Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4141 |
| ensemblid | ENSG00000166986.15 |
| hgncid | 6898 |
| symbol | MARS1 |
| name | methionyl-tRNA synthetase 1 |
| refseq_nuc | NM_004990.4 |
| refseq_prot | NP_004981.2 |
| ensembl_nuc | ENST00000262027.10 |
| ensembl_prot | ENSP00000262027.5 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 57488068 |
| end | 57516652 |
| strand | + |
| ver | v1.2 |
| region | chr12:57488068-57516652 |
| region5000 | chr12:57483068-57521652 |
| regionname0 | MARS1_chr12_57488068_57516652 |
| regionname5000 | MARS1_chr12_57483068_57521652 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 900 | 276 | 76 | 48 | 106 | 10 | 34 | 74 | MARS1_chr12_57483068_57521652 | MARS1 | MRLFV others(895): Show |
chr12 | 57483068 | 57521652 |
| a0002 | 0/0 | 900 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | MRLFV others(895): Show |
chr12 | 57483068 | 57521652 |
| a0003 | 0/0 | 900 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MARS1_chr12_57483068_57521652 | MARS1 | MRLFV others(895): Show |
chr12 | 57483068 | 57521652 |
| a0004 | 0/0 | 900 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | MRLFV others(895): Show |
chr12 | 57483068 | 57521652 |
| a0005 | 0/0 | 900 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | MRLFV others(895): Show |
chr12 | 57483068 | 57521652 |
| a0006 | 0/0 | 900 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | MRLFV others(895): Show |
chr12 | 57483068 | 57521652 |
| a0007 | 0/0 | 900 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | MRLFV others(895): Show |
chr12 | 57483068 | 57521652 |
| a0008 | 0/0 | 900 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | MRLFV others(895): Show |
chr12 | 57483068 | 57521652 |
| a0009 | 0/0 | 900 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | MRLFV others(895): Show |
chr12 | 57483068 | 57521652 |
| a0010 | 0/0 | 900 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | MRLFV others(895): Show |
chr12 | 57483068 | 57521652 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2700 | 249 | 67 | 48 | 90 | 10 | 32 | MARS1_chr12_57483068_57521652 | MARS1 | ATGAG others(2695): Show |
chr12 | 57483068 | 57521652 | ||
| a0001c0002 | 0/0 | 2700 | 11 | 0 | 0 | 10 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | ATGAG others(2695): Show |
chr12 | 57483068 | 57521652 | ||
| a0001c0003 | 0/0 | 2700 | 6 | 6 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | ATGAG others(2695): Show |
chr12 | 57483068 | 57521652 | ||
| a0001c0004 | 0/0 | 2700 | 6 | 0 | 0 | 6 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | ATGAG others(2695): Show |
chr12 | 57483068 | 57521652 | ||
| a0001c0010 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | ATGAG others(2695): Show |
chr12 | 57483068 | 57521652 | ||
| a0001c0013 | 0/0 | 2700 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | ATGAG others(2695): Show |
chr12 | 57483068 | 57521652 | ||
| a0001c0014 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | ATGAG others(2695): Show |
chr12 | 57483068 | 57521652 | ||
| a0001c0015 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | ATGAG others(2695): Show |
chr12 | 57483068 | 57521652 | ||
| a0002c0005 | 0/0 | 2700 | 3 | 3 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | ATGAG others(2695): Show |
chr12 | 57483068 | 57521652 | ||
| a0003c0006 | 0/0 | 2700 | 2 | 0 | 0 | 2 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | ATGAG others(2695): Show |
chr12 | 57483068 | 57521652 | ||
| a0004c0016 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | ATGAG others(2695): Show |
chr12 | 57483068 | 57521652 | ||
| a0005c0012 | 0/0 | 2700 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | ATGAG others(2695): Show |
chr12 | 57483068 | 57521652 | ||
| a0006c0008 | 0/0 | 2700 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | ATGAG others(2695): Show |
chr12 | 57483068 | 57521652 | ||
| a0007c0009 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | ATGAG others(2695): Show |
chr12 | 57483068 | 57521652 | ||
| a0008c0007 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | ATGAG others(2695): Show |
chr12 | 57483068 | 57521652 | ||
| a0009c0011 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | ATGAG others(2695): Show |
chr12 | 57483068 | 57521652 | ||
| a0010c0017 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | ATGAG others(2695): Show |
chr12 | 57483068 | 57521652 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2797 | 249 | 67 | 48 | 90 | 10 | 32 | MARS1_chr12_57483068_57521652 | MARS1 | ATCAG others(2792): Show |
chr12 | 57483068 | 57521652 |
| a0001c0002t0001 | 0/0 | 2797 | 11 | 0 | 0 | 10 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | ATCAG others(2792): Show |
chr12 | 57483068 | 57521652 |
| a0001c0003t0001 | 0/0 | 2797 | 6 | 6 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | ATCAG others(2792): Show |
chr12 | 57483068 | 57521652 |
| a0001c0004t0001 | 0/0 | 2797 | 6 | 0 | 0 | 6 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | ATCAG others(2792): Show |
chr12 | 57483068 | 57521652 |
| a0001c0010t0001 | 0/0 | 2797 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | ATCAG others(2792): Show |
chr12 | 57483068 | 57521652 |
| a0001c0013t0001 | 0/0 | 2797 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | ATCAG others(2792): Show |
chr12 | 57483068 | 57521652 |
| a0001c0014t0001 | 0/0 | 2797 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | ATCAG others(2792): Show |
chr12 | 57483068 | 57521652 |
| a0001c0015t0001 | 0/0 | 2797 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | ATCAG others(2792): Show |
chr12 | 57483068 | 57521652 |
| a0002c0005t0001 | 0/0 | 2797 | 3 | 3 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | ATCAG others(2792): Show |
chr12 | 57483068 | 57521652 |
| a0003c0006t0001 | 0/0 | 2797 | 2 | 0 | 0 | 2 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | ATCAG others(2792): Show |
chr12 | 57483068 | 57521652 |
| a0004c0016t0001 | 0/0 | 2797 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | ATCAG others(2792): Show |
chr12 | 57483068 | 57521652 |
| a0005c0012t0001 | 0/0 | 2797 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | ATCAG others(2792): Show |
chr12 | 57483068 | 57521652 |
| a0006c0008t0001 | 0/0 | 2797 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | ATCAG others(2792): Show |
chr12 | 57483068 | 57521652 |
| a0007c0009t0001 | 0/0 | 2797 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | ATCAG others(2792): Show |
chr12 | 57483068 | 57521652 |
| a0008c0007t0001 | 0/0 | 2797 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | ATCAG others(2792): Show |
chr12 | 57483068 | 57521652 |
| a0009c0011t0001 | 0/0 | 2797 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | ATCAG others(2792): Show |
chr12 | 57483068 | 57521652 |
| a0010c0017t0001 | 0/0 | 2797 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | ATCAG others(2792): Show |
chr12 | 57483068 | 57521652 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0135 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0180 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0003t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0003t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0003t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0003t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0004t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0004t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0004t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0004t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0010t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0013t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0014t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0001c0015t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0002c0005t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0002c0005t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0002c0005t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0003c0006t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0003c0006t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0004c0016t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0005c0012t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0006c0008t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0007c0009t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0008c0007t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0009c0011t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| a0010c0017t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | GBR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | GBR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0262 | EUR | FIN | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | FIN | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | FIN | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | FIN | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00408 | hp2 | a0001 | c0004 | t0001 | g0166 | EAS | CHS | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00438 | hp2 | a0004 | c0016 | t0001 | g0047 | EAS | CHS | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | CHS | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01081 | hp2 | a0005 | c0012 | t0001 | g0103 | AMR | PUR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01358 | hp1 | a0006 | c0008 | t0001 | g0163 | AMR | CLM | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | IBS | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0178 | AFR | ACB | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01891 | hp1 | a0001 | c0014 | t0001 | g0192 | AFR | ACB | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | KHV | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02040 | hp1 | a0007 | c0009 | t0001 | g0270 | EAS | KHV | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | KHV | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02071 | hp2 | a0001 | c0004 | t0001 | g0164 | EAS | KHV | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | KHV | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CDX | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CDX | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | KHV | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02895 | hp2 | a0001 | c0003 | t0001 | g0205 | AFR | GWD | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0204 | AFR | GWD | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02965 | hp1 | a0008 | c0007 | t0001 | g0165 | AFR | ESN | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03139 | hp2 | a0002 | c0005 | t0001 | g0246 | AFR | ESN | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | MSL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0177 | AFR | MSL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03453 | hp1 | a0001 | c0015 | t0001 | g0191 | AFR | MSL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | STU | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | STU | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03831 | hp1 | a0001 | c0013 | t0001 | g0113 | SAS | BEB | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0065 | SAS | BEB | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | STU | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | STU | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | STU | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | STU | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | STU | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | STU | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | YRI | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | YRI | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | YRI | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18942 | hp1 | a0003 | c0006 | t0001 | g0060 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18950 | hp2 | a0001 | c0004 | t0001 | g0167 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18957 | hp1 | a0001 | c0004 | t0001 | g0170 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18979 | hp1 | a0009 | c0011 | t0001 | g0027 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18980 | hp1 | a0001 | c0004 | t0001 | g0168 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18982 | hp1 | a0003 | c0006 | t0001 | g0015 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19003 | hp1 | a0001 | c0004 | t0001 | g0169 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19012 | hp1 | a0010 | c0017 | t0001 | g0274 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | LWK | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0179 | AFR | LWK | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19043 | hp1 | a0001 | c0010 | t0001 | g0048 | AFR | LWK | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19043 | hp2 | a0002 | c0005 | t0001 | g0275 | AFR | LWK | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19240 | hp1 | a0002 | c0005 | t0001 | g0239 | AFR | YRI | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0183 | AFR | YRI | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | USA | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | USA | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | LWK | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | LWK | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0135 | REF | REF | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0180 | REF | REF | MARS1_chr12_57483068_57521652 | MARS1 | chr12 | 57483068 | 57521652 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:57488136 | C | G | 1 | a0010 | 1 | NA19012.hp1 | missense_variant | MODERATE | c.46C>G | p.Leu16Val | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 1/21 | 69/2797 | 46/2703 | 16/900 | chr12 | 57488136 | |||
| chr12:57489304 | C | T | 1 | a0004 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.238C>T | p.Leu80Phe | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 3/21 | 261/2797 | 238/2703 | 80/900 | chr12 | 57489304 | |||
| chr12:57490342 | G | A | 1 | a0008 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.626G>A | p.Ser209Asn | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 6/21 | 649/2797 | 626/2703 | 209/900 | chr12 | 57490342 | |||
| chr12:57490359 | G | A | 1 | a0006 | 1 | HG01358.hp1 | missense_variant | MODERATE | c.643G>A | p.Ala215Thr | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 6/21 | 666/2797 | 643/2703 | 215/900 | chr12 | 57490359 | |||
| chr12:57490554 | C | T | 1 | a0002 | 3 | HG03139.hp2 NA19043.hp2 NA19240.hp1 |
missense_variant | MODERATE | c.680C>T | p.Thr227Ile | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/21 | 703/2797 | 680/2703 | 227/900 | chr12 | 57490554 | |||
| chr12:57500406 | G | A | 1 | a0007 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.1177G>A | p.Ala393Thr | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/21 | 1200/2797 | 1177/2703 | 393/900 | chr12 | 57500406 | |||
| chr12:57514992 | G | A | 1 | a0009 | 1 | NA18979.hp1 | missense_variant | MODERATE | c.2138G>A | p.Arg713Gln | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 17/21 | 2161/2797 | 2138/2703 | 713/900 | chr12 | 57514992 | |||
| chr12:57515034 | G | A | 1 | a0005 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.2180G>A | p.Arg727Gln | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 17/21 | 2203/2797 | 2180/2703 | 727/900 | chr12 | 57515034 | |||
| chr12:57516571 | A | C | 1 | a0003 | 2 | NA18942.hp1 NA18982.hp1 |
missense_variant | MODERATE | c.2693A>C | p.Lys898Thr | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 21/21 | 2716/2797 | 2693/2703 | 898/900 | chr12 | 57516571 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:57489958 | C | T | 1 | a0001c0004 | 6 | HG00408.hp2 HG02071.hp2 NA18950.hp2 others(3): Show |
synonymous_variant | LOW | c.477C>T | p.Pro159Pro | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 5/21 | 500/2797 | 477/2703 | 159/900 | chr12 | 57489958 | |||
| chr12:57498187 | C | T | 1 | a0001c0015 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.801C>T | p.Leu267Leu | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 8/21 | 824/2797 | 801/2703 | 267/900 | chr12 | 57498187 | |||
| chr12:57498259 | C | T | 1 | a0001c0014 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.873C>T | p.Ala291Ala | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 8/21 | 896/2797 | 873/2703 | 291/900 | chr12 | 57498259 | |||
| chr12:57511829 | A | G | 2 | a0001c0002 a0001c0004 |
17 | HG00408.hp2 HG00544.hp2 HG02015.hp2 others(14): Show |
synonymous_variant | LOW | c.1500A>G | p.Lys500Lys | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 12/21 | 1523/2797 | 1500/2703 | 500/900 | chr12 | 57511829 | |||
| chr12:57512809 | G | A | 1 | a0001c0004 | 6 | HG00408.hp2 HG02071.hp2 NA18950.hp2 others(3): Show |
synonymous_variant | LOW | c.1812G>A | p.Gly604Gly | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 15/21 | 1835/2797 | 1812/2703 | 604/900 | chr12 | 57512809 | |||
| chr12:57512839 | T | G | 1 | a0001c0010 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.1842T>G | p.Ala614Ala | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 15/21 | 1865/2797 | 1842/2703 | 614/900 | chr12 | 57512839 | |||
| chr12:57514966 | C | T | 1 | a0001c0013 | 1 | HG03831.hp1 | synonymous_variant | LOW | c.2112C>T | p.Ala704Ala | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 17/21 | 2135/2797 | 2112/2703 | 704/900 | chr12 | 57514966 | |||
| chr12:57515154 | C | A | 1 | a0001c0015 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.2209C>A | p.Arg737Arg | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 18/21 | 2232/2797 | 2209/2703 | 737/900 | chr12 | 57515154 | |||
| chr12:57516313 | G | A | 2 | a0001c0003 a0001c0015 |
7 | HG01884.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
synonymous_variant | LOW | c.2532G>A | p.Ala844Ala | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 20/21 | 2555/2797 | 2532/2703 | 844/900 | chr12 | 57516313 |
| 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 |
|---|
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:57488311 | A | G | 46 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(43): Show |
50 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.109+112A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 1/20 | chr12 | 57488311 | |||||||
| chr12:57488315 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.109+116C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 1/20 | chr12 | 57488315 | |||||||
| chr12:57488357 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.109+158C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 1/20 | chr12 | 57488357 | |||||||
| chr12:57488578 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109+379C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 1/20 | chr12 | 57488578 | |||||||
| chr12:57488684 | A | G | 13 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(10): Show |
13 | HG01167.hp2 HG01169.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.110-335A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 1/20 | chr12 | 57488684 | |||||||
| chr12:57488777 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.110-242C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 1/20 | chr12 | 57488777 | |||||||
| chr12:57488926 | A | C | 1 | a0001c0001t0001g0217 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.110-93A>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 1/20 | chr12 | 57488926 | |||||||
| chr12:57488993 | T | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0011 |
2 | HG01433.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.110-26T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 1/20 | chr12 | 57488993 | |||||||
| chr12:57489406 | A | G | 1 | a0002c0005t0001g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.280-18A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 3/20 | chr12 | 57489406 | |||||||
| chr12:57489849 | C | T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG01256.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.415-47C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 4/20 | chr12 | 57489849 | |||||||
| chr12:57489991 | C | T | 8 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(5): Show |
8 | NA18954.hp1 NA18966.hp1 NA18971.hp2 others(5): Show |
intron_variant | MODIFIER | c.490+20C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 5/20 | chr12 | 57489991 | |||||||
| chr12:57490018 | G | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.490+47G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 5/20 | chr12 | 57490018 | |||||||
| chr12:57490074 | G | A | 1 | a0001c0001t0001g0012 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.490+103G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 5/20 | chr12 | 57490074 | |||||||
| chr12:57490423 | C | G | 1 | a0006c0008t0001g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.663+44C>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 6/20 | chr12 | 57490423 | |||||||
| chr12:57490780 | C | CT | 29 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(26): Show |
29 | HG01167.hp2 HG01169.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.770+159dupT | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57490780 | ||||||
| chr12:57490780 | C | CTT | 8 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(5): Show |
8 | HG02257.hp1 HG02622.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.770+158_770+159dup others(2): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57490780 | ||||||
| chr12:57490780 | CT | C | 23 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(20): Show |
25 | HG02004.hp2 HG02055.hp1 HG02071.hp2 others(22): Show |
intron_variant | MODIFIER | c.770+159delT | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57490780 | ||||||
| chr12:57490875 | C | CT | 16 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0144 others(13): Show |
16 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(13): Show |
intron_variant | MODIFIER | c.770+249dupT | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57490875 | ||||||
| chr12:57490875 | CT | C | 54 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(51): Show |
58 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.770+249delT | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57490875 | ||||||
| chr12:57490899 | G | A | 5 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(2): Show |
5 | HG02109.hp2 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.770+255G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57490899 | |||||||
| chr12:57491217 | A | C | 1 | a0001c0014t0001g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.770+573A>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57491217 | |||||||
| chr12:57491313 | A | G | 1 | a0007c0009t0001g0270 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.770+669A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57491313 | |||||||
| chr12:57491530 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.770+886T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57491530 | |||||||
| chr12:57491620 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.770+976A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57491620 | |||||||
| chr12:57491746 | A | ACTAAGAT others(2614): Show |
1 | a0001c0001t0001g0140 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.770+1118_770+1119i others(2623): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57491746 | ||||||
| chr12:57491846 | C | T | 1 | a0001c0014t0001g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.770+1202C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57491846 | |||||||
| chr12:57491931 | T | G | 1 | a0001c0001t0001g0026 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.770+1287T>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57491931 | |||||||
| chr12:57492140 | A | AC | 6 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0235 others(3): Show |
8 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.770+1496_770+1497i others(3): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57492140 | |||||||
| chr12:57492146 | G | T | 6 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0235 others(3): Show |
8 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.770+1502G>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57492146 | |||||||
| chr12:57492147 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.770+1503C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57492147 | |||||||
| chr12:57492276 | C | CA | 14 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(11): Show |
14 | HG00408.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.770+1649dupA | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57492276 | ||||||
| chr12:57492370 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.770+1726T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57492370 | |||||||
| chr12:57492471 | A | G | 2 | a0001c0001t0001g0139 a0001c0001t0001g0154 |
2 | HG01099.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.770+1827A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57492471 | |||||||
| chr12:57492657 | C | T | 6 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(3): Show |
6 | HG00408.hp2 HG02071.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.770+2013C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57492657 | |||||||
| chr12:57492669 | T | TCA | 10 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(7): Show |
10 | HG02132.hp2 HG02135.hp2 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.770+2070_770+2071d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57492669 | ||||||
| chr12:57492669 | T | TCACA | 8 | a0001c0001t0001g0013 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
8 | HG00621.hp2 HG01358.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.770+2068_770+2071d others(6): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57492669 | ||||||
| chr12:57492669 | T | TCACACA | 4 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(1): Show |
4 | NA18954.hp1 NA18971.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+2066_770+2071d others(8): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57492669 | ||||||
| chr12:57492669 | T | TCACACAC others(1): Show |
3 | a0001c0001t0001g0199 a0001c0003t0001g0177 a0001c0003t0001g0178 |
3 | HG01884.hp2 HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.770+2064_770+2071d others(10): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57492669 | ||||||
| chr12:57492669 | T | TCTCACAC others(3): Show |
1 | a0001c0001t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.770+2026_770+2027i others(12): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57492669 | ||||||
| chr12:57492669 | TCA | T | 84 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(81): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.770+2070_770+2071d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57492669 | ||||||
| chr12:57492669 | TCACA | T | 24 | a0001c0001t0001g0023 a0001c0001t0001g0126 a0001c0001t0001g0127 others(21): Show |
24 | HG00735.hp1 HG01099.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.770+2068_770+2071d others(6): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57492669 | ||||||
| chr12:57492669 | TCACACA | T | 9 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0155 others(6): Show |
9 | HG01884.hp1 HG01943.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.770+2066_770+2071d others(8): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57492669 | ||||||
| chr12:57492669 | TCACACAC others(3): Show |
T | 4 | a0001c0001t0001g0138 a0001c0001t0001g0190 a0001c0014t0001g0192 others(1): Show |
4 | HG01891.hp1 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+2062_770+2071d others(12): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57492669 | ||||||
| chr12:57492669 | TCACACAC others(11): Show |
