Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 64087 |
| ensemblid | ENSG00000131844.17 |
| hgncid | 6937 |
| symbol | MCCC2 |
| name | methylcrotonyl-CoA carboxylase subunit 2 |
| refseq_nuc | NM_022132.5 |
| refseq_prot | NP_071415.1 |
| ensembl_nuc | ENST00000340941.11 |
| ensembl_prot | ENSP00000343657.6 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 71587340 |
| end | 71658706 |
| strand | + |
| ver | v1.2 |
| region | chr5:71587340-71658706 |
| region5000 | chr5:71582340-71663706 |
| regionname0 | MCCC2_chr5_71587340_71658706 |
| regionname5000 | MCCC2_chr5_71582340_71663706 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 563 | 346 | 81 | 59 | 156 | 8 | 40 | 116 | MCCC2_chr5_71582340_71663706 | MCCC2 | MWAVL others(558): Show |
chr5 | 71582340 | 71663706 |
| a0002 | 0/0 | 563 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | MWAVL others(558): Show |
chr5 | 71582340 | 71663706 |
| a0003 | 0/0 | 563 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | MWAVL others(558): Show |
chr5 | 71582340 | 71663706 |
| a0004 | 0/0 | 563 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | MWAVL others(558): Show |
chr5 | 71582340 | 71663706 |
| a0005 | 0/0 | 563 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | MWAVL others(558): Show |
chr5 | 71582340 | 71663706 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1689 | 296 | 58 | 48 | 148 | 6 | 35 | MCCC2_chr5_71582340_71663706 | MCCC2 | ATGTG others(1684): Show |
chr5 | 71582340 | 71663706 | ||
| a0001c0002 | 1/0 | 1689 | 43 | 21 | 8 | 7 | 2 | 4 | MCCC2_chr5_71582340_71663706 | MCCC2 | ATGTG others(1684): Show |
chr5 | 71582340 | 71663706 | ||
| a0001c0003 | 0/0 | 1689 | 3 | 2 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | ATGTG others(1684): Show |
chr5 | 71582340 | 71663706 | ||
| a0001c0006 | 0/0 | 1689 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | ATGTG others(1684): Show |
chr5 | 71582340 | 71663706 | ||
| a0001c0007 | 0/0 | 1689 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | ATGTG others(1684): Show |
chr5 | 71582340 | 71663706 | ||
| a0001c0010 | 0/0 | 1689 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | ATGTG others(1684): Show |
chr5 | 71582340 | 71663706 | ||
| a0001c0011 | 0/0 | 1689 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | ATGTG others(1684): Show |
chr5 | 71582340 | 71663706 | ||
| a0002c0005 | 0/0 | 1689 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | ATGTG others(1684): Show |
chr5 | 71582340 | 71663706 | ||
| a0003c0008 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | ATGTG others(1684): Show |
chr5 | 71582340 | 71663706 | ||
| a0004c0004 | 0/0 | 1689 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | ATGTG others(1684): Show |
chr5 | 71582340 | 71663706 | ||
| a0005c0009 | 0/0 | 1689 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | ATGTG others(1684): Show |
chr5 | 71582340 | 71663706 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3624 | 119 | 11 | 22 | 76 | 2 | 8 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0001t0002 | 0/0 | 3624 | 101 | 15 | 16 | 53 | 2 | 15 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0001t0003 | 0/0 | 3624 | 4 | 3 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0001t0004 | 0/0 | 3624 | 44 | 12 | 4 | 14 | 2 | 12 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0001t0005 | 0/0 | 3624 | 5 | 0 | 2 | 3 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0001t0006 | 0/0 | 3624 | 3 | 3 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0001t0007 | 0/0 | 3624 | 2 | 1 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0001t0008 | 0/0 | 3624 | 2 | 2 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0001t0009 | 0/0 | 3624 | 2 | 2 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0001t0010 | 0/0 | 3624 | 2 | 2 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0001t0011 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0001t0012 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0001t0013 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0001t0014 | 0/0 | 3624 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0001t0015 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0001t0017 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0001t0018 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0001t0019 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0001t0020 | 0/0 | 3624 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0001t0021 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0001t0022 | 0/1 | 3624 | 1 | 0 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0001t0023 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0002t0002 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0002t0003 | 1/0 | 3624 | 40 | 19 | 8 | 7 | 2 | 3 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0002t0016 | 0/0 | 3624 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0002t0024 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0003t0003 | 0/0 | 3624 | 3 | 2 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0006t0002 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0007t0002 | 0/0 | 3624 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0010t0004 | 0/0 | 3624 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0001c0011t0004 | 0/0 | 3624 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0002c0005t0002 | 0/0 | 3624 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0003c0008t0006 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0004c0004t0002 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| a0005c0009t0002 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | AGCTT others(3619): Show |
chr5 | 71582340 | 71663706 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0005g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0005g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0005g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0005g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0005g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0006g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0007g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0007g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0008g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0008g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0009g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0009g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0010g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0010g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0011g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0012g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0013g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0014g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0015g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0017g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0018g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0019g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0020g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0021g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0022g0113 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0001t0023g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0053 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0016g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0002t0024g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0003t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0003t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0003t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0006t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0007t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0010t0004g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0001c0011t0004g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0002c0005t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0003c0008t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0004c0004t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| a0005c0009t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0197 | EUR | GBR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00099 | hp2 | a0001 | c0002 | t0003 | g0192 | EUR | GBR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00140 | hp1 | a0001 | c0002 | t0003 | g0057 | EUR | GBR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0075 | EUR | GBR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | FIN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | FIN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00423 | hp1 | a0001 | c0001 | t0023 | g0102 | EAS | CHS | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0327 | EAS | CHS | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | CHS | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0062 | EAS | CHS | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | CHS | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00642 | hp1 | a0001 | c0001 | t0007 | g0195 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00673 | hp1 | a0001 | c0001 | t0005 | g0298 | EAS | CHS | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00733 | hp1 | a0001 | c0001 | t0020 | g0165 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00733 | hp2 | a0001 | c0001 | t0014 | g0255 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0308 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00741 | hp1 | a0001 | c0007 | t0002 | g0191 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0047 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01069 | hp1 | a0001 | c0002 | t0003 | g0024 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0314 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0072 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0073 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0315 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01074 | hp2 | a0001 | c0002 | t0003 | g0041 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0322 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01109 | hp1 | a0001 | c0002 | t0003 | g0035 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01109 | hp2 | a0002 | c0005 | t0002 | g0280 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01167 | hp2 | a0001 | c0003 | t0003 | g0193 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0306 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01192 | hp1 | a0001 | c0002 | t0003 | g0023 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01255 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0320 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0323 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01346 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0307 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01358 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0104 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0247 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0271 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01884 | hp1 | a0001 | c0001 | t0017 | g0012 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01884 | hp2 | a0001 | c0001 | t0018 | g0085 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01978 | hp1 | a0001 | c0010 | t0004 | g0248 | AMR | PEL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01981 | hp2 | a0001 | c0002 | t0003 | g0051 | AMR | PEL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02015 | hp1 | a0001 | c0002 | t0003 | g0232 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02027 | hp1 | a0001 | c0001 | t0012 | g0091 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0249 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0326 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0067 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0328 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0181 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | CDX | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0064 | EAS | CDX | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02257 | hp1 | a0001 | c0001 | t0015 | g0020 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0276 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0252 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0286 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02300 | hp1 | a0001 | c0001 | t0005 | g0275 | AMR | PEL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0211 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0066 | EAS | KHV | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0240 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02602 | hp1 | a0001 | c0002 | t0003 | g0056 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02622 | hp1 | a0001 | c0001 | t0010 | g0336 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02622 | hp2 | a0001 | c0002 | t0003 | g0036 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02647 | hp1 | a0001 | c0002 | t0003 | g0029 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02647 | hp2 | a0001 | c0002 | t0024 | g0027 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02683 | hp1 | a0001 | c0002 | t0003 | g0050 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02698 | hp1 | a0001 | c0002 | t0003 | g0084 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0076 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0205 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02717 | hp2 | a0001 | c0001 | t0021 | g0227 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0312 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0136 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0078 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0277 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02809 | hp1 | a0001 | c0001 | t0013 | g0048 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02809 | hp2 | a0001 | c0002 | t0003 | g0040 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0210 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02886 | hp2 | a0001 | c0002 | t0003 | g0028 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0209 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02895 | hp2 | a0001 | c0001 | t0009 | g0233 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0207 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0239 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0206 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0208 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0234 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02965 | hp2 | a0001 | c0002 | t0003 | g0005 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02970 | hp2 | a0001 | c0002 | t0003 | g0038 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02976 | hp1 | a0001 | c0002 | t0003 | g0037 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0285 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0058 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0241 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03041 | hp2 | a0001 | c0002 | t0003 | g0006 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03098 | hp1 | a0001 | c0001 | t0011 | g0046 | AFR | MSL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03098 | hp2 | a0001 | c0003 | t0003 | g0225 | AFR | MSL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0237 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03130 | hp2 | a0001 | c0002 | t0003 | g0253 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03195 | hp1 | a0001 | c0002 | t0003 | g0031 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0238 | AFR | MSL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03209 | hp2 | a0001 | c0002 | t0003 | g0042 | AFR | MSL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03225 | hp1 | a0001 | c0003 | t0003 | g0219 | AFR | MSL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0272 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0254 | AFR | MSL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03453 | hp2 | a0001 | c0002 | t0003 | g0223 | AFR | MSL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0251 | AFR | MSL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0235 | AFR | MSL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0100 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0077 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0299 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0074 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0194 | AFR | ESN | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03540 | hp1 | a0003 | c0008 | t0006 | g0079 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03540 | hp2 | a0001 | c0001 | t0010 | g0256 | AFR | GWD | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03579 | hp1 | a0001 | c0002 | t0003 | g0030 | AFR | MSL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0279 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0243 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | STU | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0288 | SAS | STU | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0284 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0242 | SAS | PJL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0270 | SAS | BEB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0278 | SAS | BEB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0229 | SAS | BEB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0173 | SAS | BEB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0305 | SAS | BEB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG04199 | hp1 | a0001 | c0002 | t0016 | g0052 | SAS | STU | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0246 | SAS | STU | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0069 | SAS | STU | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | STU | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0274 | SAS | STU | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG04228 | hp2 | a0001 | c0011 | t0004 | g0081 | SAS | STU | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | CHB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18906 | hp1 | a0001 | c0001 | t0019 | g0026 | AFR | YRI | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18906 | hp2 | a0001 | c0002 | t0003 | g0039 | AFR | YRI | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18941 | hp1 | a0001 | c0001 | t0005 | g0309 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18942 | hp1 | a0001 | c0002 | t0003 | g0013 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18945 | hp2 | a0001 | c0002 | t0003 | g0216 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18966 | hp2 | a0001 | c0002 | t0003 | g0054 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18981 | hp1 | a0004 | c0004 | t0002 | g0331 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18982 | hp1 | a0005 | c0009 | t0002 | g0304 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18993 | hp2 | a0001 | c0006 | t0002 | g0273 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19001 | hp1 | a0001 | c0002 | t0003 | g0218 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | LWK | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0283 | AFR | LWK | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19043 | hp1 | a0001 | c0002 | t0003 | g0005 | AFR | LWK | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | LWK | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19068 | hp1 | a0001 | c0001 | t0005 | g0297 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19081 | hp2 | a0001 | c0002 | t0003 | g0055 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19086 | hp1 | a0001 | c0002 | t0003 | g0080 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | ASW | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA20129 | hp2 | a0001 | c0001 | t0008 | g0250 | AFR | ASW | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0214 | EUR | TSI | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0257 | EUR | TSI | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0259 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02486 | hp2 | a0001 | c0002 | t0003 | g0043 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02559 | hp1 | a0001 | c0002 | t0003 | g0032 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | ACB | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | MSL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG03471 | hp2 | a0001 | c0002 | t0003 | g0006 | AFR | MSL | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0245 | AFR | USA | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | USA | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0236 | AFR | USA | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | USA | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | LWK | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| NA21309 | hp2 | a0001 | c0002 | t0003 | g0033 | AFR | LWK | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0022 | g0113 | REF | REF | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0003 | g0053 | REF | REF | MCCC2_chr5_71582340_71663706 | MCCC2 | chr5 | 71582340 | 71663706 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:71596298 | G | A | 1 | a0004 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.215G>A | p.Arg72Gln | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/17 | 301/3624 | 215/1692 | 72/563 | chr5 | 71596298 | |||
| chr5:71604443 | T | A | 1 | a0002 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.599T>A | p.Ile200Asn | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/17 | 685/3624 | 599/1692 | 200/563 | chr5 | 71604443 | |||
| chr5:71634977 | G | T | 1 | a0005 | 1 | NA18982.hp1 | missense_variant | MODERATE | c.838G>T | p.Asp280Tyr | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 9/17 | 924/3624 | 838/1692 | 280/563 | chr5 | 71634977 | |||
| chr5:71650134 | A | G | 1 | a0003 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.1439A>G | p.Asn480Ser | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/17 | 1525/3624 | 1439/1692 | 480/563 | chr5 | 71650134 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:71587515 | G | T | 1 | a0001c0011 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.90G>T | p.Ser30Ser | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/17 | 176/3624 | 90/1692 | 30/563 | chr5 | 71587515 | |||
| chr5:71626744 | A | C | 1 | a0001c0010 | 1 | HG01978.hp1 | synonymous_variant | LOW | c.729A>C | p.Gly243Gly | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/17 | 815/3624 | 729/1692 | 243/563 | chr5 | 71626744 | |||
| chr5:71632135 | T | C | 1 | a0001c0006 | 1 | NA18993.hp2 | synonymous_variant | LOW | c.753T>C | p.Thr251Thr | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/17 | 839/3624 | 753/1692 | 251/563 | chr5 | 71632135 | |||
| chr5:71635216 | T | C | 1 | a0001c0007 | 1 | HG00741.hp1 | synonymous_variant | LOW | c.969T>C | p.Ala323Ala | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/17 | 1055/3624 | 969/1692 | 323/563 | chr5 | 71635216 | |||
| chr5:71649248 | A | G | 9 | a0001c0001 a0001c0006 a0001c0007 others(6): Show |
303 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
synonymous_variant | LOW | c.1368A>G | p.Ala456Ala | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 14/17 | 1454/3624 | 1368/1692 | 456/563 | chr5 | 71649248 | |||
| chr5:71656746 | A | G | 1 | a0001c0003 | 3 | HG01167.hp2 HG03098.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.1578A>G | p.Val526Val | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 1664/3624 | 1578/1692 | 526/563 | chr5 | 71656746 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:71587388 | G | A | 1 | a0001c0001t0011 | 1 | HG03098.hp1 | 5_prime_UTR_variant | MODIFIER | c.-38G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/17 | 38 | chr5 | 71587388 | ||||||
| chr5:71587406 | C | G | 1 | a0001c0001t0010 | 2 | HG02622.hp1 HG03540.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-20C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/17 | chr5 | 71587406 | |||||||
| chr5:71656890 | T | C | 1 | a0001c0001t0012 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*30T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 30 | chr5 | 71656890 | ||||||
| chr5:71657038 | T | C | 1 | a0001c0001t0013 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*178T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 178 | chr5 | 71657038 | ||||||
| chr5:71657051 | A | T | 1 | a0001c0002t0024 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*191A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 191 | chr5 | 71657051 | ||||||
| chr5:71657064 | T | C | 1 | a0001c0001t0014 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*204T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 204 | chr5 | 71657064 | ||||||
| chr5:71657105 | T | C | 2 | a0001c0001t0007 a0001c0001t0015 |
3 | HG00642.hp1 HG02257.hp1 HG02258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*245T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 245 | chr5 | 71657105 | ||||||
| chr5:71657107 | C | T | 20 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(17): Show |
286 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
3_prime_UTR_variant | MODIFIER | c.*247C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 247 | chr5 | 71657107 | ||||||
| chr5:71657210 | C | G | 1 | a0001c0001t0009 | 2 | HG02895.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*350C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 350 | chr5 | 71657210 | ||||||
| chr5:71657238 | T | A | 1 | a0001c0002t0016 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*378T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 378 | chr5 | 71657238 | ||||||
