Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 56922 |
| ensemblid | ENSG00000078070.14 |
| hgncid | 6936 |
| symbol | MCCC1 |
| name | methylcrotonyl-CoA carboxylase subunit 1 |
| refseq_nuc | NM_020166.5 |
| refseq_prot | NP_064551.3 |
| ensembl_nuc | ENST00000265594.9 |
| ensembl_prot | ENSP00000265594.4 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 183015218 |
| end | 183099496 |
| strand | - |
| ver | v1.2 |
| region | chr3:183015218-183099496 |
| region5000 | chr3:183010218-183104496 |
| regionname0 | MCCC1_chr3_183015218_183099496 |
| regionname5000 | MCCC1_chr3_183010218_183104496 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 725 | 198 | 70 | 24 | 84 | 2 | 17 | 70 | MCCC1_chr3_183010218_183104496 | MCCC1 | MAAAS others(720): Show |
chr3 | 183010218 | 183104496 |
| a0002 | 0/1 | 725 | 138 | 16 | 38 | 60 | 6 | 17 | 42 | MCCC1_chr3_183010218_183104496 | MCCC1 | MAAAS others(720): Show |
chr3 | 183010218 | 183104496 |
| a0003 | 0/0 | 725 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | MAAAS others(720): Show |
chr3 | 183010218 | 183104496 |
| a0004 | 0/0 | 725 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | MAAAS others(720): Show |
chr3 | 183010218 | 183104496 |
| a0005 | 0/0 | 725 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MCCC1_chr3_183010218_183104496 | MCCC1 | MAAAS others(720): Show |
chr3 | 183010218 | 183104496 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2175 | 169 | 50 | 22 | 81 | 1 | 15 | MCCC1_chr3_183010218_183104496 | MCCC1 | ATGGC others(2170): Show |
chr3 | 183010218 | 183104496 | ||
| a0001c0003 | 1/0 | 2175 | 25 | 19 | 2 | 0 | 1 | 2 | MCCC1_chr3_183010218_183104496 | MCCC1 | ATGGC others(2170): Show |
chr3 | 183010218 | 183104496 | ||
| a0001c0009 | 0/0 | 2175 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | ATGGC others(2170): Show |
chr3 | 183010218 | 183104496 | ||
| a0001c0010 | 0/0 | 2175 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | ATGGC others(2170): Show |
chr3 | 183010218 | 183104496 | ||
| a0001c0011 | 0/0 | 2175 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | ATGGC others(2170): Show |
chr3 | 183010218 | 183104496 | ||
| a0001c0013 | 0/0 | 2175 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | ATGGC others(2170): Show |
chr3 | 183010218 | 183104496 | ||
| a0002c0002 | 0/1 | 2175 | 136 | 15 | 38 | 59 | 6 | 17 | MCCC1_chr3_183010218_183104496 | MCCC1 | ATGGC others(2170): Show |
chr3 | 183010218 | 183104496 | ||
| a0002c0008 | 0/0 | 2175 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | ATGGC others(2170): Show |
chr3 | 183010218 | 183104496 | ||
| a0002c0012 | 0/0 | 2175 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | ATGGC others(2170): Show |
chr3 | 183010218 | 183104496 | ||
| a0003c0005 | 0/0 | 2175 | 2 | 2 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | ATGGC others(2170): Show |
chr3 | 183010218 | 183104496 | ||
| a0003c0007 | 0/0 | 2175 | 2 | 2 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | ATGGC others(2170): Show |
chr3 | 183010218 | 183104496 | ||
| a0004c0004 | 0/0 | 2175 | 2 | 2 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | ATGGC others(2170): Show |
chr3 | 183010218 | 183104496 | ||
| a0005c0006 | 0/0 | 2175 | 2 | 0 | 0 | 2 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | ATGGC others(2170): Show |
chr3 | 183010218 | 183104496 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2454 | 168 | 49 | 22 | 81 | 1 | 15 | MCCC1_chr3_183010218_183104496 | MCCC1 | GTGGG others(2449): Show |
chr3 | 183010218 | 183104496 |
| a0001c0001t0002 | 0/0 | 2454 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | GTGGG others(2449): Show |
chr3 | 183010218 | 183104496 |
| a0001c0003t0001 | 1/0 | 2454 | 25 | 19 | 2 | 0 | 1 | 2 | MCCC1_chr3_183010218_183104496 | MCCC1 | GTGGG others(2449): Show |
chr3 | 183010218 | 183104496 |
| a0001c0009t0001 | 0/0 | 2454 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | GTGGG others(2449): Show |
chr3 | 183010218 | 183104496 |
| a0001c0010t0001 | 0/0 | 2454 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | GTGGG others(2449): Show |
chr3 | 183010218 | 183104496 |
| a0001c0011t0001 | 0/0 | 2454 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | GTGGG others(2449): Show |
chr3 | 183010218 | 183104496 |
| a0001c0013t0001 | 0/0 | 2454 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | GTGGG others(2449): Show |
chr3 | 183010218 | 183104496 |
| a0002c0002t0001 | 0/1 | 2454 | 136 | 15 | 38 | 59 | 6 | 17 | MCCC1_chr3_183010218_183104496 | MCCC1 | GTGGG others(2449): Show |
chr3 | 183010218 | 183104496 |
| a0002c0008t0003 | 0/0 | 2454 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | GTGGG others(2449): Show |
chr3 | 183010218 | 183104496 |
| a0002c0012t0001 | 0/0 | 2454 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | GTGGG others(2449): Show |
chr3 | 183010218 | 183104496 |
| a0003c0005t0001 | 0/0 | 2454 | 2 | 2 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | GTGGG others(2449): Show |
chr3 | 183010218 | 183104496 |
| a0003c0007t0001 | 0/0 | 2454 | 2 | 2 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | GTGGG others(2449): Show |
chr3 | 183010218 | 183104496 |
| a0004c0004t0001 | 0/0 | 2454 | 2 | 2 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | GTGGG others(2449): Show |
chr3 | 183010218 | 183104496 |
| a0005c0006t0001 | 0/0 | 2454 | 2 | 0 | 0 | 2 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | GTGGG others(2449): Show |
chr3 | 183010218 | 183104496 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0003t0001g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0003t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0003t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0003t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0003t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0003t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0003t0001g0194 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0003t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0003t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0003t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0003t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0003t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0003t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0009t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0010t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0011t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0001c0013t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0009 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0324 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0008t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0002c0012t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0003c0005t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0003c0005t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0003c0007t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0003c0007t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0004c0004t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0004c0004t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0005c0006t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| a0005c0006t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0113 | EUR | FIN | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0279 | EUR | FIN | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0260 | EUR | FIN | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG00323 | hp2 | a0001 | c0003 | t0001 | g0115 | EUR | FIN | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0330 | EAS | CHS | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0308 | EAS | CHS | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | CHS | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0134 | EAS | CHS | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0281 | EAS | CHS | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | CHS | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0288 | AMR | PUR | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0278 | AMR | PUR | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0311 | AMR | PUR | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0312 | AMR | PUR | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0293 | AMR | PUR | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0140 | AMR | PUR | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0061 | AMR | PUR | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0092 | AMR | PUR | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0071 | AMR | PUR | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0091 | AMR | PUR | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0084 | AMR | PUR | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0306 | AMR | PUR | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0112 | AMR | PUR | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0284 | AMR | PUR | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0083 | AMR | PUR | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0294 | AMR | PUR | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0291 | AMR | CLM | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0307 | AMR | CLM | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0266 | AMR | CLM | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0315 | AMR | CLM | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0318 | AMR | CLM | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0060 | AMR | CLM | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0320 | AMR | CLM | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0080 | AMR | CLM | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01496 | hp2 | a0001 | c0003 | t0001 | g0093 | AMR | CLM | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0114 | AFR | ACB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0070 | AFR | ACB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0209 | AFR | ACB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0290 | AMR | PEL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0135 | AMR | PEL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0136 | AMR | PEL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0287 | AMR | PEL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0283 | AMR | PEL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0130 | AMR | PEL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0295 | AMR | PEL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0138 | AMR | PEL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PEL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0289 | EAS | KHV | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0120 | EAS | KHV | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | KHV | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0280 | EAS | KHV | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0116 | EAS | KHV | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0321 | EAS | KHV | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | KHV | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | KHV | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02083 | hp2 | a0001 | c0009 | t0001 | g0310 | EAS | KHV | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0323 | EAS | KHV | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0095 | AFR | ACB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0139 | AMR | PEL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0124 | AMR | PEL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | CDX | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CDX | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0205 | AFR | ACB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0143 | AFR | ACB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02280 | hp1 | a0002 | c0008 | t0003 | g0331 | AFR | ACB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0304 | AFR | ACB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0118 | AMR | PEL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0137 | AMR | PEL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02300 | hp2 | a0001 | c0003 | t0001 | g0094 | AMR | PEL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0207 | AFR | ACB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0282 | SAS | PJL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0001 | AFR | GWD | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0079 | AFR | GWD | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0301 | SAS | PJL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0082 | AFR | GWD | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02818 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | GWD | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0142 | AFR | GWD | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02895 | hp1 | a0003 | c0005 | t0001 | g0035 | AFR | GWD | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02895 | hp2 | a0004 | c0004 | t0001 | g0329 | AFR | GWD | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02897 | hp2 | a0004 | c0004 | t0001 | g0328 | AFR | GWD | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0007 | AFR | ESN | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0144 | AFR | ESN | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02965 | hp2 | a0003 | c0007 | t0001 | g0033 | AFR | ESN | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0206 | AFR | ESN | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02970 | hp2 | a0003 | c0007 | t0001 | g0034 | AFR | ESN | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0011 | AFR | ESN | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0259 | SAS | PJL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0141 | AFR | GWD | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | ESN | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0326 | AFR | ESN | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0078 | AFR | ESN | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | ESN | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0077 | AFR | ESN | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0011 | AFR | MSL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03453 | hp2 | a0003 | c0005 | t0001 | g0036 | AFR | MSL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03486 | hp2 | a0001 | c0003 | t0001 | g0040 | AFR | MSL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0009 | SAS | PJL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0208 | AFR | ESN | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03579 | hp1 | a0001 | c0010 | t0001 | g0024 | AFR | MSL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0298 | SAS | STU | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03688 | hp2 | a0001 | c0003 | t0001 | g0196 | SAS | STU | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0074 | SAS | PJL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0072 | SAS | BEB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0297 | SAS | BEB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03927 | hp1 | a0001 | c0003 | t0001 | g0195 | SAS | BEB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0299 | SAS | BEB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0261 | SAS | STU | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0309 | SAS | STU | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0041 | SAS | BEB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | STU | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0305 | SAS | STU | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | STU | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0303 | SAS | STU | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | STU | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | STU | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18612 | hp1 | a0002 | c0012 | t0001 | g0217 | EAS | CHB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0302 | EAS | CHB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | YRI | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0001 | AFR | YRI | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0242 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0240 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18960 | hp1 | a0005 | c0006 | t0001 | g0069 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18965 | hp1 | a0001 | c0013 | t0001 | g0319 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0317 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18972 | hp1 | a0001 | c0011 | t0001 | g0174 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0314 