Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4594 |
| ensemblid | ENSG00000146085.8 |
| hgncid | 7526 |
| symbol | MMUT |
| name | methylmalonyl-CoA mutase |
| refseq_nuc | NM_000255.4 |
| refseq_prot | NP_000246.2 |
| ensembl_nuc | ENST00000274813.4 |
| ensembl_prot | ENSP00000274813.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 49430360 |
| end | 49463253 |
| strand | - |
| ver | v1.2 |
| region | chr6:49430360-49463253 |
| region5000 | chr6:49425360-49468253 |
| regionname0 | MMUT_chr6_49430360_49463253 |
| regionname5000 | MMUT_chr6_49425360_49468253 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 750 | 150 | 28 | 29 | 76 | 6 | 9 | 60 | MMUT_chr6_49425360_49468253 | MMUT | MLRAK others(745): Show |
chr6 | 49425360 | 49468253 |
| a0002 | 0/0 | 750 | 103 | 17 | 12 | 50 | 7 | 17 | 39 | MMUT_chr6_49425360_49468253 | MMUT | MLRAK others(745): Show |
chr6 | 49425360 | 49468253 |
| a0003 | 0/0 | 750 | 77 | 36 | 11 | 22 | 0 | 8 | 14 | MMUT_chr6_49425360_49468253 | MMUT | MLRAK others(745): Show |
chr6 | 49425360 | 49468253 |
| a0004 | 0/0 | 750 | 36 | 7 | 5 | 17 | 1 | 6 | 16 | MMUT_chr6_49425360_49468253 | MMUT | MLRAK others(745): Show |
chr6 | 49425360 | 49468253 |
| a0005 | 0/0 | 750 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | MLRAK others(745): Show |
chr6 | 49425360 | 49468253 |
| a0006 | 0/0 | 750 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | MLRAK others(745): Show |
chr6 | 49425360 | 49468253 |
| a0007 | 0/0 | 750 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | MLRAK others(745): Show |
chr6 | 49425360 | 49468253 |
| a0008 | 0/0 | 750 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MMUT_chr6_49425360_49468253 | MMUT | MLRAK others(745): Show |
chr6 | 49425360 | 49468253 |
| a0009 | 0/0 | 750 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MMUT_chr6_49425360_49468253 | MMUT | MLRAK others(745): Show |
chr6 | 49425360 | 49468253 |
| a0010 | 0/0 | 750 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MMUT_chr6_49425360_49468253 | MMUT | MLRAK others(745): Show |
chr6 | 49425360 | 49468253 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2250 | 130 | 28 | 24 | 63 | 6 | 7 | MMUT_chr6_49425360_49468253 | MMUT | ATGTT others(2245): Show |
chr6 | 49425360 | 49468253 | ||
| a0001c0005 | 0/0 | 2250 | 9 | 0 | 4 | 5 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | ATGTT others(2245): Show |
chr6 | 49425360 | 49468253 | ||
| a0001c0006 | 0/0 | 2250 | 8 | 0 | 0 | 8 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | ATGTT others(2245): Show |
chr6 | 49425360 | 49468253 | ||
| a0001c0008 | 0/0 | 2250 | 3 | 0 | 1 | 0 | 0 | 2 | MMUT_chr6_49425360_49468253 | MMUT | ATGTT others(2245): Show |
chr6 | 49425360 | 49468253 | ||
| a0002c0002 | 0/0 | 2250 | 102 | 17 | 12 | 50 | 6 | 17 | MMUT_chr6_49425360_49468253 | MMUT | ATGTT others(2245): Show |
chr6 | 49425360 | 49468253 | ||
| a0002c0011 | 0/0 | 2250 | 1 | 0 | 0 | 0 | 1 | 0 | MMUT_chr6_49425360_49468253 | MMUT | ATGTT others(2245): Show |
chr6 | 49425360 | 49468253 | ||
| a0003c0003 | 0/0 | 2250 | 73 | 32 | 11 | 22 | 0 | 8 | MMUT_chr6_49425360_49468253 | MMUT | ATGTT others(2245): Show |
chr6 | 49425360 | 49468253 | ||
| a0003c0007 | 0/0 | 2250 | 4 | 4 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | ATGTT others(2245): Show |
chr6 | 49425360 | 49468253 | ||
| a0004c0004 | 0/0 | 2250 | 36 | 7 | 5 | 17 | 1 | 6 | MMUT_chr6_49425360_49468253 | MMUT | ATGTT others(2245): Show |
chr6 | 49425360 | 49468253 | ||
| a0005c0015 | 0/0 | 2250 | 1 | 0 | 1 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | ATGTT others(2245): Show |
chr6 | 49425360 | 49468253 | ||
| a0006c0013 | 0/0 | 2250 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | ATGTT others(2245): Show |
chr6 | 49425360 | 49468253 | ||
| a0007c0010 | 0/0 | 2250 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | ATGTT others(2245): Show |
chr6 | 49425360 | 49468253 | ||
| a0008c0012 | 0/0 | 2250 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | ATGTT others(2245): Show |
chr6 | 49425360 | 49468253 | ||
| a0009c0009 | 0/0 | 2250 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | ATGTT others(2245): Show |
chr6 | 49425360 | 49468253 | ||
| a0010c0014 | 0/0 | 2250 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | ATGTT others(2245): Show |
chr6 | 49425360 | 49468253 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/1 | 3811 | 96 | 0 | 19 | 63 | 6 | 7 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3806): Show |
chr6 | 49425360 | 49468253 |
| a0001c0001t0003 | 1/0 | 3811 | 34 | 28 | 5 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3806): Show |
chr6 | 49425360 | 49468253 |
| a0001c0005t0002 | 0/0 | 3811 | 8 | 0 | 3 | 5 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3806): Show |
chr6 | 49425360 | 49468253 |
| a0001c0005t0011 | 0/0 | 3811 | 1 | 0 | 1 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3806): Show |
chr6 | 49425360 | 49468253 |
| a0001c0006t0002 | 0/0 | 3811 | 8 | 0 | 0 | 8 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3806): Show |
chr6 | 49425360 | 49468253 |
| a0001c0008t0003 | 0/0 | 3811 | 3 | 0 | 1 | 0 | 0 | 2 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3806): Show |
chr6 | 49425360 | 49468253 |
| a0002c0002t0001 | 0/0 | 3811 | 100 | 17 | 12 | 48 | 6 | 17 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3806): Show |
chr6 | 49425360 | 49468253 |
| a0002c0002t0012 | 0/0 | 3811 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3806): Show |
chr6 | 49425360 | 49468253 |
| a0002c0002t0014 | 0/0 | 3811 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3806): Show |
chr6 | 49425360 | 49468253 |
| a0002c0011t0001 | 0/0 | 3811 | 1 | 0 | 0 | 0 | 1 | 0 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3806): Show |
chr6 | 49425360 | 49468253 |
| a0003c0003t0001 | 0/0 | 3811 | 20 | 19 | 1 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3806): Show |
chr6 | 49425360 | 49468253 |
| a0003c0003t0003 | 0/0 | 3811 | 1 | 0 | 1 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3806): Show |
chr6 | 49425360 | 49468253 |
| a0003c0003t0004 | 0/0 | 3811 | 38 | 1 | 7 | 22 | 0 | 8 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3806): Show |
chr6 | 49425360 | 49468253 |
| a0003c0003t0005 | 0/0 | 3812 | 6 | 5 | 1 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3807): Show |
chr6 | 49425360 | 49468253 |
| a0003c0003t0007 | 0/0 | 3811 | 2 | 2 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3806): Show |
chr6 | 49425360 | 49468253 |
| a0003c0003t0008 | 0/0 | 3811 | 2 | 2 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3806): Show |
chr6 | 49425360 | 49468253 |
| a0003c0003t0009 | 0/0 | 3811 | 2 | 2 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3806): Show |
chr6 | 49425360 | 49468253 |
| a0003c0003t0010 | 0/0 | 3810 | 1 | 0 | 1 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3805): Show |
chr6 | 49425360 | 49468253 |
| a0003c0003t0013 | 0/0 | 3811 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3806): Show |
chr6 | 49425360 | 49468253 |
| a0003c0007t0003 | 0/0 | 3811 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3806): Show |
chr6 | 49425360 | 49468253 |
| a0003c0007t0006 | 0/0 | 3811 | 3 | 3 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3806): Show |
chr6 | 49425360 | 49468253 |
| a0004c0004t0003 | 0/0 | 3811 | 30 | 2 | 5 | 16 | 1 | 6 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3806): Show |
chr6 | 49425360 | 49468253 |
| a0004c0004t0004 | 0/0 | 3811 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3806): Show |
chr6 | 49425360 | 49468253 |
| a0004c0004t0005 | 0/0 | 3812 | 5 | 5 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3807): Show |
chr6 | 49425360 | 49468253 |
| a0005c0015t0002 | 0/0 | 3811 | 1 | 0 | 1 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3806): Show |
chr6 | 49425360 | 49468253 |
| a0006c0013t0003 | 0/0 | 3811 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3806): Show |
chr6 | 49425360 | 49468253 |
| a0007c0010t0003 | 0/0 | 3811 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3806): Show |
chr6 | 49425360 | 49468253 |
| a0008c0012t0002 | 0/0 | 3811 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3806): Show |
chr6 | 49425360 | 49468253 |
| a0009c0009t0002 | 0/0 | 3811 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3806): Show |
chr6 | 49425360 | 49468253 |
| a0010c0014t0002 | 0/0 | 3811 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | AGAGT others(3806): Show |
chr6 | 49425360 | 49468253 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0001 | 0/0 | 46 | 0 | 13 | 26 | 2 | 5 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0008 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0003g0006 | 1/0 | 8 | 4 | 3 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0003g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0003g0016 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0003g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0003g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0003g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0003g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0005t0002g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0005t0002g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0005t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0005t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0005t0011g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0006t0002g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0006t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0006t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0008t0003g0045 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0001c0008t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0003 | 0/0 | 23 | 2 | 6 | 10 | 3 | 2 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0005 | 0/0 | 13 | 0 | 2 | 9 | 0 | 2 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0012 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0022 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0012g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0002t0014g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0002c0011t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0004g0002 | 0/0 | 25 | 0 | 3 | 16 | 0 | 6 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0004g0047 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0004g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0004g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0004g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0005g0026 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0007g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0008g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0009g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0009g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0010g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0003t0013g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0007t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0007t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0007t0006g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0003c0007t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0004c0004t0003g0004 | 0/0 | 14 | 0 | 3 | 7 | 0 | 4 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0004c0004t0003g0020 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0004c0004t0003g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0004c0004t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0004c0004t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0004c0004t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0004c0004t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0004c0004t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0004c0004t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0004c0004t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0004c0004t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0004c0004t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0004c0004t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0004c0004t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0004c0004t0005g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0004c0004t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0004c0004t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0005c0015t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0006c0013t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0007c0010t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0008c0012t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0009c0009t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| a0010c0014t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0003 | EUR | GBR | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0003 | EUR | GBR | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG00323 | hp1 | a0004 | c0004 | t0003 | g0129 | EUR | FIN | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0104 | EUR | FIN | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG00408 | hp1 | a0003 | c0003 | t0004 | g0002 | EAS | CHS | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | CHS | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG00423 | hp1 | a0003 | c0003 | t0004 | g0002 | EAS | CHS | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | CHS | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | CHS | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | CHS | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG00558 | hp2 | a0003 | c0003 | t0004 | g0002 | EAS | CHS | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | CHS | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG00621 | hp1 | a0004 | c0004 | t0003 | g0145 | EAS | CHS | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | CHS | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG00642 | hp1 | a0004 | c0004 | t0003 | g0004 | AMR | PUR | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG00735 | hp2 | a0001 | c0005 | t0002 | g0043 | AMR | PUR | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG00741 | hp2 | a0003 | c0003 | t0001 | g0086 | AMR | PUR | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | PUR | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01081 | hp1 | a0003 | c0003 | t0004 | g0002 | AMR | PUR | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0070 | AMR | PUR | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01109 | hp2 | a0003 | c0003 | t0004 | g0002 | AMR | PUR | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0032 | AMR | PUR | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01168 | hp2 | a0003 | c0003 | t0004 | g0153 | AMR | PUR | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01243 | hp1 | a0003 | c0003 | t0003 | g0049 | AMR | PUR | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0162 | AMR | CLM | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01256 | hp1 | a0003 | c0003 | t0004 | g0151 | AMR | CLM | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01257 | hp1 | a0001 | c0008 | t0003 | g0045 | AMR | CLM | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01346 | hp2 | a0003 | c0003 | t0004 | g0154 | AMR | CLM | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01358 | hp1 | a0001 | c0005 | t0002 | g0124 | AMR | CLM | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01361 | hp1 | a0003 | c0003 | t0005 | g0026 | AMR | CLM | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01361 | hp2 | a0003 | c0003 | t0004 | g0047 | AMR | CLM | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01433 | hp1 | a0004 | c0004 | t0003 | g0020 | AMR | CLM | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | CLM | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0039 | EUR | IBS | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0022 | EUR | IBS | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0022 | EUR | IBS | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0022 | EUR | IBS | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0039 | EUR | IBS | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01884 | hp1 | a0003 | c0007 | t0006 | g0131 | AFR | ACB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01884 | hp2 | a0003 | c0003 | t0005 | g0026 | AFR | ACB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | ACB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01891 | hp2 | a0003 | c0007 | t0006 | g0133 | AFR | ACB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01928 | hp2 | a0004 | c0004 | t0003 | g0004 | AMR | PEL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01934 | hp1 | a0004 | c0004 | t0003 | g0068 | AMR | PEL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01934 | hp2 | a0004 | c0004 | t0003 | g0004 | AMR | PEL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0058 | AMR | PEL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02027 | hp1 | a0003 | c0003 | t0004 | g0002 | EAS | KHV | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | KHV | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | KHV | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02080 | hp2 | a0003 | c0003 | t0004 | g0002 | EAS | KHV | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02083 | hp1 | a0003 | c0003 | t0004 | g0002 | EAS | KHV | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | KHV | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | KHV | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | KHV | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02135 | hp2 | a0003 | c0003 | t0004 | g0002 | EAS | KHV | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0097 | AFR | ACB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02145 | hp2 | a0003 | c0003 | t0001 | g0014 | AFR | ACB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02148 | hp1 | a0001 | c0005 | t0011 | g0105 | AMR | PEL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02148 | hp2 | a0001 | c0005 | t0002 | g0043 | AMR | PEL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02155 | hp1 | a0001 | c0005 | t0002 | g0017 | EAS | CDX | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | CDX | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | CDX | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | CDX | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02257 | hp1 | a0003 | c0003 | t0001 | g0010 | AFR | ACB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | ACB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0060 | AFR | ACB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02258 | hp2 | a0003 | c0003 | t0005 | g0084 | AFR | ACB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | ACB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02300 | hp1 | a0005 | c0015 | t0002 | g0127 | AMR | PEL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02300 | hp2 | a0003 | c0003 | t0004 | g0002 | AMR | PEL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02451 | hp1 | a0003 | c0003 | t0007 | g0149 | AFR | ACB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02523 | hp1 | a0003 | c0003 | t0004 | g0156 | EAS | KHV | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0065 | SAS | PJL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0056 | SAS | PJL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02615 | hp2 | a0003 | c0007 | t0003 | g0130 | AFR | GWD | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02622 | hp2 | a0003 | c0007 | t0006 | g0132 | AFR | GWD | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02630 | hp1 | a0003 | c0003 | t0001 | g0010 | AFR | GWD | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0098 | AFR | GWD | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02647 | hp2 | a0003 | c0003 | t0008 | g0029 | AFR | GWD | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02683 | hp2 | a0001 | c0008 | t0003 | g0045 | SAS | PJL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02717 | hp1 | a0003 | c0003 | t0009 | g0087 | AFR | GWD | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02717 | hp2 | a0006 | c0013 | t0003 | g0112 | AFR | GWD | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | GWD | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02723 | hp2 | a0003 | c0003 | t0001 | g0010 | AFR | GWD | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02809 | hp1 | a0003 | c0003 | t0001 | g0037 | AFR | GWD | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02886 | hp1 | a0003 | c0003 | t0001 | g0088 | AFR | GWD | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | GWD | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02895 | hp1 | a0003 | c0003 | t0001 | g0081 | AFR | GWD | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0055 | AFR | GWD | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | GWD | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0096 | AFR | GWD | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02897 | hp1 | a0003 | c0003 | t0001 | g0014 | AFR | GWD | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | GWD | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02922 | hp1 | a0003 | c0003 | t0001 | g0038 | AFR | ESN | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0116 | AFR | ESN | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | ESN | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0050 | AFR | ESN | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02970 | hp1 | a0003 | c0003 | t0001 | g0038 | AFR | ESN | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | ESN | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | ESN | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02976 | hp2 | a0003 | c0003 | t0001 | g0014 | AFR | ESN | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03017 | hp1 | a0003 | c0003 | t0004 | g0048 | SAS | PJL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | GWD | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03130 | hp1 | a0003 | c0003 | t0007 | g0077 | AFR | ESN | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ESN | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03139 | hp1 | a0004 | c0004 | t0005 | g0147 | AFR | ESN | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0102 | AFR | ESN | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03195 | hp1 | a0004 | c0004 | t0005 | g0028 | AFR | ESN | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | ESN | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | MSL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03209 | hp2 | a0003 | c0003 | t0001 | g0010 | AFR | MSL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03225 | hp1 | a0003 | c0003 | t0001 | g0010 | AFR | MSL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | MSL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0106 | SAS | PJL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03239 | hp2 | a0003 | c0003 | t0004 | g0002 | SAS | PJL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | MSL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03453 | hp2 | a0003 | c0003 | t0005 | g0026 | AFR | MSL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03486 | hp1 | a0007 | c0010 | t0003 | g0140 | AFR | MSL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03491 | hp2 | a0003 | c0003 | t0004 | g0002 | SAS | PJL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03492 | hp1 | a0003 | c0003 | t0004 | g0002 | SAS | PJL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03492 | hp2 | a0004 | c0004 | t0003 | g0004 | SAS | PJL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03516 | hp1 | a0004 | c0004 | t0005 | g0136 | AFR | ESN | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | ESN | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03540 | hp1 | a0003 | c0003 | t0001 | g0014 | AFR | GWD | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03540 | hp2 | a0003 | c0003 | t0001 | g0089 | AFR | GWD | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0031 | SAS | PJL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0032 | SAS | PJL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03669 | hp1 | a0004 | c0004 | t0003 | g0004 | SAS | PJL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0012 | SAS | PJL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0031 | SAS | STU | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03710 | hp2 | a0003 | c0003 | t0004 | g0048 | SAS | PJL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03834 | hp1 | a0003 | c0003 | t0004 | g0002 | SAS | BEB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03834 | hp2 | a0004 | c0004 | t0003 | g0004 | SAS | BEB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03927 | hp1 | a0003 | c0003 | t0004 | g0002 | SAS | BEB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0066 | SAS | BEB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0071 | SAS | BEB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG04115 | hp1 | a0004 | c0004 | t0003 | g0004 | SAS | STU | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0012 | SAS | STU | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0012 | SAS | BEB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG04184 | hp2 | a0004 | c0004 | t0003 | g0020 | SAS | BEB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | STU | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0075 | SAS | STU | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG04204 | hp1 | a0001 | c0008 | t0003 | g0126 | SAS | STU | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG04204 | hp2 | a0003 | c0003 | t0004 | g0002 | SAS | STU | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG04228 | hp1 | a0004 | c0004 | t0003 | g0139 | SAS | STU | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0076 | SAS | STU | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18522 | hp1 | a0003 | c0003 | t0001 | g0030 | AFR | YRI | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | YRI | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | CHB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | CHB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18906 | hp1 | a0003 | c0003 | t0001 | g0080 | AFR | YRI | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18906 | hp2 | a0003 | c0003 | t0008 | g0029 | AFR | YRI | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18939 | hp2 | a0003 | c0003 | t0004 | g0152 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18940 | hp2 | a0004 | c0004 | t0003 | g0020 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18941 | hp2 | a0003 | c0003 | t0004 | g0155 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18944 | hp1 | a0002 | c0002 | t0012 | g0064 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18947 | hp1 | a0003 | c0003 | t0004 | g0158 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18948 | hp1 | a0004 | c0004 | t0003 | g0046 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18948 | hp2 | a0003 | c0003 | t0004 | g0002 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18949 | hp2 | a0003 | c0003 | t0004 | g0047 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18954 | hp1 | a0008 | c0012 | t0002 | g0117 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18957 | hp1 | a0001 | c0005 | t0002 | g0107 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18957 | hp2 | a0001 | c0006 | t0002 | g0009 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18960 | hp1 | a0001 | c0006 | t0002 | g0009 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18964 | hp2 | a0001 | c0006 | t0002 | g0009 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18966 | hp2 | a0004 | c0004 | t0003 | g0142 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18968 | hp1 | a0001 | c0006 | t0002 | g0150 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18971 | hp1 | a0004 | c0004 | t0003 | g0004 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18974 | hp1 | a0002 | c0002 | t0014 | g0074 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18974 | hp2 | a0001 | c0006 | t0002 | g0009 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18977 | hp1 | a0003 | c0003 | t0004 | g0002 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18979 | hp2 | a0004 | c0004 | t0003 | g0046 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18980 | hp2 | a0003 | c0003 | t0004 | g0002 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18984 | hp1 | a0001 | c0005 | t0002 | g0017 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18987 | hp1 | a0004 | c0004 | t0003 | g0004 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18987 | hp2 | a0001 | c0005 | t0002 | g0017 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18988 | hp1 | a0003 | c0003 | t0004 | g0002 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18988 | hp2 | a0009 | c0009 | t0002 | g0093 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18989 | hp2 | a0004 | c0004 | t0003 | g0138 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18990 | hp1 | a0010 | c0014 | t0002 | g0119 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18994 | hp1 | a0004 | c0004 | t0003 | g0004 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18994 | hp2 | a0001 | c0006 | t0002 | g0009 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18997 | hp2 | a0001 | c0006 | t0002 | g0157 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18998 | hp2 | a0001 | c0006 | t0002 | g0009 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18999 | hp2 | a0004 | c0004 | t0003 | g0020 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19004 | hp1 | a0004 | c0004 | t0003 | g0004 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19010 | hp1 | a0003 | c0003 | t0004 | g0002 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19011 | hp1 | a0003 | c0003 | t0004 | g0002 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19012 | hp2 | a0004 | c0004 | t0003 | g0004 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0134 | AFR | LWK | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | LWK | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | LWK | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19043 | hp2 | a0003 | c0003 | t0009 | g0090 | AFR | LWK | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19054 | hp2 | a0004 | c0004 | t0003 | g0144 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19056 | hp1 | a0003 | c0003 | t0004 | g0002 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19059 | hp1 | a0004 | c0004 | t0003 | g0146 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19067 | hp2 | a0004 | c0004 | t0003 | g0004 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19081 | hp2 | a0004 | c0004 | t0003 | g0004 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19082 | hp2 | a0003 | c0003 | t0004 | g0002 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19083 | hp2 | a0003 | c0003 | t0004 | g0002 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19089 | hp1 | a0001 | c0005 | t0002 | g0017 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19089 | hp2 | a0004 | c0004 | t0004 | g0137 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19090 | hp2 | a0003 | c0003 | t0004 | g0159 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | YRI | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA19240 | hp2 | a0003 | c0003 | t0001 | g0037 | AFR | YRI | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0035 | AFR | ASW | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | ASW | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0078 | EUR | TSI | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0003 | EUR | TSI | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA20805 | hp1 | a0002 | c0011 | t0001 | g0062 | EUR | TSI | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | GIH | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0054 | SAS | GIH | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG01123 | hp2 | a0003 | c0003 | t0010 | g0148 | AMR | CLM | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02109 | hp1 | a0003 | c0003 | t0013 | g0082 | AFR | ACB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02109 | hp2 | a0004 | c0004 | t0003 | g0143 | AFR | ACB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | ACB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02486 | hp2 | a0003 | c0003 | t0001 | g0030 | AFR | ACB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02559 | hp1 | a0004 | c0004 | t0005 | g0028 | AFR | ACB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG02559 | hp2 | a0003 | c0003 | t0005 | g0083 | AFR | ACB | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | MSL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0120 | AFR | MSL | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG06807 | hp1 | a0003 | c0003 | t0004 | g0135 | AFR | USA | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| HG06807 | hp2 | a0003 | c0003 | t0005 | g0085 | AFR | USA | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0035 | AFR | USA | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | USA | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA21309 | hp1 | a0004 | c0004 | t0005 | g0028 | AFR | LWK | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| NA21309 | hp2 | a0004 | c0004 | t0003 | g0141 | AFR | LWK | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0100 | REF | REF | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0006 | REF | REF | MMUT_chr6_49425360_49468253 | MMUT | chr6 | 49425360 | 49468253 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:49435569 | T | C | 4 | a0002 a0003 a0004 others(1): Show |
217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
missense_variant | MODERATE | c.2011A>G | p.Ile671Val | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/13 | 2201/3811 | 2011/2253 | 671/750 | chr6 | 49435569 | |||
| chr6:49441847 | T | C | 1 | a0008 | 1 | NA18954.hp1 | missense_variant | MODERATE | c.1801A>G | p.Ile601Val | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 10/13 | 1991/3811 | 1801/2253 | 601/750 | chr6 | 49441847 | |||
| chr6:49441871 | C | G | 1 | a0007 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.1777G>C | p.Glu593Gln | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 10/13 | 1967/3811 | 1777/2253 | 593/750 | chr6 | 49441871 | |||
| chr6:49441885 | C | A | 1 | a0006 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.1763G>T | p.Arg588Leu | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 10/13 | 1953/3811 | 1763/2253 | 588/750 | chr6 | 49441885 | |||
| chr6:49444720 | C | T | 1 | a0002 | 103 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(100): Show |
missense_variant | MODERATE | c.1595G>A | p.Arg532His | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/13 | 1785/3811 | 1595/2253 | 532/750 | chr6 | 49444720 | |||
| chr6:49447735 | C | T | 2 | a0004 a0007 |
37 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
missense_variant | MODERATE | c.1495G>A | p.Ala499Thr | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 8/13 | 1685/3811 | 1495/2253 | 499/750 | chr6 | 49447735 | |||
| chr6:49451512 | T | C | 1 | a0010 | 1 | NA18990.hp1 | missense_variant | MODERATE | c.1286A>G | p.Tyr429Cys | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 6/13 | 1476/3811 | 1286/2253 | 429/750 | chr6 | 49451512 | |||
| chr6:49457839 | G | A | 1 | a0005 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.605C>T | p.Thr202Ile | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 3/13 | 795/3811 | 605/2253 | 202/750 | chr6 | 49457839 | |||
| chr6:49457983 | C | T | 1 | a0009 | 1 | NA18988.hp2 | missense_variant | MODERATE | c.461G>A | p.Arg154His | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 3/13 | 651/3811 | 461/2253 | 154/750 | chr6 | 49457983 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:49435588 | C | T | 2 | a0001c0005 a0005c0015 |
10 | HG00735.hp2 HG01358.hp1 HG02148.hp1 others(7): Show |
synonymous_variant | LOW | c.1992G>A | p.Ala664Ala | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/13 | 2182/3811 | 1992/2253 | 664/750 | chr6 | 49435588 | |||
| chr6:49444686 | G | A | 1 | a0002c0011 | 1 | NA20805.hp1 | synonymous_variant | LOW | c.1629C>T | p.Ser543Ser | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/13 | 1819/3811 | 1629/2253 | 543/750 | chr6 | 49444686 | |||
| chr6:49457733 | T | C | 1 | a0001c0008 | 3 | HG01257.hp1 HG02683.hp2 HG04204.hp1 |
synonymous_variant | LOW | c.711A>G | p.Pro237Pro | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 3/13 | 901/3811 | 711/2253 | 237/750 | chr6 | 49457733 | |||
| chr6:49457808 | C | T | 6 | a0001c0006 a0002c0002 a0002c0011 others(3): Show |
221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
synonymous_variant | LOW | c.636G>A | p.Lys212Lys | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 3/13 | 826/3811 | 636/2253 | 212/750 | chr6 | 49457808 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:49430402 | C | T | 8 | a0001c0001t0002 a0001c0005t0002 a0001c0005t0011 others(5): Show |
116 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*1326G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 13/13 | 1326 | chr6 | 49430402 | ||||||
| chr6:49430483 | T | C | 1 | a0001c0005t0011 | 1 | HG02148.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1245A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 13/13 | 1245 | chr6 | 49430483 | ||||||
| chr6:49430503 | T | C | 1 | a0003c0003t0013 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1225A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 13/13 | 1225 | chr6 | 49430503 | ||||||
| chr6:49430620 | G | GT | 8 | a0002c0002t0001 a0002c0002t0012 a0002c0002t0014 others(5): Show |
128 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*1107dupA | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 13/13 | 1107 | chr6 | 49430620 | ||||||
| chr6:49430742 | C | T | 1 | a0002c0002t0012 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*986G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 13/13 | 986 | chr6 | 49430742 | ||||||
| chr6:49431101 | G | A | 1 | a0003c0003t0008 | 2 | HG02647.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*627C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 13/13 | 627 | chr6 | 49431101 | ||||||
| chr6:49431148 | T | C | 2 | a0003c0003t0004 a0004c0004t0004 |
39 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*580A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 13/13 | 580 | chr6 | 49431148 | ||||||
| chr6:49431170 | T | C | 1 | a0003c0003t0009 | 2 | HG02717.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*558A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 13/13 | 558 | chr6 | 49431170 | ||||||
| chr6:49431199 | T | C | 1 | a0003c0003t0007 | 2 | HG02451.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*529A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 13/13 | 529 | chr6 | 49431199 | ||||||
| chr6:49431366 | G | C | 1 | a0004c0004t0003 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*362C>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 13/13 | 362 | chr6 | 49431366 | ||||||
| chr6:49431471 | T | G | 1 | a0003c0003t0010 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*257A>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 13/13 | 257 | chr6 | 49431471 | ||||||
| chr6:49431526 | A | AT | 2 | a0003c0003t0005 a0004c0004t0005 |
11 | HG01361.hp1 HG01884.hp2 HG02258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*201dupA | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 13/13 | 201 | chr6 | 49431526 | ||||||
| chr6:49431526 | AT | A | 9 | a0002c0002t0001 a0002c0002t0012 a0002c0002t0014 others(6): Show |
129 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*201delA | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 13/13 | 201 | chr6 | 49431526 | ||||||
| chr6:49431627 | C | T | 1 | a0003c0003t0010 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*101G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 13/13 | 101 | chr6 | 49431627 | ||||||
