004g0022 a0003c0003t0004g0043 a0003c0013t0001g0319 |
3 | HG01884.hp2 HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.504+1755C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443553 | |||||||
| chr6:151443585 | C | T | 26 | a0003c0003t0001g0308 a0003c0003t0001g0309 a0003c0003t0004g0004 others(23): Show |
27 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.504+1723G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443585 | |||||||
| chr6:151443588 | C | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(87): Show |
102 | HG00099.hp1 HG00140.hp1 HG01069.hp2 others(99): Show |
intron_variant | MODIFIER | c.504+1720G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443588 | |||||||
| chr6:151443615 | T | C | 1 | a0001c0001t0002g0150 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.504+1693A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443615 | |||||||
| chr6:151443634 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.504+1674G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443634 | |||||||
| chr6:151443636 | T | C | 6 | a0004c0005t0001g0255 a0004c0005t0001g0256 a0004c0005t0001g0257 others(3): Show |
6 | HG02258.hp1 HG03041.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.504+1672A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443636 | |||||||
| chr6:151443659 | C | T | 1 | a0002c0002t0001g0098 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.504+1649G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443659 | |||||||
| chr6:151443721 | T | C | 2 | a0002c0002t0002g0046 a0002c0002t0002g0052 |
2 | HG02040.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.504+1587A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443721 | |||||||
| chr6:151443741 | C | T | 3 | a0001c0001t0001g0304 a0001c0001t0002g0303 a0001c0001t0002g0317 |
3 | HG02886.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.504+1567G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443741 | |||||||
| chr6:151443820 | C | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(61): Show |
75 | HG00099.hp1 HG01074.hp1 HG01081.hp2 others(72): Show |
intron_variant | MODIFIER | c.504+1488G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443820 | |||||||
| chr6:151444161 | T | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(87): Show |
102 | HG00099.hp1 HG00140.hp1 HG01069.hp2 others(99): Show |
intron_variant | MODIFIER | c.504+1147A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151444161 | |||||||
| chr6:151444198 | A | G | 1 | a0008c0012t0001g0239 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.504+1110T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151444198 | |||||||
| chr6:151444221 | G | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(87): Show |
102 | HG00099.hp1 HG00140.hp1 HG01069.hp2 others(99): Show |
intron_variant | MODIFIER | c.504+1087C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151444221 | |||||||
| chr6:151444285 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.504+1023C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151444285 | |||||||
| chr6:151444333 | A | G | 6 | a0001c0001t0002g0258 a0001c0001t0005g0017 a0001c0001t0005g0138 others(3): Show |
7 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+975T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151444333 | |||||||
| chr6:151444376 | G | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(41): Show |
53 | HG00099.hp1 HG01074.hp1 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.504+932C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151444376 | |||||||
| chr6:151444599 | C | G | 5 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0002g0009 others(2): Show |
6 | HG02280.hp2 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.504+709G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151444599 | |||||||
| chr6:151444650 | T | TGCCTCTT others(19): Show |
26 | a0003c0003t0001g0308 a0003c0003t0001g0309 a0003c0003t0004g0004 others(23): Show |
27 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.504+657_504+658ins others(26): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151444650 | |||||||
| chr6:151444656 | C | T | 1 | a0001c0001t0002g0214 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.504+652G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151444656 | |||||||
| chr6:151444820 | G | A | 1 | a0001c0001t0002g0180 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.504+488C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151444820 | |||||||
| chr6:151444951 | C | T | 1 | a0002c0002t0001g0097 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.504+357G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151444951 | |||||||
| chr6:151444954 | G | T | 1 | a0002c0002t0001g0097 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.504+354C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151444954 | |||||||
| chr6:151444955 | A | T | 1 | a0002c0002t0001g0097 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.504+353T>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151444955 | |||||||
| chr6:151444978 | TTTTTA | T | 6 | a0001c0001t0003g0320 a0001c0001t0003g0337 a0001c0001t0003g0342 others(3): Show |