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18985 | hp2 | a0005 | c0006 | t0001 | g0075 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18987 | hp2 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0243 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19078 | hp2 | a0002 | c0002 | t0001 | g0316 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0241 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0247 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0007 | AFR | YRI | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ASW | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0081 | AFR | ASW | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0296 | EUR | TSI | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0262 | EUR | TSI | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0258 | EUR | TSI | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0292 | EUR | TSI | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | GIH | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0068 | SAS | GIH | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0076 | AFR | ACB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0327 | AFR | ACB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | USA | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0204 | AFR | USA | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0055 | AFR | USA | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | USA | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0096 | AFR | LWK | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | LWK | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0324 | REF | REF | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0001 | g0194 | REF | REF | MCCC1_chr3_183010218_183104496 | MCCC1 | chr3 | 183010218 | 183104496 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:183020213 | G | A | 1 | a0005 | 2 | NA18960.hp1 NA18985.hp2 |
missense_variant | MODERATE | c.1894C>T | p.Pro632Ser | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/19 | 1950/2454 | 1894/2178 | 632/725 | chr3 | 183020213 | |||
| chr3:183037313 | C | T | 1 | a0003 | 4 | HG02895.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
missense_variant | MODERATE | c.1499G>A | p.Arg500Gln | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/19 | 1555/2454 | 1499/2178 | 500/725 | chr3 | 183037313 | |||
| chr3:183037421 | T | G | 2 | a0002 a0005 |
139 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(136): Show |
missense_variant | MODERATE | c.1391A>C | p.His464Pro | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/19 | 1447/2454 | 1391/2178 | 464/725 | chr3 | 183037421 | |||
| chr3:183039101 | A | C | 1 | a0004 | 2 | HG02895.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.1302T>G | p.Ile434Met | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 12/19 | 1358/2454 | 1302/2178 | 434/725 | chr3 | 183039101 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:183022447 | G | T | 1 | a0001c0011 | 1 | NA18972.hp1 | synonymous_variant | LOW | c.1839C>A | p.Ile613Ile | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 16/19 | 1895/2454 | 1839/2178 | 613/725 | chr3 | 183022447 | |||
| chr3:183022513 | G | A | 1 | a0002c0012 | 1 | NA18612.hp1 | synonymous_variant | LOW | c.1773C>T | p.Ser591Ser | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 16/19 | 1829/2454 | 1773/2178 | 591/725 | chr3 | 183022513 | |||
| chr3:183034058 | C | T | 1 | a0001c0010 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.1614G>A | p.Ser538Ser | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/19 | 1670/2454 | 1614/2178 | 538/725 | chr3 | 183034058 | |||
| chr3:183052169 | A | G | 1 | a0001c0009 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.945T>C | p.Tyr315Tyr | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/19 | 1001/2454 | 945/2178 | 315/725 | chr3 | 183052169 | |||
| chr3:183072461 | G | A | 10 | a0001c0001 a0001c0009 a0001c0010 others(7): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
synonymous_variant | LOW | c.396C>T | p.Leu132Leu | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 5/19 | 452/2454 | 396/2178 | 132/725 | chr3 | 183072461 | |||
| chr3:183072473 | T | G | 1 | a0003c0007 | 2 | HG02965.hp2 HG02970.hp2 |
synonymous_variant | LOW | c.384A>C | p.Gly128Gly | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 5/19 | 440/2454 | 384/2178 | 128/725 | chr3 | 183072473 | |||
| chr3:183092538 | G | A | 1 | a0001c0013 | 1 | NA18965.hp1 | synonymous_variant | LOW | c.144C>T | p.Asn48Asn | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/19 | 200/2454 | 144/2178 | 48/725 | chr3 | 183092538 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:183015432 | T | G | 1 | a0001c0001t0002 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 19/19 | 6 | chr3 | 183015432 | ||||||
| chr3:183099464 | T | C | 1 | a0002c0008t0003 | 1 | HG02280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-24A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/19 | 24 | chr3 | 183099464 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:183015644 | G | T | 1 | a0002c0002t0001g0262 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2050-78C>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 18/18 | chr3 | 183015644 | |||||||
| chr3:183015759 | T | C | 133 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(130): Show |
138 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.2050-193A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 18/18 | chr3 | 183015759 | |||||||
| chr3:183015911 | G | GT | 20 | a0001c0001t0001g0002 a0001c0001t0001g0053 a0001c0001t0001g0064 others(17): Show |
21 | HG00642.hp2 HG00735.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.2050-346dupA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 18/18 | chr3 | 183015911 | |||||||
| chr3:183015918 | T | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2050-352A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 18/18 | chr3 | 183015918 | |||||||
| chr3:183015924 | TG | T | 8 | a0001c0001t0001g0043 a0001c0001t0001g0154 a0001c0001t0001g0165 others(5): Show |
8 | HG00423.hp1 HG02132.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.2050-359delC | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 18/18 | chr3 | 183015924 | |||||||
| chr3:183015925 | G | T | 98 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0042 others(95): Show |
100 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.2050-359C>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 18/18 | chr3 | 183015925 | |||||||
| chr3:183015929 | T | G | 3 | a0001c0001t0001g0054 a0001c0001t0001g0086 a0001c0001t0001g0263 |
3 | HG01081.hp1 HG02886.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2050-363A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 18/18 | chr3 | 183015929 | |||||||
| chr3:183016113 | A | G | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.2050-547T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 18/18 | chr3 | 183016113 | |||||||
| chr3:183016299 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2050-733G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 18/18 | chr3 | 183016299 | |||||||
| chr3:183016354 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2050-788G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 18/18 | chr3 | 183016354 | |||||||
| chr3:183016480 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2049+786G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 18/18 | chr3 | 183016480 | |||||||
| chr3:183016584 | T | A | 14 | a0002c0002t0001g0262 a0002c0002t0001g0278 a0002c0002t0001g0279 others(11): Show |
14 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.2049+682A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 18/18 | chr3 | 183016584 | |||||||
| chr3:183016681 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2049+585C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 18/18 | chr3 | 183016681 | |||||||
| chr3:183016693 | C | A | 106 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0042 others(103): Show |
108 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(105): Show |
intron_variant | MODIFIER | c.2049+573G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 18/18 | chr3 | 183016693 | |||||||
| chr3:183016694 | G | A | 6 | a0001c0001t0001g0020 a0001c0010t0001g0024 a0003c0005t0001g0035 others(3): Show |
