Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 60488 |
| ensemblid | ENSG00000061794.13 |
| hgncid | 16635 |
| symbol | MRPS35 |
| name | mitochondrial ribosomal protein S35 |
| refseq_nuc | NM_021821.4 |
| refseq_prot | NP_068593.2 |
| ensembl_nuc | ENST00000081029.8 |
| ensembl_prot | ENSP00000081029.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 27710832 |
| end | 27756295 |
| strand | + |
| ver | v1.2 |
| region | chr12:27710832-27756295 |
| region5000 | chr12:27705832-27761295 |
| regionname0 | MRPS35_chr12_27710832_27756295 |
| regionname5000 | MRPS35_chr12_27705832_27761295 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 323 | 283 | 67 | 50 | 130 | 9 | 25 | 103 | MRPS35_chr12_27705832_27761295 | MRPS35 | MAAAA others(318): Show |
chr12 | 27705832 | 27761295 |
| a0002 | 0/0 | 323 | 60 | 0 | 10 | 40 | 3 | 7 | 28 | MRPS35_chr12_27705832_27761295 | MRPS35 | MAAAA others(318): Show |
chr12 | 27705832 | 27761295 |
| a0003 | 0/0 | 323 | 13 | 11 | 2 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | MAAAA others(318): Show |
chr12 | 27705832 | 27761295 |
| a0004 | 0/0 | 323 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | MAAAA others(318): Show |
chr12 | 27705832 | 27761295 |
| a0005 | 0/0 | 323 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | MAAAA others(318): Show |
chr12 | 27705832 | 27761295 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 969 | 283 | 67 | 50 | 130 | 9 | 25 | MRPS35_chr12_27705832_27761295 | MRPS35 | ATGGC others(964): Show |
chr12 | 27705832 | 27761295 | ||
| a0002c0002 | 0/0 | 969 | 60 | 0 | 10 | 40 | 3 | 7 | MRPS35_chr12_27705832_27761295 | MRPS35 | ATGGC others(964): Show |
chr12 | 27705832 | 27761295 | ||
| a0003c0003 | 0/0 | 969 | 12 | 10 | 2 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | ATGGC others(964): Show |
chr12 | 27705832 | 27761295 | ||
| a0003c0004 | 0/0 | 969 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | ATGGC others(964): Show |
chr12 | 27705832 | 27761295 | ||
| a0004c0005 | 0/0 | 969 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | ATGGC others(964): Show |
chr12 | 27705832 | 27761295 | ||
| a0005c0006 | 0/0 | 969 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | ATGGC others(964): Show |
chr12 | 27705832 | 27761295 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1829 | 259 | 47 | 49 | 127 | 9 | 25 | MRPS35_chr12_27705832_27761295 | MRPS35 | GTCCT others(1824): Show |
chr12 | 27705832 | 27761295 |
| a0001c0001t0003 | 0/0 | 1829 | 20 | 20 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | GTCCT others(1824): Show |
chr12 | 27705832 | 27761295 |
| a0001c0001t0004 | 0/0 | 1829 | 2 | 0 | 0 | 2 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | GTCCT others(1824): Show |
chr12 | 27705832 | 27761295 |
| a0001c0001t0005 | 0/0 | 1829 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | GTCCT others(1824): Show |
chr12 | 27705832 | 27761295 |
| a0001c0001t0006 | 0/0 | 1829 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | GTCCT others(1824): Show |
chr12 | 27705832 | 27761295 |
| a0002c0002t0001 | 0/0 | 1829 | 2 | 0 | 1 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | GTCCT others(1824): Show |
chr12 | 27705832 | 27761295 |
| a0002c0002t0002 | 0/0 | 1829 | 58 | 0 | 9 | 40 | 3 | 6 | MRPS35_chr12_27705832_27761295 | MRPS35 | GTCCT others(1824): Show |
chr12 | 27705832 | 27761295 |
| a0003c0003t0003 | 0/0 | 1829 | 12 | 10 | 2 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | GTCCT others(1824): Show |
chr12 | 27705832 | 27761295 |
| a0003c0004t0001 | 0/0 | 1829 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | GTCCT others(1824): Show |
chr12 | 27705832 | 27761295 |
| a0004c0005t0001 | 0/0 | 1829 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | GTCCT others(1824): Show |
chr12 | 27705832 | 27761295 |
| a0005c0006t0001 | 0/0 | 1829 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | GTCCT others(1824): Show |
chr12 | 27705832 | 27761295 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0020 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0125 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0152 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0003g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0005g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0001c0001t0006g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0001 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0003c0003t0003g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0003c0003t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0003c0003t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0003c0003t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0003c0003t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0003c0003t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0003c0003t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0003c0003t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0003c0003t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0003c0004t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0004c0005t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| a0005c0006t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0256 | EUR | GBR | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | GBR | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | FIN | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0201 | EUR | FIN | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0246 | EUR | FIN | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0082 | EUR | FIN | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0063 | EAS | CHS | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0055 | EAS | CHS | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0062 | EAS | CHS | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | CHS | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0075 | AMR | PUR | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0058 | AMR | PUR | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | CHS | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | PUR | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG00741 | hp2 | a0003 | c0003 | t0003 | g0184 | AMR | PUR | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01168 | hp1 | a0003 | c0003 | t0003 | g0177 | AMR | PUR | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0045 | AMR | PUR | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0011 | AMR | CLM | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | IBS | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0245 | EUR | IBS | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01884 | hp2 | a0003 | c0003 | t0003 | g0178 | AFR | ACB | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01891 | hp2 | a0003 | c0003 | t0003 | g0181 | AFR | ACB | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | PEL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0071 | AMR | PEL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0056 | AMR | PEL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | KHV | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | KHV | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | KHV | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | KHV | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | KHV | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02080 | hp1 | a0004 | c0005 | t0001 | g0118 | EAS | KHV | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0067 | EAS | KHV | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0061 | EAS | KHV | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0166 | AFR | ACB | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CDX | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CDX | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0060 | EAS | CDX | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0156 | AFR | ACB | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0079 | AFR | ACB | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0165 | AFR | ACB | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02572 | hp2 | a0003 | c0003 | t0003 | g0183 | AFR | GWD | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02615 | hp1 | a0003 | c0003 | t0003 | g0005 | AFR | GWD | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | GWD | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02630 | hp2 | a0003 | c0003 | t0003 | g0005 | AFR | GWD | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0048 | SAS | PJL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02723 | hp1 | a0003 | c0004 | t0001 | g0180 | AFR | GWD | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0159 | AFR | GWD | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02818 | hp1 | a0003 | c0003 | t0003 | g0182 | AFR | GWD | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02886 | hp1 | a0003 | c0003 | t0003 | g0179 | AFR | GWD | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02922 | hp1 | a0003 | c0003 | t0003 | g0005 | AFR | ESN | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0155 | AFR | ESN | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0059 | SAS | PJL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | MSL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | MSL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0163 | AFR | ESN | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0078 | AFR | ESN | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0311 | AFR | MSL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0310 | AFR | MSL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | MSL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0057 | SAS | PJL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03579 | hp1 | a0003 | c0003 | t0003 | g0185 | AFR | MSL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | MSL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0053 | SAS | PJL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | STU | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0054 | SAS | PJL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | BEB | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0051 | SAS | BEB | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0052 | SAS | BEB | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | BEB | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | STU | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | STU | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | BEB | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | STU | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | STU | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | STU | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | STU | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18522 | hp2 | a0003 | c0003 | t0003 | g0005 | AFR | YRI | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | CHB | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | YRI | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | YRI | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0124 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18953 | hp2 | a0001 | c0001 | t0006 | g0284 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18973 | hp1 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18992 | hp2 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA18999 | hp2 | a0005 | c0006 | t0001 | g0212 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | LWK | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | LWK | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ASW | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | ASW | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | TSI | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0042 | EUR | TSI | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA20805 | hp1 | a0002 | c0002 | t0002 | g0050 | EUR | TSI | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0011 | EUR | TSI | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | ACB | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0162 | AFR | ACB | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0164 | AFR | ACB | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | USA | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | USA | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | USA | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | USA | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0125 | REF | REF | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0152 | REF | REF | MRPS35_chr12_27705832_27761295 | MRPS35 | chr12 | 27705832 | 27761295 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:27710859 | C | A | 1 | a0003 | 13 | HG00741.hp2 HG01168.hp1 HG01884.hp2 others(10): Show |
missense_variant | MODERATE | c.16C>A | p.Leu6Ile | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/8 | 28/1829 | 16/972 | 6/323 | chr12 | 27710859 | |||
| chr12:27714794 | G | A | 1 | a0002 | 60 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(57): Show |
missense_variant | MODERATE | c.127G>A | p.Gly43Arg | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 2/8 | 139/1829 | 127/972 | 43/323 | chr12 | 27714794 | |||
| chr12:27719854 | G | C | 1 | a0004 | 1 | HG02080.hp1 | missense_variant | MODERATE | c.368G>C | p.Cys123Ser | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/8 | 380/1829 | 368/972 | 123/323 | chr12 | 27719854 | |||
| chr12:27735452 | G | C | 1 | a0005 | 1 | NA18999.hp2 | missense_variant | MODERATE | c.528G>C | p.Lys176Asn | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 6/8 | 540/1829 | 528/972 | 176/323 | chr12 | 27735452 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:27755435 | A | G | 1 | a0003c0003 | 12 | HG00741.hp2 HG01168.hp1 HG01884.hp2 others(9): Show |
synonymous_variant | LOW | c.957A>G | p.Leu319Leu | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 8/8 | 969/1829 | 957/972 | 319/323 | chr12 | 27755435 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:27710841 | G | T | 1 | a0001c0001t0004 | 2 | NA18941.hp2 NA18950.hp1 |
5_prime_UTR_variant | MODIFIER | c.-3G>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/8 | 3 | chr12 | 27710841 | ||||||
| chr12:27755670 | A | G | 1 | a0002c0002t0002 | 58 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*220A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 8/8 | 220 | chr12 | 27755670 | ||||||
| chr12:27755741 | T | G | 2 | a0001c0001t0003 a0003c0003t0003 |