| chr6:49431694 | T | C | 1 | a0003c0007t0006 | 3 | HG01884.hp1 HG01891.hp2 HG02622.hp2 |
3_prime_UTR_variant | MODIFIER | c.*34A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 13/13 | 34 | chr6 | 49431694 | ||||||
| chr6:49459489 | T | C | 1 | a0002c0002t0014 | 1 | NA18974.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-23A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 2/13 | chr6 | 49459489 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:49432003 | T | C | 1 | a0001c0006t0002g0150 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2125-147A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49432003 | |||||||
| chr6:49432074 | C | T | 3 | a0003c0003t0005g0083 a0003c0003t0005g0084 a0003c0003t0005g0085 |
3 | HG02258.hp2 HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2125-218G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49432074 | |||||||
| chr6:49432271 | G | A | 12 | a0003c0003t0004g0002 a0003c0003t0004g0047 a0003c0003t0004g0048 others(9): Show |
38 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.2125-415C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49432271 | |||||||
| chr6:49432332 | AT | A | 57 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(54): Show |
128 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.2125-477delA | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49432332 | |||||||
| chr6:49432337 | T | G | 4 | a0003c0003t0005g0026 a0003c0003t0005g0083 a0003c0003t0005g0084 others(1): Show |
6 | HG01361.hp1 HG01884.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2125-481A>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49432337 | |||||||
| chr6:49432430 | C | G | 43 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(40): Show |
103 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.2125-574G>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49432430 | |||||||
| chr6:49432481 | G | A | 1 | a0003c0003t0001g0038 | 2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2125-625C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49432481 | |||||||
| chr6:49432510 | T | C | 109 | a0001c0001t0003g0015 a0001c0001t0003g0018 a0001c0001t0003g0041 others(106): Show |
235 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.2125-654A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49432510 | |||||||
| chr6:49432524 | G | A | 101 | a0001c0001t0003g0041 a0001c0001t0003g0134 a0002c0002t0001g0003 others(98): Show |
220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.2125-668C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49432524 | |||||||
| chr6:49432532 | C | T | 1 | a0003c0003t0004g0152 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2125-676G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49432532 | |||||||
| chr6:49432548 | C | T | 1 | a0003c0003t0004g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2125-692G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49432548 | |||||||
| chr6:49432613 | T | C | 43 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(40): Show |
103 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.2125-757A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49432613 | |||||||
| chr6:49432638 | T | C | 1 | a0002c0002t0001g0070 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2125-782A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49432638 | |||||||
| chr6:49432676 | C | T | 1 | a0002c0002t0001g0031 | 2 | HG03654.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.2125-820G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49432676 | |||||||
| chr6:49432691 | T | C | 3 | a0003c0003t0001g0010 a0003c0003t0001g0088 a0003c0003t0001g0089 |
7 | HG02257.hp1 HG02630.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2125-835A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49432691 | |||||||
| chr6:49433071 | C | T | 1 | a0003c0003t0004g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2125-1215G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49433071 | |||||||
| chr6:49433082 | G | T | 57 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(54): Show |
128 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.2125-1226C>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49433082 | |||||||
| chr6:49433099 | T | C | 1 | a0001c0001t0002g0104 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2125-1243A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49433099 | |||||||
| chr6:49433468 | T | A | 3 | a0003c0003t0001g0010 a0003c0003t0001g0088 a0003c0003t0001g0089 |
7 | HG02257.hp1 HG02630.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2125-1612A>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49433468 | |||||||
| chr6:49433659 | G | A | 3 | a0003c0003t0004g0152 a0003c0003t0004g0155 a0003c0003t0004g0158 |
3 | NA18939.hp2 NA18941.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.2124+1797C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49433659 | |||||||
| chr6:49433677 | C | T | 3 | a0003c0007t0006g0131 a0003c0007t0006g0132 a0003c0007t0006g0133 |
3 | HG01884.hp1 HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2124+1779G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49433677 | |||||||
| chr6:49433786 | T | C | 4 | a0001c0001t0002g0104 a0001c0006t0002g0009 a0001c0006t0002g0150 others(1): Show |
9 | HG00323.hp2 NA18957.hp2 NA18960.hp1 others(6): Show |
intron_variant | MODIFIER | c.2124+1670A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49433786 | |||||||
| chr6:49433944 | T | C | 1 | a0003c0003t0004g0156 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2124+1512A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49433944 | |||||||
| chr6:49434070 | A | C | 1 | a0003c0003t0001g0088 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2124+1386T>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49434070 | |||||||
| chr6:49434122 | A | C | 3 | a0003c0003t0001g0014 a0003c0003t0001g0081 a0003c0003t0013g0082 |
6 | HG02109.hp1 HG02145.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2124+1334T>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49434122 | |||||||
| chr6:49434141 | C | A | 3 | a0003c0007t0006g0131 a0003c0007t0006g0132 a0003c0007t0006g0133 |
3 | HG01884.hp1 HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2124+1315G>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49434141 | |||||||
| chr6:49434156 | C | A | 1 | a0001c0001t0003g0097 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2124+1300G>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49434156 | |||||||
| chr6:49434329 | G | A | 1 | a0005c0015t0002g0127 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2124+1127C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49434329 | |||||||
| chr6:49434356 | G | A | 1 | a0004c0004t0003g0139 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2124+1100C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49434356 | |||||||
| chr6:49434499 | T | C | 1 | a0001c0001t0002g0128 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2124+957A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49434499 | |||||||
| chr6:49434606 | T | C | 17 | a0004c0004t0003g0004 a0004c0004t0003g0020 a0004c0004t0003g0046 others(14): Show |
36 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.2124+850A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49434606 | |||||||
| chr6:49434855 | A | G | 1 | a0002c0002t0001g0059 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2124+601T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49434855 | |||||||
| chr6:49434896 | C | G | 1 | a0004c0004t0003g0144 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2124+560G>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49434896 | |||||||
| chr6:49434914 | T | G | 2 | a0003c0003t0007g0077 a0003c0003t0007g0149 |
2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2124+542A>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49434914 | |||||||
| chr6:49434925 | T | C | 3 | a0004c0004t0005g0028 a0004c0004t0005g0136 a0004c0004t0005g0147 |
5 | HG02559.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2124+531A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49434925 | |||||||
| chr6:49434999 | C | T | 1 | a0004c0004t0003g0144 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2124+457G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49434999 | |||||||
| chr6:49435277 | G | T | 1 | a0002c0002t0001g0055 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2124+179C>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 12/12 | chr6 | 49435277 | |||||||
| chr6:49435941 | A | T | 1 | a0001c0001t0002g0036 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1957-318T>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49435941 | |||||||
| chr6:49435945 | A | C | 1 | a0001c0001t0002g0111 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1957-322T>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49435945 | |||||||
| chr6:49435970 | G | A | 1 | a0002c0002t0001g0060 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1957-347C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49435970 | |||||||
| chr6:49436037 | CTGAT | C | 3 | a0003c0003t0001g0010 a0003c0003t0001g0088 a0003c0003t0001g0089 |
7 | HG02257.hp1 HG02630.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1957-418_1957-415d others(6): Show |
MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49436037 | |||||||
| chr6:49436121 | A | G | 2 | a0001c0008t0003g0045 a0001c0008t0003g0126 |
3 | HG01257.hp1 HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1957-498T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49436121 | |||||||
| chr6:49436206 | C | T | 1 | a0001c0001t0002g0110 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1957-583G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49436206 | |||||||
| chr6:49436244 | A | G | 4 | a0003c0003t0005g0026 a0003c0003t0005g0083 a0003c0003t0005g0084 others(1): Show |
6 | HG01361.hp1 HG01884.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1957-621T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49436244 | |||||||
| chr6:49436273 | G | A | 1 | a0001c0001t0002g0113 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1957-650C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49436273 | |||||||
| chr6:49436277 | A | G | 1 | a0002c0002t0001g0032 | 2 | HG01167.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1957-654T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49436277 | |||||||
| chr6:49436544 | G | T | 7 | a0002c0002t0001g0005 a0002c0002t0001g0033 a0002c0002t0001g0035 others(4): Show |
21 | HG00438.hp2 HG01952.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.1957-921C>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49436544 | |||||||
| chr6:49436604 | C | CA | 10 | a0001c0001t0002g0128 a0002c0002t0001g0012 a0002c0002t0001g0053 others(7): Show |
14 | HG02132.hp2 HG02135.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1957-982dupT | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49436604 | |||||||
| chr6:49436604 | CA | C | 38 | a0003c0003t0003g0049 a0003c0003t0004g0002 a0003c0003t0004g0047 others(35): Show |
85 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.1957-982delT | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49436604 | |||||||
| chr6:49436632 | C | T | 1 | a0001c0001t0003g0016 | 4 | HG00642.hp2 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1957-1009G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49436632 | |||||||
| chr6:49436737 | A | C | 1 | a0003c0003t0008g0029 | 2 | HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1957-1114T>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49436737 | |||||||
| chr6:49436772 | C | T | 1 | a0002c0002t0001g0063 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1957-1149G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49436772 | |||||||
| chr6:49436773 | G | A | 2 | a0003c0003t0007g0077 a0003c0003t0007g0149 |
2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1957-1150C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49436773 | |||||||
| chr6:49437401 | C | T | 1 | a0003c0003t0010g0148 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1957-1778G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49437401 | |||||||
| chr6:49437670 | T | A | 3 | a0003c0007t0006g0131 a0003c0007t0006g0132 a0003c0007t0006g0133 |
3 | HG01884.hp1 HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1957-2047A>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49437670 | |||||||
| chr6:49437839 | A | G | 1 | a0007c0010t0003g0140 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1957-2216T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49437839 | |||||||
| chr6:49437860 | G | A | 1 | a0002c0002t0001g0013 | 4 | HG03195.hp2 NA19030.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1957-2237C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49437860 | |||||||
| chr6:49438109 | C | CCTT | 61 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
132 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.1956+2096_1956+209 others(7): Show |
MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49438109 | |||||||