6 | HG02109.hp2 HG02895.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2049+572C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 18/18 | chr3 | 183016694 | |||||||
| chr3:183016991 | C | G | 1 | a0002c0002t0001g0141 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2049+275G>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 18/18 | chr3 | 183016991 | |||||||
| chr3:183017029 | A | G | 1 | a0002c0008t0003g0331 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2049+237T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 18/18 | chr3 | 183017029 | |||||||
| chr3:183017235 | C | T | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.2049+31G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 18/18 | chr3 | 183017235 | |||||||
| chr3:183017358 | G | A | 1 | a0002c0002t0001g0285 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1978-21C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183017358 | |||||||
| chr3:183017394 | C | A | 317 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(314): Show |
329 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.1978-57G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183017394 | |||||||
| chr3:183017423 | T | G | 106 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0042 others(103): Show |
108 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(105): Show |
intron_variant | MODIFIER | c.1978-86A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183017423 | |||||||
| chr3:183017523 | C | T | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1978-186G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183017523 | |||||||
| chr3:183017531 | G | T | 32 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0056 others(29): Show |
33 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.1978-194C>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183017531 | |||||||
| chr3:183017624 | A | T | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1978-287T>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183017624 | |||||||
| chr3:183017654 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1978-317G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183017654 | |||||||
| chr3:183017666 | C | CAGAGGCC others(785): Show |
1 | a0001c0001t0001g0086 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1978-330_1978-329i others(794): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183017666 | |||||||
| chr3:183017706 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1978-369A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183017706 | |||||||
| chr3:183017723 | A | T | 1 | a0001c0001t0001g0086 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1978-386T>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183017723 | |||||||
| chr3:183017733 | T | A | 1 | a0001c0001t0001g0086 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1978-396A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183017733 | |||||||
| chr3:183017737 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1978-400T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183017737 | |||||||
| chr3:183017819 | T | TACTGGTC others(59): Show |
1 | a0001c0001t0001g0086 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1978-483_1978-482i others(68): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183017819 | |||||||
| chr3:183017819 | T | TACTGGTC others(26): Show |
31 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0056 others(28): Show |
32 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.1978-515_1978-483d others(35): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183017819 | |||||||
| chr3:183017819 | T | TACTGGTC others(587): Show |
1 | a0001c0001t0001g0270 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1978-483_1978-482i others(596): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183017819 | |||||||
| chr3:183017819 | T | TACTGGTC others(1214): Show |
3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG02717.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1978-483_1978-482i others(1223): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183017819 | |||||||
| chr3:183017819 | T | TACTGGTC others(92): Show |
123 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0042 others(120): Show |
125 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.1978-483_1978-482i others(101): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183017819 | |||||||
| chr3:183017819 | T | TACTGGTC others(653): Show |
143 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(140): Show |
148 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.1978-483_1978-482i others(662): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183017819 | |||||||
| chr3:183017819 | T | TACTGGTC others(686): Show |
6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG02258.hp1 HG02615.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1978-483_1978-482i others(695): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183017819 | |||||||
| chr3:183017963 | C | CAGAGGCC others(125): Show |
1 | a0001c0001t0001g0173 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1978-758_1978-627d others(134): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183017963 | |||||||
| chr3:183018087 | C | G | 1 | a0001c0001t0001g0044 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1978-750G>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018087 | |||||||
| chr3:183018095 | A | C | 1 | a0001c0001t0001g0044 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1978-758T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018095 | |||||||
| chr3:183018098 | A | T | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG02717.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1978-761T>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018098 | |||||||
| chr3:183018195 | A | G | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0173 |
3 | HG02647.hp2 HG03540.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.1978-858T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018195 | |||||||
| chr3:183018219 | G | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
4 | HG02896.hp1 HG03098.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1978-882C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018219 | |||||||
| chr3:183018248 | C | CACTGGTC others(1279): Show |
1 | a0002c0002t0001g0151 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1978-912_1978-911i others(1288): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018248 | |||||||
| chr3:183018248 | C | CACTGGTC others(1280): Show |
1 | a0002c0002t0001g0123 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1978-912_1978-911i others(1289): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018248 | |||||||
| chr3:183018248 | C | CACTGGTC others(1148): Show |
2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | NA18747.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1978-912_1978-911i others(1157): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018248 | |||||||
| chr3:183018248 | C | CACTGGTC others(983): Show |
2 | a0001c0001t0001g0265 a0001c0001t0001g0269 |
2 | NA18953.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1978-912_1978-911i others(992): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018248 | |||||||
| chr3:183018248 | C | CACTGGTC others(983): Show |
16 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0220 others(13): Show |
16 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(13): Show |
intron_variant | MODIFIER | c.1978-912_1978-911i others(992): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018248 | |||||||
| chr3:183018248 | C | CACTGGTC others(1280): Show |
8 | a0002c0002t0001g0051 a0002c0002t0001g0118 a0002c0002t0001g0122 others(5): Show |
8 | HG00438.hp1 HG00544.hp1 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.1978-912_1978-911i others(1289): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018248 | |||||||
| chr3:183018248 | C | CACTGGTC others(752): Show |
1 | a0002c0002t0001g0300 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1978-912_1978-911i others(761): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018248 | |||||||
| chr3:183018248 | C | CACTGGTC others(983): Show |
7 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(4): Show |