32 | HG00741.hp2 HG01168.hp1 HG01884.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*291T>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 8/8 | 291 | chr12 | 27755741 | ||||||
| chr12:27755948 | C | G | 1 | a0001c0001t0006 | 1 | NA18953.hp2 | 3_prime_UTR_variant | MODIFIER | c.*498C>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 8/8 | 498 | chr12 | 27755948 | ||||||
| chr12:27755969 | T | G | 1 | a0001c0001t0005 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*519T>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 8/8 | 519 | chr12 | 27755969 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:27710964 | C | G | 3 | a0001c0001t0001g0312 a0001c0001t0003g0310 a0001c0001t0003g0311 |
3 | HG03209.hp1 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.112+9C>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27710964 | |||||||
| chr12:27711076 | G | A | 7 | a0001c0001t0003g0010 a0001c0001t0003g0026 a0001c0001t0003g0027 others(4): Show |
8 | HG02109.hp1 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+121G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27711076 | |||||||
| chr12:27711303 | T | C | 47 | a0002c0002t0001g0048 a0002c0002t0001g0056 a0002c0002t0002g0001 others(44): Show |
60 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.112+348T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27711303 | |||||||
| chr12:27711408 | C | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(131): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.112+453C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27711408 | |||||||
| chr12:27711449 | C | A | 1 | a0001c0001t0001g0072 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.112+494C>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27711449 | |||||||
| chr12:27711518 | T | G | 5 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(2): Show |
5 | HG01261.hp1 HG02965.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.112+563T>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27711518 | |||||||
| chr12:27711520 | A | C | 1 | a0001c0001t0001g0186 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.112+565A>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27711520 | |||||||
| chr12:27711588 | CCTACCTG others(22): Show |
C | 1 | a0001c0001t0001g0192 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.112+634_112+662del others(29): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27711588 | |||||||
| chr12:27711784 | A | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(132): Show |
152 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.112+829A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27711784 | |||||||
| chr12:27711834 | A | G | 10 | a0003c0003t0003g0005 a0003c0003t0003g0177 a0003c0003t0003g0178 others(7): Show |
13 | HG00741.hp2 HG01168.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.112+879A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27711834 | |||||||
| chr12:27711862 | A | AATAATTG others(301): Show |
1 | a0001c0001t0001g0193 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.112+923_112+924ins others(308): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 27711862 | ||||||
| chr12:27711862 | A | AATAATTG others(304): Show |
1 | a0001c0001t0001g0194 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.112+923_112+924ins others(311): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 27711862 | ||||||
| chr12:27711862 | A | AATAATTG others(308): Show |
2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | HG01070.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.112+923_112+924ins others(315): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 27711862 | ||||||
| chr12:27711862 | A | AATAATTG others(309): Show |
57 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(54): Show |
70 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.112+923_112+924ins others(316): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 27711862 | ||||||
| chr12:27711862 | A | AATAATTG others(309): Show |
1 | a0001c0001t0001g0247 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.112+923_112+924ins others(316): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 27711862 | ||||||
| chr12:27711862 | A | AATAATTG others(310): Show |
46 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(43): Show |
49 | HG00099.hp1 HG00639.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.112+923_112+924ins others(317): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 27711862 | ||||||
| chr12:27711862 | A | AATAATTG others(311): Show |
7 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 others(4): Show |
7 | HG02738.hp2 HG03688.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.112+923_112+924ins others(318): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 27711862 | ||||||
| chr12:27711862 | A | AATAATTG others(312): Show |
2 | a0001c0001t0001g0297 a0001c0001t0001g0298 |
2 | HG06807.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.112+923_112+924ins others(319): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 27711862 | ||||||
| chr12:27711862 | A | AATAATTG others(313): Show |
2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | NA19088.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.112+923_112+924ins others(320): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 27711862 | ||||||
| chr12:27711862 | A | AATAATTG others(314): Show |
14 | a0001c0001t0001g0025 a0001c0001t0001g0187 a0001c0001t0001g0188 others(11): Show |
15 | HG00621.hp1 HG01261.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.112+923_112+924ins others(321): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 27711862 | ||||||
| chr12:27711862 | A | AATAATTG others(324): Show |
1 | a0001c0001t0001g0309 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.112+923_112+924ins others(331): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 27711862 | ||||||
| chr12:27711887 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.112+932A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27711887 | |||||||
| chr12:27711915 | C | G | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 |
3 | HG00738.hp1 HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.112+960C>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27711915 | |||||||
| chr12:27712048 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG01358.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.112+1093G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27712048 | |||||||
| chr12:27712153 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.112+1198T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27712153 | |||||||
| chr12:27712295 | A | C | 47 | a0002c0002t0001g0048 a0002c0002t0001g0056 a0002c0002t0002g0001 others(44): Show |
60 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.112+1340A>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27712295 | |||||||
| chr12:27712561 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | NA18954.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.112+1606C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27712561 | |||||||
| chr12:27712663 | A | G | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.112+1708A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27712663 | |||||||
| chr12:27712934 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.113-1846C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27712934 | |||||||
| chr12:27712953 | T | A | 1 | a0001c0001t0001g0248 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.113-1827T>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27712953 | |||||||
| chr12:27713036 | T | C | 55 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0173 others(52): Show |
68 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.113-1744T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27713036 | |||||||
| chr12:27713110 | C | A | 4 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(1): Show |
4 | HG00642.hp1 HG00738.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.113-1670C>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27713110 | |||||||
| chr12:27713295 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.113-1485C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27713295 | |||||||
| chr12:27713302 | G | A | 11 | a0002c0002t0002g0001 a0002c0002t0002g0032 a0002c0002t0002g0033 others(8): Show |
17 | HG01256.hp2 HG01258.hp2 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.113-1478G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27713302 | |||||||
| chr12:27713495 | A | G | 55 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0173 others(52): Show |
68 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.113-1285A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27713495 | |||||||
| chr12:27713512 | AAAGGCTG others(23): Show |
A | 2 | a0002c0002t0002g0069 a0002c0002t0002g0070 |
2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.113-1263_113-1234d others(32): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 27713512 | ||||||
| chr12:27713582 | A | G | 2 | a0001c0001t0003g0078 a0001c0001t0003g0079 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.113-1198A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27713582 | |||||||
| chr12:27713620 | T | C | 4 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(1): Show |
4 | HG00642.hp1 HG00738.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.113-1160T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27713620 | |||||||
| chr12:27713761 | A | G | 1 | a0001c0001t0001g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.113-1019A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27713761 | |||||||
| chr12:27713796 | T | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.113-984T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27713796 | |||||||
| chr12:27713926 | G | T | 12 | a0001c0001t0003g0010 a0001c0001t0003g0026 a0001c0001t0003g0027 others(9): Show |
13 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.113-854G>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27713926 | |||||||
| chr12:27714007 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.113-773C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27714007 | |||||||
| chr12:27714016 | A | T | 1 | a0001c0001t0001g0175 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.113-764A>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27714016 | |||||||
| chr12:27714075 | CA | C | 19 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 others(16): Show |
22 | HG00323.hp1 HG00639.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.113-686delA | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 27714075 | ||||||
| chr12:27714075 | CAA | C | 43 | a0001c0001t0001g0076 a0001c0001t0001g0157 a0001c0001t0001g0158 others(40): Show |
48 | HG00597.hp1 HG00609.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.113-687_113-686del others(2): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 27714075 | ||||||
| chr12:27714075 | CAAA | C | 28 | a0001c0001t0001g0077 a0002c0002t0001g0056 a0002c0002t0002g0001 others(25): Show |
37 | HG00609.hp1 HG00642.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.113-688_113-686del others(3): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 27714075 | ||||||
| chr12:27714088 | A | T | 12 | a0002c0002t0002g0006 a0002c0002t0002g0015 a0002c0002t0002g0061 others(9): Show |
15 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.113-692A>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27714088 | |||||||
| chr12:27714244 | T | C | 31 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0160 others(28): Show |
35 | HG00741.hp2 HG01168.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.113-536T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27714244 | |||||||
| chr12:27714634 | C | CA | 7 | a0001c0001t0001g0080 a0001c0001t0001g0157 a0001c0001t0001g0158 others(4): Show |
7 | HG02040.hp1 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.113-129dupA | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 27714634 | ||||||
| chr12:27714634 | CA | C | 8 | a0001c0001t0001g0154 a0001c0001t0001g0168 a0001c0001t0001g0171 others(5): Show |
8 | HG02258.hp2 HG02809.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.113-129delA | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 27714634 | ||||||
| chr12:27714668 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.113-112T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27714668 | |||||||
| chr12:27714766 | T | C | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG00323.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.113-14T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27714766 | |||||||
| chr12:27714773 | C | T | 217 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(214): Show |
251 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(248): Show |
splice_region_variant&intron_variant | LOW | c.113-7C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 1/7 | chr12 | 27714773 | |||||||
| chr12:27714844 | A | T | 1 | a0001c0001t0001g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.153+24A>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 2/7 | chr12 | 27714844 | |||||||
| chr12:27714939 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.153+119G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 2/7 | chr12 | 27714939 | |||||||
| chr12:27715009 | G | A | 4 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(1): Show |
4 | HG00642.hp1 HG00738.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+189G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 2/7 | chr12 | 27715009 | |||||||
| chr12:27715184 | G | A | 1 | a0002c0002t0002g0042 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.153+364G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 2/7 | chr12 | 27715184 | |||||||
| chr12:27715228 | C | T | 2 | a0001c0001t0003g0078 a0001c0001t0003g0079 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.153+408C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 2/7 | chr12 | 27715228 | |||||||
| chr12:27715229 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.153+409G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 2/7 | chr12 | 27715229 | |||||||
| chr12:27715339 | G | A | 1 | a0001c0001t0001g0301 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.153+519G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 2/7 | chr12 | 27715339 | |||||||