| chr5:71657287 | G | A | 1 | a0001c0001t0017 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*427G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 427 | chr5 | 71657287 | ||||||
| chr5:71657386 | C | T | 1 | a0001c0001t0015 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*526C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 526 | chr5 | 71657386 | ||||||
| chr5:71657437 | T | A | 2 | a0001c0001t0019 a0001c0001t0020 |
2 | HG00733.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*577T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 577 | chr5 | 71657437 | ||||||
| chr5:71657453 | G | T | 3 | a0001c0001t0004 a0001c0010t0004 a0001c0011t0004 |
46 | HG00140.hp2 HG00597.hp2 HG01070.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*593G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 593 | chr5 | 71657453 | ||||||
| chr5:71657585 | C | T | 1 | a0001c0001t0023 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*725C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 725 | chr5 | 71657585 | ||||||
| chr5:71657940 | G | T | 2 | a0001c0001t0007 a0001c0001t0015 |
3 | HG00642.hp1 HG02257.hp1 HG02258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1080G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 1080 | chr5 | 71657940 | ||||||
| chr5:71658058 | C | T | 4 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0020 others(1): Show |
122 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*1198C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 1198 | chr5 | 71658058 | ||||||
| chr5:71658103 | G | C | 24 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(21): Show |
292 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
3_prime_UTR_variant | MODIFIER | c.*1243G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 1243 | chr5 | 71658103 | ||||||
| chr5:71658207 | C | T | 1 | a0001c0001t0008 | 2 | HG03486.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1347C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 1347 | chr5 | 71658207 | ||||||
| chr5:71658241 | A | C | 3 | a0001c0001t0006 a0001c0001t0017 a0003c0008t0006 |
5 | HG01884.hp1 HG02559.hp2 HG02896.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1381A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 1381 | chr5 | 71658241 | ||||||
| chr5:71658326 | T | C | 1 | a0001c0001t0005 | 5 | HG00673.hp1 HG01496.hp2 HG02300.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1466T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 1466 | chr5 | 71658326 | ||||||
| chr5:71658433 | C | G | 5 | a0001c0001t0006 a0001c0001t0014 a0001c0001t0017 others(2): Show |
7 | HG00733.hp2 HG01884.hp1 HG01884.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1573C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 1573 | chr5 | 71658433 | ||||||
| chr5:71658564 | G | A | 1 | a0001c0001t0014 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1704G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 1704 | chr5 | 71658564 | ||||||
| chr5:71658664 | A | G | 1 | a0001c0001t0021 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1804A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 17/17 | 1804 | chr5 | 71658664 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:71587938 | A | G | 1 | a0001c0001t0010g0336 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.129+384A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71587938 | |||||||
| chr5:71588078 | G | T | 9 | a0001c0001t0002g0004 a0001c0001t0002g0328 a0001c0001t0002g0329 others(6): Show |
11 | HG02056.hp2 NA18950.hp2 NA18963.hp2 others(8): Show |
intron_variant | MODIFIER | c.129+524G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71588078 | |||||||
| chr5:71588138 | G | A | 1 | a0001c0001t0002g0011 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.129+584G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71588138 | |||||||
| chr5:71588172 | G | A | 1 | a0001c0001t0017g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.129+618G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71588172 | |||||||
| chr5:71588229 | A | G | 1 | a0001c0001t0017g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.129+675A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71588229 | |||||||
| chr5:71588268 | C | CA | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(4): Show |
7 | HG02109.hp1 HG04204.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.129+734dupA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr5 | 71588268 | ||||||
| chr5:71588268 | CA | C | 137 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(134): Show |
143 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.129+734delA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr5 | 71588268 | ||||||
| chr5:71588419 | C | A | 1 | a0001c0001t0004g0205 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.129+865C>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71588419 | |||||||
| chr5:71588487 | A | G | 3 | a0001c0001t0002g0325 a0001c0001t0002g0326 a0001c0001t0002g0327 |
3 | HG00438.hp2 HG02040.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.129+933A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71588487 | |||||||
| chr5:71588547 | C | T | 140 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(137): Show |
146 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.129+993C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71588547 | |||||||
| chr5:71588670 | T | C | 1 | a0001c0001t0015g0020 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.129+1116T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71588670 | |||||||
| chr5:71588675 | A | T | 92 | a0001c0001t0001g0260 a0001c0001t0001g0295 a0001c0001t0001g0296 others(89): Show |
97 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.129+1121A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71588675 | |||||||
| chr5:71588735 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.129+1181G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71588735 | |||||||
| chr5:71588860 | G | C | 132 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(129): Show |
138 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.129+1306G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71588860 | |||||||
| chr5:71589020 | A | G | 2 | a0001c0002t0003g0002 a0001c0002t0003g0192 |
4 | HG00099.hp2 HG01255.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+1466A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71589020 | |||||||
| chr5:71589208 | T | G | 140 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(137): Show |
146 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.129+1654T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71589208 | |||||||
| chr5:71589421 | C | T | 1 | a0001c0001t0017g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.129+1867C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71589421 | |||||||
| chr5:71589566 | A | C | 1 | a0001c0007t0002g0191 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.129+2012A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71589566 | |||||||
| chr5:71589585 | T | C | 123 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(120): Show |
129 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.129+2031T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71589585 | |||||||
| chr5:71589711 | T | C | 133 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(130): Show |
139 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.129+2157T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71589711 | |||||||
| chr5:71589776 | T | C | 1 | a0001c0007t0002g0191 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.129+2222T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71589776 | |||||||
| chr5:71589791 | A | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(114): Show |
121 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.129+2237A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71589791 | |||||||
| chr5:71590096 | C | A | 1 | a0001c0002t0003g0253 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.129+2542C>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71590096 | |||||||
| chr5:71590097 | G | T | 1 | a0001c0001t0017g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.129+2543G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71590097 | |||||||
| chr5:71590109 | A | AAC | 10 | a0001c0001t0002g0240 a0001c0001t0004g0194 a0001c0001t0004g0205 others(7): Show |
10 | HG01884.hp2 HG02572.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.129+2575_129+2576d others(4): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr5 | 71590109 | ||||||
| chr5:71590109 | AAC | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(129): Show |
136 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.129+2575_129+2576d others(4): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr5 | 71590109 | ||||||
| chr5:71590146 | C | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(240): Show |
253 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.129+2592C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71590146 | |||||||
| chr5:71590312 | T | A | 122 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(119): Show |
128 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.130-2614T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71590312 | |||||||
| chr5:71590553 | A | C | 1 | a0001c0001t0009g0234 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.130-2373A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71590553 | |||||||
| chr5:71590554 | G | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(255): Show |
268 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.130-2372G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71590554 | |||||||
| chr5:71590809 | T | G | 1 | a0001c0001t0017g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.130-2117T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71590809 | |||||||
| chr5:71590816 | C | CA | 118 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(115): Show |
124 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.130-2096dupA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr5 | 71590816 | ||||||
| chr5:71591105 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.130-1821A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71591105 | |||||||
| chr5:71591363 | A | C | 1 | a0001c0001t0007g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130-1563A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71591363 | |||||||
| chr5:71591434 | GT | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(239): Show |
252 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.130-1473delT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr5 | 71591434 | ||||||
| chr5:71591464 | T | G | 1 | a0001c0001t0015g0020 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.130-1462T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71591464 | |||||||
| chr5:71591626 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.130-1300G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71591626 | |||||||
| chr5:71591628 | G | A | 3 | a0001c0001t0001g0217 a0001c0002t0003g0216 a0001c0002t0003g0218 |
3 | NA18747.hp2 NA18945.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.130-1298G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71591628 | |||||||
| chr5:71591633 | C | G | 4 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
4 | HG00673.hp2 NA18986.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-1293C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71591633 | |||||||
| chr5:71591662 | C | T | 4 | a0001c0001t0007g0195 a0001c0001t0010g0256 a0001c0001t0010g0336 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-1264C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71591662 | |||||||
| chr5:71591668 | C | T | 2 | a0001c0002t0003g0084 a0001c0002t0003g0253 |
2 | HG02698.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.130-1258C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71591668 | |||||||
| chr5:71591732 | T | C | 259 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(256): Show |
269 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.130-1194T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71591732 | |||||||
| chr5:71591734 | G | A | 1 | a0001c0002t0003g0023 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.130-1192G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71591734 | |||||||
| chr5:71592020 | C | T | 2 | a0001c0001t0008g0250 a0001c0001t0008g0251 |
2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.130-906C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71592020 | |||||||
| chr5:71592296 | G | A | 5 | a0001c0001t0007g0195 a0001c0001t0010g0256 a0001c0001t0010g0336 others(2): Show |
5 | HG00642.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.130-630G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71592296 | |||||||
| chr5:71592397 | A | G | 1 | a0001c0001t0002g0204 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.130-529A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71592397 | |||||||
| chr5:71592415 | A | G | 259 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(256): Show |
269 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.130-511A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71592415 | |||||||
| chr5:71592838 | G | GT | 26 | a0001c0001t0001g0018 a0001c0001t0001g0175 a0001c0001t0001g0176 others(23): Show |
26 | HG00544.hp2 HG00735.hp2 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.130-72dupT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr5 | 71592838 | ||||||
| chr5:71592847 | T | C | 1 | a0001c0001t0007g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130-79T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 1/16 | chr5 | 71592847 | |||||||
| chr5:71593069 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.196+77A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71593069 | |||||||
| chr5:71593081 | C | T | 2 | a0001c0001t0008g0250 a0001c0001t0008g0251 |
2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.196+89C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71593081 | |||||||
| chr5:71593086 | G | GAT | 4 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0180 others(1): Show |
4 | HG00544.hp2 HG02071.hp1 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+97_196+98dupAT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr5 | 71593086 | ||||||
| chr5:71593090 | T | TA | 114 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): Show |
118 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.196+98_196+99insA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71593090 | |||||||
| chr5:71593091 | T | A | 2 | a0001c0001t0007g0252 a0001c0002t0003g0024 |
2 | HG01069.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.196+99T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71593091 | |||||||
| chr5:71593092 | T | A | 2 | a0001c0001t0002g0022 a0001c0001t0015g0020 |
2 | HG01243.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.196+100T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71593092 | |||||||
| chr5:71593094 | T | A | 1 | a0001c0001t0002g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.196+102T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71593094 | |||||||
| chr5:71593096 | T | A | 1 | a0001c0001t0002g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.196+104T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71593096 | |||||||
| chr5:71593298 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.196+306C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71593298 | |||||||
| chr5:71593495 | G | A | 1 | a0001c0001t0015g0020 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.196+503G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71593495 | |||||||
| chr5:71593500 | GA | G | 2 | a0001c0002t0003g0002 a0001c0002t0003g0192 |
4 | HG00099.hp2 HG01255.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+512delA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr5 | 71593500 | ||||||
| chr5:71593585 | C | T | 4 | a0001c0001t0001g0313 a0001c0001t0001g0316 a0001c0001t0002g0314 others(1): Show |
4 | HG01070.hp1 HG01074.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+593C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71593585 | |||||||
| chr5:71593790 | A | G | 10 | a0001c0001t0004g0242 a0001c0001t0004g0243 a0001c0001t0004g0244 others(7): Show |
10 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.196+798A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71593790 | |||||||
| chr5:71593960 | C | T | 4 | a0001c0001t0007g0195 a0001c0001t0010g0256 a0001c0001t0010g0336 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+968C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71593960 | |||||||
| chr5:71594043 | G | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(243): Show |
256 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.196+1051G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71594043 | |||||||
| chr5:71594178 | A | T | 4 | a0001c0001t0003g0211 a0001c0001t0004g0208 a0001c0001t0004g0209 others(1): Show |
4 | HG02451.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+1186A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71594178 | |||||||
| chr5:71594522 | C | T | 1 | a0001c0001t0017g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.196+1530C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71594522 | |||||||
| chr5:71594527 | C | CA | 242 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(239): Show |
252 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.196+1551dupA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr5 | 71594527 | ||||||
| chr5:71594565 | A | C | 10 | a0001c0001t0004g0242 a0001c0001t0004g0243 a0001c0001t0004g0244 others(7): Show |
10 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.196+1573A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71594565 | |||||||
| chr5:71594569 | T | G | 270 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(267): Show |
280 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.196+1577T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71594569 | |||||||
| chr5:71594586 | A | G | 1 | a0001c0001t0002g0229 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.196+1594A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71594586 | |||||||
| chr5:71594624 | G | A | 10 | a0001c0001t0004g0242 a0001c0001t0004g0243 a0001c0001t0004g0244 others(7): Show |
10 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.196+1632G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71594624 | |||||||
| chr5:71594625 | T | C | 1 | a0001c0001t0017g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.196+1633T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71594625 | |||||||
| chr5:71594897 | TC | T | 244 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(241): Show |
254 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.197-1382delC | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71594897 | |||||||
| chr5:71594898 | C | CT | 9 | a0001c0001t0004g0242 a0001c0001t0004g0243 a0001c0001t0004g0244 others(6): Show |
9 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.197-1367dupT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr5 | 71594898 | ||||||
| chr5:71594898 | C | T | 2 | a0001c0001t0007g0195 a0001c0001t0007g0252 |
2 | HG00642.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.197-1382C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71594898 | |||||||
| chr5:71594939 | C | T | 4 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0213 others(1): Show |
4 | HG00733.hp1 HG01099.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-1341C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71594939 | |||||||
| chr5:71594961 | C | T | 1 | a0001c0001t0007g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.197-1319C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71594961 | |||||||
| chr5:71594985 | G | GC | 246 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(243): Show |
256 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.197-1289dupC | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr5 | 71594985 | ||||||
| chr5:71595072 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(258): Show |
271 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.197-1208A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71595072 | |||||||
| chr5:71595106 | T | C | 2 | a0001c0001t0001g0087 a0001c0001t0001g0088 |
2 | NA18993.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.197-1174T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71595106 | |||||||
| chr5:71595428 | C | CA | 44 | a0001c0001t0001g0217 a0001c0001t0002g0009 a0001c0001t0002g0022 others(41): Show |
45 | HG00642.hp1 HG00738.hp2 HG01167.hp2 others(42): Show |
intron_variant | MODIFIER | c.197-834dupA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr5 | 71595428 | ||||||
| chr5:71595428 | C | CAA | 94 | a0001c0001t0001g0019 a0001c0001t0001g0159 a0001c0001t0001g0160 others(91): Show |
99 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.197-835_197-834dup others(2): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr5 | 71595428 | ||||||
| chr5:71595428 | C | CAAA | 105 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(102): Show |
109 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.197-836_197-834dup others(3): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr5 | 71595428 | ||||||
| chr5:71595428 | C | CAAAA | 6 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0175 others(3): Show |
6 | HG02027.hp1 HG03927.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-837_197-834dup others(4): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr5 | 71595428 | ||||||
| chr5:71595856 | C | G | 7 | a0001c0001t0004g0072 a0001c0001t0004g0073 a0001c0001t0004g0074 others(4): Show |
7 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.197-424C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71595856 | |||||||
| chr5:71595913 | A | T | 10 | a0001c0001t0004g0242 a0001c0001t0004g0243 a0001c0001t0004g0244 others(7): Show |
10 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.197-367A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | chr5 | 71595913 | |||||||
| chr5:71596079 | A | AT | 112 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(109): Show |
116 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.197-192dupT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr5 | 71596079 | ||||||
| chr5:71596200 | GATTAAGT | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): Show |
118 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.197-75_197-69delAG others(5): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr5 | 71596200 | ||||||
| chr5:71596659 | T | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(245): Show |
258 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.281+295T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71596659 | |||||||
| chr5:71596664 | G | C | 1 | a0001c0001t0002g0003 | 3 | HG00280.hp2 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.281+300G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71596664 | |||||||
| chr5:71596811 | G | A | 1 | a0001c0002t0024g0027 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.281+447G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71596811 | |||||||
| chr5:71596896 | T | C | 1 | a0001c0001t0007g0195 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.281+532T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71596896 | |||||||
| chr5:71596939 | C | A | 1 | a0001c0002t0003g0253 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.281+575C>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71596939 | |||||||
| chr5:71596939 | CA | C | 29 | a0001c0001t0001g0070 a0001c0001t0002g0060 a0001c0001t0002g0061 others(26): Show |
29 | HG00140.hp2 HG00597.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.281+587delA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr5 | 71596939 | ||||||
| chr5:71596981 | T | C | 1 | a0001c0002t0003g0035 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281+617T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71596981 | |||||||
| chr5:71597036 | T | C | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.281+672T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71597036 | |||||||
| chr5:71597228 | T | C | 1 | a0001c0002t0003g0036 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.281+864T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71597228 | |||||||
| chr5:71597385 | A | C | 1 | a0001c0001t0007g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.281+1021A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71597385 | |||||||
| chr5:71597511 | G | C | 2 | a0001c0001t0001g0260 a0001c0001t0002g0259 |
2 | HG01123.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.281+1147G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71597511 | |||||||
| chr5:71597524 | C | CATAGGGT others(40): Show |
1 | a0001c0011t0004g0081 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.281+1163_281+1209d others(49): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr5 | 71597524 | ||||||
| chr5:71597529 | GGTA | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(242): Show |
255 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.281+1174_281+1176d others(5): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr5 | 71597529 | ||||||
| chr5:71597635 | A | G | 1 | a0001c0001t0017g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.281+1271A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71597635 | |||||||
| chr5:71597932 | C | T | 1 | a0001c0002t0003g0033 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.281+1568C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71597932 | |||||||