6 | HG00438.hp1 NA18993.hp2 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.504+325_504+329del others(5): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151444978 | |||||||
| chr6:151445027 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(174): Show |
192 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.504+281A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151445027 | |||||||
| chr6:151445064 | A | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(46): Show |
59 | HG00099.hp1 HG01074.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.504+244T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151445064 | |||||||
| chr6:151445262 | G | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(46): Show |
59 | HG00099.hp1 HG01074.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.504+46C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151445262 | |||||||
| chr6:151446122 | G | A | 1 | a0001c0004t0001g0187 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-14-297C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151446122 | |||||||
| chr6:151446209 | G | C | 3 | a0001c0004t0001g0248 a0001c0004t0001g0249 a0001c0004t0001g0250 |
3 | HG02055.hp1 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-14-384C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151446209 | |||||||
| chr6:151446231 | G | A | 1 | a0003c0013t0001g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-14-406C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151446231 | |||||||
| chr6:151446348 | A | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(72): Show |
86 | HG00099.hp1 HG00140.hp1 HG01069.hp2 others(83): Show |
intron_variant | MODIFIER | c.-14-523T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151446348 | |||||||
| chr6:151446422 | G | GA | 11 | a0001c0001t0001g0210 a0001c0001t0002g0178 a0001c0001t0002g0209 others(8): Show |
11 | HG01175.hp2 HG01261.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-14-598dupT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151446422 | |||||||
| chr6:151446422 | GA | G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(47): Show |
59 | HG00099.hp1 HG01074.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.-14-598delT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151446422 | |||||||
| chr6:151446535 | C | T | 3 | a0003c0003t0004g0036 a0003c0003t0006g0027 a0003c0003t0006g0035 |
3 | HG02040.hp2 NA18941.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.-14-710G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151446535 | |||||||
| chr6:151446772 | A | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(246): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-14-947T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151446772 | |||||||
| chr6:151446900 | CA | C | 148 | a0001c0001t0001g0304 a0001c0001t0002g0180 a0001c0001t0002g0258 others(145): Show |
153 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(150): Show |
intron_variant | MODIFIER | c.-14-1076delT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151446900 | |||||||
| chr6:151446923 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-14-1098C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151446923 | |||||||
| chr6:151447000 | A | T | 7 | a0002c0002t0001g0045 a0002c0002t0001g0078 a0002c0002t0001g0094 others(4): Show |
7 | HG00408.hp1 NA18943.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14-1175T>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447000 | |||||||
| chr6:151447173 | G | A | 26 | a0003c0003t0001g0308 a0003c0003t0001g0309 a0003c0003t0004g0004 others(23): Show |
27 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.-14-1348C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447173 | |||||||
| chr6:151447216 | C | T | 2 | a0001c0001t0003g0343 a0001c0001t0003g0356 |
2 | HG00438.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-14-1391G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447216 | |||||||
| chr6:151447240 | T | C | 5 | a0004c0005t0001g0255 a0004c0005t0001g0256 a0004c0005t0001g0257 others(2): Show |
5 | HG03041.hp1 HG03225.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-1415A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447240 | |||||||
| chr6:151447327 | ACAAATTT others(1): Show |
A | 90 | a0001c0001t0001g0304 a0001c0001t0002g0303 a0001c0001t0002g0317 others(87): Show |
93 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.-14-1510_-14-1503d others(10): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447327 | |||||||
| chr6:151447336 | T | G | 90 | a0001c0001t0001g0304 a0001c0001t0002g0303 a0001c0001t0002g0317 others(87): Show |
93 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.-14-1511A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447336 | |||||||
| chr6:151447360 | A | G | 87 | a0002c0002t0001g0006 a0002c0002t0001g0007 a0002c0002t0001g0045 others(84): Show |
90 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.-14-1535T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447360 | |||||||
| chr6:151447397 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(174): Show |
192 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.-14-1572A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447397 | |||||||
