Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9927 |
| ensemblid | ENSG00000116688.18 |
| hgncid | 16877 |
| symbol | MFN2 |
| name | mitofusin 2 |
| refseq_nuc | NM_014874.4 |
| refseq_prot | NP_055689.1 |
| ensembl_nuc | ENST00000235329.10 |
| ensembl_prot | ENSP00000235329.5 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 11980444 |
| end | 12013508 |
| strand | + |
| ver | v1.2 |
| region | chr1:11980444-12013508 |
| region5000 | chr1:11975444-12018508 |
| regionname0 | MFN2_chr1_11980444_12013508 |
| regionname5000 | MFN2_chr1_11975444_12018508 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 757 | 389 | 91 | 64 | 172 | 14 | 46 | 134 | MFN2_chr1_11975444_12018508 | MFN2 | MSLLF others(752): Show |
chr1 | 11975444 | 12018508 |
| a0002 | 0/0 | 757 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | MSLLF others(752): Show |
chr1 | 11975444 | 12018508 |
| a0003 | 0/0 | 757 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | MSLLF others(752): Show |
chr1 | 11975444 | 12018508 |
| a0004 | 0/0 | 757 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | MSLLF others(752): Show |
chr1 | 11975444 | 12018508 |
| a0005 | 0/0 | 757 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | MSLLF others(752): Show |
chr1 | 11975444 | 12018508 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2271 | 340 | 78 | 58 | 150 | 14 | 39 | MFN2_chr1_11975444_12018508 | MFN2 | ATGTC others(2266): Show |
chr1 | 11975444 | 12018508 | ||
| a0001c0002 | 0/0 | 2271 | 21 | 1 | 3 | 12 | 0 | 5 | MFN2_chr1_11975444_12018508 | MFN2 | ATGTC others(2266): Show |
chr1 | 11975444 | 12018508 | ||
| a0001c0003 | 0/0 | 2271 | 8 | 6 | 2 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | ATGTC others(2266): Show |
chr1 | 11975444 | 12018508 | ||
| a0001c0004 | 0/0 | 2271 | 6 | 0 | 0 | 6 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | ATGTC others(2266): Show |
chr1 | 11975444 | 12018508 | ||
| a0001c0005 | 0/0 | 2271 | 3 | 3 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | ATGTC others(2266): Show |
chr1 | 11975444 | 12018508 | ||
| a0001c0006 | 0/1 | 2271 | 3 | 1 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | ATGTC others(2266): Show |
chr1 | 11975444 | 12018508 | ||
| a0001c0008 | 0/0 | 2271 | 2 | 0 | 0 | 1 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | ATGTC others(2266): Show |
chr1 | 11975444 | 12018508 | ||
| a0001c0009 | 0/0 | 2271 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | ATGTC others(2266): Show |
chr1 | 11975444 | 12018508 | ||
| a0001c0012 | 0/0 | 2271 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | ATGTC others(2266): Show |
chr1 | 11975444 | 12018508 | ||
| a0001c0013 | 0/0 | 2271 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | ATGTC others(2266): Show |
chr1 | 11975444 | 12018508 | ||
| a0001c0014 | 0/0 | 2271 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | ATGTC others(2266): Show |
chr1 | 11975444 | 12018508 | ||
| a0001c0016 | 0/0 | 2271 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | ATGTC others(2266): Show |
chr1 | 11975444 | 12018508 | ||
| a0001c0017 | 0/0 | 2271 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | ATGTC others(2266): Show |
chr1 | 11975444 | 12018508 | ||
| a0002c0007 | 0/0 | 2271 | 2 | 2 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | ATGTC others(2266): Show |
chr1 | 11975444 | 12018508 | ||
| a0003c0010 | 0/0 | 2271 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | ATGTC others(2266): Show |
chr1 | 11975444 | 12018508 | ||
| a0004c0011 | 0/0 | 2271 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | ATGTC others(2266): Show |
chr1 | 11975444 | 12018508 | ||
| a0005c0015 | 0/0 | 2271 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | ATGTC others(2266): Show |
chr1 | 11975444 | 12018508 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4407 | 123 | 26 | 27 | 48 | 6 | 16 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0001t0002 | 1/0 | 4407 | 91 | 4 | 24 | 49 | 5 | 8 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0001t0003 | 0/0 | 4407 | 59 | 0 | 5 | 41 | 2 | 11 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0001t0004 | 0/0 | 4407 | 27 | 24 | 1 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0001t0006 | 0/0 | 4407 | 6 | 5 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0001t0009 | 0/0 | 4407 | 4 | 0 | 0 | 4 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0001t0010 | 0/0 | 4407 | 3 | 3 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0001t0011 | 0/0 | 4406 | 3 | 0 | 0 | 3 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4401): Show |
chr1 | 11975444 | 12018508 |
| a0001c0001t0012 | 0/0 | 4407 | 3 | 3 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0001t0013 | 0/0 | 4407 | 3 | 3 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0001t0014 | 0/0 | 4407 | 3 | 3 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0001t0015 | 0/0 | 4407 | 3 | 3 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0001t0016 | 0/0 | 4407 | 2 | 0 | 0 | 0 | 0 | 2 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0001t0018 | 0/0 | 4407 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0001t0019 | 0/0 | 4407 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0001t0020 | 0/0 | 4406 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4401): Show |
chr1 | 11975444 | 12018508 |
| a0001c0001t0021 | 0/0 | 4407 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0001t0022 | 0/0 | 4407 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0001t0023 | 0/0 | 4408 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4403): Show |
chr1 | 11975444 | 12018508 |
| a0001c0001t0024 | 0/0 | 4407 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0001t0025 | 0/0 | 4407 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0001t0026 | 0/0 | 4407 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0001t0027 | 0/0 | 4407 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0002t0005 | 0/0 | 4407 | 16 | 1 | 3 | 7 | 0 | 5 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0002t0008 | 0/0 | 4407 | 5 | 0 | 0 | 5 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0003t0007 | 0/0 | 4408 | 6 | 5 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4403): Show |
chr1 | 11975444 | 12018508 |
| a0001c0003t0017 | 0/0 | 4408 | 2 | 1 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4403): Show |
chr1 | 11975444 | 12018508 |
| a0001c0004t0004 | 0/0 | 4407 | 6 | 0 | 0 | 6 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0005t0004 | 0/0 | 4407 | 3 | 3 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0006t0001 | 0/1 | 4407 | 3 | 1 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0008t0004 | 0/0 | 4407 | 2 | 0 | 0 | 1 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0009t0002 | 0/0 | 4407 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0012t0001 | 0/0 | 4407 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0013t0002 | 0/0 | 4407 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0014t0006 | 0/0 | 4407 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0016t0004 | 0/0 | 4407 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0001c0017t0001 | 0/0 | 4407 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0002c0007t0002 | 0/0 | 4407 | 2 | 2 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0003c0010t0002 | 0/0 | 4407 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0004c0011t0001 | 0/0 | 4407 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| a0005c0015t0008 | 0/0 | 4407 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | GTAGT others(4402): Show |
chr1 | 11975444 | 12018508 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0002 | 0/0 | 15 | 0 | 5 | 7 | 1 | 2 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0010 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0001 | 0/0 | 18 | 1 | 1 | 15 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0003 | 1/0 | 8 | 1 | 6 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0004g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0004g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0004g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0004g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0004g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0006g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0009g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0009g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0009g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0009g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0010g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0010g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0011g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0011g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0012g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0012g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0013g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0013g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0014g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0014g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0014g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0015g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0015g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0015g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0016g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0016g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0018g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0019g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0020g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0021g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0022g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0023g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0024g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0025g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0026g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0001t0027g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0002t0005g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0002t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0002t0005g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0002t0005g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0002t0005g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0002t0005g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0002t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0002t0005g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0002t0005g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0002t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0002t0005g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0002t0005g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0002t0005g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0002t0005g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0002t0005g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0002t0008g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0002t0008g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0002t0008g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0002t0008g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0002t0008g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0003t0007g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0003t0007g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0003t0007g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0003t0007g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0003t0007g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0003t0017g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0003t0017g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0004t0004g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0004t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0004t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0004t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0005t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0005t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0005t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0006t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0006t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0006t0001g0063 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0008t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0008t0004g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0009t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0012t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0013t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0014t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0016t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0001c0017t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0002c0007t0002g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0002c0007t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0003c0010t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0004c0011t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| a0005c0015t0008g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | GBR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0080 | EUR | GBR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | FIN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00280 | hp2 | a0001 | c0001 | t0024 | g0004 | EUR | FIN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | FIN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00408 | hp1 | a0001 | c0002 | t0008 | g0242 | EAS | CHS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | CHS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | CHS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | CHS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00438 | hp2 | a0001 | c0001 | t0020 | g0025 | EAS | CHS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | CHS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0226 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00733 | hp2 | a0001 | c0002 | t0005 | g0254 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0236 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0224 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01109 | hp1 | a0001 | c0003 | t0017 | g0281 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01167 | hp1 | a0001 | c0003 | t0007 | g0272 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01192 | hp1 | a0001 | c0002 | t0005 | g0253 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01192 | hp2 | a0001 | c0001 | t0006 | g0046 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | CLM | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0231 | AMR | CLM | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | CLM | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01256 | hp2 | a0001 | c0012 | t0001 | g0005 | AMR | CLM | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | CLM | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | CLM | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0146 | EUR | IBS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0098 | EUR | IBS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0061 | EUR | IBS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0223 | EUR | IBS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | IBS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0203 | EUR | IBS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0048 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0047 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0194 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02027 | hp1 | a0001 | c0002 | t0005 | g0265 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02040 | hp2 | a0001 | c0002 | t0005 | g0034 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0262 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02056 | hp1 | a0001 | c0002 | t0005 | g0245 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02056 | hp2 | a0001 | c0001 | t0011 | g0001 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02083 | hp2 | a0001 | c0004 | t0004 | g0260 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02135 | hp2 | a0001 | c0002 | t0005 | g0185 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02145 | hp1 | a0001 | c0001 | t0012 | g0291 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02145 | hp2 | a0001 | c0003 | t0007 | g0269 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CDX | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | CDX | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02257 | hp2 | a0001 | c0001 | t0010 | g0019 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02258 | hp1 | a0001 | c0001 | t0022 | g0005 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0042 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02293 | hp1 | a0001 | c0002 | t0005 | g0087 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0189 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0187 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0192 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02622 | hp2 | a0001 | c0003 | t0007 | g0271 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02630 | hp1 | a0001 | c0001 | t0014 | g0039 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0285 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0037 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0038 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02698 | hp1 | a0001 | c0001 | t0016 | g0084 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02717 | hp1 | a0001 | c0014 | t0006 | g0043 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02717 | hp2 | a0001 | c0001 | t0026 | g0261 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02723 | hp2 | a0001 | c0001 | t0015 | g0051 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0107 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02809 | hp2 | a0001 | c0016 | t0004 | g0116 