Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54456 |
| ensemblid | ENSG00000073146.17 |
| hgncid | 7201 |
| symbol | MOV10L1 |
| name | Mov10 like RISC complex RNA helicase 1 |
| refseq_nuc | NM_018995.3 |
| refseq_prot | NP_061868.1 |
| ensembl_nuc | ENST00000262794.10 |
| ensembl_prot | ENSP00000262794.5 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 50090006 |
| end | 50161687 |
| strand | + |
| ver | v1.2 |
| region | chr22:50090006-50161687 |
| region5000 | chr22:50085006-50166687 |
| regionname0 | MOV10L1_chr22_50090006_50161687 |
| regionname5000 | MOV10L1_chr22_50085006_50166687 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1211 | 189 | 67 | 31 | 63 | 8 | 18 | 54 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | MLSLA others(1206): Show |
chr22 | 50085006 | 50166687 |
| a0002 | 0/0 | 1211 | 55 | 12 | 10 | 27 | 0 | 6 | 24 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | MLSLA others(1206): Show |
chr22 | 50085006 | 50166687 |
| a0003 | 0/0 | 1211 | 44 | 3 | 11 | 19 | 3 | 8 | 17 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | MLSLA others(1206): Show |
chr22 | 50085006 | 50166687 |
| a0004 | 0/0 | 1211 | 32 | 2 | 8 | 12 | 3 | 7 | 8 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | MLSLA others(1206): Show |
chr22 | 50085006 | 50166687 |
| a0005 | 0/0 | 1211 | 32 | 0 | 0 | 29 | 0 | 3 | 22 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | MLSLA others(1206): Show |
chr22 | 50085006 | 50166687 |
| a0006 | 0/0 | 1211 | 22 | 1 | 2 | 17 | 2 | 0 | 12 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | MLSLA others(1206): Show |
chr22 | 50085006 | 50166687 |
| a0007 | 0/0 | 1211 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | MLSLA others(1206): Show |
chr22 | 50085006 | 50166687 |
| a0008 | 0/0 | 1211 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | MLSLA others(1206): Show |
chr22 | 50085006 | 50166687 |
| a0009 | 0/0 | 1211 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | MLSLA others(1206): Show |
chr22 | 50085006 | 50166687 |
| a0010 | 0/0 | 1211 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | MLSLA others(1206): Show |
chr22 | 50085006 | 50166687 |
| a0011 | 0/0 | 1211 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | MLSLA others(1206): Show |
chr22 | 50085006 | 50166687 |
| a0012 | 0/0 | 1211 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | MLSLA others(1206): Show |
chr22 | 50085006 | 50166687 |
| a0013 | 0/0 | 1211 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | MLSLA others(1206): Show |
chr22 | 50085006 | 50166687 |
| a0014 | 0/0 | 1211 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | MLSLA others(1206): Show |
chr22 | 50085006 | 50166687 |
| a0015 | 0/0 | 1211 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | MLSLA others(1206): Show |
chr22 | 50085006 | 50166687 |
| a0016 | 0/0 | 1211 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | MLSLA others(1206): Show |
chr22 | 50085006 | 50166687 |
| a0017 | 0/0 | 1211 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | MLSLA others(1206): Show |
chr22 | 50085006 | 50166687 |
| a0018 | 0/0 | 1211 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | MLSLA others(1206): Show |
chr22 | 50085006 | 50166687 |
| a0019 | 0/0 | 1211 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | MLSLA others(1206): Show |
chr22 | 50085006 | 50166687 |
| a0020 | 0/0 | 1211 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | MLSLA others(1206): Show |
chr22 | 50085006 | 50166687 |
| a0021 | 0/0 | 1211 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | MLSLA others(1206): Show |
chr22 | 50085006 | 50166687 |
| a0022 | 0/0 | 1211 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | MLSLA others(1206): Show |
chr22 | 50085006 | 50166687 |
| a0023 | 0/0 | 1211 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | MLSLA others(1206): Show |
chr22 | 50085006 | 50166687 |
| a0024 | 0/0 | 1211 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | MLSLA others(1206): Show |
chr22 | 50085006 | 50166687 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3633 | 131 | 53 | 15 | 50 | 3 | 9 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0001c0005 | 0/0 | 3633 | 27 | 4 | 5 | 11 | 1 | 6 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0001c0007 | 0/0 | 3633 | 18 | 2 | 9 | 1 | 4 | 2 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0001c0011 | 0/0 | 3633 | 8 | 7 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0001c0016 | 1/0 | 3633 | 2 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0001c0028 | 0/0 | 3633 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0001c0030 | 0/0 | 3633 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0001c0037 | 0/0 | 3633 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0002c0002 | 0/0 | 3633 | 41 | 3 | 10 | 23 | 0 | 5 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0002c0010 | 0/0 | 3633 | 9 | 9 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0002c0013 | 0/0 | 3633 | 5 | 0 | 0 | 4 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0003c0003 | 0/0 | 3633 | 36 | 2 | 9 | 19 | 2 | 4 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0003c0012 | 0/0 | 3633 | 8 | 1 | 2 | 0 | 1 | 4 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0004c0008 | 0/0 | 3633 | 17 | 1 | 5 | 4 | 2 | 5 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0004c0009 | 0/0 | 3633 | 9 | 0 | 1 | 8 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0004c0014 | 0/0 | 3633 | 4 | 1 | 1 | 0 | 0 | 2 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0004c0021 | 0/0 | 3633 | 2 | 0 | 1 | 0 | 1 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0005c0004 | 0/0 | 3633 | 29 | 0 | 0 | 26 | 0 | 3 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0005c0020 | 0/0 | 3633 | 2 | 0 | 0 | 2 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0005c0036 | 0/0 | 3633 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0006c0006 | 0/0 | 3633 | 20 | 1 | 1 | 16 | 2 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0006c0025 | 0/0 | 3633 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0006c0031 | 0/0 | 3633 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0007c0015 | 0/0 | 3633 | 3 | 0 | 2 | 0 | 1 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0008c0022 | 0/0 | 3633 | 2 | 0 | 2 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0009c0019 | 0/0 | 3633 | 2 | 2 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0010c0023 | 0/0 | 3633 | 2 | 2 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0011c0018 | 0/0 | 3633 | 2 | 0 | 0 | 2 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0012c0017 | 0/0 | 3633 | 2 | 0 | 0 | 2 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0013c0024 | 0/0 | 3633 | 2 | 0 | 0 | 2 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0014c0032 | 0/0 | 3633 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0015c0041 | 0/0 | 3633 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0016c0029 | 0/0 | 3633 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0017c0035 | 0/0 | 3633 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0018c0033 | 0/0 | 3633 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0019c0026 | 0/0 | 3633 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0020c0040 | 0/0 | 3633 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0021c0038 | 0/0 | 3633 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0022c0034 | 0/0 | 3633 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0023c0039 | 0/0 | 3633 | 1 | 0 | 0 | 0 | 1 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 | ||
| a0024c0027 | 0/0 | 3633 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATGCT others(3628): Show |
chr22 | 50085006 | 50166687 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3957 | 124 | 46 | 15 | 50 | 3 | 9 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0001c0001t0003 | 0/0 | 3957 | 7 | 7 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0001c0005t0001 | 0/0 | 3957 | 27 | 4 | 5 | 11 | 1 | 6 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0001c0007t0001 | 0/0 | 3957 | 18 | 2 | 9 | 1 | 4 | 2 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0001c0011t0001 | 0/0 | 3957 | 8 | 7 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0001c0016t0001 | 1/0 | 3957 | 2 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0001c0028t0001 | 0/0 | 3957 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0001c0030t0001 | 0/0 | 3957 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0001c0037t0001 | 0/0 | 3957 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0002c0002t0002 | 0/0 | 3966 | 40 | 3 | 10 | 22 | 0 | 5 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3961): Show |
chr22 | 50085006 | 50166687 |
| a0002c0002t0004 | 0/0 | 3967 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3962): Show |
chr22 | 50085006 | 50166687 |
| a0002c0010t0002 | 0/0 | 3966 | 9 | 9 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3961): Show |
chr22 | 50085006 | 50166687 |
| a0002c0013t0002 | 0/0 | 3966 | 4 | 0 | 0 | 3 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3961): Show |
chr22 | 50085006 | 50166687 |
| a0002c0013t0004 | 0/0 | 3967 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3962): Show |
chr22 | 50085006 | 50166687 |
| a0003c0003t0002 | 0/0 | 3966 | 34 | 2 | 9 | 17 | 2 | 4 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3961): Show |
chr22 | 50085006 | 50166687 |
| a0003c0003t0004 | 0/0 | 3967 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3962): Show |
chr22 | 50085006 | 50166687 |
| a0003c0003t0005 | 0/0 | 3967 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3962): Show |
chr22 | 50085006 | 50166687 |
| a0003c0012t0002 | 0/0 | 3966 | 8 | 1 | 2 | 0 | 1 | 4 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3961): Show |
chr22 | 50085006 | 50166687 |
| a0004c0008t0001 | 0/0 | 3957 | 17 | 1 | 5 | 4 | 2 | 5 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0004c0009t0001 | 0/0 | 3957 | 9 | 0 | 1 | 8 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0004c0014t0001 | 0/0 | 3957 | 4 | 1 | 1 | 0 | 0 | 2 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0004c0021t0001 | 0/0 | 3957 | 2 | 0 | 1 | 0 | 1 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0005c0004t0001 | 0/0 | 3957 | 29 | 0 | 0 | 26 | 0 | 3 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0005c0020t0001 | 0/0 | 3957 | 2 | 0 | 0 | 2 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0005c0036t0001 | 0/0 | 3957 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0006c0006t0001 | 0/0 | 3957 | 20 | 1 | 1 | 16 | 2 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0006c0025t0001 | 0/0 | 3957 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0006c0031t0001 | 0/0 | 3957 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0007c0015t0002 | 0/0 | 3966 | 3 | 0 | 2 | 0 | 1 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3961): Show |
chr22 | 50085006 | 50166687 |
| a0008c0022t0001 | 0/0 | 3957 | 2 | 0 | 2 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0009c0019t0001 | 0/0 | 3957 | 2 | 2 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0010c0023t0001 | 0/0 | 3957 | 2 | 2 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0011c0018t0001 | 0/0 | 3957 | 2 | 0 | 0 | 2 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0012c0017t0001 | 0/0 | 3957 | 2 | 0 | 0 | 2 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0013c0024t0002 | 0/0 | 3966 | 2 | 0 | 0 | 2 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3961): Show |
chr22 | 50085006 | 50166687 |
| a0014c0032t0001 | 0/0 | 3957 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0015c0041t0002 | 0/0 | 3966 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3961): Show |
chr22 | 50085006 | 50166687 |
| a0016c0029t0001 | 0/0 | 3957 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0017c0035t0001 | 0/0 | 3957 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0018c0033t0001 | 0/0 | 3957 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0019c0026t0001 | 0/0 | 3957 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0020c0040t0001 | 0/0 | 3957 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0021c0038t0001 | 0/0 | 3957 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0022c0034t0001 | 0/0 | 3957 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0023c0039t0001 | 0/0 | 3957 | 1 | 0 | 0 | 0 | 1 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| a0024c0027t0001 | 0/0 | 3957 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | ATTGG others(3952): Show |
chr22 | 50085006 | 50166687 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0236 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0005t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0005t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0005t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0005t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0005t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0005t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0005t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0005t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0005t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0005t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0005t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0005t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0005t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0005t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0005t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0005t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0005t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0005t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0005t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0005t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0005t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0005t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0005t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0005t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0005t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0005t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0007t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0007t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0007t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0007t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0007t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0007t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0007t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0007t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0007t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0007t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0007t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0007t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0007t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0007t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0007t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0007t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0007t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0007t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0011t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0011t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0011t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0011t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0011t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0011t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0011t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0016t0001g0190 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0016t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0028t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0030t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0001c0037t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0002g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0002t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0010t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0010t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0010t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0010t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0010t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0010t0002g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0010t0002g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0010t0002g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0010t0002g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0013t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0013t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0013t0002g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0013t0002g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0002c0013t0004g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0350 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0380 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0384 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0002g0386 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0004g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0003t0005g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0012t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0012t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0012t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0012t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0012t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0012t0002g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0012t0002g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0003c0012t0002g0378 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0008t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0008t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0008t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0008t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0008t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0008t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0008t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0008t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0008t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0008t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0008t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0008t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0008t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0008t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0008t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0008t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0009t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0009t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0009t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0009t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0009t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0009t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0009t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0009t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0009t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0014t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0014t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0014t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0014t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0021t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0004c0021t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0004t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0004t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0004t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0004t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0004t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0004t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0004t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0004t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0004t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0004t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0004t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0004t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0004t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0004t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0004t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0004t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0004t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0004t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0004t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0004t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0004t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0004t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0004t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0004t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0020t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0020t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0005c0036t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0006c0006t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0006c0006t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0006c0006t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0006c0006t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0006c0006t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0006c0006t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0006c0006t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0006c0006t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0006c0006t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0006c0006t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0006c0006t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0006c0006t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0006c0006t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0006c0006t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0006c0006t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0006c0006t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0006c0006t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0006c0006t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0006c0006t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0006c0006t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0006c0025t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0006c0031t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0007c0015t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0007c0015t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0007c0015t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0008c0022t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0008c0022t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0009c0019t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0009c0019t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0010c0023t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0010c0023t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0011c0018t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0011c0018t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0012c0017t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0012c0017t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0013c0024t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0014c0032t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0015c0041t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0016c0029t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0017c0035t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0018c0033t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0019c0026t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0020c0040t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0021c0038t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0022c0034t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0023c0039t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| a0024c0027t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0004 | c0008 | t0001 | g0103 | EUR | GBR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0268 | EUR | GBR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG00140 | hp1 | a0007 | c0015 | t0002 | g0026 | EUR | GBR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG00140 | hp2 | a0004 | c0008 | t0001 | g0086 | EUR | GBR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG00280 | hp1 | a0001 | c0007 | t0001 | g0053 | EUR | FIN | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG00280 | hp2 | a0001 | c0007 | t0001 | g0055 | EUR | FIN | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG00323 | hp1 | a0003 | c0012 | t0002 | g0319 | EUR | FIN | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG00323 | hp2 | a0001 | c0007 | t0001 | g0209 | EUR | FIN | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | CHS | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG00408 | hp2 | a0005 | c0004 | t0001 | g0090 | EAS | CHS | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | CHS | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG00438 | hp2 | a0004 | c0009 | t0001 | g0129 | EAS | CHS | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG00597 | hp1 | a0006 | c0006 | t0001 | g0259 | EAS | CHS | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0039 | EAS | CHS | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG00621 | hp1 | a0005 | c0004 | t0001 | g0091 | EAS | CHS | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0375 | EAS | CHS | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0368 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG00639 | hp2 | a0004 | c0008 | t0001 | g0120 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG00733 | hp2 | a0003 | c0003 | t0002 | g0342 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG00735 | hp1 | a0007 | c0015 | t0002 | g0027 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG00738 | hp1 | a0007 | c0015 | t0002 | g0023 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG00738 | hp2 | a0001 | c0005 | t0001 | g0181 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG00741 | hp1 | a0001 | c0007 | t0001 | g0054 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01070 | hp1 | a0014 | c0032 | t0001 | g0095 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01070 | hp2 | a0001 | c0007 | t0001 | g0230 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01074 | hp2 | a0003 | c0012 | t0002 | g0334 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01081 | hp1 | a0004 | c0008 | t0001 | g0121 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01081 | hp2 | a0003 | c0003 | t0002 | g0386 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01099 | hp1 | a0001 | c0005 | t0001 | g0198 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01099 | hp2 | a0003 | c0003 | t0002 | g0345 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01106 | hp1 | a0006 | c0031 | t0001 | g0058 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01106 | hp2 | a0004 | c0014 | t0001 | g0098 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01109 | hp1 | a0004 | c0008 | t0001 | g0109 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01168 | hp1 | a0004 | c0008 | t0001 | g0080 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0034 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01175 | hp2 | a0004 | c0008 | t0001 | g0100 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01192 | hp1 | a0001 | c0007 | t0001 | g0227 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01243 | hp1 | a0001 | c0005 | t0001 | g0172 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01243 | hp2 | a0001 | c0011 | t0001 | g0047 | AMR | PUR | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01255 | hp1 | a0004 | c0021 | t0001 | g0099 | AMR | CLM | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01256 | hp1 | a0001 | c0005 | t0001 | g0204 | AMR | CLM | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01256 | hp2 | a0001 | c0007 | t0001 | g0217 | AMR | CLM | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01257 | hp1 | a0001 | c0007 | t0001 | g0210 | AMR | CLM | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0033 | AMR | CLM | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | CLM | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | CLM | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01346 | hp2 | a0008 | c0022 | t0001 | g0134 | AMR | CLM | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01358 | hp1 | a0003 | c0012 | t0002 | g0317 | AMR | CLM | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0385 | AMR | CLM | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01361 | hp1 | a0001 | c0028 | t0001 | g0283 | AMR | CLM | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01361 | hp2 | a0001 | c0005 | t0001 | g0189 | AMR | CLM | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01496 | hp1 | a0008 | c0022 | t0001 | g0135 | AMR | CLM | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01515 | hp1 | a0003 | c0003 | t0002 | g0350 | EUR | IBS | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0051 | EUR | IBS | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01516 | hp1 | a0001 | c0005 | t0001 | g0199 | EUR | IBS | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01516 | hp2 | a0006 | c0006 | t0001 | g0069 | EUR | IBS | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | IBS | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01517 | hp2 | a0006 | c0006 | t0001 | g0070 | EUR | IBS | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01884 | hp1 | a0002 | c0010 | t0002 | g0356 | AFR | ACB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01884 | hp2 | a0009 | c0019 | t0001 | g0222 | AFR | ACB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01934 | hp1 | a0003 | c0003 | t0002 | g0360 | AMR | PEL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01934 | hp2 | a0006 | c0006 | t0001 | g0071 | AMR | PEL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0373 | AMR | PEL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01952 | hp2 | a0003 | c0003 | t0002 | g0358 | AMR | PEL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01975 | hp1 | a0001 | c0007 | t0001 | g0220 | AMR | PEL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0370 | AMR | PEL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01981 | hp1 | a0015 | c0041 | t0002 | g0036 | AMR | PEL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01981 | hp2 | a0003 | c0003 | t0002 | g0340 | AMR | PEL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01993 | hp1 | a0001 | c0007 | t0001 | g0219 | AMR | PEL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0338 | AMR | PEL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02004 | hp1 | a0003 | c0003 | t0002 | g0351 | AMR | PEL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02015 | hp1 | a0004 | c0008 | t0001 | g0127 | EAS | KHV | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02027 | hp1 | a0006 | c0006 | t0001 | g0168 | EAS | KHV | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02027 | hp2 | a0005 | c0004 | t0001 | g0101 | EAS | KHV | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02040 | hp1 | a0005 | c0004 | t0001 | g0093 | EAS | KHV | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02040 | hp2 | a0005 | c0020 | t0001 | g0112 | EAS | KHV | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02055 | hp1 | a0001 | c0011 | t0001 | g0050 | AFR | ACB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02056 | hp2 | a0004 | c0008 | t0001 | g0108 | EAS | KHV | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02074 | hp1 | a0004 | c0008 | t0001 | g0125 | EAS | KHV | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02074 | hp2 | a0001 | c0005 | t0001 | g0202 | EAS | KHV | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02080 | hp2 | a0003 | c0003 | t0002 | g0330 | EAS | KHV | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02083 | hp2 | a0003 | c0003 | t0002 | g0347 | EAS | KHV | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02132 | hp1 | a0006 | c0006 | t0001 | g0234 | EAS | KHV | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02132 | hp2 | a0005 | c0004 | t0001 | g0115 | EAS | KHV | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02135 | hp1 | a0005 | c0004 | t0001 | g0111 | EAS | KHV | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02135 | hp2 | a0006 | c0006 | t0001 | g0309 | EAS | KHV | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02145 | hp1 | a0016 | c0029 | t0001 | g0205 | AFR | ACB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02145 | hp2 | a0002 | c0010 | t0002 | g0387 | AFR | ACB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02148 | hp1 | a0003 | c0003 | t0002 | g0355 | AMR | PEL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02148 | hp2 | a0004 | c0009 | t0001 | g0314 | AMR | PEL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CDX | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CDX | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02257 | hp1 | a0017 | c0035 | t0001 | g0008 | AFR | ACB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02257 | hp2 | a0006 | c0006 | t0001 | g0221 | AFR | ACB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02258 | hp2 | a0001 | c0011 | t0001 | g0048 | AFR | ACB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0374 | AMR | PEL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02280 | hp1 | a0001 | c0011 | t0001 | g0045 | AFR | ACB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02280 | hp2 | a0004 | c0014 | t0001 | g0110 | AFR | ACB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0383 | AMR | PEL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02300 | hp1 | a0001 | c0007 | t0001 | g0218 | AMR | PEL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0376 | AMR | PEL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02451 | hp2 | a0001 | c0007 | t0001 | g0052 | AFR | ACB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02683 | hp1 | a0001 | c0005 | t0001 | g0188 | SAS | PJL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02683 | hp2 | a0003 | c0003 | t0002 | g0354 | SAS | PJL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02698 | hp1 | a0002 | c0013 | t0002 | g0043 | SAS | PJL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02735 | hp2 | a0004 | c0008 | t0001 | g0084 | SAS | PJL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02738 | hp1 | a0005 | c0004 | t0001 | g0133 | SAS | PJL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02738 | hp2 | a0003 | c0003 | t0002 | g0384 | SAS | PJL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | GWD | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02818 | hp2 | a0002 | c0010 | t0002 | g0335 | AFR | GWD | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02886 | hp2 | a0001 | c0011 | t0001 | g0004 | AFR | GWD | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02895 | hp1 | a0002 | c0010 | t0002 | g0363 | AFR | GWD | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02896 | hp2 | a0002 | c0002 | t0002 | g0035 | AFR | GWD | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02897 | hp2 | a0002 | c0010 | t0002 | g0364 | AFR | GWD | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02922 | hp1 | a0010 | c0023 | t0001 | g0232 | AFR | ESN | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02965 | hp1 | a0001 | c0005 | t0001 | g0179 | AFR | ESN | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0195 | AFR | ESN | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03017 | hp1 | a0001 | c0007 | t0001 | g0059 | SAS | PJL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03041 | hp1 | a0001 | c0011 | t0001 | g0049 | AFR | GWD | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0177 | AFR | GWD | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03098 | hp2 | a0001 | c0005 | t0001 | g0180 | AFR | MSL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | MSL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03209 | hp2 | a0001 | c0030 | t0001 | g0143 | AFR | MSL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03225 | hp2 | a0009 | c0019 | t0001 | g0223 | AFR | MSL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03239 | hp2 | a0004 | c0014 | t0001 | g0206 | SAS | PJL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0174 | AFR | MSL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03486 | hp1 | a0003 | c0003 | t0002 | g0343 | AFR | MSL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03490 | hp1 | a0004 | c0008 | t0001 | g0106 | SAS | PJL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03490 | hp2 | a0003 | c0012 | t0002 | g0321 | SAS | PJL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03491 | hp1 | a0004 | c0008 | t0001 | g0007 | SAS | PJL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03491 | hp2 | a0001 | c0007 | t0001 | g0056 | SAS | PJL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03492 | hp1 | a0004 | c0008 | t0001 | g0007 | SAS | PJL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03492 | hp2 | a0003 | c0012 | t0002 | g0320 | SAS | PJL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03516 | hp1 | a0002 | c0010 | t0002 | g0333 | AFR | ESN | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03540 | hp1 | a0002 | c0010 | t0002 | g0331 | AFR | GWD | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03540 | hp2 | a0010 | c0023 | t0001 | g0231 | AFR | GWD | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03579 | hp1 | a0001 | c0011 | t0001 | g0046 | AFR | MSL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | STU | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03688 | hp2 | a0004 | c0014 | t0001 | g0094 | SAS | STU | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03710 | hp1 | a0003 | c0003 | t0002 | g0361 | SAS | PJL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0024 | SAS | PJL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03831 | hp1 | a0003 | c0003 | t0002 | g0337 | SAS | BEB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03831 | hp2 | a0001 | c0016 | t0001 | g0191 | SAS | BEB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03834 | hp1 | a0005 | c0004 | t0001 | g0128 | SAS | BEB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | BEB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | BEB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03942 | hp2 | a0001 | c0005 | t0001 | g0164 | SAS | BEB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG04115 | hp1 | a0001 | c0005 | t0001 | g0297 | SAS | STU | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG04115 | hp2 | a0001 | c0005 | t0001 | g0167 | SAS | STU | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG04184 | hp1 | a0001 | c0005 | t0001 | g0171 | SAS | BEB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0031 | SAS | BEB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG04199 | hp1 | a0003 | c0012 | t0002 | g0378 | SAS | STU | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0022 | SAS | STU | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | STU | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG04204 | hp2 | a0004 | c0008 | t0001 | g0092 | SAS | STU | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG04228 | hp1 | a0001 | c0005 | t0001 | g0292 | SAS | STU | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG04228 | hp2 | a0003 | c0012 | t0002 | g0344 | SAS | STU | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | YRI | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18522 | hp2 | a0002 | c0010 | t0002 | g0349 | AFR | YRI | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | CHB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18747 | hp2 | a0006 | c0006 | t0001 | g0274 | EAS | CHB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18906 | hp2 | a0001 | c0011 | t0001 | g0004 | AFR | YRI | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18939 | hp2 | a0003 | c0003 | t0002 | g0382 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18941 | hp1 | a0006 | c0006 | t0001 | g0289 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18941 | hp2 | a0005 | c0004 | t0001 | g0085 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18945 | hp1 | a0005 | c0004 | t0001 | g0005 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18946 | hp1 | a0001 | c0005 | t0001 | g0272 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18946 | hp2 | a0004 | c0009 | t0001 | g0310 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18948 | hp2 | a0005 | c0004 | t0001 | g0044 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18949 | hp2 | a0005 | c0004 | t0001 | g0118 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18950 | hp2 | a0011 | c0018 | t0001 | g0075 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18952 | hp1 | a0005 | c0004 | t0001 | g0006 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18953 | hp2 | a0003 | c0003 | t0002 | g0352 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18954 | hp2 | a0003 | c0003 | t0002 | g0327 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18957 | hp1 | a0006 | c0006 | t0001 | g0244 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18957 | hp2 | a0005 | c0020 | t0001 | g0083 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18959 | hp1 | a0006 | c0006 | t0001 | g0261 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18959 | hp2 | a0005 | c0004 | t0001 | g0132 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18960 | hp1 | a0001 | c0005 | t0001 | g0165 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18960 | hp2 | a0003 | c0003 | t0002 | g0322 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18961 | hp1 | a0005 | c0004 | t0001 | g0006 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18961 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18963 | hp1 | a0018 | c0033 | t0001 | g0107 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18965 | hp1 | a0002 | c0002 | t0004 | g0016 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18965 | hp2 | a0001 | c0007 | t0001 | g0057 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18966 | hp2 | a0004 | c0009 | t0001 | g0316 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18968 | hp2 | a0004 | c0009 | t0001 | g0311 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18970 | hp2 | a0002 | c0002 | t0002 | g0372 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0369 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18973 | hp1 | a0003 | c0003 | t0004 | g0381 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18974 | hp1 | a0004 | c0009 | t0001 | g0126 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18975 | hp1 | a0003 | c0003 | t0002 | g0323 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18977 | hp1 | a0002 | c0013 | t0002 | g0336 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18980 | hp1 | a0006 | c0006 | t0001 | g0270 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18980 | hp2 | a0005 | c0004 | t0001 | g0005 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18981 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18983 | hp1 | a0003 | c0003 | t0002 | g0348 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18983 | hp2 | a0001 | c0005 | t0001 | g0169 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0339 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18985 | hp2 | a0004 | c0009 | t0001 | g0312 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18986 | hp1 | a0005 | c0004 | t0001 | g0123 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18986 | hp2 | a0006 | c0006 | t0001 | g0273 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18989 | hp1 | a0003 | c0003 | t0002 | g0326 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18990 | hp2 | a0003 | c0003 | t0002 | g0379 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18993 | hp1 | a0005 | c0004 | t0001 | g0116 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18993 | hp2 | a0001 | c0005 | t0001 | g0176 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18994 | hp1 | a0005 | c0004 | t0001 | g0130 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18995 | hp1 | a0005 | c0004 | t0001 | g0104 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18995 | hp2 | a0001 | c0005 | t0001 | g0173 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18999 | hp1 | a0001 | c0005 | t0001 | g0182 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19000 | hp1 | a0012 | c0017 | t0001 | g0275 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19000 | hp2 | a0019 | c0026 | t0001 | g0114 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19001 | hp2 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19002 | hp1 | a0005 | c0036 | t0001 | g0102 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19003 | hp1 | a0003 | c0003 | t0002 | g0353 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19005 | hp2 | a0013 | c0024 | t0002 | g0011 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19007 | hp1 | a0003 | c0003 | t0002 | g0325 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19009 | hp1 | a0001 | c0005 | t0001 | g0010 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19009 | hp2 | a0003 | c0003 | t0002 | g0328 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19010 | hp1 | a0006 | c0006 | t0001 | g0257 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19011 | hp1 | a0001 | c0037 | t0001 | g0249 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19011 | hp2 | a0005 | c0004 | t0001 | g0088 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19012 | hp2 | a0003 | c0003 | t0002 | g0357 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | LWK | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | LWK | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | LWK | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | LWK | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19054 | hp1 | a0006 | c0025 | t0001 | g0079 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19054 | hp2 | a0001 | c0005 | t0001 | g0288 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19056 | hp1 | a0005 | c0004 | t0001 | g0087 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19056 | hp2 | a0001 | c0005 | t0001 | g0203 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19058 | hp1 | a0006 | c0006 | t0001 | g0295 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19058 | hp2 | a0005 | c0004 | t0001 | g0082 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19060 | hp1 | a0006 | c0006 | t0001 | g0262 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19063 | hp2 | a0005 | c0004 | t0001 | g0119 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19066 | hp1 | a0005 | c0004 | t0001 | g0131 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19066 | hp2 | a0004 | c0009 | t0001 | g0315 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19068 | hp1 | a0020 | c0040 | t0001 | g0089 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19068 | hp2 | a0003 | c0003 | t0002 | g0359 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19070 | hp2 | a0001 | c0005 | t0001 | g0010 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19074 | hp1 | a0004 | c0009 | t0001 | g0313 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19074 | hp2 | a0021 | c0038 | t0001 | g0170 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19077 | hp1 | a0003 | c0003 | t0002 | g0324 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19080 | hp2 | a0004 | c0008 | t0001 | g0124 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0377 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19082 | hp1 | a0002 | c0013 | t0004 | g0371 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19083 | hp2 | a0022 | c0034 | t0001 | g0105 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19084 | hp1 | a0011 | c0018 | t0001 | g0076 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19084 | hp2 | a0013 | c0024 | t0002 | g0011 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19085 | hp1 | a0005 | c0004 | t0001 | g0081 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19087 | hp1 | a0005 | c0004 | t0001 | g0113 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19088 | hp1 | a0003 | c0003 | t0002 | g0362 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19088 | hp2 | a0006 | c0006 | t0001 | g0258 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19089 | hp1 | a0002 | c0013 | t0002 | g0366 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19089 | hp2 | a0005 | c0004 | t0001 | g0097 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19090 | hp1 | a0006 | c0006 | t0001 | g0298 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19091 | hp1 | a0012 | c0017 | t0001 | g0002 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19091 | hp2 | a0003 | c0003 | t0005 | g0329 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0178 | AFR | YRI | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA19240 | hp2 | a0003 | c0003 | t0002 | g0341 | AFR | YRI | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA20129 | hp1 | a0001 | c0005 | t0001 | g0166 | AFR | ASW | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ASW | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA20752 | hp1 | a0023 | c0039 | t0001 | g0187 | EUR | TSI | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA20752 | hp2 | a0004 | c0021 | t0001 | g0096 | EUR | TSI | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA20805 | hp1 | a0003 | c0003 | t0002 | g0380 | EUR | TSI | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA20805 | hp2 | a0001 | c0007 | t0001 | g0211 | EUR | TSI | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | GIH | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA20905 | hp2 | a0005 | c0004 | t0001 | g0122 | SAS | GIH | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01123 | hp1 | a0003 | c0003 | t0002 | g0346 | AMR | CLM | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG01123 | hp2 | a0001 | c0007 | t0001 | g0216 | AMR | CLM | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02109 | hp1 | a0001 | c0007 | t0001 | g0207 | AFR | ACB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0175 | AFR | ACB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0194 | AFR | ACB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02559 | hp1 | a0002 | c0010 | t0002 | g0332 | AFR | ACB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG02559 | hp2 | a0001 | c0005 | t0001 | g0197 | AFR | ACB | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03471 | hp1 | a0002 | c0002 | t0002 | g0012 | AFR | MSL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG06807 | hp1 | a0004 | c0008 | t0001 | g0117 | AFR | USA | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | USA | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18955 | hp1 | a0006 | c0006 | t0001 | g0260 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA18955 | hp2 | a0002 | c0013 | t0002 | g0365 | EAS | JPT | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | USA | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0367 | AFR | USA | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA21309 | hp1 | a0003 | c0012 | t0002 | g0318 | AFR | LWK | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| NA21309 | hp2 | a0024 | c0027 | t0001 | g0159 | AFR | LWK | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0236 | REF | REF | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| homoSapiens | grch38p0 | a0001 | c0016 | t0001 | g0190 | REF | REF | MOV10L1_chr22_50085006_50166687 | MOV10L1 | chr22 | 50085006 | 50166687 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:50090140 | A | T | 5 | a0002 a0003 a0007 others(2): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
missense_variant | MODERATE | c.52A>T | p.Thr18Ser | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/27 | 135/3957 | 52/3636 | 18/1211 | chr22 | 50090140 | |||
| chr22:50090180 | C | G | 1 | a0020 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.92C>G | p.Ala31Gly | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/27 | 175/3957 | 92/3636 | 31/1211 | chr22 | 50090180 | |||
| chr22:50092072 | A | T | 6 | a0002 a0003 a0007 others(3): Show |
107 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(104): Show |
missense_variant | MODERATE | c.169A>T | p.Met57Leu | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/27 | 252/3957 | 169/3636 | 57/1211 | chr22 | 50092072 | |||
| chr22:50099459 | A | G | 1 | a0023 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.299A>G | p.Asp100Gly | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/27 | 382/3957 | 299/3636 | 100/1211 | chr22 | 50099459 | |||
| chr22:50099528 | G | C | 1 | a0019 | 1 | NA19000.hp2 | missense_variant | MODERATE | c.368G>C | p.Cys123Ser | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/27 | 451/3957 | 368/3636 | 123/1211 | chr22 | 50099528 | |||
| chr22:50108204 | G | A | 1 | a0024 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.511G>A | p.Glu171Lys | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 4/27 | 594/3957 | 511/3636 | 171/1211 | chr22 | 50108204 | |||
| chr22:50108208 | C | G | 1 | a0021 | 1 | NA19074.hp2 | missense_variant | MODERATE | c.515C>G | p.Ala172Gly | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 4/27 | 598/3957 | 515/3636 | 172/1211 | chr22 | 50108208 | |||
| chr22:50108237 | C | T | 5 | a0002 a0003 a0007 others(2): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
missense_variant | MODERATE | c.544C>T | p.Arg182Cys | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 4/27 | 627/3957 | 544/3636 | 182/1211 | chr22 | 50108237 | |||
| chr22:50108672 | C | T | 1 | a0008 | 2 | HG01346.hp2 HG01496.hp1 |
missense_variant | MODERATE | c.571C>T | p.Leu191Phe | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/27 | 654/3957 | 571/3636 | 191/1211 | chr22 | 50108672 | |||
| chr22:50117179 | C | T | 1 | a0017 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.1282C>T | p.Leu428Phe | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/27 | 1365/3957 | 1282/3636 | 428/1211 | chr22 | 50117179 | |||
| chr22:50117257 | A | C | 9 | a0004 a0005 a0008 others(6): Show |
73 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(70): Show |
missense_variant | MODERATE | c.1360A>C | p.Ile454Leu | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/27 | 1443/3957 | 1360/3636 | 454/1211 | chr22 | 50117257 | |||
| chr22:50117267 | G | A | 1 | a0012 | 2 | NA19000.hp1 NA19091.hp1 |
missense_variant | MODERATE | c.1370G>A | p.Arg457His | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/27 | 1453/3957 | 1370/3636 | 457/1211 | chr22 | 50117267 | |||
| chr22:50117275 | T | C | 1 | a0016 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.1378T>C | p.Phe460Leu | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/27 | 1461/3957 | 1378/3636 | 460/1211 | chr22 | 50117275 | |||
| chr22:50117348 | A | G | 1 | a0022 | 1 | NA19083.hp2 | missense_variant | MODERATE | c.1451A>G | p.Lys484Arg | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/27 | 1534/3957 | 1451/3636 | 484/1211 | chr22 | 50117348 | |||
| chr22:50128420 | A | G | 1 | a0009 | 2 | HG01884.hp2 HG03225.hp2 |
missense_variant | MODERATE | c.1823A>G | p.His608Arg | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/27 | 1906/3957 | 1823/3636 | 608/1211 | chr22 | 50128420 | |||
| chr22:50134044 | G | A | 5 | a0002 a0003 a0007 others(2): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
missense_variant | MODERATE | c.1948G>A | p.Val650Ile | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 14/27 | 2031/3957 | 1948/3636 | 650/1211 | chr22 | 50134044 | |||
| chr22:50134607 | A | G | 1 | a0013 | 2 | NA19005.hp2 NA19084.hp2 |
missense_variant | MODERATE | c.2047A>G | p.Ser683Gly | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/27 | 2130/3957 | 2047/3636 | 683/1211 | chr22 | 50134607 | |||
| chr22:50142093 | A | G | 1 | a0018 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.2083A>G | p.Met695Val | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 16/27 | 2166/3957 | 2083/3636 | 695/1211 | chr22 | 50142093 | |||
| chr22:50142113 | T | A | 1 | a0015 | 1 | HG01981.hp1 | missense_variant | MODERATE | c.2103T>A | p.His701Gln | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 16/27 | 2186/3957 | 2103/3636 | 701/1211 | chr22 | 50142113 | |||
| chr22:50144197 | A | G | 13 | a0002 a0003 a0005 others(10): Show |
164 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(161): Show |
missense_variant | MODERATE | c.2459A>G | p.Gln820Arg | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/27 | 2542/3957 | 2459/3636 | 820/1211 | chr22 | 50144197 | |||
| chr22:50158183 | G | A | 1 | a0011 | 2 | NA18950.hp2 NA19084.hp1 |
missense_variant | MODERATE | c.3193G>A | p.Val1065Ile | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 23/27 | 3276/3957 | 3193/3636 | 1065/1211 | chr22 | 50158183 | |||
| chr22:50161037 | C | A | 3 | a0003 a0013 a0014 |
47 | HG00323.hp1 HG00733.hp2 HG01070.hp1 others(44): Show |
missense_variant | MODERATE | c.3536C>A | p.Ala1179Glu | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 26/27 | 3619/3957 | 3536/3636 | 1179/1211 | chr22 | 50161037 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:50099472 | C | T | 3 | a0001c0011 a0004c0014 a0008c0022 |
14 | HG01106.hp2 HG01243.hp2 HG01346.hp2 others(11): Show |
synonymous_variant | LOW | c.312C>T | p.Asp104Asp | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/27 | 395/3957 | 312/3636 | 104/1211 | chr22 | 50099472 | |||
| chr22:50099487 | T | C | 1 | a0006c0025 | 1 | NA19054.hp1 | synonymous_variant | LOW | c.327T>C | p.His109His | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/27 | 410/3957 | 327/3636 | 109/1211 | chr22 | 50099487 | |||
| chr22:50108800 | A | G | 1 | a0001c0037 | 1 | NA19011.hp1 | synonymous_variant | LOW | c.699A>G | p.Ser233Ser | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/27 | 782/3957 | 699/3636 | 233/1211 | chr22 | 50108800 | |||
| chr22:50108818 | A | G | 39 | a0001c0001 a0001c0005 a0001c0007 others(36): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
synonymous_variant | LOW | c.717A>G | p.Ala239Ala | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/27 | 800/3957 | 717/3636 | 239/1211 | chr22 | 50108818 | |||
| chr22:50115214 | A | C | 1 | a0005c0036 | 1 | NA19002.hp1 | synonymous_variant | LOW | c.1227A>C | p.Gly409Gly | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/27 | 1310/3957 | 1227/3636 | 409/1211 | chr22 | 50115214 | |||
| chr22:50117190 | C | T | 36 | a0001c0001 a0001c0007 a0001c0011 others(33): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
synonymous_variant | LOW | c.1293C>T | p.Leu431Leu | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/27 | 1376/3957 | 1293/3636 | 431/1211 | chr22 | 50117190 | |||
| chr22:50117206 | C | T | 4 | a0002c0010 a0003c0003 a0003c0012 others(1): Show |
55 | HG00323.hp1 HG00733.hp2 HG01074.hp2 others(52): Show |
synonymous_variant | LOW | c.1309C>T | p.Leu437Leu | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/27 | 1392/3957 | 1309/3636 | 437/1211 | chr22 | 50117206 | |||
| chr22:50117265 | G | C | 1 | a0001c0028 | 1 | HG01361.hp1 | synonymous_variant | LOW | c.1368G>C | p.Ala456Ala | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/27 | 1451/3957 | 1368/3636 | 456/1211 | chr22 | 50117265 | |||
| chr22:50120517 | A | G | 1 | a0003c0012 | 8 | HG00323.hp1 HG01074.hp2 HG01358.hp1 others(5): Show |
synonymous_variant | LOW | c.1470A>G | p.Gln490Gln | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/27 | 1553/3957 | 1470/3636 | 490/1211 | chr22 | 50120517 | |||
| chr22:50120592 | G | A | 1 | a0005c0020 | 2 | HG02040.hp2 NA18957.hp2 |
synonymous_variant | LOW | c.1545G>A | p.Leu515Leu | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/27 | 1628/3957 | 1545/3636 | 515/1211 | chr22 | 50120592 | |||
| chr22:50144121 | C | A | 6 | a0002c0002 a0002c0010 a0003c0003 others(3): Show |
97 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(94): Show |
synonymous_variant | LOW | c.2383C>A | p.Arg795Arg | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/27 | 2466/3957 | 2383/3636 | 795/1211 | chr22 | 50144121 | |||
| chr22:50144201 | G | A | 2 | a0003c0012 a0014c0032 |
9 | HG00323.hp1 HG01070.hp1 HG01074.hp2 others(6): Show |
synonymous_variant | LOW | c.2463G>A | p.Pro821Pro | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/27 | 2546/3957 | 2463/3636 | 821/1211 | chr22 | 50144201 | |||
| chr22:50145766 | C | T | 1 | a0001c0030 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.2583C>T | p.Ile861Ile | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/27 | 2666/3957 | 2583/3636 | 861/1211 | chr22 | 50145766 | |||
| chr22:50145772 | A | C | 9 | a0002c0002 a0002c0010 a0002c0013 others(6): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
synonymous_variant | LOW | c.2589A>C | p.Thr863Thr | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/27 | 2672/3957 | 2589/3636 | 863/1211 | chr22 | 50145772 | |||
| chr22:50149702 | C | T | 2 | a0001c0007 a0006c0031 |
19 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(16): Show |
synonymous_variant | LOW | c.2715C>T | p.Asp905Asp | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 20/27 | 2798/3957 | 2715/3636 | 905/1211 | chr22 | 50149702 | |||
| chr22:50150767 | C | A | 12 | a0004c0008 a0004c0009 a0004c0014 others(9): Show |
70 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(67): Show |
synonymous_variant | LOW | c.2760C>A | p.Gly920Gly | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 21/27 | 2843/3957 | 2760/3636 | 920/1211 | chr22 | 50150767 | |||
| chr22:50159707 | T | C | 1 | a0004c0009 | 9 | HG00438.hp2 HG02148.hp2 NA18946.hp2 others(6): Show |
synonymous_variant | LOW | c.3246T>C | p.Asn1082Asn | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 24/27 | 3329/3957 | 3246/3636 | 1082/1211 | chr22 | 50159707 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:50090054 | G | GCGGCGGG others(3): Show |
1 | a0003c0003t0005 | 1 | NA19091.hp2 | 5_prime_UTR_variant | MODIFIER | c.-29_-28insGTGACGGC others(2): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/27 | 28 | INFO_REALIGN_3_PRIME | chr22 | 50090054 | |||||
| chr22:50090054 | G | GCGGCGGT others(2): Show |
8 | a0002c0002t0002 a0002c0010t0002 a0002c0013t0002 others(5): Show |
101 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(98): Show |
5_prime_UTR_variant | MODIFIER | c.-30_-22dupGGTGACGG others(1): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/27 | 21 | INFO_REALIGN_3_PRIME | chr22 | 50090054 | |||||
| chr22:50090056 | G | T | 1 | a0001c0001t0003 | 7 | HG02109.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-33G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/27 | chr22 | 50090056 | |||||||
| chr22:50090058 | C | CGGTGACG others(3): Show |
3 | a0002c0002t0004 a0002c0013t0004 a0003c0003t0004 |
3 | NA18965.hp1 NA18973.hp1 NA19082.hp1 |
5_prime_UTR_variant | MODIFIER | c.-22_-21insGGGTGACG others(2): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/27 | 21 | INFO_REALIGN_3_PRIME | chr22 | 50090058 | |||||
| chr22:50090068 | A | G | 12 | a0002c0002t0002 a0002c0002t0004 a0002c0010t0002 others(9): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
5_prime_UTR_variant | MODIFIER | c.-21A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/27 | 21 | chr22 | 50090068 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:50090194 | C | A | 30 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(27): Show |
31 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.97+9C>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/26 | chr22 | 50090194 | |||||||
| chr22:50090457 | G | C | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | NA18990.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.97+272G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/26 | chr22 | 50090457 | |||||||
| chr22:50090487 | C | T | 72 | a0002c0002t0002g0338 a0002c0002t0002g0339 a0002c0002t0002g0367 others(69): Show |
73 | HG00323.hp1 HG00621.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.97+302C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/26 | chr22 | 50090487 | |||||||
| chr22:50090545 | C | T | 1 | a0002c0002t0002g0040 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.97+360C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/26 | chr22 | 50090545 | |||||||
| chr22:50090548 | A | C | 1 | a0002c0002t0002g0040 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.97+363A>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/26 | chr22 | 50090548 | |||||||
| chr22:50090643 | G | A | 5 | a0003c0012t0002g0317 a0003c0012t0002g0318 a0003c0012t0002g0319 others(2): Show |
5 | HG00323.hp1 HG01358.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+458G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/26 | chr22 | 50090643 | |||||||
| chr22:50090676 | T | TTG | 79 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0235 others(76): Show |
82 | HG00099.hp2 HG00438.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.97+508_97+509dupTG | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr22 | 50090676 | ||||||
| chr22:50090690 | G | T | 7 | a0004c0009t0001g0310 a0004c0009t0001g0311 a0004c0009t0001g0312 others(4): Show |
7 | HG02148.hp2 NA18946.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.97+505G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/26 | chr22 | 50090690 | |||||||
| chr22:50090705 | T | C | 102 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(99): Show |
104 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.97+520T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/26 | chr22 | 50090705 | |||||||
| chr22:50090717 | C | T | 102 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(99): Show |
104 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.97+532C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/26 | chr22 | 50090717 | |||||||
| chr22:50090719 | C | G | 102 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(99): Show |
104 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.97+534C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/26 | chr22 | 50090719 | |||||||
| chr22:50090809 | G | A | 1 | a0006c0006t0001g0168 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.97+624G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/26 | chr22 | 50090809 | |||||||
| chr22:50090878 | G | A | 1 | a0005c0004t0001g0044 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.97+693G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/26 | chr22 | 50090878 | |||||||
| chr22:50090895 | C | T | 1 | a0003c0003t0002g0386 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.97+710C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/26 | chr22 | 50090895 | |||||||
| chr22:50091012 | T | G | 7 | a0001c0011t0001g0004 a0001c0011t0001g0045 a0001c0011t0001g0046 others(4): Show |
8 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.97+827T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/26 | chr22 | 50091012 | |||||||
| chr22:50091033 | A | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.97+848A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/26 | chr22 | 50091033 | |||||||
| chr22:50091182 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.98-819C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/26 | chr22 | 50091182 | |||||||
| chr22:50091421 | T | C | 10 | a0001c0001t0001g0051 a0001c0001t0001g0060 a0001c0007t0001g0052 others(7): Show |
10 | HG00280.hp1 HG00280.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.98-580T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/26 | chr22 | 50091421 | |||||||
| chr22:50091460 | A | C | 6 | a0001c0011t0001g0004 a0001c0011t0001g0046 a0001c0011t0001g0047 others(3): Show |
7 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.98-541A>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/26 | chr22 | 50091460 | |||||||
| chr22:50091512 | C | G | 1 | a0006c0006t0001g0309 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.98-489C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/26 | chr22 | 50091512 | |||||||
| chr22:50091555 | G | T | 105 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(102): Show |
107 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.98-446G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/26 | chr22 | 50091555 | |||||||
| chr22:50091607 | C | G | 1 | a0002c0002t0002g0039 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.98-394C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/26 | chr22 | 50091607 | |||||||
| chr22:50091984 | T | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.98-17T>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 1/26 | chr22 | 50091984 | |||||||
| chr22:50092222 | G | A | 86 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0063 others(83): Show |
89 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.282+37G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50092222 | |||||||
| chr22:50092228 | G | C | 19 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0063 others(16): Show |
19 | HG01261.hp1 HG01516.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.282+43G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50092228 | |||||||
| chr22:50092369 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.282+184G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50092369 | |||||||
| chr22:50092434 | C | T | 105 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(102): Show |
107 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.282+249C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50092434 | |||||||
| chr22:50092496 | G | C | 22 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0137 others(19): Show |
24 | HG00741.hp2 HG01109.hp2 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.282+311G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50092496 | |||||||
| chr22:50092768 | T | C | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.282+583T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50092768 | |||||||
| chr22:50092775 | A | G | 131 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(128): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.282+590A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50092775 | |||||||
| chr22:50092824 | A | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.282+639A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50092824 | |||||||
| chr22:50092862 | A | G | 6 | a0001c0011t0001g0004 a0001c0011t0001g0046 a0001c0011t0001g0047 others(3): Show |
7 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.282+677A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50092862 | |||||||
| chr22:50092901 | G | C | 8 | a0001c0011t0001g0004 a0001c0011t0001g0046 a0001c0011t0001g0047 others(5): Show |
9 | HG01081.hp2 HG01168.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.282+716G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50092901 | |||||||
| chr22:50092927 | C | T | 1 | a0004c0008t0001g0007 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.282+742C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50092927 | |||||||
| chr22:50092987 | G | A | 1 | a0006c0006t0001g0234 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.282+802G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50092987 | |||||||
| chr22:50093136 | C | G | 69 | a0004c0008t0001g0007 a0004c0008t0001g0080 a0004c0008t0001g0084 others(66): Show |
72 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.282+951C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50093136 | |||||||
| chr22:50093142 | C | G | 4 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0007t0001g0227 others(1): Show |
4 | HG01070.hp2 HG01192.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.282+957C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50093142 | |||||||
| chr22:50093276 | G | T | 1 | a0002c0002t0002g0385 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.282+1091G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50093276 | |||||||
| chr22:50093288 | G | A | 8 | a0003c0003t0002g0322 a0003c0003t0002g0323 a0003c0003t0002g0324 others(5): Show |
8 | NA18954.hp2 NA18960.hp2 NA18975.hp1 others(5): Show |
intron_variant | MODIFIER | c.282+1103G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50093288 | |||||||
| chr22:50093321 | A | G | 1 | a0006c0006t0001g0309 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.282+1136A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50093321 | |||||||
| chr22:50093509 | A | ATT | 102 | a0002c0002t0002g0003 a0002c0002t0002g0013 a0002c0002t0002g0014 others(99): Show |
104 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.282+1332_282+1333d others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr22 | 50093509 | ||||||
| chr22:50093519 | C | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.282+1334C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50093519 | |||||||
| chr22:50093572 | G | A | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.282+1387G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50093572 | |||||||
| chr22:50093632 | C | G | 2 | a0008c0022t0001g0134 a0008c0022t0001g0135 |
2 | HG01346.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.282+1447C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50093632 | |||||||
| chr22:50093854 | G | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.282+1669G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50093854 | |||||||
| chr22:50094122 | T | A | 30 | a0002c0002t0002g0003 a0002c0002t0002g0013 a0002c0002t0002g0014 others(27): Show |
31 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.282+1937T>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50094122 | |||||||
| chr22:50094169 | C | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.282+1984C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50094169 | |||||||
| chr22:50094285 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.282+2100G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50094285 | |||||||
| chr22:50094353 | C | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.282+2168C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50094353 | |||||||
| chr22:50094378 | T | G | 9 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0015 others(6): Show |
9 | HG00408.hp1 HG00597.hp2 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.282+2193T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50094378 | |||||||
| chr22:50094399 | A | AT | 64 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(61): Show |
65 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.282+2232dupT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr22 | 50094399 | ||||||
| chr22:50094399 | AT | A | 95 | a0001c0001t0001g0063 a0001c0001t0001g0235 a0002c0002t0002g0003 others(92): Show |
97 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.282+2232delT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr22 | 50094399 | ||||||
| chr22:50094399 | ATT | A | 7 | a0002c0002t0002g0021 a0002c0010t0002g0331 a0002c0010t0002g0332 others(4): Show |
7 | HG01074.hp2 HG02080.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.282+2231_282+2232d others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr22 | 50094399 | ||||||
| chr22:50094551 | C | T | 10 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(7): Show |
11 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.282+2366C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50094551 | |||||||
| chr22:50094601 | G | A | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.282+2416G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50094601 | |||||||
| chr22:50094613 | A | G | 1 | a0006c0025t0001g0079 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.282+2428A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50094613 | |||||||
| chr22:50094616 | G | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.282+2431G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50094616 | |||||||
| chr22:50094620 | C | T | 33 | a0001c0001t0001g0051 a0001c0001t0001g0060 a0001c0001t0001g0136 others(30): Show |
33 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.282+2435C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50094620 | |||||||
| chr22:50094665 | C | T | 1 | a0002c0002t0002g0038 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.282+2480C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50094665 | |||||||
| chr22:50094685 | A | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.282+2500A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50094685 | |||||||
| chr22:50094688 | A | T | 1 | a0005c0004t0001g0123 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.282+2503A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50094688 | |||||||
| chr22:50094757 | A | AT | 3 | a0004c0008t0001g0120 a0004c0008t0001g0121 a0005c0004t0001g0122 |
3 | HG00639.hp2 HG01081.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.282+2573dupT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr22 | 50094757 | ||||||
| chr22:50094845 | C | G | 19 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0063 others(16): Show |
19 | HG01261.hp1 HG01516.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.282+2660C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50094845 | |||||||
| chr22:50094980 | C | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.282+2795C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50094980 | |||||||