| chr6:49438134 | A | G | 1 | a0003c0003t0004g0154 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1956+2072T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49438134 | |||||||
| chr6:49438189 | T | A | 3 | a0003c0003t0005g0083 a0003c0003t0005g0084 a0003c0003t0005g0085 |
3 | HG02258.hp2 HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1956+2017A>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49438189 | |||||||
| chr6:49438343 | G | A | 100 | a0001c0001t0003g0134 a0002c0002t0001g0003 a0002c0002t0001g0005 others(97): Show |
218 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.1956+1863C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49438343 | |||||||
| chr6:49438359 | G | A | 1 | a0003c0003t0004g0048 | 2 | HG03017.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1956+1847C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49438359 | |||||||
| chr6:49438363 | A | G | 1 | a0002c0002t0001g0065 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1956+1843T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49438363 | |||||||
| chr6:49438504 | T | A | 30 | a0003c0003t0004g0002 a0003c0003t0004g0047 a0003c0003t0004g0048 others(27): Show |
75 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.1956+1702A>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49438504 | |||||||
| chr6:49438509 | A | C | 2 | a0003c0003t0007g0077 a0003c0003t0007g0149 |
2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1956+1697T>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49438509 | |||||||
| chr6:49438554 | T | C | 2 | a0001c0001t0003g0042 a0006c0013t0003g0112 |
3 | HG02717.hp2 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1956+1652A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49438554 | |||||||
| chr6:49438635 | A | G | 99 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(96): Show |
217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.1956+1571T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49438635 | |||||||
| chr6:49438869 | C | T | 1 | a0002c0002t0001g0063 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1956+1337G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49438869 | |||||||
| chr6:49438916 | C | T | 3 | a0003c0007t0006g0131 a0003c0007t0006g0132 a0003c0007t0006g0133 |
3 | HG01884.hp1 HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1956+1290G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49438916 | |||||||
| chr6:49439098 | T | C | 1 | a0003c0003t0008g0029 | 2 | HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1956+1108A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49439098 | |||||||
| chr6:49439212 | T | C | 61 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
134 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.1956+994A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49439212 | |||||||
| chr6:49439301 | C | A | 1 | a0004c0004t0003g0141 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1956+905G>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49439301 | |||||||
| chr6:49439340 | C | G | 99 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(96): Show |
217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.1956+866G>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49439340 | |||||||
| chr6:49439356 | T | C | 96 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(93): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.1956+850A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49439356 | |||||||
| chr6:49439621 | C | T | 2 | a0002c0002t0001g0023 a0002c0002t0001g0073 |
4 | NA18747.hp2 NA18975.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1956+585G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49439621 | |||||||
| chr6:49439770 | C | A | 3 | a0003c0007t0006g0131 a0003c0007t0006g0132 a0003c0007t0006g0133 |
3 | HG01884.hp1 HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1956+436G>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49439770 | |||||||
| chr6:49439851 | G | A | 1 | a0002c0002t0001g0007 | 6 | NA18951.hp1 NA18986.hp1 NA19009.hp2 others(3): Show |
intron_variant | MODIFIER | c.1956+355C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49439851 | |||||||
| chr6:49439936 | C | T | 4 | a0003c0003t0003g0049 a0003c0003t0007g0077 a0003c0003t0007g0149 others(1): Show |
4 | HG01243.hp1 HG02451.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1956+270G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49439936 | |||||||
| chr6:49440067 | C | T | 1 | a0001c0001t0003g0120 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1956+139G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 11/12 | chr6 | 49440067 | |||||||
| chr6:49440529 | G | A | 1 | a0001c0001t0003g0018 | 4 | HG02486.hp1 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1809-176C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 10/12 | chr6 | 49440529 | |||||||
| chr6:49440638 | T | C | 1 | a0001c0001t0003g0027 | 3 | HG02257.hp2 HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1809-285A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 10/12 | chr6 | 49440638 | |||||||
| chr6:49440799 | C | A | 2 | a0003c0003t0007g0077 a0003c0003t0007g0149 |
2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1809-446G>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 10/12 | chr6 | 49440799 | |||||||
| chr6:49440914 | A | G | 7 | a0003c0003t0001g0014 a0003c0003t0001g0081 a0003c0003t0005g0026 others(4): Show |
12 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1809-561T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 10/12 | chr6 | 49440914 | |||||||
| chr6:49441275 | T | C | 1 | a0002c0002t0001g0061 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1808+565A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 10/12 | chr6 | 49441275 | |||||||
| chr6:49441399 | T | C | 3 | a0003c0003t0001g0014 a0003c0003t0001g0081 a0003c0003t0013g0082 |
6 | HG02109.hp1 HG02145.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1808+441A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 10/12 | chr6 | 49441399 | |||||||
| chr6:49441408 | G | C | 1 | a0004c0004t0003g0143 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1808+432C>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 10/12 | chr6 | 49441408 | |||||||
| chr6:49441424 | C | T | 1 | a0003c0003t0005g0084 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1808+416G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 10/12 | chr6 | 49441424 | |||||||
| chr6:49441674 | TTA | T | 2 | a0003c0003t0001g0038 a0003c0003t0001g0086 |
3 | HG00741.hp2 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1808+164_1808+165d others(4): Show |
MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 10/12 | chr6 | 49441674 | |||||||
| chr6:49441774 | G | C | 57 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(54): Show |
128 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.1808+66C>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 10/12 | chr6 | 49441774 | |||||||
| chr6:49442001 | T | A | 2 | a0003c0003t0001g0037 a0003c0003t0001g0080 |
3 | HG02809.hp1 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1677-30A>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49442001 | |||||||
| chr6:49442024 | T | C | 57 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(54): Show |
128 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.1677-53A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49442024 | |||||||
| chr6:49442135 | T | A | 57 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(54): Show |
128 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.1677-164A>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49442135 | |||||||
| chr6:49442337 | C | T | 3 | a0003c0003t0001g0014 a0003c0003t0001g0081 a0003c0003t0013g0082 |
6 | HG02109.hp1 HG02145.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1677-366G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49442337 | |||||||
| chr6:49442348 | C | T | 2 | a0003c0003t0001g0037 a0003c0003t0001g0080 |
3 | HG02809.hp1 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1677-377G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49442348 | |||||||
| chr6:49442354 | T | C | 1 | a0001c0001t0002g0123 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1677-383A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49442354 | |||||||
| chr6:49442429 | G | C | 2 | a0004c0004t0003g0138 a0004c0004t0003g0142 |
2 | NA18966.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1677-458C>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49442429 | |||||||
| chr6:49442681 | G | C | 1 | a0002c0002t0001g0033 | 2 | NA18960.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1677-710C>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49442681 | |||||||
| chr6:49442803 | C | T | 1 | a0001c0001t0003g0134 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1677-832G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49442803 | |||||||
| chr6:49442882 | G | A | 1 | a0002c0002t0001g0024 | 3 | HG00609.hp2 NA18955.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1677-911C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49442882 | |||||||
| chr6:49443023 | TA | T | 3 | a0004c0004t0005g0028 a0004c0004t0005g0136 a0004c0004t0005g0147 |
5 | HG02559.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1677-1053delT | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49443023 | |||||||
| chr6:49443081 | T | C | 3 | a0003c0007t0006g0131 a0003c0007t0006g0132 a0003c0007t0006g0133 |
3 | HG01884.hp1 HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1677-1110A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49443081 | |||||||
| chr6:49443159 | T | C | 1 | a0002c0002t0001g0031 | 2 | HG03654.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1677-1188A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49443159 | |||||||
| chr6:49443358 | C | T | 1 | a0004c0004t0003g0046 | 2 | NA18948.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1676+1281G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49443358 | |||||||
| chr6:49443420 | C | T | 2 | a0003c0003t0004g0151 a0003c0003t0004g0153 |
2 | HG01168.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.1676+1219G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49443420 | |||||||
| chr6:49443487 | G | A | 2 | a0003c0003t0003g0049 a0003c0007t0003g0130 |
2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1676+1152C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49443487 | |||||||
| chr6:49443593 | C | A | 1 | a0003c0003t0009g0087 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1676+1046G>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49443593 | |||||||
| chr6:49443594 | C | T | 1 | a0003c0003t0010g0148 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1676+1045G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49443594 | |||||||
| chr6:49443764 | G | C | 61 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
134 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.1676+875C>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49443764 | |||||||
| chr6:49443871 | G | A | 1 | a0002c0002t0001g0057 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1676+768C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49443871 | |||||||
| chr6:49443906 | A | G | 61 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
134 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.1676+733T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49443906 | |||||||
| chr6:49443967 | G | C | 1 | a0003c0003t0008g0029 | 2 | HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1676+672C>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49443967 | |||||||
| chr6:49443969 | G | A | 1 | a0001c0001t0002g0118 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1676+670C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49443969 | |||||||
| chr6:49444068 | T | C | 2 | a0003c0003t0007g0077 a0003c0003t0007g0149 |
2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1676+571A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49444068 | |||||||
| chr6:49444152 | A | G | 2 | a0003c0003t0003g0049 a0003c0007t0003g0130 |
2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1676+487T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49444152 | |||||||
| chr6:49444173 | G | A | 14 | a0004c0004t0003g0004 a0004c0004t0003g0020 a0004c0004t0003g0046 others(11): Show |
31 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1676+466C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49444173 | |||||||
| chr6:49444174 | G | T | 14 | a0004c0004t0003g0004 a0004c0004t0003g0020 a0004c0004t0003g0046 others(11): Show |
31 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1676+465C>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49444174 | |||||||
| chr6:49444237 | T | C | 2 | a0003c0003t0007g0077 a0003c0003t0007g0149 |
2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1676+402A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49444237 | |||||||
| chr6:49444309 | T | A | 2 | a0001c0005t0002g0043 a0001c0005t0002g0124 |
3 | HG00735.hp2 HG01358.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1676+330A>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49444309 | |||||||