7 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.1978-912_1978-911i others(992): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018248 | |||||||
| chr3:183018261 | A | AGAGGCCT others(26): Show |
3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0173 |
3 | HG02647.hp2 HG03540.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.1978-925_1978-924i others(35): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018261 | |||||||
| chr3:183018273 | G | C | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0227 |
3 | HG01255.hp2 HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1978-936C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018273 | |||||||
| chr3:183018274 | T | C | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0227 |
3 | HG01255.hp2 HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1978-937A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018274 | |||||||
| chr3:183018314 | T | C | 41 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0173 others(38): Show |
41 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.1978-977A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018314 | |||||||
| chr3:183018314 | T | TACTGGTC others(983): Show |
3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0227 |
3 | HG01255.hp2 HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1978-978_1978-977i others(992): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018314 | |||||||
| chr3:183018413 | C | CACTGGTC others(422): Show |
3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG02717.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1978-1077_1978-107 others(433): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018413 | |||||||
| chr3:183018413 | C | CACTGGTC others(422): Show |
2 | a0002c0002t0001g0060 a0002c0002t0001g0061 |
2 | HG01069.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1978-1077_1978-107 others(433): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018413 | |||||||
| chr3:183018413 | C | CACTGGTC others(422): Show |
99 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(96): Show |
102 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1978-1077_1978-107 others(433): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018413 | |||||||
| chr3:183018413 | C | CACTGGTC others(422): Show |
1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1978-1077_1978-107 others(433): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018413 | |||||||
| chr3:183018413 | C | CACTGGTC others(422): Show |
1 | a0001c0001t0001g0044 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1978-1077_1978-107 others(433): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018413 | |||||||
| chr3:183018413 | C | CACTGGTC others(422): Show |
103 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0042 others(100): Show |
105 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.1978-1077_1978-107 others(433): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018413 | |||||||
| chr3:183018413 | C | CACTGGTC others(719): Show |
1 | a0002c0008t0003g0331 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1978-1077_1978-107 others(730): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018413 | |||||||
| chr3:183018413 | C | CACTGGTC others(719): Show |
50 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(47): Show |
53 | HG00408.hp1 HG01069.hp1 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.1978-1077_1978-107 others(730): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018413 | |||||||
| chr3:183018413 | C | CACTGGTC others(422): Show |
4 | a0003c0005t0001g0035 a0003c0005t0001g0036 a0003c0007t0001g0033 others(1): Show |
4 | HG02895.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1978-1077_1978-107 others(433): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018413 | |||||||
| chr3:183018413 | C | T | 44 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(41): Show |
44 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.1978-1076G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018413 | |||||||
| chr3:183018516 | A | G | 317 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(314): Show |
329 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.1978-1179T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018516 | |||||||
| chr3:183018625 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1978-1288T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018625 | |||||||
| chr3:183018662 | CA | C | 61 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(58): Show |
64 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1978-1326delT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018662 | |||||||
| chr3:183018712 | T | A | 1 | a0001c0013t0001g0319 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1978-1375A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018712 | |||||||
| chr3:183018725 | T | C | 1 | a0001c0001t0001g0171 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1978-1388A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018725 | |||||||
| chr3:183018823 | A | G | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1977+1307T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018823 | |||||||
| chr3:183018863 | C | A | 5 | a0001c0010t0001g0024 a0003c0005t0001g0035 a0003c0005t0001g0036 others(2): Show |
5 | HG02895.hp1 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1977+1267G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183018863 | |||||||
| chr3:183019107 | C | T | 1 | a0002c0002t0001g0138 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1977+1023G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183019107 | |||||||
| chr3:183019127 | A | C | 1 | a0001c0001t0001g0233 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1977+1003T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183019127 | |||||||
| chr3:183019269 | C | T | 4 | a0001c0003t0001g0001 a0001c0003t0001g0204 a0001c0003t0001g0205 others(1): Show |
7 | HG02257.hp2 HG02615.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1977+861G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183019269 | |||||||
| chr3:183019309 | G | C | 1 | a0001c0001t0001g0325 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1977+821C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183019309 | |||||||
| chr3:183019420 | A | T | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1977+710T>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183019420 | |||||||
| chr3:183019433 | C | T | 1 | a0001c0010t0001g0024 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1977+697G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183019433 | |||||||
| chr3:183019482 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1977+648C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183019482 | |||||||
| chr3:183019587 | A | C | 2 | a0005c0006t0001g0069 a0005c0006t0001g0075 |
2 | NA18960.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.1977+543T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183019587 | |||||||
| chr3:183019690 | C | T | 1 | a0002c0002t0001g0288 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1977+440G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183019690 | |||||||
| chr3:183019721 | A | G | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1977+409T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183019721 | |||||||
| chr3:183019742 | C | T | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.1977+388G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183019742 | |||||||
| chr3:183019743 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1977+387C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183019743 | |||||||
| chr3:183019859 | T | A | 1 | a0001c0001t0001g0252 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1977+271A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183019859 | |||||||
| chr3:183019963 | A | T | 1 | a0001c0001t0001g0252 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1977+167T>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183019963 | |||||||
| chr3:183020017 | G | GGA | 5 | a0001c0001t0001g0221 a0001c0001t0001g0224 a0001c0001t0001g0225 others(2): Show |
5 | NA18974.hp1 NA18993.hp1 NA19065.hp2 others(2): Show |
intron_variant | MODIFIER | c.1977+111_1977+112d others(4): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183020017 | |||||||