| chr5:71598071 | C | CT | 17 | a0001c0001t0001g0070 a0001c0001t0001g0182 a0001c0001t0001g0217 others(14): Show |
17 | HG00140.hp1 HG00642.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.282-1568dupT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr5 | 71598071 | ||||||
| chr5:71598079 | T | C | 2 | a0001c0001t0001g0313 a0001c0001t0001g0316 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.282-1580T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71598079 | |||||||
| chr5:71598136 | G | A | 1 | a0001c0001t0017g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.282-1523G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71598136 | |||||||
| chr5:71598180 | T | C | 4 | a0001c0001t0001g0313 a0001c0001t0001g0316 a0001c0001t0002g0314 others(1): Show |
4 | HG01070.hp1 HG01074.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.282-1479T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71598180 | |||||||
| chr5:71598337 | G | A | 1 | a0001c0007t0002g0191 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.282-1322G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71598337 | |||||||
| chr5:71598368 | G | A | 1 | a0001c0003t0003g0219 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.282-1291G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71598368 | |||||||
| chr5:71598378 | T | A | 1 | a0001c0001t0015g0020 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.282-1281T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71598378 | |||||||
| chr5:71598417 | A | G | 1 | a0001c0001t0020g0165 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.282-1242A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71598417 | |||||||
| chr5:71598444 | A | T | 23 | a0001c0001t0003g0211 a0001c0001t0004g0208 a0001c0001t0004g0209 others(20): Show |
23 | HG00642.hp1 HG00741.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.282-1215A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71598444 | |||||||
| chr5:71598448 | T | A | 91 | a0001c0001t0001g0260 a0001c0001t0001g0295 a0001c0001t0001g0296 others(88): Show |
96 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.282-1211T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71598448 | |||||||
| chr5:71598464 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.282-1195G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71598464 | |||||||
| chr5:71598474 | C | G | 5 | a0001c0001t0001g0162 a0001c0001t0001g0182 a0001c0001t0001g0183 others(2): Show |
5 | HG00673.hp2 NA18971.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.282-1185C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71598474 | |||||||
| chr5:71598533 | G | A | 1 | a0001c0001t0002g0261 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.282-1126G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71598533 | |||||||
| chr5:71598606 | A | AT | 12 | a0001c0001t0001g0316 a0001c0001t0002g0201 a0001c0001t0002g0204 others(9): Show |
12 | HG00621.hp2 HG01168.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.282-1032dupT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr5 | 71598606 | ||||||
| chr5:71598606 | AT | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(129): Show |
136 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.282-1032delT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr5 | 71598606 | ||||||
| chr5:71598606 | ATT | A | 7 | a0001c0001t0001g0093 a0001c0001t0001g0185 a0001c0001t0004g0208 others(4): Show |
7 | HG00741.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.282-1033_282-1032d others(4): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr5 | 71598606 | ||||||
| chr5:71598606 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0007g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.282-1041_282-1032d others(12): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr5 | 71598606 | ||||||
| chr5:71598910 | C | G | 1 | a0001c0002t0003g0056 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.282-749C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71598910 | |||||||
| chr5:71598926 | A | AT | 115 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
119 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.282-720dupT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr5 | 71598926 | ||||||
| chr5:71598958 | C | T | 1 | a0001c0001t0017g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.282-701C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71598958 | |||||||
| chr5:71599133 | C | T | 120 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(117): Show |
126 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.282-526C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71599133 | |||||||
| chr5:71599136 | G | A | 5 | a0001c0001t0002g0265 a0001c0001t0002g0267 a0001c0001t0002g0268 others(2): Show |
5 | HG02155.hp1 NA18989.hp1 NA19067.hp1 others(2): Show |
intron_variant | MODIFIER | c.282-523G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71599136 | |||||||
| chr5:71599146 | T | C | 4 | a0001c0001t0001g0217 a0001c0002t0003g0216 a0001c0002t0003g0218 others(1): Show |
4 | HG02015.hp1 NA18747.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.282-513T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71599146 | |||||||
| chr5:71599238 | C | T | 9 | a0001c0001t0003g0211 a0001c0001t0004g0208 a0001c0001t0004g0209 others(6): Show |
9 | HG01884.hp2 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.282-421C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71599238 | |||||||
| chr5:71599300 | G | C | 3 | a0001c0001t0001g0164 a0001c0001t0001g0213 a0001c0001t0020g0165 |
3 | HG00733.hp1 HG01261.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.282-359G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71599300 | |||||||
| chr5:71599325 | G | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(114): Show |
121 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.282-334G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71599325 | |||||||
| chr5:71599436 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.282-223C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71599436 | |||||||
| chr5:71599451 | T | C | 1 | a0001c0001t0002g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.282-208T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71599451 | |||||||
| chr5:71599601 | G | A | 1 | a0001c0001t0007g0195 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.282-58G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 3/16 | chr5 | 71599601 | |||||||
| chr5:71599901 | C | T | 1 | a0001c0001t0002g0327 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.383+141C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71599901 | |||||||
| chr5:71600022 | C | T | 3 | a0001c0001t0002g0226 a0001c0001t0017g0012 a0001c0001t0021g0227 |
3 | HG01884.hp1 HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.383+262C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71600022 | |||||||
| chr5:71600077 | A | T | 2 | a0001c0001t0002g0226 a0001c0001t0021g0227 |
2 | HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.383+317A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71600077 | |||||||
| chr5:71600079 | C | T | 1 | a0001c0001t0004g0210 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.383+319C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71600079 | |||||||
| chr5:71600158 | C | T | 1 | a0001c0001t0007g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.383+398C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71600158 | |||||||
| chr5:71600196 | G | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0176 |
2 | HG03927.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.383+436G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71600196 | |||||||
| chr5:71600301 | T | C | 321 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(318): Show |
333 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.383+541T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71600301 | |||||||
| chr5:71600399 | C | T | 2 | a0001c0001t0014g0255 a0001c0002t0002g0254 |
2 | HG00733.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.383+639C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71600399 | |||||||
| chr5:71600564 | C | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(242): Show |
255 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.383+804C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71600564 | |||||||
| chr5:71600749 | T | A | 1 | a0001c0001t0004g0058 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.383+989T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71600749 | |||||||
| chr5:71601126 | A | C | 1 | a0001c0001t0015g0020 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.383+1366A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71601126 | |||||||
| chr5:71601228 | C | T | 2 | a0001c0001t0009g0233 a0001c0001t0009g0234 |
2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.384-1278C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71601228 | |||||||
| chr5:71601426 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0150 others(5): Show |
8 | HG02040.hp2 HG02080.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.384-1080C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71601426 | |||||||
| chr5:71601574 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.384-932C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71601574 | |||||||
| chr5:71601624 | G | T | 112 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(109): Show |
118 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.384-882G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71601624 | |||||||
| chr5:71601733 | T | C | 2 | a0001c0001t0007g0195 a0001c0001t0017g0012 |
2 | HG00642.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.384-773T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71601733 | |||||||
| chr5:71601844 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0150 a0001c0001t0001g0151 |
3 | HG02080.hp1 NA18939.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.384-662G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71601844 | |||||||
| chr5:71602129 | G | A | 1 | a0001c0001t0007g0195 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.384-377G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71602129 | |||||||
| chr5:71602217 | A | G | 2 | a0001c0001t0002g0300 a0001c0001t0002g0301 |
2 | NA18992.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.384-289A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71602217 | |||||||
| chr5:71602426 | T | C | 1 | a0001c0001t0002g0269 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.384-80T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71602426 | |||||||
| chr5:71602463 | A | G | 4 | a0001c0001t0006g0025 a0001c0001t0006g0206 a0001c0001t0006g0207 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.384-43A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 4/16 | chr5 | 71602463 | |||||||
| chr5:71602837 | A | G | 1 | a0001c0001t0002g0322 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.511+204A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71602837 | |||||||
| chr5:71602839 | A | G | 1 | a0001c0001t0007g0195 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.511+206A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71602839 | |||||||
| chr5:71602848 | C | T | 4 | a0001c0001t0004g0245 a0001c0001t0004g0246 a0001c0001t0004g0247 others(1): Show |
4 | HG01433.hp2 HG01978.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.511+215C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71602848 | |||||||
| chr5:71603040 | T | G | 2 | a0001c0001t0007g0195 a0001c0001t0017g0012 |
2 | HG00642.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.511+407T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71603040 | |||||||
| chr5:71603150 | C | T | 1 | a0001c0001t0002g0230 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.511+517C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71603150 | |||||||
| chr5:71603287 | G | A | 1 | a0001c0001t0017g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.511+654G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71603287 | |||||||
| chr5:71603407 | G | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(140): Show |
147 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.511+774G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71603407 | |||||||
| chr5:71603411 | G | T | 1 | a0001c0001t0007g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.511+778G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71603411 | |||||||
| chr5:71603415 | CA | C | 132 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0096 others(129): Show |
140 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.511+806delA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr5 | 71603415 | ||||||
| chr5:71603415 | CAA | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0016 others(126): Show |
132 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.511+805_511+806del others(2): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr5 | 71603415 | ||||||
| chr5:71603469 | A | G | 303 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(300): Show |
313 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.511+836A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71603469 | |||||||
| chr5:71603485 | C | T | 5 | a0001c0001t0002g0009 a0001c0001t0002g0224 a0001c0003t0003g0193 others(2): Show |
6 | HG01167.hp2 HG02976.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.511+852C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71603485 | |||||||
| chr5:71603692 | C | G | 1 | a0001c0002t0003g0035 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.512-664C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71603692 | |||||||
| chr5:71603811 | G | T | 2 | a0001c0001t0010g0256 a0001c0001t0010g0336 |
2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.512-545G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71603811 | |||||||
| chr5:71603854 | C | G | 1 | a0001c0001t0001g0317 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.512-502C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71603854 | |||||||
| chr5:71604109 | G | A | 1 | a0001c0001t0003g0211 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.512-247G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71604109 | |||||||
| chr5:71604165 | T | A | 2 | a0001c0001t0014g0255 a0001c0002t0002g0254 |
2 | HG00733.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.512-191T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71604165 | |||||||
| chr5:71604242 | G | A | 11 | a0001c0001t0003g0211 a0001c0001t0004g0208 a0001c0001t0004g0209 others(8): Show |
11 | HG00741.hp1 HG01884.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.512-114G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 5/16 | chr5 | 71604242 | |||||||
| chr5:71604525 | G | T | 9 | a0001c0001t0003g0211 a0001c0001t0004g0208 a0001c0001t0004g0209 others(6): Show |
9 | HG01884.hp2 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.624+57G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71604525 | |||||||
| chr5:71604582 | C | CT | 121 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
125 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.624+128dupT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71604582 | ||||||
| chr5:71604582 | CT | C | 14 | a0001c0001t0001g0070 a0001c0001t0001g0212 a0001c0001t0002g0060 others(11): Show |
14 | HG01070.hp2 HG01123.hp2 HG04204.hp1 others(11): Show |
intron_variant | MODIFIER | c.624+128delT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71604582 | ||||||
| chr5:71604730 | G | A | 1 | a0001c0001t0007g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.624+262G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71604730 | |||||||
| chr5:71604734 | C | T | 1 | a0003c0008t0006g0079 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.624+266C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71604734 | |||||||
| chr5:71604752 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.624+284C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71604752 | |||||||
| chr5:71604910 | C | T | 1 | a0001c0007t0002g0191 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.624+442C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71604910 | |||||||
| chr5:71605030 | C | T | 2 | a0001c0001t0010g0256 a0001c0001t0010g0336 |
2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.624+562C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605030 | |||||||
| chr5:71605031 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.624+563G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605031 | |||||||
| chr5:71605043 | C | T | 2 | a0001c0001t0009g0233 a0001c0001t0009g0234 |
2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.624+575C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605043 | |||||||
| chr5:71605052 | GT | G | 125 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(122): Show |
131 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.624+585delT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605052 | |||||||
| chr5:71605112 | A | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(248): Show |
261 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.624+644A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605112 | |||||||
| chr5:71605166 | G | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(254): Show |
267 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.624+698G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605166 | |||||||
| chr5:71605235 | C | A | 1 | a0001c0001t0007g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.624+767C>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605235 | |||||||
| chr5:71605426 | G | T | 1 | a0001c0001t0002g0228 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.624+958G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605426 | |||||||
| chr5:71605520 | T | C | 2 | a0001c0001t0001g0101 a0001c0001t0023g0102 |
2 | HG00423.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.624+1052T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605520 | |||||||
| chr5:71605536 | C | G | 1 | a0001c0001t0001g0147 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.624+1068C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605536 | |||||||
| chr5:71605580 | T | G | 1 | a0001c0002t0003g0013 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.624+1112T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605580 | |||||||
| chr5:71605634 | C | T | 292 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(289): Show |
302 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.624+1166C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605634 | |||||||
| chr5:71605653 | C | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(116): Show |
123 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.624+1185C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605653 | |||||||
| chr5:71605662 | G | C | 8 | a0001c0001t0004g0194 a0001c0001t0004g0205 a0001c0001t0004g0235 others(5): Show |
8 | HG02717.hp1 HG02896.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.624+1194G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605662 | |||||||
| chr5:71605930 | C | T | 1 | a0001c0001t0019g0026 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.624+1462C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71605930 | |||||||
| chr5:71606050 | C | T | 4 | a0001c0001t0001g0095 a0001c0001t0001g0146 a0001c0001t0001g0166 others(1): Show |
4 | HG03927.hp2 NA18612.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+1582C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71606050 | |||||||
| chr5:71606068 | G | C | 1 | a0001c0010t0004g0248 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.624+1600G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71606068 | |||||||
| chr5:71606129 | G | T | 244 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(241): Show |
254 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.624+1661G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71606129 | |||||||
| chr5:71606189 | G | C | 1 | a0001c0001t0004g0266 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.624+1721G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71606189 | |||||||
| chr5:71606654 | A | T | 1 | a0001c0001t0004g0069 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.624+2186A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71606654 | |||||||
| chr5:71606759 | T | C | 1 | a0001c0001t0001g0103 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.624+2291T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71606759 | |||||||
| chr5:71606760 | A | C | 1 | a0001c0002t0003g0223 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.624+2292A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71606760 | |||||||
| chr5:71606761 | A | G | 1 | a0001c0001t0001g0103 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.624+2293A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71606761 | |||||||
| chr5:71606840 | G | A | 11 | a0001c0001t0003g0211 a0001c0001t0004g0208 a0001c0001t0004g0209 others(8): Show |
11 | HG00741.hp1 HG01884.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+2372G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71606840 | |||||||
| chr5:71606904 | C | G | 1 | a0001c0002t0003g0253 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.624+2436C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71606904 | |||||||
| chr5:71607059 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.624+2591C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607059 | |||||||
| chr5:71607091 | A | C | 2 | a0001c0001t0010g0256 a0001c0001t0010g0336 |
2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.624+2623A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607091 | |||||||
| chr5:71607092 | A | C | 2 | a0001c0001t0010g0256 a0001c0001t0010g0336 |
2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.624+2624A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607092 | |||||||
| chr5:71607125 | T | C | 2 | a0001c0001t0004g0245 a0001c0001t0004g0246 |
2 | HG04199.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.624+2657T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607125 | |||||||
| chr5:71607131 | G | A | 6 | a0001c0001t0002g0010 a0001c0001t0002g0272 a0001c0001t0002g0274 others(3): Show |
7 | HG01346.hp1 HG03239.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.624+2663G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607131 | |||||||
| chr5:71607163 | T | C | 2 | a0001c0001t0002g0220 a0001c0001t0002g0228 |
2 | HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.624+2695T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607163 | |||||||
| chr5:71607277 | A | T | 1 | a0001c0001t0004g0078 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.624+2809A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607277 | |||||||
| chr5:71607292 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
124 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.624+2824G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607292 | |||||||
| chr5:71607362 | G | A | 2 | a0001c0001t0001g0189 a0001c0002t0003g0253 |
2 | HG03130.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.624+2894G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607362 | |||||||
| chr5:71607491 | C | T | 10 | a0001c0001t0004g0242 a0001c0001t0004g0243 a0001c0001t0004g0244 others(7): Show |
10 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.624+3023C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607491 | |||||||
| chr5:71607498 | T | A | 1 | a0001c0001t0019g0026 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.624+3030T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607498 | |||||||
| chr5:71607662 | T | G | 1 | a0001c0001t0007g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.624+3194T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607662 | |||||||
| chr5:71607669 | A | T | 1 | a0001c0001t0002g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.624+3201A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607669 | |||||||
| chr5:71607732 | C | T | 126 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(123): Show |
132 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.624+3264C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607732 | |||||||
| chr5:71607750 | C | T | 126 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(123): Show |
132 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.624+3282C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607750 | |||||||
| chr5:71607840 | G | A | 1 | a0001c0001t0007g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.624+3372G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607840 | |||||||
| chr5:71607881 | C | T | 113 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(110): Show |
119 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.624+3413C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607881 | |||||||
| chr5:71607882 | A | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(255): Show |
268 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.624+3414A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607882 | |||||||
| chr5:71607955 | C | T | 8 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0222 others(5): Show |
8 | HG02572.hp1 HG02717.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.624+3487C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71607955 | |||||||
| chr5:71608047 | A | G | 2 | a0001c0002t0003g0042 a0001c0002t0003g0043 |
2 | HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.624+3579A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71608047 | |||||||