| chr6:151447483 | G | A | 2 | a0001c0001t0002g0211 a0001c0001t0002g0212 |
2 | HG00639.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-14-1658C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447483 | |||||||
| chr6:151447558 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-14-1733C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447558 | |||||||
| chr6:151447565 | C | T | 26 | a0001c0004t0001g0182 a0001c0004t0001g0183 a0001c0004t0001g0184 others(23): Show |
26 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-14-1740G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447565 | |||||||
| chr6:151447764 | AGTTT | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(168): Show |
186 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.-14-1943_-14-1940d others(6): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447764 | |||||||
| chr6:151447800 | T | A | 13 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(10): Show |
15 | HG01081.hp2 HG02615.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.-14-1975A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447800 | |||||||
| chr6:151447810 | C | CT | 6 | a0001c0001t0002g0091 a0001c0001t0002g0189 a0001c0001t0002g0190 others(3): Show |
6 | HG01993.hp1 HG02572.hp1 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-1986dupA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447810 | |||||||
| chr6:151447810 | CT | C | 72 | a0001c0001t0001g0174 a0001c0001t0001g0232 a0001c0001t0002g0059 others(69): Show |
73 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.-14-1986delA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447810 | |||||||
| chr6:151447810 | CTT | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(79): Show |
93 | HG00099.hp1 HG00140.hp1 HG01069.hp2 others(90): Show |
intron_variant | MODIFIER | c.-14-1987_-14-1986d others(4): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447810 | |||||||
| chr6:151447810 | CTTT | C | 89 | a0001c0001t0002g0258 a0001c0001t0002g0317 a0001c0001t0005g0017 others(86): Show |
93 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.-14-1988_-14-1986d others(5): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447810 | |||||||
| chr6:151447836 | G | A | 1 | a0003c0013t0001g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-14-2011C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447836 | |||||||
| chr6:151447916 | C | T | 1 | a0003c0003t0004g0044 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-14-2091G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447916 | |||||||
| chr6:151447997 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(72): Show |
86 | HG00099.hp1 HG00140.hp1 HG01069.hp2 others(83): Show |
intron_variant | MODIFIER | c.-14-2172C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447997 | |||||||
| chr6:151448028 | C | A | 1 | a0001c0001t0002g0297 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-14-2203G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151448028 | |||||||
| chr6:151448085 | G | A | 1 | a0004c0005t0002g0305 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-14-2260C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151448085 | |||||||
| chr6:151448164 | T | G | 1 | a0003c0003t0004g0041 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-14-2339A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151448164 | |||||||
| chr6:151448258 | A | T | 3 | a0001c0001t0001g0304 a0001c0001t0002g0303 a0001c0001t0002g0317 |
3 | HG02886.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-14-2433T>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151448258 | |||||||
| chr6:151448403 | TC | T | 221 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(218): Show |
236 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.-14-2579delG | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151448403 | |||||||
| chr6:151448652 | A | C | 2 | a0001c0004t0001g0182 a0001c0004t0001g0183 |
2 | HG01175.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.-14-2827T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151448652 | |||||||
| chr6:151448718 | C | T | 3 | a0002c0002t0001g0064 a0002c0002t0001g0134 a0002c0002t0002g0063 |
3 | HG02683.hp1 HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-14-2893G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151448718 | |||||||
| chr6:151448878 | A | G | 120 | a0001c0001t0002g0258 a0001c0001t0002g0317 a0001c0001t0005g0017 others(117): Show |
125 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.-14-3053T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151448878 | |||||||
| chr6:151448941 | G | A | 2 | a0001c0001t0001g0304 a0001c0001t0002g0303 |
2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-15+3075C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151448941 | |||||||
| chr6:151448980 | G | A | 1 | a0001c0001t0002g0213 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-15+3036C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151448980 | |||||||
| chr6:151449001 | T | C | 22 | a0003c0003t0004g0004 a0003c0003t0004g0022 a0003c0003t0004g0024 others(19): Show |
23 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.-15+3015A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449001 | |||||||