| chr12:27715420 | C | T | 6 | a0001c0001t0001g0024 a0001c0001t0001g0248 a0001c0001t0001g0283 others(3): Show |
7 | HG00735.hp2 HG01981.hp2 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.153+600C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 2/7 | chr12 | 27715420 | |||||||
| chr12:27715437 | C | G | 1 | a0001c0001t0001g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.153+617C>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 2/7 | chr12 | 27715437 | |||||||
| chr12:27715741 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.154-550C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 2/7 | chr12 | 27715741 | |||||||
| chr12:27715918 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0241 a0001c0001t0001g0242 |
5 | HG01884.hp1 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.154-373C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 2/7 | chr12 | 27715918 | |||||||
| chr12:27716087 | G | A | 1 | a0001c0001t0001g0297 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.154-204G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 2/7 | chr12 | 27716087 | |||||||
| chr12:27716521 | CT | C | 30 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0160 others(27): Show |
34 | HG00741.hp2 HG01168.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.321+64delT | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27716521 | |||||||
| chr12:27716558 | A | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.321+100A>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27716558 | |||||||
| chr12:27716685 | C | G | 1 | a0001c0001t0001g0083 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.321+227C>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27716685 | |||||||
| chr12:27716769 | C | T | 47 | a0002c0002t0001g0048 a0002c0002t0001g0056 a0002c0002t0002g0001 others(44): Show |
60 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.321+311C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27716769 | |||||||
| chr12:27716838 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.321+380A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27716838 | |||||||
| chr12:27716993 | G | GA | 47 | a0002c0002t0001g0048 a0002c0002t0001g0056 a0002c0002t0002g0001 others(44): Show |
60 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.321+546dupA | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 27716993 | ||||||
| chr12:27717332 | T | G | 3 | a0001c0001t0001g0022 a0001c0001t0001g0250 a0001c0001t0001g0288 |
4 | HG01978.hp1 HG01993.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.321+874T>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27717332 | |||||||
| chr12:27717743 | G | A | 11 | a0001c0001t0001g0018 a0001c0001t0001g0195 a0001c0001t0001g0196 others(8): Show |
12 | HG00099.hp2 HG00280.hp2 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.321+1285G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27717743 | |||||||
| chr12:27717747 | C | T | 1 | a0001c0001t0001g0240 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.321+1289C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27717747 | |||||||
| chr12:27717790 | A | C | 2 | a0001c0001t0001g0239 a0001c0001t0001g0246 |
2 | HG00323.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.321+1332A>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27717790 | |||||||
| chr12:27717874 | G | A | 53 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0173 others(50): Show |
66 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.321+1416G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27717874 | |||||||
| chr12:27717901 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.321+1443A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27717901 | |||||||
| chr12:27717988 | A | G | 1 | a0001c0001t0005g0075 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.321+1530A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27717988 | |||||||
| chr12:27718067 | T | G | 14 | a0001c0001t0003g0010 a0001c0001t0003g0026 a0001c0001t0003g0027 others(11): Show |
15 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.321+1609T>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27718067 | |||||||
| chr12:27718093 | A | C | 1 | a0001c0001t0001g0281 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.321+1635A>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27718093 | |||||||
| chr12:27718266 | A | G | 4 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(1): Show |
4 | HG00642.hp1 HG00738.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.322-1542A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27718266 | |||||||
| chr12:27718376 | G | A | 1 | a0001c0001t0005g0075 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.322-1432G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27718376 | |||||||
| chr12:27718420 | A | G | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.322-1388A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27718420 | |||||||
| chr12:27718604 | C | A | 299 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(296): Show |
345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.322-1204C>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27718604 | |||||||
| chr12:27718759 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.322-1049A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27718759 | |||||||
| chr12:27719121 | G | C | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.322-687G>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27719121 | |||||||
| chr12:27719220 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.322-588T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27719220 | |||||||
| chr12:27719432 | C | T | 30 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0017 others(27): Show |
37 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.322-376C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27719432 | |||||||
| chr12:27719462 | C | A | 1 | a0001c0001t0001g0073 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.322-346C>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27719462 | |||||||
| chr12:27719523 | G | A | 30 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0160 others(27): Show |
34 | HG00741.hp2 HG01168.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.322-285G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27719523 | |||||||
| chr12:27719582 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.322-226C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27719582 | |||||||
| chr12:27719636 | G | A | 30 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0017 others(27): Show |
37 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.322-172G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27719636 | |||||||
| chr12:27719642 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.322-166C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27719642 | |||||||
| chr12:27719643 | G | A | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | NA18991.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.322-165G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27719643 | |||||||
| chr12:27719651 | C | T | 1 | a0001c0001t0001g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.322-157C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27719651 | |||||||
| chr12:27719672 | C | CA | 52 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0087 others(49): Show |
65 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.322-121dupA | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 27719672 | ||||||
| chr12:27719717 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.322-91T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27719717 | |||||||
| chr12:27719776 | G | A | 1 | a0002c0002t0002g0043 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.322-32G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 3/7 | chr12 | 27719776 | |||||||
| chr12:27719890 | T | A | 1 | a0001c0001t0001g0173 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.382+22T>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | chr12 | 27719890 | |||||||
| chr12:27719971 | A | G | 14 | a0001c0001t0003g0010 a0001c0001t0003g0026 a0001c0001t0003g0027 others(11): Show |
15 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.382+103A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | chr12 | 27719971 | |||||||
| chr12:27720394 | C | CA | 63 | a0001c0001t0001g0018 a0001c0001t0001g0173 a0001c0001t0001g0174 others(60): Show |
77 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.382+541dupA | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 27720394 | ||||||
| chr12:27720415 | C | T | 1 | a0001c0001t0005g0075 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.382+547C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | chr12 | 27720415 | |||||||
| chr12:27720522 | A | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.382+654A>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | chr12 | 27720522 | |||||||
| chr12:27720579 | T | G | 1 | a0001c0001t0001g0205 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.382+711T>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | chr12 | 27720579 | |||||||
| chr12:27720611 | A | G | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.382+743A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | chr12 | 27720611 | |||||||
| chr12:27720815 | T | TCTCCTTC others(315): Show |
2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.382+965_382+966ins others(322): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 27720815 | ||||||
| chr12:27720815 | T | TCTCCTTC others(316): Show |
1 | a0001c0001t0003g0159 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.382+965_382+966ins others(323): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 27720815 | ||||||
| chr12:27720815 | T | TCTCCTTC others(327): Show |
1 | a0001c0001t0003g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.382+965_382+966ins others(334): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 27720815 | ||||||
| chr12:27720815 | T | TCTCCTTC others(328): Show |
1 | a0001c0001t0003g0156 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.382+965_382+966ins others(335): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 27720815 | ||||||
| chr12:27720972 | G | A | 19 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0003g0010 others(16): Show |
20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.382+1104G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | chr12 | 27720972 | |||||||
| chr12:27721040 | G | A | 1 | a0002c0002t0002g0050 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.382+1172G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | chr12 | 27721040 | |||||||
| chr12:27721344 | T | C | 218 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(215): Show |
252 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.382+1476T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | chr12 | 27721344 | |||||||
| chr12:27721409 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.382+1541G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | chr12 | 27721409 | |||||||
| chr12:27721913 | C | A | 134 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(131): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.382+2045C>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | chr12 | 27721913 | |||||||
| chr12:27722382 | A | G | 1 | a0001c0001t0001g0279 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.383-1665A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | chr12 | 27722382 | |||||||
| chr12:27722387 | A | G | 3 | a0001c0001t0001g0021 a0001c0001t0001g0236 a0001c0001t0001g0237 |
4 | HG01106.hp1 HG01257.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-1660A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | chr12 | 27722387 | |||||||
| chr12:27722477 | G | A | 4 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(1): Show |
4 | HG00642.hp1 HG00738.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-1570G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | chr12 | 27722477 | |||||||
| chr12:27722513 | AT | A | 29 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0072 others(26): Show |
34 | HG00621.hp2 HG00673.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.383-1523delT | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 27722513 | ||||||
| chr12:27722560 | G | A | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0255 |
3 | HG02896.hp2 HG02897.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.383-1487G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | chr12 | 27722560 | |||||||
| chr12:27722574 | C | G | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.383-1473C>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | chr12 | 27722574 | |||||||
| chr12:27722644 | A | T | 1 | a0001c0001t0001g0278 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.383-1403A>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | chr12 | 27722644 | |||||||
| chr12:27722748 | G | A | 30 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0160 others(27): Show |
34 | HG00741.hp2 HG01168.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.383-1299G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | chr12 | 27722748 | |||||||
| chr12:27722995 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.383-1052G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | chr12 | 27722995 | |||||||
| chr12:27722996 | C | A | 1 | a0001c0001t0001g0256 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.383-1051C>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | chr12 | 27722996 | |||||||
| chr12:27723274 | G | GT | 8 | a0001c0001t0001g0088 a0001c0001t0001g0173 a0001c0001t0001g0174 others(5): Show |
8 | HG00642.hp1 HG00738.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.383-760dupT | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 27723274 | ||||||
| chr12:27723494 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.383-553A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | chr12 | 27723494 | |||||||
| chr12:27723621 | C | CT | 22 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0160 others(19): Show |
23 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.383-423dupT | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 27723621 | ||||||
| chr12:27723983 | A | G | 1 | a0001c0001t0001g0277 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.383-64A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 4/7 | chr12 | 27723983 | |||||||