| chr5:71608093 | C | T | 2 | a0001c0001t0007g0252 a0001c0002t0003g0223 |
2 | HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.624+3625C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71608093 | |||||||
| chr5:71608248 | C | A | 1 | a0001c0001t0007g0195 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.624+3780C>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71608248 | |||||||
| chr5:71608294 | C | G | 1 | a0001c0001t0007g0195 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.624+3826C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71608294 | |||||||
| chr5:71608397 | A | G | 1 | a0001c0001t0007g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.624+3929A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71608397 | |||||||
| chr5:71608554 | T | C | 2 | a0001c0001t0007g0195 a0001c0001t0017g0012 |
2 | HG00642.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.624+4086T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71608554 | |||||||
| chr5:71608632 | G | C | 8 | a0001c0002t0003g0002 a0001c0002t0003g0024 a0001c0002t0003g0050 others(5): Show |
10 | HG00099.hp2 HG00140.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.624+4164G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71608632 | |||||||
| chr5:71608756 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.624+4288C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71608756 | |||||||
| chr5:71608896 | C | T | 1 | a0001c0002t0024g0027 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.624+4428C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71608896 | |||||||
| chr5:71608930 | G | A | 1 | a0001c0001t0005g0275 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.624+4462G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71608930 | |||||||
| chr5:71608957 | C | G | 1 | a0001c0001t0001g0015 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.624+4489C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71608957 | |||||||
| chr5:71609000 | A | G | 1 | a0001c0001t0002g0222 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.624+4532A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609000 | |||||||
| chr5:71609117 | C | T | 1 | a0001c0001t0004g0100 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.624+4649C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609117 | |||||||
| chr5:71609160 | T | G | 2 | a0001c0001t0010g0256 a0001c0001t0010g0336 |
2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.624+4692T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609160 | |||||||
| chr5:71609186 | C | T | 1 | a0001c0001t0002g0299 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.624+4718C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609186 | |||||||
| chr5:71609257 | T | C | 1 | a0001c0001t0007g0195 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.624+4789T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609257 | |||||||
| chr5:71609267 | C | G | 2 | a0001c0001t0014g0255 a0001c0002t0002g0254 |
2 | HG00733.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.624+4799C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609267 | |||||||
| chr5:71609301 | G | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(116): Show |
123 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.624+4833G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609301 | |||||||
| chr5:71609388 | G | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(116): Show |
123 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.624+4920G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609388 | |||||||
| chr5:71609482 | A | G | 4 | a0001c0001t0004g0034 a0001c0001t0004g0067 a0001c0001t0004g0173 others(1): Show |
4 | HG02056.hp1 HG02080.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.624+5014A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609482 | |||||||
| chr5:71609582 | C | T | 258 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(255): Show |
268 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.624+5114C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609582 | |||||||
| chr5:71609802 | T | C | 1 | a0001c0001t0004g0104 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.624+5334T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609802 | |||||||
| chr5:71609817 | A | G | 1 | a0001c0001t0004g0104 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.624+5349A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609817 | |||||||
| chr5:71609827 | G | A | 1 | a0001c0001t0019g0026 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.624+5359G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609827 | |||||||
| chr5:71609834 | A | G | 2 | a0001c0001t0001g0190 a0001c0001t0019g0026 |
2 | HG01978.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.624+5366A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609834 | |||||||
| chr5:71609850 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.624+5382G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609850 | |||||||
| chr5:71609922 | C | T | 27 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0002g0199 others(24): Show |
27 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.624+5454C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71609922 | |||||||
| chr5:71610067 | G | T | 10 | a0001c0001t0004g0242 a0001c0001t0004g0243 a0001c0001t0004g0244 others(7): Show |
10 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.624+5599G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610067 | |||||||
| chr5:71610091 | C | T | 1 | a0001c0001t0004g0239 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.624+5623C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610091 | |||||||
| chr5:71610119 | T | G | 10 | a0001c0001t0004g0242 a0001c0001t0004g0243 a0001c0001t0004g0244 others(7): Show |
10 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.624+5651T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610119 | |||||||
| chr5:71610170 | G | A | 2 | a0001c0001t0010g0256 a0001c0001t0010g0336 |
2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.624+5702G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610170 | |||||||
| chr5:71610224 | C | T | 1 | a0001c0001t0002g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.624+5756C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610224 | |||||||
| chr5:71610231 | G | T | 1 | a0001c0001t0001g0189 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.624+5763G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610231 | |||||||
| chr5:71610249 | G | T | 116 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(113): Show |
122 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.624+5781G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610249 | |||||||
| chr5:71610301 | G | A | 1 | a0001c0001t0007g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.624+5833G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610301 | |||||||
| chr5:71610325 | G | A | 2 | a0001c0001t0007g0195 a0001c0001t0017g0012 |
2 | HG00642.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.624+5857G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610325 | |||||||
| chr5:71610335 | G | A | 1 | a0001c0002t0003g0253 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.624+5867G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610335 | |||||||
| chr5:71610407 | T | C | 2 | a0001c0001t0014g0255 a0001c0002t0002g0254 |
2 | HG00733.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.624+5939T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610407 | |||||||
| chr5:71610440 | C | T | 2 | a0001c0001t0004g0244 a0001c0001t0004g0249 |
2 | HG02027.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.624+5972C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610440 | |||||||
| chr5:71610541 | G | A | 1 | a0001c0007t0002g0191 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.624+6073G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610541 | |||||||
| chr5:71610558 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.624+6090G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610558 | |||||||
| chr5:71610567 | C | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(7): Show |
12 | HG00544.hp2 HG01257.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.624+6099C>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610567 | |||||||
| chr5:71610570 | A | G | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(7): Show |
12 | HG00544.hp2 HG01257.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.624+6102A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610570 | |||||||
| chr5:71610725 | G | A | 1 | a0001c0001t0002g0270 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.624+6257G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610725 | |||||||
| chr5:71610814 | G | A | 1 | a0001c0001t0002g0276 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.624+6346G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610814 | |||||||
| chr5:71610846 | C | T | 1 | a0001c0001t0002g0288 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.624+6378C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610846 | |||||||
| chr5:71610858 | T | C | 1 | a0001c0001t0007g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.624+6390T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610858 | |||||||
| chr5:71610863 | G | A | 4 | a0001c0001t0006g0025 a0001c0001t0006g0206 a0001c0001t0006g0207 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.624+6395G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610863 | |||||||
| chr5:71610992 | C | G | 1 | a0001c0001t0001g0143 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.624+6524C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610992 | |||||||
| chr5:71610999 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.624+6531C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71610999 | |||||||
| chr5:71611021 | G | A | 1 | a0001c0001t0005g0271 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.624+6553G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611021 | |||||||
| chr5:71611280 | A | G | 8 | a0001c0001t0004g0242 a0001c0001t0004g0243 a0001c0001t0004g0244 others(5): Show |
8 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.624+6812A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611280 | |||||||
| chr5:71611345 | C | T | 1 | a0001c0001t0004g0245 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.624+6877C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611345 | |||||||
| chr5:71611346 | G | A | 2 | a0001c0001t0002g0022 a0001c0001t0015g0020 |
2 | HG01243.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.624+6878G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611346 | |||||||
| chr5:71611403 | C | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(140): Show |
147 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.624+6935C>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611403 | |||||||
| chr5:71611422 | A | G | 1 | a0001c0001t0007g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.624+6954A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611422 | |||||||
| chr5:71611552 | C | G | 2 | a0001c0001t0001g0099 a0001c0001t0001g0179 |
2 | NA18941.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.624+7084C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611552 | |||||||
| chr5:71611610 | T | C | 1 | a0001c0001t0007g0195 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.624+7142T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611610 | |||||||
| chr5:71611631 | G | A | 2 | a0001c0001t0008g0250 a0001c0001t0008g0251 |
2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.624+7163G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611631 | |||||||
| chr5:71611668 | G | A | 115 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(112): Show |
121 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.624+7200G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611668 | |||||||
| chr5:71611697 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.624+7229G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611697 | |||||||
| chr5:71611711 | G | A | 115 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(112): Show |
121 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.624+7243G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611711 | |||||||
| chr5:71611799 | T | G | 7 | a0001c0002t0003g0028 a0001c0002t0003g0029 a0001c0002t0003g0030 others(4): Show |
7 | HG02559.hp1 HG02647.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.624+7331T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611799 | |||||||
| chr5:71611838 | G | T | 1 | a0001c0001t0007g0195 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.624+7370G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611838 | |||||||
| chr5:71611881 | C | T | 1 | a0001c0001t0002g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.624+7413C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611881 | |||||||
| chr5:71611890 | G | A | 1 | a0001c0001t0004g0277 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.624+7422G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611890 | |||||||
| chr5:71611986 | C | T | 1 | a0001c0001t0007g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.624+7518C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71611986 | |||||||
| chr5:71612030 | T | C | 4 | a0001c0001t0001g0313 a0001c0001t0001g0316 a0001c0001t0002g0314 others(1): Show |
4 | HG01070.hp1 HG01074.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+7562T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71612030 | |||||||
| chr5:71612033 | C | T | 1 | a0001c0001t0002g0274 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.624+7565C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71612033 | |||||||
| chr5:71612055 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.624+7587C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71612055 | |||||||
| chr5:71612159 | T | G | 1 | a0001c0001t0001g0089 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.624+7691T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71612159 | |||||||
| chr5:71612321 | A | T | 1 | a0001c0001t0004g0244 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.624+7853A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71612321 | |||||||
| chr5:71612390 | G | A | 11 | a0001c0001t0004g0058 a0001c0001t0004g0242 a0001c0001t0004g0243 others(8): Show |
11 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+7922G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71612390 | |||||||
| chr5:71612443 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.624+7975C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71612443 | |||||||
| chr5:71612472 | G | A | 1 | a0001c0001t0017g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.624+8004G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71612472 | |||||||
| chr5:71612526 | A | G | 1 | a0001c0001t0002g0287 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.624+8058A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71612526 | |||||||
| chr5:71612665 | C | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(142): Show |
149 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.624+8197C>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71612665 | |||||||
| chr5:71613268 | A | G | 1 | a0001c0001t0002g0315 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.624+8800A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71613268 | |||||||
| chr5:71613415 | A | T | 11 | a0001c0001t0004g0058 a0001c0001t0004g0242 a0001c0001t0004g0243 others(8): Show |
11 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+8947A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71613415 | |||||||
| chr5:71613521 | C | T | 11 | a0001c0001t0004g0058 a0001c0001t0004g0242 a0001c0001t0004g0243 others(8): Show |
11 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+9053C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71613521 | |||||||
| chr5:71614029 | T | TACACAC | 14 | a0001c0001t0001g0103 a0001c0001t0002g0322 a0001c0001t0004g0058 others(11): Show |
14 | HG00642.hp1 HG01099.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.624+9577_624+9582d others(8): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71614029 | ||||||
| chr5:71614029 | T | TACACACA others(1): Show |
16 | a0001c0001t0001g0086 a0001c0001t0001g0140 a0001c0001t0001g0144 others(13): Show |
16 | HG00673.hp2 HG01243.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.624+9575_624+9582d others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71614029 | ||||||
| chr5:71614029 | T | TACACACA others(3): Show |
109 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(106): Show |
113 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.624+9573_624+9582d others(12): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71614029 | ||||||
| chr5:71614029 | T | TACACACA others(5): Show |
113 | a0001c0001t0001g0019 a0001c0001t0001g0090 a0001c0001t0001g0096 others(110): Show |
119 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.624+9571_624+9582d others(14): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71614029 | ||||||
| chr5:71614029 | T | TACACACA others(7): Show |
15 | a0001c0001t0001g0214 a0001c0001t0002g0196 a0001c0001t0002g0201 others(12): Show |
15 | HG00735.hp1 HG01167.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.624+9569_624+9582d others(16): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71614029 | ||||||
| chr5:71614029 | T | TACACACA others(9): Show |
1 | a0001c0001t0002g0325 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.624+9567_624+9582d others(18): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71614029 | ||||||
| chr5:71614359 | G | A | 1 | a0002c0005t0002g0280 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.624+9891G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71614359 | |||||||
| chr5:71614442 | T | C | 260 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(257): Show |
270 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.624+9974T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71614442 | |||||||
| chr5:71614484 | C | CT | 120 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(117): Show |
125 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.624+10031dupT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71614484 | ||||||
| chr5:71614484 | C | CTTT | 9 | a0001c0001t0004g0058 a0001c0001t0004g0242 a0001c0001t0004g0243 others(6): Show |
9 | HG01433.hp2 HG01978.hp1 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.624+10029_624+1003 others(7): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71614484 | ||||||
| chr5:71614484 | CT | C | 8 | a0001c0001t0001g0094 a0001c0001t0002g0289 a0001c0001t0004g0208 others(5): Show |
8 | HG01884.hp2 HG02559.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.624+10031delT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71614484 | ||||||
| chr5:71614922 | C | G | 1 | a0001c0001t0004g0277 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.624+10454C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71614922 | |||||||
| chr5:71615035 | C | T | 1 | a0001c0002t0003g0253 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.624+10567C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71615035 | |||||||
| chr5:71615166 | C | T | 2 | a0001c0001t0007g0195 a0001c0001t0007g0252 |
2 | HG00642.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.624+10698C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71615166 | |||||||
| chr5:71615323 | C | T | 11 | a0001c0001t0004g0058 a0001c0001t0004g0242 a0001c0001t0004g0243 others(8): Show |
11 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+10855C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71615323 | |||||||
| chr5:71615532 | C | G | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.624+11064C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71615532 | |||||||
| chr5:71615570 | G | A | 11 | a0001c0001t0003g0211 a0001c0001t0004g0208 a0001c0001t0004g0209 others(8): Show |
11 | HG00741.hp1 HG01884.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.625-11070G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71615570 | |||||||
| chr5:71615696 | C | G | 1 | a0001c0001t0002g0286 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.625-10944C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71615696 | |||||||
| chr5:71615732 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.625-10908C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71615732 | |||||||
| chr5:71615956 | G | A | 2 | a0001c0001t0007g0195 a0001c0001t0007g0252 |
2 | HG00642.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.625-10684G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71615956 | |||||||
| chr5:71615967 | A | G | 1 | a0001c0001t0017g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.625-10673A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71615967 | |||||||
| chr5:71616110 | T | C | 1 | a0001c0002t0003g0084 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.625-10530T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71616110 | |||||||
| chr5:71616120 | C | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(142): Show |
149 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.625-10520C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71616120 | |||||||
| chr5:71616162 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.625-10478C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71616162 | |||||||
| chr5:71616666 | G | C | 5 | a0001c0001t0003g0045 a0001c0001t0003g0047 a0001c0001t0003g0049 others(2): Show |
5 | HG00741.hp2 HG02258.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.625-9974G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71616666 | |||||||
| chr5:71616676 | T | C | 2 | a0001c0001t0007g0195 a0001c0001t0007g0252 |
2 | HG00642.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.625-9964T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71616676 | |||||||
| chr5:71616716 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.625-9924C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71616716 | |||||||
| chr5:71616854 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(143): Show |
150 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.625-9786C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71616854 | |||||||
| chr5:71616982 | A | G | 2 | a0001c0001t0007g0195 a0001c0001t0007g0252 |
2 | HG00642.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.625-9658A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71616982 | |||||||
| chr5:71617042 | CA | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(116): Show |
123 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.625-9594delA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71617042 | ||||||
| chr5:71617227 | T | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
124 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.625-9413T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71617227 | |||||||
| chr5:71617471 | C | T | 2 | a0001c0003t0003g0193 a0001c0003t0003g0225 |
2 | HG01167.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.625-9169C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71617471 | |||||||
| chr5:71617612 | T | C | 2 | a0001c0001t0014g0255 a0001c0002t0002g0254 |
2 | HG00733.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.625-9028T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71617612 | |||||||
| chr5:71617854 | A | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(142): Show |
149 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.625-8786A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71617854 | |||||||
| chr5:71618081 | G | C | 115 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(112): Show |
121 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.625-8559G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71618081 | |||||||
| chr5:71618236 | T | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
124 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.625-8404T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71618236 | |||||||
| chr5:71618437 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(143): Show |
150 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.625-8203C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71618437 | |||||||
| chr5:71618462 | ATTCT | A | 10 | a0001c0001t0001g0260 a0001c0001t0002g0003 a0001c0001t0002g0197 others(7): Show |
12 | HG00099.hp1 HG00280.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.625-8166_625-8163d others(6): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618462 | ||||||
| chr5:71618488 | T | TCTTC | 8 | a0001c0001t0002g0270 a0001c0001t0002g0286 a0001c0001t0002g0315 others(5): Show |
10 | HG01074.hp1 HG01109.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-8092_625-8089d others(6): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618488 | ||||||
| chr5:71618488 | T | TCTTCCTT others(1): Show |
5 | a0001c0001t0002g0319 a0001c0002t0003g0028 a0001c0002t0003g0038 others(2): Show |
5 | HG02074.hp2 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.625-8096_625-8089d others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618488 | ||||||
| chr5:71618488 | T | TCTTCCTT others(5): Show |
1 | a0001c0002t0003g0037 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.625-8100_625-8089d others(14): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618488 | ||||||
| chr5:71618488 | TCTTC | T | 45 | a0001c0001t0001g0313 a0001c0001t0001g0316 a0001c0001t0001g0317 others(42): Show |