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02818 | hp1 | a0001 | c0001 | t0010 | g0096 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0188 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0169 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02895 | hp2 | a0001 | c0005 | t0004 | g0283 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0171 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0126 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0273 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02965 | hp2 | a0002 | c0007 | t0002 | g0008 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0041 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02970 | hp2 | a0001 | c0001 | t0013 | g0033 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02976 | hp1 | a0001 | c0001 | t0012 | g0036 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0186 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03017 | hp2 | a0001 | c0002 | t0005 | g0246 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03098 | hp1 | a0001 | c0003 | t0007 | g0035 | AFR | MSL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03130 | hp2 | a0001 | c0001 | t0014 | g0040 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03195 | hp1 | a0001 | c0001 | t0010 | g0019 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03195 | hp2 | a0001 | c0005 | t0004 | g0284 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03209 | hp1 | a0001 | c0001 | t0014 | g0045 | AFR | MSL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03209 | hp2 | a0001 | c0001 | t0013 | g0241 | AFR | MSL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03239 | hp2 | a0001 | c0001 | t0018 | g0103 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03453 | hp1 | a0002 | c0007 | t0002 | g0001 | AFR | MSL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03453 | hp2 | a0001 | c0001 | t0027 | g0052 | AFR | MSL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03486 | hp2 | a0001 | c0003 | t0017 | g0282 | AFR | MSL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0120 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0121 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0286 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03516 | hp2 | a0001 | c0001 | t0013 | g0033 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03540 | hp1 | a0001 | c0003 | t0007 | g0035 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0191 | AFR | MSL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0287 | AFR | MSL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0031 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03654 | hp2 | a0001 | c0002 | t0005 | g0247 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03669 | hp1 | a0001 | c0002 | t0005 | g0244 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0220 | SAS | STU | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03688 | hp2 | a0001 | c0002 | t0005 | g0243 | SAS | STU | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0155 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03710 | hp1 | a0001 | c0001 | t0019 | g0104 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0202 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0197 | SAS | BEB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03834 | hp2 | a0001 | c0002 | t0005 | g0250 | SAS | BEB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0264 | SAS | BEB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | BEB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03942 | hp2 | a0001 | c0001 | t0016 | g0086 | SAS | BEB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0280 | SAS | BEB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0184 | SAS | BEB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0214 | SAS | STU | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | STU | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | STU | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG04228 | hp2 | a0001 | c0008 | t0004 | g0259 | SAS | STU | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | YRI | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18522 | hp2 | a0001 | c0001 | t0015 | g0050 | AFR | YRI | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | CHB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0167 | AFR | YRI | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18906 | hp2 | a0001 | c0002 | t0005 | g0055 | AFR | YRI | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18939 | hp2 | a0001 | c0017 | t0001 | g0049 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18946 | hp1 | a0001 | c0001 | t0009 | g0032 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18952 | hp1 | a0001 | c0001 | t0009 | g0147 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18952 | hp2 | a0001 | c0004 | t0004 | g0015 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18953 | hp1 | a0001 | c0001 | t0023 | g0199 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18967 | hp2 | a0001 | c0004 | t0004 | g0258 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18970 | hp1 | a0001 | c0004 | t0004 | g0256 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18973 | hp2 | a0001 | c0002 | t0008 | g0251 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18977 | hp2 | a0001 | c0002 | t0005 | g0268 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18978 | hp1 | a0001 | c0001 | t0021 | g0179 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18985 | hp2 | a0001 | c0002 | t0005 | g0249 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18990 | hp1 | a0001 | c0004 | t0004 | g0015 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18991 | hp1 | a0001 | c0001 | t0009 | g0221 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18993 | hp1 | a0001 | c0001 | t0011 | g0009 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18993 | hp2 | a0004 | c0011 | t0001 | g0177 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18994 | hp2 | a0001 | c0008 | t0004 | g0257 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19010 | hp1 | a0001 | c0002 | t0005 | g0034 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0044 | AFR | LWK | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19058 | hp2 | a0001 | c0002 | t0008 | g0267 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19068 | hp1 | a0001 | c0002 | t0008 | g0252 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19074 | hp2 | a0001 | c0001 | t0011 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19080 | hp1 | a0005 | c0015 | t0008 | g0248 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19082 | hp1 | a0001 | c0013 | t0002 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19082 | hp2 | a0001 | c0004 | t0004 | g0015 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19083 | hp1 | a0001 | c0001 | t0009 | g0135 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19089 | hp2 | a0001 | c0002 | t0008 | g0266 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19090 | hp2 | a0001 | c0009 | t0002 | g0255 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0097 | AFR | YRI | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0095 | EUR | TSI | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | GIH | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA20905 | hp2 | a0001 | c0006 | t0001 | g0017 | SAS | GIH | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02109 | hp2 | a0001 | c0001 | t0012 | g0036 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02486 | hp1 | a0001 | c0006 | t0001 | g0012 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02559 | hp1 | a0001 | c0001 | t0015 | g0053 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG02559 | hp2 | a0001 | c0001 | t0025 | g0290 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03471 | hp1 | a0001 | c0005 | t0004 | g0119 | AFR | MSL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0190 | AFR | MSL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG06807 | hp1 | a0003 | c0010 | t0002 | g0289 | AFR | USA | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| HG06807 | hp2 | a0001 | c0003 | t0007 | g0270 | AFR | USA | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | USA | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | USA | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0170 | AFR | LWK | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | LWK | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| homoSapiens | chm13v2 | a0001 | c0006 | t0001 | g0063 | REF | REF | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0003 | REF | REF | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:12002088 | C | T | 1 | a0005 | 1 | NA19080.hp1 | missense_variant | MODERATE | c.1145C>T | p.Ala382Val | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/19 | 1335/4407 | 1145/2274 | 382/757 | chr1 | 12002088 | |||
| chr1:12004010 | G | A | 1 | a0002 | 2 | HG02965.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.1179G>A | p.Met393Ile | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 12/19 | 1369/4407 | 1179/2274 | 393/757 | chr1 | 12004010 | |||
| chr1:12004030 | G | A | 1 | a0003 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.1199G>A | p.Arg400Gln | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 12/19 | 1389/4407 | 1199/2274 | 400/757 | chr1 | 12004030 | |||
| chr1:12004923 | G | A | 1 | a0004 | 1 | NA18993.hp2 | missense_variant | MODERATE | c.1491G>A | p.Met497Ile | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 14/19 | 1681/4407 | 1491/2274 | 497/757 | chr1 | 12004923 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:11989318 | C | A | 2 | a0001c0004 a0001c0009 |
7 | HG02083.hp2 NA18952.hp2 NA18967.hp2 others(4): Show |
synonymous_variant | LOW | c.150C>A | p.Ile50Ile | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/19 | 340/4407 | 150/2274 | 50/757 | chr1 | 11989318 | |||
| chr1:11989327 | C | T | 1 | a0001c0003 | 8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
synonymous_variant | LOW | c.159C>T | p.Ser53Ser | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/19 | 349/4407 | 159/2274 | 53/757 | chr1 | 11989327 | |||
| chr1:11989333 | C | T | 3 | a0001c0004 a0001c0008 a0001c0009 |
9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
synonymous_variant | LOW | c.165C>T | p.Thr55Thr | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/19 | 355/4407 | 165/2274 | 55/757 | chr1 | 11989333 | |||
| chr1:11996225 | C | T | 1 | a0001c0017 | 1 | NA18939.hp2 | synonymous_variant | LOW | c.381C>T | p.Gly127Gly | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/19 | 571/4407 | 381/2274 | 127/757 | chr1 | 11996225 | |||
| chr1:11996252 | A | T | 3 | a0001c0004 a0001c0008 a0001c0009 |
9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
synonymous_variant | LOW | c.408A>T | p.Val136Val | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/19 | 598/4407 | 408/2274 | 136/757 | chr1 | 11996252 | |||
| chr1:11999023 | C | T | 1 | a0001c0016 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.744C>T | p.Leu248Leu | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/19 | 934/4407 | 744/2274 | 248/757 | chr1 | 11999023 | |||
| chr1:12001541 | C | T | 1 | a0001c0006 | 2 | HG02486.hp1 NA20905.hp2 |
synonymous_variant | LOW | c.957C>T | p.Gly319Gly | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 9/19 | 1147/4407 | 957/2274 | 319/757 | chr1 | 12001541 | |||
| chr1:12001773 | C | T | 1 | a0001c0005 | 3 | HG02895.hp2 HG03195.hp2 HG03471.hp1 |
synonymous_variant | LOW | c.975C>T | p.Gly325Gly | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 10/19 | 1165/4407 | 975/2274 | 325/757 | chr1 | 12001773 | |||
| chr1:12005784 | C | T | 4 | a0001c0002 a0001c0004 a0001c0008 others(1): Show |
30 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(27): Show |
synonymous_variant | LOW | c.1569C>T | p.Ser523Ser | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 15/19 | 1759/4407 | 1569/2274 | 523/757 | chr1 | 12005784 | |||
| chr1:12006549 | C | T | 1 | a0001c0014 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.1728C>T | p.Pro576Pro | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 16/19 | 1918/4407 | 1728/2274 | 576/757 | chr1 | 12006549 | |||
| chr1:12006567 | C | G | 1 | a0001c0013 | 1 | NA19082.hp1 | synonymous_variant | LOW | c.1746C>G | p.Ala582Ala | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 16/19 | 1936/4407 | 1746/2274 | 582/757 | chr1 | 12006567 | |||
| chr1:12007100 | C | G | 1 | a0001c0012 | 1 | HG01256.hp2 | synonymous_variant | LOW | c.1920C>G | p.Leu640Leu | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/19 | 2110/4407 | 1920/2274 | 640/757 | chr1 | 12007100 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:11982039 | C | T | 2 | a0001c0001t0015 a0001c0001t0027 |
4 | HG02559.hp1 HG02723.hp2 HG03453.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-80C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/19 | 7130 | chr1 | 11982039 | ||||||
| chr1:12011579 | C | T | 1 | a0001c0001t0027 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 14 | chr1 | 12011579 | ||||||
| chr1:12011623 | A | G | 30 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(27): Show |
286 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(283): Show |
3_prime_UTR_variant | MODIFIER | c.*58A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 58 | chr1 | 12011623 | ||||||
| chr1:12011656 | G | C | 1 | a0001c0001t0021 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*91G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 91 | chr1 | 12011656 | ||||||
| chr1:12011784 | C | CTT | 2 | a0001c0001t0011 a0001c0001t0020 |
4 | HG00438.hp2 HG02056.hp2 NA18993.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*221_*222dupTT | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 223 | INFO_REALIGN_3_PRIME | chr1 | 12011784 | |||||
| chr1:12011796 | G | A | 2 | a0001c0001t0012 a0001c0001t0013 |
6 | HG02109.hp2 HG02145.hp1 HG02970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*231G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 231 | chr1 | 12011796 | ||||||
| chr1:12011815 | C | G | 1 | a0001c0001t0026 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*250C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 250 | chr1 | 12011815 | ||||||
| chr1:12011869 | A | G | 1 | a0001c0001t0013 | 3 | HG02970.hp2 HG03209.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*304A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 304 | chr1 | 12011869 | ||||||
| chr1:12012295 | C | T | 3 | a0001c0001t0006 a0001c0001t0025 a0001c0014t0006 |
8 | HG01192.hp2 HG02280.hp1 HG02559.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*730C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 730 | chr1 | 12012295 | ||||||
| chr1:12012342 | T | C | 1 | a0001c0003t0007 | 6 | HG01167.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*777T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 777 | chr1 | 12012342 | ||||||
| chr1:12012461 | G | C | 16 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0009 others(13): Show |
213 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*896G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 896 | chr1 | 12012461 | ||||||
| chr1:12012477 | C | T | 3 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0024 |
64 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*912C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 912 | chr1 | 12012477 | ||||||
| chr1:12012599 | C | T | 1 | a0001c0001t0010 | 3 | HG02257.hp2 HG02818.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1034C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 1034 | chr1 | 12012599 | ||||||
| chr1:12012624 | A | G | 1 | a0001c0001t0019 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1059A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 1059 | chr1 | 12012624 | ||||||
| chr1:12012665 | A | G | 6 | a0001c0001t0016 a0001c0001t0019 a0001c0001t0024 others(3): Show |
26 | HG00280.hp2 HG00408.hp1 HG00733.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1100A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 1100 | chr1 | 12012665 | ||||||
| chr1:12012726 | C | A | 1 | a0001c0003t0007 | 6 | HG01167.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1161C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 1161 | chr1 | 12012726 | ||||||
| chr1:12012875 | G | A | 1 | a0001c0001t0026 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1310G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 1310 | chr1 | 12012875 | ||||||
| chr1:12012900 | C | T | 1 | a0001c0001t0025 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1335C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 1335 | chr1 | 12012900 | ||||||
| chr1:12013104 | G | A | 1 | a0001c0001t0022 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1539G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 1539 | chr1 | 12013104 | ||||||
| chr1:12013127 | G | A | 1 | a0001c0001t0018 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1562G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 1562 | chr1 | 12013127 | ||||||
| chr1:12013141 | C | T | 3 | a0001c0001t0006 a0001c0001t0014 a0001c0014t0006 |
10 | HG01192.hp2 HG02280.hp1 HG02630.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1576C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 1576 | chr1 | 12013141 | ||||||
| chr1:12013194 | G | GA | 3 | a0001c0001t0023 a0001c0003t0007 a0001c0003t0017 |
9 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1640dupA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 1641 | INFO_REALIGN_3_PRIME | chr1 | 12013194 | |||||
| chr1:12013359 | ATTG | A | 2 | a0001c0001t0011 a0001c0001t0020 |
4 | HG00438.hp2 HG02056.hp2 NA18993.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1800_*1802delGTT | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 1800 | INFO_REALIGN_3_PRIME | chr1 | 12013359 | |||||