| chr22:50094993 | C | T | 33 | a0001c0001t0001g0051 a0001c0001t0001g0060 a0001c0001t0001g0136 others(30): Show |
33 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.282+2808C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50094993 | |||||||
| chr22:50095002 | G | A | 3 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | HG03688.hp1 NA18973.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.282+2817G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50095002 | |||||||
| chr22:50095077 | C | T | 1 | a0002c0002t0002g0020 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.282+2892C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50095077 | |||||||
| chr22:50095119 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.282+2934G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50095119 | |||||||
| chr22:50095318 | G | A | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.282+3133G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50095318 | |||||||
| chr22:50095331 | G | A | 3 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | HG00733.hp1 HG02698.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.282+3146G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50095331 | |||||||
| chr22:50095432 | A | T | 1 | a0005c0004t0001g0119 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.282+3247A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50095432 | |||||||
| chr22:50095665 | C | T | 2 | a0002c0002t0002g0019 a0002c0002t0002g0020 |
2 | NA18969.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.282+3480C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50095665 | |||||||
| chr22:50095850 | A | G | 1 | a0001c0007t0001g0230 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.283-3593A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50095850 | |||||||
| chr22:50095862 | T | C | 1 | a0001c0001t0001g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.283-3581T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50095862 | |||||||
| chr22:50095884 | G | A | 1 | a0024c0027t0001g0159 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.283-3559G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50095884 | |||||||
| chr22:50096110 | A | G | 1 | a0002c0002t0002g0383 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.283-3333A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50096110 | |||||||
| chr22:50096111 | C | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0153 a0001c0001t0001g0154 others(1): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-3332C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50096111 | |||||||
| chr22:50096153 | C | A | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.283-3290C>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50096153 | |||||||
| chr22:50096364 | A | G | 2 | a0002c0002t0002g0021 a0002c0002t0002g0037 |
2 | NA18942.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.283-3079A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50096364 | |||||||
| chr22:50096382 | C | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | NA18990.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.283-3061C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50096382 | |||||||
| chr22:50096406 | G | C | 1 | a0001c0007t0001g0052 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.283-3037G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50096406 | |||||||
| chr22:50096445 | A | G | 3 | a0001c0005t0001g0197 a0001c0005t0001g0198 a0001c0005t0001g0199 |
3 | HG01099.hp1 HG01516.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.283-2998A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50096445 | |||||||
| chr22:50096480 | T | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.283-2963T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50096480 | |||||||
| chr22:50096523 | G | T | 32 | a0001c0001t0001g0051 a0001c0001t0001g0060 a0001c0001t0001g0136 others(29): Show |
32 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.283-2920G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50096523 | |||||||
| chr22:50096578 | T | C | 1 | a0001c0007t0001g0053 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.283-2865T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50096578 | |||||||
| chr22:50096794 | T | A | 1 | a0001c0007t0001g0054 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.283-2649T>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50096794 | |||||||
| chr22:50096887 | A | G | 104 | a0001c0001t0001g0196 a0002c0002t0002g0003 a0002c0002t0002g0012 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.283-2556A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50096887 | |||||||
| chr22:50097005 | T | C | 10 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(7): Show |
11 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.283-2438T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50097005 | |||||||
| chr22:50097360 | C | G | 1 | a0005c0004t0001g0118 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.283-2083C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50097360 | |||||||
| chr22:50097442 | T | C | 1 | a0005c0004t0001g0081 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.283-2001T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50097442 | |||||||
| chr22:50097498 | T | C | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.283-1945T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50097498 | |||||||
| chr22:50097603 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.283-1840T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50097603 | |||||||
| chr22:50097632 | G | A | 28 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(25): Show |
28 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.283-1811G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50097632 | |||||||
| chr22:50097699 | T | G | 8 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0063 others(5): Show |
8 | HG01261.hp1 HG02004.hp2 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.283-1744T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50097699 | |||||||
| chr22:50097702 | G | A | 5 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-1741G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50097702 | |||||||
| chr22:50097801 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.283-1642G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50097801 | |||||||
| chr22:50097819 | G | A | 1 | a0001c0005t0001g0164 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.283-1624G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50097819 | |||||||
| chr22:50097823 | C | A | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.283-1620C>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50097823 | |||||||
| chr22:50097856 | C | G | 1 | a0001c0001t0001g0308 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.283-1587C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50097856 | |||||||
| chr22:50098000 | A | ATTTTTTT others(184): Show |
1 | a0004c0008t0001g0117 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.283-1435_283-1434i others(193): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr22 | 50098000 | ||||||
| chr22:50098025 | T | C | 1 | a0004c0008t0001g0117 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.283-1418T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50098025 | |||||||
| chr22:50098090 | A | G | 1 | a0004c0008t0001g0080 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.283-1353A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50098090 | |||||||
| chr22:50098117 | A | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.283-1326A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50098117 | |||||||
| chr22:50098214 | T | TTATTAAG others(16): Show |
1 | a0001c0001t0001g0141 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.283-1227_283-1226i others(25): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr22 | 50098214 | ||||||
| chr22:50098214 | TTAAG | T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0137 others(20): Show |
25 | HG00741.hp2 HG01109.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.283-1226_283-1223d others(6): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr22 | 50098214 | ||||||
| chr22:50098218 | G | GTATTAAG others(20): Show |
142 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0235 others(139): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.283-1200_283-1174d others(29): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr22 | 50098218 | ||||||
| chr22:50098218 | G | GTATTAAG others(47): Show |
4 | a0004c0008t0001g0080 a0004c0008t0001g0106 a0006c0006t0001g0274 others(1): Show |
4 | HG01168.hp1 HG02145.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-1174_283-1173i others(56): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr22 | 50098218 | ||||||
| chr22:50098218 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.283-1225G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50098218 | |||||||
| chr22:50098218 | GTATTAAG others(20): Show |
G | 1 | a0001c0005t0001g0182 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.283-1200_283-1174d others(29): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr22 | 50098218 | ||||||
| chr22:50098243 | A | AATTATTA others(16): Show |
1 | a0005c0004t0001g0116 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.283-1198_283-1176d others(25): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr22 | 50098243 | ||||||
| chr22:50098267 | A | C | 5 | a0001c0007t0001g0216 a0001c0007t0001g0217 a0001c0007t0001g0218 others(2): Show |
5 | HG01123.hp2 HG01256.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-1176A>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50098267 | |||||||
| chr22:50098268 | AT | A | 5 | a0001c0007t0001g0216 a0001c0007t0001g0217 a0001c0007t0001g0218 others(2): Show |
5 | HG01123.hp2 HG01256.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-1174delT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50098268 | |||||||
| chr22:50098271 | A | T | 5 | a0001c0007t0001g0216 a0001c0007t0001g0217 a0001c0007t0001g0218 others(2): Show |
5 | HG01123.hp2 HG01256.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-1172A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50098271 | |||||||
| chr22:50098272 | C | CTT | 217 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(214): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.283-1171_283-1170i others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50098272 | |||||||
| chr22:50098272 | C | T | 5 | a0001c0007t0001g0216 a0001c0007t0001g0217 a0001c0007t0001g0218 others(2): Show |
5 | HG01123.hp2 HG01256.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-1171C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50098272 | |||||||
| chr22:50098337 | T | C | 222 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(219): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.283-1106T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50098337 | |||||||
| chr22:50098432 | G | T | 1 | a0016c0029t0001g0205 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.283-1011G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50098432 | |||||||
| chr22:50098498 | T | C | 19 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0063 others(16): Show |
19 | HG01261.hp1 HG01516.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.283-945T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50098498 | |||||||
| chr22:50098561 | G | A | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.283-882G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50098561 | |||||||
| chr22:50098566 | C | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.283-877C>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50098566 | |||||||
| chr22:50098574 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.283-869T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50098574 | |||||||
| chr22:50098670 | A | T | 2 | a0001c0001t0003g0194 a0001c0001t0003g0195 |
2 | HG02486.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.283-773A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50098670 | |||||||
| chr22:50098729 | T | C | 1 | a0005c0004t0001g0081 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.283-714T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50098729 | |||||||
| chr22:50098771 | G | A | 1 | a0005c0004t0001g0082 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.283-672G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50098771 | |||||||
| chr22:50098806 | A | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.283-637A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50098806 | |||||||
| chr22:50098977 | A | G | 3 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | HG03688.hp1 NA18973.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.283-466A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50098977 | |||||||
| chr22:50099253 | T | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.283-190T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50099253 | |||||||
| chr22:50099317 | C | T | 3 | a0006c0006t0001g0221 a0009c0019t0001g0222 a0009c0019t0001g0223 |
3 | HG01884.hp2 HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.283-126C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50099317 | |||||||
| chr22:50099323 | C | T | 30 | a0001c0001t0001g0051 a0001c0001t0001g0060 a0001c0001t0001g0136 others(27): Show |
30 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.283-120C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 2/26 | chr22 | 50099323 | |||||||
| chr22:50099745 | G | A | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.442+143G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50099745 | |||||||
| chr22:50099762 | A | G | 29 | a0002c0002t0002g0003 a0002c0002t0002g0013 a0002c0002t0002g0014 others(26): Show |
30 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.442+160A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50099762 | |||||||
| chr22:50099762 | A | T | 1 | a0002c0002t0002g0018 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.442+160A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50099762 | |||||||
| chr22:50099815 | T | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.442+213T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50099815 | |||||||
| chr22:50099836 | A | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.442+234A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50099836 | |||||||
| chr22:50099842 | A | G | 2 | a0001c0001t0001g0140 a0001c0001t0001g0193 |
2 | HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.442+240A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50099842 | |||||||
| chr22:50099979 | TTTTTTG | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.442+401_442+406del others(6): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr22 | 50099979 | ||||||
| chr22:50100010 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.442+408G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50100010 | |||||||
| chr22:50100159 | TTTTTTGT others(507): Show |
T | 1 | a0015c0041t0002g0036 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.442+565_442+1078de others(1): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr22 | 50100159 | ||||||
| chr22:50100208 | G | A | 1 | a0001c0011t0001g0045 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.442+606G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50100208 | |||||||
| chr22:50100252 | T | C | 102 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(99): Show |
104 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.442+650T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50100252 | |||||||
| chr22:50100255 | A | G | 1 | a0002c0013t0004g0371 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.442+653A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50100255 | |||||||
| chr22:50100271 | G | A | 1 | a0001c0007t0001g0059 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.442+669G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50100271 | |||||||
| chr22:50100292 | C | T | 2 | a0001c0001t0001g0241 a0001c0001t0001g0256 |
2 | NA18942.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.442+690C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50100292 | |||||||
| chr22:50100504 | T | A | 2 | a0002c0010t0002g0349 a0002c0010t0002g0387 |
2 | HG02145.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.442+902T>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50100504 | |||||||
| chr22:50100510 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.442+908T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50100510 | |||||||
| chr22:50100596 | C | G | 4 | a0001c0005t0001g0197 a0001c0005t0001g0198 a0001c0005t0001g0199 others(1): Show |
4 | HG01099.hp1 HG01256.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.442+994C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50100596 | |||||||
| chr22:50100747 | T | C | 166 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(163): Show |
169 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.442+1145T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50100747 | |||||||
| chr22:50100800 | C | T | 4 | a0001c0001t0003g0192 a0006c0006t0001g0221 a0009c0019t0001g0222 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.442+1198C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50100800 | |||||||
| chr22:50100984 | T | C | 154 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(151): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.442+1382T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50100984 | |||||||
| chr22:50101085 | C | T | 1 | a0016c0029t0001g0205 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.442+1483C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50101085 | |||||||
| chr22:50101531 | T | C | 1 | a0001c0005t0001g0165 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.442+1929T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50101531 | |||||||
| chr22:50101579 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.442+1977G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50101579 | |||||||
| chr22:50101579 | G | GCCTGATC others(1): Show |
103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.442+1977_442+1978i others(10): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50101579 | |||||||
| chr22:50101700 | C | T | 7 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(4): Show |
7 | HG01496.hp2 HG02717.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.442+2098C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50101700 | |||||||
| chr22:50101800 | C | CT | 22 | a0001c0001t0001g0051 a0001c0001t0001g0060 a0001c0007t0001g0052 others(19): Show |
22 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.442+2199dupT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr22 | 50101800 | ||||||
| chr22:50101920 | G | A | 30 | a0002c0002t0002g0003 a0002c0002t0002g0013 a0002c0002t0002g0014 others(27): Show |
31 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.442+2318G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50101920 | |||||||
| chr22:50101961 | C | T | 1 | a0005c0004t0001g0118 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.442+2359C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50101961 | |||||||
| chr22:50102026 | A | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.442+2424A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50102026 | |||||||
| chr22:50102245 | A | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.442+2643A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50102245 | |||||||
| chr22:50102337 | T | C | 11 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(8): Show |
12 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.442+2735T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50102337 | |||||||
| chr22:50102348 | C | T | 8 | a0001c0011t0001g0004 a0001c0011t0001g0046 a0001c0011t0001g0047 others(5): Show |
9 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.442+2746C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50102348 | |||||||
| chr22:50102508 | C | A | 1 | a0002c0013t0002g0336 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.442+2906C>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50102508 | |||||||
| chr22:50102522 | A | G | 2 | a0009c0019t0001g0222 a0009c0019t0001g0223 |
2 | HG01884.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.442+2920A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50102522 | |||||||
| chr22:50102574 | A | C | 1 | a0005c0004t0001g0115 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.442+2972A>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50102574 | |||||||
| chr22:50102833 | A | G | 163 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(160): Show |
166 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.442+3231A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50102833 | |||||||
| chr22:50102870 | C | A | 1 | a0001c0007t0001g0055 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.442+3268C>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50102870 | |||||||
| chr22:50102987 | A | G | 72 | a0002c0002t0002g0338 a0002c0002t0002g0339 a0002c0002t0002g0367 others(69): Show |
73 | HG00323.hp1 HG00621.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.442+3385A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50102987 | |||||||
| chr22:50103062 | G | A | 1 | a0003c0003t0002g0322 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.442+3460G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50103062 | |||||||
| chr22:50103081 | G | T | 9 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(6): Show |
9 | HG02080.hp1 NA18747.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.442+3479G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50103081 | |||||||
| chr22:50103207 | G | A | 1 | a0004c0009t0001g0313 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.442+3605G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50103207 | |||||||
| chr22:50103284 | T | C | 1 | a0015c0041t0002g0036 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.442+3682T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50103284 | |||||||
| chr22:50103432 | C | A | 1 | a0001c0001t0001g0061 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.442+3830C>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50103432 | |||||||
| chr22:50103488 | T | C | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.442+3886T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50103488 | |||||||
| chr22:50103693 | A | G | 102 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(99): Show |
104 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.442+4091A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50103693 | |||||||
| chr22:50103708 | C | G | 1 | a0015c0041t0002g0036 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.442+4106C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50103708 | |||||||
| chr22:50103882 | A | G | 1 | a0002c0002t0002g0035 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.443-4254A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50103882 | |||||||
| chr22:50104114 | C | G | 1 | a0002c0010t0002g0335 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.443-4022C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50104114 | |||||||
| chr22:50104463 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.443-3673G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50104463 | |||||||
| chr22:50104887 | C | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.443-3249C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50104887 | |||||||
| chr22:50104891 | C | CT | 16 | a0001c0001t0001g0051 a0001c0001t0001g0060 a0001c0001t0001g0239 others(13): Show |
16 | HG00280.hp1 HG00280.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.443-3228dupT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr22 | 50104891 | ||||||
| chr22:50104891 | CT | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0137 others(128): Show |
135 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.443-3228delT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr22 | 50104891 | ||||||
| chr22:50104965 | C | T | 1 | a0003c0003t0002g0380 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.443-3171C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50104965 | |||||||
| chr22:50104967 | T | C | 379 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(376): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.443-3169T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50104967 | |||||||
| chr22:50105182 | A | G | 3 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0215 |
3 | HG02717.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.443-2954A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50105182 | |||||||
| chr22:50105204 | T | C | 1 | a0003c0003t0002g0337 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.443-2932T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50105204 | |||||||
| chr22:50105302 | A | G | 6 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(3): Show |
6 | HG02615.hp2 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.443-2834A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50105302 | |||||||
| chr22:50105331 | T | C | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.443-2805T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50105331 | |||||||
| chr22:50105335 | C | A | 1 | a0001c0001t0001g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.443-2801C>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50105335 | |||||||
| chr22:50105355 | G | A | 25 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0063 others(22): Show |
25 | HG00323.hp2 HG01123.hp2 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.443-2781G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50105355 | |||||||
| chr22:50105417 | C | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.443-2719C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50105417 | |||||||
| chr22:50105568 | C | T | 9 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(6): Show |
9 | HG02080.hp1 NA18747.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.443-2568C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50105568 | |||||||
| chr22:50105571 | T | C | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.443-2565T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50105571 | |||||||
| chr22:50105775 | G | A | 1 | a0004c0009t0001g0314 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.443-2361G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50105775 | |||||||
| chr22:50105860 | A | G | 2 | a0009c0019t0001g0222 a0009c0019t0001g0223 |
2 | HG01884.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.443-2276A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50105860 | |||||||
| chr22:50106008 | T | C | 3 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | HG03688.hp1 NA18973.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.443-2128T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50106008 | |||||||
| chr22:50106271 | T | C | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.443-1865T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50106271 | |||||||
| chr22:50106285 | G | C | 3 | a0001c0005t0001g0164 a0001c0005t0001g0167 a0024c0027t0001g0159 |
3 | HG03942.hp2 HG04115.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.443-1851G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50106285 | |||||||
| chr22:50106301 | C | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.443-1835C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50106301 | |||||||
| chr22:50106312 | AC | A | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.443-1820delC | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr22 | 50106312 | ||||||
| chr22:50106325 | C | CT | 167 | a0001c0001t0001g0064 a0001c0001t0001g0149 a0001c0001t0001g0150 others(164): Show |
173 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.443-1788dupT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr22 | 50106325 | ||||||
| chr22:50106325 | C | CTT | 48 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0063 others(45): Show |
48 | HG00597.hp2 HG01109.hp1 HG01123.hp2 others(45): Show |
intron_variant | MODIFIER | c.443-1789_443-1788d others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr22 | 50106325 | ||||||
| chr22:50106325 | C | CTTT | 19 | a0001c0001t0001g0051 a0001c0001t0001g0060 a0001c0001t0001g0077 others(16): Show |
19 | HG00280.hp1 HG00280.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.443-1790_443-1788d others(5): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr22 | 50106325 | ||||||
| chr22:50106325 | CTTTTTTT others(7): Show |
C | 1 | a0016c0029t0001g0205 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.443-1801_443-1788d others(16): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr22 | 50106325 | ||||||
| chr22:50106460 | T | C | 4 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 others(1): Show |
4 | HG00733.hp1 HG02698.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.443-1676T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50106460 | |||||||
| chr22:50106659 | C | T | 5 | a0003c0012t0002g0317 a0003c0012t0002g0318 a0003c0012t0002g0319 others(2): Show |
5 | HG00323.hp1 HG01358.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.443-1477C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50106659 | |||||||
| chr22:50106699 | C | CT | 12 | a0001c0001t0001g0063 a0001c0001t0001g0150 a0001c0001t0001g0151 others(9): Show |
13 | HG01109.hp2 HG02055.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.443-1417dupT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr22 | 50106699 | ||||||
| chr22:50106699 | CT | C | 10 | a0001c0001t0001g0228 a0001c0001t0001g0246 a0001c0001t0001g0247 others(7): Show |
10 | HG01123.hp2 HG01256.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.443-1417delT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr22 | 50106699 | ||||||
| chr22:50106699 | CTTT | C | 99 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(96): Show |
101 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.443-1419_443-1417d others(5): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr22 | 50106699 | ||||||
| chr22:50106759 | TGGCTCAA others(4): Show |
T | 1 | a0001c0007t0001g0217 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.443-1370_443-1360d others(13): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr22 | 50106759 | ||||||
| chr22:50106769 | T | G | 11 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(8): Show |
12 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.443-1367T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50106769 | |||||||
| chr22:50106794 | C | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.443-1342C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50106794 | |||||||
| chr22:50106795 | G | A | 2 | a0001c0007t0001g0210 a0001c0007t0001g0211 |
2 | HG01257.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.443-1341G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50106795 | |||||||
| chr22:50106827 | G | T | 1 | a0005c0004t0001g0087 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.443-1309G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50106827 | |||||||
| chr22:50106850 | T | C | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.443-1286T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50106850 | |||||||
| chr22:50106937 | ATGATCCA others(354): Show |
A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0193 |
2 | HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.443-1145_443-785de others(1): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr22 | 50106937 | ||||||
| chr22:50106954 | G | A | 2 | a0005c0020t0001g0083 a0005c0020t0001g0112 |
2 | HG02040.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.443-1182G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50106954 | |||||||
| chr22:50106992 | T | C | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.443-1144T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50106992 | |||||||
| chr22:50106996 | C | T | 1 | a0003c0003t0002g0382 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.443-1140C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50106996 | |||||||
| chr22:50107095 | G | A | 1 | a0004c0009t0001g0129 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.443-1041G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50107095 | |||||||
| chr22:50107113 | C | T | 1 | a0004c0008t0001g0080 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.443-1023C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50107113 | |||||||
| chr22:50107168 | G | T | 78 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0156 others(75): Show |
80 | HG00099.hp2 HG00438.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.443-968G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50107168 | |||||||
| chr22:50107175 | C | T | 2 | a0003c0003t0002g0382 a0003c0003t0004g0381 |
2 | NA18939.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.443-961C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50107175 | |||||||
| chr22:50107205 | G | T | 1 | a0001c0001t0001g0268 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.443-931G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50107205 | |||||||
| chr22:50107214 | A | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.443-922A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50107214 | |||||||
| chr22:50107259 | A | G | 48 | a0002c0002t0002g0003 a0002c0002t0002g0013 a0002c0002t0002g0014 others(45): Show |
49 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.443-877A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50107259 | |||||||
| chr22:50107275 | C | T | 4 | a0001c0011t0001g0004 a0001c0011t0001g0048 a0001c0011t0001g0049 others(1): Show |
4 | HG02055.hp1 HG02258.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.443-861C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50107275 | |||||||
| chr22:50107287 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.443-849C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50107287 | |||||||
| chr22:50107305 | A | G | 48 | a0002c0002t0002g0003 a0002c0002t0002g0013 a0002c0002t0002g0014 others(45): Show |
49 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.443-831A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50107305 | |||||||
| chr22:50107383 | A | G | 1 | a0001c0005t0001g0292 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.443-753A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50107383 | |||||||
| chr22:50107594 | C | T | 1 | a0001c0005t0001g0181 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.443-542C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50107594 | |||||||
| chr22:50107644 | G | A | 5 | a0001c0007t0001g0216 a0001c0007t0001g0217 a0001c0007t0001g0218 others(2): Show |
5 | HG01123.hp2 HG01256.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.443-492G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50107644 | |||||||
| chr22:50107656 | G | C | 4 | a0001c0001t0001g0077 a0006c0006t0001g0069 a0006c0006t0001g0070 others(1): Show |
4 | HG01516.hp2 HG01517.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.443-480G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50107656 | |||||||
| chr22:50107666 | G | A | 1 | a0001c0007t0001g0209 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.443-470G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50107666 | |||||||
| chr22:50107669 | C | T | 49 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(46): Show |
50 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.443-467C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50107669 | |||||||
| chr22:50107756 | T | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.443-380T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50107756 | |||||||
| chr22:50107826 | C | T | 1 | a0002c0002t0002g0040 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.443-310C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50107826 | |||||||
| chr22:50107835 | G | A | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.443-301G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50107835 | |||||||
| chr22:50107866 | C | T | 1 | a0001c0005t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.443-270C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50107866 | |||||||
| chr22:50107989 | G | A | 1 | a0003c0012t0002g0317 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.443-147G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50107989 | |||||||
| chr22:50108001 | C | T | 1 | a0003c0012t0002g0334 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.443-135C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50108001 | |||||||
| chr22:50108038 | G | A | 21 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(18): Show |
21 | HG01261.hp1 HG01515.hp2 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.443-98G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50108038 | |||||||
| chr22:50108056 | G | A | 3 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | HG00733.hp1 HG02698.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.443-80G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 3/26 | chr22 | 50108056 | |||||||
| chr22:50108259 | G | A | 1 | a0007c0015t0002g0023 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.555+11G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 4/26 | chr22 | 50108259 | |||||||
| chr22:50108359 | G | C | 22 | a0001c0007t0001g0052 a0001c0007t0001g0053 a0001c0007t0001g0054 others(19): Show |
22 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.555+111G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 4/26 | chr22 | 50108359 | |||||||
| chr22:50108368 | T | C | 21 | a0001c0001t0001g0051 a0001c0001t0001g0060 a0001c0007t0001g0052 others(18): Show |
21 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.555+120T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 4/26 | chr22 | 50108368 | |||||||
| chr22:50108415 | T | A | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.555+167T>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 4/26 | chr22 | 50108415 | |||||||
| chr22:50108439 | G | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.555+191G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 4/26 | chr22 | 50108439 | |||||||
| chr22:50108471 | C | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.556-186C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 4/26 | chr22 | 50108471 | |||||||
| chr22:50108495 | A | G | 2 | a0009c0019t0001g0222 a0009c0019t0001g0223 |