| chr3:183020036 | A | C | 8 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(5): Show |
8 | HG01891.hp2 HG02055.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1977+94T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 17/18 | chr3 | 183020036 | |||||||
| chr3:183020318 | T | A | 1 | a0001c0001t0001g0166 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1870-81A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 16/18 | chr3 | 183020318 | |||||||
| chr3:183020371 | A | C | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1870-134T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 16/18 | chr3 | 183020371 | |||||||
| chr3:183020499 | G | A | 73 | a0002c0002t0001g0009 a0002c0002t0001g0010 a0002c0002t0001g0029 others(70): Show |
75 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.1870-262C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 16/18 | chr3 | 183020499 | |||||||
| chr3:183020504 | C | T | 1 | a0001c0001t0001g0025 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1870-267G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 16/18 | chr3 | 183020504 | |||||||
| chr3:183020505 | G | A | 1 | a0001c0011t0001g0174 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1870-268C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 16/18 | chr3 | 183020505 | |||||||
| chr3:183020585 | T | C | 1 | a0003c0005t0001g0035 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1870-348A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 16/18 | chr3 | 183020585 | |||||||
| chr3:183020693 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0107 |
2 | HG02040.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1870-456C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 16/18 | chr3 | 183020693 | |||||||
| chr3:183020781 | T | C | 73 | a0001c0001t0001g0160 a0002c0002t0001g0009 a0002c0002t0001g0010 others(70): Show |
75 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.1870-544A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 16/18 | chr3 | 183020781 | |||||||
| chr3:183020851 | G | A | 2 | a0002c0002t0001g0293 a0002c0002t0001g0294 |
2 | HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1870-614C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 16/18 | chr3 | 183020851 | |||||||
| chr3:183020933 | G | A | 16 | a0001c0001t0001g0044 a0001c0001t0001g0197 a0001c0001t0001g0198 others(13): Show |
20 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.1870-696C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 16/18 | chr3 | 183020933 | |||||||
| chr3:183020965 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1870-728G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 16/18 | chr3 | 183020965 | |||||||
| chr3:183021588 | C | T | 106 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0037 others(103): Show |
108 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(105): Show |
intron_variant | MODIFIER | c.1869+829G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 16/18 | chr3 | 183021588 | |||||||
| chr3:183021785 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1869+632G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 16/18 | chr3 | 183021785 | |||||||
| chr3:183021950 | C | G | 73 | a0002c0002t0001g0009 a0002c0002t0001g0010 a0002c0002t0001g0029 others(70): Show |
75 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.1869+467G>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 16/18 | chr3 | 183021950 | |||||||
| chr3:183022048 | G | T | 61 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(58): Show |
64 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1869+369C>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 16/18 | chr3 | 183022048 | |||||||
| chr3:183022066 | G | A | 8 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(5): Show |
8 | HG01891.hp2 HG02055.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1869+351C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 16/18 | chr3 | 183022066 | |||||||
| chr3:183022162 | T | C | 38 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0039 others(35): Show |
39 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.1869+255A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 16/18 | chr3 | 183022162 | |||||||
| chr3:183022325 | C | T | 1 | a0001c0003t0001g0196 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1869+92G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 16/18 | chr3 | 183022325 | |||||||
| chr3:183022701 | G | T | 1 | a0001c0001t0001g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1732-147C>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183022701 | |||||||
| chr3:183022912 | G | C | 1 | a0002c0008t0003g0331 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1732-358C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183022912 | |||||||
| chr3:183022929 | A | G | 1 | a0002c0002t0001g0131 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1732-375T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183022929 | |||||||
| chr3:183022974 | C | CA | 32 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0056 others(29): Show |
33 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.1732-421dupT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183022974 | |||||||
| chr3:183023013 | T | C | 32 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0056 others(29): Show |
33 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.1732-459A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183023013 | |||||||
| chr3:183023030 | A | G | 1 | a0001c0001t0001g0276 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1732-476T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183023030 | |||||||
| chr3:183023144 | T | G | 1 | a0002c0002t0001g0317 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1732-590A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183023144 | |||||||
| chr3:183023145 | G | T | 1 | a0002c0002t0001g0317 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1732-591C>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183023145 | |||||||
| chr3:183023295 | G | A | 8 | a0001c0001t0001g0044 a0001c0001t0001g0197 a0001c0001t0001g0198 others(5): Show |
8 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.1732-741C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183023295 | |||||||
| chr3:183023567 | A | C | 1 | a0002c0002t0001g0317 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1732-1013T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183023567 | |||||||
| chr3:183023570 | C | T | 1 | a0002c0002t0001g0317 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1732-1016G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183023570 | |||||||
| chr3:183023574 | G | C | 1 | a0002c0002t0001g0317 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1732-1020C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183023574 | |||||||
| chr3:183023576 | C | T | 1 | a0002c0002t0001g0317 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1732-1022G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183023576 | |||||||
| chr3:183023577 | A | G | 1 | a0002c0002t0001g0317 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1732-1023T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183023577 | |||||||
| chr3:183023610 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1732-1056C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183023610 | |||||||
| chr3:183023612 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1732-1058G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183023612 | |||||||
| chr3:183023665 | A | G | 1 | a0002c0002t0001g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1732-1111T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183023665 | |||||||
| chr3:183023942 | T | C | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG02717.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1732-1388A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183023942 | |||||||
| chr3:183024069 | A | G | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1732-1515T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183024069 | |||||||
| chr3:183024086 | A | T | 2 | a0002c0002t0001g0297 a0002c0002t0001g0298 |
2 | HG03688.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1732-1532T>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183024086 | |||||||