T | 1 | a0001c0001t0001g0162 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.770+2054_770+2071d others(20): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57492669 | ||||||
| chr12:57492669 | TCACACAC others(17): Show |
T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(52): Show |
59 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.770+2048_770+2071d others(26): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57492669 | ||||||
| chr12:57492669 | TCACACAC others(21): Show |
T | 1 | a0001c0001t0001g0232 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.770+2044_770+2071d others(30): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57492669 | ||||||
| chr12:57492675 | A | T | 1 | a0008c0007t0001g0165 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.770+2031A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57492675 | |||||||
| chr12:57492679 | A | T | 1 | a0001c0001t0001g0174 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.770+2035A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57492679 | |||||||
| chr12:57492682 | C | G | 1 | a0001c0001t0001g0198 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.770+2038C>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57492682 | |||||||
| chr12:57492712 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.770+2068C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57492712 | |||||||
| chr12:57492826 | A | G | 56 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(53): Show |
60 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.770+2182A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57492826 | |||||||
| chr12:57493152 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.770+2508A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493152 | |||||||
| chr12:57493170 | T | G | 1 | a0001c0001t0001g0221 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.770+2526T>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493170 | |||||||
| chr12:57493235 | T | C | 1 | a0001c0015t0001g0191 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.770+2591T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493235 | |||||||
| chr12:57493290 | G | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0043 a0001c0001t0001g0044 |
3 | NA18954.hp2 NA18990.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.770+2646G>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493290 | |||||||
| chr12:57493319 | ATATAT | A | 6 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(3): Show |
6 | HG02109.hp2 HG02922.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.770+2681_770+2685d others(7): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493319 | ||||||
| chr12:57493334 | T | C | 1 | a0001c0001t0001g0146 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.770+2690T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493334 | |||||||
| chr12:57493347 | ATATATAT | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(52): Show |
59 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.770+2709_770+2715d others(9): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493347 | ||||||
| chr12:57493353 | A | G | 1 | a0001c0004t0001g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.770+2709A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493353 | |||||||
| chr12:57493354 | T | A | 1 | a0001c0004t0001g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.770+2710T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493354 | |||||||
| chr12:57493360 | G | A | 2 | a0001c0001t0001g0213 a0001c0004t0001g0167 |
2 | NA18950.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.770+2716G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493360 | |||||||
| chr12:57493365 | G | A | 2 | a0001c0001t0001g0213 a0001c0004t0001g0167 |
2 | NA18950.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.770+2721G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493365 | |||||||
| chr12:57493370 | A | G | 49 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(46): Show |
53 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.770+2726A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493370 | |||||||
| chr12:57493375 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.770+2731T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493375 | |||||||
| chr12:57493376 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.770+2732A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493376 | |||||||
| chr12:57493378 | T | A | 1 | a0001c0001t0001g0265 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.770+2734T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493378 | |||||||
| chr12:57493378 | T | C | 1 | a0001c0001t0001g0010 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.770+2734T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493378 | |||||||
| chr12:57493379 | A | T | 1 | a0001c0001t0001g0265 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.770+2735A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493379 | |||||||
| chr12:57493382 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.770+2738T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493382 | |||||||
| chr12:57493384 | A | G | 1 | a0001c0014t0001g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.770+2740A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493384 | |||||||
| chr12:57493384 | ATATATTA others(5): Show |
A | 1 | a0001c0001t0001g0203 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.770+2741_770+2752d others(14): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493384 | |||||||
| chr12:57493389 | T | TATTATAT others(49): Show |
1 | a0001c0004t0001g0168 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.770+2745_770+2746i others(58): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493389 | |||||||
| chr12:57493390 | T | A | 52 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(49): Show |
56 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.770+2746T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493390 | |||||||
| chr12:57493391 | A | T | 3 | a0001c0001t0001g0213 a0001c0004t0001g0169 a0001c0004t0001g0170 |
3 | NA18957.hp1 NA19003.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.770+2747A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493391 | |||||||
| chr12:57493392 | TATATAAT others(33): Show |
T | 1 | a0001c0001t0001g0243 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.770+2754_770+2793d others(42): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493392 | ||||||
| chr12:57493392 | TATATAAT others(52): Show |
T | 1 | a0001c0001t0001g0269 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.770+2754_770+2812d others(61): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493392 | ||||||
| chr12:57493393 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.770+2749A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493393 | |||||||
| chr12:57493397 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.770+2753A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493397 | |||||||
| chr12:57493397 | AATATATG others(2): Show |
A | 4 | a0001c0001t0001g0255 a0001c0001t0001g0260 a0001c0001t0001g0262 others(1): Show |
4 | HG00280.hp1 HG03710.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.770+2759_770+2767d others(11): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493397 | ||||||
| chr12:57493398 | A | T | 48 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(45): Show |
52 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.770+2754A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493398 | |||||||
| chr12:57493401 | T | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0235 others(3): Show |
8 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.770+2757T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493401 | |||||||
| chr12:57493402 | ATG | A | 43 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(40): Show |
47 | HG00438.hp1 HG00597.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.770+2760_770+2761d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493402 | ||||||
| chr12:57493404 | G | A | 9 | a0001c0001t0001g0125 a0001c0001t0001g0213 a0001c0004t0001g0164 others(6): Show |
9 | HG00408.hp2 HG01891.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.770+2760G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493404 | |||||||
| chr12:57493405 | T | A | 45 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(42): Show |
49 | HG00438.hp1 HG00597.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.770+2761T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493405 | |||||||
| chr12:57493407 | A | T | 4 | a0001c0001t0001g0255 a0001c0001t0001g0260 a0001c0001t0001g0262 others(1): Show |
4 | HG00280.hp1 HG03710.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.770+2763A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493407 | |||||||
| chr12:57493410 | T | A | 1 | a0001c0004t0001g0169 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.770+2766T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493410 | |||||||
| chr12:57493410 | T | G | 1 | a0001c0004t0001g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.770+2766T>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493410 | |||||||
| chr12:57493411 | A | AAT | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.770+2772_770+2773d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493411 | ||||||
| chr12:57493411 | A | T | 2 | a0001c0004t0001g0167 a0001c0004t0001g0169 |
2 | NA18950.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.770+2767A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493411 | |||||||
| chr12:57493412 | A | T | 4 | a0001c0001t0001g0213 a0001c0004t0001g0164 a0001c0004t0001g0166 others(1): Show |
4 | HG00408.hp2 HG02071.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.770+2768A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493412 | |||||||
| chr12:57493413 | TATATTAT others(31): Show |
T | 10 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0244 others(7): Show |
10 | HG01192.hp1 HG02040.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.770+2774_770+2811d others(40): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493413 | ||||||
| chr12:57493417 | T | A | 5 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(2): Show |
5 | HG00408.hp2 HG02071.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.770+2773T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493417 | |||||||
| chr12:57493418 | T | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(36): Show |
43 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.770+2774T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493418 | |||||||
| chr12:57493419 | A | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(31): Show |
38 | HG00438.hp1 HG00597.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.770+2775A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493419 | |||||||
| chr12:57493422 | T | C | 11 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0235 others(8): Show |
13 | HG02055.hp1 HG02056.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.770+2778T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493422 | |||||||
| chr12:57493422 | TG | T | 4 | a0001c0001t0001g0255 a0001c0001t0001g0260 a0001c0001t0001g0262 others(1): Show |
4 | HG00280.hp1 HG03710.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.770+2779delG | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493422 | |||||||
| chr12:57493423 | G | A | 42 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(39): Show |
46 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.770+2779G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493423 | |||||||
| chr12:57493424 | A | T | 2 | a0001c0001t0001g0213 a0001c0004t0001g0169 |
2 | NA19003.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.770+2780A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493424 | |||||||
| chr12:57493426 | ATG | A | 25 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0242 others(22): Show |
27 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.770+2784_770+2785d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493426 | ||||||
| chr12:57493427 | TG | T | 4 | a0001c0001t0001g0255 a0001c0001t0001g0260 a0001c0001t0001g0262 others(1): Show |
4 | HG00280.hp1 HG03710.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.770+2784delG | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493427 | |||||||
| chr12:57493428 | G | A | 16 | a0001c0001t0001g0002 a0001c0001t0001g0125 a0001c0001t0001g0213 others(13): Show |
18 | HG00741.hp1 HG01256.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.770+2784G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493428 | |||||||
| chr12:57493430 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.770+2786A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493430 | |||||||
| chr12:57493431 | T | A | 14 | a0001c0001t0001g0002 a0001c0001t0001g0215 a0001c0001t0001g0234 others(11): Show |
16 | HG00741.hp1 HG01256.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.770+2787T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493431 | |||||||
| chr12:57493432 | A | ATAATATA others(42): Show |
1 | a0001c0004t0001g0169 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.770+2788_770+2789i others(51): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493432 | |||||||
| chr12:57493432 | A | T | 15 | a0001c0001t0001g0002 a0001c0001t0001g0125 a0001c0001t0001g0215 others(12): Show |
17 | HG00741.hp1 HG01256.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.770+2788A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493432 | |||||||
| chr12:57493433 | A | T | 4 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(1): Show |
4 | HG00408.hp2 HG02071.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+2789A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493433 | |||||||
| chr12:57493434 | TATATTAC others(48): Show |
T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0123 |
2 | NA18941.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.770+2795_770+2849d others(57): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493434 | ||||||
| chr12:57493436 | TATTAC | T | 7 | a0001c0001t0001g0255 a0001c0001t0001g0260 a0001c0001t0001g0262 others(4): Show |
7 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.770+2795_770+2799d others(7): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493436 | ||||||
| chr12:57493437 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.770+2793A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493437 | |||||||
| chr12:57493438 | T | A | 2 | a0001c0001t0001g0125 a0001c0004t0001g0167 |
2 | HG03654.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.770+2794T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493438 | |||||||
| chr12:57493438 | T | G | 3 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0170 |
3 | HG00408.hp2 HG02071.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.770+2794T>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493438 | |||||||
| chr12:57493438 | T | TAATATAA others(7): Show |
2 | a0001c0001t0001g0080 a0009c0011t0001g0027 |
2 | HG00423.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.770+2794_770+2795i others(16): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493438 | |||||||
| chr12:57493438 | TTACATAA others(17): Show |
T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(132): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.770+2797_770+2820d others(26): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493438 | ||||||
| chr12:57493438 | TTACATAA others(24): Show |
T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0145 a0001c0001t0001g0152 |
3 | HG00733.hp1 HG01346.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.770+2797_770+2827d others(33): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493438 | ||||||
| chr12:57493438 | TTACATAA others(127): Show |
T | 1 | a0001c0001t0001g0232 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.770+2797_770+2930d others(2): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493438 | ||||||
| chr12:57493439 | T | A | 45 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(42): Show |
48 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.770+2795T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493439 | |||||||
| chr12:57493440 | A | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0242 others(18): Show |
23 | HG00438.hp1 HG00597.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.770+2796A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493440 | |||||||
| chr12:57493441 | C | T | 95 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(92): Show |
98 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.770+2797C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493441 | |||||||
| chr12:57493443 | T | A | 15 | a0001c0001t0001g0002 a0001c0001t0001g0215 a0001c0001t0001g0234 others(12): Show |
17 | HG01256.hp1 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.770+2799T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493443 | |||||||
| chr12:57493444 | A | T | 15 | a0001c0001t0001g0002 a0001c0001t0001g0215 a0001c0001t0001g0234 others(12): Show |
17 | HG01256.hp1 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.770+2800A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493444 | |||||||
| chr12:57493445 | A | T | 2 | a0001c0001t0001g0125 a0008c0007t0001g0165 |
2 | HG02965.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.770+2801A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493445 | |||||||
| chr12:57493446 | TATATA | T | 4 | a0001c0001t0001g0255 a0001c0001t0001g0260 a0001c0001t0001g0262 others(1): Show |
4 | HG00280.hp1 HG03710.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.770+2808_770+2812d others(7): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493446 | ||||||
| chr12:57493448 | T | C | 5 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(2): Show |
5 | HG02109.hp2 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.770+2804T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493448 | |||||||
| chr12:57493449 | A | G | 2 | a0001c0001t0001g0080 a0009c0011t0001g0027 |
2 | HG00423.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.770+2805A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493449 | |||||||
| chr12:57493450 | T | A | 16 | a0001c0001t0001g0002 a0001c0001t0001g0215 a0001c0001t0001g0234 others(13): Show |
18 | HG00741.hp1 HG01256.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.770+2806T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493450 | |||||||
| chr12:57493451 | A | AAT | 25 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0242 others(22): Show |
27 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.770+2812_770+2813d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493451 | ||||||
| chr12:57493451 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.770+2807A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493451 | |||||||
| chr12:57493451 | A | T | 21 | a0001c0001t0001g0002 a0001c0001t0001g0081 a0001c0001t0001g0215 others(18): Show |
23 | HG00741.hp1 HG01256.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.770+2807A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493451 | |||||||
| chr12:57493452 | A | T | 1 | a0001c0001t0001g0213 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.770+2808A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493452 | |||||||
| chr12:57493453 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.770+2809T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493453 | |||||||
| chr12:57493454 | ATAT | A | 16 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0023 others(13): Show |
16 | HG00423.hp1 HG01168.hp2 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.770+2814_770+2816d others(5): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493454 | ||||||
| chr12:57493454 | ATATTATA others(65): Show |
A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0082 a0001c0001t0001g0085 others(4): Show |
8 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(5): Show |
intron_variant | MODIFIER | c.770+2814_770+2885d others(74): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493454 | ||||||
| chr12:57493455 | T | A | 2 | a0001c0003t0001g0204 a0001c0003t0001g0205 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.770+2811T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493455 | |||||||
| chr12:57493456 | A | T | 2 | a0001c0003t0001g0204 a0001c0003t0001g0205 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.770+2812A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493456 | |||||||
| chr12:57493457 | T | A | 3 | a0001c0001t0001g0125 a0001c0003t0001g0204 a0001c0003t0001g0205 |
3 | HG02895.hp2 HG02897.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.770+2813T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493457 | |||||||
| chr12:57493457 | TTATAATA others(7): Show |
T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0174 |
2 | HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.770+2838_770+2851d others(16): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493457 | ||||||
| chr12:57493457 | TTATAATA others(38): Show |
T | 3 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 |
3 | HG02109.hp2 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.770+2838_770+2882d others(47): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493457 | ||||||
| chr12:57493458 | T | A | 1 | a0008c0007t0001g0165 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.770+2814T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493458 | |||||||
| chr12:57493458 | T | G | 1 | a0001c0001t0001g0213 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.770+2814T>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493458 | |||||||
| chr12:57493460 | T | C | 20 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0235 others(17): Show |
22 | HG02055.hp1 HG02056.hp2 HG02083.hp1 others(19): Show |
intron_variant | MODIFIER | c.770+2816T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493460 | |||||||
| chr12:57493461 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.770+2817A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493461 | |||||||
| chr12:57493462 | A | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0125 |
2 | HG01361.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.770+2818A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493462 | |||||||
| chr12:57493463 | T | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(132): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.770+2819T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493463 | |||||||
| chr12:57493463 | T | G | 1 | a0001c0001t0001g0210 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.770+2819T>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493463 | |||||||
| chr12:57493464 | A | ATATAATA others(10): Show |
1 | a0001c0001t0001g0198 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.770+2821_770+2837d others(19): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493464 | ||||||
| chr12:57493464 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.770+2820A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493464 | |||||||
| chr12:57493466 | A | G | 17 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0023 others(14): Show |
17 | HG00423.hp1 HG01168.hp2 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.770+2822A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493466 | |||||||
| chr12:57493470 | T | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0145 a0001c0001t0001g0152 |
3 | HG00733.hp1 HG01346.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.770+2826T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493470 | |||||||
| chr12:57493471 | A | ATAT | 9 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0083 others(6): Show |
9 | HG01168.hp2 HG02109.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.770+2828_770+2830d others(5): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493471 | ||||||
| chr12:57493471 | A | ATATAATA others(3): Show |
7 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0206 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.770+2828_770+2837d others(12): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493471 | ||||||
| chr12:57493471 | A | ATATAATA others(27): Show |
1 | a0001c0001t0001g0219 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.770+2837_770+2838i others(36): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493471 | ||||||
| chr12:57493471 | A | ATATAATA others(75): Show |
1 | a0001c0001t0001g0230 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.770+2837_770+2838i others(84): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493471 | ||||||
| chr12:57493474 | TAATA | T | 12 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0023 others(9): Show |
12 | HG00423.hp1 HG01943.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.770+2831_770+2834d others(6): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493474 | |||||||
| chr12:57493475 | AAT | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0080 others(36): Show |
42 | HG00280.hp1 HG00423.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.770+2837_770+2838d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493475 | ||||||
| chr12:57493476 | A | T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0081 a0001c0001t0001g0216 others(12): Show |
16 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.770+2832A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493476 | |||||||
| chr12:57493477 | T | C | 2 | a0001c0001t0001g0176 a0001c0001t0001g0187 |
2 | HG02717.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.770+2833T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493477 | |||||||
| chr12:57493478 | A | ATAT | 9 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0201 others(6): Show |
9 | HG02055.hp2 HG02615.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.770+2835_770+2837d others(5): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493478 | ||||||
| chr12:57493478 | A | T | 36 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0234 others(33): Show |
39 | HG00280.hp1 HG00733.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.770+2834A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493478 | |||||||
| chr12:57493479 | T | C | 4 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0250 others(1): Show |
4 | HG02622.hp1 HG03139.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+2835T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493479 | |||||||
| chr12:57493480 | A | G | 1 | a0001c0001t0001g0214 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.770+2836A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493480 | |||||||
| chr12:57493481 | T | A | 14 | a0001c0001t0001g0008 a0001c0001t0001g0216 a0001c0001t0001g0217 others(11): Show |
15 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.770+2837T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493481 | |||||||
| chr12:57493481 | T | C | 15 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0235 others(12): Show |
17 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.770+2837T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493481 | |||||||
| chr12:57493481 | T | TATTAC | 3 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0170 |
3 | HG00408.hp2 HG02071.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.770+2838_770+2839i others(7): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493481 | ||||||
| chr12:57493481 | TAATA | T | 5 | a0001c0001t0001g0197 a0001c0001t0001g0223 a0001c0003t0001g0177 others(2): Show |