| chr12:27724233 | T | A | 4 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(1): Show |
4 | HG00642.hp1 HG00738.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.522+47T>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27724233 | |||||||
| chr12:27724630 | C | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(132): Show |
152 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.522+444C>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27724630 | |||||||
| chr12:27724637 | G | A | 2 | a0001c0001t0003g0078 a0001c0001t0003g0079 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.522+451G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27724637 | |||||||
| chr12:27724702 | C | G | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG00738.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.522+516C>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27724702 | |||||||
| chr12:27724731 | A | G | 47 | a0002c0002t0001g0048 a0002c0002t0001g0056 a0002c0002t0002g0001 others(44): Show |
60 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.522+545A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27724731 | |||||||
| chr12:27724744 | GA | G | 8 | a0002c0002t0001g0048 a0002c0002t0002g0011 a0002c0002t0002g0042 others(5): Show |
9 | HG01192.hp2 HG01255.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.522+570delA | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27724744 | ||||||
| chr12:27724770 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.522+584C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27724770 | |||||||
| chr12:27724806 | T | G | 1 | a0001c0001t0001g0206 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.522+620T>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27724806 | |||||||
| chr12:27724822 | A | G | 8 | a0002c0002t0001g0048 a0002c0002t0002g0011 a0002c0002t0002g0042 others(5): Show |
9 | HG01192.hp2 HG01255.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.522+636A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27724822 | |||||||
| chr12:27725163 | C | G | 1 | a0001c0001t0001g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.522+977C>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27725163 | |||||||
| chr12:27725321 | C | G | 35 | a0002c0002t0001g0048 a0002c0002t0001g0056 a0002c0002t0002g0001 others(32): Show |
45 | HG00609.hp1 HG00642.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.522+1135C>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27725321 | |||||||
| chr12:27725371 | G | A | 4 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(1): Show |
4 | HG00642.hp1 HG00738.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.522+1185G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27725371 | |||||||
| chr12:27725501 | T | C | 12 | a0001c0001t0003g0010 a0001c0001t0003g0026 a0001c0001t0003g0027 others(9): Show |
13 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.522+1315T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27725501 | |||||||
| chr12:27725542 | G | A | 47 | a0002c0002t0001g0048 a0002c0002t0001g0056 a0002c0002t0002g0001 others(44): Show |
60 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.522+1356G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27725542 | |||||||
| chr12:27725798 | C | CT | 20 | a0001c0001t0001g0108 a0001c0001t0001g0119 a0001c0001t0001g0120 others(17): Show |
20 | HG00642.hp1 HG00738.hp1 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.522+1637dupT | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27725798 | ||||||
| chr12:27725798 | CT | C | 45 | a0001c0001t0001g0021 a0001c0001t0001g0076 a0001c0001t0001g0077 others(42): Show |
50 | HG00408.hp1 HG01106.hp1 HG01168.hp1 others(47): Show |
intron_variant | MODIFIER | c.522+1637delT | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27725798 | ||||||
| chr12:27725798 | CTT | C | 118 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(115): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.522+1636_522+1637d others(4): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27725798 | ||||||
| chr12:27725895 | A | G | 49 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0002c0002t0001g0048 others(46): Show |
62 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.522+1709A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27725895 | |||||||
| chr12:27725915 | C | G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | NA19012.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.522+1729C>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27725915 | |||||||
| chr12:27725975 | A | G | 1 | a0001c0001t0001g0247 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.522+1789A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27725975 | |||||||
| chr12:27725993 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.522+1807A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27725993 | |||||||
| chr12:27726009 | CAT | C | 8 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(5): Show |
8 | HG02559.hp2 HG02602.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.522+1824_522+1825d others(4): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27726009 | |||||||
| chr12:27726012 | G | C | 8 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(5): Show |
8 | HG02559.hp2 HG02602.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.522+1826G>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27726012 | |||||||
| chr12:27726015 | GC | G | 8 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(5): Show |
8 | HG02559.hp2 HG02602.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.522+1832delC | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27726015 | ||||||
| chr12:27726042 | T | C | 47 | a0002c0002t0001g0048 a0002c0002t0001g0056 a0002c0002t0002g0001 others(44): Show |
60 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.522+1856T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27726042 | |||||||
| chr12:27726209 | T | G | 6 | a0001c0001t0001g0025 a0001c0001t0001g0257 a0001c0001t0001g0258 others(3): Show |
7 | HG00621.hp1 NA18940.hp1 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.522+2023T>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27726209 | |||||||
| chr12:27726610 | A | G | 5 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0003g0155 others(2): Show |
5 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.522+2424A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27726610 | |||||||
| chr12:27726900 | A | G | 10 | a0003c0003t0003g0005 a0003c0003t0003g0177 a0003c0003t0003g0178 others(7): Show |
13 | HG00741.hp2 HG01168.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.522+2714A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27726900 | |||||||
| chr12:27726916 | T | G | 1 | a0001c0001t0001g0198 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.522+2730T>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27726916 | |||||||
| chr12:27726960 | C | CT | 130 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(127): Show |
146 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.522+2792dupT | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27726960 | ||||||
| chr12:27726960 | C | CTT | 11 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(8): Show |
11 | HG00408.hp2 HG00642.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.522+2791_522+2792d others(4): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27726960 | ||||||
| chr12:27727153 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.522+2967G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27727153 | |||||||
| chr12:27727162 | C | T | 1 | a0001c0001t0001g0283 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.522+2976C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27727162 | |||||||
| chr12:27727759 | C | T | 1 | a0001c0001t0005g0075 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.522+3573C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27727759 | |||||||
| chr12:27728148 | T | A | 3 | a0002c0002t0002g0051 a0002c0002t0002g0052 a0002c0002t0002g0059 |
3 | HG03017.hp1 HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.522+3962T>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27728148 | |||||||
| chr12:27728217 | T | C | 20 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0160 others(17): Show |
21 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.522+4031T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27728217 | |||||||
| chr12:27728272 | C | G | 4 | a0001c0001t0001g0227 a0001c0001t0001g0239 a0001c0001t0001g0245 others(1): Show |
4 | HG00323.hp1 HG01175.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.522+4086C>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27728272 | |||||||
| chr12:27728575 | A | C | 47 | a0002c0002t0001g0048 a0002c0002t0001g0056 a0002c0002t0002g0001 others(44): Show |
60 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.522+4389A>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27728575 | |||||||
| chr12:27728902 | A | C | 47 | a0002c0002t0001g0048 a0002c0002t0001g0056 a0002c0002t0002g0001 others(44): Show |
60 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.522+4716A>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27728902 | |||||||
| chr12:27729109 | G | A | 4 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(1): Show |
4 | HG00642.hp1 HG00738.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.522+4923G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27729109 | |||||||
| chr12:27729147 | T | C | 5 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0199 others(2): Show |
5 | HG00280.hp2 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.522+4961T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27729147 | |||||||
| chr12:27729358 | G | A | 27 | a0002c0002t0001g0056 a0002c0002t0002g0001 a0002c0002t0002g0012 others(24): Show |
36 | HG00609.hp1 HG00642.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.522+5172G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27729358 | |||||||
| chr12:27729490 | T | C | 5 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0003g0155 others(2): Show |
5 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.522+5304T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27729490 | |||||||
| chr12:27729827 | C | T | 3 | a0001c0001t0003g0164 a0001c0001t0003g0165 a0001c0001t0003g0166 |
3 | HG02145.hp1 HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.523-5620C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27729827 | |||||||
| chr12:27729954 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.523-5493A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27729954 | |||||||
| chr12:27729998 | T | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0194 a0001c0001t0001g0259 others(1): Show |
5 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.523-5449T>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27729998 | |||||||
| chr12:27730240 | A | G | 53 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0173 others(50): Show |
66 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.523-5207A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27730240 | |||||||
| chr12:27730248 | A | G | 53 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0173 others(50): Show |
66 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.523-5199A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27730248 | |||||||
| chr12:27730332 | T | C | 4 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(1): Show |
4 | HG00642.hp1 HG00738.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.523-5115T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27730332 | |||||||
| chr12:27730362 | CTTG | C | 29 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0017 others(26): Show |
36 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.523-5080_523-5078d others(5): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27730362 | ||||||
| chr12:27730517 | C | T | 12 | a0001c0001t0001g0025 a0001c0001t0001g0226 a0001c0001t0001g0258 others(9): Show |
13 | HG02015.hp2 HG03540.hp1 HG03704.hp2 others(10): Show |
intron_variant | MODIFIER | c.523-4930C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27730517 | |||||||
| chr12:27730595 | G | A | 20 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0160 others(17): Show |
21 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.523-4852G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27730595 | |||||||
| chr12:27730713 | C | T | 4 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.523-4734C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27730713 | |||||||
| chr12:27730766 | C | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(131): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.523-4681C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27730766 | |||||||
| chr12:27730796 | C | G | 10 | a0003c0003t0003g0005 a0003c0003t0003g0177 a0003c0003t0003g0178 others(7): Show |
13 | HG00741.hp2 HG01168.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.523-4651C>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27730796 | |||||||
| chr12:27730873 | C | G | 217 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(214): Show |
251 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.523-4574C>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27730873 | |||||||
| chr12:27730903 | G | C | 1 | a0001c0001t0003g0026 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.523-4544G>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27730903 | |||||||
| chr12:27730999 | T | C | 3 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 |
3 | HG00558.hp1 NA18948.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.523-4448T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27730999 | |||||||
| chr12:27731116 | A | G | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.523-4331A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27731116 | |||||||
| chr12:27731217 | G | A | 16 | a0001c0001t0001g0025 a0001c0001t0001g0187 a0001c0001t0001g0188 others(13): Show |
17 | HG01261.hp1 HG02015.hp2 HG02965.hp2 others(14): Show |
intron_variant | MODIFIER | c.523-4230G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27731217 | |||||||