49 | HG00280.hp2 HG00609.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.625-8092_625-8089d others(6): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618488 | ||||||
| chr5:71618488 | TCTTCCTT others(1): Show |
T | 48 | a0001c0001t0001g0070 a0001c0001t0001g0217 a0001c0001t0001g0295 others(45): Show |
49 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.625-8096_625-8089d others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618488 | ||||||
| chr5:71618488 | TCTTCCTT others(5): Show |
T | 46 | a0001c0001t0001g0260 a0001c0001t0002g0010 a0001c0001t0002g0060 others(43): Show |
47 | HG00438.hp2 HG00673.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.625-8100_625-8089d others(14): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618488 | ||||||
| chr5:71618488 | TCTTCCTT others(9): Show |
T | 9 | a0001c0001t0002g0230 a0001c0001t0002g0285 a0001c0001t0002g0306 others(6): Show |
9 | HG01168.hp1 HG01358.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.625-8104_625-8089d others(18): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618488 | ||||||
| chr5:71618488 | TCTTCCTT others(13): Show |
T | 8 | a0001c0001t0002g0221 a0001c0001t0002g0226 a0001c0001t0002g0299 others(5): Show |
8 | HG01261.hp1 HG01884.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.625-8108_625-8089d others(22): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618488 | ||||||
| chr5:71618488 | TCTTCCTT others(17): Show |
T | 3 | a0001c0001t0006g0025 a0001c0001t0006g0207 a0001c0001t0007g0195 |
3 | HG00642.hp1 HG02559.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.625-8112_625-8089d others(26): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618488 | ||||||
| chr5:71618488 | TCTTCCTT others(21): Show |
T | 13 | a0001c0001t0001g0101 a0001c0001t0001g0111 a0001c0001t0002g0092 others(10): Show |
13 | HG00280.hp1 HG01433.hp2 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.625-8116_625-8089d others(30): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618488 | ||||||
| chr5:71618488 | TCTTCCTT others(25): Show |
T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(116): Show |
123 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.625-8120_625-8089d others(34): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618488 | ||||||
| chr5:71618488 | TCTTCCTT others(29): Show |
T | 1 | a0001c0001t0001g0163 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.625-8124_625-8089d others(38): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618488 | ||||||
| chr5:71618488 | TCTTCCTT others(37): Show |
T | 1 | a0003c0008t0006g0079 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.625-8132_625-8089d others(46): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618488 | ||||||
| chr5:71618494 | TTCCTTCC others(3): Show |
T | 1 | a0001c0001t0006g0206 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.625-8145_625-8136d others(12): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71618494 | |||||||
| chr5:71618501 | C | CTTCCTTC others(5): Show |
1 | a0001c0002t0003g0050 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.625-8128_625-8127i others(14): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618501 | ||||||
| chr5:71618503 | T | TCCTTCCT others(5): Show |
1 | a0001c0002t0003g0253 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.625-8126_625-8125i others(14): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618503 | ||||||
| chr5:71618512 | CCTTCCTT others(33): Show |
C | 1 | a0001c0001t0001g0103 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.625-8124_625-8085d others(42): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618512 | ||||||
| chr5:71618548 | C | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(144): Show |
151 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.625-8092C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71618548 | |||||||
| chr5:71618548 | CCTTT | C | 3 | a0001c0002t0003g0002 a0001c0002t0003g0051 a0001c0002t0003g0192 |
5 | HG00099.hp2 HG01255.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.625-8081_625-8078d others(6): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71618548 | ||||||
| chr5:71618552 | T | C | 3 | a0001c0002t0003g0024 a0001c0002t0003g0050 a0001c0002t0003g0057 |
3 | HG00140.hp1 HG01069.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.625-8088T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71618552 | |||||||
| chr5:71618607 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.625-8033G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71618607 | |||||||
| chr5:71618624 | T | G | 271 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(268): Show |
281 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.625-8016T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71618624 | |||||||
| chr5:71618655 | G | A | 10 | a0001c0001t0003g0211 a0001c0001t0004g0208 a0001c0001t0004g0209 others(7): Show |
10 | HG01884.hp1 HG01884.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-7985G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71618655 | |||||||
| chr5:71619117 | C | T | 3 | a0001c0001t0010g0256 a0001c0001t0010g0336 a0001c0002t0003g0253 |
3 | HG02622.hp1 HG03130.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.625-7523C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71619117 | |||||||
| chr5:71619227 | A | G | 1 | a0001c0001t0002g0283 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.625-7413A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71619227 | |||||||
| chr5:71619256 | T | G | 1 | a0001c0002t0003g0033 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.625-7384T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71619256 | |||||||
| chr5:71619346 | C | T | 2 | a0001c0001t0009g0233 a0001c0001t0009g0234 |
2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.625-7294C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71619346 | |||||||
| chr5:71619583 | C | T | 1 | a0001c0001t0002g0278 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.625-7057C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71619583 | |||||||
| chr5:71619661 | G | A | 1 | a0001c0001t0002g0278 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.625-6979G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71619661 | |||||||
| chr5:71619718 | A | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
119 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.625-6922A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71619718 | |||||||
| chr5:71619761 | G | A | 3 | a0001c0001t0010g0256 a0001c0001t0010g0336 a0001c0002t0003g0253 |
3 | HG02622.hp1 HG03130.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.625-6879G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71619761 | |||||||
| chr5:71619787 | C | T | 5 | a0001c0001t0002g0009 a0001c0001t0002g0224 a0001c0003t0003g0193 others(2): Show |
6 | HG01167.hp2 HG02976.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.625-6853C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71619787 | |||||||
| chr5:71619884 | G | C | 3 | a0001c0001t0010g0256 a0001c0001t0010g0336 a0001c0002t0003g0253 |
3 | HG02622.hp1 HG03130.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.625-6756G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71619884 | |||||||
| chr5:71619915 | C | T | 1 | a0001c0002t0003g0035 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.625-6725C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71619915 | |||||||
| chr5:71619948 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.625-6692G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71619948 | |||||||
| chr5:71619990 | C | CA | 22 | a0001c0001t0002g0082 a0001c0001t0002g0202 a0001c0001t0002g0279 others(19): Show |
24 | HG00099.hp2 HG00140.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.625-6637dupA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71619990 | ||||||
| chr5:71620028 | G | A | 1 | a0001c0001t0004g0257 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.625-6612G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71620028 | |||||||
| chr5:71620099 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.625-6541A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71620099 | |||||||
| chr5:71620117 | A | G | 1 | a0001c0001t0002g0306 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.625-6523A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71620117 | |||||||
| chr5:71620150 | A | G | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.625-6490A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71620150 | |||||||
| chr5:71620165 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.625-6475A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71620165 | |||||||
| chr5:71620439 | C | T | 3 | a0001c0001t0001g0093 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | NA18942.hp2 NA18982.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.625-6201C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71620439 | |||||||
| chr5:71620445 | A | G | 15 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0002g0199 others(12): Show |
15 | HG00423.hp2 HG00438.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.625-6195A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71620445 | |||||||
| chr5:71620564 | C | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
124 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.625-6076C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71620564 | |||||||
| chr5:71620779 | A | G | 13 | a0001c0001t0002g0279 a0001c0001t0004g0058 a0001c0001t0004g0242 others(10): Show |
13 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.625-5861A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71620779 | |||||||
| chr5:71620807 | C | T | 2 | a0001c0001t0019g0026 a0001c0007t0002g0191 |
2 | HG00741.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.625-5833C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71620807 | |||||||
| chr5:71621029 | A | G | 13 | a0001c0001t0002g0279 a0001c0001t0004g0058 a0001c0001t0004g0242 others(10): Show |
13 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.625-5611A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71621029 | |||||||
| chr5:71621147 | C | G | 2 | a0001c0001t0001g0087 a0001c0001t0001g0088 |
2 | NA18993.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.625-5493C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71621147 | |||||||
| chr5:71621192 | GAGAAAGA others(9): Show |
G | 1 | a0001c0002t0003g0035 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.625-5445_625-5430d others(18): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71621192 | ||||||
| chr5:71621198 | G | T | 1 | a0001c0001t0003g0211 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.625-5442G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71621198 | |||||||
| chr5:71621343 | T | A | 12 | a0001c0001t0004g0058 a0001c0001t0004g0242 a0001c0001t0004g0243 others(9): Show |
12 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.625-5297T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71621343 | |||||||
| chr5:71621457 | G | A | 14 | a0001c0001t0003g0211 a0001c0001t0004g0208 a0001c0001t0004g0209 others(11): Show |
14 | HG00642.hp1 HG00741.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.625-5183G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71621457 | |||||||
| chr5:71621477 | G | A | 2 | a0001c0001t0019g0026 a0001c0007t0002g0191 |
2 | HG00741.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.625-5163G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71621477 | |||||||
| chr5:71621479 | A | G | 1 | a0001c0001t0002g0092 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.625-5161A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71621479 | |||||||
| chr5:71621502 | G | A | 1 | a0001c0001t0002g0276 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.625-5138G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71621502 | |||||||
| chr5:71621639 | A | G | 1 | a0001c0001t0002g0229 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.625-5001A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71621639 | |||||||
| chr5:71621895 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.625-4745G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71621895 | |||||||
| chr5:71622068 | G | A | 113 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(110): Show |
119 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.625-4572G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71622068 | |||||||
| chr5:71622118 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(133): Show |
140 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.625-4522C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71622118 | |||||||
| chr5:71622219 | C | T | 1 | a0001c0010t0004g0248 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.625-4421C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71622219 | |||||||
| chr5:71622270 | T | TA | 135 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(132): Show |
139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.625-4360dupA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71622270 | ||||||
| chr5:71622286 | C | T | 12 | a0001c0001t0003g0211 a0001c0001t0004g0208 a0001c0001t0004g0209 others(9): Show |
12 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.625-4354C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71622286 | |||||||
| chr5:71622339 | A | G | 1 | a0001c0001t0002g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.625-4301A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71622339 | |||||||
| chr5:71622435 | G | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(115): Show |
122 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.625-4205G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71622435 | |||||||
| chr5:71622449 | T | C | 10 | a0001c0001t0003g0211 a0001c0001t0004g0208 a0001c0001t0004g0209 others(7): Show |
10 | HG01884.hp1 HG01884.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-4191T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71622449 | |||||||
| chr5:71622754 | C | T | 1 | a0001c0007t0002g0191 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.625-3886C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71622754 | |||||||
| chr5:71622832 | C | T | 1 | a0001c0001t0009g0233 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.625-3808C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71622832 | |||||||
| chr5:71622903 | G | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
130 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.625-3737G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71622903 | |||||||
| chr5:71622992 | C | T | 2 | a0001c0001t0010g0256 a0001c0001t0010g0336 |
2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.625-3648C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71622992 | |||||||
| chr5:71622997 | C | T | 4 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
4 | HG00673.hp2 NA18986.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-3643C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71622997 | |||||||
| chr5:71623076 | A | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
124 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.625-3564A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71623076 | |||||||
| chr5:71623258 | T | C | 14 | a0001c0001t0003g0211 a0001c0001t0004g0208 a0001c0001t0004g0209 others(11): Show |
14 | HG00642.hp1 HG00741.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.625-3382T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71623258 | |||||||
| chr5:71623357 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(115): Show |
122 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.625-3283C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71623357 | |||||||
| chr5:71623459 | G | A | 10 | a0001c0001t0003g0211 a0001c0001t0004g0208 a0001c0001t0004g0209 others(7): Show |
10 | HG01884.hp1 HG01884.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-3181G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71623459 | |||||||
| chr5:71623967 | C | T | 2 | a0001c0001t0019g0026 a0001c0007t0002g0191 |
2 | HG00741.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.625-2673C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71623967 | |||||||
| chr5:71623999 | G | A | 1 | a0003c0008t0006g0079 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.625-2641G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71623999 | |||||||
| chr5:71624181 | G | A | 1 | a0001c0001t0002g0263 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.625-2459G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71624181 | |||||||
| chr5:71624266 | A | G | 1 | a0001c0001t0004g0243 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.625-2374A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71624266 | |||||||
| chr5:71624308 | A | G | 2 | a0001c0001t0007g0195 a0001c0001t0007g0252 |
2 | HG00642.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.625-2332A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71624308 | |||||||
| chr5:71624344 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.625-2296C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71624344 | |||||||
| chr5:71624400 | C | T | 14 | a0001c0001t0003g0211 a0001c0001t0004g0208 a0001c0001t0004g0209 others(11): Show |
14 | HG00642.hp1 HG00741.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.625-2240C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71624400 | |||||||
| chr5:71624426 | G | A | 2 | a0001c0001t0008g0250 a0001c0001t0008g0251 |
2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.625-2214G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71624426 | |||||||
| chr5:71624455 | G | A | 1 | a0001c0001t0002g0300 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.625-2185G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71624455 | |||||||
| chr5:71624645 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.625-1995G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71624645 | |||||||
| chr5:71624663 | T | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
126 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.625-1977T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71624663 | |||||||
| chr5:71624674 | G | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(268): Show |
281 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.625-1966G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71624674 | |||||||
| chr5:71624690 | TTTC | T | 11 | a0001c0001t0004g0208 a0001c0001t0004g0209 a0001c0001t0004g0210 others(8): Show |
11 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.625-1947_625-1945d others(5): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71624690 | ||||||
| chr5:71624693 | CT | C | 190 | a0001c0001t0001g0070 a0001c0001t0001g0217 a0001c0001t0001g0260 others(187): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.625-1928delT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71624693 | ||||||
| chr5:71624693 | CTT | C | 6 | a0001c0001t0002g0314 a0001c0001t0004g0014 a0001c0001t0019g0026 others(3): Show |
6 | HG00140.hp1 HG00741.hp1 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.625-1929_625-1928d others(4): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71624693 | ||||||
| chr5:71624693 | CTTT | C | 6 | a0001c0001t0001g0089 a0001c0001t0001g0094 a0001c0001t0002g0092 others(3): Show |
6 | HG00733.hp2 HG03139.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.625-1930_625-1928d others(5): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71624693 | ||||||
| chr5:71624693 | CTTTT | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(113): Show |
120 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.625-1931_625-1928d others(6): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71624693 | ||||||
| chr5:71624844 | G | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(133): Show |
140 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.625-1796G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71624844 | |||||||
| chr5:71625304 | G | GTCCTTTG others(4): Show |
1 | a0001c0001t0001g0094 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.625-1335_625-1325d others(13): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr5 | 71625304 | ||||||
| chr5:71625349 | G | A | 1 | a0001c0001t0010g0256 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.625-1291G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71625349 | |||||||
| chr5:71625668 | A | C | 13 | a0001c0001t0002g0279 a0001c0001t0004g0058 a0001c0001t0004g0242 others(10): Show |
13 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.625-972A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71625668 | |||||||
| chr5:71625680 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.625-960A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71625680 | |||||||
| chr5:71625750 | A | G | 2 | a0001c0001t0009g0233 a0001c0001t0009g0234 |
2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.625-890A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71625750 | |||||||
| chr5:71625941 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(131): Show |
138 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.625-699G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71625941 | |||||||
| chr5:71625946 | G | A | 2 | a0001c0001t0010g0256 a0001c0001t0010g0336 |
2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.625-694G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71625946 | |||||||
| chr5:71626032 | C | T | 2 | a0001c0001t0019g0026 a0001c0007t0002g0191 |
2 | HG00741.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.625-608C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71626032 | |||||||
| chr5:71626301 | C | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(129): Show |
136 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.625-339C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71626301 | |||||||
| chr5:71626395 | C | T | 10 | a0001c0001t0003g0211 a0001c0001t0004g0208 a0001c0001t0004g0209 others(7): Show |
10 | HG01884.hp1 HG01884.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-245C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 6/16 | chr5 | 71626395 | |||||||
| chr5:71626789 | G | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(268): Show |
281 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.738+36G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71626789 | |||||||
| chr5:71626885 | C | T | 38 | a0001c0001t0001g0016 a0001c0001t0001g0070 a0001c0001t0001g0150 others(35): Show |
38 | HG00140.hp2 HG00597.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.738+132C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71626885 | |||||||
| chr5:71626982 | A | C | 1 | a0001c0002t0003g0013 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.738+229A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71626982 | |||||||
| chr5:71627069 | A | C | 1 | a0001c0001t0002g0136 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.738+316A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71627069 | |||||||
| chr5:71627141 | G | T | 131 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(128): Show |
137 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.738+388G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71627141 | |||||||
| chr5:71627179 | G | C | 116 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(113): Show |
122 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.738+426G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71627179 | |||||||
| chr5:71627179 | G | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(131): Show |
138 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.738+426G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71627179 | |||||||
| chr5:71627336 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(131): Show |
138 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.738+583T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71627336 | |||||||
| chr5:71627531 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(131): Show |
138 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.738+778C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71627531 | |||||||
| chr5:71627600 | T | C | 1 | a0001c0001t0002g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.738+847T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71627600 | |||||||
| chr5:71627628 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(131): Show |
138 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.738+875G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71627628 | |||||||
| chr5:71627801 | C | A | 1 | a0001c0002t0003g0253 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.738+1048C>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71627801 | |||||||
| chr5:71627825 | C | CT | 17 | a0001c0001t0002g0231 a0001c0001t0002g0258 a0001c0001t0003g0211 others(14): Show |
17 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.738+1083dupT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr5 | 71627825 | ||||||
| chr5:71628004 | C | T | 13 | a0001c0001t0003g0211 a0001c0001t0004g0208 a0001c0001t0004g0209 others(10): Show |
13 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.738+1251C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71628004 | |||||||
| chr5:71628124 | A | G | 1 | a0001c0001t0002g0258 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.738+1371A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71628124 | |||||||
| chr5:71628140 | G | T | 124 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(121): Show |
130 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.738+1387G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71628140 | |||||||