2 | HG01884.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.556-162A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 4/26 | chr22 | 50108495 | |||||||
| chr22:50108532 | G | A | 3 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | HG03688.hp1 NA18973.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.556-125G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 4/26 | chr22 | 50108532 | |||||||
| chr22:50108542 | A | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.556-115A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 4/26 | chr22 | 50108542 | |||||||
| chr22:50108602 | C | T | 19 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0063 others(16): Show |
19 | HG01261.hp1 HG01516.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.556-55C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 4/26 | chr22 | 50108602 | |||||||
| chr22:50108929 | G | A | 1 | a0006c0006t0001g0221 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.743+85G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50108929 | |||||||
| chr22:50108960 | C | T | 54 | a0002c0010t0002g0331 a0002c0010t0002g0332 a0002c0010t0002g0333 others(51): Show |
55 | HG00323.hp1 HG00733.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.743+116C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50108960 | |||||||
| chr22:50109100 | C | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.743+256C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50109100 | |||||||
| chr22:50109129 | T | C | 234 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(231): Show |
240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.743+285T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50109129 | |||||||
| chr22:50109251 | T | G | 1 | a0001c0001t0001g0252 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.743+407T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50109251 | |||||||
| chr22:50109283 | A | G | 98 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0014 others(95): Show |
99 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.743+439A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50109283 | |||||||
| chr22:50109435 | C | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.743+591C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50109435 | |||||||
| chr22:50109451 | T | C | 1 | a0001c0001t0001g0290 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.743+607T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50109451 | |||||||
| chr22:50109466 | G | A | 1 | a0004c0008t0001g0120 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.743+622G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50109466 | |||||||
| chr22:50109492 | AC | A | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.743+652delC | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr22 | 50109492 | ||||||
| chr22:50109527 | C | T | 1 | a0004c0008t0001g0084 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.743+683C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50109527 | |||||||
| chr22:50109556 | G | A | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.743+712G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50109556 | |||||||
| chr22:50109560 | G | A | 5 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.743+716G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50109560 | |||||||
| chr22:50109595 | C | T | 1 | a0005c0004t0001g0123 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.743+751C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50109595 | |||||||
| chr22:50109623 | A | G | 1 | a0002c0013t0002g0043 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.743+779A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50109623 | |||||||
| chr22:50109627 | C | T | 2 | a0002c0010t0002g0363 a0002c0010t0002g0364 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.743+783C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50109627 | |||||||
| chr22:50109670 | C | CA | 44 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(41): Show |
44 | HG01109.hp1 HG01261.hp1 HG01515.hp2 others(41): Show |
intron_variant | MODIFIER | c.743+848dupA | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr22 | 50109670 | ||||||
| chr22:50109670 | CA | C | 99 | a0001c0001t0001g0252 a0002c0002t0002g0003 a0002c0002t0002g0012 others(96): Show |
101 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.743+848delA | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr22 | 50109670 | ||||||
| chr22:50109670 | CAA | C | 6 | a0002c0002t0002g0033 a0002c0002t0002g0034 a0002c0002t0002g0035 others(3): Show |
6 | HG01168.hp2 HG01257.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.743+847_743+848del others(2): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr22 | 50109670 | ||||||
| chr22:50109670 | CAAAAAAA | C | 10 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(7): Show |
11 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.743+842_743+848del others(7): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr22 | 50109670 | ||||||
| chr22:50109767 | A | T | 1 | a0001c0001t0001g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.743+923A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50109767 | |||||||
| chr22:50109785 | C | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.743+941C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50109785 | |||||||
| chr22:50109796 | C | T | 7 | a0005c0004t0001g0006 a0005c0004t0001g0081 a0005c0004t0001g0087 others(4): Show |
8 | NA18949.hp2 NA18952.hp1 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.743+952C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50109796 | |||||||
| chr22:50109841 | T | TA | 48 | a0002c0002t0002g0003 a0002c0002t0002g0013 a0002c0002t0002g0014 others(45): Show |
49 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.743+1003dupA | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr22 | 50109841 | ||||||
| chr22:50109848 | T | A | 102 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(99): Show |
104 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.743+1004T>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50109848 | |||||||
| chr22:50109888 | C | A | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.743+1044C>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50109888 | |||||||
| chr22:50109942 | A | G | 2 | a0001c0007t0001g0054 a0001c0007t0001g0056 |
2 | HG00741.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.743+1098A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50109942 | |||||||
| chr22:50110175 | C | T | 3 | a0001c0005t0001g0166 a0001c0005t0001g0179 a0001c0005t0001g0180 |
3 | HG02965.hp1 HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.743+1331C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50110175 | |||||||
| chr22:50110178 | G | A | 1 | a0016c0029t0001g0205 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.743+1334G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50110178 | |||||||
| chr22:50110197 | A | C | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.743+1353A>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50110197 | |||||||
| chr22:50110223 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.743+1379G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50110223 | |||||||
| chr22:50110279 | C | A | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.743+1435C>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50110279 | |||||||
| chr22:50110309 | C | T | 105 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(102): Show |
107 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.743+1465C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50110309 | |||||||
| chr22:50110318 | C | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.743+1474C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50110318 | |||||||
| chr22:50110344 | G | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.743+1500G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50110344 | |||||||
| chr22:50110362 | T | A | 1 | a0001c0005t0001g0188 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.743+1518T>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50110362 | |||||||
| chr22:50110396 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.743+1552C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50110396 | |||||||
| chr22:50110397 | C | T | 1 | a0003c0003t0002g0384 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.743+1553C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50110397 | |||||||
| chr22:50110414 | A | T | 1 | a0001c0005t0001g0288 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.743+1570A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50110414 | |||||||
| chr22:50110420 | G | A | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.743+1576G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50110420 | |||||||
| chr22:50110448 | C | CA | 28 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(25): Show |
28 | HG01175.hp1 HG01261.hp1 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.743+1618dupA | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr22 | 50110448 | ||||||
| chr22:50110523 | G | C | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.743+1679G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50110523 | |||||||
| chr22:50110556 | T | C | 234 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(231): Show |
240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.743+1712T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50110556 | |||||||
| chr22:50110723 | G | A | 1 | a0006c0006t0001g0221 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.743+1879G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50110723 | |||||||
| chr22:50110748 | C | T | 7 | a0002c0002t0002g0021 a0002c0002t0002g0025 a0002c0002t0002g0029 others(4): Show |
7 | NA18942.hp1 NA18949.hp1 NA18999.hp2 others(4): Show |
intron_variant | MODIFIER | c.743+1904C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50110748 | |||||||
| chr22:50110764 | C | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.743+1920C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50110764 | |||||||
| chr22:50110848 | T | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.743+2004T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50110848 | |||||||
| chr22:50110887 | C | T | 1 | a0001c0005t0001g0297 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.743+2043C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50110887 | |||||||
| chr22:50110911 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.743+2067A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50110911 | |||||||
| chr22:50110935 | TA | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.743+2102delA | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr22 | 50110935 | ||||||
| chr22:50111009 | C | T | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.743+2165C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50111009 | |||||||
| chr22:50111231 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.743+2387A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50111231 | |||||||
| chr22:50111431 | T | C | 1 | a0003c0003t0002g0341 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.744-2217T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50111431 | |||||||
| chr22:50111459 | G | GT | 3 | a0002c0002t0002g0029 a0002c0002t0002g0030 a0002c0002t0002g0032 |
3 | NA18949.hp1 NA19001.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.744-2188dupT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr22 | 50111459 | ||||||
| chr22:50111486 | C | CT | 104 | a0001c0001t0001g0061 a0001c0001t0001g0136 a0001c0001t0001g0139 others(101): Show |
106 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(103): Show |
intron_variant | MODIFIER | c.744-2135dupT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr22 | 50111486 | ||||||
| chr22:50111486 | C | CTT | 44 | a0001c0001t0001g0062 a0001c0001t0001g0208 a0001c0001t0001g0233 others(41): Show |
45 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.744-2136_744-2135d others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr22 | 50111486 | ||||||
| chr22:50111486 | C | CTTT | 12 | a0002c0002t0002g0017 a0002c0002t0002g0018 a0002c0002t0002g0019 others(9): Show |
12 | HG00597.hp2 HG00621.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.744-2137_744-2135d others(5): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr22 | 50111486 | ||||||
| chr22:50111486 | C | T | 1 | a0002c0002t0002g0376 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.744-2162C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50111486 | |||||||
| chr22:50111486 | CT | C | 22 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(19): Show |
22 | HG01261.hp1 HG01515.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.744-2135delT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr22 | 50111486 | ||||||
| chr22:50111486 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0224 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.744-2147_744-2135d others(15): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr22 | 50111486 | ||||||
| chr22:50111486 | CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | NA18973.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.744-2148_744-2135d others(16): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr22 | 50111486 | ||||||
| chr22:50111486 | CTTTTTTT others(8): Show |
C | 1 | a0020c0040t0001g0089 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.744-2149_744-2135d others(17): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr22 | 50111486 | ||||||
| chr22:50111535 | G | A | 3 | a0001c0005t0001g0010 a0001c0005t0001g0288 a0001c0005t0001g0292 |
4 | HG04228.hp1 NA19009.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.744-2113G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50111535 | |||||||
| chr22:50111584 | A | G | 5 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.744-2064A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50111584 | |||||||
| chr22:50111703 | C | T | 1 | a0001c0005t0001g0189 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.744-1945C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50111703 | |||||||
| chr22:50111892 | G | C | 3 | a0001c0005t0001g0164 a0001c0005t0001g0167 a0024c0027t0001g0159 |
3 | HG03942.hp2 HG04115.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.744-1756G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50111892 | |||||||
| chr22:50111984 | G | A | 70 | a0004c0008t0001g0007 a0004c0008t0001g0080 a0004c0008t0001g0084 others(67): Show |
73 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.744-1664G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50111984 | |||||||
| chr22:50112033 | T | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.744-1615T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50112033 | |||||||
| chr22:50112060 | G | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0235 others(73): Show |
78 | HG00099.hp2 HG00438.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.744-1588G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50112060 | |||||||
| chr22:50112073 | T | C | 1 | a0004c0014t0001g0110 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.744-1575T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50112073 | |||||||
| chr22:50112163 | C | T | 1 | a0002c0002t0002g0028 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.744-1485C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50112163 | |||||||
| chr22:50112379 | C | T | 28 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(25): Show |
28 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.744-1269C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50112379 | |||||||
| chr22:50112520 | G | A | 2 | a0001c0007t0001g0216 a0001c0007t0001g0217 |
2 | HG01123.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.744-1128G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50112520 | |||||||
| chr22:50112584 | C | T | 6 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(3): Show |
6 | HG01496.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.744-1064C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50112584 | |||||||
| chr22:50112698 | T | C | 1 | a0002c0002t0002g0040 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.744-950T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50112698 | |||||||
| chr22:50112756 | C | T | 1 | a0001c0007t0001g0059 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.744-892C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50112756 | |||||||
| chr22:50112771 | G | A | 3 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | HG03688.hp1 NA18973.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.744-877G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50112771 | |||||||
| chr22:50112780 | C | G | 1 | a0004c0008t0001g0080 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.744-868C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50112780 | |||||||
| chr22:50112809 | G | A | 1 | a0002c0002t0002g0376 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.744-839G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50112809 | |||||||
| chr22:50112883 | A | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.744-765A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50112883 | |||||||
| chr22:50113126 | G | A | 1 | a0002c0002t0002g0035 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.744-522G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50113126 | |||||||
| chr22:50113145 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.744-503G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50113145 | |||||||
| chr22:50113246 | T | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG01255.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.744-402T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50113246 | |||||||
| chr22:50113280 | G | C | 1 | a0001c0001t0001g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.744-368G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50113280 | |||||||
| chr22:50113288 | C | T | 1 | a0002c0002t0002g0017 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.744-360C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50113288 | |||||||
| chr22:50113395 | A | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.744-253A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50113395 | |||||||
| chr22:50113473 | G | A | 2 | a0011c0018t0001g0075 a0011c0018t0001g0076 |
2 | NA18950.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.744-175G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50113473 | |||||||
| chr22:50113478 | C | G | 1 | a0001c0001t0001g0042 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.744-170C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50113478 | |||||||
| chr22:50113543 | G | A | 21 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(18): Show |
21 | HG01261.hp1 HG01515.hp2 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.744-105G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50113543 | |||||||
| chr22:50113583 | C | T | 1 | a0002c0002t0002g0375 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.744-65C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 5/26 | chr22 | 50113583 | |||||||
| chr22:50113849 | C | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.884+61C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 6/26 | chr22 | 50113849 | |||||||
| chr22:50113905 | ATCTTT | A | 4 | a0001c0007t0001g0216 a0001c0007t0001g0217 a0001c0007t0001g0219 others(1): Show |
4 | HG01123.hp2 HG01256.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.884+124_884+128del others(5): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr22 | 50113905 | ||||||
| chr22:50113912 | C | CT | 17 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0149 others(14): Show |
17 | HG00597.hp2 HG00735.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.884+148dupT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr22 | 50113912 | ||||||
| chr22:50113912 | CT | C | 63 | a0001c0001t0001g0051 a0001c0001t0001g0136 a0001c0001t0001g0208 others(60): Show |
63 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.884+148delT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr22 | 50113912 | ||||||
| chr22:50113912 | CTT | C | 9 | a0001c0011t0001g0004 a0001c0011t0001g0045 a0001c0011t0001g0046 others(6): Show |
10 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.884+147_884+148del others(2): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr22 | 50113912 | ||||||
| chr22:50113920 | T | C | 67 | a0004c0008t0001g0007 a0004c0008t0001g0086 a0004c0008t0001g0092 others(64): Show |
70 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.884+132T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 6/26 | chr22 | 50113920 | |||||||
| chr22:50113921 | T | C | 1 | a0004c0008t0001g0084 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.884+133T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 6/26 | chr22 | 50113921 | |||||||
| chr22:50113954 | C | T | 3 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0215 |
3 | HG02717.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.884+166C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 6/26 | chr22 | 50113954 | |||||||
| chr22:50113956 | T | C | 1 | a0016c0029t0001g0205 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.884+168T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 6/26 | chr22 | 50113956 | |||||||
| chr22:50113958 | G | C | 1 | a0016c0029t0001g0205 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.884+170G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 6/26 | chr22 | 50113958 | |||||||
| chr22:50113981 | C | T | 10 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(7): Show |
11 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.884+193C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 6/26 | chr22 | 50113981 | |||||||
| chr22:50114003 | C | T | 6 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(3): Show |
6 | HG01496.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.884+215C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 6/26 | chr22 | 50114003 | |||||||
| chr22:50114011 | C | T | 1 | a0006c0006t0001g0221 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.884+223C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 6/26 | chr22 | 50114011 | |||||||
| chr22:50114084 | A | C | 1 | a0002c0002t0002g0038 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.884+296A>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 6/26 | chr22 | 50114084 | |||||||
| chr22:50114108 | C | T | 1 | a0001c0007t0001g0230 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.885-273C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 6/26 | chr22 | 50114108 | |||||||
| chr22:50114166 | C | G | 1 | a0001c0001t0001g0136 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.885-215C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 6/26 | chr22 | 50114166 | |||||||
| chr22:50114212 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.885-169C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 6/26 | chr22 | 50114212 | |||||||
| chr22:50114307 | T | C | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.885-74T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 6/26 | chr22 | 50114307 | |||||||
| chr22:50114656 | C | T | 3 | a0001c0001t0003g0174 a0001c0001t0003g0175 a0001c0001t0003g0178 |
3 | HG02109.hp2 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1126+34C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 7/26 | chr22 | 50114656 | |||||||
| chr22:50114719 | C | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1126+97C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 7/26 | chr22 | 50114719 | |||||||
| chr22:50114847 | C | G | 6 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(3): Show |
6 | HG01496.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1126+225C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 7/26 | chr22 | 50114847 | |||||||
| chr22:50114889 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1127-225G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 7/26 | chr22 | 50114889 | |||||||
| chr22:50114935 | A | G | 1 | a0004c0009t0001g0313 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1127-179A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 7/26 | chr22 | 50114935 | |||||||
| chr22:50115085 | A | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1127-29A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 7/26 | chr22 | 50115085 | |||||||
| chr22:50115304 | G | T | 2 | a0003c0003t0002g0382 a0003c0003t0004g0381 |
2 | NA18939.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1259+58G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | chr22 | 50115304 | |||||||
| chr22:50115336 | G | A | 6 | a0001c0011t0001g0004 a0001c0011t0001g0046 a0001c0011t0001g0047 others(3): Show |
7 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1259+90G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | chr22 | 50115336 | |||||||
| chr22:50115403 | A | G | 1 | a0002c0002t0002g0038 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1259+157A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | chr22 | 50115403 | |||||||
| chr22:50115433 | G | A | 210 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(207): Show |
216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.1259+187G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | chr22 | 50115433 | |||||||
| chr22:50115559 | A | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0078 |
2 | NA19064.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1259+313A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | chr22 | 50115559 | |||||||
| chr22:50115625 | G | C | 61 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(58): Show |
62 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.1259+379G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | chr22 | 50115625 | |||||||
| chr22:50115761 | C | T | 5 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1259+515C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | chr22 | 50115761 | |||||||
| chr22:50115830 | C | T | 10 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(7): Show |
11 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1259+584C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | chr22 | 50115830 | |||||||
| chr22:50115835 | G | A | 140 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(137): Show |
143 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.1259+589G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | chr22 | 50115835 | |||||||
| chr22:50115840 | G | A | 1 | a0001c0007t0001g0227 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1259+594G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | chr22 | 50115840 | |||||||
| chr22:50115855 | G | A | 1 | a0003c0003t0002g0341 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1259+609G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | chr22 | 50115855 | |||||||
| chr22:50115892 | T | C | 2 | a0005c0004t0001g0090 a0005c0004t0001g0111 |
2 | HG00408.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1259+646T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | chr22 | 50115892 | |||||||
| chr22:50115916 | G | A | 1 | a0006c0006t0001g0221 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1259+670G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | chr22 | 50115916 | |||||||
| chr22:50115918 | C | G | 1 | a0016c0029t0001g0205 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1259+672C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | chr22 | 50115918 | |||||||
| chr22:50115931 | G | C | 1 | a0001c0001t0001g0255 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1259+685G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | chr22 | 50115931 | |||||||
| chr22:50115970 | G | T | 1 | a0001c0005t0001g0165 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1259+724G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | chr22 | 50115970 | |||||||
| chr22:50116049 | C | T | 1 | a0016c0029t0001g0205 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1259+803C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | chr22 | 50116049 | |||||||
| chr22:50116050 | G | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0241 a0001c0001t0001g0256 |
4 | HG02015.hp2 HG03669.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1259+804G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | chr22 | 50116050 | |||||||
| chr22:50116193 | C | CT | 54 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(51): Show |
55 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.1260-949dupT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr22 | 50116193 | ||||||
| chr22:50116303 | T | C | 1 | a0002c0002t0002g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1260-854T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | chr22 | 50116303 | |||||||
| chr22:50116334 | C | G | 1 | a0003c0003t0005g0329 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1260-823C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | chr22 | 50116334 | |||||||
| chr22:50116395 | C | G | 7 | a0001c0001t0003g0174 a0001c0001t0003g0175 a0001c0001t0003g0177 others(4): Show |
7 | HG02109.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1260-762C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | chr22 | 50116395 | |||||||
| chr22:50116446 | C | CA | 109 | a0001c0001t0001g0041 a0001c0001t0001g0294 a0001c0005t0001g0176 others(106): Show |
111 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.1260-696dupA | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr22 | 50116446 | ||||||
| chr22:50116446 | C | CAA | 6 | a0002c0002t0002g0031 a0002c0002t0002g0375 a0002c0002t0002g0383 others(3): Show |
6 | HG00621.hp2 HG02293.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1260-697_1260-696d others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr22 | 50116446 | ||||||
| chr22:50116472 | G | A | 1 | a0006c0006t0001g0221 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1260-685G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | chr22 | 50116472 | |||||||
| chr22:50116659 | A | G | 4 | a0002c0002t0002g0025 a0002c0002t0002g0029 a0002c0002t0002g0030 others(1): Show |
4 | NA18949.hp1 NA18999.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260-498A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | chr22 | 50116659 | |||||||
| chr22:50116660 | C | CT | 21 | a0001c0001t0001g0063 a0001c0001t0001g0074 a0001c0001t0001g0150 others(18): Show |
21 | HG01109.hp2 HG01891.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1260-474dupT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr22 | 50116660 | ||||||
| chr22:50116660 | C | CTT | 54 | a0004c0008t0001g0007 a0004c0008t0001g0084 a0004c0008t0001g0086 others(51): Show |
57 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.1260-475_1260-474d others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr22 | 50116660 | ||||||
| chr22:50116660 | C | CTTT | 15 | a0004c0008t0001g0080 a0004c0008t0001g0108 a0004c0009t0001g0314 others(12): Show |
15 | HG00621.hp1 HG01106.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.1260-476_1260-474d others(5): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr22 | 50116660 | ||||||
| chr22:50116660 | CT | C | 13 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0002c0002t0002g0012 others(10): Show |
13 | HG01981.hp2 HG02145.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1260-474delT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr22 | 50116660 | ||||||
| chr22:50116660 | CTT | C | 47 | a0001c0001t0001g0213 a0001c0007t0001g0227 a0002c0010t0002g0356 others(44): Show |
48 | HG00323.hp1 HG00733.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.1260-475_1260-474d others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr22 | 50116660 | ||||||
| chr22:50116660 | CTTT | C | 20 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(17): Show |
20 | HG00280.hp1 HG00280.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.1260-476_1260-474d others(5): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr22 | 50116660 | ||||||
| chr22:50116870 | G | T | 125 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(122): Show |
127 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1260-287G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | chr22 | 50116870 | |||||||
| chr22:50117057 | G | C | 378 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(375): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.1260-100G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | chr22 | 50117057 | |||||||
| chr22:50117062 | AACTCTGT others(1): Show |
A | 18 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0141 others(15): Show |
20 | HG00741.hp2 HG01109.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.1260-91_1260-84del others(8): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr22 | 50117062 | ||||||
| chr22:50117396 | T | A | 17 | a0003c0003t0002g0341 a0003c0003t0002g0342 a0003c0003t0002g0343 others(14): Show |
17 | HG00323.hp1 HG00733.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.1454+45T>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50117396 | |||||||
| chr22:50117441 | C | T | 1 | a0016c0029t0001g0205 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1454+90C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50117441 | |||||||
| chr22:50117476 | G | A | 1 | a0004c0008t0001g0080 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1454+125G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50117476 | |||||||
| chr22:50117540 | C | G | 1 | a0006c0006t0001g0270 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1454+189C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50117540 | |||||||
| chr22:50117554 | G | A | 2 | a0005c0020t0001g0083 a0005c0020t0001g0112 |
2 | HG02040.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1454+203G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50117554 | |||||||
| chr22:50117572 | C | T | 28 | a0003c0003t0002g0322 a0003c0003t0002g0323 a0003c0003t0002g0324 others(25): Show |
29 | HG01081.hp2 HG01099.hp2 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.1454+221C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50117572 | |||||||
| chr22:50117690 | C | T | 11 | a0001c0001t0001g0253 a0001c0001t0001g0299 a0001c0001t0001g0300 others(8): Show |
11 | HG01975.hp2 HG02056.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1454+339C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50117690 | |||||||
| chr22:50117712 | C | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1454+361C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50117712 | |||||||
| chr22:50117833 | T | C | 23 | a0001c0001t0001g0235 a0001c0001t0001g0246 a0001c0001t0001g0247 others(20): Show |
23 | HG00597.hp1 HG02027.hp1 HG02132.hp1 others(20): Show |
intron_variant | MODIFIER | c.1454+482T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50117833 | |||||||
| chr22:50117902 | C | T | 13 | a0001c0007t0001g0052 a0001c0007t0001g0053 a0001c0007t0001g0054 others(10): Show |
13 | HG00280.hp1 HG00280.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.1454+551C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50117902 | |||||||
| chr22:50117903 | G | A | 1 | a0002c0002t0002g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1454+552G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50117903 | |||||||
| chr22:50117986 | A | T | 1 | a0002c0002t0002g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1454+635A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50117986 | |||||||
| chr22:50118058 | G | A | 22 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(19): Show |
22 | HG00280.hp1 HG00280.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.1454+707G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50118058 | |||||||
| chr22:50118188 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1454+837G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50118188 | |||||||
| chr22:50118223 | C | CCATTGTT others(5): Show |
125 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(122): Show |
127 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1454+875_1454+886d others(14): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr22 | 50118223 | ||||||
| chr22:50118293 | G | T | 1 | a0001c0005t0001g0188 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1454+942G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50118293 | |||||||
| chr22:50118307 | G | A | 49 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(46): Show |
50 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.1454+956G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50118307 | |||||||
| chr22:50118358 | A | G | 131 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(128): Show |
133 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.1454+1007A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50118358 | |||||||
| chr22:50118386 | A | G | 131 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(128): Show |
133 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.1454+1035A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50118386 | |||||||
| chr22:50118520 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1454+1169A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50118520 | |||||||
| chr22:50118691 | C | A | 131 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(128): Show |
133 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.1454+1340C>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50118691 | |||||||
| chr22:50118806 | T | G | 70 | a0004c0008t0001g0007 a0004c0008t0001g0080 a0004c0008t0001g0084 others(67): Show |
73 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.1454+1455T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50118806 | |||||||
| chr22:50118895 | G | A | 2 | a0002c0010t0002g0331 a0002c0010t0002g0335 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1454+1544G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50118895 | |||||||
| chr22:50118923 | T | C | 1 | a0003c0003t0002g0350 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1454+1572T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50118923 | |||||||
| chr22:50118978 | A | G | 82 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(79): Show |
83 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1455-1524A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50118978 | |||||||
| chr22:50119002 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | NA18990.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1455-1500G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50119002 | |||||||