| chr6:49444358 | A | G | 1 | a0004c0004t0003g0068 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1676+281T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49444358 | |||||||
| chr6:49444445 | T | C | 1 | a0001c0001t0002g0113 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1676+194A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49444445 | |||||||
| chr6:49444562 | T | G | 34 | a0003c0003t0004g0002 a0003c0003t0004g0047 a0003c0003t0004g0048 others(31): Show |
81 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.1676+77A>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 9/12 | chr6 | 49444562 | |||||||
| chr6:49445034 | CAT | C | 20 | a0003c0003t0001g0038 a0003c0003t0001g0086 a0004c0004t0003g0004 others(17): Show |
40 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1561-282_1561-281d others(4): Show |
MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 8/12 | chr6 | 49445034 | |||||||
| chr6:49445197 | T | C | 1 | a0001c0001t0002g0122 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1561-443A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 8/12 | chr6 | 49445197 | |||||||
| chr6:49445283 | T | A | 1 | a0001c0001t0002g0044 | 2 | NA18950.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1561-529A>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 8/12 | chr6 | 49445283 | |||||||
| chr6:49445293 | A | G | 1 | a0007c0010t0003g0140 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1561-539T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 8/12 | chr6 | 49445293 | |||||||
| chr6:49445512 | C | T | 2 | a0003c0003t0003g0049 a0003c0007t0003g0130 |
2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1561-758G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 8/12 | chr6 | 49445512 | |||||||
| chr6:49445531 | G | C | 99 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(96): Show |
217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.1561-777C>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 8/12 | chr6 | 49445531 | |||||||
| chr6:49445559 | A | T | 1 | a0001c0001t0002g0109 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1561-805T>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 8/12 | chr6 | 49445559 | |||||||
| chr6:49445576 | G | A | 99 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(96): Show |
217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.1561-822C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 8/12 | chr6 | 49445576 | |||||||
| chr6:49445678 | G | C | 99 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(96): Show |
217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.1561-924C>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 8/12 | chr6 | 49445678 | |||||||
| chr6:49445762 | A | G | 1 | a0002c0002t0001g0058 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1561-1008T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 8/12 | chr6 | 49445762 | |||||||
| chr6:49445798 | C | T | 3 | a0003c0003t0001g0014 a0003c0003t0001g0081 a0003c0003t0013g0082 |
6 | HG02109.hp1 HG02145.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1561-1044G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 8/12 | chr6 | 49445798 | |||||||
| chr6:49446263 | A | G | 14 | a0004c0004t0003g0004 a0004c0004t0003g0020 a0004c0004t0003g0046 others(11): Show |
31 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1560+1407T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 8/12 | chr6 | 49446263 | |||||||
| chr6:49446278 | G | A | 1 | a0002c0002t0001g0063 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1560+1392C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 8/12 | chr6 | 49446278 | |||||||
| chr6:49446522 | T | G | 43 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(40): Show |
103 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1560+1148A>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 8/12 | chr6 | 49446522 | |||||||
| chr6:49446603 | A | G | 1 | a0002c0002t0014g0074 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1560+1067T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 8/12 | chr6 | 49446603 | |||||||
| chr6:49446706 | T | C | 2 | a0003c0003t0003g0049 a0003c0007t0003g0130 |
2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1560+964A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 8/12 | chr6 | 49446706 | |||||||
| chr6:49447157 | T | C | 1 | a0001c0001t0003g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1560+513A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 8/12 | chr6 | 49447157 | |||||||
| chr6:49447330 | C | T | 57 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(54): Show |
128 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.1560+340G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 8/12 | chr6 | 49447330 | |||||||
| chr6:49447482 | T | G | 1 | a0002c0002t0012g0064 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1560+188A>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 8/12 | chr6 | 49447482 | |||||||
| chr6:49447546 | T | C | 2 | a0003c0003t0003g0049 a0003c0007t0003g0130 |
2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1560+124A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 8/12 | chr6 | 49447546 | |||||||
| chr6:49447590 | G | A | 1 | a0004c0004t0003g0144 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1560+80C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 8/12 | chr6 | 49447590 | |||||||
| chr6:49447638 | T | TA | 43 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(40): Show |
103 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1560+31dupT | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 8/12 | chr6 | 49447638 | |||||||
| chr6:49447638 | T | TAA | 17 | a0003c0003t0001g0010 a0003c0003t0001g0014 a0003c0003t0001g0030 others(14): Show |
30 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1560+30_1560+31dup others(2): Show |
MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 8/12 | chr6 | 49447638 | |||||||
| chr6:49447638 | TA | T | 10 | a0001c0001t0002g0095 a0001c0001t0002g0108 a0001c0001t0002g0121 others(7): Show |
15 | HG01884.hp1 HG02622.hp2 HG06807.hp1 others(12): Show |
intron_variant | MODIFIER | c.1560+31delT | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 8/12 | chr6 | 49447638 | |||||||
| chr6:49447827 | C | T | 1 | a0003c0003t0007g0149 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1445-42G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 7/12 | chr6 | 49447827 | |||||||
| chr6:49447932 | A | T | 1 | a0001c0001t0002g0106 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1445-147T>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 7/12 | chr6 | 49447932 | |||||||
| chr6:49448123 | G | A | 1 | a0001c0001t0002g0036 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1445-338C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 7/12 | chr6 | 49448123 | |||||||
| chr6:49448156 | A | G | 2 | a0001c0005t0011g0105 a0005c0015t0002g0127 |
2 | HG02148.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1445-371T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 7/12 | chr6 | 49448156 | |||||||
| chr6:49448290 | C | A | 7 | a0003c0003t0001g0014 a0003c0003t0001g0081 a0003c0003t0005g0026 others(4): Show |
12 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1445-505G>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 7/12 | chr6 | 49448290 | |||||||
| chr6:49448338 | T | G | 2 | a0003c0003t0007g0077 a0003c0003t0007g0149 |
2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1444+478A>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 7/12 | chr6 | 49448338 | |||||||
| chr6:49448391 | A | G | 1 | a0001c0001t0003g0096 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1444+425T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 7/12 | chr6 | 49448391 | |||||||
| chr6:49448615 | A | C | 3 | a0003c0003t0001g0014 a0003c0003t0001g0081 a0003c0003t0013g0082 |
6 | HG02109.hp1 HG02145.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1444+201T>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 7/12 | chr6 | 49448615 | |||||||
| chr6:49448615 | A | G | 1 | a0003c0003t0001g0080 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1444+201T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 7/12 | chr6 | 49448615 | |||||||
| chr6:49448625 | C | A | 2 | a0001c0001t0002g0036 a0001c0001t0002g0078 |
3 | HG01167.hp2 HG01169.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1444+191G>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 7/12 | chr6 | 49448625 | |||||||
| chr6:49448639 | T | C | 1 | a0003c0003t0004g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1444+177A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 7/12 | chr6 | 49448639 | |||||||
| chr6:49448747 | T | C | 2 | a0003c0003t0007g0077 a0003c0003t0007g0149 |
2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1444+69A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 7/12 | chr6 | 49448747 | |||||||
| chr6:49448935 | G | A | 2 | a0001c0001t0002g0114 a0001c0001t0002g0163 |
2 | NA18971.hp2 NA19001.hp1 |
splice_region_variant&intron_variant | LOW | c.1333-8C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 6/12 | chr6 | 49448935 | |||||||
| chr6:49448945 | A | C | 3 | a0003c0003t0001g0014 a0003c0003t0001g0081 a0003c0003t0013g0082 |
6 | HG02109.hp1 HG02145.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1333-18T>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 6/12 | chr6 | 49448945 | |||||||
| chr6:49449020 | AT | A | 7 | a0003c0003t0001g0014 a0003c0003t0001g0081 a0003c0003t0005g0026 others(4): Show |
12 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1333-94delA | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 6/12 | chr6 | 49449020 | |||||||
| chr6:49449090 | T | C | 1 | a0001c0001t0003g0134 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1333-163A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 6/12 | chr6 | 49449090 | |||||||
| chr6:49449112 | T | C | 43 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(40): Show |
103 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1333-185A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 6/12 | chr6 | 49449112 | |||||||
| chr6:49449205 | T | C | 3 | a0003c0003t0001g0010 a0003c0003t0001g0088 a0003c0003t0001g0089 |
7 | HG02257.hp1 HG02630.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1333-278A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 6/12 | chr6 | 49449205 | |||||||
| chr6:49449217 | C | T | 2 | a0003c0003t0007g0077 a0003c0003t0007g0149 |
2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1333-290G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 6/12 | chr6 | 49449217 | |||||||
| chr6:49449246 | G | A | 2 | a0003c0003t0007g0077 a0003c0003t0007g0149 |
2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1333-319C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 6/12 | chr6 | 49449246 | |||||||
| chr6:49449373 | A | T | 1 | a0003c0003t0004g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1333-446T>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 6/12 | chr6 | 49449373 | |||||||
| chr6:49449497 | AAAG | A | 31 | a0003c0003t0004g0002 a0003c0003t0004g0047 a0003c0003t0004g0048 others(28): Show |
76 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1333-573_1333-571d others(5): Show |
MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 6/12 | chr6 | 49449497 | |||||||
| chr6:49449783 | A | C | 1 | a0001c0001t0002g0040 | 2 | HG00741.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1333-856T>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 6/12 | chr6 | 49449783 | |||||||
| chr6:49449809 | G | A | 1 | a0003c0003t0004g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1333-882C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 6/12 | chr6 | 49449809 | |||||||
| chr6:49449837 | C | T | 1 | a0004c0004t0003g0139 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1333-910G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 6/12 | chr6 | 49449837 | |||||||
| chr6:49450095 | G | C | 1 | a0002c0002t0001g0065 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1333-1168C>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 6/12 | chr6 | 49450095 | |||||||
| chr6:49450145 | C | T | 3 | a0003c0003t0001g0014 a0003c0003t0001g0081 a0003c0003t0013g0082 |
6 | HG02109.hp1 HG02145.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1333-1218G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 6/12 | chr6 | 49450145 | |||||||
| chr6:49450229 | T | TA | 10 | a0001c0001t0002g0115 a0001c0001t0003g0102 a0001c0001t0003g0116 others(7): Show |
15 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1332+1236dupT | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 6/12 | chr6 | 49450229 | |||||||
| chr6:49450229 | TA | T | 11 | a0001c0001t0002g0099 a0001c0001t0002g0103 a0001c0001t0002g0104 others(8): Show |
13 | HG00323.hp1 HG00323.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.1332+1236delT | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 6/12 | chr6 | 49450229 | |||||||
| chr6:49450289 | C | T | 1 | a0001c0001t0003g0102 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1332+1177G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 6/12 | chr6 | 49450289 | |||||||
| chr6:49450391 | A | G | 2 | a0003c0003t0001g0030 a0003c0003t0008g0029 |