| chr1:12013395 | C | T | 1 | a0001c0001t0009 | 4 | NA18946.hp1 NA18952.hp1 NA18991.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1830C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 1830 | chr1 | 12013395 | ||||||
| chr1:12013431 | G | C | 1 | a0001c0001t0020 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1866G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 1866 | chr1 | 12013431 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:11980585 | G | A | 11 | a0001c0001t0004g0047 a0001c0001t0006g0037 a0001c0001t0006g0038 others(8): Show |
11 | HG01192.hp2 HG01891.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-150+101G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11980585 | |||||||
| chr1:11980621 | G | A | 1 | a0001c0001t0004g0048 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-150+137G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11980621 | |||||||
| chr1:11980657 | G | C | 1 | a0001c0001t0006g0037 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-150+173G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11980657 | |||||||
| chr1:11980698 | C | T | 1 | a0001c0001t0003g0292 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-150+214C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11980698 | |||||||
| chr1:11980715 | C | T | 10 | a0001c0001t0001g0288 a0001c0001t0004g0285 a0001c0001t0004g0286 others(7): Show |
11 | HG01070.hp1 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-150+231C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11980715 | |||||||
| chr1:11980719 | G | A | 1 | a0001c0017t0001g0049 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-150+235G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11980719 | |||||||
| chr1:11980720 | C | G | 1 | a0001c0017t0001g0049 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-150+236C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11980720 | |||||||
| chr1:11980725 | C | T | 1 | a0001c0017t0001g0049 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-150+241C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11980725 | |||||||
| chr1:11980739 | C | A | 1 | a0001c0001t0006g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-150+255C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11980739 | |||||||
| chr1:11980747 | A | C | 2 | a0001c0003t0017g0281 a0001c0003t0017g0282 |
2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-150+263A>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11980747 | |||||||
| chr1:11980764 | A | G | 2 | a0001c0001t0001g0279 a0001c0001t0003g0280 |
2 | HG03491.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-150+280A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11980764 | |||||||
| chr1:11980812 | G | A | 2 | a0001c0005t0004g0283 a0001c0005t0004g0284 |
2 | HG02895.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-150+328G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11980812 | |||||||
| chr1:11980974 | G | C | 2 | a0001c0003t0017g0281 a0001c0003t0017g0282 |
2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-150+490G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11980974 | |||||||
| chr1:11981100 | C | A | 4 | a0001c0001t0015g0050 a0001c0001t0015g0051 a0001c0001t0015g0053 others(1): Show |
4 | HG02559.hp1 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-150+616C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981100 | |||||||
| chr1:11981171 | G | T | 1 | a0001c0001t0002g0278 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-150+687G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981171 | |||||||
| chr1:11981202 | A | C | 1 | a0001c0017t0001g0049 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-150+718A>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981202 | |||||||
| chr1:11981203 | T | G | 1 | a0001c0001t0014g0039 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-150+719T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981203 | |||||||
| chr1:11981242 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-149-728C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981242 | |||||||
| chr1:11981367 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-149-603C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981367 | |||||||
| chr1:11981505 | C | T | 2 | a0001c0003t0017g0281 a0001c0003t0017g0282 |
2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-149-465C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981505 | |||||||
| chr1:11981696 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-149-274A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981696 | |||||||
| chr1:11981709 | A | G | 1 | a0001c0001t0004g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-149-261A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981709 | |||||||
| chr1:11981720 | A | G | 1 | a0001c0001t0003g0274 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-149-250A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981720 | |||||||
| chr1:11981783 | C | T | 1 | a0001c0001t0004g0273 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-149-187C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981783 | |||||||
| chr1:11981801 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-149-169T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981801 | |||||||
| chr1:11981816 | T | G | 1 | a0001c0017t0001g0049 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-149-154T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981816 | |||||||
| chr1:11981832 | C | T | 5 | a0001c0003t0007g0035 a0001c0003t0007g0269 a0001c0003t0007g0270 others(2): Show |
6 | HG01167.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-149-138C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981832 | |||||||
| chr1:11981920 | G | GTTTTGTT others(3): Show |
1 | a0001c0002t0005g0055 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-149-46_-149-45ins others(10): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11981920 | ||||||
| chr1:11981920 | G | GTTTTTT | 11 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(8): Show |
11 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-149-43_-149-38dup others(6): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11981920 | ||||||
| chr1:11981920 | G | GTTTTTTT | 91 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(88): Show |
116 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.-149-44_-149-38dup others(7): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11981920 | ||||||
| chr1:11981920 | G | GTTTTTTT others(1): Show |
99 | a0001c0001t0001g0030 a0001c0001t0001g0198 a0001c0001t0001g0200 others(96): Show |
117 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.-149-45_-149-38dup others(8): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11981920 | ||||||
| chr1:11981920 | G | GTTTTTTT others(2): Show |
21 | a0001c0001t0002g0262 a0001c0001t0003g0263 a0001c0001t0003g0264 others(18): Show |
21 | HG01109.hp1 HG02027.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.-149-46_-149-38dup others(9): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11981920 | ||||||
| chr1:11981920 | G | GTTTTTTT others(3): Show |
1 | a0001c0001t0006g0046 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-149-47_-149-38dup others(10): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11981920 | ||||||
| chr1:11981940 | G | T | 8 | a0001c0002t0005g0055 a0001c0004t0004g0015 a0001c0004t0004g0256 others(5): Show |
10 | HG02083.hp2 HG04228.hp2 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.-149-30G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981940 | |||||||
| chr1:11981955 | T | G | 11 | a0001c0001t0004g0047 a0001c0001t0006g0037 a0001c0001t0006g0038 others(8): Show |
11 | HG01192.hp2 HG01891.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-149-15T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981955 | |||||||
| chr1:11982204 | A | G | 220 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(217): Show |
262 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.-5+90A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11982204 | |||||||
| chr1:11982241 | C | T | 21 | a0001c0001t0013g0033 a0001c0001t0013g0241 a0001c0002t0005g0034 others(18): Show |
23 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-5+127C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11982241 | |||||||
| chr1:11982386 | C | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(187): Show |
226 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.-5+272C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11982386 | |||||||
| chr1:11982449 | T | C | 203 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(200): Show |
242 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.-5+335T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11982449 | |||||||
| chr1:11982497 | A | G | 1 | a0003c0010t0002g0289 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-5+383A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11982497 | |||||||
| chr1:11982682 | C | T | 3 | a0001c0001t0004g0285 a0001c0001t0004g0286 a0001c0001t0004g0287 |
3 | HG02630.hp2 HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-5+568C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11982682 | |||||||
| chr1:11982698 | G | A | 155 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
189 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.-5+584G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11982698 | |||||||
| chr1:11982880 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-5+766G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11982880 | |||||||
| chr1:11983120 | G | A | 2 | a0001c0001t0003g0120 a0001c0001t0003g0121 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-5+1006G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11983120 | |||||||
| chr1:11983134 | G | A | 5 | a0001c0001t0003g0193 a0001c0001t0003g0194 a0001c0001t0003g0195 others(2): Show |
5 | HG01934.hp1 NA18963.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+1020G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11983134 | |||||||
| chr1:11983197 | C | T | 10 | a0001c0001t0004g0014 a0001c0001t0004g0190 a0001c0001t0004g0191 others(7): Show |
12 | HG02280.hp2 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-5+1083C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11983197 | |||||||
| chr1:11983217 | G | A | 4 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0059 others(1): Show |
4 | NA18940.hp1 NA18945.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+1103G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11983217 | |||||||
| chr1:11983324 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-5+1210G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11983324 | |||||||
| chr1:11983412 | T | C | 21 | a0001c0001t0013g0033 a0001c0001t0013g0241 a0001c0002t0005g0034 others(18): Show |
23 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-5+1298T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11983412 | |||||||
| chr1:11983525 | T | C | 1 | a0001c0001t0003g0197 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-5+1411T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11983525 | |||||||
| chr1:11983600 | T | A | 1 | a0001c0001t0002g0061 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-5+1486T>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11983600 | |||||||
| chr1:11983660 | G | A | 191 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(188): Show |
227 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.-5+1546G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11983660 | |||||||
| chr1:11983807 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-5+1693G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11983807 | |||||||
| chr1:11983820 | G | A | 7 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0064 others(4): Show |
11 | HG01099.hp2 HG01123.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5+1706G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11983820 | |||||||
| chr1:11983869 | G | A | 1 | a0001c0001t0004g0190 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-5+1755G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11983869 | |||||||
| chr1:11984107 | C | T | 203 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(200): Show |
242 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.-5+1993C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11984107 | |||||||
| chr1:11984294 | G | A | 3 | a0001c0001t0012g0036 a0001c0001t0012g0291 a0003c0010t0002g0289 |
4 | HG02109.hp2 HG02145.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+2180G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11984294 | |||||||
| chr1:11984323 | T | C | 1 | a0001c0001t0002g0069 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-5+2209T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11984323 | |||||||
| chr1:11984366 | GGAGA | G | 7 | a0001c0004t0004g0015 a0001c0004t0004g0256 a0001c0004t0004g0258 others(4): Show |
9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-5+2256_-5+2259del others(4): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11984366 | ||||||
| chr1:11984506 | G | T | 7 | a0001c0004t0004g0015 a0001c0004t0004g0256 a0001c0004t0004g0258 others(4): Show |
9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-5+2392G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11984506 | |||||||
| chr1:11984615 | C | A | 5 | a0001c0003t0007g0035 a0001c0003t0007g0269 a0001c0003t0007g0270 others(2): Show |
6 | HG01167.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+2501C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11984615 | |||||||
| chr1:11984858 | C | T | 1 | a0001c0001t0004g0190 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-5+2744C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11984858 | |||||||
| chr1:11984868 | G | A | 1 | a0001c0001t0004g0190 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-5+2754G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11984868 | |||||||
| chr1:11984953 | C | T | 2 | a0001c0003t0017g0281 a0001c0003t0017g0282 |
2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-5+2839C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11984953 | |||||||
| chr1:11985074 | G | A | 7 | a0001c0004t0004g0015 a0001c0004t0004g0256 a0001c0004t0004g0258 others(4): Show |
9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-5+2960G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985074 | |||||||
| chr1:11985096 | C | T | 1 | a0001c0001t0002g0056 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-5+2982C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985096 | |||||||
| chr1:11985455 | C | CT | 15 | a0001c0001t0002g0026 a0001c0001t0002g0060 a0001c0001t0002g0068 others(12): Show |
16 | HG00423.hp2 HG01109.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.-5+3368dupT | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11985455 | ||||||
| chr1:11985455 | C | CTT | 9 | a0001c0001t0004g0014 a0001c0001t0004g0189 a0001c0001t0004g0190 others(6): Show |
12 | HG01167.hp1 HG02280.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-5+3367_-5+3368dup others(2): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11985455 | ||||||
| chr1:11985455 | CT | C | 21 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0076 others(18): Show |
24 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.-5+3368delT | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11985455 | ||||||
| chr1:11985455 | CTTTTT | C | 11 | a0001c0001t0004g0047 a0001c0001t0006g0037 a0001c0001t0006g0038 others(8): Show |
11 | HG01192.hp2 HG01891.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5+3364_-5+3368del others(5): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11985455 | ||||||
| chr1:11985455 | CTTTTTTT | C | 6 | a0001c0004t0004g0015 a0001c0004t0004g0256 a0001c0004t0004g0258 others(3): Show |
8 | HG04228.hp2 NA18952.hp2 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5+3362_-5+3368del others(7): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11985455 | ||||||
| chr1:11985455 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0002g0070 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-5+3359_-5+3368del others(10): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11985455 | ||||||
| chr1:11985482 | T | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
131 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.-5+3368T>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985482 | |||||||
| chr1:11985482 | T | TA | 67 | a0001c0001t0001g0054 a0001c0001t0001g0111 a0001c0001t0001g0112 others(64): Show |
75 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.-5+3371dupA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11985482 | ||||||
| chr1:11985482 | T | TTA | 27 | a0001c0001t0003g0184 a0001c0001t0003g0236 a0001c0001t0003g0237 others(24): Show |
28 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5+3368_-5+3369ins others(2): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985482 | |||||||
| chr1:11985495 | TTCGC | T | 3 | a0001c0001t0003g0183 a0001c0001t0003g0235 a0001c0001t0003g0240 |
3 | NA18981.hp2 NA19085.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-5+3384_-5+3387del others(4): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11985495 | ||||||
| chr1:11985498 | G | T | 203 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(200): Show |
243 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.-5+3384G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985498 | |||||||
| chr1:11985540 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-5+3426C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985540 | |||||||
| chr1:11985615 | C | T | 7 | a0001c0004t0004g0015 a0001c0004t0004g0256 a0001c0004t0004g0258 others(4): Show |
9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-5+3501C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985615 | |||||||
| chr1:11985656 | C | T | 1 | a0001c0001t0019g0104 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-4-3509C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985656 | |||||||