| chr22:50119034 | G | A | 54 | a0002c0010t0002g0331 a0002c0010t0002g0332 a0002c0010t0002g0333 others(51): Show |
55 | HG00323.hp1 HG00733.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.1455-1468G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50119034 | |||||||
| chr22:50119162 | AC | A | 12 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(9): Show |
13 | HG01243.hp2 HG02055.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1455-1335delC | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr22 | 50119162 | ||||||
| chr22:50119170 | G | T | 1 | a0001c0005t0001g0288 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1455-1332G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50119170 | |||||||
| chr22:50119185 | G | A | 1 | a0001c0007t0001g0053 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1455-1317G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50119185 | |||||||
| chr22:50119211 | C | T | 54 | a0002c0010t0002g0331 a0002c0010t0002g0332 a0002c0010t0002g0333 others(51): Show |
55 | HG00323.hp1 HG00733.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.1455-1291C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50119211 | |||||||
| chr22:50119411 | A | G | 19 | a0001c0007t0001g0052 a0001c0007t0001g0053 a0001c0007t0001g0054 others(16): Show |
19 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.1455-1091A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50119411 | |||||||
| chr22:50119733 | T | G | 1 | a0001c0005t0001g0181 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1455-769T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50119733 | |||||||
| chr22:50119977 | C | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1455-525C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50119977 | |||||||
| chr22:50120076 | G | A | 131 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(128): Show |
133 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.1455-426G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50120076 | |||||||
| chr22:50120094 | G | A | 3 | a0002c0013t0002g0336 a0002c0013t0002g0365 a0002c0013t0004g0371 |
3 | NA18955.hp2 NA18977.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1455-408G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50120094 | |||||||
| chr22:50120112 | G | T | 3 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | HG03688.hp1 NA18973.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1455-390G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50120112 | |||||||
| chr22:50120273 | C | T | 1 | a0016c0029t0001g0205 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1455-229C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 9/26 | chr22 | 50120273 | |||||||
| chr22:50120818 | G | A | 131 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(128): Show |
133 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.1569+202G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50120818 | |||||||
| chr22:50121148 | G | A | 1 | a0006c0006t0001g0221 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1569+532G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50121148 | |||||||
| chr22:50121374 | G | A | 384 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(381): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.1569+758G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50121374 | |||||||
| chr22:50121409 | C | G | 131 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(128): Show |
133 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.1569+793C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50121409 | |||||||
| chr22:50121470 | AT | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0152 a0001c0001t0001g0153 others(3): Show |
8 | HG00741.hp2 HG01891.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1569+855delT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50121470 | |||||||
| chr22:50121524 | G | A | 19 | a0001c0007t0001g0052 a0001c0007t0001g0053 a0001c0007t0001g0054 others(16): Show |
19 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.1569+908G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50121524 | |||||||
| chr22:50121550 | G | A | 1 | a0006c0006t0001g0221 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1569+934G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50121550 | |||||||
| chr22:50121671 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1569+1055G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50121671 | |||||||
| chr22:50121746 | A | G | 2 | a0006c0006t0001g0262 a0006c0006t0001g0298 |
2 | NA19060.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1569+1130A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50121746 | |||||||
| chr22:50121769 | G | A | 2 | a0001c0001t0001g0290 a0001c0028t0001g0283 |
2 | HG01361.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1569+1153G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50121769 | |||||||
| chr22:50121789 | A | G | 10 | a0003c0003t0002g0337 a0003c0003t0002g0340 a0003c0003t0002g0351 others(7): Show |
11 | HG01934.hp1 HG01981.hp2 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.1569+1173A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50121789 | |||||||
| chr22:50121914 | G | A | 1 | a0001c0001t0001g0225 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1569+1298G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50121914 | |||||||
| chr22:50121929 | T | G | 1 | a0002c0002t0002g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1569+1313T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50121929 | |||||||
| chr22:50121943 | C | T | 131 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(128): Show |
133 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.1569+1327C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50121943 | |||||||
| chr22:50122036 | C | T | 45 | a0003c0003t0002g0322 a0003c0003t0002g0323 a0003c0003t0002g0324 others(42): Show |
46 | HG00323.hp1 HG00733.hp2 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.1569+1420C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50122036 | |||||||
| chr22:50122340 | G | T | 111 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(108): Show |
113 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.1569+1724G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50122340 | |||||||
| chr22:50122442 | T | G | 1 | a0006c0006t0001g0257 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1569+1826T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50122442 | |||||||
| chr22:50122723 | TTTTCTTT others(1): Show |
T | 131 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(128): Show |
133 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.1569+2127_1569+213 others(12): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr22 | 50122723 | ||||||
| chr22:50122773 | T | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1569+2157T>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50122773 | |||||||
| chr22:50122789 | A | T | 6 | a0004c0008t0001g0106 a0004c0009t0001g0315 a0005c0004t0001g0128 others(3): Show |
6 | HG01346.hp2 HG01496.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1569+2173A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50122789 | |||||||
| chr22:50122793 | A | T | 59 | a0004c0008t0001g0007 a0004c0008t0001g0084 a0004c0008t0001g0086 others(56): Show |
61 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.1569+2177A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50122793 | |||||||
| chr22:50122797 | A | T | 82 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(79): Show |
86 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1569+2181A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50122797 | |||||||
| chr22:50122797 | AT | A | 131 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(128): Show |
133 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.1569+2186delT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr22 | 50122797 | ||||||
| chr22:50122873 | G | A | 10 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(7): Show |
11 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1569+2257G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50122873 | |||||||
| chr22:50122935 | G | A | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1569+2319G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50122935 | |||||||
| chr22:50122988 | A | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1569+2372A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50122988 | |||||||
| chr22:50123027 | C | T | 20 | a0001c0007t0001g0052 a0001c0007t0001g0053 a0001c0007t0001g0054 others(17): Show |
20 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.1570-2365C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50123027 | |||||||
| chr22:50123155 | C | T | 70 | a0004c0008t0001g0007 a0004c0008t0001g0080 a0004c0008t0001g0084 others(67): Show |
73 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.1570-2237C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50123155 | |||||||
| chr22:50123161 | G | A | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1570-2231G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50123161 | |||||||
| chr22:50123196 | C | CA | 53 | a0001c0001t0001g0002 a0001c0001t0001g0156 a0001c0001t0001g0208 others(50): Show |
54 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.1570-2174dupA | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr22 | 50123196 | ||||||
| chr22:50123196 | C | CAA | 12 | a0001c0007t0001g0052 a0001c0007t0001g0207 a0001c0007t0001g0209 others(9): Show |
12 | HG00323.hp2 HG01070.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.1570-2175_1570-217 others(6): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr22 | 50123196 | ||||||
| chr22:50123196 | C | CAAA | 7 | a0001c0007t0001g0053 a0001c0007t0001g0055 a0001c0007t0001g0056 others(4): Show |
7 | HG00280.hp1 HG00280.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.1570-2176_1570-217 others(7): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr22 | 50123196 | ||||||
| chr22:50123196 | CA | C | 27 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(24): Show |
27 | HG01261.hp1 HG01515.hp2 HG01516.hp2 others(24): Show |
intron_variant | MODIFIER | c.1570-2174delA | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr22 | 50123196 | ||||||
| chr22:50123196 | CAAA | C | 9 | a0002c0002t0002g0012 a0002c0002t0002g0383 a0002c0013t0004g0371 others(6): Show |
9 | HG02293.hp2 HG03471.hp1 NA18954.hp2 others(6): Show |
intron_variant | MODIFIER | c.1570-2176_1570-217 others(7): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr22 | 50123196 | ||||||
| chr22:50123196 | CAAAA | C | 91 | a0002c0002t0002g0003 a0002c0002t0002g0013 a0002c0002t0002g0014 others(88): Show |
93 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.1570-2177_1570-217 others(8): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr22 | 50123196 | ||||||
| chr22:50123369 | T | G | 49 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(46): Show |
49 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.1570-2023T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50123369 | |||||||
| chr22:50123372 | A | G | 1 | a0006c0006t0001g0221 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1570-2020A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50123372 | |||||||
| chr22:50123421 | A | G | 2 | a0001c0001t0001g0208 a0001c0001t0001g0215 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1570-1971A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50123421 | |||||||
| chr22:50123478 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1570-1914C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50123478 | |||||||
| chr22:50123570 | G | A | 4 | a0001c0001t0001g0077 a0006c0006t0001g0069 a0006c0006t0001g0070 others(1): Show |
4 | HG01516.hp2 HG01517.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.1570-1822G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50123570 | |||||||
| chr22:50123581 | T | G | 1 | a0001c0001t0001g0263 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1570-1811T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50123581 | |||||||
| chr22:50123655 | A | G | 2 | a0004c0021t0001g0096 a0004c0021t0001g0099 |
2 | HG01255.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1570-1737A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50123655 | |||||||
| chr22:50123692 | C | T | 8 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1570-1700C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50123692 | |||||||
| chr22:50123882 | G | C | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1570-1510G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50123882 | |||||||
| chr22:50124374 | A | C | 49 | a0002c0002t0002g0003 a0002c0002t0002g0013 a0002c0002t0002g0014 others(46): Show |
50 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.1570-1018A>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50124374 | |||||||
| chr22:50124464 | A | G | 2 | a0001c0001t0001g0140 a0001c0001t0001g0193 |
2 | HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1570-928A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50124464 | |||||||
| chr22:50124478 | G | T | 1 | a0002c0002t0002g0035 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1570-914G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50124478 | |||||||
| chr22:50124516 | C | T | 28 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(25): Show |
28 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1570-876C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50124516 | |||||||
| chr22:50124523 | G | C | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1570-869G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50124523 | |||||||
| chr22:50124587 | C | G | 1 | a0001c0001t0001g0160 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1570-805C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50124587 | |||||||
| chr22:50124594 | A | G | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0150 |
3 | HG01109.hp2 HG01255.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1570-798A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50124594 | |||||||
| chr22:50124711 | T | C | 164 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(161): Show |
167 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1570-681T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50124711 | |||||||
| chr22:50124765 | C | T | 28 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(25): Show |
28 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1570-627C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50124765 | |||||||
| chr22:50124787 | C | G | 1 | a0004c0008t0001g0086 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1570-605C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50124787 | |||||||
| chr22:50124924 | G | A | 4 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0213 others(1): Show |
4 | HG01496.hp2 HG02717.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1570-468G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50124924 | |||||||
| chr22:50124947 | A | G | 8 | a0001c0001t0001g0051 a0001c0001t0001g0060 a0001c0001t0001g0072 others(5): Show |
8 | HG01515.hp2 HG01517.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.1570-445A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50124947 | |||||||
| chr22:50125076 | T | C | 1 | a0001c0007t0001g0053 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1570-316T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50125076 | |||||||
| chr22:50125141 | G | A | 7 | a0001c0001t0001g0243 a0001c0001t0001g0264 a0001c0001t0001g0266 others(4): Show |
7 | NA18974.hp2 NA18981.hp1 NA18994.hp2 others(4): Show |
intron_variant | MODIFIER | c.1570-251G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50125141 | |||||||
| chr22:50125155 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1570-237C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50125155 | |||||||
| chr22:50125166 | G | A | 1 | a0002c0002t0002g0021 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1570-226G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50125166 | |||||||
| chr22:50125279 | C | T | 70 | a0004c0008t0001g0007 a0004c0008t0001g0080 a0004c0008t0001g0084 others(67): Show |
73 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.1570-113C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50125279 | |||||||
| chr22:50125286 | G | A | 1 | a0002c0002t0002g0372 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1570-106G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50125286 | |||||||
| chr22:50125287 | C | T | 1 | a0002c0002t0002g0013 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1570-105C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 10/26 | chr22 | 50125287 | |||||||
| chr22:50125716 | T | A | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1747+147T>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 11/26 | chr22 | 50125716 | |||||||
| chr22:50125752 | G | T | 131 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(128): Show |
133 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.1747+183G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 11/26 | chr22 | 50125752 | |||||||
| chr22:50125755 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1747+186G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 11/26 | chr22 | 50125755 | |||||||
| chr22:50125765 | G | A | 3 | a0001c0001t0003g0174 a0001c0001t0003g0175 a0001c0001t0003g0178 |
3 | HG02109.hp2 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1747+196G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 11/26 | chr22 | 50125765 | |||||||
| chr22:50125783 | G | T | 19 | a0001c0007t0001g0052 a0001c0007t0001g0053 a0001c0007t0001g0054 others(16): Show |
19 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.1747+214G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 11/26 | chr22 | 50125783 | |||||||
| chr22:50125799 | G | T | 1 | a0005c0004t0001g0116 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1747+230G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 11/26 | chr22 | 50125799 | |||||||
| chr22:50125809 | G | A | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1747+240G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 11/26 | chr22 | 50125809 | |||||||
| chr22:50125888 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1748-314C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 11/26 | chr22 | 50125888 | |||||||
| chr22:50125951 | C | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1748-251C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 11/26 | chr22 | 50125951 | |||||||
| chr22:50125954 | A | AT | 111 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(108): Show |
113 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.1748-237dupT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr22 | 50125954 | ||||||
| chr22:50125984 | A | G | 352 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(349): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.1748-218A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 11/26 | chr22 | 50125984 | |||||||
| chr22:50125990 | C | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1748-212C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 11/26 | chr22 | 50125990 | |||||||
| chr22:50126013 | C | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1748-189C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 11/26 | chr22 | 50126013 | |||||||
| chr22:50126035 | G | A | 1 | a0003c0003t0002g0342 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1748-167G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 11/26 | chr22 | 50126035 | |||||||
| chr22:50126081 | T | C | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1748-121T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 11/26 | chr22 | 50126081 | |||||||
| chr22:50126106 | T | C | 70 | a0004c0008t0001g0007 a0004c0008t0001g0080 a0004c0008t0001g0084 others(67): Show |
73 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.1748-96T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 11/26 | chr22 | 50126106 | |||||||
| chr22:50126107 | T | G | 1 | a0001c0005t0001g0288 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1748-95T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 11/26 | chr22 | 50126107 | |||||||
| chr22:50126154 | T | A | 1 | a0001c0011t0001g0050 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1748-48T>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 11/26 | chr22 | 50126154 | |||||||
| chr22:50126189 | A | AT | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
splice_region_variant&intron_variant | LOW | c.1748-7dupT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr22 | 50126189 | ||||||
| chr22:50126309 | A | G | 1 | a0001c0001t0001g0287 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1818+37A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50126309 | |||||||
| chr22:50126321 | C | A | 2 | a0001c0007t0001g0210 a0001c0007t0001g0211 |
2 | HG01257.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1818+49C>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50126321 | |||||||
| chr22:50126343 | C | T | 1 | a0005c0004t0001g0044 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1818+71C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50126343 | |||||||
| chr22:50126445 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1818+173A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50126445 | |||||||
| chr22:50126494 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1818+222T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50126494 | |||||||
| chr22:50126602 | GCT | G | 8 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1818+333_1818+334d others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr22 | 50126602 | ||||||
| chr22:50126675 | G | T | 4 | a0001c0005t0001g0197 a0001c0005t0001g0198 a0001c0005t0001g0199 others(1): Show |
4 | HG01099.hp1 HG01256.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1818+403G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50126675 | |||||||
| chr22:50126701 | TTACTGGT others(4): Show |
T | 1 | a0001c0007t0001g0227 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1818+440_1818+450d others(13): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr22 | 50126701 | ||||||
| chr22:50126787 | A | T | 1 | a0001c0001t0001g0291 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1818+515A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50126787 | |||||||
| chr22:50126885 | A | G | 234 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(231): Show |
240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.1818+613A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50126885 | |||||||
| chr22:50126938 | C | T | 164 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(161): Show |
167 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1818+666C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50126938 | |||||||
| chr22:50126953 | C | G | 1 | a0001c0001t0001g0196 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1818+681C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50126953 | |||||||
| chr22:50127050 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1818+778G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50127050 | |||||||
| chr22:50127090 | G | A | 3 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | HG00733.hp1 HG02698.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1818+818G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50127090 | |||||||
| chr22:50127154 | A | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1818+882A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50127154 | |||||||
| chr22:50127209 | A | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1818+937A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50127209 | |||||||
| chr22:50127260 | G | A | 48 | a0002c0002t0002g0003 a0002c0002t0002g0013 a0002c0002t0002g0014 others(45): Show |
49 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1818+988G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50127260 | |||||||
| chr22:50127291 | C | T | 1 | a0003c0003t0002g0384 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1818+1019C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50127291 | |||||||
| chr22:50127326 | G | A | 21 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(18): Show |
21 | HG01261.hp1 HG01515.hp2 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.1818+1054G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50127326 | |||||||
| chr22:50127479 | A | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1819-937A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50127479 | |||||||
| chr22:50127482 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1819-934C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50127482 | |||||||
| chr22:50127496 | C | T | 1 | a0004c0008t0001g0100 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1819-920C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50127496 | |||||||
| chr22:50127541 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1819-875C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50127541 | |||||||
| chr22:50127684 | T | C | 1 | a0002c0002t0002g0022 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1819-732T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50127684 | |||||||
| chr22:50127753 | T | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1819-663T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50127753 | |||||||
| chr22:50127778 | T | TTG | 101 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(98): Show |
103 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.1819-638_1819-637i others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50127778 | |||||||
| chr22:50127779 | G | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1819-637G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50127779 | |||||||
| chr22:50127780 | T | G | 2 | a0001c0001t0001g0140 a0001c0001t0001g0193 |
2 | HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1819-636T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50127780 | |||||||
| chr22:50127801 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1819-615C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50127801 | |||||||
| chr22:50127835 | C | T | 11 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(8): Show |
12 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1819-581C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50127835 | |||||||
| chr22:50127858 | C | T | 22 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(19): Show |
22 | HG01261.hp1 HG01515.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.1819-558C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50127858 | |||||||
| chr22:50127914 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1819-502A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50127914 | |||||||
| chr22:50127967 | C | T | 1 | a0001c0028t0001g0283 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1819-449C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50127967 | |||||||
| chr22:50128015 | G | A | 1 | a0006c0006t0001g0071 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1819-401G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50128015 | |||||||
| chr22:50128166 | A | G | 1 | a0001c0005t0001g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1819-250A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50128166 | |||||||
| chr22:50128205 | G | C | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1819-211G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50128205 | |||||||
| chr22:50128249 | C | G | 1 | a0001c0001t0001g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1819-167C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50128249 | |||||||
| chr22:50128288 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1819-128T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50128288 | |||||||
| chr22:50128309 | A | G | 1 | a0016c0029t0001g0205 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1819-107A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50128309 | |||||||
| chr22:50128310 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1819-106T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50128310 | |||||||
| chr22:50128352 | T | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1819-64T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50128352 | |||||||
| chr22:50128357 | CTAGA | C | 11 | a0005c0004t0001g0006 a0005c0004t0001g0081 a0005c0004t0001g0085 others(8): Show |
12 | HG02027.hp2 NA18941.hp2 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.1819-56_1819-53del others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr22 | 50128357 | ||||||
| chr22:50128378 | T | C | 4 | a0001c0001t0003g0174 a0001c0001t0003g0175 a0001c0001t0003g0178 others(1): Show |
4 | HG02109.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1819-38T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50128378 | |||||||
| chr22:50128406 | C | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1819-10C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 12/26 | chr22 | 50128406 | |||||||
| chr22:50128540 | C | CT | 34 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0139 others(31): Show |
35 | HG01243.hp1 HG01243.hp2 HG01361.hp2 others(32): Show |
intron_variant | MODIFIER | c.1910+55dupT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr22 | 50128540 | ||||||
| chr22:50128540 | CT | C | 148 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0041 others(145): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.1910+55delT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr22 | 50128540 | ||||||
| chr22:50128540 | CTTTTTTT others(4): Show |
C | 48 | a0002c0002t0002g0003 a0002c0002t0002g0013 a0002c0002t0002g0014 others(45): Show |
49 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1910+45_1910+55del others(11): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr22 | 50128540 | ||||||
| chr22:50128609 | A | G | 19 | a0001c0007t0001g0052 a0001c0007t0001g0053 a0001c0007t0001g0054 others(16): Show |
19 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.1910+102A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50128609 | |||||||
| chr22:50128712 | T | C | 1 | a0016c0029t0001g0205 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1910+205T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50128712 | |||||||
| chr22:50128785 | C | T | 1 | a0002c0002t0002g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1910+278C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50128785 | |||||||
| chr22:50128839 | G | A | 54 | a0002c0010t0002g0331 a0002c0010t0002g0332 a0002c0010t0002g0333 others(51): Show |
55 | HG00323.hp1 HG00733.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.1910+332G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50128839 | |||||||
| chr22:50128845 | C | CT | 8 | a0001c0001t0001g0051 a0001c0001t0001g0060 a0001c0001t0001g0072 others(5): Show |
8 | HG01515.hp2 HG01517.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.1910+351dupT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr22 | 50128845 | ||||||
| chr22:50128905 | G | A | 2 | a0005c0004t0001g0128 a0005c0004t0001g0133 |
2 | HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1910+398G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50128905 | |||||||
| chr22:50128906 | A | T | 1 | a0004c0009t0001g0126 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1910+399A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50128906 | |||||||
| chr22:50128916 | G | C | 352 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(349): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.1910+409G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50128916 | |||||||
| chr22:50128976 | CTT | C | 6 | a0001c0001t0001g0139 a0001c0001t0001g0144 a0001c0001t0001g0145 others(3): Show |
6 | HG02717.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1910+471_1910+472d others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr22 | 50128976 | ||||||
| chr22:50129027 | G | A | 7 | a0001c0001t0003g0174 a0001c0001t0003g0175 a0001c0001t0003g0177 others(4): Show |
7 | HG02109.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1910+520G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50129027 | |||||||
| chr22:50129178 | G | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1910+671G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50129178 | |||||||
| chr22:50129179 | T | C | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1910+672T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50129179 | |||||||
| chr22:50129181 | T | C | 1 | a0005c0004t0001g0101 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1910+674T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50129181 | |||||||
| chr22:50129235 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1910+728G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50129235 | |||||||
| chr22:50129384 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1910+877T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50129384 | |||||||
| chr22:50129465 | T | A | 1 | a0001c0005t0001g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1910+958T>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50129465 | |||||||
| chr22:50129604 | G | A | 1 | a0005c0004t0001g0113 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1910+1097G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50129604 | |||||||
| chr22:50129638 | A | G | 20 | a0001c0007t0001g0052 a0001c0007t0001g0053 a0001c0007t0001g0054 others(17): Show |
20 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.1910+1131A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50129638 | |||||||
| chr22:50129654 | A | T | 2 | a0008c0022t0001g0134 a0008c0022t0001g0135 |
2 | HG01346.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1910+1147A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50129654 | |||||||
| chr22:50129680 | C | T | 1 | a0004c0009t0001g0316 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1910+1173C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50129680 | |||||||
| chr22:50129737 | G | C | 1 | a0001c0001t0001g0286 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1910+1230G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50129737 | |||||||
| chr22:50129854 | C | T | 1 | a0001c0007t0001g0230 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1910+1347C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50129854 | |||||||
| chr22:50129922 | T | C | 6 | a0001c0011t0001g0004 a0001c0011t0001g0046 a0001c0011t0001g0047 others(3): Show |
7 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1910+1415T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50129922 | |||||||
| chr22:50129966 | C | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1910+1459C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50129966 | |||||||
| chr22:50129993 | G | C | 1 | a0005c0004t0001g0088 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1910+1486G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50129993 | |||||||
| chr22:50130045 | G | A | 1 | a0004c0014t0001g0094 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1910+1538G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50130045 | |||||||
| chr22:50130092 | A | G | 75 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0235 others(72): Show |
77 | HG00099.hp2 HG00438.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.1910+1585A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50130092 | |||||||
| chr22:50130134 | G | C | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1910+1627G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50130134 | |||||||
| chr22:50130142 | G | A | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1910+1635G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50130142 | |||||||
| chr22:50130206 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1910+1699C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50130206 | |||||||
| chr22:50130213 | T | G | 1 | a0001c0001t0001g0245 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1910+1706T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50130213 | |||||||
| chr22:50130311 | C | A | 1 | a0001c0001t0001g0266 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1910+1804C>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50130311 | |||||||
| chr22:50130323 | A | G | 1 | a0003c0003t0002g0326 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1910+1816A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50130323 | |||||||
| chr22:50130324 | G | C | 1 | a0003c0003t0002g0326 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1910+1817G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50130324 | |||||||
| chr22:50130417 | A | C | 11 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(8): Show |
12 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1910+1910A>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50130417 | |||||||
| chr22:50130477 | C | T | 23 | a0001c0001t0001g0235 a0001c0001t0001g0246 a0001c0001t0001g0247 others(20): Show |
23 | HG00597.hp1 HG02027.hp1 HG02132.hp1 others(20): Show |
intron_variant | MODIFIER | c.1910+1970C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50130477 | |||||||
| chr22:50130572 | C | T | 2 | a0009c0019t0001g0222 a0009c0019t0001g0223 |
2 | HG01884.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1910+2065C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50130572 | |||||||
| chr22:50130577 | AG | A | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1910+2076delG | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr22 | 50130577 | ||||||
| chr22:50130585 | A | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1910+2078A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50130585 | |||||||
| chr22:50130673 | GGAT | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1910+2172_1910+217 others(7): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr22 | 50130673 | ||||||
| chr22:50130728 | A | C | 1 | a0001c0016t0001g0191 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1910+2221A>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50130728 | |||||||
| chr22:50130773 | G | A | 5 | a0001c0001t0001g0253 a0001c0001t0001g0299 a0001c0001t0001g0301 others(2): Show |
5 | HG02056.hp1 NA18963.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.1910+2266G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50130773 | |||||||
| chr22:50130846 | G | A | 2 | a0001c0001t0001g0302 a0004c0008t0001g0117 |