| chr3:183024106 | C | T | 1 | a0002c0002t0001g0137 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1732-1552G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183024106 | |||||||
| chr3:183024280 | A | G | 1 | a0002c0002t0001g0076 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1731+1475T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183024280 | |||||||
| chr3:183024285 | A | G | 8 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(5): Show |
8 | HG01891.hp2 HG02055.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1731+1470T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183024285 | |||||||
| chr3:183024618 | C | CA | 305 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(302): Show |
313 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.1731+1136dupT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183024618 | |||||||
| chr3:183025071 | C | T | 1 | a0002c0002t0001g0306 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1731+684G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183025071 | |||||||
| chr3:183025135 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0161 a0001c0001t0001g0162 |
4 | HG00639.hp1 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1731+620C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183025135 | |||||||
| chr3:183025231 | T | C | 38 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0039 others(35): Show |
39 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.1731+524A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183025231 | |||||||
| chr3:183025260 | C | T | 53 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(50): Show |
56 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.1731+495G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183025260 | |||||||
| chr3:183025309 | C | T | 8 | a0001c0001t0001g0044 a0001c0001t0001g0197 a0001c0001t0001g0198 others(5): Show |
8 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.1731+446G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183025309 | |||||||
| chr3:183025479 | C | A | 71 | a0002c0002t0001g0009 a0002c0002t0001g0010 a0002c0002t0001g0029 others(68): Show |
73 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.1731+276G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 15/18 | chr3 | 183025479 | |||||||
| chr3:183025879 | C | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02896.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1682-75G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183025879 | |||||||
| chr3:183026045 | TTTTGA | T | 32 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0056 others(29): Show |
33 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.1682-246_1682-242d others(7): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183026045 | |||||||
| chr3:183026147 | A | T | 1 | a0001c0001t0001g0159 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1682-343T>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183026147 | |||||||
| chr3:183026640 | G | T | 1 | a0002c0002t0001g0321 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1682-836C>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183026640 | |||||||
| chr3:183027047 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1682-1243G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183027047 | |||||||
| chr3:183027194 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1682-1390A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183027194 | |||||||
| chr3:183027295 | A | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0172 |
2 | HG01074.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1682-1491T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183027295 | |||||||
| chr3:183027343 | A | G | 276 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(273): Show |
283 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.1682-1539T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183027343 | |||||||
| chr3:183027750 | C | T | 1 | a0002c0002t0001g0302 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1682-1946G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183027750 | |||||||
| chr3:183027942 | T | C | 32 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0056 others(29): Show |
33 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.1682-2138A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183027942 | |||||||
| chr3:183027969 | A | T | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1682-2165T>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183027969 | |||||||
| chr3:183028025 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1682-2221A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183028025 | |||||||
| chr3:183028283 | C | A | 2 | a0002c0002t0001g0091 a0002c0002t0001g0092 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1682-2479G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183028283 | |||||||
| chr3:183028361 | G | C | 1 | a0002c0002t0001g0266 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1682-2557C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183028361 | |||||||
| chr3:183028420 | C | T | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0042 others(102): Show |
107 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.1682-2616G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183028420 | |||||||
| chr3:183028839 | T | A | 5 | a0002c0002t0001g0005 a0002c0002t0001g0050 a0002c0002t0001g0122 others(2): Show |
6 | NA18940.hp2 NA18963.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.1682-3035A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183028839 | |||||||
| chr3:183028966 | C | T | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG02717.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1682-3162G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183028966 | |||||||
| chr3:183029029 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0087 |
2 | HG01257.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1682-3225G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183029029 | |||||||
| chr3:183029061 | T | C | 3 | a0001c0001t0001g0101 a0001c0001t0001g0168 a0001c0001t0001g0173 |
3 | NA18972.hp2 NA18992.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1682-3257A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183029061 | |||||||
| chr3:183029184 | G | A | 1 | a0002c0002t0001g0118 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1682-3380C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183029184 | |||||||
| chr3:183029277 | A | C | 2 | a0001c0001t0001g0181 a0001c0001t0001g0286 |
2 | NA18953.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1682-3473T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183029277 | |||||||
| chr3:183029469 | T | C | 1 | a0001c0001t0001g0212 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1682-3665A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183029469 | |||||||
| chr3:183029506 | A | G | 3 | a0001c0001t0001g0101 a0001c0001t0001g0168 a0001c0001t0001g0173 |
3 | NA18972.hp2 NA18992.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1682-3702T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183029506 | |||||||
| chr3:183029583 | T | A | 8 | a0001c0001t0001g0044 a0001c0001t0001g0197 a0001c0001t0001g0198 others(5): Show |
8 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.1682-3779A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183029583 | |||||||
| chr3:183029690 | AT | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0042 others(102): Show |
107 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.1682-3887delA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183029690 | |||||||
| chr3:183029764 | A | G | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1682-3960T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183029764 | |||||||
| chr3:183030029 | C | A | 5 | a0001c0010t0001g0024 a0003c0005t0001g0035 a0003c0005t0001g0036 others(2): Show |
5 | HG02895.hp1 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1681+3962G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183030029 | |||||||
| chr3:183030030 | T | A | 5 | a0001c0010t0001g0024 a0003c0005t0001g0035 a0003c0005t0001g0036 others(2): Show |