5 | HG01884.hp2 HG02572.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.770+2838_770+2841d others(6): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493481 | |||||||
| chr12:57493481 | TAATATAT others(21): Show |
T | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.770+2838_770+2865d others(30): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493481 | |||||||
| chr12:57493482 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.770+2838A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493482 | |||||||
| chr12:57493482 | A | T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0216 a0001c0001t0001g0217 others(12): Show |
16 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.770+2838A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493482 | |||||||
| chr12:57493483 | A | T | 1 | a0001c0001t0001g0215 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.770+2839A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493483 | |||||||
| chr12:57493484 | T | C | 4 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0190 others(1): Show |
4 | HG02559.hp1 HG02615.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+2840T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493484 | |||||||
| chr12:57493486 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.770+2842T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493486 | |||||||
| chr12:57493487 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(136): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.770+2843A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493487 | |||||||
| chr12:57493487 | ATAATATA others(363): Show |
A | 1 | a0001c0015t0001g0191 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.770+2845_770+3214d others(2): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493487 | ||||||
| chr12:57493488 | T | A | 15 | a0001c0001t0001g0008 a0001c0001t0001g0215 a0001c0001t0001g0216 others(12): Show |
16 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.770+2844T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493488 | |||||||
| chr12:57493489 | A | AAT | 5 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0168 others(2): Show |
5 | HG00408.hp2 HG02071.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.770+2850_770+2851d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493489 | ||||||
| chr12:57493489 | A | T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0215 a0001c0001t0001g0216 others(12): Show |
16 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.770+2845A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493489 | |||||||
| chr12:57493490 | ATATATTA others(29): Show |
A | 1 | a0001c0001t0001g0037 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.770+2851_770+2886d others(38): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493490 | ||||||
| chr12:57493492 | ATAT | A | 3 | a0001c0001t0001g0197 a0001c0001t0001g0213 a0001c0001t0001g0223 |
3 | HG02572.hp1 HG02572.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.770+2852_770+2854d others(5): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493492 | ||||||
| chr12:57493495 | T | A | 8 | a0001c0001t0001g0032 a0001c0001t0001g0045 a0001c0001t0001g0046 others(5): Show |
8 | HG01168.hp2 HG01256.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.770+2851T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493495 | |||||||
| chr12:57493495 | T | TAA | 7 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0049 others(4): Show |
7 | HG01361.hp1 HG02451.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.770+2851_770+2852i others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493495 | |||||||
| chr12:57493495 | T | TAATATAT others(45): Show |
1 | a0001c0001t0001g0186 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.770+2851_770+2852i others(54): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493495 | |||||||
| chr12:57493495 | TTATA | T | 40 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0014 others(37): Show |
43 | HG00280.hp1 HG00423.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.770+2852_770+2855d others(6): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493495 | |||||||
| chr12:57493496 | T | A | 11 | a0001c0001t0001g0080 a0001c0001t0001g0194 a0001c0001t0001g0196 others(8): Show |
11 | HG00423.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.770+2852T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493496 | |||||||
| chr12:57493496 | TATAATAT others(34): Show |
T | 1 | a0001c0010t0001g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.770+2856_770+2896d others(43): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493496 | ||||||
| chr12:57493497 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.770+2853A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493497 | |||||||
| chr12:57493498 | T | C | 8 | a0001c0001t0001g0245 a0001c0004t0001g0164 a0001c0004t0001g0166 others(5): Show |
8 | HG00408.hp2 HG01891.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.770+2854T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493498 | |||||||
| chr12:57493500 | A | T | 12 | a0001c0001t0001g0080 a0001c0001t0001g0194 a0001c0001t0001g0196 others(9): Show |
12 | HG00423.hp2 HG01256.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.770+2856A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493500 | |||||||
| chr12:57493501 | T | A | 12 | a0001c0001t0001g0080 a0001c0001t0001g0194 a0001c0001t0001g0196 others(9): Show |
12 | HG00423.hp2 HG01256.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.770+2857T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493501 | |||||||
| chr12:57493501 | TA | T | 40 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0014 others(37): Show |
43 | HG00280.hp1 HG00423.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.770+2858delA | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493501 | |||||||
| chr12:57493502 | A | ATATAATA others(8): Show |
1 | a0001c0001t0001g0222 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.770+2867_770+2868i others(17): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493502 | ||||||
| chr12:57493502 | A | T | 14 | a0001c0001t0001g0080 a0001c0001t0001g0083 a0001c0001t0001g0084 others(11): Show |
14 | HG00423.hp2 HG01256.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.770+2858A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493502 | |||||||
| chr12:57493504 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.770+2860A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493504 | |||||||
| chr12:57493505 | T | C | 23 | a0001c0001t0001g0002 a0001c0001t0001g0215 a0001c0001t0001g0234 others(20): Show |
25 | HG00280.hp1 HG01256.hp1 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.770+2861T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493505 | |||||||
| chr12:57493509 | A | ATAT | 5 | a0001c0001t0001g0176 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | HG02257.hp2 HG02717.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.770+2866_770+2868d others(5): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493509 | ||||||
| chr12:57493509 | A | ATATAATA others(3): Show |
2 | a0001c0001t0001g0203 a0001c0003t0001g0179 |
2 | HG02895.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.770+2866_770+2875d others(12): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493509 | ||||||
| chr12:57493509 | A | ATATAT | 9 | a0001c0001t0001g0008 a0001c0001t0001g0242 a0001c0001t0001g0245 others(6): Show |
10 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.770+2869_770+2870i others(7): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493509 | ||||||
| chr12:57493511 | ATAATATA others(4): Show |
A | 1 | a0001c0001t0001g0110 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.770+2868_770+2878d others(13): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493511 | |||||||
| chr12:57493512 | T | TATTAC | 4 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(1): Show |
4 | HG00408.hp2 HG02071.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+2869_770+2870i others(7): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493512 | ||||||
| chr12:57493513 | AATATATA others(12): Show |
A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.770+2875_770+2893d others(21): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493513 | ||||||
| chr12:57493514 | A | T | 4 | a0001c0001t0001g0101 a0001c0001t0001g0131 a0001c0001t0001g0250 others(1): Show |
4 | HG00558.hp1 HG02040.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.770+2870A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493514 | |||||||
| chr12:57493514 | ATATATAA others(5): Show |
A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(68): Show |
76 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.770+2875_770+2886d others(14): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493514 | ||||||
| chr12:57493515 | TATATA | T | 39 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0215 others(36): Show |
42 | HG00280.hp1 HG00733.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.770+2877_770+2881d others(7): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493515 | ||||||
| chr12:57493516 | A | ATAT | 4 | a0001c0001t0001g0198 a0001c0001t0001g0221 a0001c0001t0001g0230 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+2873_770+2875d others(5): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493516 | ||||||
| chr12:57493516 | ATATAATA others(3): Show |
A | 1 | a0001c0001t0001g0141 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.770+2883_770+2892d others(12): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493516 | ||||||
| chr12:57493517 | T | C | 2 | a0001c0001t0001g0250 a0001c0001t0001g0271 |
2 | HG03139.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.770+2873T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493517 | |||||||
| chr12:57493518 | A | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0081 a0001c0001t0001g0123 |
3 | HG01361.hp1 NA18941.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.770+2874A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493518 | |||||||
| chr12:57493518 | ATAAT | A | 63 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(60): Show |
64 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(61): Show |
intron_variant | MODIFIER | c.770+2875_770+2878d others(6): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493518 | |||||||
| chr12:57493518 | ATAATATA others(9): Show |
A | 5 | a0001c0001t0001g0031 a0001c0001t0001g0079 a0001c0001t0001g0132 others(2): Show |
5 | HG01071.hp2 HG01099.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.770+2875_770+2890d others(18): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493518 | |||||||
| chr12:57493520 | A | AAT | 13 | a0001c0001t0001g0008 a0001c0001t0001g0242 a0001c0001t0001g0245 others(10): Show |
14 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(11): Show |
intron_variant | MODIFIER | c.770+2881_770+2882d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493520 | ||||||
| chr12:57493520 | A | T | 21 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0049 others(18): Show |
21 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.770+2876A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493520 | |||||||
| chr12:57493521 | A | T | 2 | a0001c0004t0001g0168 a0001c0004t0001g0169 |
2 | NA18980.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.770+2877A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493521 | |||||||
| chr12:57493523 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.770+2879A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493523 | |||||||
| chr12:57493524 | T | A | 20 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0049 others(17): Show |
20 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.770+2880T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493524 | |||||||
| chr12:57493524 | T | C | 2 | a0001c0004t0001g0168 a0001c0004t0001g0169 |
2 | NA18980.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.770+2880T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493524 | |||||||
| chr12:57493525 | A | T | 20 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0049 others(17): Show |
20 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.770+2881A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493525 | |||||||
| chr12:57493525 | AT | A | 65 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(62): Show |
66 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.770+2883delT | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493525 | ||||||
| chr12:57493526 | T | A | 22 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0049 others(19): Show |
22 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.770+2882T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493526 | |||||||
| chr12:57493526 | T | TTATAATA others(10): Show |
1 | a0001c0001t0001g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.770+2898_770+2899i others(19): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493526 | ||||||
| chr12:57493529 | T | C | 21 | a0001c0001t0001g0002 a0001c0001t0001g0215 a0001c0001t0001g0216 others(18): Show |
23 | HG00408.hp2 HG01256.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.770+2885T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493529 | |||||||
| chr12:57493530 | A | T | 1 | a0009c0011t0001g0027 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.770+2886A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493530 | |||||||
| chr12:57493535 | A | G | 7 | a0001c0001t0001g0004 a0001c0001t0001g0082 a0001c0001t0001g0085 others(4): Show |
8 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(5): Show |
intron_variant | MODIFIER | c.770+2891A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493535 | |||||||
| chr12:57493536 | TA | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0079 a0001c0001t0001g0132 others(2): Show |
5 | HG01071.hp2 HG01099.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.770+2894delA | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493536 | ||||||
| chr12:57493537 | A | AAT | 52 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(49): Show |
56 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.770+2898_770+2899d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493537 | ||||||
| chr12:57493537 | A | T | 1 | a0001c0001t0001g0099 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.770+2893A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493537 | |||||||
| chr12:57493538 | A | T | 3 | a0001c0001t0001g0080 a0001c0001t0001g0250 a0001c0001t0001g0271 |
3 | HG00423.hp2 HG03139.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.770+2894A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493538 | |||||||
| chr12:57493540 | A | T | 1 | a0009c0011t0001g0027 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.770+2896A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493540 | |||||||
| chr12:57493541 | T | A | 1 | a0009c0011t0001g0027 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.770+2897T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493541 | |||||||
| chr12:57493543 | T | A | 4 | a0001c0001t0001g0250 a0001c0001t0001g0271 a0001c0004t0001g0168 others(1): Show |
4 | HG03139.hp1 NA18980.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.770+2899T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493543 | |||||||
| chr12:57493543 | T | TAA | 5 | a0001c0001t0001g0123 a0001c0001t0001g0194 a0001c0001t0001g0196 others(2): Show |
5 | HG02615.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.770+2899_770+2900i others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493543 | |||||||
| chr12:57493544 | T | A | 6 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0186 others(3): Show |
6 | HG01168.hp2 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.770+2900T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493544 | |||||||
| chr12:57493546 | T | C | 31 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(28): Show |
35 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.770+2902T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493546 | |||||||
| chr12:57493548 | A | T | 11 | a0001c0001t0001g0036 a0001c0001t0001g0078 a0001c0001t0001g0186 others(8): Show |
11 | HG00621.hp2 HG02015.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.770+2904A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493548 | |||||||
| chr12:57493549 | T | A | 5 | a0001c0001t0001g0186 a0001c0001t0001g0224 a0001c0001t0001g0250 others(2): Show |
5 | HG02055.hp2 HG02257.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.770+2905T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493549 | |||||||
| chr12:57493550 | A | T | 3 | a0001c0001t0001g0186 a0001c0001t0001g0224 a0001c0003t0001g0179 |
3 | HG02055.hp2 HG02257.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.770+2906A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493550 | |||||||
| chr12:57493553 | T | C | 2 | a0001c0014t0001g0192 a0009c0011t0001g0027 |
2 | HG01891.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.770+2909T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493553 | |||||||
| chr12:57493554 | A | ATT | 11 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0023 others(8): Show |
11 | HG00423.hp1 HG01943.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.770+2910_770+2911i others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493554 | |||||||
| chr12:57493554 | AAT | A | 3 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 |
3 | HG02109.hp2 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.770+2916_770+2917d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493554 | ||||||
| chr12:57493555 | A | T | 1 | a0001c0001t0001g0197 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.770+2911A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493555 | |||||||
| chr12:57493555 | ATATATAA others(5): Show |
A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0082 a0001c0001t0001g0233 |
4 | HG00597.hp2 NA18950.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+2916_770+2927d others(14): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493555 | ||||||
| chr12:57493556 | TATATA | T | 29 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0216 others(26): Show |
29 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.770+2918_770+2922d others(7): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493556 | ||||||
| chr12:57493560 | T | A | 4 | a0001c0001t0001g0174 a0001c0001t0001g0215 a0001c0001t0001g0250 others(1): Show |
4 | HG01256.hp1 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.770+2916T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493560 | |||||||
| chr12:57493560 | T | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG01168.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.770+2916T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493560 | |||||||
| chr12:57493560 | TAATATAT others(7): Show |
T | 2 | a0001c0001t0001g0176 a0008c0007t0001g0165 |
2 | HG02965.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.770+2917_770+2930d others(16): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493560 | |||||||
| chr12:57493561 | A | AAT | 5 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(2): Show |
5 | HG00408.hp2 HG01891.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.770+2922_770+2923d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493561 | ||||||
| chr12:57493561 | A | T | 5 | a0001c0001t0001g0020 a0001c0001t0001g0174 a0001c0001t0001g0215 others(2): Show |
5 | HG01256.hp1 HG02698.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.770+2917A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493561 | |||||||
| chr12:57493561 | AATATATT others(5): Show |
A | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0004c0016t0001g0047 |
3 | HG00438.hp2 HG00621.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.770+2923_770+2934d others(14): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493561 | ||||||
| chr12:57493562 | A | T | 19 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(16): Show |
23 | HG00438.hp1 HG00597.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.770+2918A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493562 | |||||||
| chr12:57493563 | T | A | 1 | a0001c0001t0001g0197 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.770+2919T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493563 | |||||||
| chr12:57493563 | TATATTAT others(23): Show |
T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG00423.hp1 HG01943.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.770+2920_770+2949d others(32): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493563 | |||||||
| chr12:57493564 | A | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0050 a0001c0001t0001g0153 others(3): Show |
6 | HG02451.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.770+2920A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493564 | |||||||
| chr12:57493565 | T | A | 6 | a0001c0001t0001g0023 a0001c0001t0001g0050 a0001c0001t0001g0153 others(3): Show |
6 | HG02451.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.770+2921T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493565 | |||||||
| chr12:57493565 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.770+2921T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493565 | |||||||
| chr12:57493567 | T | A | 22 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(19): Show |
26 | HG00438.hp1 HG00597.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.770+2923T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493567 | |||||||
| chr12:57493567 | T | TA | 6 | a0001c0001t0001g0023 a0001c0001t0001g0050 a0001c0001t0001g0153 others(3): Show |
6 | HG02451.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.770+2923_770+2924i others(3): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493567 | |||||||
| chr12:57493567 | TTATAA | T | 3 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 |
3 | HG02109.hp2 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.770+2928_770+2932d others(7): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493567 | ||||||
| chr12:57493568 | T | A | 1 | a0001c0001t0001g0245 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.770+2924T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493568 | |||||||
| chr12:57493568 | TATA | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0077 a0001c0001t0001g0122 others(1): Show |
4 | HG02735.hp1 HG03098.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.770+2928_770+2930d others(5): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493568 | ||||||
| chr12:57493570 | T | C | 18 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0235 others(15): Show |
18 | HG00408.hp2 HG00733.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.770+2926T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493570 | |||||||
| chr12:57493571 | A | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG01168.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.770+2927A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493571 | |||||||
| chr12:57493572 | A | T | 19 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(16): Show |
23 | HG00438.hp1 HG00597.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.770+2928A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493572 | |||||||
| chr12:57493573 | T | A | 19 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(16): Show |
23 | HG00438.hp1 HG00597.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.770+2929T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493573 | |||||||
| chr12:57493576 | A | G | 3 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 |
3 | HG02109.hp2 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.770+2932A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493576 | |||||||
| chr12:57493577 | T | C | 6 | a0001c0001t0001g0023 a0001c0001t0001g0050 a0001c0001t0001g0153 others(3): Show |
6 | HG02451.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.770+2933T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493577 | |||||||
| chr12:57493578 | A | T | 7 | a0001c0001t0001g0022 a0001c0001t0001g0045 a0001c0001t0001g0046 others(4): Show |
7 | HG01168.hp2 HG01243.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.770+2934A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493578 | |||||||
| chr12:57493579 | A | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(143): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.770+2935A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493579 | |||||||
| chr12:57493580 | TATATA | T | 24 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0238 others(21): Show |
24 | HG00280.hp1 HG01192.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.770+2942_770+2946d others(7): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493580 | ||||||
| chr12:57493581 | ATATAATA others(3): Show |
A | 1 | a0001c0001t0001g0217 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.770+2948_770+2957d others(12): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493581 | ||||||
| chr12:57493584 | T | A | 19 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(16): Show |
23 | HG00438.hp1 HG00597.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.770+2940T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493584 | |||||||
| chr12:57493584 | T | C | 4 | a0001c0001t0001g0197 a0001c0003t0001g0177 a0001c0003t0001g0178 others(1): Show |
4 | HG01884.hp2 HG02572.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.770+2940T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493584 | |||||||
| chr12:57493585 | A | AAT | 7 | a0001c0001t0001g0245 a0001c0003t0001g0177 a0001c0003t0001g0178 others(4): Show |
7 | HG00408.hp2 HG01884.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.770+2946_770+2947d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493585 | ||||||
| chr12:57493585 | A | ATT | 4 | a0001c0001t0001g0023 a0001c0001t0001g0050 a0001c0001t0001g0153 others(1): Show |
4 | HG02451.hp1 HG03225.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+2941_770+2942i others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493585 | |||||||
| chr12:57493585 | A | T | 22 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(19): Show |
26 | HG00438.hp1 HG00597.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.770+2941A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493585 | |||||||
| chr12:57493585 | AATATATT others(5): Show |
A | 1 | a0001c0001t0001g0259 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.770+2947_770+2958d others(14): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493585 | ||||||
| chr12:57493586 | A | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(146): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.770+2942A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493586 | |||||||
| chr12:57493587 | T | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(137): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.770+2943T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493587 | |||||||
| chr12:57493587 | TATATTA | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0077 a0001c0001t0001g0121 others(2): Show |
5 | HG01243.hp1 HG01358.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.770+2944_770+2949d others(8): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493587 | |||||||
| chr12:57493588 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.770+2944A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493588 | |||||||
| chr12:57493588 | A | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0231 |
3 | HG01168.hp2 HG02109.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.770+2944A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493588 | |||||||