2 | HG02080.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1910+2339G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50130846 | |||||||
| chr22:50130975 | C | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1910+2468C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50130975 | |||||||
| chr22:50131014 | A | C | 1 | a0006c0025t0001g0079 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1910+2507A>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50131014 | |||||||
| chr22:50131022 | G | A | 8 | a0001c0007t0001g0052 a0001c0007t0001g0053 a0001c0007t0001g0054 others(5): Show |
8 | HG00280.hp1 HG00280.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.1910+2515G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50131022 | |||||||
| chr22:50131054 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1910+2547G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50131054 | |||||||
| chr22:50131063 | A | AT | 7 | a0001c0001t0001g0215 a0001c0005t0001g0197 a0001c0005t0001g0198 others(4): Show |
7 | HG00280.hp1 HG01099.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1910+2575dupT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr22 | 50131063 | ||||||
| chr22:50131063 | AT | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0061 others(140): Show |
147 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(144): Show |
intron_variant | MODIFIER | c.1910+2575delT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr22 | 50131063 | ||||||
| chr22:50131063 | ATT | A | 161 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0140 others(158): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.1910+2574_1910+257 others(6): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr22 | 50131063 | ||||||
| chr22:50131063 | ATTT | A | 23 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(20): Show |
23 | HG01261.hp1 HG01515.hp2 HG01516.hp2 others(20): Show |
intron_variant | MODIFIER | c.1910+2573_1910+257 others(7): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr22 | 50131063 | ||||||
| chr22:50131187 | T | C | 5 | a0001c0007t0001g0210 a0001c0007t0001g0211 a0001c0007t0001g0227 others(2): Show |
5 | HG01070.hp2 HG01192.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1910+2680T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50131187 | |||||||
| chr22:50131191 | G | A | 4 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0007t0001g0052 others(1): Show |
4 | HG02451.hp2 HG03471.hp2 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.1910+2684G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50131191 | |||||||
| chr22:50131238 | A | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0152 a0001c0001t0001g0153 others(106): Show |
113 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.1910+2731A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50131238 | |||||||
| chr22:50131290 | A | T | 6 | a0003c0003t0002g0330 a0003c0003t0002g0347 a0003c0003t0002g0348 others(3): Show |
6 | HG02080.hp2 HG02083.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.1911-2717A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50131290 | |||||||
| chr22:50131361 | C | T | 163 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(160): Show |
166 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1911-2646C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50131361 | |||||||
| chr22:50131672 | T | C | 1 | a0001c0016t0001g0191 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1911-2335T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50131672 | |||||||
| chr22:50131709 | A | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1911-2298A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50131709 | |||||||
| chr22:50131722 | GA | G | 68 | a0001c0001t0001g0301 a0004c0008t0001g0007 a0004c0008t0001g0080 others(65): Show |
71 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.1911-2272delA | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr22 | 50131722 | ||||||
| chr22:50131734 | AAG | A | 42 | a0003c0003t0002g0322 a0003c0003t0002g0323 a0003c0003t0002g0324 others(39): Show |
43 | HG00323.hp1 HG00733.hp2 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1911-2271_1911-227 others(6): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr22 | 50131734 | ||||||
| chr22:50131735 | AG | A | 59 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(56): Show |
60 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.1911-2271delG | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50131735 | |||||||
| chr22:50131767 | G | T | 1 | a0003c0003t0002g0326 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1911-2240G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50131767 | |||||||
| chr22:50131852 | C | T | 1 | a0004c0008t0001g0007 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1911-2155C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50131852 | |||||||
| chr22:50131854 | C | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1911-2153C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50131854 | |||||||
| chr22:50131932 | A | G | 164 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(161): Show |
167 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1911-2075A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50131932 | |||||||
| chr22:50131937 | G | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1911-2070G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50131937 | |||||||
| chr22:50131999 | G | A | 49 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(46): Show |
50 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.1911-2008G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50131999 | |||||||
| chr22:50132169 | A | G | 1 | a0002c0002t0002g0028 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1911-1838A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50132169 | |||||||
| chr22:50132326 | G | C | 3 | a0001c0007t0001g0054 a0001c0007t0001g0056 a0006c0031t0001g0058 |
3 | HG00741.hp1 HG01106.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1911-1681G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50132326 | |||||||
| chr22:50132375 | A | G | 1 | a0003c0003t0004g0381 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1911-1632A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50132375 | |||||||
| chr22:50132423 | A | G | 239 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0041 others(236): Show |
244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1911-1584A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50132423 | |||||||
| chr22:50132444 | G | T | 164 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(161): Show |
167 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1911-1563G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50132444 | |||||||
| chr22:50132448 | A | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1911-1559A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50132448 | |||||||
| chr22:50132524 | G | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1911-1483G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50132524 | |||||||
| chr22:50132534 | C | CAG | 164 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(161): Show |
167 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1911-1472_1911-147 others(6): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr22 | 50132534 | ||||||
| chr22:50132558 | A | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1911-1449A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50132558 | |||||||
| chr22:50132605 | G | A | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1911-1402G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50132605 | |||||||
| chr22:50132692 | C | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1911-1315C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50132692 | |||||||
| chr22:50132731 | G | C | 164 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(161): Show |
167 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1911-1276G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50132731 | |||||||
| chr22:50132742 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1911-1265T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50132742 | |||||||
| chr22:50132950 | T | C | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1911-1057T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50132950 | |||||||
| chr22:50132960 | C | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1911-1047C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50132960 | |||||||
| chr22:50133013 | C | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1911-994C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50133013 | |||||||
| chr22:50133041 | A | AAAAAC | 101 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(98): Show |
103 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.1911-962_1911-961i others(7): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr22 | 50133041 | ||||||
| chr22:50133059 | T | A | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1911-948T>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50133059 | |||||||
| chr22:50133101 | C | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1911-906C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50133101 | |||||||
| chr22:50133241 | G | A | 4 | a0001c0001t0001g0077 a0006c0006t0001g0069 a0006c0006t0001g0070 others(1): Show |
4 | HG01516.hp2 HG01517.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.1911-766G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50133241 | |||||||
| chr22:50133354 | G | A | 2 | a0010c0023t0001g0231 a0010c0023t0001g0232 |
2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1911-653G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50133354 | |||||||
| chr22:50133454 | T | TA | 9 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0004c0008t0001g0106 others(6): Show |
9 | HG00408.hp2 HG01981.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.1911-536dupA | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr22 | 50133454 | ||||||
| chr22:50133454 | TA | T | 54 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(51): Show |
54 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.1911-536delA | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr22 | 50133454 | ||||||
| chr22:50133468 | A | G | 53 | a0002c0010t0002g0331 a0002c0010t0002g0332 a0002c0010t0002g0333 others(50): Show |
54 | HG00323.hp1 HG00733.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.1911-539A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50133468 | |||||||
| chr22:50133506 | CT | C | 113 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(110): Show |
116 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1911-491delT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr22 | 50133506 | ||||||
| chr22:50133718 | A | T | 1 | a0003c0003t0002g0326 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1911-289A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50133718 | |||||||
| chr22:50133719 | T | A | 1 | a0003c0003t0002g0326 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1911-288T>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50133719 | |||||||
| chr22:50133745 | T | C | 28 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(25): Show |
28 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1911-262T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50133745 | |||||||
| chr22:50133878 | T | C | 1 | a0003c0003t0002g0337 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1911-129T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50133878 | |||||||
| chr22:50133977 | A | G | 70 | a0004c0008t0001g0007 a0004c0008t0001g0080 a0004c0008t0001g0084 others(67): Show |
73 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.1911-30A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 13/26 | chr22 | 50133977 | |||||||
| chr22:50134317 | T | TCA | 102 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(99): Show |
104 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.1970-213_1970-212i others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 14/26 | chr22 | 50134317 | |||||||
| chr22:50134318 | T | C | 1 | a0003c0003t0002g0326 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1970-212T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 14/26 | chr22 | 50134318 | |||||||
| chr22:50134319 | A | T | 102 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(99): Show |
104 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.1970-211A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 14/26 | chr22 | 50134319 | |||||||
| chr22:50134321 | G | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1970-209G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 14/26 | chr22 | 50134321 | |||||||
| chr22:50134322 | A | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1970-208A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 14/26 | chr22 | 50134322 | |||||||
| chr22:50134323 | A | G | 102 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(99): Show |
104 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.1970-207A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 14/26 | chr22 | 50134323 | |||||||
| chr22:50134323 | A | T | 1 | a0003c0003t0002g0326 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1970-207A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 14/26 | chr22 | 50134323 | |||||||
| chr22:50134336 | G | A | 1 | a0004c0008t0001g0080 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1970-194G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 14/26 | chr22 | 50134336 | |||||||
| chr22:50134341 | A | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1970-189A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 14/26 | chr22 | 50134341 | |||||||
| chr22:50134652 | T | G | 102 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(99): Show |
104 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.2070+22T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50134652 | |||||||
| chr22:50134654 | C | G | 1 | a0003c0003t0002g0326 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2070+24C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50134654 | |||||||
| chr22:50134679 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2070+49C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50134679 | |||||||
| chr22:50134694 | A | G | 2 | a0002c0010t0002g0331 a0002c0010t0002g0335 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2070+64A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50134694 | |||||||
| chr22:50134737 | G | A | 1 | a0003c0003t0002g0345 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2070+107G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50134737 | |||||||
| chr22:50134745 | G | A | 1 | a0001c0005t0001g0203 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2070+115G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50134745 | |||||||
| chr22:50134794 | C | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.2070+164C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50134794 | |||||||
| chr22:50135031 | T | G | 1 | a0003c0003t0002g0326 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2070+401T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50135031 | |||||||
| chr22:50135032 | G | T | 1 | a0003c0003t0002g0326 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2070+402G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50135032 | |||||||
| chr22:50135063 | GAGTGCAG others(7): Show |
G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.2070+435_2070+448d others(16): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr22 | 50135063 | ||||||
| chr22:50135183 | T | G | 70 | a0004c0008t0001g0007 a0004c0008t0001g0080 a0004c0008t0001g0084 others(67): Show |
73 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.2070+553T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50135183 | |||||||
| chr22:50135261 | C | T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.2070+631C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50135261 | |||||||
| chr22:50135306 | C | A | 1 | a0003c0003t0002g0326 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2070+676C>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50135306 | |||||||
| chr22:50135601 | A | G | 11 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(8): Show |
12 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.2070+971A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50135601 | |||||||
| chr22:50135715 | C | A | 2 | a0001c0007t0001g0210 a0001c0007t0001g0211 |
2 | HG01257.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2070+1085C>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50135715 | |||||||
| chr22:50135750 | CA | C | 8 | a0001c0001t0001g0051 a0001c0001t0001g0160 a0001c0001t0001g0254 others(5): Show |
8 | HG01515.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2070+1137delA | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr22 | 50135750 | ||||||
| chr22:50135797 | G | C | 21 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(18): Show |
21 | HG01261.hp1 HG01515.hp2 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.2070+1167G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50135797 | |||||||
| chr22:50135850 | T | C | 11 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0139 others(8): Show |
11 | HG02258.hp1 HG02451.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2070+1220T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50135850 | |||||||
| chr22:50135959 | T | A | 54 | a0002c0010t0002g0331 a0002c0010t0002g0332 a0002c0010t0002g0333 others(51): Show |
55 | HG00323.hp1 HG00733.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.2070+1329T>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50135959 | |||||||
| chr22:50136134 | C | T | 1 | a0004c0009t0001g0314 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2070+1504C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50136134 | |||||||
| chr22:50136153 | T | C | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2070+1523T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50136153 | |||||||
| chr22:50136202 | C | T | 1 | a0010c0023t0001g0231 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2070+1572C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50136202 | |||||||
| chr22:50136495 | A | G | 19 | a0001c0007t0001g0052 a0001c0007t0001g0053 a0001c0007t0001g0054 others(16): Show |
19 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.2070+1865A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50136495 | |||||||
| chr22:50136866 | C | T | 1 | a0001c0001t0003g0195 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2070+2236C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50136866 | |||||||
| chr22:50136931 | A | G | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2070+2301A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50136931 | |||||||
| chr22:50136970 | T | C | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2070+2340T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50136970 | |||||||
| chr22:50137167 | C | A | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2070+2537C>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50137167 | |||||||
| chr22:50137195 | A | G | 1 | a0005c0004t0001g0119 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2070+2565A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50137195 | |||||||
| chr22:50137205 | C | A | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2070+2575C>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50137205 | |||||||
| chr22:50137206 | C | G | 1 | a0003c0003t0002g0326 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2070+2576C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50137206 | |||||||
| chr22:50137207 | G | C | 1 | a0003c0003t0002g0326 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2070+2577G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50137207 | |||||||
| chr22:50137266 | G | T | 1 | a0001c0005t0001g0203 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2070+2636G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50137266 | |||||||
| chr22:50137336 | C | G | 4 | a0004c0008t0001g0106 a0004c0008t0001g0117 a0004c0021t0001g0096 others(1): Show |
4 | HG01255.hp1 HG03490.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2070+2706C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50137336 | |||||||
| chr22:50137496 | G | A | 1 | a0003c0003t0002g0355 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2070+2866G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50137496 | |||||||
| chr22:50137591 | G | A | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2070+2961G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50137591 | |||||||
| chr22:50137619 | C | T | 1 | a0002c0002t0002g0021 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2070+2989C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50137619 | |||||||
| chr22:50137654 | A | G | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2070+3024A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50137654 | |||||||
| chr22:50137670 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2070+3040G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50137670 | |||||||
| chr22:50137695 | ACT | A | 5 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2070+3068_2070+306 others(6): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr22 | 50137695 | ||||||
| chr22:50137727 | C | CATATATA others(24): Show |
2 | a0004c0008t0001g0125 a0004c0008t0001g0127 |
2 | HG02015.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.2070+3103_2070+313 others(35): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr22 | 50137727 | ||||||
| chr22:50137733 | T | C | 21 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(18): Show |
21 | HG01261.hp1 HG01515.hp2 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.2070+3103T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50137733 | |||||||
| chr22:50137733 | T | TATATTTT others(24): Show |
66 | a0001c0001t0001g0233 a0001c0001t0001g0277 a0001c0001t0001g0278 others(63): Show |
69 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.2070+3180_2070+321 others(35): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr22 | 50137733 | ||||||
| chr22:50137733 | T | TATATTTT others(55): Show |
7 | a0004c0008t0001g0086 a0004c0008t0001g0100 a0004c0008t0001g0108 others(4): Show |
7 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.2070+3149_2070+321 others(66): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr22 | 50137733 | ||||||
| chr22:50137733 | T | TATATTTT others(86): Show |
5 | a0004c0014t0001g0098 a0004c0014t0001g0110 a0004c0014t0001g0206 others(2): Show |
5 | HG01106.hp2 HG01346.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.2070+3118_2070+321 others(97): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr22 | 50137733 | ||||||
| chr22:50137733 | T | TATATTTT others(117): Show |
1 | a0004c0014t0001g0094 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2070+3210_2070+321 others(128): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr22 | 50137733 | ||||||
| chr22:50137733 | TATATTTT others(24): Show |
T | 19 | a0001c0007t0001g0052 a0001c0007t0001g0053 a0001c0007t0001g0054 others(16): Show |
19 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.2070+3180_2070+321 others(35): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr22 | 50137733 | ||||||
| chr22:50137741 | A | T | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2070+3111A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50137741 | |||||||
| chr22:50137748 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2070+3118T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50137748 | |||||||
| chr22:50137748 | T | TACATATA others(24): Show |
2 | a0001c0001t0001g0051 a0001c0001t0001g0060 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2070+3148_2070+314 others(35): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr22 | 50137748 | ||||||
| chr22:50137758 | A | C | 13 | a0003c0003t0002g0342 a0003c0003t0002g0350 a0003c0003t0002g0355 others(10): Show |
13 | HG00323.hp1 HG00733.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.2070+3128A>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50137758 | |||||||
| chr22:50137770 | T | A | 1 | a0001c0001t0001g0009 | 2 | HG02015.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.2070+3140T>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50137770 | |||||||
| chr22:50137770 | T | TTATATAT others(24): Show |
1 | a0005c0004t0001g0087 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2070+3170_2070+317 others(35): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr22 | 50137770 | ||||||
| chr22:50137770 | TTA | T | 104 | a0001c0001t0001g0284 a0002c0002t0002g0003 a0002c0002t0002g0012 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2070+3149_2070+315 others(6): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr22 | 50137770 | ||||||
| chr22:50137770 | TTATATAT others(26): Show |
T | 1 | a0002c0002t0002g0038 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2070+3149_2070+318 others(37): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr22 | 50137770 | ||||||
| chr22:50137779 | T | C | 21 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(18): Show |
21 | HG01261.hp1 HG01515.hp2 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.2070+3149T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50137779 | |||||||
| chr22:50137783 | TATATAAA others(51): Show |
T | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.2070+3159_2070+321 others(62): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr22 | 50137783 | ||||||
| chr22:50137810 | T | C | 21 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(18): Show |
21 | HG01261.hp1 HG01515.hp2 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.2070+3180T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50137810 | |||||||
| chr22:50137828 | T | C | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2070+3198T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50137828 | |||||||
| chr22:50137829 | A | ATTTTATA others(23): Show |
2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2070+3213_2070+324 others(34): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr22 | 50137829 | ||||||
| chr22:50137953 | G | T | 1 | a0004c0008t0001g0124 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2070+3323G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50137953 | |||||||
| chr22:50137954 | G | A | 1 | a0004c0008t0001g0124 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2070+3324G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50137954 | |||||||
| chr22:50137956 | T | A | 1 | a0004c0008t0001g0124 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2070+3326T>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50137956 | |||||||
| chr22:50138011 | C | T | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0196 |
3 | HG02258.hp1 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2070+3381C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50138011 | |||||||
| chr22:50138290 | C | T | 1 | a0004c0009t0001g0315 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2070+3660C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50138290 | |||||||
| chr22:50138789 | C | G | 1 | a0003c0003t0002g0326 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2071-3292C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50138789 | |||||||
| chr22:50138790 | G | C | 1 | a0003c0003t0002g0326 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2071-3291G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50138790 | |||||||
| chr22:50138795 | C | A | 2 | a0001c0001t0001g0277 a0001c0001t0001g0287 |
2 | HG01074.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.2071-3286C>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50138795 | |||||||
| chr22:50138895 | G | A | 10 | a0002c0002t0002g0338 a0002c0002t0002g0367 a0002c0002t0002g0368 others(7): Show |
10 | HG00621.hp2 HG00639.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.2071-3186G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50138895 | |||||||
| chr22:50138945 | G | A | 10 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(7): Show |
11 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2071-3136G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50138945 | |||||||
| chr22:50139005 | AT | A | 10 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0193 others(7): Show |
10 | HG00323.hp2 HG02486.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2071-3061delT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr22 | 50139005 | ||||||
| chr22:50139092 | A | G | 55 | a0002c0010t0002g0331 a0002c0010t0002g0332 a0002c0010t0002g0333 others(52): Show |
56 | HG00323.hp1 HG00733.hp2 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.2071-2989A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50139092 | |||||||
| chr22:50139147 | C | T | 1 | a0002c0002t0002g0372 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2071-2934C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50139147 | |||||||
| chr22:50139184 | C | T | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2071-2897C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50139184 | |||||||
| chr22:50139253 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2071-2828C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50139253 | |||||||
| chr22:50139609 | A | G | 1 | a0006c0006t0001g0259 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2071-2472A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50139609 | |||||||
| chr22:50139646 | G | A | 49 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(46): Show |
50 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2071-2435G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50139646 | |||||||
| chr22:50139875 | C | T | 27 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(24): Show |
27 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.2071-2206C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50139875 | |||||||
| chr22:50139957 | G | A | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2071-2124G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50139957 | |||||||
| chr22:50140015 | G | A | 1 | a0003c0003t0002g0341 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2071-2066G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50140015 | |||||||
| chr22:50140021 | A | T | 27 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(24): Show |
27 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.2071-2060A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50140021 | |||||||
| chr22:50140074 | A | G | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2071-2007A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50140074 | |||||||
| chr22:50140193 | A | G | 1 | a0002c0002t0002g0034 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2071-1888A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50140193 | |||||||
| chr22:50140356 | T | C | 1 | a0019c0026t0001g0114 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2071-1725T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50140356 | |||||||
| chr22:50140384 | A | G | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.2071-1697A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50140384 | |||||||
| chr22:50140584 | T | C | 1 | a0006c0006t0001g0260 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2071-1497T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50140584 | |||||||
| chr22:50140690 | C | T | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2071-1391C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50140690 | |||||||
| chr22:50140729 | C | CT | 8 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.2071-1341dupT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr22 | 50140729 | ||||||
| chr22:50140729 | C | CTTTT | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.2071-1344_2071-134 others(8): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr22 | 50140729 | ||||||
| chr22:50140741 | G | T | 1 | a0003c0003t0002g0326 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2071-1340G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50140741 | |||||||
| chr22:50140774 | G | A | 1 | a0005c0004t0001g0088 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2071-1307G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50140774 | |||||||
| chr22:50140785 | C | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0235 others(73): Show |
78 | HG00099.hp2 HG00438.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.2071-1296C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50140785 | |||||||
| chr22:50141052 | CT | C | 21 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(18): Show |
21 | HG01261.hp1 HG01515.hp2 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.2071-1017delT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr22 | 50141052 | ||||||
| chr22:50141060 | T | G | 8 | a0001c0001t0001g0290 a0001c0028t0001g0283 a0003c0003t0002g0330 others(5): Show |
8 | HG01361.hp1 HG02080.hp2 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.2071-1021T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50141060 | |||||||
| chr22:50141061 | T | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0141 others(17): Show |
22 | HG00741.hp2 HG01109.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.2071-1020T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50141061 | |||||||
| chr22:50141083 | G | C | 1 | a0001c0007t0001g0057 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2071-998G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50141083 | |||||||
| chr22:50141121 | G | T | 1 | a0002c0002t0002g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2071-960G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50141121 | |||||||
| chr22:50141146 | G | T | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2071-935G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50141146 | |||||||
| chr22:50141328 | G | A | 2 | a0001c0001t0001g0290 a0001c0028t0001g0283 |
2 | HG01361.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2071-753G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50141328 | |||||||
| chr22:50141328 | G | T | 1 | a0001c0007t0001g0057 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2071-753G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50141328 | |||||||
| chr22:50141335 | CTT | C | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2071-735_2071-734d others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr22 | 50141335 | ||||||
| chr22:50141377 | T | C | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2071-704T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50141377 | |||||||
| chr22:50141472 | G | T | 1 | a0002c0002t0002g0377 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2071-609G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50141472 | |||||||
| chr22:50141495 | A | AT | 13 | a0001c0001t0001g0140 a0001c0001t0001g0307 a0001c0001t0003g0174 others(10): Show |
13 | HG02074.hp1 HG02109.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.2071-570dupT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr22 | 50141495 | ||||||
| chr22:50141495 | A | ATTTT | 41 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(38): Show |
42 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.2071-573_2071-570d others(6): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr22 | 50141495 | ||||||
| chr22:50141495 | A | ATTTTT | 6 | a0002c0002t0002g0033 a0002c0002t0002g0372 a0002c0002t0002g0385 others(3): Show |
6 | HG01257.hp2 HG01358.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.2071-574_2071-570d others(7): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr22 | 50141495 | ||||||
| chr22:50141495 | A | ATTTTTT | 48 | a0002c0010t0002g0331 a0002c0010t0002g0332 a0002c0010t0002g0333 others(45): Show |
49 | HG00323.hp1 HG00733.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.2071-575_2071-570d others(8): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr22 | 50141495 | ||||||
| chr22:50141495 | A | ATTTTTTT | 6 | a0002c0010t0002g0387 a0003c0003t0002g0346 a0003c0003t0002g0348 others(3): Show |
6 | HG01123.hp1 HG02145.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.2071-576_2071-570d others(9): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr22 | 50141495 | ||||||
| chr22:50141495 | AT | A | 33 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(30): Show |
33 | HG01261.hp1 HG01496.hp2 HG01515.hp2 others(30): Show |
intron_variant | MODIFIER | c.2071-570delT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr22 | 50141495 | ||||||
| chr22:50141495 | ATT | A | 11 | a0001c0001t0001g0214 a0001c0001t0001g0224 a0001c0001t0001g0225 others(8): Show |
12 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.2071-571_2071-570d others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr22 | 50141495 | ||||||
| chr22:50141512 | G | T | 1 | a0003c0003t0002g0326 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2071-569G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50141512 | |||||||
| chr22:50141573 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2071-508C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50141573 | |||||||
| chr22:50141615 | T | C | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2071-466T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50141615 | |||||||
| chr22:50141620 | G | A | 6 | a0001c0011t0001g0004 a0001c0011t0001g0046 a0001c0011t0001g0047 others(3): Show |
7 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2071-461G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50141620 | |||||||
| chr22:50141634 | C | T | 20 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(17): Show |
20 | HG01261.hp1 HG01515.hp2 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.2071-447C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50141634 | |||||||
| chr22:50141684 | G | C | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.2071-397G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50141684 | |||||||
| chr22:50141715 | C | A | 1 | a0003c0003t0002g0326 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2071-366C>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50141715 | |||||||
| chr22:50141839 | C | G | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0149 others(1): Show |
4 | HG02717.hp1 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2071-242C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50141839 | |||||||