| chr6:151449060 | C | CA | 74 | a0001c0001t0001g0002 a0001c0001t0001g0092 a0001c0001t0001g0219 others(71): Show |
77 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.-15+2955dupT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449060 | |||||||
| chr6:151449060 | C | CAA | 81 | a0001c0001t0001g0227 a0001c0001t0001g0232 a0001c0001t0001g0299 others(78): Show |
82 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.-15+2954_-15+2955d others(4): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449060 | |||||||
| chr6:151449060 | C | CAAA | 35 | a0001c0001t0001g0304 a0001c0001t0002g0303 a0002c0002t0001g0072 others(32): Show |
37 | HG01069.hp2 HG01071.hp1 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.-15+2953_-15+2955d others(5): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449060 | |||||||
| chr6:151449060 | C | CAAAAAAA others(1): Show |
6 | a0001c0001t0001g0008 a0001c0001t0001g0143 a0001c0001t0001g0148 others(3): Show |
7 | HG01081.hp2 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15+2948_-15+2955d others(10): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449060 | |||||||
| chr6:151449060 | C | CAAAAAAA others(2): Show |
10 | a0001c0001t0001g0149 a0001c0001t0001g0154 a0001c0001t0001g0155 others(7): Show |
13 | HG02280.hp2 HG02559.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.-15+2947_-15+2955d others(11): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449060 | |||||||
| chr6:151449060 | C | CAAAAAAA others(3): Show |
3 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 |
3 | HG03098.hp2 HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-15+2946_-15+2955d others(12): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449060 | |||||||
| chr6:151449060 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0159 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-15+2945_-15+2955d others(13): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449060 | |||||||
| chr6:151449060 | C | CAAAAAAA others(6): Show |
1 | a0001c0004t0008g0365 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-15+2943_-15+2955d others(15): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449060 | |||||||
| chr6:151449060 | C | CAAAAAAA others(7): Show |
1 | a0001c0004t0008g0366 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-15+2942_-15+2955d others(16): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449060 | |||||||
| chr6:151449060 | CA | C | 13 | a0001c0001t0001g0014 a0001c0001t0001g0140 a0001c0001t0001g0141 others(10): Show |
14 | HG01255.hp1 HG02155.hp1 HG03239.hp1 others(11): Show |
intron_variant | MODIFIER | c.-15+2955delT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449060 | |||||||
| chr6:151449060 | CAA | C | 18 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(15): Show |
23 | HG00099.hp1 HG01074.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.-15+2954_-15+2955d others(4): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449060 | |||||||
| chr6:151449097 | G | A | 1 | a0001c0001t0005g0259 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-15+2919C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449097 | |||||||
| chr6:151449164 | C | T | 26 | a0003c0003t0001g0308 a0003c0003t0001g0309 a0003c0003t0004g0004 others(23): Show |
27 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.-15+2852G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449164 | |||||||
| chr6:151449294 | G | A | 1 | a0001c0001t0002g0317 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-15+2722C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449294 | |||||||
| chr6:151449368 | C | T | 207 | a0001c0001t0001g0092 a0001c0001t0001g0304 a0001c0001t0002g0059 others(204): Show |
213 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.-15+2648G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449368 | |||||||
| chr6:151449369 | G | GA | 49 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(46): Show |
59 | HG00099.hp1 HG00438.hp1 HG01074.hp1 others(56): Show |
intron_variant | MODIFIER | c.-15+2646dupT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449369 | |||||||
| chr6:151449369 | G | GAA | 6 | a0001c0001t0001g0145 a0001c0001t0001g0177 a0001c0001t0001g0253 others(3): Show |
6 | HG02723.hp2 NA18979.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+2645_-15+2646d others(4): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449369 | |||||||
| chr6:151449369 | GA | G | 32 | a0001c0001t0002g0258 a0001c0001t0003g0331 a0001c0001t0005g0017 others(29): Show |
34 | HG00140.hp1 HG00621.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.-15+2646delT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449369 | |||||||
| chr6:151449372 | A | C | 5 | a0001c0001t0002g0258 a0001c0001t0005g0017 a0001c0001t0005g0259 others(2): Show |
6 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+2644T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449372 | |||||||
| chr6:151449637 | C | T | 2 | a0001c0001t0002g0147 a0001c0001t0002g0235 |
2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-15+2379G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449637 | |||||||
| chr6:151449656 | T | TC | 9 | a0001c0001t0003g0331 a0001c0001t0003g0332 a0001c0001t0003g0362 others(6): Show |