| chr5:71628156 | C | T | 1 | a0001c0007t0002g0191 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.738+1403C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71628156 | |||||||
| chr5:71628273 | C | T | 2 | a0001c0001t0002g0289 a0001c0001t0002g0290 |
2 | NA18957.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.738+1520C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71628273 | |||||||
| chr5:71628320 | G | A | 1 | a0001c0001t0002g0302 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.738+1567G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71628320 | |||||||
| chr5:71628586 | G | C | 125 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(122): Show |
131 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.738+1833G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71628586 | |||||||
| chr5:71628710 | G | A | 3 | a0001c0001t0007g0195 a0001c0001t0007g0252 a0001c0001t0015g0020 |
3 | HG00642.hp1 HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.738+1957G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71628710 | |||||||
| chr5:71628831 | A | G | 1 | a0001c0001t0002g0220 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.738+2078A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71628831 | |||||||
| chr5:71628853 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.738+2100G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71628853 | |||||||
| chr5:71629043 | T | C | 2 | a0001c0001t0009g0233 a0001c0001t0009g0234 |
2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.738+2290T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71629043 | |||||||
| chr5:71629203 | C | CA | 134 | a0001c0001t0001g0114 a0001c0001t0001g0217 a0001c0001t0001g0260 others(131): Show |
140 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.738+2462dupA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr5 | 71629203 | ||||||
| chr5:71629219 | A | G | 133 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(130): Show |
139 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.738+2466A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71629219 | |||||||
| chr5:71629717 | A | C | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.739-2404A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71629717 | |||||||
| chr5:71629735 | C | CATT | 3 | a0001c0001t0001g0135 a0001c0001t0001g0142 a0001c0001t0001g0145 |
3 | HG02683.hp2 NA18972.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.739-2360_739-2358d others(5): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr5 | 71629735 | ||||||
| chr5:71629735 | C | CATTATTA others(5): Show |
1 | a0001c0001t0010g0256 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.739-2369_739-2358d others(14): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr5 | 71629735 | ||||||
| chr5:71629735 | CATTATT | C | 132 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(129): Show |
138 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.739-2363_739-2358d others(8): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr5 | 71629735 | ||||||
| chr5:71630290 | A | G | 6 | a0001c0001t0004g0242 a0001c0001t0004g0245 a0001c0001t0004g0246 others(3): Show |
6 | HG01433.hp2 HG01978.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.739-1831A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71630290 | |||||||
| chr5:71630433 | C | T | 13 | a0001c0001t0002g0279 a0001c0001t0004g0058 a0001c0001t0004g0242 others(10): Show |
13 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.739-1688C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71630433 | |||||||
| chr5:71630549 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(136): Show |
143 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.739-1572A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71630549 | |||||||
| chr5:71630605 | T | C | 1 | a0001c0002t0003g0023 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.739-1516T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71630605 | |||||||
| chr5:71630627 | G | C | 1 | a0001c0001t0009g0233 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.739-1494G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71630627 | |||||||
| chr5:71630732 | A | G | 109 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(106): Show |
115 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.739-1389A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71630732 | |||||||
| chr5:71630928 | A | C | 4 | a0001c0001t0003g0211 a0001c0001t0004g0208 a0001c0001t0004g0209 others(1): Show |
4 | HG02451.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.739-1193A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71630928 | |||||||
| chr5:71630991 | A | G | 1 | a0001c0001t0004g0239 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.739-1130A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71630991 | |||||||
| chr5:71631171 | G | T | 1 | a0001c0001t0001g0134 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.739-950G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71631171 | |||||||
| chr5:71631349 | C | T | 1 | a0003c0008t0006g0079 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.739-772C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71631349 | |||||||
| chr5:71631538 | C | CT | 50 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(47): Show |
50 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.739-563dupT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr5 | 71631538 | ||||||
| chr5:71631538 | CTTT | C | 120 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(117): Show |
126 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.739-565_739-563del others(3): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr5 | 71631538 | ||||||
| chr5:71631615 | A | G | 4 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 others(1): Show |
4 | HG00597.hp2 HG02155.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.739-506A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71631615 | |||||||
| chr5:71631676 | G | T | 1 | a0001c0001t0002g0269 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.739-445G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71631676 | |||||||
| chr5:71631753 | C | G | 262 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(259): Show |
272 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.739-368C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71631753 | |||||||
| chr5:71631859 | C | T | 108 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(105): Show |
114 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.739-262C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71631859 | |||||||
| chr5:71631860 | G | T | 1 | a0001c0001t0004g0247 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.739-261G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71631860 | |||||||
| chr5:71631920 | C | T | 3 | a0001c0001t0002g0231 a0001c0001t0019g0026 a0001c0007t0002g0191 |
3 | HG00741.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.739-201C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71631920 | |||||||
| chr5:71632029 | G | A | 124 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(121): Show |
130 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.739-92G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71632029 | |||||||
| chr5:71632030 | G | C | 13 | a0001c0001t0002g0279 a0001c0001t0004g0058 a0001c0001t0004g0242 others(10): Show |
13 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.739-91G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71632030 | |||||||
| chr5:71632096 | C | T | 10 | a0001c0001t0003g0211 a0001c0001t0004g0208 a0001c0001t0004g0209 others(7): Show |
10 | HG01884.hp1 HG01884.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.739-25C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 7/16 | chr5 | 71632096 | |||||||
| chr5:71632256 | C | T | 124 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(121): Show |
130 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.803+71C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71632256 | |||||||
| chr5:71632424 | T | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(116): Show |
123 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.803+239T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71632424 | |||||||
| chr5:71632474 | G | A | 4 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
4 | HG00673.hp2 NA18986.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.803+289G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71632474 | |||||||
| chr5:71632583 | C | T | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG00423.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.803+398C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71632583 | |||||||
| chr5:71632621 | G | A | 257 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(254): Show |
267 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.803+436G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71632621 | |||||||
| chr5:71632697 | CA | C | 8 | a0001c0001t0004g0194 a0001c0001t0004g0205 a0001c0001t0004g0235 others(5): Show |
8 | HG02717.hp1 HG02896.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.803+514delA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71632697 | ||||||
| chr5:71632738 | G | A | 124 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(121): Show |
130 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.803+553G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71632738 | |||||||
| chr5:71632819 | C | T | 1 | a0001c0007t0002g0191 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.803+634C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71632819 | |||||||
| chr5:71632840 | A | G | 2 | a0001c0001t0010g0256 a0001c0001t0010g0336 |
2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.803+655A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71632840 | |||||||
| chr5:71633091 | T | A | 1 | a0001c0001t0002g0092 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.803+906T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633091 | |||||||
| chr5:71633091 | T | TTA | 6 | a0001c0002t0003g0028 a0001c0002t0003g0031 a0001c0002t0003g0032 others(3): Show |
6 | HG01109.hp1 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.803+946_803+947dup others(2): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | ||||||
| chr5:71633091 | T | TTATA | 3 | a0001c0002t0003g0030 a0001c0002t0003g0033 a0001c0002t0016g0052 |
3 | HG03579.hp1 HG04199.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.803+944_803+947dup others(4): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | ||||||
| chr5:71633091 | T | TTATATAT others(1): Show |
4 | a0001c0001t0003g0211 a0001c0002t0003g0037 a0001c0002t0003g0043 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.803+940_803+947dup others(8): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | ||||||
| chr5:71633091 | T | TTATATAT others(3): Show |
1 | a0001c0002t0003g0055 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.803+938_803+947dup others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | ||||||
| chr5:71633091 | T | TTATATAT others(5): Show |
2 | a0001c0001t0007g0252 a0001c0002t0003g0036 |
2 | HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.803+936_803+947dup others(12): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | ||||||
| chr5:71633091 | T | TTATATAT others(7): Show |
6 | a0001c0001t0004g0208 a0001c0001t0004g0209 a0001c0002t0003g0029 others(3): Show |
6 | HG02647.hp1 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.803+934_803+947dup others(14): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | ||||||
| chr5:71633091 | T | TTATATAT others(9): Show |
3 | a0001c0002t0003g0006 a0001c0002t0003g0038 a0001c0002t0003g0042 |
4 | HG02970.hp2 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.803+932_803+947dup others(16): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | ||||||
| chr5:71633091 | T | TTATATAT others(11): Show |
1 | a0001c0002t0003g0005 | 2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.803+930_803+947dup others(18): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | ||||||
| chr5:71633091 | T | TTTTATAT others(3): Show |
1 | a0001c0001t0018g0085 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.803+907_803+908ins others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | ||||||
| chr5:71633091 | TTA | T | 11 | a0001c0001t0004g0014 a0001c0001t0004g0044 a0001c0001t0004g0065 others(8): Show |
11 | HG00099.hp2 HG00140.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.803+946_803+947del others(2): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | ||||||
| chr5:71633091 | TTATA | T | 27 | a0001c0001t0001g0070 a0001c0001t0002g0060 a0001c0001t0002g0061 others(24): Show |
27 | HG00140.hp2 HG00597.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.803+944_803+947del others(4): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | ||||||
| chr5:71633091 | TTATATA | T | 8 | a0001c0001t0002g0279 a0001c0001t0004g0067 a0001c0001t0004g0072 others(5): Show |
8 | HG01070.hp2 HG01071.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.803+942_803+947del others(6): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | ||||||
| chr5:71633091 | TTATATAT others(1): Show |
T | 7 | a0001c0001t0004g0058 a0001c0001t0004g0243 a0001c0001t0004g0244 others(4): Show |
7 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.803+940_803+947del others(8): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | ||||||
| chr5:71633091 | TTATATAT others(3): Show |
T | 1 | a0001c0001t0001g0214 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.803+938_803+947del others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | ||||||
| chr5:71633091 | TTATATAT others(5): Show |
T | 1 | a0001c0001t0001g0172 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.803+936_803+947del others(12): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | ||||||
| chr5:71633091 | TTATATAT others(9): Show |
T | 3 | a0001c0001t0014g0255 a0001c0002t0002g0254 a0001c0003t0003g0225 |
3 | HG00733.hp2 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.803+932_803+947del others(16): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | ||||||
| chr5:71633091 | TTATATAT others(11): Show |
T | 2 | a0001c0001t0002g0221 a0001c0001t0002g0291 |
2 | HG03195.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.803+930_803+947del others(18): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | ||||||
| chr5:71633091 | TTATATAT others(13): Show |
T | 103 | a0001c0001t0001g0217 a0001c0001t0001g0260 a0001c0001t0001g0295 others(100): Show |
109 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.803+928_803+947del others(20): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | ||||||
| chr5:71633091 | TTATATAT others(15): Show |
T | 10 | a0001c0001t0004g0194 a0001c0001t0004g0205 a0001c0001t0004g0235 others(7): Show |
10 | HG02717.hp1 HG02896.hp2 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.803+926_803+947del others(22): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | ||||||
| chr5:71633091 | TTATATAT others(17): Show |
T | 2 | a0001c0001t0006g0206 a0001c0001t0006g0207 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.803+924_803+947del others(24): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633091 | ||||||
| chr5:71633093 | A | T | 5 | a0001c0001t0002g0231 a0001c0001t0007g0195 a0001c0001t0015g0020 others(2): Show |
5 | HG00642.hp1 HG00741.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.803+908A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633093 | |||||||
| chr5:71633101 | A | T | 2 | a0001c0001t0004g0247 a0001c0010t0004g0248 |
2 | HG01433.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.803+916A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633101 | |||||||
| chr5:71633106 | TATATATA others(4): Show |
T | 1 | a0001c0002t0003g0013 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.803+922_803+932del others(11): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633106 | |||||||
| chr5:71633107 | ATATATAT others(19): Show |
A | 1 | a0001c0007t0002g0191 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.803+924_803+949del others(26): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633107 | ||||||
| chr5:71633109 | ATATATAT others(17): Show |
A | 1 | a0001c0001t0002g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.803+926_803+949del others(24): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633109 | ||||||
| chr5:71633117 | A | T | 1 | a0001c0001t0001g0214 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.803+932A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633117 | |||||||
| chr5:71633119 | A | T | 3 | a0001c0001t0001g0172 a0001c0001t0001g0214 a0001c0002t0003g0013 |
3 | NA18942.hp1 NA18948.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.803+934A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633119 | |||||||
| chr5:71633119 | ATATATAT others(7): Show |
A | 1 | a0001c0001t0019g0026 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.803+936_803+949del others(14): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633119 | ||||||
| chr5:71633121 | A | T | 5 | a0001c0001t0001g0172 a0001c0001t0001g0214 a0001c0001t0002g0022 others(2): Show |
5 | HG01243.hp1 HG03486.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.803+936A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633121 | |||||||
| chr5:71633123 | A | ATTTTTTT others(3): Show |
2 | a0001c0001t0001g0164 a0001c0001t0001g0213 |
2 | HG01261.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.803+939_803+940ins others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633123 | ||||||
| chr5:71633123 | A | T | 8 | a0001c0001t0001g0019 a0001c0001t0001g0126 a0001c0001t0001g0172 others(5): Show |
8 | HG01243.hp1 HG02109.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.803+938A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633123 | |||||||
| chr5:71633125 | A | ATTTTTTT others(3): Show |
2 | a0001c0001t0001g0098 a0001c0001t0001g0101 |
2 | NA18991.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.803+941_803+942ins others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633125 | ||||||
| chr5:71633125 | A | T | 10 | a0001c0001t0001g0019 a0001c0001t0001g0126 a0001c0001t0001g0164 others(7): Show |
10 | HG01243.hp1 HG01261.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.803+940A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633125 | |||||||
| chr5:71633127 | A | ATATTTTT others(8): Show |
1 | a0001c0001t0001g0151 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.803+945_803+946ins others(15): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633127 | ||||||
| chr5:71633127 | A | ATTTTTTT others(2): Show |
8 | a0001c0001t0001g0089 a0001c0001t0001g0093 a0001c0001t0001g0109 others(5): Show |
8 | HG01168.hp2 HG02922.hp1 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.803+943_803+944ins others(9): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633127 | ||||||
| chr5:71633127 | A | ATTTTTTT others(3): Show |
34 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(31): Show |
38 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.803+943_803+944ins others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633127 | ||||||
| chr5:71633127 | A | ATTTTTTT others(4): Show |
3 | a0001c0001t0001g0148 a0001c0001t0001g0186 a0001c0001t0004g0100 |
3 | HG01981.hp1 HG03490.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.803+943_803+944ins others(11): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633127 | ||||||
| chr5:71633127 | A | ATTTTTTT others(5): Show |
3 | a0001c0001t0001g0133 a0001c0001t0001g0140 a0001c0001t0001g0154 |
3 | HG02015.hp2 HG02040.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.803+943_803+944ins others(12): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633127 | ||||||
| chr5:71633127 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0001g0174 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.803+943_803+944ins others(13): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633127 | ||||||
| chr5:71633127 | A | ATTTTTTT others(7): Show |
1 | a0001c0001t0001g0163 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.803+943_803+944ins others(14): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633127 | ||||||
| chr5:71633127 | A | T | 21 | a0001c0001t0001g0019 a0001c0001t0001g0096 a0001c0001t0001g0098 others(18): Show |
21 | HG00642.hp2 HG00733.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.803+942A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633127 | |||||||
| chr5:71633128 | T | TTTTTTTT others(3): Show |
2 | a0001c0001t0008g0250 a0001c0001t0008g0251 |
2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.803+943_803+944ins others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633128 | |||||||
| chr5:71633129 | A | ATTTTTTT others(3): Show |
3 | a0001c0001t0001g0108 a0001c0001t0001g0143 a0001c0001t0001g0187 |
3 | NA18947.hp2 NA18967.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.803+945_803+946ins others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633129 | ||||||
| chr5:71633129 | A | ATTTTTTT others(4): Show |
5 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0128 others(2): Show |
5 | HG00280.hp1 HG02004.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.803+945_803+946ins others(11): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633129 | ||||||
| chr5:71633129 | A | ATTTTTTT others(5): Show |
13 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(10): Show |
13 | HG00621.hp1 HG01123.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.803+945_803+946ins others(12): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633129 | ||||||
| chr5:71633129 | A | ATTTTTTT others(7): Show |
1 | a0001c0001t0001g0120 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.803+945_803+946ins others(14): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633129 | ||||||
| chr5:71633129 | A | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(72): Show |
79 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.803+944A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633129 | |||||||
| chr5:71633131 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0167 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.803+947_803+948ins others(23): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | ||||||
| chr5:71633131 | A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0160 a0001c0001t0001g0313 |
2 | HG01169.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.803+947_803+948ins others(24): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | ||||||
| chr5:71633131 | A | ATATATAT others(3): Show |
1 | a0001c0001t0006g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.803+947_803+948ins others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | ||||||
| chr5:71633131 | A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0115 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.803+947_803+948ins others(22): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | ||||||
| chr5:71633131 | A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0156 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.803+947_803+948ins others(22): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | ||||||
| chr5:71633131 | A | ATATATTT others(4): Show |
1 | a0001c0001t0001g0116 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.803+947_803+948ins others(11): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | ||||||
| chr5:71633131 | A | ATATATTT others(13): Show |
2 | a0001c0001t0001g0127 a0001c0001t0001g0317 |
2 | NA19012.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.803+947_803+948ins others(20): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | ||||||
| chr5:71633131 | A | ATATTTTT others(8): Show |
1 | a0001c0001t0001g0175 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.803+947_803+948ins others(15): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | ||||||
| chr5:71633131 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0117 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.803+951_803+952ins others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | ||||||
| chr5:71633131 | A | ATTTTTTT others(4): Show |
2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.803+951_803+952ins others(11): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | ||||||
| chr5:71633131 | A | ATTTTTTT others(7): Show |
2 | a0001c0001t0001g0016 a0001c0001t0001g0150 |
2 | NA18939.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.803+951_803+952ins others(14): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | ||||||
| chr5:71633131 | A | ATTTTTTT others(11): Show |
1 | a0001c0001t0001g0157 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.803+951_803+952ins others(18): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | ||||||
| chr5:71633131 | A | ATTTTTTT others(6): Show |
3 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0134 |
3 | NA18984.hp2 NA18993.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.803+951_803+952ins others(13): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | ||||||
| chr5:71633131 | A | ATTTTTTT others(7): Show |
3 | a0001c0001t0001g0153 a0001c0001t0001g0178 a0001c0001t0004g0104 |
3 | HG00735.hp2 HG01433.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.803+951_803+952ins others(14): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | ||||||
| chr5:71633131 | A | ATTTTTTT others(8): Show |
1 | a0001c0001t0001g0114 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.803+951_803+952ins others(15): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | ||||||