4 | HG02486.hp2 HG02647.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1332+1075T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 6/12 | chr6 | 49450391 | |||||||
| chr6:49450417 | A | G | 1 | a0001c0001t0002g0036 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1332+1049T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 6/12 | chr6 | 49450417 | |||||||
| chr6:49450698 | C | G | 2 | a0003c0003t0003g0049 a0003c0007t0003g0130 |
2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1332+768G>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 6/12 | chr6 | 49450698 | |||||||
| chr6:49450902 | G | A | 2 | a0003c0003t0001g0038 a0003c0003t0001g0086 |
3 | HG00741.hp2 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1332+564C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 6/12 | chr6 | 49450902 | |||||||
| chr6:49451021 | G | A | 6 | a0001c0001t0002g0008 a0001c0001t0002g0011 a0001c0001t0002g0094 others(3): Show |
15 | HG00408.hp2 HG01993.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.1332+445C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 6/12 | chr6 | 49451021 | |||||||
| chr6:49451038 | T | G | 1 | a0003c0003t0004g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1332+428A>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 6/12 | chr6 | 49451038 | |||||||
| chr6:49451144 | A | G | 1 | a0003c0003t0010g0148 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1332+322T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 6/12 | chr6 | 49451144 | |||||||
| chr6:49451356 | T | A | 1 | a0002c0002t0001g0067 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1332+110A>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 6/12 | chr6 | 49451356 | |||||||
| chr6:49451726 | G | A | 1 | a0001c0001t0003g0120 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1084-12C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49451726 | |||||||
| chr6:49451764 | T | C | 5 | a0001c0001t0002g0019 a0001c0001t0002g0092 a0001c0001t0002g0121 others(2): Show |
8 | HG00621.hp2 HG02074.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.1084-50A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49451764 | |||||||
| chr6:49451783 | C | T | 2 | a0003c0003t0009g0087 a0003c0003t0009g0090 |
2 | HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1084-69G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49451783 | |||||||
| chr6:49451909 | T | C | 18 | a0004c0004t0003g0004 a0004c0004t0003g0020 a0004c0004t0003g0046 others(15): Show |
37 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1084-195A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49451909 | |||||||
| chr6:49451931 | T | C | 3 | a0003c0007t0006g0131 a0003c0007t0006g0132 a0003c0007t0006g0133 |
3 | HG01884.hp1 HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1084-217A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49451931 | |||||||
| chr6:49452151 | A | G | 61 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(58): Show |
134 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.1084-437T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49452151 | |||||||
| chr6:49452355 | C | T | 3 | a0003c0003t0001g0014 a0003c0003t0001g0081 a0003c0003t0013g0082 |
6 | HG02109.hp1 HG02145.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1084-641G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49452355 | |||||||
| chr6:49452426 | G | A | 3 | a0003c0003t0001g0010 a0003c0003t0001g0088 a0003c0003t0001g0089 |
7 | HG02257.hp1 HG02630.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1084-712C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49452426 | |||||||
| chr6:49452484 | C | T | 1 | a0002c0002t0001g0054 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1084-770G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49452484 | |||||||
| chr6:49452493 | T | C | 79 | a0001c0001t0002g0123 a0002c0002t0001g0003 a0002c0002t0001g0005 others(76): Show |
171 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.1084-779A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49452493 | |||||||
| chr6:49452535 | A | G | 62 | a0001c0001t0002g0036 a0002c0002t0001g0003 a0002c0002t0001g0005 others(59): Show |
136 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.1084-821T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49452535 | |||||||
| chr6:49452837 | C | G | 7 | a0003c0003t0001g0014 a0003c0003t0001g0081 a0003c0003t0005g0026 others(4): Show |
12 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1083+748G>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49452837 | |||||||
| chr6:49452847 | C | T | 36 | a0001c0006t0002g0009 a0001c0006t0002g0150 a0001c0006t0002g0157 others(33): Show |
86 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.1083+738G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49452847 | |||||||
| chr6:49452874 | T | C | 1 | a0002c0002t0001g0034 | 2 | HG00558.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.1083+711A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49452874 | |||||||
| chr6:49452974 | TGA | T | 3 | a0003c0003t0001g0010 a0003c0003t0001g0088 a0003c0003t0001g0089 |
7 | HG02257.hp1 HG02630.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1083+609_1083+610d others(4): Show |
MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49452974 | |||||||
| chr6:49453035 | C | G | 1 | a0001c0001t0002g0101 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1083+550G>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49453035 | |||||||
| chr6:49453039 | G | GT | 57 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0011 others(54): Show |
137 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.1083+545dupA | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49453039 | |||||||
| chr6:49453043 | T | G | 1 | a0003c0003t0010g0148 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1083+542A>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49453043 | |||||||
| chr6:49453045 | T | G | 60 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(57): Show |
133 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.1083+540A>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49453045 | |||||||
| chr6:49453059 | T | G | 64 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(61): Show |
137 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.1083+526A>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49453059 | |||||||
| chr6:49453059 | T | TG | 33 | a0001c0006t0002g0009 a0001c0006t0002g0150 a0001c0006t0002g0157 others(30): Show |
79 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.1083+525_1083+526i others(3): Show |
MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49453059 | |||||||
| chr6:49453059 | T | TTG | 3 | a0003c0003t0004g0047 a0004c0004t0003g0020 a0004c0004t0005g0136 |
7 | HG01361.hp2 HG01433.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1083+525_1083+526i others(4): Show |
MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49453059 | |||||||
| chr6:49453103 | G | A | 1 | a0003c0003t0004g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1083+482C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49453103 | |||||||
| chr6:49453155 | C | T | 1 | a0003c0003t0001g0037 | 2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1083+430G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49453155 | |||||||
| chr6:49453198 | C | T | 1 | a0002c0002t0001g0031 | 2 | HG03654.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1083+387G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49453198 | |||||||
| chr6:49453233 | T | G | 62 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(59): Show |
135 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.1083+352A>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49453233 | |||||||
| chr6:49453247 | G | A | 1 | a0002c0002t0001g0069 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1083+338C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49453247 | |||||||
| chr6:49453420 | T | G | 1 | a0002c0002t0001g0070 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1083+165A>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49453420 | |||||||
| chr6:49453526 | C | CA | 2 | a0003c0003t0001g0037 a0003c0003t0001g0080 |
3 | HG02809.hp1 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1083+58dupT | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49453526 | |||||||
| chr6:49453528 | G | A | 62 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(59): Show |
135 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.1083+57C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49453528 | |||||||
| chr6:49453535 | T | A | 2 | a0002c0002t0001g0025 a0002c0002t0001g0071 |
4 | HG01891.hp1 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1083+50A>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49453535 | |||||||
| chr6:49453544 | A | G | 1 | a0003c0003t0007g0077 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1083+41T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49453544 | |||||||
| chr6:49453565 | A | G | 4 | a0003c0007t0003g0130 a0003c0007t0006g0131 a0003c0007t0006g0132 others(1): Show |
4 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1083+20T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 5/12 | chr6 | 49453565 | |||||||
| chr6:49453769 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.912-13G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 4/12 | chr6 | 49453769 | |||||||
| chr6:49453866 | G | A | 32 | a0001c0006t0002g0009 a0001c0006t0002g0150 a0001c0006t0002g0157 others(29): Show |
82 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.912-110C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 4/12 | chr6 | 49453866 | |||||||
| chr6:49453886 | A | C | 1 | a0003c0003t0004g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.912-130T>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 4/12 | chr6 | 49453886 | |||||||
| chr6:49453894 | G | A | 104 | a0001c0001t0003g0015 a0001c0001t0003g0134 a0001c0006t0002g0009 others(101): Show |
230 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.912-138C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 4/12 | chr6 | 49453894 | |||||||
| chr6:49454165 | T | C | 1 | a0003c0003t0003g0049 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.912-409A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 4/12 | chr6 | 49454165 | |||||||
| chr6:49454309 | T | C | 1 | a0001c0005t0002g0124 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.912-553A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 4/12 | chr6 | 49454309 | |||||||
| chr6:49454568 | G | A | 1 | a0002c0002t0001g0072 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.912-812C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 4/12 | chr6 | 49454568 | |||||||
| chr6:49454723 | A | G | 1 | a0003c0003t0010g0148 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.912-967T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 4/12 | chr6 | 49454723 | |||||||
| chr6:49454778 | G | T | 3 | a0001c0001t0003g0096 a0001c0001t0003g0097 a0001c0001t0003g0098 |
3 | HG02145.hp1 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.912-1022C>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 4/12 | chr6 | 49454778 | |||||||
| chr6:49454806 | G | A | 2 | a0001c0001t0002g0011 a0001c0001t0002g0094 |
6 | HG00408.hp2 HG02155.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.912-1050C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 4/12 | chr6 | 49454806 | |||||||
| chr6:49454971 | G | A | 1 | a0002c0002t0001g0073 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.911+1109C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 4/12 | chr6 | 49454971 | |||||||
| chr6:49455133 | A | T | 1 | a0001c0001t0002g0079 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.911+947T>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 4/12 | chr6 | 49455133 | |||||||
| chr6:49455134 | AT | A | 4 | a0003c0003t0001g0038 a0003c0003t0001g0086 a0003c0003t0009g0087 others(1): Show |
5 | HG00741.hp2 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.911+945delA | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 4/12 | chr6 | 49455134 | |||||||
| chr6:49455135 | T | A | 57 | a0001c0001t0002g0001 a0001c0001t0002g0092 a0001c0008t0003g0045 others(54): Show |
121 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.911+945A>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 4/12 | chr6 | 49455135 | |||||||
| chr6:49455137 | T | A | 5 | a0003c0003t0001g0038 a0003c0003t0001g0086 a0003c0003t0001g0089 others(2): Show |
6 | HG00741.hp2 HG02717.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.911+943A>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 4/12 | chr6 | 49455137 | |||||||
| chr6:49455168 | A | G | 2 | a0001c0001t0002g0095 a0001c0001t0002g0125 |
2 | NA18962.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.911+912T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 4/12 | chr6 | 49455168 | |||||||
| chr6:49455278 | T | C | 32 | a0001c0006t0002g0009 a0001c0006t0002g0150 a0001c0006t0002g0157 others(29): Show |
82 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.911+802A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 4/12 | chr6 | 49455278 | |||||||
| chr6:49455305 | G | A | 1 | a0004c0004t0005g0147 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.911+775C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 4/12 | chr6 | 49455305 | |||||||