| chr22:50141973 | A | T | 1 | a0001c0001t0001g0239 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2071-108A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 15/26 | chr22 | 50141973 | |||||||
| chr22:50142265 | G | T | 21 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(18): Show |
21 | HG01261.hp1 HG01515.hp2 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.2179+76G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 16/26 | chr22 | 50142265 | |||||||
| chr22:50142270 | C | T | 55 | a0002c0010t0002g0331 a0002c0010t0002g0332 a0002c0010t0002g0333 others(52): Show |
56 | HG00323.hp1 HG00733.hp2 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.2179+81C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 16/26 | chr22 | 50142270 | |||||||
| chr22:50142447 | T | A | 1 | a0003c0003t0002g0326 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2179+258T>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 16/26 | chr22 | 50142447 | |||||||
| chr22:50142475 | G | A | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2179+286G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 16/26 | chr22 | 50142475 | |||||||
| chr22:50142665 | T | TA | 14 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(11): Show |
15 | HG01243.hp2 HG01255.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2180-365dupA | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr22 | 50142665 | ||||||
| chr22:50142692 | C | G | 1 | a0002c0002t0002g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2180-351C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 16/26 | chr22 | 50142692 | |||||||
| chr22:50142728 | C | T | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2180-315C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 16/26 | chr22 | 50142728 | |||||||
| chr22:50142808 | G | C | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2180-235G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 16/26 | chr22 | 50142808 | |||||||
| chr22:50142823 | G | C | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2180-220G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 16/26 | chr22 | 50142823 | |||||||
| chr22:50142870 | G | A | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2180-173G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 16/26 | chr22 | 50142870 | |||||||
| chr22:50142962 | C | T | 12 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(9): Show |
13 | HG01243.hp2 HG01255.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2180-81C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 16/26 | chr22 | 50142962 | |||||||
| chr22:50142963 | G | A | 9 | a0002c0010t0002g0331 a0002c0010t0002g0332 a0002c0010t0002g0333 others(6): Show |
9 | HG01884.hp1 HG02145.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.2180-80G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 16/26 | chr22 | 50142963 | |||||||
| chr22:50143278 | T | C | 106 | a0001c0001t0001g0241 a0001c0001t0001g0256 a0002c0002t0002g0003 others(103): Show |
108 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.2358+57T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 17/26 | chr22 | 50143278 | |||||||
| chr22:50143461 | C | A | 103 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(100): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.2358+240C>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 17/26 | chr22 | 50143461 | |||||||
| chr22:50143530 | C | T | 2 | a0002c0010t0002g0349 a0002c0010t0002g0387 |
2 | HG02145.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2358+309C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 17/26 | chr22 | 50143530 | |||||||
| chr22:50143617 | C | T | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2358+396C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 17/26 | chr22 | 50143617 | |||||||
| chr22:50143646 | G | A | 32 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0061 others(29): Show |
34 | HG00741.hp2 HG01109.hp2 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.2358+425G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 17/26 | chr22 | 50143646 | |||||||
| chr22:50143665 | C | T | 1 | a0002c0002t0002g0025 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2359-432C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 17/26 | chr22 | 50143665 | |||||||
| chr22:50143727 | C | T | 1 | a0001c0001t0001g0276 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2359-370C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 17/26 | chr22 | 50143727 | |||||||
| chr22:50143798 | G | A | 6 | a0003c0012t0002g0317 a0003c0012t0002g0318 a0003c0012t0002g0319 others(3): Show |
6 | HG00323.hp1 HG01070.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.2359-299G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 17/26 | chr22 | 50143798 | |||||||
| chr22:50143808 | G | A | 73 | a0001c0005t0001g0165 a0001c0007t0001g0216 a0001c0007t0001g0217 others(70): Show |
76 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.2359-289G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 17/26 | chr22 | 50143808 | |||||||
| chr22:50143824 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2359-273C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 17/26 | chr22 | 50143824 | |||||||
| chr22:50143849 | ACT | A | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2359-245_2359-244d others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr22 | 50143849 | ||||||
| chr22:50143903 | T | G | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2359-194T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 17/26 | chr22 | 50143903 | |||||||
| chr22:50143987 | C | T | 1 | a0005c0004t0001g0122 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2359-110C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 17/26 | chr22 | 50143987 | |||||||
| chr22:50144037 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2359-60C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 17/26 | chr22 | 50144037 | |||||||
| chr22:50144053 | G | A | 1 | a0016c0029t0001g0205 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2359-44G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 17/26 | chr22 | 50144053 | |||||||
| chr22:50144294 | A | T | 1 | a0021c0038t0001g0170 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2505+51A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144294 | |||||||
| chr22:50144346 | A | G | 1 | a0001c0005t0001g0169 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2505+103A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144346 | |||||||
| chr22:50144439 | C | A | 19 | a0001c0005t0001g0171 a0001c0005t0001g0197 a0002c0010t0002g0349 others(16): Show |
19 | HG00140.hp2 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.2505+196C>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144439 | |||||||
| chr22:50144449 | CTG | C | 183 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0072 others(180): Show |
188 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.2505+211_2505+212d others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr22 | 50144449 | ||||||
| chr22:50144587 | G | GT | 54 | a0001c0001t0001g0265 a0002c0010t0002g0331 a0002c0010t0002g0332 others(51): Show |
56 | HG00323.hp1 HG00733.hp2 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.2505+356dupT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr22 | 50144587 | ||||||
| chr22:50144587 | GTT | G | 80 | a0001c0001t0001g0072 a0001c0001t0001g0224 a0001c0001t0001g0225 others(77): Show |
82 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.2505+355_2505+356d others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr22 | 50144587 | ||||||
| chr22:50144592 | T | G | 25 | a0001c0001t0001g0142 a0001c0001t0001g0268 a0001c0005t0001g0172 others(22): Show |
25 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(22): Show |
intron_variant | MODIFIER | c.2505+349T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144592 | |||||||
| chr22:50144594 | T | G | 79 | a0001c0001t0001g0072 a0001c0001t0001g0224 a0001c0001t0001g0225 others(76): Show |
81 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.2505+351T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144594 | |||||||
| chr22:50144616 | G | C | 1 | a0002c0010t0002g0335 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2505+373G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144616 | |||||||
| chr22:50144620 | C | T | 1 | a0006c0006t0001g0071 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2505+377C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144620 | |||||||
| chr22:50144631 | A | G | 2 | a0002c0002t0002g0037 a0016c0029t0001g0205 |
2 | HG02145.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2505+388A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144631 | |||||||
| chr22:50144642 | C | T | 1 | a0016c0029t0001g0205 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2505+399C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144642 | |||||||
| chr22:50144643 | A | G | 4 | a0001c0001t0001g0247 a0001c0007t0001g0059 a0002c0002t0002g0037 others(1): Show |
4 | HG02145.hp1 HG02293.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.2505+400A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144643 | |||||||
| chr22:50144644 | T | C | 2 | a0001c0007t0001g0059 a0016c0029t0001g0205 |
2 | HG02145.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.2505+401T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144644 | |||||||
| chr22:50144644 | T | G | 1 | a0002c0002t0002g0037 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2505+401T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144644 | |||||||
| chr22:50144674 | C | T | 6 | a0003c0003t0002g0330 a0003c0003t0002g0347 a0003c0003t0002g0348 others(3): Show |
6 | HG02080.hp2 HG02083.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.2505+431C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144674 | |||||||
| chr22:50144675 | A | G | 7 | a0001c0001t0001g0142 a0003c0003t0002g0330 a0003c0003t0002g0347 others(4): Show |
7 | HG02080.hp2 HG02083.hp2 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.2505+432A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144675 | |||||||
| chr22:50144707 | A | G | 26 | a0001c0001t0001g0268 a0001c0001t0001g0287 a0001c0001t0001g0294 others(23): Show |
26 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.2505+464A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144707 | |||||||
| chr22:50144743 | G | A | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 |
3 | HG01261.hp1 HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.2505+500G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144743 | |||||||
| chr22:50144774 | A | C | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.2505+531A>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144774 | |||||||
| chr22:50144774 | A | G | 2 | a0001c0001t0001g0074 a0001c0001t0001g0078 |
2 | NA19064.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.2505+531A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144774 | |||||||
| chr22:50144782 | C | T | 2 | a0003c0003t0002g0341 a0003c0003t0002g0343 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2505+539C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144782 | |||||||
| chr22:50144783 | G | A | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0002c0010t0002g0349 others(1): Show |
4 | HG02004.hp2 HG02145.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.2505+540G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144783 | |||||||
| chr22:50144803 | G | A | 43 | a0001c0001t0001g0253 a0002c0002t0002g0013 a0002c0002t0002g0014 others(40): Show |
43 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.2505+560G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144803 | |||||||
| chr22:50144803 | G | C | 1 | a0006c0025t0001g0079 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2505+560G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144803 | |||||||
| chr22:50144816 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0041 others(61): Show |
67 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.2505+573C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144816 | |||||||
| chr22:50144817 | A | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0041 others(247): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.2505+574A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144817 | |||||||
| chr22:50144823 | T | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0041 others(247): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.2505+580T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144823 | |||||||
| chr22:50144824 | G | A | 68 | a0001c0001t0001g0042 a0001c0001t0001g0136 a0001c0001t0001g0208 others(65): Show |
70 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.2505+581G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144824 | |||||||
| chr22:50144828 | G | A | 68 | a0001c0001t0001g0042 a0001c0001t0001g0136 a0001c0001t0001g0208 others(65): Show |
70 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.2505+585G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144828 | |||||||
| chr22:50144832 | C | G | 1 | a0001c0007t0001g0055 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2505+589C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144832 | |||||||
| chr22:50144832 | C | T | 205 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0063 others(202): Show |
210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.2505+589C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144832 | |||||||
| chr22:50144833 | G | A | 1 | a0002c0013t0002g0043 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2505+590G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144833 | |||||||
| chr22:50144842 | A | G | 3 | a0002c0013t0002g0336 a0002c0013t0002g0365 a0002c0013t0004g0371 |
3 | NA18955.hp2 NA18977.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.2505+599A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144842 | |||||||
| chr22:50144854 | T | G | 1 | a0003c0012t0002g0317 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2505+611T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144854 | |||||||
| chr22:50144860 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2505+617C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144860 | |||||||
| chr22:50144872 | T | C | 1 | a0002c0013t0002g0043 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2505+629T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144872 | |||||||
| chr22:50144932 | G | A | 13 | a0001c0001t0001g0072 a0001c0001t0001g0224 a0001c0001t0001g0225 others(10): Show |
14 | HG01243.hp2 HG01255.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2505+689G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50144932 | |||||||
| chr22:50145069 | A | C | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2506-620A>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50145069 | |||||||
| chr22:50145236 | C | G | 1 | a0002c0013t0002g0366 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2506-453C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50145236 | |||||||
| chr22:50145253 | G | A | 102 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(99): Show |
104 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.2506-436G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50145253 | |||||||
| chr22:50145290 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2506-399C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50145290 | |||||||
| chr22:50145315 | C | G | 358 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(355): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.2506-374C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50145315 | |||||||
| chr22:50145342 | A | T | 1 | a0001c0005t0001g0176 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2506-347A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50145342 | |||||||
| chr22:50145432 | T | C | 1 | a0006c0006t0001g0221 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2506-257T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50145432 | |||||||
| chr22:50145494 | T | A | 1 | a0001c0001t0001g0285 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2506-195T>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50145494 | |||||||
| chr22:50145539 | A | G | 1 | a0002c0002t0002g0369 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2506-150A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 18/26 | chr22 | 50145539 | |||||||
| chr22:50145819 | C | T | 20 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(17): Show |
20 | HG01261.hp1 HG01515.hp2 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.2627+9C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50145819 | |||||||
| chr22:50145832 | C | A | 13 | a0001c0001t0001g0072 a0001c0001t0001g0224 a0001c0001t0001g0225 others(10): Show |
14 | HG01243.hp2 HG01255.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2627+22C>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50145832 | |||||||
| chr22:50145833 | G | A | 1 | a0003c0003t0002g0361 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2627+23G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50145833 | |||||||
| chr22:50145850 | G | C | 8 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.2627+40G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50145850 | |||||||
| chr22:50145939 | G | A | 1 | a0004c0008t0001g0092 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2627+129G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50145939 | |||||||
| chr22:50145950 | G | C | 1 | a0001c0005t0001g0176 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2627+140G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50145950 | |||||||
| chr22:50145987 | C | T | 19 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0141 others(16): Show |
21 | HG00741.hp2 HG01109.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.2627+177C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50145987 | |||||||
| chr22:50146059 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2627+249G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50146059 | |||||||
| chr22:50146148 | A | AGGCCTGG others(6): Show |
104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2627+345_2627+346i others(15): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50146148 | ||||||
| chr22:50146179 | C | CT | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2627+369_2627+370i others(3): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50146179 | |||||||
| chr22:50146197 | G | A | 1 | a0010c0023t0001g0231 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2627+387G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50146197 | |||||||
| chr22:50146247 | G | T | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2627+437G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50146247 | |||||||
| chr22:50146252 | G | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0196 |
3 | HG02258.hp1 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2627+442G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50146252 | |||||||
| chr22:50146264 | C | T | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2627+454C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50146264 | |||||||
| chr22:50146319 | G | A | 1 | a0002c0002t0002g0013 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2627+509G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50146319 | |||||||
| chr22:50146366 | G | T | 1 | a0002c0002t0004g0016 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2627+556G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50146366 | |||||||
| chr22:50146372 | G | A | 82 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(79): Show |
84 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.2627+562G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50146372 | |||||||
| chr22:50146391 | C | A | 3 | a0007c0015t0002g0023 a0007c0015t0002g0026 a0007c0015t0002g0027 |
3 | HG00140.hp1 HG00735.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.2627+581C>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50146391 | |||||||
| chr22:50146519 | C | T | 1 | a0023c0039t0001g0187 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2627+709C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50146519 | |||||||
| chr22:50146707 | G | A | 1 | a0006c0006t0001g0221 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2627+897G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50146707 | |||||||
| chr22:50146745 | T | G | 114 | a0001c0001t0001g0072 a0001c0001t0001g0224 a0001c0001t0001g0225 others(111): Show |
117 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.2627+935T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50146745 | |||||||
| chr22:50146804 | G | A | 2 | a0011c0018t0001g0075 a0011c0018t0001g0076 |
2 | NA18950.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2627+994G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50146804 | |||||||
| chr22:50146908 | C | G | 1 | a0003c0012t0002g0317 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2627+1098C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50146908 | |||||||
| chr22:50146985 | G | A | 2 | a0005c0020t0001g0083 a0005c0020t0001g0112 |
2 | HG02040.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.2627+1175G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50146985 | |||||||
| chr22:50147013 | C | G | 108 | a0001c0001t0001g0008 a0001c0001t0001g0151 a0002c0002t0002g0003 others(105): Show |
110 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.2627+1203C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147013 | |||||||
| chr22:50147099 | G | A | 70 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0235 others(67): Show |
72 | HG00099.hp2 HG00438.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.2627+1289G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147099 | |||||||
| chr22:50147166 | G | A | 98 | a0001c0001t0001g0008 a0001c0001t0001g0151 a0002c0002t0002g0003 others(95): Show |
100 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.2627+1356G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147166 | |||||||
| chr22:50147175 | G | GGCAGGCC others(89): Show |
1 | a0001c0005t0001g0292 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2627+1387_2627+148 others(100): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147175 | ||||||
| chr22:50147175 | G | GGCAGGCC others(41): Show |
9 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0007t0001g0219 others(6): Show |
9 | HG00597.hp2 HG01891.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.2627+1386_2627+138 others(52): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147175 | ||||||
| chr22:50147175 | G | GGCAGGCC others(89): Show |
1 | a0004c0008t0001g0092 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2627+1386_2627+138 others(100): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147175 | ||||||
| chr22:50147175 | G | GGCAGGCC others(137): Show |
1 | a0002c0002t0002g0018 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2627+1386_2627+138 others(148): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147175 | ||||||
| chr22:50147175 | G | GGCAGGCC others(185): Show |
2 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
2 | HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2627+1386_2627+138 others(196): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147175 | ||||||
| chr22:50147175 | G | GGCAGGCC others(233): Show |
2 | a0002c0002t0002g0019 a0003c0003t0004g0381 |
2 | NA18969.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.2627+1386_2627+138 others(244): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147175 | ||||||
| chr22:50147175 | G | GGCAGGCC others(281): Show |
1 | a0010c0023t0001g0231 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2627+1386_2627+138 others(292): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147175 | ||||||
| chr22:50147175 | G | GGCAGGCC others(425): Show |
1 | a0001c0001t0001g0072 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2627+1386_2627+138 others(436): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147175 | ||||||
| chr22:50147175 | G | GGCAGGCC others(473): Show |
1 | a0010c0023t0001g0232 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2627+1386_2627+138 others(484): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147175 | ||||||
| chr22:50147175 | GGCAGGCC others(41): Show |
G | 27 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0290 others(24): Show |
27 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.2627+1387_2627+143 others(52): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147175 | ||||||
| chr22:50147175 | GGCAGGCC others(89): Show |
G | 23 | a0001c0001t0001g0136 a0001c0001t0001g0141 a0001c0001t0001g0142 others(20): Show |
24 | HG00280.hp1 HG00621.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.2627+1387_2627+148 others(100): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147175 | ||||||
| chr22:50147175 | GGCAGGCC others(137): Show |
G | 36 | a0001c0001t0001g0145 a0001c0001t0001g0208 a0001c0001t0001g0224 others(33): Show |
36 | HG00140.hp1 HG00280.hp2 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.2627+1387_2627+153 others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147175 | ||||||
| chr22:50147175 | GGCAGGCC others(185): Show |
G | 27 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0147 others(24): Show |
29 | HG00741.hp1 HG01070.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.2627+1387_2627+157 others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147175 | ||||||
| chr22:50147175 | GGCAGGCC others(233): Show |
G | 28 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(25): Show |
29 | HG00741.hp2 HG01496.hp2 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.2627+1387_2627+162 others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147175 | ||||||
| chr22:50147175 | GGCAGGCC others(281): Show |
G | 24 | a0001c0001t0001g0008 a0001c0001t0001g0064 a0001c0001t0001g0065 others(21): Show |
25 | HG00408.hp1 HG01243.hp1 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.2627+1387_2627+167 others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147175 | ||||||
| chr22:50147175 | GGCAGGCC others(329): Show |
G | 5 | a0001c0030t0001g0143 a0003c0003t0002g0340 a0003c0003t0002g0354 others(2): Show |
5 | HG00323.hp1 HG01981.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2627+1387_2627+172 others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147175 | ||||||
| chr22:50147197 | A | ACTCTGTG others(41): Show |
1 | a0004c0009t0001g0315 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2627+1754_2627+180 others(52): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147197 | ||||||
| chr22:50147197 | A | ACTCTGTG others(89): Show |
5 | a0001c0001t0001g0286 a0004c0008t0001g0121 a0005c0004t0001g0044 others(2): Show |
5 | HG01081.hp1 HG03239.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.2627+1706_2627+180 others(100): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147197 | ||||||
| chr22:50147197 | A | ACTCTGTG others(137): Show |
1 | a0005c0004t0001g0115 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2627+1658_2627+180 others(148): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147197 | ||||||
| chr22:50147197 | A | ACTCTGTG others(185): Show |
1 | a0004c0014t0001g0098 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2627+1610_2627+180 others(196): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147197 | ||||||
| chr22:50147197 | A | ACTCTGTG others(233): Show |
1 | a0001c0001t0001g0183 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2627+1562_2627+180 others(244): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147197 | ||||||
| chr22:50147197 | A | G | 27 | a0001c0001t0001g0072 a0001c0001t0001g0161 a0001c0001t0001g0162 others(24): Show |
27 | HG00597.hp2 HG00733.hp2 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.2627+1387A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147197 | |||||||
| chr22:50147197 | ACTCTGTG others(41): Show |
A | 13 | a0001c0001t0001g0062 a0001c0001t0001g0158 a0001c0001t0001g0277 others(10): Show |
13 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.2627+1754_2627+180 others(52): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147197 | ||||||
| chr22:50147197 | ACTCTGTG others(89): Show |
A | 36 | a0001c0001t0001g0146 a0001c0001t0001g0196 a0001c0001t0001g0238 others(33): Show |
36 | HG00408.hp2 HG00438.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.2627+1706_2627+180 others(100): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147197 | ||||||
| chr22:50147197 | ACTCTGTG others(137): Show |
A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0061 others(17): Show |
21 | HG00099.hp1 HG01516.hp1 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.2627+1658_2627+180 others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147197 | ||||||
| chr22:50147197 | ACTCTGTG others(185): Show |
A | 23 | a0001c0001t0001g0009 a0001c0001t0001g0140 a0001c0001t0001g0247 others(20): Show |
23 | HG01346.hp1 HG01361.hp2 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.2627+1610_2627+180 others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147197 | ||||||
| chr22:50147197 | ACTCTGTG others(233): Show |
A | 63 | a0001c0001t0001g0138 a0001c0001t0001g0193 a0001c0001t0001g0235 others(60): Show |
64 | HG00438.hp1 HG00597.hp1 HG01168.hp1 others(61): Show |
intron_variant | MODIFIER | c.2627+1562_2627+180 others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147197 | ||||||
| chr22:50147197 | ACTCTGTG others(281): Show |
A | 7 | a0001c0001t0001g0268 a0001c0005t0001g0010 a0001c0005t0001g0165 others(4): Show |
7 | HG00099.hp2 HG01243.hp2 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.2627+1514_2627+180 others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147197 | ||||||
| chr22:50147197 | ACTCTGTG others(329): Show |
A | 3 | a0001c0005t0001g0166 a0001c0005t0001g0179 a0001c0005t0001g0180 |
3 | HG02965.hp1 HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2627+1466_2627+180 others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147197 | ||||||
| chr22:50147245 | G | GCTCTGTG others(233): Show |
1 | a0001c0016t0001g0191 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2627+1482_2627+148 others(244): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147245 | ||||||
| chr22:50147245 | G | GCTCTGTG others(233): Show |
1 | a0004c0021t0001g0099 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2627+1674_2627+167 others(244): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147245 | ||||||
| chr22:50147278 | C | CGCTCTCT others(521): Show |
1 | a0009c0019t0001g0222 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2627+1801_2627+180 others(532): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147278 | ||||||
| chr22:50147278 | C | T | 1 | a0001c0001t0001g0284 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2627+1468C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147278 | |||||||
| chr22:50147282 | C | G | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG01074.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2627+1472C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147282 | |||||||
| chr22:50147293 | G | A | 3 | a0001c0005t0001g0292 a0001c0016t0001g0191 a0004c0008t0001g0100 |
3 | HG01175.hp2 HG03831.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2627+1483G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147293 | |||||||
| chr22:50147326 | C | CGCTCTCT others(233): Show |
1 | a0001c0001t0001g0185 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2627+1755_2627+175 others(244): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147326 | ||||||
| chr22:50147326 | C | CGCTCTCT others(281): Show |
2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2627+1563_2627+156 others(292): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147326 | ||||||
| chr22:50147326 | C | T | 2 | a0002c0010t0002g0331 a0002c0010t0002g0335 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2627+1516C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147326 | |||||||
| chr22:50147330 | C | G | 1 | a0001c0001t0001g0285 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2627+1520C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147330 | |||||||
| chr22:50147340 | C | CGCTCTGT others(329): Show |
1 | a0001c0001t0001g0139 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2627+1755_2627+175 others(340): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147340 | ||||||
| chr22:50147341 | G | A | 1 | a0001c0016t0001g0191 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2627+1531G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147341 | |||||||
| chr22:50147341 | G | GCTCTGTG others(89): Show |
1 | a0004c0009t0001g0316 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2627+1626_2627+162 others(100): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147341 | ||||||
| chr22:50147374 | C | T | 5 | a0001c0001t0001g0214 a0002c0010t0002g0331 a0002c0010t0002g0332 others(2): Show |
5 | HG02559.hp1 HG02723.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2627+1564C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147374 | |||||||
| chr22:50147388 | C | T | 1 | a0002c0002t0002g0374 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2627+1578C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147388 | |||||||
| chr22:50147389 | G | A | 6 | a0001c0001t0001g0287 a0001c0005t0001g0181 a0001c0005t0001g0198 others(3): Show |
6 | HG00738.hp2 HG01099.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.2627+1579G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147389 | |||||||
| chr22:50147422 | C | T | 8 | a0001c0001t0001g0062 a0002c0002t0002g0012 a0002c0010t0002g0332 others(5): Show |
8 | HG01884.hp1 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2627+1612C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147422 | |||||||
| chr22:50147426 | C | G | 1 | a0001c0001t0001g0287 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2627+1616C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147426 | |||||||
| chr22:50147436 | C | CGCTCTGT others(233): Show |
1 | a0001c0001t0001g0184 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2627+1755_2627+175 others(244): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147436 | ||||||
| chr22:50147437 | G | A | 5 | a0001c0005t0001g0176 a0001c0005t0001g0197 a0001c0005t0001g0199 others(2): Show |
5 | HG00280.hp1 HG01516.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.2627+1627G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147437 | |||||||
| chr22:50147437 | G | GCTCTGTG others(521): Show |
1 | a0001c0001t0001g0160 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2627+1770_2627+177 others(532): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147437 | ||||||
| chr22:50147470 | C | CGCTCTCT others(521): Show |
1 | a0009c0019t0001g0223 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2627+1801_2627+180 others(532): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147470 | ||||||
| chr22:50147470 | C | T | 3 | a0001c0001t0001g0146 a0002c0010t0002g0349 a0002c0010t0002g0387 |
3 | HG02145.hp2 HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2627+1660C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147470 | |||||||
| chr22:50147471 | G | A | 1 | a0002c0002t0002g0003 | 2 | HG04204.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2627+1661G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147471 | |||||||
| chr22:50147474 | C | G | 1 | a0001c0001t0001g0294 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2627+1664C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147474 | |||||||
| chr22:50147477 | TCAGAGGC others(135): Show |
T | 1 | a0002c0013t0004g0371 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2627+1675_2627+181 others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147477 | ||||||
| chr22:50147485 | G | A | 7 | a0001c0005t0001g0171 a0001c0005t0001g0173 a0001c0005t0001g0182 others(4): Show |
7 | HG01099.hp1 HG01361.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.2627+1675G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147485 | |||||||
| chr22:50147518 | C | T | 4 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0158 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2627+1708C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147518 | |||||||
| chr22:50147519 | G | A | 5 | a0002c0002t0002g0003 a0002c0002t0002g0024 a0002c0002t0002g0031 others(2): Show |
6 | HG01168.hp2 HG01257.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.2627+1709G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147519 | |||||||
| chr22:50147533 | G | A | 16 | a0001c0005t0001g0010 a0001c0005t0001g0164 a0001c0005t0001g0167 others(13): Show |
16 | HG00280.hp1 HG01255.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.2627+1723G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147533 | |||||||
| chr22:50147533 | G | GCTCTGTG others(89): Show |
1 | a0003c0003t0002g0342 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2627+1801_2627+180 others(100): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147533 | ||||||
| chr22:50147566 | C | CGCTCTCT others(137): Show |
1 | a0001c0001t0001g0162 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2627+1801_2627+180 others(148): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50147566 | ||||||
| chr22:50147566 | C | T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0137 others(8): Show |
13 | HG02280.hp1 HG02622.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.2627+1756C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147566 | |||||||
| chr22:50147573 | T | C | 1 | a0003c0003t0002g0353 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2627+1763T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147573 | |||||||
| chr22:50147634 | C | G | 113 | a0001c0001t0001g0077 a0002c0002t0002g0003 a0002c0002t0002g0013 others(110): Show |
116 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.2627+1824C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147634 | |||||||
| chr22:50147673 | CA | C | 4 | a0001c0001t0001g0072 a0001c0001t0001g0224 a0001c0001t0001g0225 others(1): Show |
4 | HG03688.hp1 NA18970.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.2627+1864delA | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147673 | |||||||
| chr22:50147703 | A | G | 1 | a0004c0009t0001g0313 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2627+1893A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147703 | |||||||
| chr22:50147986 | G | C | 105 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(102): Show |