9 | HG00609.hp1 HG01261.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15+2359dupG | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449656 | |||||||
| chr6:151449660 | CA | C | 3 | a0001c0001t0001g0304 a0001c0001t0002g0303 a0003c0003t0012g0262 |
3 | HG02486.hp2 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-15+2355delT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449660 | |||||||
| chr6:151449661 | A | C | 180 | a0001c0001t0001g0092 a0001c0001t0002g0059 a0001c0001t0002g0073 others(177): Show |
186 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.-15+2355T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449661 | |||||||
| chr6:151449662 | C | CG | 20 | a0001c0001t0002g0076 a0001c0001t0002g0258 a0001c0001t0003g0324 others(17): Show |
20 | HG00408.hp1 HG00621.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-15+2353dupC | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449662 | |||||||
| chr6:151449663 | G | C | 4 | a0001c0001t0001g0304 a0001c0001t0002g0303 a0002c0002t0002g0054 others(1): Show |
4 | HG02486.hp2 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+2353C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449663 | |||||||
| chr6:151449667 | CCCCTCTC others(10): Show |
C | 1 | a0003c0003t0004g0041 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-15+2332_-15+2348d others(19): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449667 | |||||||
| chr6:151449679 | C | G | 11 | a0001c0001t0002g0258 a0001c0001t0005g0017 a0001c0001t0005g0259 others(8): Show |
12 | HG02109.hp2 HG02258.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.-15+2337G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449679 | |||||||
| chr6:151449840 | G | T | 1 | a0002c0002t0001g0075 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-15+2176C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449840 | |||||||
| chr6:151449981 | C | T | 11 | a0001c0001t0003g0323 a0001c0001t0003g0324 a0001c0001t0003g0325 others(8): Show |
11 | HG00099.hp2 HG00323.hp2 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15+2035G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449981 | |||||||
| chr6:151450018 | G | A | 81 | a0001c0001t0001g0092 a0001c0001t0002g0059 a0001c0001t0002g0076 others(78): Show |
82 | HG00408.hp1 HG00609.hp2 HG01109.hp2 others(79): Show |
intron_variant | MODIFIER | c.-15+1998C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450018 | |||||||
| chr6:151450043 | G | A | 11 | a0001c0001t0002g0258 a0001c0001t0005g0017 a0001c0001t0005g0259 others(8): Show |
12 | HG02109.hp2 HG02258.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.-15+1973C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450043 | |||||||
| chr6:151450052 | GCCTCTGC others(32): Show |
G | 1 | a0001c0001t0002g0263 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-15+1925_-15+1963d others(41): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450052 | |||||||
| chr6:151450072 | C | A | 1 | a0001c0001t0002g0317 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-15+1944G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450072 | |||||||
| chr6:151450134 | GCCCGGCC others(33): Show |
G | 98 | a0001c0001t0001g0092 a0001c0001t0002g0059 a0001c0001t0002g0073 others(95): Show |
101 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.-15+1842_-15+1881d others(42): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450134 | |||||||
| chr6:151450141 | C | T | 1 | a0004c0005t0002g0305 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-15+1875G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450141 | |||||||
| chr6:151450168 | A | G | 112 | a0001c0001t0001g0304 a0001c0001t0002g0258 a0001c0001t0002g0303 others(109): Show |
115 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-15+1848T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450168 | |||||||
| chr6:151450291 | C | T | 12 | a0001c0004t0001g0182 a0001c0004t0001g0183 a0001c0004t0001g0184 others(9): Show |
12 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-15+1725G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450291 | |||||||
| chr6:151450322 | C | CGGTCT | 28 | a0001c0001t0002g0258 a0001c0001t0005g0017 a0001c0001t0005g0259 others(25): Show |
30 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.-15+1693_-15+1694i others(7): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450322 | |||||||
| chr6:151450357 | T | G | 7 | a0001c0001t0001g0302 a0001c0001t0002g0016 a0001c0001t0002g0147 others(4): Show |
8 | HG01884.hp2 HG01891.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15+1659A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450357 | |||||||
| chr6:151450359 | GGGGTCAG others(37): Show |
G | 5 | a0001c0001t0002g0258 a0001c0001t0005g0017 a0001c0001t0005g0259 others(2): Show |
6 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+1613_-15+1656d others(46): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450359 | |||||||
| chr6:151450361 | GGTCAGCC others(118): Show |
G | 1 | a0001c0001t0003g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-15+1530_-15+1654d others(2): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450361 | |||||||
| chr6:151450407 | GGTCAGCC others(72): Show |