| chr12:27731218 | G | T | 1 | a0001c0001t0001g0194 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.523-4229G>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27731218 | |||||||
| chr12:27731349 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.523-4098A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27731349 | |||||||
| chr12:27731631 | C | T | 10 | a0003c0003t0003g0005 a0003c0003t0003g0177 a0003c0003t0003g0178 others(7): Show |
13 | HG00741.hp2 HG01168.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.523-3816C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27731631 | |||||||
| chr12:27731671 | C | T | 1 | a0001c0001t0001g0299 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.523-3776C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27731671 | |||||||
| chr12:27731872 | G | A | 54 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0173 others(51): Show |
67 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.523-3575G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27731872 | |||||||
| chr12:27731906 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.523-3541A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27731906 | |||||||
| chr12:27732075 | A | G | 2 | a0001c0001t0001g0268 a0001c0001t0001g0278 |
2 | NA18973.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.523-3372A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27732075 | |||||||
| chr12:27732265 | A | C | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | NA18954.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.523-3182A>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27732265 | |||||||
| chr12:27732474 | C | T | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.523-2973C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27732474 | |||||||
| chr12:27732498 | A | G | 1 | a0003c0003t0003g0182 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.523-2949A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27732498 | |||||||
| chr12:27732671 | T | A | 1 | a0001c0001t0001g0255 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.523-2776T>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27732671 | |||||||
| chr12:27732799 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.523-2648A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27732799 | |||||||
| chr12:27732875 | C | A | 1 | a0001c0001t0001g0126 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.523-2572C>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27732875 | |||||||
| chr12:27732885 | T | G | 1 | a0001c0001t0001g0252 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.523-2562T>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27732885 | |||||||
| chr12:27732987 | GAT | G | 3 | a0001c0001t0001g0089 a0001c0001t0001g0228 a0001c0001t0003g0156 |
3 | HG02080.hp2 HG02258.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.523-2407_523-2406d others(4): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27732987 | ||||||
| chr12:27732987 | GATAT | G | 9 | a0001c0001t0001g0091 a0001c0001t0001g0106 a0001c0001t0001g0147 others(6): Show |
9 | HG00741.hp2 HG01168.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.523-2409_523-2406d others(6): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27732987 | ||||||
| chr12:27732987 | GATATAT | G | 13 | a0001c0001t0001g0016 a0001c0001t0001g0092 a0001c0001t0001g0093 others(10): Show |
16 | HG00639.hp1 HG01175.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.523-2411_523-2406d others(8): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27732987 | ||||||
| chr12:27732987 | GATATATA others(1): Show |
G | 25 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0094 others(22): Show |
28 | HG00609.hp1 HG01081.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.523-2413_523-2406d others(10): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27732987 | ||||||
| chr12:27732987 | GATATATA others(3): Show |
G | 32 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0084 others(29): Show |
40 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.523-2415_523-2406d others(12): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27732987 | ||||||
| chr12:27732987 | GATATATA others(5): Show |
G | 22 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0088 others(19): Show |
27 | HG00642.hp1 HG00673.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.523-2417_523-2406d others(14): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27732987 | ||||||
| chr12:27732987 | GATATATA others(7): Show |
G | 21 | a0001c0001t0001g0004 a0001c0001t0001g0080 a0001c0001t0001g0085 others(18): Show |
25 | HG00558.hp1 HG01123.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.523-2419_523-2406d others(16): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27732987 | ||||||
| chr12:27732987 | GATATATA others(9): Show |
G | 12 | a0001c0001t0001g0072 a0001c0001t0001g0117 a0001c0001t0001g0134 others(9): Show |
13 | HG00597.hp2 HG01891.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.523-2421_523-2406d others(18): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27732987 | ||||||
| chr12:27732987 | GATATATA others(11): Show |
G | 20 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0073 others(17): Show |
23 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.523-2423_523-2406d others(20): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27732987 | ||||||
| chr12:27732987 | GATATATA others(13): Show |
G | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.523-2425_523-2406d others(22): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27732987 | ||||||
| chr12:27732987 | GATATATA others(15): Show |
G | 1 | a0001c0001t0001g0145 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.523-2427_523-2406d others(24): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27732987 | ||||||
| chr12:27732987 | GATATATA others(21): Show |
G | 2 | a0001c0001t0001g0153 a0002c0002t0002g0067 |
2 | HG02055.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.523-2433_523-2406d others(30): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27732987 | ||||||
| chr12:27732987 | GATATATA others(29): Show |
G | 124 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(121): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.523-2441_523-2406d others(38): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27732987 | ||||||
| chr12:27732987 | GATATATA others(31): Show |
G | 8 | a0001c0001t0001g0024 a0001c0001t0001g0104 a0001c0001t0001g0222 others(5): Show |
9 | HG00735.hp2 HG01361.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.523-2443_523-2406d others(40): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27732987 | ||||||
| chr12:27732993 | T | G | 1 | a0002c0002t0002g0033 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.523-2454T>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27732993 | |||||||
| chr12:27732995 | T | G | 1 | a0002c0002t0002g0034 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.523-2452T>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27732995 | |||||||
| chr12:27732997 | T | G | 1 | a0002c0002t0002g0039 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.523-2450T>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27732997 | |||||||
| chr12:27732999 | T | G | 8 | a0002c0002t0002g0001 a0002c0002t0002g0032 a0002c0002t0002g0035 others(5): Show |
14 | HG01256.hp2 HG01258.hp2 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.523-2448T>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27732999 | |||||||
| chr12:27733018 | A | ATATCTAT others(5): Show |
1 | a0002c0002t0002g0066 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.523-2426_523-2425i others(14): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27733018 | ||||||
| chr12:27733022 | A | C | 1 | a0002c0002t0002g0066 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.523-2425A>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27733022 | |||||||
| chr12:27733024 | A | C | 1 | a0002c0002t0002g0058 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.523-2423A>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27733024 | |||||||
| chr12:27733026 | A | ATCTATAT others(5): Show |
2 | a0002c0002t0002g0069 a0002c0002t0002g0070 |
2 | NA18944.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.523-2420_523-2419i others(14): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27733026 | ||||||
| chr12:27733026 | A | ATCTATCT others(7): Show |
2 | a0002c0002t0002g0015 a0002c0002t0002g0065 |
3 | HG02027.hp2 HG02056.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.523-2420_523-2419i others(16): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27733026 | ||||||
| chr12:27733026 | A | C | 2 | a0002c0002t0002g0066 a0002c0002t0002g0067 |
2 | HG02129.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.523-2421A>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27733026 | |||||||
| chr12:27733030 | A | ATATCTAT others(5): Show |
1 | a0002c0002t0002g0006 | 3 | HG00673.hp2 NA18957.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.523-2414_523-2413i others(14): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27733030 | ||||||
| chr12:27733030 | A | ATATCTAT others(13): Show |
1 | a0002c0002t0002g0062 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.523-2414_523-2413i others(22): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27733030 | ||||||
| chr12:27733030 | A | ATCTATCT others(7): Show |
1 | a0002c0002t0002g0063 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.523-2416_523-2415i others(16): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27733030 | ||||||
| chr12:27733030 | A | C | 7 | a0002c0002t0002g0015 a0002c0002t0002g0064 a0002c0002t0002g0065 others(4): Show |
8 | HG02027.hp2 HG02056.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.523-2417A>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27733030 | |||||||
| chr12:27733034 | A | ATATCTAT others(9): Show |
1 | a0002c0002t0002g0068 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.523-2410_523-2409i others(18): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27733034 | ||||||
| chr12:27733034 | A | ATC | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0002c0002t0002g0053 |
3 | HG02896.hp2 HG02897.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.523-2412_523-2411i others(4): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27733034 | ||||||
| chr12:27733034 | A | ATCTATCT others(11): Show |
1 | a0002c0002t0002g0061 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.523-2412_523-2411i others(20): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27733034 | ||||||
| chr12:27733034 | A | C | 16 | a0001c0001t0001g0173 a0002c0002t0001g0056 a0002c0002t0002g0006 others(13): Show |
20 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.523-2413A>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27733034 | |||||||
| chr12:27733038 | A | C | 45 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0173 others(42): Show |
58 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.523-2409A>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27733038 | |||||||
| chr12:27733040 | A | C | 1 | a0001c0001t0001g0259 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.523-2407A>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27733040 | |||||||
| chr12:27733284 | A | G | 28 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0160 others(25): Show |
32 | HG00741.hp2 HG01168.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.523-2163A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27733284 | |||||||
| chr12:27733467 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.523-1980T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27733467 | |||||||
| chr12:27733499 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.523-1948A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27733499 | |||||||
| chr12:27734242 | C | CT | 50 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0174 others(47): Show |
63 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.523-1188dupT | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27734242 | ||||||
| chr12:27734242 | CTT | C | 31 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0160 others(28): Show |
35 | HG00642.hp1 HG00738.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.523-1189_523-1188d others(4): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 27734242 | ||||||
| chr12:27734266 | G | A | 3 | a0001c0001t0003g0164 a0001c0001t0003g0310 a0001c0001t0003g0311 |
3 | HG02559.hp1 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.523-1181G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27734266 | |||||||
| chr12:27734530 | C | T | 27 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0003g0010 others(24): Show |
31 | HG00741.hp2 HG01168.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.523-917C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27734530 | |||||||
| chr12:27734538 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.523-909G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27734538 | |||||||
| chr12:27734616 | T | G | 294 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(291): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.523-831T>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27734616 | |||||||
| chr12:27734701 | G | A | 3 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0005g0075 |
3 | HG00642.hp1 HG00738.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.523-746G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27734701 | |||||||
| chr12:27734738 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.523-709C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27734738 | |||||||
| chr12:27735106 | A | G | 1 | a0001c0001t0003g0031 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.523-341A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27735106 | |||||||
| chr12:27735122 | C | T | 5 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(2): Show |
5 | HG00642.hp1 HG00738.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.523-325C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27735122 | |||||||
| chr12:27735334 | T | C | 2 | a0001c0001t0001g0211 a0002c0002t0001g0056 |
2 | HG01981.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.523-113T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27735334 | |||||||
| chr12:27735410 | G | T | 1 | a0001c0001t0001g0220 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.523-37G>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 5/7 | chr12 | 27735410 | |||||||