108 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.2628-1629G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147986 | |||||||
| chr22:50147991 | C | T | 20 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(17): Show |
20 | HG01261.hp1 HG01515.hp2 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.2628-1624C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50147991 | |||||||
| chr22:50148008 | G | A | 1 | a0002c0002t0002g0022 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2628-1607G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50148008 | |||||||
| chr22:50148023 | C | T | 1 | a0002c0002t0002g0031 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2628-1592C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50148023 | |||||||
| chr22:50148036 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2628-1579C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50148036 | |||||||
| chr22:50148244 | G | C | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2628-1371G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50148244 | |||||||
| chr22:50148292 | G | T | 1 | a0016c0029t0001g0205 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2628-1323G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50148292 | |||||||
| chr22:50148299 | G | A | 1 | a0005c0020t0001g0083 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2628-1316G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50148299 | |||||||
| chr22:50148374 | G | C | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2628-1241G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50148374 | |||||||
| chr22:50148385 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2628-1230G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50148385 | |||||||
| chr22:50148429 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2628-1186A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50148429 | |||||||
| chr22:50148438 | G | A | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2628-1177G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50148438 | |||||||
| chr22:50148476 | C | A | 7 | a0001c0011t0001g0004 a0001c0011t0001g0045 a0001c0011t0001g0046 others(4): Show |
8 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.2628-1139C>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50148476 | |||||||
| chr22:50148558 | C | G | 97 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(94): Show |
100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.2628-1057C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50148558 | |||||||
| chr22:50148663 | C | CT | 12 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0213 others(9): Show |
12 | HG01496.hp2 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2628-936dupT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50148663 | ||||||
| chr22:50148663 | CT | C | 120 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(117): Show |
121 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.2628-936delT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr22 | 50148663 | ||||||
| chr22:50148855 | G | A | 1 | a0001c0007t0001g0057 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2628-760G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50148855 | |||||||
| chr22:50148866 | G | A | 1 | a0001c0007t0001g0054 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2628-749G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50148866 | |||||||
| chr22:50148885 | T | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0041 others(266): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.2628-730T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50148885 | |||||||
| chr22:50148915 | C | T | 46 | a0003c0003t0002g0322 a0003c0003t0002g0323 a0003c0003t0002g0324 others(43): Show |
47 | HG00323.hp1 HG00733.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.2628-700C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50148915 | |||||||
| chr22:50148922 | C | T | 20 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(17): Show |
20 | HG01261.hp1 HG01515.hp2 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.2628-693C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50148922 | |||||||
| chr22:50148987 | G | A | 1 | a0001c0007t0001g0216 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2628-628G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50148987 | |||||||
| chr22:50149033 | G | T | 10 | a0002c0002t0002g0012 a0002c0010t0002g0331 a0002c0010t0002g0332 others(7): Show |
10 | HG01884.hp1 HG02145.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2628-582G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50149033 | |||||||
| chr22:50149364 | C | T | 1 | a0004c0009t0001g0126 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2628-251C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50149364 | |||||||
| chr22:50149396 | G | C | 1 | a0001c0001t0001g0293 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2628-219G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50149396 | |||||||
| chr22:50149400 | G | A | 6 | a0001c0011t0001g0004 a0001c0011t0001g0046 a0001c0011t0001g0047 others(3): Show |
7 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2628-215G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50149400 | |||||||
| chr22:50149493 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2628-122C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50149493 | |||||||
| chr22:50149527 | T | C | 2 | a0004c0008t0001g0084 a0004c0008t0001g0092 |
2 | HG02735.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2628-88T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50149527 | |||||||
| chr22:50149550 | T | G | 120 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(117): Show |
123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.2628-65T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 19/26 | chr22 | 50149550 | |||||||
| chr22:50149724 | G | A | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2727+10G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 20/26 | chr22 | 50149724 | |||||||
| chr22:50149734 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2727+20T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 20/26 | chr22 | 50149734 | |||||||
| chr22:50149858 | G | T | 1 | a0001c0001t0001g0042 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2727+144G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 20/26 | chr22 | 50149858 | |||||||
| chr22:50149884 | G | A | 44 | a0002c0002t0002g0003 a0002c0002t0002g0013 a0002c0002t0002g0014 others(41): Show |
45 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.2727+170G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 20/26 | chr22 | 50149884 | |||||||
| chr22:50149893 | T | G | 1 | a0001c0005t0001g0169 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2727+179T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 20/26 | chr22 | 50149893 | |||||||
| chr22:50149969 | G | A | 1 | a0001c0005t0001g0165 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2727+255G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 20/26 | chr22 | 50149969 | |||||||
| chr22:50149996 | C | T | 1 | a0001c0005t0001g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2727+282C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 20/26 | chr22 | 50149996 | |||||||
| chr22:50150041 | A | T | 67 | a0004c0008t0001g0007 a0004c0008t0001g0080 a0004c0008t0001g0084 others(64): Show |
70 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.2727+327A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 20/26 | chr22 | 50150041 | |||||||
| chr22:50150046 | A | G | 69 | a0004c0008t0001g0007 a0004c0008t0001g0080 a0004c0008t0001g0084 others(66): Show |
72 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.2727+332A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 20/26 | chr22 | 50150046 | |||||||
| chr22:50150068 | C | T | 1 | a0015c0041t0002g0036 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2727+354C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 20/26 | chr22 | 50150068 | |||||||
| chr22:50150168 | T | C | 1 | a0002c0002t0002g0374 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2727+454T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 20/26 | chr22 | 50150168 | |||||||
| chr22:50150279 | G | C | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2728-456G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 20/26 | chr22 | 50150279 | |||||||
| chr22:50150298 | C | T | 1 | a0001c0011t0001g0050 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2728-437C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 20/26 | chr22 | 50150298 | |||||||
| chr22:50150347 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2728-388C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 20/26 | chr22 | 50150347 | |||||||
| chr22:50150572 | C | T | 1 | a0003c0003t0002g0359 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2728-163C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 20/26 | chr22 | 50150572 | |||||||
| chr22:50150614 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2728-121C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 20/26 | chr22 | 50150614 | |||||||
| chr22:50150692 | G | A | 5 | a0002c0002t0002g0003 a0002c0002t0002g0024 a0002c0002t0002g0031 others(2): Show |
6 | HG01168.hp2 HG01257.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.2728-43G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 20/26 | chr22 | 50150692 | |||||||
| chr22:50150926 | G | A | 1 | a0001c0001t0001g0303 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2892+27G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 21/26 | chr22 | 50150926 | |||||||
| chr22:50151118 | G | A | 1 | a0001c0011t0001g0045 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2892+219G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 21/26 | chr22 | 50151118 | |||||||
| chr22:50151147 | A | G | 239 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(236): Show |
245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.2892+248A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 21/26 | chr22 | 50151147 | |||||||
| chr22:50151200 | TCTC | T | 20 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(17): Show |
20 | HG01261.hp1 HG01515.hp2 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.2892+305_2892+307d others(5): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr22 | 50151200 | ||||||
| chr22:50151578 | G | GT | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2892+679_2892+680i others(3): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 21/26 | chr22 | 50151578 | |||||||
| chr22:50151608 | C | T | 46 | a0003c0003t0002g0322 a0003c0003t0002g0323 a0003c0003t0002g0324 others(43): Show |
47 | HG00323.hp1 HG00733.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.2892+709C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 21/26 | chr22 | 50151608 | |||||||
| chr22:50151677 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2892+778C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 21/26 | chr22 | 50151677 | |||||||
| chr22:50151721 | G | T | 1 | a0001c0001t0001g0150 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2892+822G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 21/26 | chr22 | 50151721 | |||||||
| chr22:50151763 | G | A | 1 | a0016c0029t0001g0205 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2892+864G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 21/26 | chr22 | 50151763 | |||||||
| chr22:50151857 | G | A | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2892+958G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 21/26 | chr22 | 50151857 | |||||||
| chr22:50151890 | C | A | 1 | a0001c0001t0001g0212 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2892+991C>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 21/26 | chr22 | 50151890 | |||||||
| chr22:50151902 | C | A | 13 | a0001c0001t0001g0072 a0001c0001t0001g0224 a0001c0001t0001g0225 others(10): Show |
14 | HG01243.hp2 HG01255.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2892+1003C>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 21/26 | chr22 | 50151902 | |||||||
| chr22:50151945 | G | A | 2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | NA19070.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.2892+1046G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 21/26 | chr22 | 50151945 | |||||||
| chr22:50151964 | C | T | 19 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(16): Show |
19 | HG01515.hp2 HG01516.hp2 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.2892+1065C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 21/26 | chr22 | 50151964 | |||||||
| chr22:50152042 | G | A | 65 | a0004c0008t0001g0007 a0004c0008t0001g0080 a0004c0008t0001g0084 others(62): Show |
68 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.2893-1003G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 21/26 | chr22 | 50152042 | |||||||
| chr22:50152076 | A | G | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2893-969A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 21/26 | chr22 | 50152076 | |||||||
| chr22:50152108 | C | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2893-937C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 21/26 | chr22 | 50152108 | |||||||
| chr22:50152114 | C | T | 67 | a0004c0008t0001g0007 a0004c0008t0001g0080 a0004c0008t0001g0084 others(64): Show |
70 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.2893-931C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 21/26 | chr22 | 50152114 | |||||||
| chr22:50152137 | AACAG | A | 46 | a0003c0003t0002g0322 a0003c0003t0002g0323 a0003c0003t0002g0324 others(43): Show |
47 | HG00323.hp1 HG00733.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.2893-903_2893-900d others(6): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr22 | 50152137 | ||||||
| chr22:50152205 | G | A | 13 | a0001c0001t0001g0072 a0001c0001t0001g0224 a0001c0001t0001g0225 others(10): Show |
14 | HG01243.hp2 HG01255.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2893-840G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 21/26 | chr22 | 50152205 | |||||||
| chr22:50152308 | C | T | 6 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(3): Show |
6 | HG02257.hp2 HG02717.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2893-737C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 21/26 | chr22 | 50152308 | |||||||
| chr22:50152460 | A | G | 1 | a0016c0029t0001g0205 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2893-585A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 21/26 | chr22 | 50152460 | |||||||
| chr22:50152574 | G | T | 219 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(216): Show |
224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.2893-471G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 21/26 | chr22 | 50152574 | |||||||
| chr22:50152781 | G | A | 1 | a0001c0007t0001g0052 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2893-264G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 21/26 | chr22 | 50152781 | |||||||
| chr22:50153030 | A | G | 12 | a0001c0001t0001g0243 a0001c0001t0001g0264 a0001c0001t0001g0266 others(9): Show |
12 | HG00438.hp1 NA18945.hp2 NA18953.hp1 others(9): Show |
intron_variant | MODIFIER | c.2893-15A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 21/26 | chr22 | 50153030 | |||||||
| chr22:50153041 | G | A | 5 | a0002c0002t0002g0003 a0002c0002t0002g0024 a0002c0002t0002g0031 others(2): Show |
6 | HG01168.hp2 HG01257.hp2 HG03710.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.2893-4G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 21/26 | chr22 | 50153041 | |||||||
| chr22:50153239 | G | A | 2 | a0001c0001t0001g0266 a0016c0029t0001g0205 |
2 | HG02145.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.3066+21G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50153239 | |||||||
| chr22:50153249 | G | A | 7 | a0001c0011t0001g0004 a0001c0011t0001g0045 a0001c0011t0001g0046 others(4): Show |
8 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.3066+31G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50153249 | |||||||
| chr22:50153254 | G | A | 67 | a0004c0008t0001g0007 a0004c0008t0001g0080 a0004c0008t0001g0084 others(64): Show |
70 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.3066+36G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50153254 | |||||||
| chr22:50153404 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3066+186T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50153404 | |||||||
| chr22:50153435 | A | G | 352 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(349): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.3066+217A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50153435 | |||||||
| chr22:50153528 | C | T | 20 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(17): Show |
20 | HG01261.hp1 HG01515.hp2 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.3066+310C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50153528 | |||||||
| chr22:50153535 | A | G | 238 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(235): Show |
244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.3066+317A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50153535 | |||||||
| chr22:50153596 | C | T | 5 | a0001c0007t0001g0216 a0001c0007t0001g0217 a0001c0007t0001g0218 others(2): Show |
5 | HG01123.hp2 HG01256.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.3066+378C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50153596 | |||||||
| chr22:50153608 | C | G | 3 | a0001c0001t0003g0177 a0001c0001t0003g0194 a0001c0001t0003g0195 |
3 | HG02486.hp1 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3066+390C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50153608 | |||||||
| chr22:50153634 | C | T | 6 | a0003c0012t0002g0317 a0003c0012t0002g0318 a0003c0012t0002g0319 others(3): Show |
6 | HG00323.hp1 HG01070.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.3066+416C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50153634 | |||||||
| chr22:50153697 | C | T | 94 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(91): Show |
97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.3066+479C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50153697 | |||||||
| chr22:50153706 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3066+488C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50153706 | |||||||
| chr22:50153754 | G | A | 5 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 others(2): Show |
5 | HG00099.hp2 HG00733.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.3066+536G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50153754 | |||||||
| chr22:50153829 | T | C | 1 | a0001c0007t0001g0230 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.3066+611T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50153829 | |||||||
| chr22:50153931 | G | C | 1 | a0001c0001t0001g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3066+713G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50153931 | |||||||
| chr22:50153934 | C | T | 1 | a0001c0007t0001g0227 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3066+716C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50153934 | |||||||
| chr22:50154088 | G | A | 19 | a0001c0007t0001g0052 a0001c0007t0001g0053 a0001c0007t0001g0054 others(16): Show |
19 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.3066+870G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50154088 | |||||||
| chr22:50154095 | G | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0193 |
2 | HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.3066+877G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50154095 | |||||||
| chr22:50154211 | G | A | 5 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3066+993G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50154211 | |||||||
| chr22:50154304 | C | T | 1 | a0005c0004t0001g0101 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3066+1086C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50154304 | |||||||
| chr22:50154402 | A | T | 1 | a0014c0032t0001g0095 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.3066+1184A>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50154402 | |||||||
| chr22:50154402 | AT | A | 10 | a0001c0001t0001g0051 a0001c0001t0001g0243 a0001c0005t0001g0179 others(7): Show |
10 | HG01099.hp1 HG01257.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.3066+1197delT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr22 | 50154402 | ||||||
| chr22:50154403 | T | A | 1 | a0005c0004t0001g0088 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.3066+1185T>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50154403 | |||||||
| chr22:50154547 | G | A | 1 | a0001c0005t0001g0167 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3066+1329G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50154547 | |||||||
| chr22:50154797 | T | G | 67 | a0004c0008t0001g0007 a0004c0008t0001g0080 a0004c0008t0001g0084 others(64): Show |
70 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.3066+1579T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50154797 | |||||||
| chr22:50155263 | G | GT | 54 | a0001c0001t0001g0151 a0001c0001t0001g0250 a0001c0001t0001g0294 others(51): Show |
55 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.3066+2060dupT | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr22 | 50155263 | ||||||
| chr22:50155263 | G | GTT | 40 | a0001c0001t0001g0072 a0001c0001t0001g0224 a0001c0001t0001g0225 others(37): Show |
41 | HG00621.hp2 HG00639.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.3066+2059_3066+206 others(6): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr22 | 50155263 | ||||||
| chr22:50155312 | G | C | 20 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(17): Show |
20 | HG01261.hp1 HG01515.hp2 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.3066+2094G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50155312 | |||||||
| chr22:50155323 | C | T | 1 | a0016c0029t0001g0205 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3066+2105C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50155323 | |||||||
| chr22:50155432 | C | T | 104 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(101): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.3066+2214C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50155432 | |||||||
| chr22:50155464 | T | C | 2 | a0002c0002t0002g0019 a0002c0002t0002g0020 |
2 | NA18969.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.3066+2246T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50155464 | |||||||
| chr22:50155595 | A | G | 14 | a0001c0001t0001g0072 a0001c0001t0001g0224 a0001c0001t0001g0225 others(11): Show |
15 | HG01243.hp2 HG01255.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.3066+2377A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50155595 | |||||||
| chr22:50155869 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3067-2188A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50155869 | |||||||
| chr22:50155910 | T | G | 46 | a0003c0003t0002g0322 a0003c0003t0002g0323 a0003c0003t0002g0324 others(43): Show |
47 | HG00323.hp1 HG00733.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.3067-2147T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50155910 | |||||||
| chr22:50155936 | A | G | 5 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(2): Show |
5 | HG01891.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3067-2121A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50155936 | |||||||
| chr22:50156031 | G | A | 1 | a0016c0029t0001g0205 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3067-2026G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50156031 | |||||||
| chr22:50156049 | C | CTCAT | 5 | a0002c0010t0002g0331 a0002c0010t0002g0332 a0002c0010t0002g0333 others(2): Show |
5 | HG02145.hp1 HG02559.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.3067-1983_3067-198 others(8): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr22 | 50156049 | ||||||
| chr22:50156343 | T | G | 14 | a0001c0001t0001g0072 a0001c0001t0001g0224 a0001c0001t0001g0225 others(11): Show |
15 | HG01243.hp2 HG01255.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.3067-1714T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50156343 | |||||||
| chr22:50156406 | A | G | 184 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(181): Show |
189 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.3067-1651A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50156406 | |||||||
| chr22:50156550 | C | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0240 a0001c0001t0001g0242 others(6): Show |
10 | HG02083.hp1 HG02165.hp2 NA18966.hp1 others(7): Show |
intron_variant | MODIFIER | c.3067-1507C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50156550 | |||||||
| chr22:50156640 | C | T | 1 | a0016c0029t0001g0205 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3067-1417C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50156640 | |||||||
| chr22:50156753 | T | A | 46 | a0003c0003t0002g0322 a0003c0003t0002g0323 a0003c0003t0002g0324 others(43): Show |
47 | HG00323.hp1 HG00733.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.3067-1304T>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50156753 | |||||||
| chr22:50156827 | C | T | 58 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(55): Show |
59 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.3067-1230C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50156827 | |||||||
| chr22:50156937 | G | C | 69 | a0004c0008t0001g0007 a0004c0008t0001g0080 a0004c0008t0001g0084 others(66): Show |
72 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.3067-1120G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50156937 | |||||||
| chr22:50156946 | A | C | 1 | a0005c0004t0001g0133 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3067-1111A>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50156946 | |||||||
| chr22:50156956 | G | A | 1 | a0001c0001t0003g0194 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3067-1101G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50156956 | |||||||
| chr22:50157004 | T | C | 1 | a0001c0007t0001g0220 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3067-1053T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50157004 | |||||||
| chr22:50157006 | C | T | 12 | a0001c0001t0001g0072 a0001c0001t0001g0224 a0001c0001t0001g0225 others(9): Show |
13 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.3067-1051C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50157006 | |||||||
| chr22:50157024 | C | T | 20 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(17): Show |
20 | HG01261.hp1 HG01515.hp2 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.3067-1033C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50157024 | |||||||
| chr22:50157190 | G | T | 2 | a0001c0001t0003g0174 a0001c0001t0003g0175 |
2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3067-867G>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50157190 | |||||||
| chr22:50157193 | C | T | 80 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0156 others(77): Show |
82 | HG00099.hp2 HG00438.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.3067-864C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50157193 | |||||||
| chr22:50157212 | T | G | 75 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(72): Show |
78 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.3067-845T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50157212 | |||||||
| chr22:50157270 | TC | T | 47 | a0001c0001t0001g0241 a0003c0003t0002g0322 a0003c0003t0002g0323 others(44): Show |
48 | HG00323.hp1 HG00733.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.3067-781delC | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr22 | 50157270 | ||||||
| chr22:50157301 | T | C | 1 | a0001c0005t0001g0169 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3067-756T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50157301 | |||||||
| chr22:50157413 | T | C | 264 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0041 others(261): Show |
272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.3067-644T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50157413 | |||||||
| chr22:50157484 | G | A | 46 | a0003c0003t0002g0322 a0003c0003t0002g0323 a0003c0003t0002g0324 others(43): Show |
47 | HG00323.hp1 HG00733.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.3067-573G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50157484 | |||||||
| chr22:50157625 | T | G | 46 | a0003c0003t0002g0322 a0003c0003t0002g0323 a0003c0003t0002g0324 others(43): Show |
47 | HG00323.hp1 HG00733.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.3067-432T>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50157625 | |||||||
| chr22:50157676 | G | A | 4 | a0001c0005t0001g0197 a0001c0005t0001g0198 a0001c0005t0001g0199 others(1): Show |
4 | HG01099.hp1 HG01256.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3067-381G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50157676 | |||||||
| chr22:50157761 | C | CA | 26 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0233 others(23): Show |
26 | HG00140.hp1 HG01257.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.3067-276dupA | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr22 | 50157761 | ||||||
| chr22:50157761 | C | CAA | 83 | a0002c0002t0002g0003 a0002c0002t0002g0013 a0002c0002t0002g0014 others(80): Show |
85 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.3067-277_3067-276d others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr22 | 50157761 | ||||||
| chr22:50157761 | CA | C | 25 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0042 others(22): Show |
25 | HG01261.hp1 HG01515.hp2 HG01516.hp2 others(22): Show |
intron_variant | MODIFIER | c.3067-276delA | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr22 | 50157761 | ||||||
| chr22:50157761 | CAA | C | 93 | a0001c0001t0001g0067 a0001c0001t0001g0136 a0001c0001t0001g0208 others(90): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.3067-277_3067-276d others(4): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr22 | 50157761 | ||||||
| chr22:50157811 | C | T | 1 | a0001c0001t0003g0174 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3067-246C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50157811 | |||||||
| chr22:50157838 | C | G | 46 | a0003c0003t0002g0322 a0003c0003t0002g0323 a0003c0003t0002g0324 others(43): Show |
47 | HG00323.hp1 HG00733.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.3067-219C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50157838 | |||||||
| chr22:50157847 | G | A | 9 | a0002c0010t0002g0331 a0002c0010t0002g0332 a0002c0010t0002g0333 others(6): Show |
9 | HG01884.hp1 HG02145.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.3067-210G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | chr22 | 50157847 | |||||||
| chr22:50157889 | C | CATT | 46 | a0003c0003t0002g0322 a0003c0003t0002g0323 a0003c0003t0002g0324 others(43): Show |
47 | HG00323.hp1 HG00733.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.3067-167_3067-165d others(5): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr22 | 50157889 | ||||||
| chr22:50158240 | G | C | 1 | a0001c0005t0001g0176 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.3216+34G>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 23/26 | chr22 | 50158240 | |||||||
| chr22:50158334 | G | A | 1 | a0006c0006t0001g0221 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3216+128G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 23/26 | chr22 | 50158334 | |||||||
| chr22:50158374 | C | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0151 a0017c0035t0001g0008 |
3 | HG02055.hp2 HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3216+168C>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 23/26 | chr22 | 50158374 | |||||||
| chr22:50158482 | T | C | 6 | a0001c0001t0001g0001 a0001c0001t0001g0152 a0001c0001t0001g0153 others(3): Show |
8 | HG00741.hp2 HG01891.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.3216+276T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 23/26 | chr22 | 50158482 | |||||||
| chr22:50158561 | G | A | 1 | a0001c0007t0001g0056 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3216+355G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 23/26 | chr22 | 50158561 | |||||||
| chr22:50158575 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3216+369A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 23/26 | chr22 | 50158575 | |||||||
| chr22:50158922 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3216+716C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 23/26 | chr22 | 50158922 | |||||||
| chr22:50159037 | C | T | 19 | a0001c0007t0001g0052 a0001c0007t0001g0053 a0001c0007t0001g0054 others(16): Show |
19 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.3217-641C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 23/26 | chr22 | 50159037 | |||||||
| chr22:50159084 | G | A | 1 | a0002c0002t0002g0032 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.3217-594G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 23/26 | chr22 | 50159084 | |||||||
| chr22:50159116 | A | G | 352 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(349): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.3217-562A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 23/26 | chr22 | 50159116 | |||||||
| chr22:50159169 | G | A | 1 | a0001c0005t0001g0202 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3217-509G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 23/26 | chr22 | 50159169 | |||||||
| chr22:50159339 | C | T | 1 | a0002c0002t0002g0035 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3217-339C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 23/26 | chr22 | 50159339 | |||||||
| chr22:50159550 | C | T | 46 | a0003c0003t0002g0322 a0003c0003t0002g0323 a0003c0003t0002g0324 others(43): Show |
47 | HG00323.hp1 HG00733.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.3217-128C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 23/26 | chr22 | 50159550 | |||||||
| chr22:50159559 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3217-119G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 23/26 | chr22 | 50159559 | |||||||
| chr22:50159601 | C | CA | 81 | a0001c0001t0001g0146 a0002c0002t0002g0003 a0002c0002t0002g0012 others(78): Show |
83 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.3217-65dupA | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr22 | 50159601 | ||||||
| chr22:50159804 | C | T | 4 | a0001c0001t0001g0051 a0001c0001t0001g0060 a0011c0018t0001g0075 others(1): Show |
4 | HG01515.hp2 HG01517.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.3324+19C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 24/26 | chr22 | 50159804 | |||||||
| chr22:50159867 | G | A | 20 | a0001c0007t0001g0052 a0001c0007t0001g0053 a0001c0007t0001g0054 others(17): Show |
20 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.3324+82G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 24/26 | chr22 | 50159867 | |||||||
| chr22:50159869 | A | G | 8 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.3324+84A>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 24/26 | chr22 | 50159869 | |||||||
| chr22:50159914 | C | T | 3 | a0001c0001t0003g0177 a0001c0001t0003g0194 a0001c0001t0003g0195 |
3 | HG02486.hp1 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3324+129C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 24/26 | chr22 | 50159914 | |||||||
| chr22:50160047 | C | T | 58 | a0002c0002t0002g0003 a0002c0002t0002g0012 a0002c0002t0002g0013 others(55): Show |
59 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.3324+262C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 24/26 | chr22 | 50160047 | |||||||
| chr22:50160122 | G | A | 94 | a0001c0001t0001g0136 a0001c0001t0001g0208 a0001c0001t0001g0212 others(91): Show |
97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.3324+337G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 24/26 | chr22 | 50160122 | |||||||
| chr22:50160136 | C | T | 3 | a0001c0005t0001g0164 a0001c0005t0001g0167 a0024c0027t0001g0159 |
3 | HG03942.hp2 HG04115.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3324+351C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 24/26 | chr22 | 50160136 | |||||||
| chr22:50160137 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3324+352G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 24/26 | chr22 | 50160137 | |||||||
| chr22:50160223 | T | TC | 12 | a0001c0001t0001g0146 a0001c0001t0001g0151 a0001c0001t0001g0253 others(9): Show |
12 | HG00621.hp2 HG00735.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.3324+444dupC | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr22 | 50160223 | ||||||
| chr22:50160277 | C | T | 1 | a0001c0011t0001g0045 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3325-411C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 24/26 | chr22 | 50160277 | |||||||
| chr22:50160339 | C | T | 13 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0063 others(10): Show |
13 | HG01261.hp1 HG01516.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.3325-349C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 24/26 | chr22 | 50160339 | |||||||
| chr22:50160536 | G | A | 3 | a0001c0001t0003g0174 a0001c0001t0003g0175 a0001c0001t0003g0178 |
3 | HG02109.hp2 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3325-152G>A | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 24/26 | chr22 | 50160536 | |||||||
| chr22:50160682 | T | C | 69 | a0004c0008t0001g0007 a0004c0008t0001g0080 a0004c0008t0001g0084 others(66): Show |
72 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(69): Show |
splice_region_variant&intron_variant | LOW | c.3325-6T>C | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 24/26 | chr22 | 50160682 | |||||||
| chr22:50160899 | C | T | 20 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(17): Show |
20 | HG01261.hp1 HG01515.hp2 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.3463-65C>T | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 25/26 | chr22 | 50160899 | |||||||
| chr22:50160915 | A | ATG | 6 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(3): Show |
6 | HG02145.hp1 HG02717.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.3463-48_3463-47dup others(2): Show |
MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chr22 | 50160915 | ||||||
| chr22:50161137 | C | G | 1 | a0003c0003t0002g0386 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3554+82C>G | MOV10L1 | ENSG00000073146.17 | transcript | ENST00000262794.10 | protein_coding | 26/26 | chr22 | 50161137 |