G | 44 | a0001c0001t0003g0021 a0001c0001t0003g0320 a0001c0001t0003g0321 others(41): Show |
45 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.-15+1530_-15+1608d others(81): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450407 | |||||||
| chr6:151450408 | GTCAGCCC others(71): Show |
G | 2 | a0001c0004t0008g0365 a0001c0004t0008g0366 |
2 | HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-15+1530_-15+1607d others(80): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450408 | |||||||
| chr6:151450422 | CGGCCAGC others(26): Show |
C | 8 | a0001c0001t0002g0258 a0001c0001t0005g0017 a0001c0001t0005g0259 others(5): Show |
9 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.-15+1561_-15+1593d others(35): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450422 | |||||||
| chr6:151450431 | A | G | 1 | a0003c0003t0001g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-15+1585T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450431 | |||||||
| chr6:151450436 | G | A | 1 | a0001c0001t0003g0341 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-15+1580C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450436 | |||||||
| chr6:151450439 | T | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(201): Show |
218 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.-15+1577A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450439 | |||||||
| chr6:151450442 | G | A | 1 | a0003c0013t0001g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-15+1574C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450442 | |||||||
| chr6:151450455 | G | GGGGTCAG others(10): Show |
2 | a0002c0002t0001g0120 a0002c0002t0002g0053 |
2 | HG03831.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.-15+1560_-15+1561i others(19): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450455 | |||||||
| chr6:151450455 | G | GGGTCAGC others(9): Show |
186 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(183): Show |
200 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.-15+1560_-15+1561i others(18): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450455 | |||||||
| chr6:151450455 | G | GGGTTAGC others(9): Show |
11 | a0001c0004t0001g0182 a0001c0004t0001g0183 a0001c0004t0001g0184 others(8): Show |
11 | HG01175.hp1 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-15+1560_-15+1561i others(18): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450455 | |||||||
| chr6:151450455 | G | GTCAGCCC others(52): Show |
1 | a0001c0001t0003g0341 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-15+1560_-15+1561i others(61): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450455 | |||||||
| chr6:151450456 | GGCCAGCC others(23): Show |
G | 3 | a0001c0004t0011g0181 a0003c0003t0004g0024 a0003c0003t0004g0025 |
3 | HG01884.hp1 HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-15+1530_-15+1559d others(32): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450456 | |||||||
| chr6:151450458 | C | T | 1 | a0002c0002t0002g0063 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-15+1558G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450458 | |||||||
| chr6:151450461 | G | GCCCCCCG others(10): Show |
1 | a0002c0002t0002g0063 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-15+1554_-15+1555i others(19): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450461 | |||||||
| chr6:151450467 | G | A | 1 | a0001c0001t0003g0341 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-15+1549C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450467 | |||||||
| chr6:151450477 | A | G | 1 | a0001c0001t0003g0341 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-15+1539T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450477 | |||||||
| chr6:151450489 | C | T | 1 | a0001c0004t0011g0181 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-15+1527G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450489 | |||||||
| chr6:151450509 | C | T | 1 | a0001c0001t0001g0299 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-15+1507G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450509 | |||||||
| chr6:151450518 | C | T | 1 | a0001c0001t0003g0333 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-15+1498G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450518 | |||||||
| chr6:151450525 | G | A | 3 | a0001c0004t0011g0181 a0003c0003t0004g0024 a0003c0003t0004g0025 |
3 | HG01884.hp1 HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-15+1491C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450525 | |||||||
| chr6:151450529 | TGGGGGGT others(42): Show |
T | 1 | a0001c0001t0002g0015 | 2 | NA18971.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.-15+1438_-15+1486d others(51): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450529 | |||||||
| chr6:151450534 | G | T | 3 | a0001c0004t0011g0181 a0003c0003t0004g0024 a0003c0003t0004g0025 |
3 | HG01884.hp1 HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-15+1482C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450534 | |||||||
| chr6:151450546 | G | A | 1 | a0002c0002t0001g0137 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-15+1470C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450546 | |||||||
| chr6:151450564 | TCCGGGAG others(25): Show |
T | 2 | a0001c0004t0008g0365 a0001c0004t0008g0366 |