| chr5:71633131 | A | ATTTTTTT others(11): Show |
1 | a0001c0001t0001g0118 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.803+951_803+952ins others(18): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633131 | ||||||
| chr5:71633131 | A | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(98): Show |
105 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.803+946A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633131 | |||||||
| chr5:71633132 | T | TATATATA others(12): Show |
1 | a0001c0001t0007g0195 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.803+947_803+948ins others(19): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633132 | |||||||
| chr5:71633133 | T | A | 7 | a0001c0001t0003g0211 a0001c0001t0004g0208 a0001c0001t0004g0209 others(4): Show |
7 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.803+948T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633133 | |||||||
| chr5:71633134 | T | A | 1 | a0001c0001t0007g0195 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.803+949T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633134 | |||||||
| chr5:71633135 | T | A | 2 | a0001c0001t0004g0210 a0003c0008t0006g0079 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.803+950T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633135 | |||||||
| chr5:71633137 | A | ATATATAT others(3): Show |
1 | a0001c0001t0004g0210 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.803+953_803+954ins others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633137 | ||||||
| chr5:71633137 | A | T | 12 | a0001c0001t0001g0088 a0001c0001t0001g0098 a0001c0001t0001g0110 others(9): Show |
12 | HG00280.hp1 HG01884.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.803+952A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633137 | |||||||
| chr5:71633292 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.803+1107A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633292 | |||||||
| chr5:71633306 | T | C | 1 | a0001c0001t0002g0264 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.803+1121T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633306 | |||||||
| chr5:71633326 | G | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(116): Show |
123 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.803+1141G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633326 | |||||||
| chr5:71633484 | A | G | 1 | a0001c0001t0002g0284 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.803+1299A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633484 | |||||||
| chr5:71633551 | AT | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(121): Show |
128 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.803+1377delT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr5 | 71633551 | ||||||
| chr5:71633683 | A | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(253): Show |
266 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.804-1260A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633683 | |||||||
| chr5:71633743 | G | A | 2 | a0001c0001t0014g0255 a0001c0002t0002g0254 |
2 | HG00733.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.804-1200G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633743 | |||||||
| chr5:71633912 | A | G | 2 | a0001c0001t0008g0250 a0001c0001t0008g0251 |
2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.804-1031A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633912 | |||||||
| chr5:71633930 | T | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(255): Show |
268 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.804-1013T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71633930 | |||||||
| chr5:71634219 | T | C | 1 | a0003c0008t0006g0079 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.804-724T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71634219 | |||||||
| chr5:71634270 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.804-673C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71634270 | |||||||
| chr5:71634391 | T | C | 2 | a0001c0001t0014g0255 a0001c0002t0002g0254 |
2 | HG00733.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.804-552T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71634391 | |||||||
| chr5:71634453 | A | G | 1 | a0001c0001t0002g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.804-490A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71634453 | |||||||
| chr5:71634626 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.804-317C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71634626 | |||||||
| chr5:71634682 | T | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(253): Show |
266 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.804-261T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 8/16 | chr5 | 71634682 | |||||||
| chr5:71635069 | T | G | 1 | a0001c0001t0004g0067 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.903+27T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 9/16 | chr5 | 71635069 | |||||||
| chr5:71635139 | A | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
124 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.904-12A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 9/16 | chr5 | 71635139 | |||||||
| chr5:71635285 | T | G | 13 | a0001c0001t0003g0211 a0001c0001t0004g0208 a0001c0001t0004g0209 others(10): Show |
13 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.999+39T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71635285 | |||||||
| chr5:71635407 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.999+161G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71635407 | |||||||
| chr5:71635436 | G | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(191): Show |
198 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.999+190G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71635436 | |||||||
| chr5:71635558 | T | C | 2 | a0001c0001t0014g0255 a0001c0002t0002g0254 |
2 | HG00733.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.999+312T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71635558 | |||||||
| chr5:71635917 | G | T | 1 | a0001c0002t0002g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.999+671G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71635917 | |||||||
| chr5:71635946 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.999+700G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71635946 | |||||||
| chr5:71636040 | A | G | 4 | a0001c0001t0001g0217 a0001c0002t0003g0216 a0001c0002t0003g0218 others(1): Show |
4 | HG02015.hp1 NA18747.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.999+794A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71636040 | |||||||
| chr5:71636056 | G | A | 245 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(242): Show |
255 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.999+810G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71636056 | |||||||
| chr5:71636129 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0010g0336 |
2 | HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.999+883G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71636129 | |||||||
| chr5:71636165 | A | G | 1 | a0001c0001t0004g0249 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.999+919A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71636165 | |||||||
| chr5:71636175 | G | A | 245 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(242): Show |
255 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.999+929G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71636175 | |||||||
| chr5:71636434 | G | A | 1 | a0001c0001t0020g0165 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.999+1188G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71636434 | |||||||
| chr5:71636699 | C | CAAAT | 3 | a0001c0001t0007g0195 a0001c0001t0010g0256 a0001c0001t0010g0336 |
3 | HG00642.hp1 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.999+1473_999+1476d others(6): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr5 | 71636699 | ||||||
| chr5:71636821 | G | A | 1 | a0001c0001t0004g0058 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.999+1575G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71636821 | |||||||
| chr5:71636900 | T | C | 8 | a0001c0001t0004g0194 a0001c0001t0004g0205 a0001c0001t0004g0236 others(5): Show |
8 | HG02257.hp1 HG02717.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.999+1654T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71636900 | |||||||
| chr5:71636986 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.999+1740C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71636986 | |||||||
| chr5:71636987 | G | A | 1 | a0001c0001t0002g0136 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.999+1741G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71636987 | |||||||
| chr5:71637084 | G | A | 2 | a0001c0002t0003g0223 a0001c0002t0003g0253 |
2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.999+1838G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71637084 | |||||||
| chr5:71637169 | T | C | 1 | a0001c0001t0001g0317 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.999+1923T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71637169 | |||||||
| chr5:71637201 | A | G | 2 | a0001c0001t0014g0255 a0001c0002t0002g0254 |
2 | HG00733.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.999+1955A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71637201 | |||||||
| chr5:71637690 | A | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(116): Show |
123 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.999+2444A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71637690 | |||||||
| chr5:71637731 | T | A | 7 | a0001c0001t0006g0025 a0001c0001t0006g0206 a0001c0001t0006g0207 others(4): Show |
7 | HG00733.hp2 HG01884.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.999+2485T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71637731 | |||||||
| chr5:71637870 | G | A | 4 | a0001c0001t0004g0208 a0001c0001t0004g0209 a0001c0001t0004g0210 others(1): Show |
4 | HG02698.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.999+2624G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71637870 | |||||||
| chr5:71637928 | A | G | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.999+2682A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71637928 | |||||||
| chr5:71637963 | C | T | 1 | a0001c0001t0017g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.999+2717C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71637963 | |||||||
| chr5:71637964 | G | A | 116 | a0001c0001t0001g0070 a0001c0001t0002g0003 a0001c0001t0002g0004 others(113): Show |
122 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.999+2718G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71637964 | |||||||
| chr5:71637992 | A | G | 17 | a0001c0001t0003g0211 a0001c0001t0004g0208 a0001c0001t0004g0209 others(14): Show |
17 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.999+2746A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71637992 | |||||||
| chr5:71638089 | A | T | 2 | a0001c0001t0008g0250 a0001c0001t0008g0251 |
2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.999+2843A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71638089 | |||||||
| chr5:71638314 | A | G | 10 | a0001c0001t0002g0009 a0001c0001t0002g0220 a0001c0001t0002g0221 others(7): Show |
11 | HG02572.hp1 HG02717.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.1000-2689A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71638314 | |||||||
| chr5:71638324 | T | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(74): Show |
81 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1000-2679T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71638324 | |||||||
| chr5:71638459 | C | T | 33 | a0001c0001t0002g0231 a0001c0001t0003g0045 a0001c0001t0003g0047 others(30): Show |
33 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1000-2544C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71638459 | |||||||
| chr5:71638460 | G | A | 2 | a0001c0002t0003g0028 a0001c0002t0003g0029 |
2 | HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1000-2543G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71638460 | |||||||
| chr5:71638473 | C | CAGATCTG others(59): Show |
1 | a0001c0001t0004g0078 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1000-2526_1000-246 others(70): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr5 | 71638473 | ||||||
| chr5:71638560 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1000-2443G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71638560 | |||||||
| chr5:71638696 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1000-2307T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71638696 | |||||||
| chr5:71638767 | C | T | 1 | a0001c0002t0003g0080 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1000-2236C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71638767 | |||||||
| chr5:71638877 | G | A | 129 | a0001c0001t0001g0070 a0001c0001t0002g0003 a0001c0001t0002g0004 others(126): Show |
135 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.1000-2126G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71638877 | |||||||
| chr5:71639004 | T | C | 30 | a0001c0001t0003g0045 a0001c0001t0003g0047 a0001c0001t0003g0049 others(27): Show |
30 | HG00140.hp2 HG00597.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1000-1999T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71639004 | |||||||
| chr5:71639075 | C | T | 6 | a0001c0001t0006g0025 a0001c0001t0006g0206 a0001c0001t0006g0207 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000-1928C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71639075 | |||||||
| chr5:71639077 | T | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(134): Show |
141 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.1000-1926T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71639077 | |||||||
| chr5:71639192 | C | T | 1 | a0001c0001t0015g0020 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1000-1811C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71639192 | |||||||
| chr5:71639382 | T | C | 3 | a0001c0001t0004g0208 a0001c0001t0004g0209 a0001c0001t0004g0210 |
3 | HG02886.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1000-1621T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71639382 | |||||||
| chr5:71639561 | C | T | 8 | a0001c0002t0003g0002 a0001c0002t0003g0024 a0001c0002t0003g0050 others(5): Show |
10 | HG00099.hp2 HG00140.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.1000-1442C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71639561 | |||||||
| chr5:71639590 | T | C | 1 | a0001c0011t0004g0081 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1000-1413T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71639590 | |||||||
| chr5:71639700 | T | C | 1 | a0001c0001t0005g0275 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1000-1303T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71639700 | |||||||
| chr5:71639816 | A | C | 7 | a0001c0001t0006g0025 a0001c0001t0006g0206 a0001c0001t0006g0207 others(4): Show |
7 | HG00733.hp2 HG01884.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1000-1187A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71639816 | |||||||
| chr5:71640382 | AT | A | 229 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(226): Show |
237 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(234): Show |
intron_variant | MODIFIER | c.1000-600delT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr5 | 71640382 | ||||||
| chr5:71640382 | ATT | A | 61 | a0001c0001t0001g0019 a0001c0001t0001g0111 a0001c0001t0001g0134 others(58): Show |
61 | HG00140.hp2 HG00280.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.1000-601_1000-600d others(4): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr5 | 71640382 | ||||||
| chr5:71640583 | G | A | 1 | a0001c0001t0002g0269 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1000-420G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71640583 | |||||||
| chr5:71640704 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0019g0026 a0001c0007t0002g0191 |
3 | HG00741.hp1 HG02109.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1000-299G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71640704 | |||||||
| chr5:71640753 | G | A | 1 | a0001c0001t0002g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1000-250G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71640753 | |||||||
| chr5:71640766 | T | G | 1 | a0001c0001t0019g0026 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1000-237T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71640766 | |||||||
| chr5:71640816 | C | G | 122 | a0001c0001t0001g0070 a0001c0001t0002g0003 a0001c0001t0002g0004 others(119): Show |
128 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.1000-187C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71640816 | |||||||
| chr5:71640852 | T | C | 1 | a0001c0001t0004g0100 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1000-151T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 10/16 | chr5 | 71640852 | |||||||
| chr5:71641104 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1072+29A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71641104 | |||||||
| chr5:71641133 | T | G | 7 | a0001c0001t0006g0025 a0001c0001t0006g0206 a0001c0001t0006g0207 others(4): Show |
7 | HG00733.hp2 HG01884.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1072+58T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71641133 | |||||||
| chr5:71641282 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1072+207G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71641282 | |||||||
| chr5:71641378 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1072+303C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71641378 | |||||||
| chr5:71641625 | A | G | 2 | a0001c0001t0007g0195 a0001c0001t0007g0252 |
2 | HG00642.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1072+550A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71641625 | |||||||
| chr5:71641697 | A | G | 1 | a0001c0001t0014g0255 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1072+622A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71641697 | |||||||
| chr5:71641815 | A | G | 5 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0119 others(2): Show |
5 | HG02083.hp1 NA18957.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1072+740A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71641815 | |||||||
| chr5:71642137 | G | A | 26 | a0001c0001t0003g0211 a0001c0001t0004g0208 a0001c0001t0004g0209 others(23): Show |
26 | HG00733.hp2 HG01167.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1072+1062G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71642137 | |||||||
| chr5:71642265 | C | T | 226 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(223): Show |
236 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.1072+1190C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71642265 | |||||||
| chr5:71642270 | A | T | 1 | a0001c0001t0014g0255 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1072+1195A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71642270 | |||||||
| chr5:71642318 | G | T | 1 | a0001c0002t0002g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1072+1243G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71642318 | |||||||
| chr5:71642440 | G | A | 2 | a0001c0001t0002g0278 a0001c0001t0002g0288 |
2 | HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1072+1365G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71642440 | |||||||
| chr5:71642550 | A | T | 2 | a0001c0001t0009g0233 a0001c0001t0009g0234 |
2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1073-1269A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71642550 | |||||||
| chr5:71642559 | T | C | 6 | a0001c0001t0006g0025 a0001c0001t0006g0206 a0001c0001t0006g0207 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1073-1260T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71642559 | |||||||
| chr5:71642649 | C | G | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1073-1170C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71642649 | |||||||
| chr5:71642857 | A | G | 2 | a0001c0001t0004g0245 a0001c0001t0004g0246 |
2 | HG04199.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1073-962A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71642857 | |||||||
| chr5:71642927 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1073-892C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71642927 | |||||||
| chr5:71642954 | G | C | 91 | a0001c0001t0001g0070 a0001c0001t0002g0003 a0001c0001t0002g0004 others(88): Show |
96 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1073-865G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71642954 | |||||||
| chr5:71642963 | A | G | 1 | a0001c0002t0003g0035 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1073-856A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71642963 | |||||||
| chr5:71642981 | C | T | 30 | a0001c0001t0003g0045 a0001c0001t0003g0047 a0001c0001t0003g0049 others(27): Show |
30 | HG00140.hp2 HG00597.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1073-838C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71642981 | |||||||
| chr5:71643055 | A | G | 1 | a0001c0001t0004g0245 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1073-764A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71643055 | |||||||
| chr5:71643125 | A | G | 7 | a0001c0001t0006g0025 a0001c0001t0006g0206 a0001c0001t0006g0207 others(4): Show |
7 | HG00733.hp2 HG01884.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1073-694A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71643125 | |||||||
| chr5:71643202 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1073-617C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71643202 | |||||||
| chr5:71643264 | C | T | 1 | a0001c0001t0004g0067 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1073-555C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71643264 | |||||||
| chr5:71643303 | T | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(217): Show |
230 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1073-516T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71643303 | |||||||
| chr5:71643360 | C | G | 2 | a0001c0001t0008g0250 a0001c0001t0008g0251 |
2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1073-459C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71643360 | |||||||
| chr5:71643412 | A | G | 2 | a0001c0001t0008g0250 a0001c0001t0008g0251 |
2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1073-407A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71643412 | |||||||
| chr5:71643610 | G | A | 253 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(250): Show |
263 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.1073-209G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71643610 | |||||||
| chr5:71643645 | A | G | 1 | a0001c0001t0017g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1073-174A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71643645 | |||||||
| chr5:71643690 | A | T | 1 | a0001c0001t0009g0233 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1073-129A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71643690 | |||||||
| chr5:71643721 | G | C | 1 | a0001c0001t0018g0085 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1073-98G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71643721 | |||||||
| chr5:71643741 | G | A | 1 | a0001c0001t0002g0264 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1073-78G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 11/16 | chr5 | 71643741 | |||||||
| chr5:71643958 | A | G | 3 | a0001c0002t0003g0054 a0001c0002t0003g0055 a0001c0002t0003g0080 |
3 | NA18966.hp2 NA19081.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1149+63A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71643958 | |||||||
| chr5:71644032 | C | CGT | 3 | a0001c0001t0004g0104 a0001c0001t0008g0250 a0001c0001t0008g0251 |
3 | HG01433.hp1 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1149+137_1149+138i others(4): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71644032 | |||||||
| chr5:71644033 | A | ATG | 26 | a0001c0001t0001g0021 a0001c0001t0001g0105 a0001c0001t0001g0111 others(23): Show |
26 | HG00280.hp1 HG00438.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1149+175_1149+176d others(4): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr5 | 71644033 | ||||||
| chr5:71644033 | A | ATGTG | 144 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(141): Show |
150 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.1149+173_1149+176d others(6): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr5 | 71644033 | ||||||
| chr5:71644033 | A | ATGTGTG | 53 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0093 others(50): Show |
55 | HG00544.hp1 HG00544.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1149+171_1149+176d others(8): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr5 | 71644033 | ||||||
| chr5:71644033 | A | ATGTGTGT others(1): Show |
13 | a0001c0001t0001g0135 a0001c0001t0001g0172 a0001c0001t0002g0010 others(10): Show |
14 | HG00735.hp1 HG02155.hp1 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.1149+169_1149+176d others(10): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr5 | 71644033 | ||||||
| chr5:71644033 | A | ATGTGTGT others(3): Show |
16 | a0001c0001t0002g0022 a0001c0001t0004g0014 a0001c0001t0004g0034 others(13): Show |
16 | HG00140.hp2 HG00597.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1149+167_1149+176d others(12): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr5 | 71644033 | ||||||
| chr5:71644033 | A | ATGTGTGT others(5): Show |