| chr1:11985725 | C | T | 21 | a0001c0001t0013g0033 a0001c0001t0013g0241 a0001c0002t0005g0034 others(18): Show |
23 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-4-3440C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985725 | |||||||
| chr1:11985757 | C | T | 2 | a0001c0001t0013g0033 a0001c0001t0013g0241 |
3 | HG02970.hp2 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-4-3408C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985757 | |||||||
| chr1:11985783 | A | G | 5 | a0001c0003t0007g0035 a0001c0003t0007g0269 a0001c0003t0007g0270 others(2): Show |
6 | HG01167.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4-3382A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985783 | |||||||
| chr1:11985833 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-4-3332G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985833 | |||||||
| chr1:11985850 | A | G | 1 | a0001c0005t0004g0119 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-4-3315A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985850 | |||||||
| chr1:11985861 | A | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0074 |
2 | HG00639.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-4-3304A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985861 | |||||||
| chr1:11985878 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-4-3287C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985878 | |||||||
| chr1:11985902 | T | A | 1 | a0001c0001t0010g0019 | 2 | HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-4-3263T>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985902 | |||||||
| chr1:11986006 | G | T | 206 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(203): Show |
246 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.-4-3159G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11986006 | |||||||
| chr1:11986032 | G | A | 78 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(75): Show |
106 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.-4-3133G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11986032 | |||||||
| chr1:11986277 | C | G | 198 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(195): Show |
237 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.-4-2888C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11986277 | |||||||
| chr1:11986490 | G | A | 10 | a0001c0001t0004g0014 a0001c0001t0004g0190 a0001c0001t0004g0191 others(7): Show |
12 | HG02280.hp2 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-4-2675G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11986490 | |||||||
| chr1:11986591 | C | CT | 21 | a0001c0001t0001g0168 a0001c0001t0001g0208 a0001c0001t0002g0262 others(18): Show |
24 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.-4-2557dupT | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11986591 | ||||||
| chr1:11986591 | CT | C | 8 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0158 others(5): Show |
8 | HG00408.hp2 HG01978.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4-2557delT | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11986591 | ||||||
| chr1:11986626 | T | C | 2 | a0001c0001t0001g0054 a0001c0001t0004g0273 |
2 | HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-4-2539T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11986626 | |||||||
| chr1:11986701 | G | A | 7 | a0001c0003t0007g0035 a0001c0003t0007g0269 a0001c0003t0007g0270 others(4): Show |
8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4-2464G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11986701 | |||||||
| chr1:11986710 | C | T | 10 | a0001c0001t0004g0014 a0001c0001t0004g0190 a0001c0001t0004g0191 others(7): Show |
12 | HG02280.hp2 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-4-2455C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11986710 | |||||||
| chr1:11986772 | G | A | 21 | a0001c0001t0013g0033 a0001c0001t0013g0241 a0001c0002t0005g0034 others(18): Show |
23 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-4-2393G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11986772 | |||||||
| chr1:11986823 | C | T | 91 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(88): Show |
120 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.-4-2342C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11986823 | |||||||
| chr1:11986971 | T | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(203): Show |
246 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.-4-2194T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11986971 | |||||||
| chr1:11987139 | G | GTC | 213 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(210): Show |
255 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(252): Show |
intron_variant | MODIFIER | c.-4-2024_-4-2023dup others(2): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11987139 | ||||||
| chr1:11987176 | T | C | 213 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(210): Show |
255 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(252): Show |
intron_variant | MODIFIER | c.-4-1989T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11987176 | |||||||
| chr1:11987247 | G | A | 5 | a0001c0003t0007g0035 a0001c0003t0007g0269 a0001c0003t0007g0270 others(2): Show |
6 | HG01167.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4-1918G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11987247 | |||||||
| chr1:11987302 | ACT | A | 21 | a0001c0001t0013g0033 a0001c0001t0013g0241 a0001c0002t0005g0034 others(18): Show |
23 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-4-1860_-4-1859del others(2): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11987302 | ||||||
| chr1:11987311 | C | CA | 10 | a0001c0001t0002g0077 a0001c0001t0002g0078 a0001c0001t0002g0105 others(7): Show |
12 | HG02080.hp2 HG02083.hp2 HG04228.hp2 others(9): Show |
intron_variant | MODIFIER | c.-4-1838dupA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11987311 | ||||||
| chr1:11987311 | CA | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(199): Show |
242 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.-4-1838delA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11987311 | ||||||
| chr1:11987370 | C | T | 21 | a0001c0001t0013g0033 a0001c0001t0013g0241 a0001c0002t0005g0034 others(18): Show |
23 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-4-1795C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11987370 | |||||||
| chr1:11987560 | G | C | 7 | a0001c0004t0004g0015 a0001c0004t0004g0256 a0001c0004t0004g0258 others(4): Show |
9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4-1605G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11987560 | |||||||
| chr1:11987572 | G | A | 2 | a0001c0001t0013g0033 a0001c0001t0013g0241 |
3 | HG02970.hp2 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-4-1593G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11987572 | |||||||
| chr1:11987587 | G | A | 10 | a0001c0001t0004g0014 a0001c0001t0004g0190 a0001c0001t0004g0191 others(7): Show |
12 | HG02280.hp2 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-4-1578G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11987587 | |||||||
| chr1:11987629 | C | CA | 5 | a0001c0001t0001g0125 a0001c0001t0001g0157 a0001c0001t0003g0204 others(2): Show |
5 | HG01169.hp2 HG01975.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-1535dupA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11987629 | ||||||
| chr1:11987629 | C | CAA | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
222 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.-4-1535_-4-1534ins others(2): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11987629 | ||||||
| chr1:11987629 | C | CAAA | 26 | a0001c0001t0001g0062 a0001c0001t0001g0111 a0001c0001t0001g0129 others(23): Show |
28 | HG00738.hp2 HG01109.hp1 HG01934.hp1 others(25): Show |
intron_variant | MODIFIER | c.-4-1535_-4-1534ins others(3): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11987629 | ||||||
| chr1:11987631 | G | A | 213 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(210): Show |
255 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(252): Show |
intron_variant | MODIFIER | c.-4-1534G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11987631 | |||||||
| chr1:11987672 | G | A | 7 | a0001c0003t0007g0035 a0001c0003t0007g0269 a0001c0003t0007g0270 others(4): Show |
8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4-1493G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11987672 | |||||||
| chr1:11987763 | C | T | 7 | a0001c0003t0007g0035 a0001c0003t0007g0269 a0001c0003t0007g0270 others(4): Show |
8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4-1402C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11987763 | |||||||
| chr1:11988022 | C | T | 1 | a0001c0001t0002g0069 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-4-1143C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988022 | |||||||
| chr1:11988042 | T | C | 1 | a0001c0001t0002g0079 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-4-1123T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988042 | |||||||
| chr1:11988044 | T | C | 1 | a0001c0001t0002g0079 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-4-1121T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988044 | |||||||
| chr1:11988045 | G | A | 1 | a0001c0001t0002g0079 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-4-1120G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988045 | |||||||
| chr1:11988048 | G | C | 1 | a0001c0001t0002g0079 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-4-1117G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988048 | |||||||
| chr1:11988050 | A | C | 1 | a0001c0001t0002g0079 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-4-1115A>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988050 | |||||||
| chr1:11988054 | C | A | 1 | a0001c0001t0002g0079 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-4-1111C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988054 | |||||||
| chr1:11988056 | G | T | 1 | a0001c0001t0002g0079 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-4-1109G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988056 | |||||||
| chr1:11988058 | G | T | 1 | a0001c0001t0002g0079 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-4-1107G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988058 | |||||||
| chr1:11988061 | A | G | 1 | a0001c0001t0002g0079 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-4-1104A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988061 | |||||||
| chr1:11988073 | A | G | 206 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(203): Show |
246 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.-4-1092A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988073 | |||||||
| chr1:11988080 | GTT | G | 50 | a0001c0001t0001g0218 a0001c0001t0001g0228 a0001c0001t0003g0004 others(47): Show |
58 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.-4-1081_-4-1080del others(2): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11988080 | ||||||
| chr1:11988082 | T | G | 1 | a0001c0004t0004g0256 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-4-1083T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988082 | |||||||
| chr1:11988082 | T | TTGTG | 13 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0144 others(10): Show |
15 | HG02083.hp2 HG02132.hp1 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.-4-1082_-4-1081ins others(4): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11988082 | ||||||
| chr1:11988082 | T | TTGTGTG | 112 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(109): Show |
138 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.-4-1082_-4-1081ins others(6): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11988082 | ||||||
| chr1:11988082 | T | TTGTGTGT others(1): Show |
28 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0054 others(25): Show |
31 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.-4-1082_-4-1081ins others(8): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11988082 | ||||||
| chr1:11988082 | T | TTGTGTGT others(3): Show |
6 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0149 others(3): Show |
6 | HG00140.hp1 HG01123.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4-1082_-4-1081ins others(10): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11988082 | ||||||
| chr1:11988082 | T | TTGTGTGT others(5): Show |
3 | a0001c0001t0006g0037 a0001c0001t0006g0041 a0001c0001t0006g0046 |
3 | HG01192.hp2 HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-4-1082_-4-1081ins others(12): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11988082 | ||||||
| chr1:11988084 | T | G | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
197 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.-4-1081T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988084 | |||||||
| chr1:11988084 | T | TTG | 3 | a0001c0001t0004g0014 a0001c0001t0004g0190 a0001c0001t0004g0192 |
5 | HG02280.hp2 HG02572.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-1057_-4-1056dup others(2): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11988084 | ||||||
| chr1:11988086 | G | T | 1 | a0001c0005t0004g0283 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-4-1079G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988086 | |||||||
| chr1:11988108 | G | T | 3 | a0001c0001t0002g0078 a0001c0001t0002g0101 a0001c0001t0003g0214 |
3 | HG02080.hp2 HG02735.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-4-1057G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988108 | |||||||
| chr1:11988247 | G | A | 3 | a0001c0001t0012g0036 a0001c0001t0012g0291 a0003c0010t0002g0289 |
4 | HG02109.hp2 HG02145.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-918G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988247 | |||||||
| chr1:11988267 | A | G | 7 | a0001c0004t0004g0015 a0001c0004t0004g0256 a0001c0004t0004g0258 others(4): Show |
9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4-898A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988267 | |||||||
| chr1:11988403 | G | GT | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
198 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.-4-745dupT | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11988403 | ||||||
| chr1:11988403 | G | GTT | 59 | a0001c0001t0001g0124 a0001c0001t0001g0128 a0001c0001t0001g0173 others(56): Show |
67 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.-4-746_-4-745dupTT | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11988403 | ||||||
| chr1:11988409 | T | G | 7 | a0001c0004t0004g0015 a0001c0004t0004g0256 a0001c0004t0004g0258 others(4): Show |
9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4-756T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988409 | |||||||
| chr1:11988425 | A | G | 1 | a0001c0001t0003g0197 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-4-740A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988425 | |||||||
| chr1:11988532 | C | T | 6 | a0001c0001t0002g0262 a0001c0001t0004g0029 a0001c0001t0004g0186 others(3): Show |
7 | HG02055.hp1 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4-633C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988532 | |||||||
| chr1:11988538 | C | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(162): Show |
202 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.-4-627C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988538 | |||||||
| chr1:11988608 | G | A | 7 | a0001c0004t0004g0015 a0001c0004t0004g0256 a0001c0004t0004g0258 others(4): Show |
9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4-557G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988608 | |||||||
| chr1:11988614 | G | A | 2 | a0001c0001t0002g0080 a0001c0001t0002g0106 |
2 | HG00140.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-4-551G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988614 | |||||||
| chr1:11988619 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-4-546C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988619 | |||||||
| chr1:11988826 | A | G | 213 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(210): Show |
255 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(252): Show |
intron_variant | MODIFIER | c.-4-339A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988826 | |||||||
| chr1:11988944 | C | A | 2 | a0001c0001t0004g0014 a0001c0001t0004g0192 |
4 | HG02280.hp2 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-221C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988944 | |||||||
| chr1:11989014 | C | G | 1 | a0001c0001t0001g0013 | 3 | HG02071.hp2 NA19080.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-4-151C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11989014 | |||||||
| chr1:11989120 | C | T | 1 | a0001c0001t0002g0024 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-4-45C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11989120 | |||||||
| chr1:11989561 | CAT | C | 7 | a0001c0003t0007g0035 a0001c0003t0007g0269 a0001c0003t0007g0270 others(4): Show |
8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.175+219_175+220del others(2): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11989561 | |||||||
| chr1:11989651 | C | A | 3 | a0001c0001t0003g0213 a0001c0001t0003g0216 a0001c0001t0003g0217 |
3 | NA18970.hp2 NA19011.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.175+308C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11989651 | |||||||
| chr1:11989779 | C | T | 1 | a0001c0001t0026g0261 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.175+436C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11989779 | |||||||
| chr1:11989814 | A | T | 1 | a0001c0001t0002g0070 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.175+471A>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11989814 | |||||||
| chr1:11989858 | A | G | 2 | a0001c0002t0005g0253 a0001c0002t0005g0254 |