2 | HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-15+1420_-15+1451d others(34): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450564 | |||||||
| chr6:151450629 | C | T | 2 | a0003c0003t0004g0024 a0003c0003t0004g0025 |
2 | HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-15+1387G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450629 | |||||||
| chr6:151450639 | C | T | 31 | a0001c0001t0002g0258 a0001c0001t0005g0017 a0001c0001t0005g0259 others(28): Show |
33 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.-15+1377G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450639 | |||||||
| chr6:151450657 | T | A | 2 | a0003c0003t0004g0024 a0003c0003t0004g0025 |
2 | HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-15+1359A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450657 | |||||||
| chr6:151450658 | G | T | 5 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0002g0009 others(2): Show |
6 | HG02280.hp2 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+1358C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450658 | |||||||
| chr6:151450676 | C | T | 2 | a0003c0003t0004g0024 a0003c0003t0004g0025 |
2 | HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-15+1340G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450676 | |||||||
| chr6:151450702 | A | G | 3 | a0001c0001t0014g0339 a0003c0003t0004g0024 a0003c0003t0004g0025 |
3 | HG00408.hp2 HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-15+1314T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450702 | |||||||
| chr6:151450704 | T | C | 259 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(256): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.-15+1312A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450704 | |||||||
| chr6:151450726 | A | C | 3 | a0001c0001t0014g0339 a0003c0003t0004g0024 a0003c0003t0004g0025 |
3 | HG00408.hp2 HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-15+1290T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450726 | |||||||
| chr6:151450728 | G | A | 3 | a0001c0001t0014g0339 a0003c0003t0004g0024 a0003c0003t0004g0025 |
3 | HG00408.hp2 HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-15+1288C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450728 | |||||||
| chr6:151450729 | G | T | 3 | a0001c0001t0014g0339 a0003c0003t0004g0024 a0003c0003t0004g0025 |
3 | HG00408.hp2 HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-15+1287C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450729 | |||||||
| chr6:151450750 | G | A | 3 | a0001c0001t0014g0339 a0003c0003t0004g0024 a0003c0003t0004g0025 |
3 | HG00408.hp2 HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-15+1266C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450750 | |||||||
| chr6:151450751 | T | G | 3 | a0001c0001t0014g0339 a0003c0003t0004g0024 a0003c0003t0004g0025 |
3 | HG00408.hp2 HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-15+1265A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450751 | |||||||
| chr6:151450755 | AGAAAGGG others(2): Show |
A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(26): Show |
35 | HG00099.hp1 HG01074.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.-15+1252_-15+1260d others(11): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450755 | |||||||
| chr6:151450771 | G | T | 113 | a0001c0001t0001g0092 a0001c0001t0002g0059 a0001c0001t0002g0073 others(110): Show |
116 | HG00408.hp1 HG00408.hp2 HG00609.hp2 others(113): Show |
intron_variant | MODIFIER | c.-15+1245C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450771 | |||||||
| chr6:151450778 | A | G | 113 | a0001c0001t0001g0092 a0001c0001t0002g0059 a0001c0001t0002g0073 others(110): Show |
116 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.-15+1238T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450778 | |||||||
| chr6:151450804 | T | G | 1 | a0001c0001t0002g0307 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-15+1212A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450804 | |||||||
| chr6:151450809 | G | T | 19 | a0003c0003t0004g0004 a0003c0003t0004g0024 a0003c0003t0004g0025 others(16): Show |
20 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.-15+1207C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450809 | |||||||
| chr6:151450908 | C | T | 5 | a0001c0001t0002g0258 a0001c0001t0005g0017 a0001c0001t0005g0259 others(2): Show |
6 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+1108G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450908 | |||||||
| chr6:151450927 | T | G | 5 | a0002c0002t0001g0130 a0002c0002t0001g0131 a0002c0002t0001g0132 others(2): Show |
5 | HG01975.hp2 HG01993.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15+1089A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450927 | |||||||
| chr6:151450984 | A | G | 31 | a0001c0001t0002g0258 a0001c0001t0005g0017 a0001c0001t0005g0259 others(28): Show |
33 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.-15+1032T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450984 | |||||||
| chr6:151451004 | C | T | 1 | a0003c0003t0004g0004 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-15+1012G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451004 | |||||||