| chr12:57493589 | T | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0231 |
3 | HG01168.hp2 HG02109.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.770+2945T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493589 | |||||||
| chr12:57493589 | TATTA | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(137): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.770+2946_770+2949d others(6): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493589 | |||||||
| chr12:57493591 | T | A | 5 | a0001c0001t0001g0235 a0001c0001t0001g0243 a0001c0001t0001g0251 others(2): Show |
5 | HG00733.hp2 HG00735.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.770+2947T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493591 | |||||||
| chr12:57493591 | T | TA | 7 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0198 others(4): Show |
7 | HG01168.hp2 HG02109.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.770+2947_770+2948i others(3): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493591 | |||||||
| chr12:57493591 | T | TATTATAT others(35): Show |
1 | a0001c0003t0001g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.770+2947_770+2948i others(44): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493591 | |||||||
| chr12:57493591 | TTATAATA | T | 9 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(6): Show |
9 | HG02109.hp2 HG02622.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.770+2965_770+2971d others(9): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493591 | ||||||
| chr12:57493592 | T | A | 1 | a0001c0001t0001g0197 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.770+2948T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493592 | |||||||
| chr12:57493593 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.770+2949A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493593 | |||||||
| chr12:57493593 | A | T | 1 | a0001c0001t0001g0197 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.770+2949A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493593 | |||||||
| chr12:57493594 | T | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0053 |
2 | NA19079.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.770+2950T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493594 | |||||||
| chr12:57493594 | T | C | 22 | a0001c0001t0001g0216 a0001c0001t0001g0240 a0001c0001t0001g0241 others(19): Show |
22 | HG00280.hp1 HG00408.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.770+2950T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493594 | |||||||
| chr12:57493595 | A | AT | 7 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0001g0050 others(4): Show |
7 | HG01361.hp1 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.770+2951_770+2952i others(3): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493595 | |||||||
| chr12:57493595 | A | T | 4 | a0001c0001t0001g0198 a0001c0001t0001g0221 a0001c0003t0001g0179 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.770+2951A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493595 | |||||||
| chr12:57493596 | A | T | 8 | a0001c0001t0001g0175 a0001c0001t0001g0235 a0001c0001t0001g0243 others(5): Show |
8 | HG00733.hp2 HG00735.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.770+2952A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493596 | |||||||
| chr12:57493597 | T | A | 6 | a0001c0001t0001g0175 a0001c0001t0001g0235 a0001c0001t0001g0243 others(3): Show |
6 | HG00733.hp2 HG00735.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.770+2953T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493597 | |||||||
| chr12:57493598 | A | ATAT | 7 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0222 others(4): Show |
7 | HG02055.hp2 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.770+2955_770+2957d others(5): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493598 | ||||||
| chr12:57493598 | A | ATATAATA others(3): Show |
2 | a0001c0003t0001g0204 a0001c0003t0001g0205 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.770+2955_770+2964d others(12): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493598 | ||||||
| chr12:57493598 | A | ATATAATA others(10): Show |
3 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0203 |
3 | HG02615.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.770+2966_770+2982d others(19): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493598 | ||||||
| chr12:57493598 | A | ATATAATA others(59): Show |
1 | a0001c0001t0001g0225 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.770+2982_770+2983i others(68): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493598 | ||||||
| chr12:57493598 | A | ATATAATA others(106): Show |
1 | a0001c0001t0001g0206 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.770+2982_770+2983i others(115): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493598 | ||||||
| chr12:57493598 | A | T | 1 | a0001c0001t0001g0259 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.770+2954A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493598 | |||||||
| chr12:57493599 | T | A | 6 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0001g0050 others(3): Show |
6 | HG01361.hp1 HG02451.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.770+2955T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493599 | |||||||
| chr12:57493600 | A | ATATTATA others(6): Show |
1 | a0001c0001t0001g0020 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.770+2958_770+2959i others(15): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493600 | ||||||
| chr12:57493600 | A | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0001g0050 others(3): Show |
6 | HG01361.hp1 HG02451.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.770+2956A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493600 | |||||||
| chr12:57493601 | T | C | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0174 others(1): Show |
4 | HG01168.hp2 HG02109.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.770+2957T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493601 | |||||||
| chr12:57493602 | A | T | 3 | a0001c0001t0001g0197 a0001c0003t0001g0177 a0001c0003t0001g0178 |
3 | HG01884.hp2 HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.770+2958A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493602 | |||||||
| chr12:57493603 | A | T | 2 | a0001c0004t0001g0168 a0001c0004t0001g0169 |
2 | NA18980.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.770+2959A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493603 | |||||||
| chr12:57493604 | TATATA | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(31): Show |
38 | HG00280.hp1 HG00597.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.770+2966_770+2970d others(7): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493604 | ||||||
| chr12:57493608 | T | A | 8 | a0001c0001t0001g0217 a0001c0001t0001g0235 a0001c0001t0001g0243 others(5): Show |
8 | HG00733.hp2 HG00735.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.770+2964T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493608 | |||||||
| chr12:57493608 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(148): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.770+2964T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493608 | |||||||
| chr12:57493609 | A | AAT | 7 | a0001c0001t0001g0197 a0001c0001t0001g0215 a0001c0001t0001g0242 others(4): Show |
7 | HG00438.hp1 HG01256.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.770+2970_770+2971d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493609 | ||||||
| chr12:57493609 | A | AATATAAT others(94): Show |
1 | a0001c0004t0001g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.770+2970_770+2971i others(103): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493609 | ||||||
| chr12:57493609 | A | ATT | 3 | a0001c0001t0001g0221 a0001c0003t0001g0179 a0001c0003t0001g0183 |
3 | HG02647.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.770+2965_770+2966i others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493609 | |||||||
| chr12:57493609 | A | T | 10 | a0001c0001t0001g0217 a0001c0001t0001g0230 a0001c0001t0001g0235 others(7): Show |
10 | HG00733.hp2 HG00735.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.770+2965A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493609 | |||||||
| chr12:57493610 | A | T | 6 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0174 others(3): Show |
6 | HG01168.hp2 HG02056.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.770+2966A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493610 | |||||||
| chr12:57493612 | ATAT | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(149): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.770+2972_770+2974d others(5): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493612 | ||||||
| chr12:57493614 | A | ACAAT | 7 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0032 others(4): Show |
7 | HG01361.hp1 HG02451.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.770+2970_770+2971i others(6): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493614 | |||||||
| chr12:57493614 | AT | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0174 |
3 | HG01168.hp2 HG03098.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.770+2972delT | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493614 | ||||||
| chr12:57493615 | T | A | 10 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0032 others(7): Show |
10 | HG01361.hp1 HG01943.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.770+2971T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493615 | |||||||
| chr12:57493615 | T | TAA | 5 | a0001c0001t0001g0216 a0001c0004t0001g0164 a0001c0004t0001g0166 others(2): Show |
5 | HG00408.hp2 HG01891.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.770+2971_770+2972i others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493615 | |||||||
| chr12:57493615 | T | TATTATAT others(33): Show |
2 | a0001c0003t0001g0177 a0001c0003t0001g0178 |
2 | HG01884.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.770+2971_770+2972i others(42): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493615 | |||||||
| chr12:57493617 | A | G | 11 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0215 others(8): Show |
14 | HG00438.hp1 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.770+2973A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493617 | |||||||
| chr12:57493618 | T | C | 7 | a0001c0001t0001g0087 a0001c0001t0001g0238 a0001c0001t0001g0241 others(4): Show |
7 | HG01192.hp1 HG03017.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.770+2974T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493618 | |||||||
| chr12:57493619 | A | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG01168.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.770+2975A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493619 | |||||||
| chr12:57493619 | AAT | A | 3 | a0001c0001t0001g0221 a0004c0016t0001g0047 a0009c0011t0001g0027 |
3 | HG00438.hp2 HG02647.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.770+2982_770+2983d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493619 | ||||||
| chr12:57493620 | A | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(156): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.770+2976A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493620 | |||||||
| chr12:57493621 | T | A | 1 | a0001c0001t0001g0198 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.770+2977T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493621 | |||||||
| chr12:57493626 | ATT | A | 12 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0174 others(9): Show |
14 | HG00597.hp1 HG00741.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.770+2983_770+2984d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493626 | |||||||
| chr12:57493627 | T | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0197 a0001c0001t0001g0215 others(33): Show |
38 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.770+2983T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493627 | |||||||
| chr12:57493628 | T | A | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.770+2984T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493628 | |||||||
| chr12:57493630 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.770+2986T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493630 | |||||||
| chr12:57493631 | AT | A | 17 | a0001c0001t0001g0216 a0001c0001t0001g0244 a0001c0001t0001g0245 others(14): Show |
17 | HG00280.hp1 HG00408.hp2 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.770+2988delT | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493631 | |||||||
| chr12:57493634 | TA | T | 4 | a0001c0001t0001g0121 a0001c0001t0001g0234 a0002c0005t0001g0239 others(1): Show |
4 | HG01243.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+2992delA | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493634 | ||||||
| chr12:57493634 | TAATTAAT others(1): Show |
T | 5 | a0001c0001t0001g0235 a0001c0001t0001g0241 a0001c0001t0001g0243 others(2): Show |
5 | HG00733.hp2 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.770+2991_770+2998d others(10): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493634 | |||||||
| chr12:57493635 | A | T | 23 | a0001c0001t0001g0002 a0001c0001t0001g0198 a0001c0001t0001g0217 others(20): Show |
25 | HG00438.hp1 HG00735.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.770+2991A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493635 | |||||||
| chr12:57493635 | AAT | A | 12 | a0001c0001t0001g0244 a0001c0001t0001g0255 a0001c0001t0001g0260 others(9): Show |
12 | HG00280.hp1 HG02040.hp1 HG03710.hp1 others(9): Show |
intron_variant | MODIFIER | c.770+2992_770+2993d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493635 | |||||||
| chr12:57493636 | A | T | 8 | a0001c0001t0001g0216 a0001c0001t0001g0234 a0001c0001t0001g0245 others(5): Show |
8 | HG00408.hp2 HG02056.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.770+2992A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493636 | |||||||
| chr12:57493636 | AT | A | 17 | a0001c0001t0001g0002 a0001c0001t0001g0198 a0001c0001t0001g0217 others(14): Show |
19 | HG00438.hp1 HG01192.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.770+2994delT | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493636 | ||||||
| chr12:57493637 | T | A | 5 | a0001c0001t0001g0216 a0001c0001t0001g0245 a0001c0004t0001g0164 others(2): Show |
5 | HG00408.hp2 HG02056.hp2 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.770+2993T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493637 | |||||||
| chr12:57493637 | T | G | 3 | a0001c0001t0001g0234 a0002c0005t0001g0239 a0002c0005t0001g0246 |
3 | HG03041.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.770+2993T>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493637 | |||||||
| chr12:57493637 | T | TAATATAT others(9): Show |
1 | a0001c0001t0001g0231 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.770+2993_770+2994i others(18): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493637 | |||||||
| chr12:57493637 | T | TACATATT others(25): Show |
2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG01168.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.770+2993_770+2994i others(34): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493637 | |||||||
| chr12:57493637 | T | TATATAAT others(40): Show |
2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.770+2993_770+2994i others(49): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493637 | |||||||
| chr12:57493638 | T | A | 14 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0247 others(11): Show |
16 | HG00597.hp1 HG00741.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.770+2994T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493638 | |||||||
| chr12:57493638 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.770+2994T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493638 | |||||||
| chr12:57493639 | A | AT | 5 | a0001c0003t0001g0177 a0001c0003t0001g0178 a0001c0004t0001g0167 others(2): Show |
5 | HG01884.hp2 HG03225.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.770+2995_770+2996i others(3): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493639 | |||||||
| chr12:57493639 | A | T | 12 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0215 others(9): Show |
14 | HG00597.hp1 HG00741.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.770+2995A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493639 | |||||||
| chr12:57493640 | A | T | 4 | a0001c0001t0001g0198 a0001c0001t0001g0221 a0001c0001t0001g0231 others(1): Show |
4 | HG02109.hp1 HG02647.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+2996A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493640 | |||||||
| chr12:57493642 | A | AT | 11 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0247 others(8): Show |
13 | HG00597.hp1 HG00741.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.770+2999dupT | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493642 | ||||||
| chr12:57493644 | A | G | 13 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0235 others(10): Show |
15 | HG00597.hp1 HG00741.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.770+3000A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493644 | |||||||
| chr12:57493645 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.770+3001T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493645 | |||||||
| chr12:57493646 | A | T | 6 | a0001c0001t0001g0174 a0001c0003t0001g0177 a0001c0003t0001g0178 others(3): Show |
6 | HG01884.hp2 HG03098.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.770+3002A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493646 | |||||||
| chr12:57493647 | A | T | 15 | a0001c0001t0001g0197 a0001c0001t0001g0216 a0001c0001t0001g0244 others(12): Show |
15 | HG00280.hp1 HG02040.hp1 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.770+3003A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493647 | |||||||
| chr12:57493649 | A | ATAATATA others(78): Show |
1 | a0001c0004t0001g0170 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.770+3007_770+3008i others(87): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493649 | ||||||
| chr12:57493649 | A | ATAATATA others(97): Show |
2 | a0001c0004t0001g0164 a0001c0004t0001g0166 |
2 | HG00408.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.770+3007_770+3008i others(106): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493649 | ||||||
| chr12:57493649 | A | ATAT | 5 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0004t0001g0167 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.770+3007_770+3008i others(5): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493649 | ||||||
| chr12:57493649 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.770+3005A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493649 | |||||||
| chr12:57493650 | TAC | T | 15 | a0001c0001t0001g0197 a0001c0001t0001g0216 a0001c0001t0001g0244 others(12): Show |
15 | HG00280.hp1 HG02040.hp1 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.770+3008_770+3009d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493650 | ||||||
| chr12:57493652 | C | T | 52 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(49): Show |
56 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.770+3008C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493652 | |||||||
| chr12:57493654 | A | T | 9 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0197 others(6): Show |
9 | HG01168.hp2 HG02109.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.770+3010A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493654 | |||||||
| chr12:57493654 | ATATATAT | A | 16 | a0001c0001t0001g0038 a0001c0001t0001g0194 a0001c0001t0001g0196 others(13): Show |
16 | HG02055.hp2 HG02257.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.770+3025_770+3031d others(9): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493654 | ||||||
| chr12:57493658 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.770+3014A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493658 | |||||||
| chr12:57493660 | A | T | 1 | a0001c0003t0001g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.770+3016A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493660 | |||||||
| chr12:57493661 | T | A | 28 | a0001c0001t0001g0002 a0001c0001t0001g0197 a0001c0001t0001g0215 others(25): Show |
30 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.770+3017T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493661 | |||||||
| chr12:57493661 | TTATATAT others(2): Show |
T | 4 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0186 others(1): Show |
4 | HG02129.hp2 HG02257.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+3033_770+3041d others(11): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493661 | ||||||
| chr12:57493662 | T | A | 9 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0126 others(6): Show |
9 | HG00735.hp1 HG01106.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.770+3018T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493662 | |||||||
| chr12:57493662 | T | TGTA | 3 | a0001c0001t0001g0217 a0001c0001t0001g0253 a0001c0014t0001g0192 |
3 | HG01891.hp1 HG02622.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.770+3018_770+3019i others(5): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493662 | |||||||
| chr12:57493663 | A | ATATATAT others(103): Show |
2 | a0001c0003t0001g0204 a0001c0003t0001g0205 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.770+3024_770+3025i others(112): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493663 | ||||||
| chr12:57493663 | A | ATATATTA others(41): Show |
2 | a0001c0003t0001g0177 a0001c0003t0001g0178 |
2 | HG01884.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.770+3028_770+3029i others(50): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493663 | ||||||
| chr12:57493663 | A | ATATTATA others(5): Show |
1 | a0001c0003t0001g0183 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.770+3022_770+3023i others(14): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493663 | ||||||
| chr12:57493663 | A | G | 1 | a0002c0005t0001g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.770+3019A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493663 | |||||||
| chr12:57493663 | A | T | 6 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0198 others(3): Show |
6 | HG01168.hp2 HG02109.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.770+3019A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493663 | |||||||
| chr12:57493665 | ATATTAT | A | 14 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0235 others(11): Show |
16 | HG00597.hp1 HG00741.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.770+3022_770+3027d others(8): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493665 | |||||||
| chr12:57493665 | ATATTATA others(6): Show |
A | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.770+3022_770+3034d others(15): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493665 | |||||||
| chr12:57493667 | ATTATATA others(183): Show |
A | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.770+3030_770+3219d others(2): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493667 | ||||||
| chr12:57493668 | T | A | 1 | a0001c0001t0001g0216 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.770+3024T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493668 | |||||||
| chr12:57493668 | TTATATAT others(135): Show |
T | 3 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 |
3 | HG02109.hp2 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.770+3030_770+3171d others(2): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493668 | ||||||
| chr12:57493669 | T | A | 13 | a0001c0001t0001g0076 a0001c0001t0001g0203 a0001c0001t0001g0217 others(10): Show |
13 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.770+3025T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493669 | |||||||
| chr12:57493669 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.770+3025T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493669 | |||||||
| chr12:57493669 | T | TATA | 6 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(3): Show |
6 | HG00408.hp2 HG02071.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.770+3026_770+3028d others(5): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493669 | ||||||
| chr12:57493669 | T | TATATATA others(18): Show |
1 | a0001c0001t0001g0050 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.770+3032_770+3033i others(27): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493669 | ||||||
| chr12:57493670 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.770+3026A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493670 | |||||||
| chr12:57493671 | T | TA | 4 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0251 others(1): Show |
4 | HG00438.hp1 HG00735.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+3028dupA | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493671 | ||||||
| chr12:57493672 | ATATATT | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0215 a0001c0001t0001g0234 others(21): Show |
26 | HG00280.hp1 HG00733.hp2 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.770+3029_770+3034d others(8): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493672 | |||||||
| chr12:57493673 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.770+3029T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493673 | |||||||
| chr12:57493676 | A | G | 1 | a0001c0001t0001g0216 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.770+3032A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493676 | |||||||
| chr12:57493677 | T | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0223 |
2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.770+3033T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493677 | |||||||
| chr12:57493677 | TTATA | T | 3 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0245 |
3 | HG02056.hp2 HG03239.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.770+3038_770+3041d others(6): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493677 | ||||||
| chr12:57493678 | T | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0216 others(19): Show |
24 | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.770+3034T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493678 | |||||||
| chr12:57493681 | A | ATAT | 6 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(3): Show |
6 | HG00408.hp2 HG02071.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.770+3038_770+3040d others(5): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493681 | ||||||
| chr12:57493684 | T | A | 1 | a0001c0001t0001g0230 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.770+3040T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493684 | |||||||
| chr12:57493684 | T | C | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.770+3040T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493684 | |||||||
| chr12:57493685 | A | T | 4 | a0001c0001t0001g0050 a0001c0001t0001g0076 a0001c0001t0001g0131 others(1): Show |
4 | HG02040.hp2 HG03704.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+3041A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493685 | |||||||
| chr12:57493686 | A | T | 1 | a0001c0001t0001g0174 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.770+3042A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493686 | |||||||
| chr12:57493688 | A | G | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.770+3044A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493688 | |||||||
| chr12:57493689 | T | C | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.770+3045T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493689 | |||||||