2 | HG00733.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.175+515A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11989858 | |||||||
| chr1:11990004 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.175+661T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11990004 | |||||||
| chr1:11990169 | A | G | 2 | a0001c0001t0004g0047 a0001c0001t0025g0290 |
2 | HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.175+826A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11990169 | |||||||
| chr1:11990577 | T | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(203): Show |
246 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.175+1234T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11990577 | |||||||
| chr1:11990872 | C | T | 2 | a0001c0001t0013g0033 a0001c0001t0013g0241 |
3 | HG02970.hp2 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.175+1529C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11990872 | |||||||
| chr1:11990891 | G | A | 1 | a0001c0001t0018g0103 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.175+1548G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11990891 | |||||||
| chr1:11990929 | T | C | 14 | a0001c0003t0007g0035 a0001c0003t0007g0269 a0001c0003t0007g0270 others(11): Show |
17 | HG01109.hp1 HG01167.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.175+1586T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11990929 | |||||||
| chr1:11991071 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.176-1484C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11991071 | |||||||
| chr1:11991279 | G | A | 7 | a0001c0003t0007g0035 a0001c0003t0007g0269 a0001c0003t0007g0270 others(4): Show |
8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.176-1276G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11991279 | |||||||
| chr1:11991361 | C | T | 7 | a0001c0001t0001g0168 a0001c0001t0004g0048 a0001c0001t0004g0126 others(4): Show |
7 | HG01884.hp2 HG02886.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.176-1194C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11991361 | |||||||
| chr1:11991462 | C | G | 7 | a0001c0004t0004g0015 a0001c0004t0004g0256 a0001c0004t0004g0258 others(4): Show |
9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.176-1093C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11991462 | |||||||
| chr1:11991651 | G | A | 52 | a0001c0001t0001g0218 a0001c0001t0001g0228 a0001c0001t0003g0004 others(49): Show |
60 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.176-904G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11991651 | |||||||
| chr1:11991690 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.176-865C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11991690 | |||||||
| chr1:11991706 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.176-849C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11991706 | |||||||
| chr1:11991780 | C | T | 1 | a0001c0002t0005g0055 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.176-775C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11991780 | |||||||
| chr1:11991822 | G | A | 1 | a0001c0002t0008g0242 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.176-733G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11991822 | |||||||
| chr1:11991840 | C | T | 1 | a0001c0001t0002g0067 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.176-715C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11991840 | |||||||
| chr1:11991841 | G | A | 1 | a0001c0002t0005g0055 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.176-714G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11991841 | |||||||
| chr1:11991855 | C | T | 2 | a0001c0003t0007g0269 a0001c0003t0007g0270 |
2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.176-700C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11991855 | |||||||
| chr1:11991873 | C | G | 224 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(221): Show |
268 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.176-682C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11991873 | |||||||
| chr1:11991910 | C | A | 12 | a0001c0001t0004g0047 a0001c0001t0006g0037 a0001c0001t0006g0038 others(9): Show |
12 | HG01192.hp2 HG01891.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.176-645C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11991910 | |||||||
| chr1:11991923 | C | CA | 28 | a0001c0001t0001g0009 a0001c0001t0001g0083 a0001c0001t0002g0009 others(25): Show |
33 | HG00140.hp2 HG00280.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.176-603dupA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | ||||||
| chr1:11991923 | C | CAA | 11 | a0001c0001t0001g0028 a0001c0001t0001g0158 a0001c0001t0001g0165 others(8): Show |
12 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.176-604_176-603dup others(2): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | ||||||
| chr1:11991923 | C | CAAA | 45 | a0001c0001t0001g0018 a0001c0001t0001g0054 a0001c0001t0001g0117 others(42): Show |
53 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.176-605_176-603dup others(3): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | ||||||
| chr1:11991923 | C | CAAAA | 30 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0114 others(27): Show |
33 | HG00323.hp2 HG00735.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.176-606_176-603dup others(4): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | ||||||
| chr1:11991923 | C | CAAAAA | 22 | a0001c0001t0001g0002 a0001c0001t0001g0030 a0001c0001t0001g0073 others(19): Show |
37 | HG00558.hp1 HG00597.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.176-607_176-603dup others(5): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | ||||||
| chr1:11991923 | C | CAAAAAA | 37 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0017 others(34): Show |
43 | HG00609.hp1 HG00639.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.176-608_176-603dup others(6): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | ||||||
| chr1:11991923 | C | CAAAAAAA | 17 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0127 others(14): Show |
20 | HG00558.hp2 HG00639.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.176-609_176-603dup others(7): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | ||||||
| chr1:11991923 | C | CAAAAAAA others(1): Show |
8 | a0001c0001t0001g0012 a0001c0001t0001g0062 a0001c0001t0001g0132 others(5): Show |
9 | HG00735.hp2 HG01169.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.176-610_176-603dup others(8): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | ||||||
| chr1:11991923 | C | CAAAAAAA others(2): Show |
9 | a0001c0001t0001g0175 a0001c0001t0013g0033 a0001c0002t0005g0249 others(6): Show |
10 | HG00408.hp1 HG00733.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.176-611_176-603dup others(9): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | ||||||
| chr1:11991923 | C | CAAAAAAA others(3): Show |
9 | a0001c0001t0002g0262 a0001c0001t0013g0241 a0001c0002t0005g0034 others(6): Show |
10 | HG01192.hp1 HG02027.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.176-612_176-603dup others(10): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | ||||||
| chr1:11991923 | C | CAAAAAAA others(4): Show |
1 | a0001c0002t0005g0245 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.176-613_176-603dup others(11): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | ||||||
| chr1:11991923 | C | CAAAAAAA others(5): Show |
1 | a0001c0002t0008g0266 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.176-614_176-603dup others(12): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | ||||||
| chr1:11991923 | C | CAAAAAAA others(12): Show |
1 | a0001c0002t0005g0244 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.176-621_176-603dup others(19): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | ||||||
| chr1:11991923 | C | CAAAAAAA others(13): Show |
1 | a0001c0002t0005g0243 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.176-622_176-603dup others(20): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | ||||||
| chr1:11991923 | CA | C | 20 | a0001c0001t0001g0076 a0001c0001t0002g0023 a0001c0001t0002g0066 others(17): Show |
24 | HG01515.hp2 HG01993.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.176-603delA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | ||||||
| chr1:11991923 | CAAAAAAA others(2): Show |
C | 7 | a0001c0001t0003g0155 a0001c0004t0004g0015 a0001c0004t0004g0256 others(4): Show |
9 | HG02083.hp2 HG03704.hp2 HG04228.hp2 others(6): Show |
intron_variant | MODIFIER | c.176-611_176-603del others(9): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | ||||||
| chr1:11991923 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0124 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.176-614_176-603del others(12): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | ||||||
| chr1:11991923 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0004g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.176-617_176-603del others(15): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | ||||||
| chr1:11992216 | C | T | 3 | a0001c0001t0003g0183 a0001c0001t0003g0235 a0001c0001t0003g0240 |
3 | NA18981.hp2 NA19085.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.176-339C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11992216 | |||||||
| chr1:11992217 | G | A | 1 | a0001c0001t0002g0262 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.176-338G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11992217 | |||||||
| chr1:11992230 | G | A | 7 | a0001c0004t0004g0015 a0001c0004t0004g0256 a0001c0004t0004g0258 others(4): Show |
9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.176-325G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11992230 | |||||||
| chr1:11992254 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.176-301T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11992254 | |||||||
| chr1:11992299 | T | G | 7 | a0001c0004t0004g0015 a0001c0004t0004g0256 a0001c0004t0004g0258 others(4): Show |
9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.176-256T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11992299 | |||||||
| chr1:11992348 | G | A | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(292): Show |
373 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(370): Show |
intron_variant | MODIFIER | c.176-207G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11992348 | |||||||
| chr1:11992355 | G | T | 2 | a0001c0003t0017g0281 a0001c0003t0017g0282 |
2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.176-200G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11992355 | |||||||
| chr1:11992376 | C | A | 6 | a0001c0001t0002g0262 a0001c0001t0004g0029 a0001c0001t0004g0186 others(3): Show |
7 | HG02055.hp1 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.176-179C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11992376 | |||||||
| chr1:11992496 | C | G | 7 | a0001c0003t0007g0035 a0001c0003t0007g0269 a0001c0003t0007g0270 others(4): Show |
8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.176-59C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11992496 | |||||||
| chr1:11992722 | T | C | 1 | a0001c0001t0004g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.311+32T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11992722 | |||||||
| chr1:11992883 | G | GCCTCGAC others(3): Show |
1 | a0001c0001t0003g0234 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.311+197_311+206dup others(10): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11992883 | ||||||
| chr1:11992967 | C | CT | 86 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0076 others(83): Show |
123 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.311+289dupT | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11992967 | ||||||
| chr1:11992967 | C | CTT | 14 | a0001c0002t0005g0034 a0001c0002t0005g0055 a0001c0002t0005g0185 others(11): Show |
17 | HG01109.hp1 HG01167.hp1 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.311+288_311+289dup others(2): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11992967 | ||||||
| chr1:11992967 | C | CTTT | 30 | a0001c0001t0004g0047 a0001c0001t0004g0273 a0001c0001t0006g0037 others(27): Show |
31 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.311+287_311+289dup others(3): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11992967 | ||||||
| chr1:11992967 | C | CTTTT | 71 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(68): Show |
79 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.311+286_311+289dup others(4): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11992967 | ||||||
| chr1:11992967 | C | CTTTTT | 91 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(88): Show |
120 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.311+285_311+289dup others(5): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11992967 | ||||||
| chr1:11993005 | A | G | 2 | a0001c0003t0017g0281 a0001c0003t0017g0282 |
2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.311+315A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993005 | |||||||
| chr1:11993043 | C | T | 213 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(210): Show |
255 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(252): Show |
intron_variant | MODIFIER | c.311+353C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993043 | |||||||
| chr1:11993068 | ACCAGTCT others(255): Show |
A | 7 | a0001c0004t0004g0015 a0001c0004t0004g0256 a0001c0004t0004g0258 others(4): Show |
9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.311+379_311+640del | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993068 | |||||||
| chr1:11993081 | G | A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0030 a0001c0001t0001g0125 others(3): Show |
9 | HG01258.hp2 HG01346.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.311+391G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993081 | |||||||
| chr1:11993136 | C | G | 1 | a0001c0002t0005g0246 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.311+446C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993136 | |||||||
| chr1:11993171 | TCTA | T | 4 | a0001c0001t0003g0004 a0001c0001t0003g0031 a0001c0001t0003g0212 others(1): Show |
4 | HG02129.hp2 NA18957.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.311+484_311+486del others(3): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11993171 | ||||||
| chr1:11993207 | T | C | 198 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(195): Show |
237 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.311+517T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993207 | |||||||
| chr1:11993334 | G | A | 10 | a0001c0001t0004g0014 a0001c0001t0004g0190 a0001c0001t0004g0191 others(7): Show |
12 | HG02280.hp2 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.311+644G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993334 | |||||||
| chr1:11993418 | C | CA | 9 | a0001c0001t0001g0090 a0001c0001t0002g0089 a0001c0003t0007g0035 others(6): Show |
10 | HG01109.hp1 HG01167.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.311+737dupA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11993418 | ||||||
| chr1:11993644 | AGAATGGT others(2): Show |
A | 7 | a0001c0004t0004g0015 a0001c0004t0004g0256 a0001c0004t0004g0258 others(4): Show |
9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.311+958_311+966del others(9): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11993644 | ||||||
| chr1:11993660 | C | CG | 7 | a0001c0003t0007g0035 a0001c0003t0007g0269 a0001c0003t0007g0270 others(4): Show |
8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.311+970_311+971ins others(1): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993660 | |||||||
| chr1:11993661 | A | G | 213 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(210): Show |
255 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(252): Show |
intron_variant | MODIFIER | c.311+971A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993661 | |||||||
| chr1:11993668 | G | A | 7 | a0001c0004t0004g0015 a0001c0004t0004g0256 a0001c0004t0004g0258 others(4): Show |
9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.311+978G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993668 | |||||||
| chr1:11993733 | C | CA | 6 | a0001c0001t0002g0001 a0001c0001t0002g0068 a0001c0001t0002g0069 others(3): Show |
6 | HG01346.hp1 HG03516.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.311+1060dupA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11993733 | ||||||
| chr1:11993733 | CA | C | 200 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(197): Show |
240 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.311+1060delA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11993733 | ||||||
| chr1:11993733 | CAAAAA | C | 7 | a0001c0004t0004g0015 a0001c0004t0004g0256 a0001c0004t0004g0258 others(4): Show |
8 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.311+1056_311+1060d others(7): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11993733 | ||||||
| chr1:11993774 | T | G | 2 | a0001c0002t0005g0246 a0001c0002t0005g0247 |
2 | HG03017.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.311+1084T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993774 | |||||||
| chr1:11993826 | T | C | 1 | a0001c0001t0003g0204 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.311+1136T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993826 | |||||||
| chr1:11993865 | G | A | 14 | a0001c0003t0007g0035 a0001c0003t0007g0269 a0001c0003t0007g0270 others(11): Show |
17 | HG01109.hp1 HG01167.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.311+1175G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993865 | |||||||
| chr1:11993940 | G | A | 7 | a0001c0003t0007g0035 a0001c0003t0007g0269 a0001c0003t0007g0270 others(4): Show |
8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.311+1250G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993940 | |||||||