| chr12:27735660 | G | C | 1 | a0001c0001t0001g0260 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.632+104G>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 6/7 | chr12 | 27735660 | |||||||
| chr12:27736048 | G | A | 1 | a0001c0001t0001g0240 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.632+492G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 6/7 | chr12 | 27736048 | |||||||
| chr12:27736154 | A | T | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0210 |
3 | HG00738.hp1 HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.632+598A>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 6/7 | chr12 | 27736154 | |||||||
| chr12:27736190 | G | A | 2 | a0001c0001t0001g0304 a0001c0001t0001g0305 |
2 | HG02015.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.632+634G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 6/7 | chr12 | 27736190 | |||||||
| chr12:27736310 | G | T | 1 | a0001c0001t0001g0219 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.632+754G>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 6/7 | chr12 | 27736310 | |||||||
| chr12:27736348 | T | C | 1 | a0001c0001t0003g0078 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.632+792T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 6/7 | chr12 | 27736348 | |||||||
| chr12:27736409 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.632+853C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 6/7 | chr12 | 27736409 | |||||||
| chr12:27736481 | T | C | 1 | a0001c0001t0001g0247 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.632+925T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 6/7 | chr12 | 27736481 | |||||||
| chr12:27736500 | CT | C | 179 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(176): Show |
208 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.632+957delT | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 27736500 | ||||||
| chr12:27736553 | G | T | 1 | a0001c0001t0001g0207 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.633-986G>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 6/7 | chr12 | 27736553 | |||||||
| chr12:27736554 | G | T | 1 | a0001c0001t0001g0207 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.633-985G>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 6/7 | chr12 | 27736554 | |||||||
| chr12:27737134 | C | T | 33 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0160 others(30): Show |
37 | HG00642.hp1 HG00738.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.633-405C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 6/7 | chr12 | 27737134 | |||||||
| chr12:27737306 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.633-233C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 6/7 | chr12 | 27737306 | |||||||
| chr12:27737333 | C | T | 5 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(2): Show |
5 | HG00642.hp1 HG00738.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.633-206C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 6/7 | chr12 | 27737333 | |||||||
| chr12:27737402 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.633-137C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 6/7 | chr12 | 27737402 | |||||||
| chr12:27737444 | C | G | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.633-95C>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 6/7 | chr12 | 27737444 | |||||||
| chr12:27737448 | A | G | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.633-91A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 6/7 | chr12 | 27737448 | |||||||
| chr12:27737522 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.633-17C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 6/7 | chr12 | 27737522 | |||||||
| chr12:27737523 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.633-16G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 6/7 | chr12 | 27737523 | |||||||
| chr12:27737731 | T | C | 2 | a0001c0001t0001g0231 a0001c0001t0001g0261 |
2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.702+123T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27737731 | |||||||
| chr12:27738236 | A | C | 1 | a0001c0001t0001g0219 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.702+628A>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27738236 | |||||||
| chr12:27738447 | T | G | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.702+839T>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27738447 | |||||||
| chr12:27738498 | T | G | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | NA18954.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.702+890T>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27738498 | |||||||
| chr12:27738633 | A | T | 1 | a0001c0001t0001g0186 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.702+1025A>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27738633 | |||||||
| chr12:27738913 | C | CT | 33 | a0001c0001t0001g0143 a0001c0001t0001g0157 a0001c0001t0001g0158 others(30): Show |
37 | HG00741.hp2 HG01168.hp1 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.702+1323dupT | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27738913 | ||||||
| chr12:27738913 | CT | C | 11 | a0001c0001t0001g0134 a0001c0001t0001g0145 a0001c0001t0001g0169 others(8): Show |
11 | HG00323.hp1 HG01257.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.702+1323delT | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27738913 | ||||||
| chr12:27738969 | A | T | 81 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0157 others(78): Show |
98 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.702+1361A>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27738969 | |||||||
| chr12:27739049 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.702+1441A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27739049 | |||||||
| chr12:27739150 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.702+1542G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27739150 | |||||||
| chr12:27739220 | A | C | 1 | a0001c0001t0005g0075 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.702+1612A>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27739220 | |||||||
| chr12:27739641 | A | G | 39 | a0002c0002t0001g0056 a0002c0002t0002g0001 a0002c0002t0002g0006 others(36): Show |
51 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.702+2033A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27739641 | |||||||
| chr12:27739828 | C | A | 1 | a0001c0001t0001g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.702+2220C>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27739828 | |||||||
| chr12:27739973 | A | T | 130 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(127): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.702+2365A>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27739973 | |||||||
| chr12:27740039 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.702+2431G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27740039 | |||||||
| chr12:27740047 | G | A | 1 | a0002c0002t0002g0042 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.702+2439G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27740047 | |||||||
| chr12:27740066 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.702+2458C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27740066 | |||||||
| chr12:27740068 | G | A | 1 | a0002c0002t0002g0054 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.702+2460G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27740068 | |||||||
| chr12:27740134 | A | G | 27 | a0002c0002t0001g0056 a0002c0002t0002g0001 a0002c0002t0002g0012 others(24): Show |
36 | HG00609.hp1 HG00642.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.702+2526A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27740134 | |||||||
| chr12:27740240 | T | G | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.702+2632T>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27740240 | |||||||
| chr12:27740267 | CT | C | 51 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(48): Show |
64 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.702+2673delT | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27740267 | ||||||
| chr12:27740413 | G | A | 49 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0017 others(46): Show |
56 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.702+2805G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27740413 | |||||||
| chr12:27740715 | A | G | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.702+3107A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27740715 | |||||||
| chr12:27740942 | G | A | 1 | a0002c0002t0002g0014 | 2 | HG00735.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.702+3334G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27740942 | |||||||
| chr12:27741038 | G | A | 3 | a0002c0002t0002g0043 a0002c0002t0002g0046 a0002c0002t0002g0047 |
3 | NA18962.hp2 NA19005.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.702+3430G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27741038 | |||||||
| chr12:27741039 | G | A | 3 | a0002c0002t0002g0011 a0002c0002t0002g0042 a0002c0002t0002g0045 |
4 | HG01192.hp2 HG01255.hp1 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.702+3431G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27741039 | |||||||
| chr12:27741093 | G | A | 2 | a0001c0001t0001g0203 a0001c0001t0001g0309 |
2 | HG01192.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.702+3485G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27741093 | |||||||
| chr12:27741100 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.702+3492G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27741100 | |||||||
| chr12:27741119 | G | C | 5 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(2): Show |
5 | HG00642.hp1 HG00738.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.702+3511G>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27741119 | |||||||
| chr12:27741178 | T | A | 4 | a0001c0001t0001g0109 a0001c0001t0001g0114 a0001c0001t0001g0274 others(1): Show |
4 | HG01257.hp1 HG01258.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.702+3570T>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27741178 | |||||||
| chr12:27741243 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.702+3635C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27741243 | |||||||
| chr12:27741254 | C | T | 2 | a0001c0001t0001g0266 a0001c0001t0001g0298 |
2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.702+3646C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27741254 | |||||||
| chr12:27741339 | C | CT | 81 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0157 others(78): Show |
98 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.702+3731_702+3732i others(3): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27741339 | |||||||
| chr12:27741947 | G | C | 1 | a0001c0001t0001g0256 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.702+4339G>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27741947 | |||||||
| chr12:27742100 | T | C | 46 | a0002c0002t0001g0056 a0002c0002t0002g0001 a0002c0002t0002g0006 others(43): Show |
59 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.702+4492T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27742100 | |||||||
| chr12:27742328 | C | A | 1 | a0001c0001t0001g0286 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.702+4720C>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27742328 | |||||||
| chr12:27742331 | T | G | 1 | a0001c0001t0001g0286 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.702+4723T>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27742331 | |||||||
| chr12:27742332 | T | TTGAATGT others(6): Show |
1 | a0001c0001t0001g0286 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.702+4725_702+4726i others(15): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27742332 | ||||||
| chr12:27742415 | G | A | 3 | a0001c0001t0003g0163 a0001c0001t0003g0165 a0001c0001t0003g0166 |
3 | HG02145.hp1 HG02451.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.702+4807G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27742415 | |||||||
| chr12:27742437 | A | G | 75 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0003g0010 others(72): Show |
92 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.702+4829A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27742437 | |||||||
| chr12:27742698 | C | G | 1 | a0002c0002t0002g0063 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.702+5090C>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27742698 | |||||||
| chr12:27742963 | C | T | 1 | a0002c0002t0002g0012 | 2 | HG02015.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.702+5355C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27742963 | |||||||
| chr12:27743182 | C | T | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0173 |
3 | HG00738.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.702+5574C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27743182 | |||||||
| chr12:27743216 | A | C | 1 | a0001c0001t0001g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.702+5608A>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27743216 | |||||||
| chr12:27743294 | A | G | 213 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(210): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.702+5686A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27743294 | |||||||
| chr12:27743331 | C | T | 7 | a0002c0002t0002g0011 a0002c0002t0002g0042 a0002c0002t0002g0043 others(4): Show |
8 | HG01192.hp2 HG01255.hp1 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.702+5723C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27743331 | |||||||
| chr12:27743357 | A | T | 1 | a0001c0001t0001g0103 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.702+5749A>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27743357 | |||||||
| chr12:27743375 | T | C | 81 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0173 others(78): Show |
98 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.702+5767T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27743375 | |||||||
| chr12:27743385 | G | A | 3 | a0001c0001t0001g0227 a0001c0001t0001g0239 a0001c0001t0001g0246 |
3 | HG00323.hp1 HG01175.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.702+5777G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27743385 | |||||||