| chr12:57493693 | T | A | 31 | a0001c0001t0001g0002 a0001c0001t0001g0217 a0001c0001t0001g0223 others(28): Show |
33 | HG00280.hp1 HG01891.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.770+3049T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493693 | |||||||
| chr12:57493693 | TTATATAT others(5): Show |
T | 1 | a0001c0001t0001g0271 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.770+3055_770+3066d others(14): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493693 | ||||||
| chr12:57493696 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.770+3052T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493696 | |||||||
| chr12:57493697 | ATATT | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0267 a0001c0001t0001g0269 |
3 | HG01192.hp1 HG01891.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.770+3054_770+3057d others(6): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493697 | |||||||
| chr12:57493698 | T | A | 4 | a0001c0001t0001g0237 a0001c0001t0001g0241 a0001c0001t0001g0242 others(1): Show |
4 | HG00438.hp1 HG00733.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+3054T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493698 | |||||||
| chr12:57493699 | A | T | 4 | a0001c0001t0001g0237 a0001c0001t0001g0241 a0001c0001t0001g0242 others(1): Show |
4 | HG00438.hp1 HG00733.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+3055A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493699 | |||||||
| chr12:57493700 | T | A | 4 | a0001c0001t0001g0237 a0001c0001t0001g0241 a0001c0001t0001g0242 others(1): Show |
4 | HG00438.hp1 HG00733.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+3056T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493700 | |||||||
| chr12:57493701 | T | A | 4 | a0001c0001t0001g0216 a0001c0001t0001g0228 a0001c0001t0001g0229 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.770+3057T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493701 | |||||||
| chr12:57493702 | A | G | 13 | a0001c0001t0001g0244 a0001c0001t0001g0253 a0001c0001t0001g0255 others(10): Show |
13 | HG00280.hp1 HG02040.hp1 HG03710.hp1 others(10): Show |
intron_variant | MODIFIER | c.770+3058A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493702 | |||||||
| chr12:57493702 | A | T | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.770+3058A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493702 | |||||||
| chr12:57493703 | TA | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0267 a0001c0001t0001g0269 |
3 | HG01192.hp1 HG01891.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.770+3061delA | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493703 | ||||||
| chr12:57493704 | A | ATATATTA others(113): Show |
1 | a0008c0007t0001g0165 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.770+3060_770+3061i others(122): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493704 | |||||||
| chr12:57493704 | A | T | 1 | a0001c0001t0001g0050 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.770+3060A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493704 | |||||||
| chr12:57493704 | AATATATT | A | 32 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0032 others(29): Show |
32 | HG00544.hp1 HG00621.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.770+3079_770+3085d others(9): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493704 | ||||||
| chr12:57493705 | A | T | 1 | a0001c0001t0001g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.770+3061A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493705 | |||||||
| chr12:57493705 | ATATAT | A | 20 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0238 others(17): Show |
20 | HG00280.hp1 HG01256.hp1 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.770+3067_770+3071d others(7): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493705 | ||||||
| chr12:57493706 | T | A | 1 | a0001c0001t0001g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.770+3062T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493706 | |||||||
| chr12:57493710 | T | A | 7 | a0001c0001t0001g0035 a0001c0001t0001g0228 a0001c0001t0001g0229 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.770+3066T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493710 | |||||||
| chr12:57493710 | T | TAA | 21 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
25 | HG00597.hp1 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.770+3066_770+3067i others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493710 | |||||||
| chr12:57493710 | T | TATTATAA | 5 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(2): Show |
5 | HG00408.hp2 HG02071.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.770+3066_770+3067i others(9): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493710 | |||||||
| chr12:57493711 | T | A | 10 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0076 others(7): Show |
10 | HG00438.hp1 HG00621.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.770+3067T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493711 | |||||||
| chr12:57493712 | A | ATATAT | 8 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0199 others(5): Show |
8 | HG02257.hp1 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.770+3074_770+3078d others(7): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493712 | ||||||
| chr12:57493712 | A | T | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG00438.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.770+3068A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493712 | |||||||
| chr12:57493716 | A | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0142 |
2 | HG00558.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.770+3072A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493716 | |||||||
| chr12:57493717 | T | A | 54 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(51): Show |
58 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.770+3073T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493717 | |||||||
| chr12:57493718 | T | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0076 others(5): Show |
8 | HG00621.hp2 HG01891.hp1 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.770+3074T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493718 | |||||||
| chr12:57493718 | T | TATA | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.770+3075_770+3077d others(5): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493718 | ||||||
| chr12:57493718 | T | TATAATAT others(3): Show |
1 | a0001c0001t0001g0086 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.770+3077_770+3078i others(12): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493718 | ||||||
| chr12:57493719 | A | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0076 others(2): Show |
5 | HG00621.hp2 HG02015.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.770+3075A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493719 | |||||||
| chr12:57493721 | A | G | 1 | a0001c0004t0001g0166 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.770+3077A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493721 | |||||||
| chr12:57493722 | T | A | 6 | a0001c0001t0001g0031 a0001c0001t0001g0151 a0001c0001t0001g0156 others(3): Show |
7 | HG02056.hp1 HG03540.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.770+3078T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493722 | |||||||
| chr12:57493723 | A | T | 6 | a0001c0001t0001g0031 a0001c0001t0001g0151 a0001c0001t0001g0156 others(3): Show |
7 | HG02056.hp1 HG03540.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.770+3079A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493723 | |||||||
| chr12:57493723 | AT | A | 7 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0076 others(4): Show |
7 | HG00621.hp2 HG02015.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.770+3081delT | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493723 | ||||||
| chr12:57493723 | ATTATATT others(99): Show |
A | 1 | a0001c0001t0001g0059 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.770+3081_770+3186d others(2): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493723 | ||||||
| chr12:57493724 | T | A | 9 | a0001c0001t0001g0031 a0001c0001t0001g0151 a0001c0001t0001g0156 others(6): Show |
10 | HG00438.hp1 HG02056.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.770+3080T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493724 | |||||||
| chr12:57493724 | T | TAATA | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.770+3080_770+3081i others(6): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493724 | |||||||
| chr12:57493724 | T | TATATTGT others(4): Show |
1 | a0001c0014t0001g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.770+3080_770+3081i others(13): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493724 | |||||||
| chr12:57493726 | A | G | 3 | a0001c0001t0001g0245 a0001c0001t0001g0267 a0001c0001t0001g0269 |
3 | HG01192.hp1 HG02056.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.770+3082A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493726 | |||||||
| chr12:57493727 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.770+3083T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493727 | |||||||
| chr12:57493728 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.770+3084A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493728 | |||||||
| chr12:57493728 | A | T | 1 | a0001c0001t0001g0174 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.770+3084A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493728 | |||||||
| chr12:57493729 | T | A | 83 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(80): Show |
88 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.770+3085T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493729 | |||||||
| chr12:57493730 | T | A | 4 | a0001c0001t0001g0237 a0001c0001t0001g0241 a0001c0001t0001g0242 others(1): Show |
4 | HG00438.hp1 HG02818.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+3086T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493730 | |||||||
| chr12:57493731 | A | T | 4 | a0001c0001t0001g0237 a0001c0001t0001g0241 a0001c0001t0001g0242 others(1): Show |
4 | HG00438.hp1 HG02818.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+3087A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493731 | |||||||
| chr12:57493733 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.770+3089A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493733 | |||||||
| chr12:57493735 | A | ATT | 5 | a0001c0001t0001g0031 a0001c0001t0001g0156 a0001c0002t0001g0005 others(2): Show |
6 | HG03540.hp1 NA18960.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.770+3091_770+3092i others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493735 | |||||||
| chr12:57493735 | A | T | 7 | a0001c0001t0001g0013 a0001c0001t0001g0035 a0001c0001t0001g0036 others(4): Show |
7 | HG00621.hp2 HG01891.hp2 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.770+3091A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493735 | |||||||
| chr12:57493736 | A | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(129): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.770+3092A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493736 | |||||||
| chr12:57493736 | ATATATAT others(46): Show |
A | 1 | a0002c0005t0001g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.770+3105_770+3157d others(55): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493736 | ||||||
| chr12:57493737 | T | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.770+3093T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493737 | |||||||
| chr12:57493738 | A | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.770+3094A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493738 | |||||||
| chr12:57493742 | A | T | 1 | a0001c0001t0001g0086 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.770+3098A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493742 | |||||||
| chr12:57493742 | ATT | A | 7 | a0001c0001t0001g0093 a0001c0001t0001g0217 a0001c0001t0001g0235 others(4): Show |
7 | HG00438.hp1 HG00733.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.770+3099_770+3100d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493742 | |||||||
| chr12:57493743 | T | A | 15 | a0001c0001t0001g0086 a0001c0001t0001g0244 a0001c0001t0001g0253 others(12): Show |
15 | HG00280.hp1 HG02040.hp1 HG02965.hp1 others(12): Show |
intron_variant | MODIFIER | c.770+3099T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493743 | |||||||
| chr12:57493743 | TTATATAC others(27): Show |
T | 2 | a0002c0005t0001g0239 a0002c0005t0001g0275 |
2 | NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.770+3105_770+3138d others(36): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493743 | ||||||
| chr12:57493744 | T | A | 1 | a0001c0001t0001g0151 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.770+3100T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493744 | |||||||
| chr12:57493745 | A | T | 1 | a0001c0001t0001g0151 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.770+3101A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493745 | |||||||
| chr12:57493745 | ATATACAT | A | 11 | a0001c0001t0001g0244 a0001c0001t0001g0255 a0001c0001t0001g0260 others(8): Show |
11 | HG00280.hp1 HG02040.hp1 HG03710.hp1 others(8): Show |
intron_variant | MODIFIER | c.770+3106_770+3112d others(9): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493745 | ||||||
| chr12:57493746 | T | TATAATAT others(1): Show |
5 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(2): Show |
5 | HG00408.hp2 HG02071.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.770+3105_770+3106i others(10): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493746 | ||||||
| chr12:57493747 | ATACATTA others(4): Show |
A | 14 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0215 others(11): Show |
16 | HG00597.hp1 HG00735.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.770+3104_770+3114d others(13): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493747 | |||||||
| chr12:57493747 | ATACATTA others(6): Show |
A | 2 | a0001c0001t0001g0267 a0001c0001t0001g0269 |
2 | HG01192.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.770+3104_770+3116d others(15): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493747 | |||||||
| chr12:57493747 | ATACATTA others(29): Show |
A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0236 others(1): Show |
6 | HG02258.hp2 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.770+3104_770+3139d others(38): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493747 | |||||||
| chr12:57493747 | ATACATTA others(66): Show |
A | 1 | a0001c0001t0001g0247 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.770+3104_770+3176d others(75): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493747 | |||||||
| chr12:57493748 | TAC | T | 5 | a0001c0001t0001g0045 a0001c0001t0001g0142 a0001c0001t0001g0216 others(2): Show |
5 | HG01168.hp2 HG01192.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.770+3106_770+3107d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493748 | ||||||
| chr12:57493749 | A | T | 3 | a0001c0002t0001g0005 a0001c0002t0001g0095 a0001c0002t0001g0129 |
4 | NA18960.hp1 NA18979.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+3105A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493749 | |||||||
| chr12:57493750 | C | A | 3 | a0001c0002t0001g0005 a0001c0002t0001g0095 a0001c0002t0001g0129 |
4 | NA18960.hp1 NA18979.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+3106C>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493750 | |||||||
| chr12:57493750 | C | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.770+3106C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493750 | |||||||
| chr12:57493751 | A | T | 10 | a0001c0001t0001g0086 a0001c0001t0001g0118 a0001c0001t0001g0122 others(7): Show |
11 | HG01167.hp1 HG02056.hp1 HG02735.hp1 others(8): Show |
intron_variant | MODIFIER | c.770+3107A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493751 | |||||||
| chr12:57493752 | T | A | 19 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0076 others(16): Show |
20 | HG00621.hp2 HG01167.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.770+3108T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493752 | |||||||
| chr12:57493752 | T | TTA | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.770+3112_770+3113d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493752 | ||||||
| chr12:57493752 | T | TTATATTA others(7): Show |
2 | a0001c0003t0001g0204 a0001c0003t0001g0205 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.770+3119_770+3120i others(16): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493752 | ||||||
| chr12:57493756 | ATT | A | 4 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0235 others(1): Show |
4 | HG00733.hp2 HG02055.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.770+3113_770+3114d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493756 | |||||||
| chr12:57493757 | T | A | 6 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0241 others(3): Show |
6 | HG00438.hp1 HG02818.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.770+3113T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493757 | |||||||
| chr12:57493757 | TTA | T | 3 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0221 |
3 | HG02572.hp1 HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.770+3121_770+3122d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493757 | ||||||
| chr12:57493758 | T | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.770+3114T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493758 | |||||||
| chr12:57493758 | T | TATATATA others(4): Show |
1 | a0001c0001t0001g0050 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.770+3124_770+3125i others(13): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493758 | ||||||
| chr12:57493759 | A | T | 5 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0076 others(2): Show |
5 | HG00621.hp2 HG01891.hp2 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.770+3115A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493759 | |||||||
| chr12:57493763 | A | T | 1 | a0001c0001t0001g0238 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.770+3119A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493763 | |||||||
| chr12:57493764 | TATTATA | T | 10 | a0001c0001t0001g0244 a0001c0001t0001g0255 a0001c0001t0001g0260 others(7): Show |
10 | HG00280.hp1 HG02040.hp1 HG03710.hp1 others(7): Show |
intron_variant | MODIFIER | c.770+3121_770+3126d others(8): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493764 | |||||||
| chr12:57493766 | T | A | 27 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0197 others(24): Show |
30 | HG00408.hp2 HG00597.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.770+3122T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493766 | |||||||
| chr12:57493766 | TTATATAT others(46): Show |
T | 1 | a0001c0001t0001g0132 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.770+3128_770+3180d others(55): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493766 | ||||||
| chr12:57493767 | T | A | 6 | a0001c0001t0001g0238 a0001c0001t0001g0253 a0001c0001t0001g0267 others(3): Show |
6 | HG01192.hp1 HG03540.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.770+3123T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493767 | |||||||
| chr12:57493770 | A | ATAT | 6 | a0001c0001t0001g0245 a0001c0004t0001g0164 a0001c0004t0001g0166 others(3): Show |
6 | HG00408.hp2 HG02056.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.770+3127_770+3129d others(5): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493770 | ||||||
| chr12:57493770 | ATATAAT | A | 5 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0076 others(2): Show |
5 | HG00621.hp2 HG01891.hp2 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.770+3127_770+3132d others(8): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493770 | |||||||
| chr12:57493773 | TAATA | T | 14 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0240 others(11): Show |
16 | HG00597.hp1 HG00733.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.770+3130_770+3133d others(6): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493773 | |||||||
| chr12:57493774 | A | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(140): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.770+3130A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493774 | |||||||
| chr12:57493775 | A | T | 5 | a0001c0001t0001g0231 a0001c0001t0001g0237 a0001c0001t0001g0241 others(2): Show |
5 | HG00438.hp1 HG02109.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.770+3131A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493775 | |||||||
| chr12:57493776 | T | TA | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(129): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.770+3133dupA | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493776 | ||||||
| chr12:57493776 | T | TAATATAT others(11): Show |
1 | a0001c0001t0001g0088 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.770+3133_770+3134i others(20): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493776 | ||||||
| chr12:57493776 | T | TATATATT others(10): Show |
5 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0089 others(2): Show |
5 | NA18943.hp1 NA18974.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.770+3142_770+3143i others(19): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493776 | ||||||
| chr12:57493776 | T | TATATATT others(10): Show |
5 | a0001c0001t0001g0225 a0001c0003t0001g0177 a0001c0003t0001g0178 others(2): Show |
5 | HG01884.hp2 HG03041.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.770+3133_770+3149d others(19): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493776 | ||||||
| chr12:57493776 | T | TATATATT others(27): Show |
1 | a0001c0001t0001g0054 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.770+3149_770+3150i others(36): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493776 | ||||||
| chr12:57493776 | T | TATATATT others(34): Show |
2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | HG02735.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.770+3149_770+3150i others(43): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493776 | ||||||
| chr12:57493776 | T | TATATTAT others(1): Show |
3 | a0001c0002t0001g0005 a0001c0002t0001g0095 a0001c0002t0001g0129 |
4 | NA18960.hp1 NA18979.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+3136_770+3137i others(10): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493776 | ||||||
| chr12:57493777 | A | ATATATTA others(5): Show |
2 | a0001c0001t0001g0020 a0006c0008t0001g0163 |
2 | HG01358.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.770+3139_770+3150d others(14): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493777 | ||||||
| chr12:57493780 | T | A | 1 | a0001c0001t0001g0248 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.770+3136T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493780 | |||||||
| chr12:57493782 | T | A | 37 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0086 others(34): Show |
39 | HG00280.hp1 HG00408.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.770+3138T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493782 | |||||||
| chr12:57493782 | T | TTATATAT others(10): Show |
3 | a0001c0001t0001g0055 a0001c0001t0001g0058 a0001c0001t0001g0085 |
3 | HG00621.hp1 HG01358.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.770+3149_770+3150i others(19): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493782 | ||||||
| chr12:57493782 | T | TTATATAT others(36): Show |
4 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0223 others(1): Show |
4 | HG02055.hp2 HG02572.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.770+3149_770+3150i others(45): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493782 | ||||||
| chr12:57493782 | T | TTATATAT others(104): Show |
1 | a0001c0001t0001g0222 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.770+3149_770+3150i others(113): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493782 | ||||||
| chr12:57493783 | T | A | 3 | a0001c0001t0001g0174 a0001c0001t0001g0231 a0001c0001t0001g0235 |
3 | HG02055.hp1 HG02109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.770+3139T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493783 | |||||||
| chr12:57493783 | T | TATATATT others(3): Show |
3 | a0001c0001t0001g0032 a0001c0001t0001g0057 a0001c0001t0001g0226 |
3 | HG01071.hp1 HG03209.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.770+3140_770+3149d others(12): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493783 | ||||||
| chr12:57493783 | T | TATATATT others(10): Show |
2 | a0001c0001t0001g0056 a0001c0001t0001g0214 |
2 | HG00544.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.770+3149_770+3150i others(19): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493783 | ||||||
| chr12:57493784 | A | T | 1 | a0001c0001t0001g0231 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.770+3140A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493784 | |||||||
| chr12:57493785 | TATATTAT others(86): Show |
T | 1 | a0001c0001t0001g0242 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.770+3146_770+3238d others(95): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493785 | ||||||
| chr12:57493786 | ATATTATA others(31): Show |
A | 1 | a0001c0001t0001g0249 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.770+3146_770+3183d others(40): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493786 | ||||||
| chr12:57493787 | T | A | 1 | a0001c0001t0001g0238 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.770+3143T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493787 | |||||||
| chr12:57493787 | TATTATAT others(84): Show |
T | 3 | a0001c0001t0001g0237 a0001c0001t0001g0241 a0001c0001t0001g0271 |
3 | HG02818.hp2 HG03654.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.770+3146_770+3236d others(93): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493787 | ||||||
| chr12:57493788 | A | T | 1 | a0001c0001t0001g0238 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.770+3144A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493788 | |||||||
| chr12:57493789 | T | A | 35 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0186 others(32): Show |
37 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.770+3145T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493789 | |||||||
| chr12:57493789 | T | TTATAATA others(38): Show |
11 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0199 others(8): Show |
11 | HG02257.hp1 HG02615.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.770+3149_770+3150i others(47): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493789 | ||||||
| chr12:57493789 | TTA | T | 3 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0094 |
3 | HG00741.hp2 HG02129.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.770+3151_770+3152d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493789 | ||||||
| chr12:57493790 | T | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0235 others(2): Show |
7 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.770+3146T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493790 | |||||||
| chr12:57493790 | T | C | 1 | a0001c0001t0001g0008 | 2 | NA19007.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.770+3146T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493790 | |||||||
| chr12:57493790 | T | TATA | 6 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0228 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.770+3147_770+3149d others(5): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493790 | ||||||