| chr6:49455326 | C | G | 4 | a0003c0007t0003g0130 a0003c0007t0006g0131 a0003c0007t0006g0132 others(1): Show |
4 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.911+754G>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 4/12 | chr6 | 49455326 | |||||||
| chr6:49455522 | T | A | 1 | a0003c0003t0007g0077 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.911+558A>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 4/12 | chr6 | 49455522 | |||||||
| chr6:49455592 | G | A | 1 | a0001c0001t0002g0125 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.911+488C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 4/12 | chr6 | 49455592 | |||||||
| chr6:49455713 | C | T | 2 | a0003c0003t0007g0077 a0003c0003t0007g0149 |
2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.911+367G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 4/12 | chr6 | 49455713 | |||||||
| chr6:49455834 | G | C | 98 | a0001c0006t0002g0009 a0001c0006t0002g0150 a0001c0006t0002g0157 others(95): Show |
221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.911+246C>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 4/12 | chr6 | 49455834 | |||||||
| chr6:49456002 | A | T | 1 | a0001c0001t0002g0094 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.911+78T>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 4/12 | chr6 | 49456002 | |||||||
| chr6:49456358 | T | C | 1 | a0003c0003t0009g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.754-121A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 3/12 | chr6 | 49456358 | |||||||
| chr6:49456406 | G | T | 4 | a0003c0007t0003g0130 a0003c0007t0006g0131 a0003c0007t0006g0132 others(1): Show |
4 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.754-169C>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 3/12 | chr6 | 49456406 | |||||||
| chr6:49456597 | C | T | 1 | a0003c0003t0004g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.754-360G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 3/12 | chr6 | 49456597 | |||||||
| chr6:49456679 | T | A | 1 | a0001c0008t0003g0126 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.754-442A>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 3/12 | chr6 | 49456679 | |||||||
| chr6:49456755 | C | T | 1 | a0001c0001t0002g0039 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.754-518G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 3/12 | chr6 | 49456755 | |||||||
| chr6:49456790 | C | T | 1 | a0003c0003t0003g0049 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.754-553G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 3/12 | chr6 | 49456790 | |||||||
| chr6:49456799 | T | C | 1 | a0002c0002t0001g0021 | 3 | HG02896.hp1 HG02897.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.754-562A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 3/12 | chr6 | 49456799 | |||||||
| chr6:49457107 | C | T | 2 | a0001c0006t0002g0009 a0001c0006t0002g0150 |
7 | NA18957.hp2 NA18960.hp1 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.753+584G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 3/12 | chr6 | 49457107 | |||||||
| chr6:49457109 | T | C | 1 | a0002c0002t0001g0035 | 2 | NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.753+582A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 3/12 | chr6 | 49457109 | |||||||
| chr6:49457129 | G | A | 1 | a0003c0003t0001g0086 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.753+562C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 3/12 | chr6 | 49457129 | |||||||
| chr6:49457130 | T | C | 1 | a0003c0003t0004g0158 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.753+561A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 3/12 | chr6 | 49457130 | |||||||
| chr6:49457136 | G | T | 1 | a0002c0002t0001g0051 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.753+555C>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 3/12 | chr6 | 49457136 | |||||||
| chr6:49457183 | C | T | 4 | a0003c0007t0003g0130 a0003c0007t0006g0131 a0003c0007t0006g0132 others(1): Show |
4 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.753+508G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 3/12 | chr6 | 49457183 | |||||||
| chr6:49458099 | G | A | 1 | a0003c0003t0010g0148 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.386-41C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 2/12 | chr6 | 49458099 | |||||||
| chr6:49458115 | G | A | 1 | a0001c0001t0002g0128 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.386-57C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 2/12 | chr6 | 49458115 | |||||||
| chr6:49458305 | G | A | 102 | a0001c0006t0002g0009 a0001c0006t0002g0150 a0001c0006t0002g0157 others(99): Show |
225 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.386-247C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 2/12 | chr6 | 49458305 | |||||||
| chr6:49458600 | C | T | 1 | a0003c0003t0009g0087 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.385+482G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 2/12 | chr6 | 49458600 | |||||||
| chr6:49458622 | C | T | 3 | a0002c0002t0001g0021 a0002c0002t0001g0050 a0002c0002t0001g0162 |
5 | HG01255.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.385+460G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 2/12 | chr6 | 49458622 | |||||||
| chr6:49458768 | C | T | 2 | a0003c0003t0001g0030 a0003c0003t0008g0029 |
4 | HG02486.hp2 HG02647.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+314G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 2/12 | chr6 | 49458768 | |||||||
| chr6:49458786 | T | C | 1 | a0003c0003t0009g0087 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.385+296A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 2/12 | chr6 | 49458786 | |||||||
| chr6:49458898 | C | T | 4 | a0003c0007t0003g0130 a0003c0007t0006g0131 a0003c0007t0006g0132 others(1): Show |
4 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+184G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 2/12 | chr6 | 49458898 | |||||||
| chr6:49459017 | A | C | 4 | a0003c0003t0001g0014 a0003c0003t0001g0081 a0003c0003t0013g0082 others(1): Show |
7 | HG00323.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.385+65T>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 2/12 | chr6 | 49459017 | |||||||
| chr6:49459068 | C | T | 1 | a0003c0003t0007g0077 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.385+14G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 2/12 | chr6 | 49459068 | |||||||
| chr6:49459531 | A | T | 1 | a0001c0001t0003g0015 | 4 | HG02615.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39-26T>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49459531 | |||||||
| chr6:49459696 | T | C | 103 | a0001c0001t0003g0134 a0001c0006t0002g0009 a0001c0006t0002g0150 others(100): Show |
226 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.-39-191A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49459696 | |||||||
| chr6:49459792 | T | A | 2 | a0003c0003t0009g0087 a0003c0003t0009g0090 |
2 | HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-39-287A>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49459792 | |||||||
| chr6:49459819 | C | A | 1 | a0002c0002t0001g0075 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-39-314G>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49459819 | |||||||
| chr6:49459844 | G | C | 1 | a0003c0003t0005g0026 | 3 | HG01361.hp1 HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-39-339C>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49459844 | |||||||
| chr6:49459942 | A | G | 65 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(62): Show |
138 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.-39-437T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49459942 | |||||||
| chr6:49460009 | C | T | 7 | a0003c0003t0001g0014 a0003c0003t0001g0081 a0003c0003t0005g0026 others(4): Show |
12 | HG01361.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-39-504G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49460009 | |||||||
| chr6:49460205 | A | G | 62 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(59): Show |
135 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.-39-700T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49460205 | |||||||
| chr6:49460278 | T | G | 1 | a0003c0003t0010g0148 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-39-773A>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49460278 | |||||||
| chr6:49460414 | A | G | 1 | a0001c0001t0002g0078 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-39-909T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49460414 | |||||||
| chr6:49460647 | G | C | 62 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(59): Show |
135 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.-39-1142C>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49460647 | |||||||
| chr6:49460661 | C | T | 2 | a0003c0003t0001g0037 a0003c0003t0001g0080 |
3 | HG02809.hp1 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-39-1156G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49460661 | |||||||
| chr6:49460755 | A | T | 1 | a0003c0003t0008g0029 | 2 | HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-39-1250T>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49460755 | |||||||
| chr6:49460973 | T | G | 3 | a0003c0003t0001g0010 a0003c0003t0001g0088 a0003c0003t0001g0089 |
7 | HG02257.hp1 HG02630.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-39-1468A>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49460973 | |||||||
| chr6:49461042 | G | A | 65 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(62): Show |
138 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.-39-1537C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49461042 | |||||||
| chr6:49461251 | T | C | 2 | a0003c0003t0007g0077 a0003c0003t0007g0149 |
2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-39-1746A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49461251 | |||||||
| chr6:49461331 | A | G | 1 | a0001c0001t0002g0092 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-40+1772T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49461331 | |||||||
| chr6:49461451 | C | T | 1 | a0001c0001t0002g0091 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-40+1652G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49461451 | |||||||
| chr6:49461524 | T | C | 1 | a0003c0003t0009g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-40+1579A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49461524 | |||||||
| chr6:49461535 | G | A | 1 | a0002c0002t0001g0076 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-40+1568C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49461535 | |||||||
| chr6:49461551 | C | T | 62 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(59): Show |
135 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.-40+1552G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49461551 | |||||||
| chr6:49461578 | G | C | 1 | a0003c0003t0004g0159 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-40+1525C>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49461578 | |||||||
| chr6:49461594 | C | T | 3 | a0001c0001t0002g0036 a0001c0001t0002g0078 a0001c0001t0002g0079 |
4 | HG01167.hp2 HG01169.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40+1509G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49461594 | |||||||
| chr6:49461778 | C | T | 1 | a0003c0003t0007g0077 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-40+1325G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49461778 | |||||||
| chr6:49461993 | C | A | 14 | a0001c0006t0002g0009 a0001c0006t0002g0150 a0001c0006t0002g0157 others(11): Show |
45 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.-40+1110G>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49461993 | |||||||
| chr6:49462194 | A | G | 1 | a0003c0003t0003g0049 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-40+909T>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49462194 | |||||||
| chr6:49462369 | C | G | 46 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0007 others(43): Show |
108 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.-40+734G>C | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49462369 | |||||||
| chr6:49462504 | C | T | 1 | a0003c0003t0003g0049 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-40+599G>A | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49462504 | |||||||
| chr6:49462728 | T | C | 1 | a0001c0001t0002g0160 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-40+375A>G | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49462728 | |||||||
| chr6:49462901 | G | A | 1 | a0002c0002t0001g0161 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-40+202C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49462901 | |||||||
| chr6:49463043 | G | A | 1 | a0002c0002t0001g0162 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-40+60C>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49463043 | |||||||
| chr6:49463089 | T | A | 1 | a0001c0001t0002g0163 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-40+14A>T | MMUT | ENSG00000146085.8 | transcript | ENST00000274813.4 | protein_coding | 1/12 | chr6 | 49463089 |