| chr6:151451043 | T | G | 1 | a0001c0001t0001g0254 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-15+973A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451043 | |||||||
| chr6:151451110 | G | T | 1 | a0001c0001t0002g0179 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-15+906C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451110 | |||||||
| chr6:151451150 | A | G | 3 | a0004c0005t0001g0255 a0004c0005t0001g0256 a0004c0005t0001g0257 |
3 | HG03041.hp1 HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-15+866T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451150 | |||||||
| chr6:151451198 | T | TA | 92 | a0001c0001t0001g0092 a0001c0001t0002g0073 a0001c0001t0002g0074 others(89): Show |
95 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.-15+817dupT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451198 | |||||||
| chr6:151451198 | T | TAA | 19 | a0001c0001t0003g0324 a0001c0001t0003g0325 a0001c0001t0003g0326 others(16): Show |
19 | HG00099.hp2 HG00438.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.-15+816_-15+817dup others(2): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451198 | |||||||
| chr6:151451198 | T | TAAA | 29 | a0001c0001t0003g0021 a0001c0001t0003g0341 a0001c0001t0003g0342 others(26): Show |
30 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.-15+815_-15+817dup others(3): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451198 | |||||||
| chr6:151451198 | TA | T | 87 | a0001c0001t0001g0002 a0001c0001t0001g0192 a0001c0001t0001g0207 others(84): Show |
91 | HG00423.hp2 HG00621.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.-15+817delT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451198 | |||||||
| chr6:151451198 | TAA | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(41): Show |
53 | HG00099.hp1 HG01081.hp2 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.-15+816_-15+817del others(2): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451198 | |||||||
| chr6:151451198 | TAAA | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0142 a0001c0001t0001g0143 others(2): Show |
6 | HG01074.hp1 HG02572.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+815_-15+817del others(3): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451198 | |||||||
| chr6:151451199 | A | T | 1 | a0003c0003t0004g0004 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-15+817T>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451199 | |||||||
| chr6:151451212 | A | C | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | NA18987.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-15+804T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451212 | |||||||
| chr6:151451220 | C | A | 2 | a0001c0001t0002g0312 a0001c0001t0002g0313 |
2 | NA18963.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.-15+796G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451220 | |||||||
| chr6:151451222 | C | A | 2 | a0001c0001t0002g0312 a0001c0001t0002g0313 |
2 | NA18963.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.-15+794G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451222 | |||||||
| chr6:151451260 | T | A | 97 | a0001c0001t0001g0092 a0001c0001t0002g0059 a0001c0001t0002g0073 others(94): Show |
100 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.-15+756A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451260 | |||||||
| chr6:151451373 | A | G | 1 | a0001c0001t0002g0139 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-15+643T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451373 | |||||||
| chr6:151451434 | A | G | 97 | a0001c0001t0001g0092 a0001c0001t0002g0059 a0001c0001t0002g0073 others(94): Show |
100 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.-15+582T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451434 | |||||||
| chr6:151451450 | A | G | 2 | a0002c0002t0001g0056 a0002c0002t0010g0057 |
2 | HG02132.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.-15+566T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451450 | |||||||
| chr6:151451468 | C | T | 11 | a0002c0002t0001g0051 a0002c0002t0002g0005 a0002c0002t0002g0046 others(8): Show |
12 | HG02040.hp1 NA18954.hp2 NA18979.hp2 others(9): Show |
intron_variant | MODIFIER | c.-15+548G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451468 | |||||||
| chr6:151451469 | G | A | 3 | a0001c0004t0001g0314 a0001c0004t0001g0315 a0001c0004t0001g0316 |
3 | HG01891.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-15+547C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451469 | |||||||
| chr6:151451488 | G | A | 1 | a0001c0001t0002g0317 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-15+528C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451488 | |||||||
| chr6:151451538 | A | G | 1 | a0002c0002t0001g0045 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-15+478T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451538 | |||||||
| chr6:151451620 | G | A | 1 | a0001c0001t0002g0318 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-15+396C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451620 | |||||||
| chr6:151451977 | G | A | 1 | a0003c0013t0001g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-15+39C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451977 |