| chr12:57493792 | T | TA | 6 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(3): Show |
6 | HG00408.hp2 HG01891.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.770+3149dupA | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493792 | ||||||
| chr12:57493793 | ATATTATA others(10): Show |
A | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG01256.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.770+3153_770+3169d others(19): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493793 | ||||||
| chr12:57493794 | T | A | 2 | a0001c0001t0001g0267 a0001c0001t0001g0269 |
2 | HG01192.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.770+3150T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493794 | |||||||
| chr12:57493795 | A | T | 2 | a0001c0001t0001g0267 a0001c0001t0001g0269 |
2 | HG01192.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.770+3151A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493795 | |||||||
| chr12:57493796 | T | A | 8 | a0001c0001t0001g0045 a0001c0001t0001g0083 a0001c0001t0001g0084 others(5): Show |
8 | HG00741.hp2 HG01168.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.770+3152T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493796 | |||||||
| chr12:57493796 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.770+3152T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493796 | |||||||
| chr12:57493796 | T | TA | 6 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(3): Show |
6 | HG00408.hp2 HG01891.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.770+3152_770+3153i others(3): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493796 | |||||||
| chr12:57493797 | T | A | 1 | a0001c0001t0001g0174 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.770+3153T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493797 | |||||||
| chr12:57493800 | ATTATATA others(51): Show |
A | 1 | a0001c0001t0001g0238 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.770+3158_770+3215d others(60): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493800 | ||||||
| chr12:57493801 | T | A | 38 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(35): Show |
42 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.770+3157T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493801 | |||||||
| chr12:57493802 | T | A | 6 | a0001c0001t0001g0045 a0001c0001t0001g0093 a0001c0001t0001g0096 others(3): Show |
6 | HG01168.hp2 HG01192.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.770+3158T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493802 | |||||||
| chr12:57493803 | A | T | 5 | a0001c0001t0001g0045 a0001c0001t0001g0093 a0001c0001t0001g0096 others(2): Show |
5 | HG01168.hp2 HG01192.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.770+3159A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493803 | |||||||
| chr12:57493803 | ATATAATG others(26): Show |
A | 3 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0221 |
3 | HG02572.hp1 HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.770+3166_770+3198d others(35): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493803 | ||||||
| chr12:57493805 | ATAATG | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0240 others(5): Show |
10 | HG00741.hp1 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.770+3164_770+3168d others(7): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493805 | ||||||
| chr12:57493807 | A | T | 1 | a0001c0010t0001g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.770+3163A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493807 | |||||||
| chr12:57493807 | AAT | A | 6 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(3): Show |
6 | HG00408.hp2 HG01891.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.770+3164_770+3165d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493807 | |||||||
| chr12:57493808 | A | T | 9 | a0001c0001t0001g0045 a0001c0001t0001g0083 a0001c0001t0001g0084 others(6): Show |
9 | HG00741.hp2 HG01168.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.770+3164A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493808 | |||||||
| chr12:57493809 | T | A | 5 | a0001c0001t0001g0045 a0001c0001t0001g0093 a0001c0001t0001g0096 others(2): Show |
5 | HG01168.hp2 HG01192.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.770+3165T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493809 | |||||||
| chr12:57493809 | T | TATATATT others(5): Show |
1 | a0001c0001t0001g0046 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.770+3165_770+3166i others(14): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493809 | |||||||
| chr12:57493810 | G | A | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.770+3166G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493810 | |||||||
| chr12:57493810 | G | T | 12 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0093 others(9): Show |
12 | HG00408.hp2 HG01168.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.770+3166G>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493810 | |||||||
| chr12:57493815 | TTA | T | 4 | a0001c0001t0001g0030 a0001c0001t0001g0064 a0001c0001t0001g0072 others(1): Show |
4 | HG03710.hp2 HG04184.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.770+3179_770+3180d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493815 | ||||||
| chr12:57493815 | TTATA | T | 3 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0094 |
3 | HG00741.hp2 HG02129.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.770+3177_770+3180d others(6): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493815 | ||||||
| chr12:57493816 | T | A | 2 | a0001c0001t0001g0231 a0001c0010t0001g0048 |
2 | HG02109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.770+3172T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493816 | |||||||
| chr12:57493819 | AT | A | 31 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0235 others(28): Show |
33 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.770+3176delT | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493819 | |||||||
| chr12:57493819 | ATATAT | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0240 others(4): Show |
9 | HG00741.hp1 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.770+3186_770+3190d others(7): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493819 | ||||||
| chr12:57493822 | T | A | 1 | a0001c0004t0001g0170 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.770+3178T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493822 | |||||||
| chr12:57493822 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.770+3178T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493822 | |||||||
| chr12:57493823 | A | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(149): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.770+3179A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493823 | |||||||
| chr12:57493823 | AT | A | 32 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0235 others(29): Show |
34 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.770+3181delT | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493823 | ||||||
| chr12:57493824 | T | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(149): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.770+3180T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493824 | |||||||
| chr12:57493824 | T | TTATATAA others(125): Show |
1 | a0001c0001t0001g0230 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.770+3185_770+3186i others(134): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493824 | ||||||
| chr12:57493828 | A | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.770+3184A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493828 | |||||||
| chr12:57493829 | T | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.770+3185T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493829 | |||||||
| chr12:57493829 | T | TATTA | 6 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(3): Show |
6 | HG00408.hp2 HG01891.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.770+3185_770+3186i others(6): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493829 | |||||||
| chr12:57493830 | T | A | 25 | a0001c0001t0001g0013 a0001c0001t0001g0083 a0001c0001t0001g0084 others(22): Show |
25 | HG00741.hp2 HG01258.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.770+3186T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493830 | |||||||
| chr12:57493830 | T | C | 1 | a0001c0001t0001g0273 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.770+3186T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493830 | |||||||
| chr12:57493831 | ATATAT | A | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0231 |
3 | HG01256.hp1 HG02109.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.770+3192_770+3196d others(7): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493831 | ||||||
| chr12:57493833 | ATAT | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0083 a0001c0001t0001g0084 others(6): Show |
9 | HG00741.hp2 HG01258.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.770+3193_770+3195d others(5): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493833 | ||||||
| chr12:57493835 | A | AAT | 5 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0093 others(2): Show |
5 | HG01168.hp2 HG01192.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.770+3191_770+3192i others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493835 | |||||||
| chr12:57493835 | A | AATATATT others(28): Show |
1 | a0001c0001t0001g0226 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.770+3191_770+3192i others(37): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493835 | |||||||
| chr12:57493835 | A | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0230 |
2 | HG02056.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.770+3191A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493835 | |||||||
| chr12:57493836 | T | A | 8 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0093 others(5): Show |
8 | HG01168.hp2 HG01192.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.770+3192T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493836 | |||||||
| chr12:57493836 | T | TATTA | 11 | a0001c0001t0001g0030 a0001c0001t0001g0064 a0001c0001t0001g0072 others(8): Show |
11 | HG02257.hp1 HG02615.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.770+3192_770+3193i others(6): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493836 | |||||||
| chr12:57493836 | T | TATTATAT others(4): Show |
1 | a0001c0001t0001g0174 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.770+3192_770+3193i others(13): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493836 | |||||||
| chr12:57493836 | T | TATTATAT others(119): Show |
2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.770+3192_770+3193i others(128): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493836 | |||||||
| chr12:57493836 | T | TATTATAT others(2): Show |
11 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0222 others(8): Show |
11 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.770+3192_770+3193i others(11): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493836 | |||||||
| chr12:57493836 | T | TATTATAT others(9): Show |
1 | a0008c0007t0001g0165 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.770+3192_770+3193i others(18): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493836 | |||||||
| chr12:57493839 | TA | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0059 others(5): Show |
10 | HG00558.hp2 HG00741.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.770+3197delA | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493839 | ||||||
| chr12:57493840 | A | AT | 7 | a0001c0001t0001g0249 a0001c0004t0001g0164 a0001c0004t0001g0166 others(4): Show |
7 | HG00408.hp2 HG01891.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.770+3196_770+3197i others(3): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493840 | |||||||
| chr12:57493841 | A | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.770+3197A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493841 | |||||||
| chr12:57493843 | A | AT | 6 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(3): Show |
6 | HG00408.hp2 HG01891.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.770+3200dupT | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493843 | ||||||
| chr12:57493844 | TATA | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0235 others(26): Show |
30 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.770+3204_770+3206d others(5): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493844 | ||||||
| chr12:57493847 | A | T | 1 | a0001c0001t0001g0249 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.770+3203A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493847 | |||||||
| chr12:57493848 | A | T | 9 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0240 others(6): Show |
11 | HG00741.hp1 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.770+3204A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493848 | |||||||
| chr12:57493852 | ATATATTT others(4): Show |
A | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG01256.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.770+3214_770+3224d others(13): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493852 | ||||||
| chr12:57493853 | T | TA | 8 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0053 others(5): Show |
8 | HG01891.hp1 HG02056.hp1 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.770+3210dupA | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493853 | ||||||
| chr12:57493853 | TA | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0235 others(26): Show |
30 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.770+3210delA | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493853 | |||||||
| chr12:57493854 | AT | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.770+3211delT | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493854 | |||||||
| chr12:57493855 | T | TTATAATA others(64): Show |
1 | a0001c0004t0001g0170 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.770+3211_770+3212i others(73): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493855 | |||||||
| chr12:57493855 | TATTTATA others(3): Show |
T | 1 | a0002c0005t0001g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.770+3212_770+3221d others(12): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493855 | |||||||
| chr12:57493858 | T | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.770+3214T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493858 | |||||||
| chr12:57493859 | T | A | 1 | a0001c0014t0001g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.770+3215T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493859 | |||||||
| chr12:57493860 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.770+3216A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493860 | |||||||
| chr12:57493863 | T | A | 150 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.770+3219T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493863 | |||||||
| chr12:57493863 | TTATATAA others(2): Show |
T | 11 | a0001c0001t0001g0013 a0001c0001t0001g0045 a0001c0001t0001g0046 others(8): Show |
11 | HG00558.hp2 HG01168.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.770+3233_770+3241d others(11): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493863 | ||||||
| chr12:57493864 | TA | T | 7 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0053 others(4): Show |
7 | HG02056.hp1 HG03710.hp2 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.770+3221delA | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493864 | |||||||
| chr12:57493867 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.770+3223A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493867 | |||||||
| chr12:57493869 | A | ATATTT | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.770+3225_770+3226i others(7): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493869 | |||||||
| chr12:57493869 | A | T | 3 | a0001c0001t0001g0012 a0003c0006t0001g0015 a0006c0008t0001g0163 |
3 | HG01358.hp1 NA18982.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.770+3225A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493869 | |||||||
| chr12:57493869 | AAT | A | 8 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0053 others(5): Show |
8 | HG02056.hp1 HG02965.hp1 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.770+3233_770+3234d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493869 | ||||||
| chr12:57493870 | A | T | 32 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0235 others(29): Show |
34 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.770+3226A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493870 | |||||||
| chr12:57493871 | T | A | 1 | a0001c0001t0001g0269 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.770+3227T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493871 | |||||||
| chr12:57493872 | A | AT | 147 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.770+3229dupT | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493872 | ||||||
| chr12:57493872 | A | ATATAATA others(20): Show |
1 | a0001c0001t0001g0094 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.770+3232_770+3233i others(29): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493872 | ||||||
| chr12:57493872 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0049 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.770+3234_770+3235i others(15): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493872 | ||||||
| chr12:57493872 | A | ATATATTA others(39): Show |
1 | a0006c0008t0001g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.770+3233_770+3234i others(48): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493872 | ||||||
| chr12:57493872 | A | T | 9 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0040 others(6): Show |
9 | HG02056.hp1 HG02135.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.770+3228A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493872 | |||||||
| chr12:57493875 | TATA | T | 31 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0235 others(28): Show |
33 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.770+3235_770+3237d others(5): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493875 | ||||||
| chr12:57493884 | T | A | 10 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(7): Show |
10 | HG00408.hp2 HG01256.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.770+3240T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493884 | |||||||
| chr12:57493885 | A | AT | 10 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(7): Show |
10 | HG00408.hp2 HG01256.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.770+3241_770+3242i others(3): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493885 | |||||||
| chr12:57493885 | A | T | 37 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0235 others(34): Show |
39 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.770+3241A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493885 | |||||||
| chr12:57493886 | A | T | 10 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0227 others(7): Show |
12 | HG00741.hp1 HG01168.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.770+3242A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493886 | |||||||
| chr12:57493888 | ATATATTT others(36): Show |
A | 9 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0240 others(6): Show |
11 | HG00741.hp1 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.770+3250_770+3292d others(45): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493888 | ||||||
| chr12:57493898 | G | A | 47 | a0001c0001t0001g0002 a0001c0001t0001g0215 a0001c0001t0001g0216 others(44): Show |
49 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.770+3254G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493898 | |||||||
| chr12:57493899 | TTATATAA others(2): Show |
T | 6 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0034 others(3): Show |
6 | HG01433.hp2 HG01515.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.770+3279_770+3287d others(11): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493899 | ||||||
| chr12:57493908 | A | ATATATAA others(12): Show |
1 | a0001c0014t0001g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.770+3278_770+3279i others(21): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493908 | ||||||
| chr12:57493912 | A | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0153 a0001c0001t0001g0155 others(1): Show |
4 | HG01884.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+3268A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493912 | |||||||
| chr12:57493913 | T | A | 4 | a0001c0003t0001g0177 a0001c0003t0001g0178 a0001c0003t0001g0179 others(1): Show |
4 | HG01884.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+3269T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493913 | |||||||
| chr12:57493914 | A | T | 4 | a0001c0003t0001g0177 a0001c0003t0001g0178 a0001c0003t0001g0179 others(1): Show |
4 | HG01884.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+3270A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493914 | |||||||
| chr12:57493917 | A | AT | 4 | a0001c0003t0001g0177 a0001c0003t0001g0178 a0001c0003t0001g0179 others(1): Show |
4 | HG01884.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+3274dupT | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493917 | ||||||
| chr12:57493923 | A | T | 47 | a0001c0001t0001g0002 a0001c0001t0001g0062 a0001c0001t0001g0102 others(44): Show |
49 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.770+3279A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493923 | |||||||
| chr12:57493924 | ATATATAT | A | 46 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0215 others(43): Show |
48 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.770+3295_770+3301d others(9): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493924 | ||||||
| chr12:57493931 | T | TTA | 3 | a0001c0001t0001g0061 a0001c0001t0001g0217 a0001c0014t0001g0192 |
3 | HG01891.hp1 HG02622.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.770+3293_770+3294d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57493931 | ||||||
| chr12:57493945 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.770+3301T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493945 | |||||||
| chr12:57493948 | A | T | 1 | a0001c0001t0001g0232 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.770+3304A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493948 | |||||||
| chr12:57493952 | TTTAATTT others(19): Show |
T | 1 | a0001c0001t0001g0121 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.770+3309_770+3334d others(28): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493952 | |||||||
| chr12:57493984 | T | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.770+3340T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57493984 | |||||||
| chr12:57494080 | C | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0033 others(4): Show |
8 | HG01978.hp1 HG02300.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.770+3436C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57494080 | |||||||
| chr12:57494208 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.770+3564G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57494208 | |||||||
| chr12:57494321 | T | A | 6 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0258 others(3): Show |
6 | HG00597.hp1 HG00733.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.770+3677T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57494321 | |||||||
| chr12:57494325 | T | C | 2 | a0001c0001t0001g0202 a0001c0001t0001g0206 |
2 | HG02257.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.770+3681T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57494325 | |||||||
| chr12:57494328 | C | CT | 13 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0084 others(10): Show |
13 | HG00323.hp1 HG00408.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.770+3701dupT | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57494328 | ||||||
| chr12:57494328 | C | T | 1 | a0009c0011t0001g0027 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.770+3684C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57494328 | |||||||
| chr12:57494328 | CT | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(61): Show |
68 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.770+3701delT | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57494328 | ||||||
| chr12:57494370 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.770+3726C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57494370 | |||||||
| chr12:57494421 | G | A | 25 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0197 others(22): Show |
25 | HG01167.hp2 HG01169.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.771-3736G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57494421 | |||||||
| chr12:57494442 | C | G | 3 | a0001c0001t0001g0002 a0001c0001t0001g0237 a0001c0001t0001g0243 |
5 | HG02451.hp2 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.771-3715C>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57494442 | |||||||
| chr12:57494485 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.771-3672G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57494485 | |||||||
| chr12:57494494 | A | AT | 57 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0030 others(54): Show |
57 | HG00597.hp2 HG00735.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.771-3638dupT | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57494494 | ||||||
| chr12:57494494 | AT | A | 16 | a0001c0001t0001g0013 a0001c0001t0001g0029 a0001c0001t0001g0045 others(13): Show |
16 | HG01167.hp1 HG01167.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.771-3638delT | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57494494 | ||||||
| chr12:57494521 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.771-3636G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57494521 | |||||||
| chr12:57494588 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.771-3569G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57494588 | |||||||
| chr12:57494812 | G | A | 56 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(53): Show |
60 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.771-3345G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57494812 | |||||||
| chr12:57495033 | A | AC | 32 | a0001c0001t0001g0040 a0001c0001t0001g0046 a0001c0001t0001g0055 others(29): Show |
32 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.771-3124_771-3123i others(3): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57495033 | |||||||
| chr12:57495034 | T | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.771-3123T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57495034 | |||||||
| chr12:57495034 | T | G | 34 | a0001c0001t0001g0040 a0001c0001t0001g0046 a0001c0001t0001g0055 others(31): Show |
34 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.771-3123T>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57495034 | |||||||
| chr12:57495035 | G | C | 1 | a0009c0011t0001g0027 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.771-3122G>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57495035 | |||||||
| chr12:57495046 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.771-3111C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57495046 | |||||||
| chr12:57495083 | C | T | 4 | a0001c0003t0001g0177 a0001c0003t0001g0178 a0001c0003t0001g0179 others(1): Show |
4 | HG01884.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.771-3074C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57495083 | |||||||