| chr1:11993973 | G | A | 223 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
267 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.311+1283G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993973 | |||||||
| chr1:11994025 | G | A | 1 | a0001c0001t0006g0041 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.311+1335G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11994025 | |||||||
| chr1:11994244 | C | G | 4 | a0001c0001t0004g0029 a0001c0001t0004g0186 a0001c0001t0004g0187 others(1): Show |
5 | HG02572.hp1 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.311+1554C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11994244 | |||||||
| chr1:11994264 | A | G | 1 | a0001c0001t0002g0068 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.311+1574A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11994264 | |||||||
| chr1:11994302 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.311+1612A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11994302 | |||||||
| chr1:11994331 | G | C | 6 | a0001c0001t0004g0285 a0001c0001t0004g0286 a0001c0001t0004g0287 others(3): Show |
6 | HG02630.hp2 HG02895.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.311+1641G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11994331 | |||||||
| chr1:11994463 | G | A | 2 | a0001c0001t0001g0138 a0004c0011t0001g0177 |
2 | NA18960.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.312-1693G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11994463 | |||||||
| chr1:11994507 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.312-1649A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11994507 | |||||||
| chr1:11994538 | C | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0074 |
2 | HG00639.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.312-1618C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11994538 | |||||||
| chr1:11994583 | C | G | 1 | a0001c0001t0001g0275 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.312-1573C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11994583 | |||||||
| chr1:11994584 | C | T | 7 | a0001c0003t0007g0035 a0001c0003t0007g0269 a0001c0003t0007g0270 others(4): Show |
8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.312-1572C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11994584 | |||||||
| chr1:11994589 | C | CA | 6 | a0001c0004t0004g0015 a0001c0004t0004g0256 a0001c0004t0004g0258 others(3): Show |
8 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.312-1555dupA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11994589 | ||||||
| chr1:11994615 | A | G | 10 | a0001c0001t0004g0014 a0001c0001t0004g0190 a0001c0001t0004g0191 others(7): Show |
12 | HG02280.hp2 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.312-1541A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11994615 | |||||||
| chr1:11994691 | C | A | 2 | a0001c0001t0010g0019 a0001c0001t0010g0096 |
3 | HG02257.hp2 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.312-1465C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11994691 | |||||||
| chr1:11994854 | A | G | 213 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(210): Show |
255 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(252): Show |
intron_variant | MODIFIER | c.312-1302A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11994854 | |||||||
| chr1:11995165 | G | A | 1 | a0001c0001t0016g0084 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.312-991G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11995165 | |||||||
| chr1:11995357 | G | A | 5 | a0001c0003t0007g0035 a0001c0003t0007g0269 a0001c0003t0007g0270 others(2): Show |
6 | HG01167.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.312-799G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11995357 | |||||||
| chr1:11995398 | T | C | 7 | a0001c0004t0004g0015 a0001c0004t0004g0256 a0001c0004t0004g0258 others(4): Show |
9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.312-758T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11995398 | |||||||
| chr1:11995406 | G | A | 7 | a0001c0003t0007g0035 a0001c0003t0007g0269 a0001c0003t0007g0270 others(4): Show |
8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.312-750G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11995406 | |||||||
| chr1:11995432 | C | A | 7 | a0001c0004t0004g0015 a0001c0004t0004g0256 a0001c0004t0004g0258 others(4): Show |
9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.312-724C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11995432 | |||||||
| chr1:11995642 | T | TA | 7 | a0001c0003t0007g0035 a0001c0003t0007g0269 a0001c0003t0007g0270 others(4): Show |
8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.312-503dupA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11995642 | ||||||
| chr1:11995643 | A | G | 7 | a0001c0004t0004g0015 a0001c0004t0004g0256 a0001c0004t0004g0258 others(4): Show |
9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.312-513A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11995643 | |||||||
| chr1:11995665 | T | G | 1 | a0001c0001t0002g0064 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.312-491T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11995665 | |||||||
| chr1:11995706 | A | G | 2 | a0001c0001t0004g0014 a0001c0001t0004g0192 |
4 | HG02280.hp2 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.312-450A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11995706 | |||||||
| chr1:11995917 | C | T | 2 | a0001c0001t0001g0054 a0001c0001t0004g0273 |
2 | HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.312-239C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11995917 | |||||||
| chr1:11996010 | T | C | 7 | a0001c0004t0004g0015 a0001c0004t0004g0256 a0001c0004t0004g0258 others(4): Show |
9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.312-146T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11996010 | |||||||
| chr1:11996018 | C | G | 12 | a0001c0001t0004g0047 a0001c0001t0006g0037 a0001c0001t0006g0038 others(9): Show |
12 | HG01192.hp2 HG01891.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.312-138C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11996018 | |||||||
| chr1:11996383 | C | T | 206 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(203): Show |
246 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.474+65C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11996383 | |||||||
| chr1:11996404 | A | C | 3 | a0001c0001t0015g0050 a0001c0001t0015g0051 a0001c0001t0015g0053 |
3 | HG02559.hp1 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.474+86A>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11996404 | |||||||
| chr1:11996406 | G | C | 2 | a0001c0005t0004g0119 a0001c0005t0004g0284 |
2 | HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.474+88G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11996406 | |||||||
| chr1:11996596 | A | G | 7 | a0001c0003t0007g0035 a0001c0003t0007g0269 a0001c0003t0007g0270 others(4): Show |
8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.474+278A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11996596 | |||||||
| chr1:11996678 | G | A | 3 | a0001c0001t0003g0184 a0001c0001t0003g0202 a0001c0001t0003g0220 |
3 | HG03688.hp1 HG03710.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.474+360G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11996678 | |||||||
| chr1:11996725 | G | C | 2 | a0001c0001t0002g0081 a0001c0001t0002g0085 |
2 | HG02074.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.474+407G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11996725 | |||||||
| chr1:11996758 | T | C | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(290): Show |
371 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(368): Show |
intron_variant | MODIFIER | c.474+440T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11996758 | |||||||
| chr1:11996760 | G | C | 1 | a0001c0002t0008g0267 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.474+442G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11996760 | |||||||
| chr1:11996888 | A | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(203): Show |
246 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.475-409A>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11996888 | |||||||
| chr1:11997025 | C | T | 1 | a0001c0001t0003g0231 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.475-272C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11997025 | |||||||
| chr1:11997026 | G | A | 1 | a0001c0001t0003g0216 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.475-271G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11997026 | |||||||
| chr1:11997038 | C | CA | 8 | a0001c0001t0002g0011 a0001c0001t0002g0091 a0001c0001t0002g0107 others(5): Show |
9 | HG01175.hp2 HG02280.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.475-240dupA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 11997038 | ||||||
| chr1:11997038 | CA | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(194): Show |
238 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.475-240delA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 11997038 | ||||||
| chr1:11997038 | CAA | C | 7 | a0001c0001t0001g0168 a0001c0001t0004g0048 a0001c0001t0004g0126 others(4): Show |
7 | HG01884.hp2 HG02886.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.475-241_475-240del others(2): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 11997038 | ||||||
| chr1:11997065 | T | G | 5 | a0001c0003t0007g0035 a0001c0003t0007g0269 a0001c0003t0007g0270 others(2): Show |
6 | HG01167.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.475-232T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11997065 | |||||||
| chr1:11997101 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.475-196G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11997101 | |||||||
| chr1:11997230 | C | G | 2 | a0001c0002t0008g0252 a0005c0015t0008g0248 |
2 | NA19068.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.475-67C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11997230 | |||||||
| chr1:11997254 | G | C | 1 | a0001c0001t0006g0037 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.475-43G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11997254 | |||||||
| chr1:11997264 | C | T | 7 | a0001c0004t0004g0015 a0001c0004t0004g0256 a0001c0004t0004g0258 others(4): Show |
9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.475-33C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11997264 | |||||||
| chr1:11997525 | T | A | 1 | a0001c0001t0026g0261 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.599+104T>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11997525 | |||||||
| chr1:11997530 | A | G | 2 | a0001c0003t0017g0281 a0001c0003t0017g0282 |
2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.599+109A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11997530 | |||||||
| chr1:11997536 | A | C | 7 | a0001c0003t0007g0035 a0001c0003t0007g0269 a0001c0003t0007g0270 others(4): Show |
8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.599+115A>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11997536 | |||||||
| chr1:11997675 | G | A | 3 | a0001c0001t0016g0084 a0001c0001t0016g0086 a0001c0001t0019g0104 |
3 | HG02698.hp1 HG03710.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.599+254G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11997675 | |||||||
| chr1:11997736 | G | C | 1 | a0001c0003t0017g0281 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.599+315G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11997736 | |||||||
| chr1:11997853 | A | C | 1 | a0001c0001t0002g0099 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.599+432A>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11997853 | |||||||
| chr1:11997856 | A | C | 1 | a0001c0001t0002g0099 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.599+435A>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11997856 | |||||||
| chr1:11997879 | C | CT | 22 | a0001c0001t0002g0059 a0001c0001t0002g0082 a0001c0001t0004g0014 others(19): Show |
26 | HG01884.hp2 HG02083.hp2 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.599+480dupT | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 11997879 | ||||||
| chr1:11997879 | C | CTTT | 156 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(153): Show |
194 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.599+478_599+480dup others(3): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 11997879 | ||||||
| chr1:11997879 | C | CTTTT | 12 | a0001c0001t0001g0018 a0001c0001t0001g0136 a0001c0001t0001g0151 others(9): Show |
13 | HG00597.hp1 HG00738.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.599+477_599+480dup others(4): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 11997879 | ||||||
| chr1:11997879 | CT | C | 6 | a0001c0001t0002g0092 a0001c0001t0002g0278 a0001c0003t0007g0035 others(3): Show |
7 | HG01070.hp2 HG01167.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.599+480delT | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 11997879 | ||||||
| chr1:11997914 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.599+493T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11997914 | |||||||
| chr1:11997915 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.599+494G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11997915 | |||||||
| chr1:11997917 | T | C | 12 | a0001c0001t0004g0047 a0001c0001t0006g0037 a0001c0001t0006g0038 others(9): Show |
12 | HG01192.hp2 HG01891.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.599+496T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11997917 | |||||||
| chr1:11997952 | C | T | 1 | a0001c0001t0004g0189 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.599+531C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11997952 | |||||||
| chr1:11997989 | T | C | 1 | a0001c0002t0005g0246 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.599+568T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11997989 | |||||||
| chr1:11998028 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.599+607T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998028 | |||||||
| chr1:11998029 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.599+608G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998029 | |||||||
| chr1:11998031 | C | A | 1 | a0001c0001t0001g0275 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.599+610C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998031 | |||||||
| chr1:11998072 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.599+651C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998072 | |||||||
| chr1:11998111 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.600-659T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998111 | |||||||
| chr1:11998118 | A | G | 5 | a0001c0001t0001g0111 a0001c0001t0001g0276 a0001c0001t0002g0109 others(2): Show |
5 | HG02257.hp1 HG02559.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.600-652A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998118 | |||||||
| chr1:11998134 | A | G | 54 | a0001c0001t0001g0151 a0001c0001t0001g0164 a0001c0001t0001g0205 others(51): Show |
63 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.600-636A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998134 | |||||||
| chr1:11998158 | G | A | 1 | a0001c0001t0002g0101 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.600-612G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998158 | |||||||
| chr1:11998162 | A | G | 1 | a0001c0001t0002g0101 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.600-608A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998162 | |||||||
| chr1:11998173 | T | C | 2 | a0001c0001t0002g0262 a0001c0001t0004g0097 |
2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.600-597T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998173 | |||||||
| chr1:11998480 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.600-290G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998480 | |||||||
| chr1:11998497 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.600-273G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998497 | |||||||
| chr1:11998523 | G | A | 12 | a0001c0001t0004g0047 a0001c0001t0006g0037 a0001c0001t0006g0038 others(9): Show |
12 | HG01192.hp2 HG01891.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.600-247G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998523 | |||||||
| chr1:11998549 | AAAAAC | A | 210 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
253 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.600-199_600-195del others(5): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 11998549 | ||||||
| chr1:11998654 | G | A | 1 | a0001c0001t0001g0027 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.600-116G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998654 | |||||||
| chr1:11998685 | C | T | 8 | a0001c0001t0001g0228 a0001c0001t0003g0032 a0001c0001t0003g0211 others(5): Show |
8 | NA18946.hp1 NA18952.hp1 NA18967.hp1 others(5): Show |
intron_variant | MODIFIER | c.600-85C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998685 | |||||||
| chr1:11998745 | T | C | 27 | a0001c0002t0005g0034 a0001c0002t0005g0055 a0001c0002t0005g0087 others(24): Show |
30 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.600-25T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998745 | |||||||
| chr1:11998936 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.709-52G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 7/18 | chr1 | 11998936 | |||||||
| chr1:11998953 | G | A | 1 | a0001c0001t0003g0226 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.709-35G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 7/18 | chr1 | 11998953 | |||||||
| chr1:11999303 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.816+208C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 11999303 | |||||||