| chr12:27743685 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.702+6077G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27743685 | |||||||
| chr12:27744102 | T | G | 213 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(210): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.702+6494T>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27744102 | |||||||
| chr12:27744103 | T | C | 213 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(210): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.702+6495T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27744103 | |||||||
| chr12:27744176 | T | C | 301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.702+6568T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27744176 | |||||||
| chr12:27744319 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.702+6711C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27744319 | |||||||
| chr12:27744321 | C | T | 3 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 |
3 | HG00558.hp1 NA18948.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.702+6713C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27744321 | |||||||
| chr12:27744439 | CA | C | 7 | a0001c0001t0003g0010 a0001c0001t0003g0027 a0001c0001t0003g0028 others(4): Show |
8 | HG02109.hp2 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.702+6841delA | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27744439 | ||||||
| chr12:27744491 | T | C | 213 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(210): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.702+6883T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27744491 | |||||||
| chr12:27744604 | C | T | 4 | a0001c0001t0001g0090 a0001c0001t0001g0230 a0001c0001t0001g0240 others(1): Show |
4 | HG00408.hp2 HG03688.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+6996C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27744604 | |||||||
| chr12:27744605 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0289 |
3 | HG00639.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.702+6997G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27744605 | |||||||
| chr12:27744698 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.702+7090A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27744698 | |||||||
| chr12:27744792 | A | C | 1 | a0001c0001t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.702+7184A>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27744792 | |||||||
| chr12:27744867 | G | GT | 132 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(129): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.702+7267dupT | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27744867 | ||||||
| chr12:27744892 | A | T | 5 | a0001c0001t0001g0088 a0001c0001t0001g0101 a0001c0001t0001g0103 others(2): Show |
5 | NA18940.hp2 NA18969.hp2 NA19065.hp2 others(2): Show |
intron_variant | MODIFIER | c.702+7284A>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27744892 | |||||||
| chr12:27744893 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.702+7285A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27744893 | |||||||
| chr12:27744994 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.702+7386C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27744994 | |||||||
| chr12:27745017 | G | T | 48 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0002c0002t0001g0056 others(45): Show |
61 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.702+7409G>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27745017 | |||||||
| chr12:27745170 | A | G | 2 | a0001c0001t0001g0273 a0001c0001t0001g0276 |
2 | NA18945.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.702+7562A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27745170 | |||||||
| chr12:27745331 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.702+7723G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27745331 | |||||||
| chr12:27745526 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.702+7918A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27745526 | |||||||
| chr12:27745568 | CT | C | 29 | a0001c0001t0001g0196 a0001c0001t0003g0010 a0001c0001t0003g0026 others(26): Show |
33 | HG00741.hp2 HG01168.hp1 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.702+7971delT | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27745568 | ||||||
| chr12:27745579 | T | A | 1 | a0001c0001t0001g0086 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.702+7971T>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27745579 | |||||||
| chr12:27745652 | T | A | 2 | a0001c0001t0003g0078 a0001c0001t0003g0079 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.702+8044T>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27745652 | |||||||
| chr12:27745674 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.702+8066T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27745674 | |||||||
| chr12:27745720 | T | C | 213 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(210): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.702+8112T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27745720 | |||||||
| chr12:27745961 | A | G | 1 | a0001c0001t0001g0297 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.702+8353A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27745961 | |||||||
| chr12:27746259 | G | A | 3 | a0001c0001t0001g0203 a0001c0001t0001g0243 a0001c0001t0001g0309 |
3 | HG01192.hp1 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.702+8651G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27746259 | |||||||
| chr12:27746264 | T | C | 3 | a0002c0002t0002g0033 a0002c0002t0002g0034 a0002c0002t0002g0039 |
3 | NA18950.hp2 NA19010.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.702+8656T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27746264 | |||||||
| chr12:27746275 | G | A | 1 | a0002c0002t0002g0068 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.702+8667G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27746275 | |||||||
| chr12:27746302 | T | C | 48 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0002c0002t0001g0056 others(45): Show |
61 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.702+8694T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27746302 | |||||||
| chr12:27746338 | C | CA | 76 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0003g0010 others(73): Show |
93 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.702+8731dupA | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27746338 | ||||||
| chr12:27746342 | A | G | 11 | a0001c0001t0003g0010 a0001c0001t0003g0026 a0001c0001t0003g0027 others(8): Show |
12 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.702+8734A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27746342 | |||||||
| chr12:27746600 | A | G | 1 | a0002c0002t0002g0057 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.703-8581A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27746600 | |||||||
| chr12:27746724 | G | C | 213 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(210): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.703-8457G>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27746724 | |||||||
| chr12:27746725 | G | A | 1 | a0002c0002t0002g0035 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.703-8456G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27746725 | |||||||
| chr12:27746885 | A | G | 1 | a0001c0001t0001g0299 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.703-8296A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27746885 | |||||||
| chr12:27747069 | T | A | 5 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(2): Show |
5 | HG00642.hp1 HG00738.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-8112T>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27747069 | |||||||
| chr12:27747113 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.703-8068A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27747113 | |||||||
| chr12:27747194 | G | A | 1 | a0005c0006t0001g0212 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.703-7987G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27747194 | |||||||
| chr12:27747474 | A | AAAATTTA others(7): Show |
47 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0157 others(44): Show |
49 | HG00099.hp1 HG00735.hp2 HG01978.hp1 others(46): Show |
intron_variant | MODIFIER | c.703-7706_703-7693d others(16): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27747474 | ||||||
| chr12:27747507 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.703-7674G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27747507 | |||||||
| chr12:27747525 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.703-7656T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27747525 | |||||||
| chr12:27747898 | T | C | 7 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0173 others(4): Show |
7 | HG00642.hp1 HG00738.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.703-7283T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27747898 | |||||||
| chr12:27747914 | A | G | 1 | a0001c0001t0005g0075 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.703-7267A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27747914 | |||||||
| chr12:27748119 | T | C | 46 | a0002c0002t0001g0056 a0002c0002t0002g0001 a0002c0002t0002g0006 others(43): Show |
59 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.703-7062T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27748119 | |||||||
| chr12:27748296 | T | C | 131 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(128): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.703-6885T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27748296 | |||||||
| chr12:27748438 | G | GGT | 21 | a0001c0001t0001g0009 a0001c0001t0001g0106 a0001c0001t0001g0107 others(18): Show |
23 | HG00280.hp2 HG01070.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.703-6711_703-6710d others(4): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27748438 | ||||||
| chr12:27748438 | G | GGTGT | 49 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(46): Show |
55 | HG00621.hp2 HG00673.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.703-6713_703-6710d others(6): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27748438 | ||||||
| chr12:27748438 | G | GGTGTGT | 84 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0018 others(81): Show |
96 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.703-6715_703-6710d others(8): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27748438 | ||||||
| chr12:27748438 | G | GGTGTGTG others(1): Show |
12 | a0001c0001t0001g0020 a0001c0001t0001g0202 a0001c0001t0001g0216 others(9): Show |
13 | HG01175.hp2 HG01433.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.703-6717_703-6710d others(10): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27748438 | ||||||
| chr12:27748438 | G | GGTGTGTG others(3): Show |
3 | a0001c0001t0001g0223 a0001c0001t0001g0225 a0001c0001t0001g0249 |
3 | HG02451.hp1 HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.703-6719_703-6710d others(12): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27748438 | ||||||
| chr12:27748438 | G | GTGT | 3 | a0001c0001t0001g0217 a0001c0001t0001g0241 a0001c0001t0001g0242 |
3 | HG02922.hp2 HG03041.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.703-6743_703-6742i others(5): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27748438 | |||||||
| chr12:27748438 | GGT | G | 37 | a0001c0001t0001g0113 a0001c0001t0001g0149 a0001c0001t0001g0174 others(34): Show |
42 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.703-6711_703-6710d others(4): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27748438 | ||||||
| chr12:27748438 | GGTGT | G | 39 | a0001c0001t0003g0026 a0001c0001t0003g0155 a0001c0001t0003g0156 others(36): Show |
51 | HG00609.hp1 HG00642.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.703-6713_703-6710d others(6): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27748438 | ||||||
| chr12:27748584 | T | TTAAAATG others(341): Show |
1 | a0001c0001t0001g0153 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.703-6582_703-6581i others(350): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27748584 | ||||||
| chr12:27748596 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.703-6585T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27748596 | |||||||
| chr12:27748627 | G | T | 1 | a0001c0001t0001g0137 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.703-6554G>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27748627 | |||||||
| chr12:27748813 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.703-6368G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27748813 | |||||||
| chr12:27749063 | A | T | 1 | a0001c0001t0001g0157 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.703-6118A>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27749063 | |||||||
| chr12:27749138 | A | AT | 18 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0081 others(15): Show |
18 | HG00558.hp1 HG01243.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.703-6033dupT | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27749138 | ||||||
| chr12:27749138 | AT | A | 212 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(209): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.703-6033delT | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27749138 | ||||||
| chr12:27749261 | C | T | 37 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0192 others(34): Show |
39 | HG00735.hp2 HG01978.hp1 HG01981.hp2 others(36): Show |
intron_variant | MODIFIER | c.703-5920C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27749261 | |||||||
| chr12:27749329 | C | CA | 76 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0003g0010 others(73): Show |
93 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.703-5843dupA | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27749329 | ||||||
| chr12:27749599 | A | G | 213 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(210): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.703-5582A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27749599 | |||||||
| chr12:27750060 | G | A | 3 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0190 |
3 | HG03041.hp1 HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.703-5121G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27750060 | |||||||