| chr12:57495102 | A | C | 1 | a0001c0001t0001g0265 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.771-3055A>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57495102 | |||||||
| chr12:57495103 | C | A | 1 | a0001c0001t0001g0265 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.771-3054C>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57495103 | |||||||
| chr12:57495138 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.771-3019C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57495138 | |||||||
| chr12:57495185 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.771-2972C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57495185 | |||||||
| chr12:57495214 | C | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(52): Show |
59 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.771-2943C>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57495214 | |||||||
| chr12:57495228 | T | C | 4 | a0001c0001t0001g0022 a0001c0001t0001g0077 a0001c0001t0001g0087 others(1): Show |
4 | HG02735.hp1 HG03017.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.771-2929T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57495228 | |||||||
| chr12:57495244 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.771-2913C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57495244 | |||||||
| chr12:57495257 | G | A | 1 | a0001c0001t0001g0244 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.771-2900G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57495257 | |||||||
| chr12:57495266 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.771-2891C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57495266 | |||||||
| chr12:57495294 | G | A | 55 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(52): Show |
56 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.771-2863G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57495294 | |||||||
| chr12:57495297 | C | G | 1 | a0001c0001t0001g0121 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.771-2860C>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57495297 | |||||||
| chr12:57495373 | CGGGCAGA others(30): Show |
C | 5 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(2): Show |
5 | HG02109.hp2 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.771-2768_771-2732d others(39): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57495373 | ||||||
| chr12:57495445 | C | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
54 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.771-2712C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57495445 | |||||||
| chr12:57495460 | G | T | 1 | a0001c0001t0001g0251 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.771-2697G>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57495460 | |||||||
| chr12:57495593 | C | CG | 7 | a0001c0001t0001g0033 a0001c0001t0001g0141 a0001c0001t0001g0151 others(4): Show |
7 | HG00741.hp1 HG02056.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.771-2560dupG | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57495593 | ||||||
| chr12:57495593 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.771-2564C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57495593 | |||||||
| chr12:57495601 | C | T | 6 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(3): Show |
6 | HG00408.hp2 HG02071.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.771-2556C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57495601 | |||||||
| chr12:57495677 | C | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.771-2480C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57495677 | |||||||
| chr12:57495807 | C | T | 46 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(43): Show |
50 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.771-2350C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57495807 | |||||||
| chr12:57495865 | C | T | 3 | a0001c0001t0001g0176 a0001c0001t0001g0232 a0001c0001t0001g0241 |
3 | HG02647.hp2 HG02965.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.771-2292C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57495865 | |||||||
| chr12:57495970 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.771-2187G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57495970 | |||||||
| chr12:57496082 | T | A | 1 | a0009c0011t0001g0027 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.771-2075T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57496082 | |||||||
| chr12:57496091 | A | G | 3 | a0002c0005t0001g0239 a0002c0005t0001g0246 a0002c0005t0001g0275 |
3 | HG03139.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.771-2066A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57496091 | |||||||
| chr12:57496137 | T | C | 56 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(53): Show |
60 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.771-2020T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57496137 | |||||||
| chr12:57496164 | A | G | 1 | a0001c0001t0001g0044 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.771-1993A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57496164 | |||||||
| chr12:57496177 | CT | C | 12 | a0001c0001t0001g0029 a0001c0001t0001g0059 a0001c0001t0001g0101 others(9): Show |
12 | HG00558.hp1 HG00558.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.771-1966delT | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 57496177 | ||||||
| chr12:57496324 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.771-1833C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57496324 | |||||||
| chr12:57496480 | A | T | 1 | a0009c0011t0001g0027 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.771-1677A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57496480 | |||||||
| chr12:57496486 | A | T | 6 | a0001c0001t0001g0050 a0001c0001t0001g0056 a0001c0001t0001g0061 others(3): Show |
6 | HG00544.hp1 HG02683.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.771-1671A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57496486 | |||||||
| chr12:57496536 | T | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.771-1621T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57496536 | |||||||
| chr12:57496774 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG00621.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.771-1383C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57496774 | |||||||
| chr12:57496918 | T | G | 1 | a0001c0001t0001g0023 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.771-1239T>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57496918 | |||||||
| chr12:57496937 | A | G | 30 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0197 others(27): Show |
30 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.771-1220A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57496937 | |||||||
| chr12:57497042 | G | C | 1 | a0009c0011t0001g0027 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.771-1115G>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57497042 | |||||||
| chr12:57497400 | A | G | 30 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0197 others(27): Show |
30 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.771-757A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57497400 | |||||||
| chr12:57497447 | G | T | 1 | a0001c0001t0001g0232 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.771-710G>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57497447 | |||||||
| chr12:57497524 | C | A | 6 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(3): Show |
6 | HG00408.hp2 HG02071.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.771-633C>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57497524 | |||||||
| chr12:57497581 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.771-576T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57497581 | |||||||
| chr12:57497690 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.771-467C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57497690 | |||||||
| chr12:57497713 | C | G | 46 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(43): Show |
50 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.771-444C>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57497713 | |||||||
| chr12:57497774 | G | A | 1 | a0001c0002t0001g0143 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.771-383G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57497774 | |||||||
| chr12:57497868 | A | G | 1 | a0001c0001t0001g0247 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.771-289A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57497868 | |||||||
| chr12:57497918 | G | C | 1 | a0001c0001t0001g0271 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.771-239G>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57497918 | |||||||
| chr12:57498021 | T | C | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(261): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.771-136T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | chr12 | 57498021 | |||||||
| chr12:57498315 | C | CG | 4 | a0001c0001t0001g0121 a0001c0001t0001g0199 a0001c0001t0001g0224 others(1): Show |
4 | HG00741.hp1 HG01243.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.887+45dupG | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr12 | 57498315 | ||||||
| chr12:57498391 | C | A | 4 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(1): Show |
4 | HG02109.hp2 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.888-29C>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 8/20 | chr12 | 57498391 | |||||||
| chr12:57498717 | T | G | 6 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(3): Show |
6 | HG00408.hp2 HG02071.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1091+94T>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | chr12 | 57498717 | |||||||
| chr12:57499016 | G | T | 56 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(53): Show |
60 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1091+393G>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | chr12 | 57499016 | |||||||
| chr12:57499061 | C | A | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(260): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1091+438C>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | chr12 | 57499061 | |||||||
| chr12:57499066 | C | T | 56 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(53): Show |
60 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1091+443C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | chr12 | 57499066 | |||||||
| chr12:57499071 | G | A | 3 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0121 |
3 | HG00140.hp1 HG01243.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1091+448G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | chr12 | 57499071 | |||||||
| chr12:57499089 | G | C | 1 | a0001c0001t0001g0257 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1091+466G>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | chr12 | 57499089 | |||||||
| chr12:57499090 | C | G | 1 | a0001c0001t0001g0257 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1091+467C>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | chr12 | 57499090 | |||||||
| chr12:57499182 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1091+559G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | chr12 | 57499182 | |||||||
| chr12:57499284 | C | CA | 41 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0033 others(38): Show |
43 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.1091+684dupA | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr12 | 57499284 | ||||||
| chr12:57499371 | G | A | 6 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(3): Show |
6 | HG00408.hp2 HG02071.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1091+748G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | chr12 | 57499371 | |||||||
| chr12:57499386 | G | A | 4 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(1): Show |
4 | HG02109.hp2 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1091+763G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | chr12 | 57499386 | |||||||
| chr12:57499439 | C | CA | 64 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0033 others(61): Show |
66 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.1091+831dupA | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr12 | 57499439 | ||||||
| chr12:57499486 | C | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0090 others(1): Show |
4 | NA18943.hp1 NA18974.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.1092-835C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | chr12 | 57499486 | |||||||
| chr12:57499492 | T | G | 6 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(3): Show |
6 | HG00408.hp2 HG02071.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1092-829T>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | chr12 | 57499492 | |||||||
| chr12:57499601 | C | CA | 10 | a0001c0001t0001g0171 a0001c0001t0001g0174 a0001c0001t0001g0190 others(7): Show |
10 | HG00408.hp2 HG01891.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1092-704dupA | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr12 | 57499601 | ||||||
| chr12:57499601 | CA | C | 9 | a0001c0001t0001g0008 a0001c0001t0001g0071 a0001c0001t0001g0237 others(6): Show |
10 | HG00280.hp1 HG00438.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.1092-704delA | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr12 | 57499601 | ||||||
| chr12:57499601 | CAA | C | 6 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0258 others(3): Show |
6 | HG00597.hp1 HG00733.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1092-705_1092-704d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr12 | 57499601 | ||||||
| chr12:57499602 | A | C | 1 | a0001c0001t0001g0207 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1092-719A>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | chr12 | 57499602 | |||||||
| chr12:57499620 | G | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.1092-701G>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | chr12 | 57499620 | |||||||
| chr12:57499643 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0102 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1092-678G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | chr12 | 57499643 | |||||||
| chr12:57499781 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1092-540C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | chr12 | 57499781 | |||||||
| chr12:57499822 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1092-499C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | chr12 | 57499822 | |||||||
| chr12:57499836 | A | G | 56 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(53): Show |
60 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1092-485A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | chr12 | 57499836 | |||||||
| chr12:57499919 | C | A | 1 | a0001c0001t0001g0151 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1092-402C>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | chr12 | 57499919 | |||||||
| chr12:57500005 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1092-316A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | chr12 | 57500005 | |||||||
| chr12:57500084 | A | C | 1 | a0001c0001t0001g0257 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1092-237A>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | chr12 | 57500084 | |||||||
| chr12:57500189 | G | C | 1 | a0001c0001t0001g0257 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1092-132G>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | chr12 | 57500189 | |||||||
| chr12:57500190 | C | G | 1 | a0001c0001t0001g0257 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1092-131C>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | chr12 | 57500190 | |||||||
| chr12:57500269 | G | C | 1 | a0008c0007t0001g0165 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1092-52G>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 9/20 | chr12 | 57500269 | |||||||
| chr12:57500549 | C | G | 1 | a0001c0001t0001g0104 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1293+27C>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57500549 | |||||||
| chr12:57501069 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1293+547T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57501069 | |||||||
| chr12:57501075 | G | T | 1 | a0001c0001t0001g0116 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1293+553G>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57501075 | |||||||
| chr12:57501152 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1293+630C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57501152 | |||||||
| chr12:57501158 | G | T | 1 | a0001c0001t0001g0227 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1293+636G>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57501158 | |||||||
| chr12:57501175 | G | C | 1 | a0001c0001t0001g0176 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1293+653G>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57501175 | |||||||
| chr12:57501292 | C | T | 1 | a0001c0014t0001g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1293+770C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57501292 | |||||||
| chr12:57501476 | C | A | 8 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0199 others(5): Show |
8 | HG02257.hp1 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1293+954C>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57501476 | |||||||
| chr12:57501638 | G | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1293+1116G>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57501638 | |||||||
| chr12:57501835 | A | C | 1 | a0001c0001t0001g0012 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1293+1313A>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57501835 | |||||||
| chr12:57501898 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1293+1376G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57501898 | |||||||
| chr12:57501999 | C | CA | 6 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(3): Show |
6 | HG02109.hp2 HG02922.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1293+1487dupA | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr12 | 57501999 | ||||||
| chr12:57502231 | C | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0237 a0001c0001t0001g0243 |
5 | HG02451.hp2 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1293+1709C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57502231 | |||||||
| chr12:57502290 | G | A | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 |
3 | HG01256.hp1 HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1293+1768G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57502290 | |||||||
| chr12:57502357 | G | A | 1 | a0001c0002t0001g0100 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1293+1835G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57502357 | |||||||
| chr12:57502400 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1294-1825A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57502400 | |||||||
| chr12:57502445 | G | T | 1 | a0001c0001t0001g0257 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1294-1780G>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57502445 | |||||||
| chr12:57502586 | A | G | 1 | a0001c0015t0001g0191 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1294-1639A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57502586 | |||||||
| chr12:57502670 | C | T | 56 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(53): Show |
60 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1294-1555C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57502670 | |||||||
| chr12:57502705 | C | CA | 10 | a0001c0001t0001g0024 a0001c0001t0001g0032 a0001c0001t0001g0046 others(7): Show |
10 | HG01358.hp2 HG02735.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1294-1503dupA | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr12 | 57502705 | ||||||
| chr12:57502705 | CA | C | 51 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(48): Show |
55 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.1294-1503delA | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr12 | 57502705 | ||||||
| chr12:57502727 | C | CA | 7 | a0001c0001t0001g0212 a0001c0001t0001g0222 a0001c0001t0001g0228 others(4): Show |
7 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1294-1496dupA | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr12 | 57502727 | ||||||
| chr12:57502730 | C | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(136): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1294-1495C>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57502730 | |||||||
| chr12:57502730 | C | CA | 13 | a0001c0001t0001g0046 a0001c0001t0001g0092 a0001c0001t0001g0094 others(10): Show |
13 | HG00741.hp2 HG01099.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.1294-1493dupA | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr12 | 57502730 | ||||||
| chr12:57502733 | C | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(235): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1294-1492C>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57502733 | |||||||
| chr12:57502744 | C | A | 3 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 |
3 | HG00735.hp1 HG01106.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1294-1481C>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57502744 | |||||||
| chr12:57502778 | C | T | 1 | a0009c0011t0001g0027 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1294-1447C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57502778 | |||||||
| chr12:57502779 | G | A | 4 | a0001c0003t0001g0177 a0001c0003t0001g0178 a0001c0003t0001g0179 others(1): Show |
4 | HG01884.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1294-1446G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57502779 | |||||||
| chr12:57502837 | A | G | 6 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(3): Show |
6 | HG00408.hp2 HG02071.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1294-1388A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57502837 | |||||||
| chr12:57502903 | A | G | 4 | a0001c0001t0001g0034 a0001c0001t0001g0059 a0001c0001t0001g0151 others(1): Show |
4 | HG00558.hp2 HG02056.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1294-1322A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57502903 | |||||||
| chr12:57503020 | C | T | 4 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(1): Show |
4 | HG02109.hp2 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1294-1205C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57503020 | |||||||
| chr12:57503028 | A | AAAC | 7 | a0001c0001t0001g0176 a0001c0004t0001g0164 a0001c0004t0001g0166 others(4): Show |
7 | HG00408.hp2 HG02071.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1294-1173_1294-117 others(7): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr12 | 57503028 | ||||||
| chr12:57503086 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1294-1139G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57503086 | |||||||
| chr12:57503321 | C | T | 1 | a0001c0014t0001g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1294-904C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57503321 | |||||||
| chr12:57503491 | C | T | 56 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(53): Show |
60 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1294-734C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57503491 | |||||||
| chr12:57503512 | C | T | 46 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(43): Show |
50 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1294-713C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57503512 | |||||||
| chr12:57503564 | T | C | 2 | a0001c0001t0001g0062 a0001c0001t0001g0102 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1294-661T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57503564 | |||||||
| chr12:57503595 | C | T | 2 | a0001c0001t0001g0018 a0001c0014t0001g0192 |
2 | HG01891.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1294-630C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57503595 | |||||||
| chr12:57503600 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0122 |
2 | HG02735.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1294-625G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57503600 | |||||||
| chr12:57503684 | G | C | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG02622.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1294-541G>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57503684 | |||||||
| chr12:57503836 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0040 a0001c0001t0001g0041 |
3 | HG02132.hp2 HG02135.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1294-389G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57503836 | |||||||
| chr12:57504176 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1294-49C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57504176 | |||||||
| chr12:57504219 | T | A | 1 | a0001c0001t0001g0219 | 1 | HG02809.hp1 | splice_region_variant&intron_variant | LOW | c.1294-6T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 10/20 | chr12 | 57504219 | |||||||
| chr12:57504335 | G | A | 6 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(3): Show |
6 | HG00408.hp2 HG02071.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1368+36G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57504335 | |||||||
| chr12:57504695 | A | AT | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1368+421dupT | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 57504695 | ||||||
| chr12:57504695 | A | ATT | 25 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0035 others(22): Show |
25 | HG00140.hp1 HG00621.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1368+420_1368+421d others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 57504695 | ||||||
| chr12:57504695 | AT | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0064 others(30): Show |
36 | HG00408.hp2 HG01168.hp1 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.1368+421delT | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 57504695 | ||||||
| chr12:57504743 | G | A | 9 | a0001c0001t0001g0244 a0001c0001t0001g0249 a0001c0001t0001g0261 others(6): Show |
9 | HG02040.hp1 HG02083.hp1 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.1368+444G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57504743 | |||||||
| chr12:57504812 | T | G | 6 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(3): Show |
6 | HG00408.hp2 HG02071.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1368+513T>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57504812 | |||||||
| chr12:57504817 | C | T | 1 | a0008c0007t0001g0165 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1368+518C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57504817 | |||||||
| chr12:57504847 | G | T | 1 | a0001c0001t0001g0104 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1368+548G>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57504847 | |||||||
| chr12:57504849 | G | A | 2 | a0001c0001t0001g0197 a0001c0001t0001g0198 |
2 | HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1368+550G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57504849 | |||||||
| chr12:57504852 | T | C | 56 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(53): Show |
60 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1368+553T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57504852 | |||||||
| chr12:57504993 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1368+694C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57504993 | |||||||
| chr12:57505036 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1368+737A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57505036 | |||||||