| chr1:11999355 | C | T | 95 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(92): Show |
124 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.816+260C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 11999355 | |||||||
| chr1:11999441 | G | A | 27 | a0001c0002t0005g0034 a0001c0002t0005g0055 a0001c0002t0005g0087 others(24): Show |
30 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.816+346G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 11999441 | |||||||
| chr1:11999491 | A | G | 21 | a0001c0002t0005g0034 a0001c0002t0005g0055 a0001c0002t0005g0087 others(18): Show |
22 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.816+396A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 11999491 | |||||||
| chr1:11999546 | C | T | 1 | a0001c0001t0004g0189 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.816+451C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 11999546 | |||||||
| chr1:11999689 | C | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0146 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.816+594C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 11999689 | |||||||
| chr1:11999726 | A | G | 5 | a0001c0003t0007g0035 a0001c0003t0007g0269 a0001c0003t0007g0270 others(2): Show |
6 | HG01167.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.816+631A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 11999726 | |||||||
| chr1:11999810 | G | A | 4 | a0001c0001t0012g0036 a0001c0001t0012g0291 a0001c0001t0013g0033 others(1): Show |
6 | HG02109.hp2 HG02145.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.816+715G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 11999810 | |||||||
| chr1:11999832 | C | T | 1 | a0001c0001t0003g0211 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.816+737C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 11999832 | |||||||
| chr1:11999883 | A | G | 1 | a0001c0001t0002g0099 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.816+788A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 11999883 | |||||||
| chr1:11999912 | G | T | 2 | a0001c0001t0002g0020 a0001c0001t0002g0102 |
3 | NA18945.hp2 NA18959.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.816+817G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 11999912 | |||||||
| chr1:12000098 | C | CA | 210 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
253 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.816+1009dupA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr1 | 12000098 | ||||||
| chr1:12000216 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.816+1121G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 12000216 | |||||||
| chr1:12000279 | A | G | 228 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(225): Show |
273 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.817-1122A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 12000279 | |||||||
| chr1:12000297 | A | G | 7 | a0001c0003t0007g0035 a0001c0003t0007g0269 a0001c0003t0007g0270 others(4): Show |
8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.817-1104A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 12000297 | |||||||
| chr1:12000436 | C | T | 2 | a0001c0003t0017g0281 a0001c0003t0017g0282 |
2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.817-965C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 12000436 | |||||||
| chr1:12000444 | C | T | 3 | a0001c0001t0003g0203 a0001c0001t0003g0223 a0001c0001t0003g0236 |
3 | HG00735.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.817-957C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 12000444 | |||||||
| chr1:12000466 | G | A | 4 | a0001c0001t0012g0036 a0001c0001t0012g0291 a0001c0001t0013g0033 others(1): Show |
6 | HG02109.hp2 HG02145.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.817-935G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 12000466 | |||||||
| chr1:12000508 | T | C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(172): Show |
214 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.817-893T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 12000508 | |||||||
| chr1:12000508 | T | G | 1 | a0001c0001t0003g0230 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.817-893T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 12000508 | |||||||
| chr1:12000547 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.817-854A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 12000547 | |||||||
| chr1:12000705 | C | T | 1 | a0001c0001t0002g0088 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.817-696C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 12000705 | |||||||
| chr1:12000812 | A | G | 34 | a0001c0002t0005g0034 a0001c0002t0005g0055 a0001c0002t0005g0087 others(31): Show |
38 | HG00408.hp1 HG00733.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.817-589A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 12000812 | |||||||
| chr1:12000841 | C | T | 1 | a0001c0001t0002g0070 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.817-560C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 12000841 | |||||||
| chr1:12001035 | T | C | 1 | a0001c0005t0004g0283 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.817-366T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 12001035 | |||||||
| chr1:12001573 | G | A | 4 | a0001c0001t0004g0048 a0001c0001t0004g0126 a0001c0001t0004g0170 others(1): Show |
4 | HG01884.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.970+19G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 9/18 | chr1 | 12001573 | |||||||
| chr1:12001605 | G | A | 2 | a0001c0001t0002g0093 a0001c0001t0002g0094 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.970+51G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 9/18 | chr1 | 12001605 | |||||||
| chr1:12001941 | C | G | 6 | a0001c0001t0004g0285 a0001c0001t0004g0286 a0001c0001t0004g0287 others(3): Show |
6 | HG02630.hp2 HG02895.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1039-41C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 10/18 | chr1 | 12001941 | |||||||
| chr1:12001960 | T | C | 22 | a0001c0001t0001g0074 a0001c0002t0005g0034 a0001c0002t0005g0055 others(19): Show |
23 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.1039-22T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 10/18 | chr1 | 12001960 | |||||||
| chr1:12001963 | G | A | 18 | a0001c0001t0001g0168 a0001c0001t0004g0014 a0001c0001t0004g0048 others(15): Show |
20 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.1039-19G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 10/18 | chr1 | 12001963 | |||||||
| chr1:12002122 | A | G | 1 | a0001c0005t0004g0119 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1160+19A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12002122 | |||||||
| chr1:12002148 | A | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
253 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.1160+45A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12002148 | |||||||
| chr1:12002304 | C | G | 176 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(173): Show |
215 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1160+201C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12002304 | |||||||
| chr1:12002344 | T | C | 1 | a0001c0003t0007g0272 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1160+241T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12002344 | |||||||
| chr1:12002418 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1160+315G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12002418 | |||||||
| chr1:12002450 | T | G | 172 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(169): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1160+347T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12002450 | |||||||
| chr1:12002919 | G | A | 1 | a0001c0002t0005g0055 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1160+816G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12002919 | |||||||
| chr1:12002975 | C | T | 1 | a0001c0001t0026g0261 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1160+872C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12002975 | |||||||
| chr1:12003083 | AT | A | 32 | a0001c0002t0005g0034 a0001c0002t0005g0055 a0001c0002t0005g0087 others(29): Show |
36 | HG00408.hp1 HG00733.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1161-899delT | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 12003083 | ||||||
| chr1:12003141 | G | A | 12 | a0001c0001t0001g0168 a0001c0001t0004g0014 a0001c0001t0004g0048 others(9): Show |
14 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1161-851G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12003141 | |||||||
| chr1:12003174 | TC | T | 27 | a0001c0002t0005g0034 a0001c0002t0005g0055 a0001c0002t0005g0087 others(24): Show |
30 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.1161-816delC | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 12003174 | ||||||
| chr1:12003216 | C | T | 4 | a0001c0001t0012g0036 a0001c0001t0012g0291 a0001c0001t0013g0033 others(1): Show |
6 | HG02109.hp2 HG02145.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1161-776C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12003216 | |||||||
| chr1:12003237 | A | AT | 32 | a0001c0002t0005g0034 a0001c0002t0005g0055 a0001c0002t0005g0087 others(29): Show |
36 | HG00408.hp1 HG00733.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1161-754dupT | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 12003237 | ||||||
| chr1:12003250 | C | T | 1 | a0001c0001t0002g0061 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1161-742C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12003250 | |||||||
| chr1:12003533 | G | A | 4 | a0001c0001t0012g0036 a0001c0001t0012g0291 a0001c0001t0013g0033 others(1): Show |
6 | HG02109.hp2 HG02145.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1161-459G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12003533 | |||||||
| chr1:12003556 | C | T | 1 | a0001c0001t0002g0095 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1161-436C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12003556 | |||||||
| chr1:12003589 | A | G | 2 | a0001c0001t0001g0054 a0001c0001t0004g0273 |
2 | HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1161-403A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12003589 | |||||||
| chr1:12003664 | C | CA | 45 | a0001c0001t0001g0118 a0001c0001t0001g0141 a0001c0001t0001g0161 others(42): Show |
48 | HG00408.hp1 HG00733.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.1161-312dupA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 12003664 | ||||||
| chr1:12003664 | C | CAA | 6 | a0001c0004t0004g0015 a0001c0004t0004g0256 a0001c0004t0004g0258 others(3): Show |
8 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1161-313_1161-312d others(4): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 12003664 | ||||||
| chr1:12003664 | CA | C | 5 | a0001c0001t0002g0094 a0001c0001t0012g0036 a0001c0001t0012g0291 others(2): Show |
7 | HG01256.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161-312delA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 12003664 | ||||||
| chr1:12003795 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1161-197C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12003795 | |||||||
| chr1:12003922 | T | C | 1 | a0001c0001t0002g0078 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1161-70T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12003922 | |||||||
| chr1:12004160 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1287+42C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 12/18 | chr1 | 12004160 | |||||||
| chr1:12004164 | T | C | 1 | a0001c0001t0004g0189 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1287+46T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 12/18 | chr1 | 12004164 | |||||||
| chr1:12004266 | C | G | 6 | a0001c0004t0004g0015 a0001c0004t0004g0256 a0001c0004t0004g0258 others(3): Show |
8 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1287+148C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 12/18 | chr1 | 12004266 | |||||||
| chr1:12004711 | A | C | 3 | a0001c0001t0016g0084 a0001c0001t0016g0086 a0001c0001t0019g0104 |
3 | HG02698.hp1 HG03710.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1392+98A>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 13/18 | chr1 | 12004711 | |||||||
| chr1:12004760 | G | A | 5 | a0001c0001t0001g0134 a0001c0001t0001g0139 a0001c0001t0001g0142 others(2): Show |
5 | NA18959.hp2 NA19005.hp1 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.1393-65G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 13/18 | chr1 | 12004760 | |||||||
| chr1:12004769 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1393-56G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 13/18 | chr1 | 12004769 | |||||||
| chr1:12004769 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1393-56G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 13/18 | chr1 | 12004769 | |||||||
| chr1:12005113 | A | G | 27 | a0001c0002t0005g0034 a0001c0002t0005g0055 a0001c0002t0005g0087 others(24): Show |
30 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.1495+186A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 14/18 | chr1 | 12005113 | |||||||
| chr1:12005163 | C | A | 1 | a0001c0001t0006g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1495+236C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 14/18 | chr1 | 12005163 | |||||||
| chr1:12005237 | C | T | 5 | a0001c0001t0004g0029 a0001c0001t0004g0186 a0001c0001t0004g0187 others(2): Show |
6 | HG02451.hp2 HG02572.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1495+310C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 14/18 | chr1 | 12005237 | |||||||
| chr1:12005565 | C | T | 1 | a0001c0001t0002g0278 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1496-146C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 14/18 | chr1 | 12005565 | |||||||
| chr1:12005677 | T | C | 3 | a0001c0001t0015g0050 a0001c0001t0015g0051 a0001c0001t0015g0053 |
3 | HG02559.hp1 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1496-34T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 14/18 | chr1 | 12005677 | |||||||
| chr1:12005968 | G | C | 4 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0166 others(1): Show |
4 | HG01243.hp2 HG02615.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1716+37G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 15/18 | chr1 | 12005968 | |||||||
| chr1:12006021 | C | CCT | 18 | a0001c0001t0001g0168 a0001c0001t0004g0014 a0001c0001t0004g0048 others(15): Show |
20 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.1716+91_1716+92dup others(2): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 12006021 | ||||||
| chr1:12006056 | C | T | 18 | a0001c0001t0001g0168 a0001c0001t0004g0014 a0001c0001t0004g0048 others(15): Show |
20 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.1716+125C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 15/18 | chr1 | 12006056 | |||||||
| chr1:12006161 | T | TA | 183 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(180): Show |
223 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.1716+233dupA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 12006161 | ||||||
| chr1:12006215 | T | TACGACTA others(315): Show |
1 | a0001c0008t0004g0257 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1716+295_1716+296i others(324): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 12006215 | ||||||
| chr1:12006215 | T | TACGACTA others(316): Show |
1 | a0001c0004t0004g0258 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1716+295_1716+296i others(325): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 12006215 | ||||||
| chr1:12006215 | T | TACGACTA others(317): Show |
3 | a0001c0004t0004g0015 a0001c0004t0004g0260 a0001c0008t0004g0259 |
5 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1716+295_1716+296i others(326): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 12006215 | ||||||
| chr1:12006215 | T | TACGACTA others(318): Show |
1 | a0001c0004t0004g0256 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1716+295_1716+296i others(327): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 12006215 | ||||||
| chr1:12006267 | A | G | 27 | a0001c0002t0005g0034 a0001c0002t0005g0055 a0001c0002t0005g0087 others(24): Show |
30 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.1717-271A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 15/18 | chr1 | 12006267 | |||||||
| chr1:12006354 | C | T | 1 | a0001c0001t0004g0189 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1717-184C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 15/18 | chr1 | 12006354 | |||||||
| chr1:12006361 | T | C | 13 | a0001c0001t0004g0047 a0001c0001t0006g0037 a0001c0001t0006g0038 others(10): Show |
13 | HG01192.hp2 HG01891.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1717-177T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 15/18 | chr1 | 12006361 | |||||||
| chr1:12006504 | G | A | 1 | a0001c0001t0027g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1717-34G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 15/18 | chr1 | 12006504 | |||||||
| chr1:12006756 | T | C | 22 | a0001c0001t0003g0222 a0001c0001t0003g0227 a0001c0002t0005g0034 others(19): Show |
23 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.1872+63T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 16/18 | chr1 | 12006756 | |||||||
| chr1:12006838 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1872+145C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 16/18 | chr1 | 12006838 | |||||||
| chr1:12006899 | C | G | 7 | a0001c0003t0007g0035 a0001c0003t0007g0269 a0001c0003t0007g0270 others(4): Show |
8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1873-154C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 16/18 | chr1 | 12006899 | |||||||
| chr1:12006987 | T | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(162): Show |