| chr12:27750639 | CA | C | 81 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0173 others(78): Show |
98 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.703-4534delA | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27750639 | ||||||
| chr12:27750761 | T | C | 76 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0003g0010 others(73): Show |
93 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.703-4420T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27750761 | |||||||
| chr12:27750769 | T | C | 213 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(210): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.703-4412T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27750769 | |||||||
| chr12:27750959 | T | C | 131 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0017 others(128): Show |
155 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.703-4222T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27750959 | |||||||
| chr12:27751053 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.703-4128A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27751053 | |||||||
| chr12:27751102 | C | CA | 30 | a0001c0001t0001g0107 a0001c0001t0001g0113 a0001c0001t0001g0129 others(27): Show |
31 | HG00280.hp2 HG00438.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.703-4055dupA | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27751102 | ||||||
| chr12:27751102 | C | CAA | 96 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(93): Show |
111 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.703-4056_703-4055d others(4): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27751102 | ||||||
| chr12:27751102 | C | CAAA | 56 | a0001c0001t0001g0008 a0001c0001t0001g0135 a0001c0001t0001g0157 others(53): Show |
67 | HG00099.hp1 HG00544.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.703-4057_703-4055d others(5): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27751102 | ||||||
| chr12:27751102 | CA | C | 9 | a0001c0001t0001g0109 a0001c0001t0001g0112 a0001c0001t0001g0170 others(6): Show |
9 | HG00558.hp1 HG00738.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.703-4055delA | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27751102 | ||||||
| chr12:27751122 | A | G | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.703-4059A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27751122 | |||||||
| chr12:27751124 | A | AAAAAG | 11 | a0002c0002t0002g0006 a0002c0002t0002g0015 a0002c0002t0002g0061 others(8): Show |
14 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.703-4055_703-4054i others(7): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27751124 | ||||||
| chr12:27751125 | A | AAAAGAAA others(19): Show |
1 | a0001c0001t0001g0303 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.703-4055_703-4054i others(28): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27751125 | ||||||
| chr12:27751240 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.703-3941G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27751240 | |||||||
| chr12:27751273 | A | G | 28 | a0001c0001t0003g0010 a0001c0001t0003g0026 a0001c0001t0003g0027 others(25): Show |
32 | HG00741.hp2 HG01168.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.703-3908A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27751273 | |||||||
| chr12:27751526 | C | T | 7 | a0001c0001t0003g0010 a0001c0001t0003g0027 a0001c0001t0003g0028 others(4): Show |
8 | HG02109.hp2 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.703-3655C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27751526 | |||||||
| chr12:27751631 | T | C | 227 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(224): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.703-3550T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27751631 | |||||||
| chr12:27751636 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.703-3545G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27751636 | |||||||
| chr12:27751656 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.703-3525C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27751656 | |||||||
| chr12:27751761 | C | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.703-3420C>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27751761 | |||||||
| chr12:27751862 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.703-3319C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27751862 | |||||||
| chr12:27751886 | G | A | 4 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0210 others(1): Show |
4 | HG00642.hp1 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.703-3295G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27751886 | |||||||
| chr12:27751909 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.703-3272C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27751909 | |||||||
| chr12:27752088 | AT | A | 185 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(182): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.703-3092delT | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27752088 | |||||||
| chr12:27752089 | T | A | 27 | a0001c0001t0001g0285 a0002c0002t0001g0056 a0002c0002t0002g0001 others(24): Show |
36 | HG00609.hp1 HG00642.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.703-3092T>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27752089 | |||||||
| chr12:27752093 | A | T | 212 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(209): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.703-3088A>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27752093 | |||||||
| chr12:27752112 | A | G | 297 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(294): Show |
342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.703-3069A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27752112 | |||||||
| chr12:27752265 | G | C | 1 | a0001c0001t0001g0115 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.703-2916G>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27752265 | |||||||
| chr12:27752277 | G | A | 213 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(210): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.703-2904G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27752277 | |||||||
| chr12:27752312 | G | A | 308 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.703-2869G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27752312 | |||||||
| chr12:27752410 | T | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.703-2771T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27752410 | |||||||
| chr12:27752524 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.703-2657C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27752524 | |||||||
| chr12:27752566 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.703-2615G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27752566 | |||||||
| chr12:27752575 | A | G | 4 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0210 others(1): Show |
4 | HG00642.hp1 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.703-2606A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27752575 | |||||||
| chr12:27752670 | T | C | 2 | a0001c0001t0003g0078 a0001c0001t0003g0079 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.703-2511T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27752670 | |||||||
| chr12:27752684 | G | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.703-2497G>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27752684 | |||||||
| chr12:27752728 | C | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(131): Show |
150 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.703-2453C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27752728 | |||||||
| chr12:27752757 | A | G | 167 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(164): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.703-2424A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27752757 | |||||||
| chr12:27752889 | A | G | 1 | a0002c0002t0002g0012 | 2 | HG02015.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.703-2292A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27752889 | |||||||
| chr12:27753036 | T | C | 45 | a0002c0002t0002g0001 a0002c0002t0002g0006 a0002c0002t0002g0011 others(42): Show |
58 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.703-2145T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27753036 | |||||||
| chr12:27753056 | G | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0210 |
2 | HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.703-2125G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27753056 | |||||||
| chr12:27753070 | T | A | 45 | a0002c0002t0002g0001 a0002c0002t0002g0006 a0002c0002t0002g0011 others(42): Show |
58 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.703-2111T>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27753070 | |||||||
| chr12:27753074 | A | T | 45 | a0002c0002t0002g0001 a0002c0002t0002g0006 a0002c0002t0002g0011 others(42): Show |
58 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.703-2107A>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27753074 | |||||||
| chr12:27753075 | G | A | 45 | a0002c0002t0002g0001 a0002c0002t0002g0006 a0002c0002t0002g0011 others(42): Show |
58 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.703-2106G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27753075 | |||||||
| chr12:27753076 | AGGACACA others(5): Show |
A | 6 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0145 others(3): Show |
6 | HG01123.hp2 HG01346.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.703-2102_703-2091d others(14): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27753076 | ||||||
| chr12:27753348 | T | C | 1 | a0001c0001t0001g0216 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.703-1833T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27753348 | |||||||
| chr12:27753368 | T | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.703-1813T>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27753368 | |||||||
| chr12:27753372 | CTAT | C | 45 | a0002c0002t0002g0001 a0002c0002t0002g0006 a0002c0002t0002g0011 others(42): Show |
58 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.703-1804_703-1802d others(5): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27753372 | ||||||
| chr12:27753645 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.703-1536A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27753645 | |||||||
| chr12:27753708 | G | T | 12 | a0002c0002t0002g0006 a0002c0002t0002g0015 a0002c0002t0002g0061 others(9): Show |
15 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.703-1473G>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27753708 | |||||||
| chr12:27753717 | GA | G | 45 | a0002c0002t0002g0001 a0002c0002t0002g0006 a0002c0002t0002g0011 others(42): Show |
58 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.703-1456delA | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27753717 | ||||||
| chr12:27753904 | G | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(160): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.703-1277G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27753904 | |||||||
| chr12:27753945 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.703-1236A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27753945 | |||||||
| chr12:27753990 | A | T | 135 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(132): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.703-1191A>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27753990 | |||||||
| chr12:27754058 | G | A | 45 | a0002c0002t0002g0001 a0002c0002t0002g0006 a0002c0002t0002g0011 others(42): Show |
58 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.703-1123G>A | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27754058 | |||||||
| chr12:27754078 | A | G | 1 | a0001c0001t0001g0130 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.703-1103A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27754078 | |||||||
| chr12:27754091 | T | C | 1 | a0001c0001t0003g0026 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.703-1090T>C | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27754091 | |||||||
| chr12:27754733 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.703-448C>T | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27754733 | |||||||
| chr12:27754765 | C | CA | 6 | a0001c0001t0001g0073 a0001c0001t0001g0077 a0001c0001t0001g0099 others(3): Show |
6 | HG01358.hp1 HG02109.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.703-395dupA | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27754765 | ||||||
| chr12:27754765 | C | CAA | 16 | a0001c0001t0001g0174 a0001c0001t0001g0210 a0001c0001t0003g0010 others(13): Show |
17 | HG00642.hp1 HG02109.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.703-396_703-395dup others(2): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27754765 | ||||||
| chr12:27754765 | C | CAAA | 10 | a0001c0001t0003g0166 a0003c0003t0003g0005 a0003c0003t0003g0177 others(7): Show |
13 | HG00741.hp2 HG01168.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.703-397_703-395dup others(3): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27754765 | ||||||
| chr12:27754765 | CA | C | 25 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0109 others(22): Show |
27 | HG00323.hp1 HG00621.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.703-395delA | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27754765 | ||||||
| chr12:27754765 | CAA | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.703-396_703-395del others(2): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27754765 | ||||||
| chr12:27754765 | CAAA | C | 46 | a0001c0001t0001g0196 a0002c0002t0002g0001 a0002c0002t0002g0006 others(43): Show |
59 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.703-397_703-395del others(3): Show |
MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27754765 | ||||||
| chr12:27755086 | G | GA | 60 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0159 others(57): Show |
76 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.703-84dupA | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 27755086 | ||||||
| chr12:27755131 | A | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0129 |
2 | HG02602.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.703-50A>G | MRPS35 | ENSG00000061794.13 | transcript | ENST00000081029.8 | protein_coding | 7/7 | chr12 | 27755131 |