| chr12:57505159 | G | A | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(260): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1368+860G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57505159 | |||||||
| chr12:57505164 | G | GT | 58 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(55): Show |
62 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.1368+879dupT | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 57505164 | ||||||
| chr12:57505202 | C | T | 5 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0187 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1368+903C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57505202 | |||||||
| chr12:57505323 | G | A | 218 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(215): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1368+1024G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57505323 | |||||||
| chr12:57505913 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1368+1614A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57505913 | |||||||
| chr12:57505994 | C | T | 5 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(2): Show |
5 | HG02109.hp2 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1368+1695C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57505994 | |||||||
| chr12:57506006 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1368+1707C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57506006 | |||||||
| chr12:57506028 | T | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0053 |
2 | NA19079.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1368+1729T>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57506028 | |||||||
| chr12:57506558 | G | A | 46 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(43): Show |
50 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1368+2259G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57506558 | |||||||
| chr12:57506698 | A | T | 1 | a0001c0001t0001g0218 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1368+2399A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57506698 | |||||||
| chr12:57506707 | C | T | 6 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(3): Show |
6 | HG00408.hp2 HG02071.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1368+2408C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57506707 | |||||||
| chr12:57506766 | TC | T | 56 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(53): Show |
60 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1368+2470delC | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 57506766 | ||||||
| chr12:57506850 | CT | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(61): Show |
68 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.1368+2570delT | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 57506850 | ||||||
| chr12:57506900 | G | T | 13 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0235 others(10): Show |
15 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1368+2601G>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57506900 | |||||||
| chr12:57506918 | A | T | 1 | a0001c0001t0001g0150 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1368+2619A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57506918 | |||||||
| chr12:57506997 | G | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
54 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.1368+2698G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57506997 | |||||||
| chr12:57507034 | T | A | 1 | a0001c0002t0001g0065 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1368+2735T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57507034 | |||||||
| chr12:57507083 | T | C | 50 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
54 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.1368+2784T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57507083 | |||||||
| chr12:57507140 | A | C | 9 | a0001c0001t0001g0244 a0001c0001t0001g0249 a0001c0001t0001g0261 others(6): Show |
9 | HG02040.hp1 HG02083.hp1 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.1368+2841A>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57507140 | |||||||
| chr12:57507287 | A | G | 56 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(53): Show |
60 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1368+2988A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57507287 | |||||||
| chr12:57507393 | AGGCAGAG others(123): Show |
A | 1 | a0001c0001t0001g0243 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1368+3126_1368+325 others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 57507393 | ||||||
| chr12:57507425 | T | C | 262 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(259): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.1368+3126T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57507425 | |||||||
| chr12:57507453 | C | T | 3 | a0001c0001t0001g0171 a0001c0001t0001g0173 a0001c0001t0001g0175 |
3 | HG02922.hp1 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1368+3154C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57507453 | |||||||
| chr12:57507457 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1368+3158C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57507457 | |||||||
| chr12:57507461 | GCGGCTGG others(219): Show |
G | 4 | a0001c0002t0001g0063 a0001c0002t0001g0065 a0001c0002t0001g0108 others(1): Show |
4 | HG00544.hp2 HG02015.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1368+3181_1368+340 others(4): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 57507461 | ||||||
| chr12:57507484 | ACC | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(214): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1368+3194_1368+319 others(6): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 57507484 | ||||||
| chr12:57507488 | C | G | 1 | a0001c0001t0001g0071 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1368+3189C>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57507488 | |||||||
| chr12:57507507 | C | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(221): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1368+3208C>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57507507 | |||||||
| chr12:57507577 | ACCTCCCG others(41): Show |
A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(140): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.1368+3340_1368+338 others(52): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 57507577 | ||||||
| chr12:57507602 | G | T | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 |
3 | HG01256.hp1 HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1368+3303G>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57507602 | |||||||
| chr12:57507615 | CCCCCCAC others(40): Show |
C | 1 | a0001c0001t0001g0112 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1368+3322_1368+336 others(51): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 57507615 | ||||||
| chr12:57507635 | C | T | 6 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(3): Show |
6 | HG00408.hp2 HG02071.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1368+3336C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57507635 | |||||||
| chr12:57507639 | GCGGCTGG others(41): Show |
G | 26 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0034 others(23): Show |
27 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(24): Show |
intron_variant | MODIFIER | c.1368+3388_1368+343 others(52): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 57507639 | ||||||
| chr12:57507640 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0064 a0001c0001t0001g0072 |
3 | HG03710.hp2 HG04184.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1368+3341C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57507640 | |||||||
| chr12:57507662 | GCCCCCCA others(88): Show |
G | 6 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(3): Show |
6 | HG00408.hp2 HG02071.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1368+3388_1368+348 others(99): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 57507662 | ||||||
| chr12:57507663 | CCCCCCAC others(40): Show |
C | 1 | a0001c0013t0001g0113 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1368+3370_1368+341 others(51): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 57507663 | ||||||
| chr12:57507668 | C | A | 4 | a0001c0003t0001g0177 a0001c0003t0001g0178 a0001c0003t0001g0179 others(1): Show |
4 | HG01884.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1368+3369C>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57507668 | |||||||
| chr12:57507683 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1368+3384C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57507683 | |||||||
| chr12:57507687 | A | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1368+3388A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57507687 | |||||||
| chr12:57507774 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1368+3475C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57507774 | |||||||
| chr12:57507798 | A | G | 7 | a0001c0001t0001g0174 a0001c0004t0001g0164 a0001c0004t0001g0166 others(4): Show |
7 | HG00408.hp2 HG02071.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1368+3499A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57507798 | |||||||
| chr12:57507837 | G | A | 1 | a0008c0007t0001g0165 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1368+3538G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57507837 | |||||||
| chr12:57507927 | GCTCCTCA others(33): Show |
G | 1 | a0001c0001t0001g0075 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1368+3645_1368+368 others(44): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 57507927 | ||||||
| chr12:57507956 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1368+3657C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57507956 | |||||||
| chr12:57508050 | A | T | 4 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(1): Show |
4 | HG03130.hp1 HG03239.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1369-3648A>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57508050 | |||||||
| chr12:57508106 | A | G | 56 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(53): Show |
60 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1369-3592A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57508106 | |||||||
| chr12:57508214 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1369-3484C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57508214 | |||||||
| chr12:57508266 | C | T | 2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1369-3432C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57508266 | |||||||
| chr12:57508302 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1369-3396A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57508302 | |||||||
| chr12:57508337 | C | T | 6 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(3): Show |
6 | HG00408.hp2 HG02071.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1369-3361C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57508337 | |||||||
| chr12:57508428 | G | GCTGGCGG others(4): Show |
6 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(3): Show |
6 | HG00408.hp2 HG02071.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1369-3262_1369-325 others(15): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 57508428 | ||||||
| chr12:57508470 | C | G | 66 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(63): Show |
71 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1369-3228C>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57508470 | |||||||
| chr12:57508531 | C | G | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | NA18971.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1369-3167C>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57508531 | |||||||
| chr12:57508571 | G | T | 2 | a0001c0001t0001g0020 a0006c0008t0001g0163 |
2 | HG01358.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1369-3127G>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57508571 | |||||||
| chr12:57508630 | C | G | 1 | a0001c0001t0001g0039 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1369-3068C>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57508630 | |||||||
| chr12:57508630 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1369-3068C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57508630 | |||||||
| chr12:57508699 | A | AGGGTAGA others(1): Show |
6 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0187 others(3): Show |
6 | HG02559.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1369-2997_1369-299 others(12): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 57508699 | ||||||
| chr12:57508699 | A | AGGTAGAG | 6 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(3): Show |
6 | HG00408.hp2 HG02071.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1369-2982_1369-297 others(11): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 57508699 | ||||||
| chr12:57508699 | A | AGGTAGAG others(7): Show |
56 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0023 others(53): Show |
58 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1369-2989_1369-297 others(18): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 57508699 | ||||||
| chr12:57508699 | A | AGGTAGAG others(6): Show |
10 | a0001c0001t0001g0066 a0001c0001t0001g0149 a0001c0001t0001g0194 others(7): Show |
10 | HG00639.hp2 HG02257.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1369-2991_1369-299 others(17): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 57508699 | ||||||
| chr12:57508699 | A | AGGTAGAG others(13): Show |
165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1369-2991_1369-299 others(24): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 57508699 | ||||||
| chr12:57508699 | A | AGGTAGAG others(19): Show |
26 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0034 others(23): Show |
27 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(24): Show |
intron_variant | MODIFIER | c.1369-2991_1369-299 others(30): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 57508699 | ||||||
| chr12:57508722 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1369-2976G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57508722 | |||||||
| chr12:57508833 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1369-2865A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57508833 | |||||||
| chr12:57508844 | A | G | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(260): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1369-2854A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57508844 | |||||||
| chr12:57508893 | A | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0153 a0001c0001t0001g0155 others(1): Show |
4 | HG01884.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1369-2805A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57508893 | |||||||
| chr12:57509098 | T | A | 1 | a0001c0001t0001g0012 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1369-2600T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57509098 | |||||||
| chr12:57509157 | A | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0257 |
3 | HG00741.hp1 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1369-2541A>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57509157 | |||||||
| chr12:57509195 | A | C | 1 | a0001c0001t0001g0176 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1369-2503A>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57509195 | |||||||
| chr12:57509300 | T | G | 49 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(46): Show |
53 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.1369-2398T>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57509300 | |||||||
| chr12:57509514 | C | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0054 a0001c0001t0001g0067 |
3 | NA18941.hp1 NA19002.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1369-2184C>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57509514 | |||||||
| chr12:57509609 | C | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0043 a0001c0001t0001g0044 |
3 | NA18954.hp2 NA18990.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1369-2089C>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57509609 | |||||||
| chr12:57509872 | A | G | 1 | a0001c0014t0001g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1369-1826A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57509872 | |||||||
| chr12:57510194 | C | T | 1 | a0001c0002t0001g0108 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1369-1504C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57510194 | |||||||
| chr12:57510211 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1369-1487C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57510211 | |||||||
| chr12:57510332 | C | T | 6 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(3): Show |
6 | HG00408.hp2 HG02071.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1369-1366C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57510332 | |||||||
| chr12:57510343 | C | T | 6 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0167 others(3): Show |
6 | HG00408.hp2 HG02071.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1369-1355C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57510343 | |||||||
| chr12:57510387 | G | A | 46 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(43): Show |
50 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1369-1311G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57510387 | |||||||
| chr12:57510453 | GC | G | 3 | a0001c0004t0001g0164 a0001c0004t0001g0166 a0001c0004t0001g0170 |
3 | HG00408.hp2 HG02071.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.1369-1244delC | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57510453 | |||||||
| chr12:57510700 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1369-998G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57510700 | |||||||
| chr12:57510793 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1369-905C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57510793 | |||||||
| chr12:57511048 | G | C | 1 | a0001c0001t0001g0131 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1369-650G>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57511048 | |||||||
| chr12:57511070 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1369-628T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57511070 | |||||||
| chr12:57511142 | T | TA | 251 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(248): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1369-543dupA | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 57511142 | ||||||
| chr12:57511156 | T | A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0235 others(3): Show |
8 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1369-542T>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57511156 | |||||||
| chr12:57511214 | C | T | 25 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0197 others(22): Show |
25 | HG01167.hp2 HG01169.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1369-484C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57511214 | |||||||
| chr12:57511239 | C | G | 5 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(2): Show |
5 | HG02109.hp2 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1369-459C>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57511239 | |||||||
| chr12:57511379 | T | G | 1 | a0001c0001t0001g0003 | 2 | NA18998.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1369-319T>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57511379 | |||||||
| chr12:57511502 | A | C | 1 | a0001c0001t0001g0176 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1369-196A>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57511502 | |||||||
| chr12:57511503 | G | A | 32 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(29): Show |
33 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.1369-195G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57511503 | |||||||
| chr12:57511534 | G | C | 30 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0197 others(27): Show |
30 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.1369-164G>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57511534 | |||||||
| chr12:57511566 | G | C | 50 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
54 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.1369-132G>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57511566 | |||||||
| chr12:57511629 | A | G | 17 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0219 others(14): Show |
17 | HG01167.hp2 HG01169.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1369-69A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 11/20 | chr12 | 57511629 | |||||||
| chr12:57511904 | A | G | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(260): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1539+36A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 12/20 | chr12 | 57511904 | |||||||
| chr12:57512227 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1636-9T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 13/20 | chr12 | 57512227 | |||||||
| chr12:57512360 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02293.hp1 | splice_region_variant&intron_variant | LOW | c.1753+7A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 14/20 | chr12 | 57512360 | |||||||
| chr12:57512499 | G | A | 16 | a0001c0002t0001g0005 a0001c0002t0001g0063 a0001c0002t0001g0065 others(13): Show |
17 | HG00408.hp2 HG00544.hp2 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.1753+146G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 14/20 | chr12 | 57512499 | |||||||
| chr12:57513110 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1967+146G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 15/20 | chr12 | 57513110 | |||||||
| chr12:57513408 | C | T | 5 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(2): Show |
5 | HG02109.hp2 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1967+444C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 15/20 | chr12 | 57513408 | |||||||
| chr12:57513614 | C | CA | 25 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0040 others(22): Show |
26 | HG00140.hp2 HG00741.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1967+669dupA | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr12 | 57513614 | ||||||
| chr12:57513614 | C | CAAA | 15 | a0001c0002t0001g0005 a0001c0002t0001g0063 a0001c0002t0001g0065 others(12): Show |
16 | HG00408.hp2 HG00544.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.1967+667_1967+669d others(5): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr12 | 57513614 | ||||||
| chr12:57513614 | CA | C | 7 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0003t0001g0177 others(4): Show |
7 | HG01433.hp2 HG01515.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1967+669delA | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr12 | 57513614 | ||||||
| chr12:57513755 | T | G | 1 | a0001c0001t0001g0201 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1967+791T>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 15/20 | chr12 | 57513755 | |||||||
| chr12:57513763 | C | T | 3 | a0001c0001t0001g0219 a0001c0001t0001g0222 a0001c0001t0001g0223 |
3 | HG02572.hp2 HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1967+799C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 15/20 | chr12 | 57513763 | |||||||
| chr12:57513855 | G | T | 4 | a0001c0003t0001g0177 a0001c0003t0001g0178 a0001c0003t0001g0179 others(1): Show |
4 | HG01884.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1968-865G>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 15/20 | chr12 | 57513855 | |||||||
| chr12:57513962 | T | C | 3 | a0001c0001t0001g0002 a0001c0001t0001g0237 a0001c0001t0001g0243 |
5 | HG02451.hp2 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1968-758T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 15/20 | chr12 | 57513962 | |||||||
| chr12:57513986 | C | G | 18 | a0001c0001t0001g0009 a0001c0001t0001g0244 a0001c0001t0001g0245 others(15): Show |
19 | HG00741.hp1 HG01168.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.1968-734C>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 15/20 | chr12 | 57513986 | |||||||
| chr12:57514059 | C | CA | 18 | a0001c0001t0001g0034 a0001c0001t0001g0093 a0001c0002t0001g0005 others(15): Show |
19 | HG00408.hp2 HG00544.hp2 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.1968-647dupA | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr12 | 57514059 | ||||||
| chr12:57514074 | T | G | 1 | a0001c0001t0001g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1968-646T>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 15/20 | chr12 | 57514074 | |||||||
| chr12:57514157 | C | CT | 6 | a0001c0001t0001g0045 a0001c0001t0001g0096 a0001c0001t0001g0097 others(3): Show |
6 | HG01168.hp2 HG02135.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.1968-546dupT | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr12 | 57514157 | ||||||
| chr12:57514214 | G | A | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1968-506G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 15/20 | chr12 | 57514214 | |||||||
| chr12:57514556 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1968-164T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 15/20 | chr12 | 57514556 | |||||||
| chr12:57514689 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1968-31T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 15/20 | chr12 | 57514689 | |||||||
| chr12:57514906 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2100-48T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 16/20 | chr12 | 57514906 | |||||||
| chr12:57515067 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2204+9G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 17/20 | chr12 | 57515067 | |||||||
| chr12:57515068 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2204+10C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 17/20 | chr12 | 57515068 | |||||||
| chr12:57515081 | C | T | 2 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
2 | HG02129.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.2204+23C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 17/20 | chr12 | 57515081 | |||||||
| chr12:57515501 | T | C | 16 | a0001c0002t0001g0005 a0001c0002t0001g0063 a0001c0002t0001g0065 others(13): Show |
17 | HG00408.hp2 HG00544.hp2 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.2391+165T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 18/20 | chr12 | 57515501 | |||||||
| chr12:57515615 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2391+279G>A | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 18/20 | chr12 | 57515615 | |||||||
| chr12:57515731 | C | T | 4 | a0001c0001t0001g0260 a0001c0001t0001g0262 a0001c0001t0001g0264 others(1): Show |
4 | HG00280.hp1 HG01192.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.2392-189C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 18/20 | chr12 | 57515731 | |||||||
| chr12:57515886 | A | G | 1 | a0008c0007t0001g0165 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2392-34A>G | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 18/20 | chr12 | 57515886 | |||||||
| chr12:57516385 | T | C | 2 | a0001c0001t0001g0139 a0001c0001t0001g0154 |
2 | HG01099.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.2556+48T>C | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 20/20 | chr12 | 57516385 | |||||||
| chr12:57516403 | C | T | 1 | a0002c0005t0001g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2557-32C>T | MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 20/20 | chr12 | 57516403 |