202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1873-66T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 16/18 | chr1 | 12006987 | |||||||
| chr1:12007014 | C | T | 1 | a0001c0001t0003g0194 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1873-39C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 16/18 | chr1 | 12007014 | |||||||
| chr1:12007279 | G | C | 4 | a0001c0001t0012g0036 a0001c0001t0012g0291 a0001c0001t0013g0033 others(1): Show |
6 | HG02109.hp2 HG02145.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2069+30G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12007279 | |||||||
| chr1:12007331 | C | T | 27 | a0001c0002t0005g0034 a0001c0002t0005g0055 a0001c0002t0005g0087 others(24): Show |
30 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.2069+82C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12007331 | |||||||
| chr1:12007441 | C | T | 1 | a0001c0001t0026g0261 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2069+192C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12007441 | |||||||
| chr1:12007448 | G | T | 7 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0064 others(4): Show |
11 | HG01099.hp2 HG01123.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.2069+199G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12007448 | |||||||
| chr1:12007652 | T | G | 27 | a0001c0002t0005g0034 a0001c0002t0005g0055 a0001c0002t0005g0087 others(24): Show |
30 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.2069+403T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12007652 | |||||||
| chr1:12007669 | T | G | 1 | a0001c0002t0005g0245 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2069+420T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12007669 | |||||||
| chr1:12007749 | A | T | 6 | a0001c0001t0004g0285 a0001c0001t0004g0286 a0001c0001t0004g0287 others(3): Show |
6 | HG02630.hp2 HG02895.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.2069+500A>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12007749 | |||||||
| chr1:12007775 | T | C | 10 | a0001c0001t0006g0037 a0001c0001t0006g0038 a0001c0001t0006g0041 others(7): Show |
10 | HG01192.hp2 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.2069+526T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12007775 | |||||||
| chr1:12007778 | T | C | 4 | a0001c0001t0012g0036 a0001c0001t0012g0291 a0001c0001t0013g0033 others(1): Show |
6 | HG02109.hp2 HG02145.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2069+529T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12007778 | |||||||
| chr1:12007837 | A | G | 176 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(173): Show |
215 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.2069+588A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12007837 | |||||||
| chr1:12008081 | C | G | 3 | a0001c0001t0015g0050 a0001c0001t0015g0051 a0001c0001t0015g0053 |
3 | HG02559.hp1 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2069+832C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008081 | |||||||
| chr1:12008185 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2069+936T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008185 | |||||||
| chr1:12008225 | G | A | 6 | a0001c0004t0004g0015 a0001c0004t0004g0256 a0001c0004t0004g0258 others(3): Show |
8 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.2069+976G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008225 | |||||||
| chr1:12008230 | C | T | 3 | a0001c0005t0004g0119 a0001c0005t0004g0283 a0001c0005t0004g0284 |
3 | HG02895.hp2 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2069+981C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008230 | |||||||
| chr1:12008322 | T | C | 34 | a0001c0002t0005g0034 a0001c0002t0005g0055 a0001c0002t0005g0087 others(31): Show |
38 | HG00408.hp1 HG00733.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2069+1073T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008322 | |||||||
| chr1:12008326 | T | C | 1 | a0001c0001t0015g0050 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2069+1077T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008326 | |||||||
| chr1:12008328 | G | A | 2 | a0001c0003t0017g0281 a0001c0003t0017g0282 |
2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2069+1079G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008328 | |||||||
| chr1:12008350 | C | T | 3 | a0001c0001t0003g0203 a0001c0001t0003g0223 a0001c0001t0003g0236 |
3 | HG00735.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2069+1101C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008350 | |||||||
| chr1:12008351 | G | A | 21 | a0001c0002t0005g0034 a0001c0002t0005g0055 a0001c0002t0005g0087 others(18): Show |
22 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.2069+1102G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008351 | |||||||
| chr1:12008367 | G | A | 3 | a0001c0001t0001g0027 a0001c0001t0001g0136 a0001c0001t0001g0146 |
4 | HG01069.hp1 HG01071.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.2069+1118G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008367 | |||||||
| chr1:12008394 | G | A | 172 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(169): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.2069+1145G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008394 | |||||||
| chr1:12008423 | AC | A | 198 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(195): Show |
241 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.2070-1161delC | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 12008423 | ||||||
| chr1:12008424 | CCCCCCCC others(41): Show |
C | 12 | a0001c0001t0004g0047 a0001c0001t0006g0037 a0001c0001t0006g0038 others(9): Show |
12 | HG01192.hp2 HG01891.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.2070-1161_2070-111 others(52): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 12008424 | ||||||
| chr1:12008428 | C | T | 3 | a0001c0001t0003g0213 a0001c0001t0003g0216 a0001c0001t0003g0217 |
3 | NA18970.hp2 NA19011.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.2070-1164C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008428 | |||||||
| chr1:12008446 | C | T | 1 | a0001c0001t0003g0225 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2070-1146C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008446 | |||||||
| chr1:12008454 | C | T | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.2070-1138C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008454 | |||||||
| chr1:12008463 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0276 |
2 | HG02257.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2070-1129C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008463 | |||||||
| chr1:12008468 | A | G | 216 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(213): Show |
261 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2070-1124A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008468 | |||||||
| chr1:12008489 | C | T | 160 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(157): Show |
197 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.2070-1103C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008489 | |||||||
| chr1:12008532 | C | T | 172 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(169): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.2070-1060C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008532 | |||||||
| chr1:12008544 | G | A | 4 | a0001c0001t0012g0036 a0001c0001t0012g0291 a0001c0001t0013g0033 others(1): Show |
6 | HG02109.hp2 HG02145.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2070-1048G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008544 | |||||||
| chr1:12008599 | C | T | 57 | a0001c0001t0001g0228 a0001c0001t0003g0004 a0001c0001t0003g0031 others(54): Show |
65 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.2070-993C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008599 | |||||||
| chr1:12008603 | T | C | 228 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(225): Show |
273 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.2070-989T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008603 | |||||||
| chr1:12008607 | C | T | 6 | a0001c0004t0004g0015 a0001c0004t0004g0256 a0001c0004t0004g0258 others(3): Show |
8 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.2070-985C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008607 | |||||||
| chr1:12008609 | G | A | 1 | a0001c0001t0004g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2070-983G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008609 | |||||||
| chr1:12008635 | TCA | T | 5 | a0001c0001t0004g0029 a0001c0001t0004g0186 a0001c0001t0004g0187 others(2): Show |
6 | HG02451.hp2 HG02572.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2070-954_2070-953d others(4): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 12008635 | ||||||
| chr1:12008684 | T | C | 7 | a0001c0003t0007g0035 a0001c0003t0007g0269 a0001c0003t0007g0270 others(4): Show |
8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2070-908T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008684 | |||||||
| chr1:12008761 | C | T | 1 | a0001c0001t0006g0042 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2070-831C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008761 | |||||||
| chr1:12008769 | G | A | 27 | a0001c0002t0005g0034 a0001c0002t0005g0055 a0001c0002t0005g0087 others(24): Show |
30 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.2070-823G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008769 | |||||||
| chr1:12008795 | T | C | 34 | a0001c0002t0005g0034 a0001c0002t0005g0055 a0001c0002t0005g0087 others(31): Show |
38 | HG00408.hp1 HG00733.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2070-797T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008795 | |||||||
| chr1:12008798 | G | T | 1 | a0001c0001t0001g0218 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2070-794G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008798 | |||||||
| chr1:12008800 | C | CG | 3 | a0001c0001t0002g0021 a0001c0001t0003g0240 a0001c0001t0009g0135 |
4 | NA18969.hp2 NA18981.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.2070-788dupG | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 12008800 | ||||||
| chr1:12008813 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2070-779G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008813 | |||||||
| chr1:12008884 | T | C | 235 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(232): Show |
281 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.2070-708T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008884 | |||||||
| chr1:12008885 | G | A | 7 | a0001c0001t0001g0072 a0001c0004t0004g0015 a0001c0004t0004g0256 others(4): Show |
9 | HG00639.hp1 HG02083.hp2 HG04228.hp2 others(6): Show |
intron_variant | MODIFIER | c.2070-707G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008885 | |||||||
| chr1:12008928 | G | A | 1 | a0001c0001t0003g0238 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2070-664G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008928 | |||||||
| chr1:12008955 | C | G | 1 | a0001c0001t0001g0145 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2070-637C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008955 | |||||||
| chr1:12008964 | G | A | 27 | a0001c0002t0005g0034 a0001c0002t0005g0055 a0001c0002t0005g0087 others(24): Show |
30 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.2070-628G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008964 | |||||||
| chr1:12009004 | C | T | 3 | a0001c0005t0004g0119 a0001c0005t0004g0283 a0001c0005t0004g0284 |
3 | HG02895.hp2 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2070-588C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12009004 | |||||||
| chr1:12009068 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2070-524C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12009068 | |||||||
| chr1:12009073 | G | A | 27 | a0001c0002t0005g0034 a0001c0002t0005g0055 a0001c0002t0005g0087 others(24): Show |
30 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.2070-519G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12009073 | |||||||
| chr1:12009082 | C | T | 1 | a0001c0001t0025g0290 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2070-510C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12009082 | |||||||
| chr1:12009187 | G | A | 1 | a0001c0001t0004g0190 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2070-405G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12009187 | |||||||
| chr1:12009197 | AGGGAGAG others(28): Show |
A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0150 |
2 | HG02165.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.2070-382_2070-348d others(37): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 12009197 | ||||||
| chr1:12009221 | G | A | 1 | a0001c0001t0003g0197 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2070-371G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12009221 | |||||||
| chr1:12009529 | C | T | 7 | a0001c0003t0007g0035 a0001c0003t0007g0269 a0001c0003t0007g0270 others(4): Show |
8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2070-63C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12009529 | |||||||
| chr1:12009547 | C | T | 1 | a0001c0001t0002g0091 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2070-45C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12009547 | |||||||
| chr1:12009741 | T | C | 34 | a0001c0002t0005g0034 a0001c0002t0005g0055 a0001c0002t0005g0087 others(31): Show |
38 | HG00408.hp1 HG00733.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2204+15T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12009741 | |||||||
| chr1:12009805 | C | T | 1 | a0001c0001t0003g0216 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2204+79C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12009805 | |||||||
| chr1:12009844 | A | G | 2 | a0001c0003t0017g0281 a0001c0003t0017g0282 |
2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2204+118A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12009844 | |||||||
| chr1:12010173 | G | T | 1 | a0001c0001t0003g0236 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2204+447G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12010173 | |||||||
| chr1:12010231 | C | T | 3 | a0001c0005t0004g0119 a0001c0005t0004g0283 a0001c0005t0004g0284 |
3 | HG02895.hp2 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2204+505C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12010231 | |||||||
| chr1:12010235 | G | A | 172 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(169): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.2204+509G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12010235 | |||||||
| chr1:12010515 | G | T | 12 | a0001c0001t0001g0168 a0001c0001t0004g0014 a0001c0001t0004g0048 others(9): Show |
14 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.2204+789G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12010515 | |||||||
| chr1:12010855 | G | C | 12 | a0001c0001t0001g0168 a0001c0001t0004g0014 a0001c0001t0004g0048 others(9): Show |
14 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.2205-641G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12010855 | |||||||
| chr1:12010863 | T | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
253 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.2205-633T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12010863 | |||||||
| chr1:12010919 | C | T | 7 | a0001c0003t0007g0035 a0001c0003t0007g0269 a0001c0003t0007g0270 others(4): Show |
8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2205-577C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12010919 | |||||||
| chr1:12011025 | GC | G | 34 | a0001c0002t0005g0034 a0001c0002t0005g0055 a0001c0002t0005g0087 others(31): Show |
38 | HG00408.hp1 HG00733.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2205-463delC | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 12011025 | ||||||
| chr1:12011033 | C | T | 20 | a0001c0002t0005g0034 a0001c0002t0005g0087 a0001c0002t0005g0185 others(17): Show |
21 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.2205-463C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12011033 | |||||||
| chr1:12011035 | C | T | 27 | a0001c0002t0005g0034 a0001c0002t0005g0055 a0001c0002t0005g0087 others(24): Show |
30 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.2205-461C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12011035 | |||||||
| chr1:12011376 | C | G | 70 | a0001c0001t0001g0228 a0001c0001t0003g0004 a0001c0001t0003g0031 others(67): Show |
78 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.2205-120C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12011376 | |||||||
| chr1:12011458 | T | G | 1 | a0001c0001t0021g0179 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2205-38T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12011458 | |||||||
| chr1:12011478 | A | G | 1 | a0001c0001t0021g0179 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2205-18A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12011478 | |||||||
| chr1:12011479 | G | C | 1 | a0001c0001t0021g0179 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2205-17G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12011479 | |||||||
| chr1:12011481 | A | C | 1 | a0001c0001t0021g0179 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2205-15A>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12011481 | |||||||
| chr1:12011482 | C | A | 1 | a0001c0001t0021g0179 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2205-14C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12011482 | |||||||
| chr1:12011483 | C | A | 7 | a0001c0001t0004g0285 a0001c0001t0004g0286 a0001c0001t0004g0287 others(4): Show |
7 | HG02630.hp2 HG02895.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.2205-13C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12011483 |