1 | a0001c0001t0004g0078 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1149+165_1149+176d others(14): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr5 | 71644033 | ||||||
| chr5:71644033 | A | ATGTGTGT others(7): Show |
1 | a0001c0001t0004g0065 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1149+163_1149+176d others(16): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr5 | 71644033 | ||||||
| chr5:71644033 | A | ATGTGTGT others(9): Show |
1 | a0001c0001t0004g0067 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1149+161_1149+176d others(18): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr5 | 71644033 | ||||||
| chr5:71644033 | A | G | 11 | a0001c0001t0004g0104 a0001c0001t0006g0025 a0001c0001t0006g0206 others(8): Show |
11 | HG00733.hp2 HG00741.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.1149+138A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71644033 | |||||||
| chr5:71644033 | ATG | A | 4 | a0001c0001t0003g0211 a0001c0001t0010g0256 a0001c0001t0010g0336 others(1): Show |
4 | HG01192.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1149+175_1149+176d others(4): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr5 | 71644033 | ||||||
| chr5:71644060 | TGTGTGTG others(7): Show |
T | 2 | a0001c0001t0007g0195 a0001c0001t0007g0252 |
2 | HG00642.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1149+167_1149+180d others(16): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr5 | 71644060 | ||||||
| chr5:71644062 | TGTGTGTG others(5): Show |
T | 11 | a0001c0001t0002g0009 a0001c0001t0002g0220 a0001c0001t0002g0221 others(8): Show |
12 | HG02257.hp1 HG02572.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.1149+169_1149+180d others(14): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr5 | 71644062 | ||||||
| chr5:71644070 | T | C | 2 | a0001c0002t0003g0006 a0001c0002t0024g0027 |
2 | HG02647.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1149+175T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71644070 | |||||||
| chr5:71644070 | TGC | T | 5 | a0001c0001t0002g0060 a0001c0001t0002g0282 a0001c0001t0004g0238 others(2): Show |
5 | HG01255.hp1 HG02738.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1149+181_1149+182d others(4): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr5 | 71644070 | ||||||
| chr5:71644070 | TGCGC | T | 6 | a0001c0001t0006g0025 a0001c0001t0006g0206 a0001c0001t0006g0207 others(3): Show |
6 | HG00733.hp2 HG01884.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1149+179_1149+182d others(6): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr5 | 71644070 | ||||||
| chr5:71644072 | C | T | 258 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(255): Show |
267 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1149+177C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71644072 | |||||||
| chr5:71644074 | C | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(208): Show |
220 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.1149+179C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71644074 | |||||||
| chr5:71644466 | A | G | 1 | a0001c0002t0003g0035 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1149+571A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71644466 | |||||||
| chr5:71644747 | T | C | 2 | a0001c0001t0009g0233 a0001c0001t0009g0234 |
2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1149+852T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71644747 | |||||||
| chr5:71644976 | T | A | 6 | a0001c0001t0006g0025 a0001c0001t0006g0206 a0001c0001t0006g0207 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1149+1081T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71644976 | |||||||
| chr5:71645002 | G | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0167 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1149+1107G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71645002 | |||||||
| chr5:71645210 | G | A | 1 | a0001c0006t0002g0273 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1150-1001G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71645210 | |||||||
| chr5:71645254 | C | T | 10 | a0001c0001t0004g0058 a0001c0001t0004g0242 a0001c0001t0004g0243 others(7): Show |
10 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.1150-957C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71645254 | |||||||
| chr5:71645267 | G | A | 37 | a0001c0001t0002g0092 a0001c0001t0002g0231 a0001c0001t0003g0045 others(34): Show |
37 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1150-944G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71645267 | |||||||
| chr5:71645458 | T | G | 1 | a0001c0001t0001g0215 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1150-753T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71645458 | |||||||
| chr5:71645555 | A | G | 1 | a0001c0001t0002g0092 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1150-656A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71645555 | |||||||
| chr5:71645685 | C | T | 1 | a0001c0001t0002g0003 | 3 | HG00280.hp2 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1150-526C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71645685 | |||||||
| chr5:71646064 | T | TA | 272 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(269): Show |
282 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.1150-135dupA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr5 | 71646064 | ||||||
| chr5:71646106 | G | T | 2 | a0001c0001t0009g0233 a0001c0001t0009g0234 |
2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1150-105G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71646106 | |||||||
| chr5:71646135 | T | G | 1 | a0001c0002t0003g0035 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1150-76T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 12/16 | chr5 | 71646135 | |||||||
| chr5:71646338 | C | T | 2 | a0001c0001t0008g0250 a0001c0001t0008g0251 |
2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1216+61C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71646338 | |||||||
| chr5:71646440 | A | G | 3 | a0001c0001t0007g0195 a0001c0001t0007g0252 a0001c0001t0015g0020 |
3 | HG00642.hp1 HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1216+163A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71646440 | |||||||
| chr5:71646509 | G | A | 37 | a0001c0001t0002g0092 a0001c0001t0002g0231 a0001c0001t0003g0045 others(34): Show |
37 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1216+232G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71646509 | |||||||
| chr5:71646611 | C | T | 1 | a0001c0001t0002g0270 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1216+334C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71646611 | |||||||
| chr5:71646700 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1216+423A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71646700 | |||||||
| chr5:71646742 | T | G | 1 | a0001c0001t0014g0255 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1216+465T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71646742 | |||||||
| chr5:71646777 | A | G | 1 | a0001c0001t0002g0312 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1216+500A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71646777 | |||||||
| chr5:71646858 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0003g0049 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1216+581G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71646858 | |||||||
| chr5:71646928 | T | C | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1216+651T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71646928 | |||||||
| chr5:71647246 | G | A | 1 | a0001c0001t0002g0139 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1216+969G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71647246 | |||||||
| chr5:71647257 | G | A | 1 | a0001c0001t0014g0255 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1216+980G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71647257 | |||||||
| chr5:71647354 | A | G | 25 | a0001c0001t0004g0014 a0001c0001t0004g0034 a0001c0001t0004g0044 others(22): Show |
25 | HG00140.hp2 HG00597.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.1216+1077A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71647354 | |||||||
| chr5:71647400 | A | T | 1 | a0001c0001t0014g0255 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1216+1123A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71647400 | |||||||
| chr5:71647411 | T | C | 1 | a0001c0001t0002g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1216+1134T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71647411 | |||||||
| chr5:71647660 | G | T | 1 | a0001c0001t0019g0026 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1216+1383G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71647660 | |||||||
| chr5:71647920 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1217-1177C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71647920 | |||||||
| chr5:71647978 | T | G | 2 | a0001c0001t0007g0195 a0001c0001t0007g0252 |
2 | HG00642.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1217-1119T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71647978 | |||||||
| chr5:71648292 | G | C | 1 | a0001c0001t0001g0107 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1217-805G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71648292 | |||||||
| chr5:71648431 | T | C | 1 | a0001c0001t0001g0018 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1217-666T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71648431 | |||||||
| chr5:71648794 | G | A | 6 | a0001c0001t0006g0025 a0001c0001t0006g0206 a0001c0001t0006g0207 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1217-303G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71648794 | |||||||
| chr5:71648949 | T | C | 3 | a0001c0001t0003g0211 a0001c0001t0010g0256 a0001c0001t0010g0336 |
3 | HG02451.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1217-148T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71648949 | |||||||
| chr5:71648952 | C | T | 4 | a0001c0001t0006g0025 a0001c0001t0006g0206 a0001c0001t0006g0207 others(1): Show |
4 | HG01884.hp1 HG02559.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1217-145C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71648952 | |||||||
| chr5:71649018 | C | T | 2 | a0001c0001t0008g0250 a0001c0001t0008g0251 |
2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1217-79C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71649018 | |||||||
| chr5:71649090 | C | G | 1 | a0001c0002t0024g0027 | 1 | HG02647.hp2 | splice_region_variant&intron_variant | LOW | c.1217-7C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 13/16 | chr5 | 71649090 | |||||||
| chr5:71649344 | A | C | 1 | a0001c0001t0002g0229 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1373+91A>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 14/16 | chr5 | 71649344 | |||||||
| chr5:71649356 | G | C | 1 | a0001c0001t0002g0290 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1373+103G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 14/16 | chr5 | 71649356 | |||||||
| chr5:71649384 | A | G | 1 | a0001c0001t0014g0255 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1373+131A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 14/16 | chr5 | 71649384 | |||||||
| chr5:71649626 | C | T | 1 | a0001c0001t0002g0328 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1373+373C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 14/16 | chr5 | 71649626 | |||||||
| chr5:71649636 | G | A | 2 | a0001c0001t0009g0233 a0001c0001t0009g0234 |
2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1373+383G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 14/16 | chr5 | 71649636 | |||||||
| chr5:71649814 | C | G | 1 | a0001c0001t0001g0317 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1374-255C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 14/16 | chr5 | 71649814 | |||||||
| chr5:71650024 | T | C | 1 | a0001c0001t0001g0295 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1374-45T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 14/16 | chr5 | 71650024 | |||||||
| chr5:71650286 | G | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(114): Show |
121 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1488+103G>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71650286 | |||||||
| chr5:71650296 | G | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): Show |
118 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.1488+113G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71650296 | |||||||
| chr5:71650444 | C | T | 1 | a0001c0001t0004g0034 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1488+261C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71650444 | |||||||
| chr5:71650495 | C | T | 224 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(221): Show |
234 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.1488+312C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71650495 | |||||||
| chr5:71650496 | G | T | 3 | a0001c0001t0004g0208 a0001c0001t0004g0209 a0001c0001t0004g0210 |
3 | HG02886.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1488+313G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71650496 | |||||||
| chr5:71650503 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1488+320C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71650503 | |||||||
| chr5:71650641 | T | TTTTA | 3 | a0001c0001t0004g0208 a0001c0001t0004g0209 a0001c0001t0004g0210 |
3 | HG02886.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1488+478_1488+481d others(6): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr5 | 71650641 | ||||||
| chr5:71650680 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1488+497G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71650680 | |||||||
| chr5:71650712 | G | A | 48 | a0001c0001t0002g0092 a0001c0001t0002g0231 a0001c0001t0002g0279 others(45): Show |
48 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1488+529G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71650712 | |||||||
| chr5:71650718 | G | A | 2 | a0001c0003t0003g0193 a0001c0003t0003g0225 |
2 | HG01167.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1488+535G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71650718 | |||||||
| chr5:71650758 | T | C | 1 | a0001c0001t0002g0307 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1488+575T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71650758 | |||||||
| chr5:71650809 | T | C | 285 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(282): Show |
295 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.1488+626T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71650809 | |||||||
| chr5:71650885 | G | T | 1 | a0001c0001t0008g0251 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1488+702G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71650885 | |||||||
| chr5:71651046 | T | C | 275 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(272): Show |
285 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.1488+863T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71651046 | |||||||
| chr5:71651047 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1488+864G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71651047 | |||||||
| chr5:71651323 | G | GA | 3 | a0001c0001t0007g0195 a0001c0001t0007g0252 a0001c0001t0015g0020 |
3 | HG00642.hp1 HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1488+1143dupA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr5 | 71651323 | ||||||
| chr5:71651423 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1488+1240G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71651423 | |||||||
| chr5:71651459 | T | C | 274 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(271): Show |
284 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.1489-1210T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71651459 | |||||||
| chr5:71651474 | T | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(221): Show |
234 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.1489-1195T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71651474 | |||||||
| chr5:71651690 | T | C | 1 | a0001c0001t0002g0222 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1489-979T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71651690 | |||||||
| chr5:71651723 | T | C | 2 | a0001c0001t0009g0233 a0001c0001t0009g0234 |
2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1489-946T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71651723 | |||||||
| chr5:71651837 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1489-832C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71651837 | |||||||
| chr5:71652194 | T | C | 1 | a0001c0007t0002g0191 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1489-475T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71652194 | |||||||
| chr5:71652436 | C | T | 268 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(265): Show |
278 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.1489-233C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71652436 | |||||||
| chr5:71652558 | T | G | 268 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(265): Show |
278 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.1489-111T>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 15/16 | chr5 | 71652558 | |||||||
| chr5:71652827 | G | A | 274 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(271): Show |
284 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.1574+73G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71652827 | |||||||
| chr5:71652991 | G | A | 90 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0010 others(87): Show |
95 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1574+237G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71652991 | |||||||
| chr5:71653052 | G | T | 1 | a0001c0001t0001g0155 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1574+298G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71653052 | |||||||
| chr5:71653218 | C | T | 268 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(265): Show |
278 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.1574+464C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71653218 | |||||||
| chr5:71653282 | C | A | 1 | a0001c0001t0007g0195 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1574+528C>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71653282 | |||||||
| chr5:71653383 | T | TC | 3 | a0001c0001t0003g0211 a0001c0001t0010g0256 a0001c0001t0010g0336 |
3 | HG02451.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1574+630dupC | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr5 | 71653383 | ||||||
| chr5:71653418 | A | AGACTAAT others(51): Show |
1 | a0001c0001t0002g0270 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1574+665_1574+722d others(60): Show |
MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr5 | 71653418 | ||||||
| chr5:71653593 | T | A | 4 | a0001c0001t0002g0060 a0001c0001t0002g0071 a0001c0001t0002g0082 others(1): Show |
4 | NA18943.hp2 NA18948.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.1574+839T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71653593 | |||||||
| chr5:71653628 | T | C | 3 | a0001c0001t0004g0208 a0001c0001t0004g0209 a0001c0001t0004g0210 |
3 | HG02886.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1574+874T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71653628 | |||||||
| chr5:71653651 | A | T | 1 | a0001c0001t0002g0272 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1574+897A>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71653651 | |||||||
| chr5:71653678 | G | A | 1 | a0001c0001t0004g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1574+924G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71653678 | |||||||
| chr5:71653823 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1574+1069C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71653823 | |||||||
| chr5:71653850 | CA | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(266): Show |
279 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.1574+1113delA | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr5 | 71653850 | ||||||
| chr5:71654086 | C | T | 1 | a0003c0008t0006g0079 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1574+1332C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71654086 | |||||||
| chr5:71654091 | G | A | 3 | a0001c0001t0007g0195 a0001c0001t0007g0252 a0001c0001t0015g0020 |
3 | HG00642.hp1 HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1574+1337G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71654091 | |||||||
| chr5:71654466 | T | A | 8 | a0001c0001t0004g0194 a0001c0001t0004g0205 a0001c0001t0004g0235 others(5): Show |
8 | HG02717.hp1 HG02896.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1574+1712T>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71654466 | |||||||
| chr5:71654479 | A | G | 1 | a0001c0001t0004g0058 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1574+1725A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71654479 | |||||||
| chr5:71654557 | G | T | 1 | a0001c0001t0014g0255 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1574+1803G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71654557 | |||||||
| chr5:71654763 | G | A | 3 | a0001c0001t0007g0195 a0001c0001t0007g0252 a0001c0001t0015g0020 |
3 | HG00642.hp1 HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1575-1980G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71654763 | |||||||
| chr5:71654836 | G | T | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1575-1907G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71654836 | |||||||
| chr5:71654837 | A | AT | 6 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0184 others(3): Show |
6 | HG00673.hp2 HG01978.hp1 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.1575-1888dupT | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr5 | 71654837 | ||||||
| chr5:71654911 | T | C | 284 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(281): Show |
294 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.1575-1832T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71654911 | |||||||
| chr5:71654959 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1575-1784C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71654959 | |||||||
| chr5:71654992 | G | A | 1 | a0001c0001t0014g0255 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1575-1751G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71654992 | |||||||
| chr5:71655080 | C | T | 3 | a0001c0001t0003g0211 a0001c0001t0010g0256 a0001c0001t0010g0336 |
3 | HG02451.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1575-1663C>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71655080 | |||||||
| chr5:71655105 | A | G | 1 | a0001c0001t0002g0312 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1575-1638A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71655105 | |||||||
| chr5:71655114 | A | G | 1 | a0001c0001t0019g0026 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1575-1629A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71655114 | |||||||
| chr5:71655220 | C | A | 1 | a0001c0001t0002g0312 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1575-1523C>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71655220 | |||||||
| chr5:71655405 | T | C | 3 | a0001c0001t0002g0231 a0001c0001t0019g0026 a0001c0007t0002g0191 |
3 | HG00741.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1575-1338T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71655405 | |||||||
| chr5:71655406 | C | G | 271 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(268): Show |
281 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.1575-1337C>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71655406 | |||||||
| chr5:71655471 | G | T | 3 | a0001c0001t0007g0195 a0001c0001t0007g0252 a0001c0001t0015g0020 |
3 | HG00642.hp1 HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1575-1272G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71655471 | |||||||
| chr5:71655826 | A | G | 19 | a0001c0001t0002g0279 a0001c0001t0004g0058 a0001c0001t0004g0194 others(16): Show |
19 | HG01433.hp2 HG01978.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.1575-917A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71655826 | |||||||
| chr5:71656104 | G | T | 272 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(269): Show |
282 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.1575-639G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71656104 | |||||||
| chr5:71656154 | G | T | 1 | a0001c0001t0002g0092 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1575-589G>T | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71656154 | |||||||
| chr5:71656356 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1575-387G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71656356 | |||||||
| chr5:71656543 | T | C | 1 | a0001c0001t0002g0299 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1575-200T>C | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71656543 | |||||||
| chr5:71656590 | G | A | 2 | a0001c0001t0008g0250 a0001c0001t0008g0251 |
2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1575-153G>A | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71656590 | |||||||
| chr5:71656639 | A | G | 1 | a0001c0002t0002g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1575-104A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71656639 | |||||||
| chr5:71656679 | A | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(237): Show |
250 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.1575-64A>G | MCCC2 | ENSG00000131844.17 | transcript | ENST00000340941.11 | protein_coding | 16/16 | chr5 | 71656679 |