5 | HG02895.hp1 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1681+3961A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183030030 | |||||||
| chr3:183030030 | T | C | 303 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(300): Show |
311 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.1681+3961A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183030030 | |||||||
| chr3:183030086 | T | C | 1 | a0002c0008t0003g0331 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1681+3905A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183030086 | |||||||
| chr3:183030148 | A | G | 1 | a0002c0002t0001g0138 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1681+3843T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183030148 | |||||||
| chr3:183030222 | C | T | 14 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(11): Show |
14 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1681+3769G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183030222 | |||||||
| chr3:183030243 | A | G | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1681+3748T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183030243 | |||||||
| chr3:183030340 | A | C | 7 | a0002c0002t0001g0076 a0002c0002t0001g0077 a0002c0002t0001g0078 others(4): Show |
7 | HG01433.hp2 HG02486.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1681+3651T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183030340 | |||||||
| chr3:183030521 | T | C | 3 | a0001c0003t0001g0093 a0001c0003t0001g0094 a0001c0003t0001g0115 |
3 | HG00323.hp2 HG01496.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1681+3470A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183030521 | |||||||
| chr3:183030659 | G | A | 8 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(5): Show |
8 | HG01891.hp2 HG02055.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1681+3332C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183030659 | |||||||
| chr3:183030707 | A | T | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0042 others(102): Show |
107 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.1681+3284T>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183030707 | |||||||
| chr3:183030741 | GA | G | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0042 others(102): Show |
107 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.1681+3249delT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183030741 | |||||||
| chr3:183030936 | G | A | 1 | a0001c0003t0001g0040 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1681+3055C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183030936 | |||||||
| chr3:183030995 | C | A | 1 | a0002c0002t0001g0330 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1681+2996G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183030995 | |||||||
| chr3:183031024 | T | C | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1681+2967A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183031024 | |||||||
| chr3:183031247 | T | G | 1 | a0001c0001t0001g0163 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1681+2744A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183031247 | |||||||
| chr3:183031253 | T | G | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1681+2738A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183031253 | |||||||
| chr3:183031364 | G | C | 1 | a0002c0002t0001g0029 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1681+2627C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183031364 | |||||||
| chr3:183031382 | T | C | 1 | a0001c0001t0001g0325 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1681+2609A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183031382 | |||||||
| chr3:183031441 | G | A | 8 | a0001c0001t0001g0044 a0001c0001t0001g0197 a0001c0001t0001g0198 others(5): Show |
8 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.1681+2550C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183031441 | |||||||
| chr3:183031491 | C | CT | 135 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(132): Show |
139 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.1681+2499dupA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183031491 | |||||||
| chr3:183031491 | C | CTT | 127 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(124): Show |
131 | HG00438.hp1 HG00544.hp2 HG00639.hp1 others(128): Show |
intron_variant | MODIFIER | c.1681+2498_1681+249 others(6): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183031491 | |||||||
| chr3:183031491 | C | CTTT | 51 | a0001c0001t0001g0042 a0001c0001t0001g0046 a0001c0001t0001g0053 others(48): Show |
51 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.1681+2497_1681+249 others(7): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183031491 | |||||||
| chr3:183031578 | A | G | 1 | a0002c0002t0001g0266 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1681+2413T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183031578 | |||||||
| chr3:183031731 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1681+2260G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183031731 | |||||||
| chr3:183031788 | G | A | 1 | a0001c0010t0001g0024 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1681+2203C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183031788 | |||||||
| chr3:183031808 | CT | C | 292 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(289): Show |
300 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.1681+2182delA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183031808 | |||||||
| chr3:183031968 | C | T | 134 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(131): Show |
139 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.1681+2023G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183031968 | |||||||
| chr3:183032058 | T | C | 1 | a0002c0002t0001g0081 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1681+1933A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183032058 | |||||||
| chr3:183032107 | A | G | 1 | a0002c0002t0001g0073 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1681+1884T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183032107 | |||||||
| chr3:183032243 | T | C | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG02717.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1681+1748A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183032243 | |||||||
| chr3:183032256 | C | T | 5 | a0002c0002t0001g0290 a0002c0002t0001g0291 a0002c0002t0001g0293 others(2): Show |
5 | HG00738.hp1 HG01175.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.1681+1735G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183032256 | |||||||
| chr3:183032327 | G | A | 58 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(55): Show |
59 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.1681+1664C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183032327 | |||||||
| chr3:183032735 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1681+1256C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183032735 | |||||||
| chr3:183032750 | T | G | 8 | a0001c0001t0001g0044 a0001c0001t0001g0197 a0001c0001t0001g0198 others(5): Show |
8 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.1681+1241A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183032750 | |||||||
| chr3:183032767 | G | A | 11 | a0001c0001t0001g0044 a0001c0001t0001g0197 a0001c0001t0001g0198 others(8): Show |
11 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.1681+1224C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183032767 | |||||||
| chr3:183032775 | G | A | 1 | a0002c0002t0001g0264 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1681+1216C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183032775 | |||||||
| chr3:183032873 | C | CA | 48 | a0001c0001t0001g0026 a0001c0001t0001g0273 a0001c0010t0001g0024 others(45): Show |
49 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.1681+1117dupT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183032873 | |||||||
| chr3:183032873 | C | CAA | 8 | a0001c0001t0001g0020 a0002c0002t0001g0119 a0002c0002t0001g0149 others(5): Show |
8 | HG02109.hp2 HG02895.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1681+1116_1681+111 others(6): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183032873 | |||||||
| chr3:183032873 | CA | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0022 others(97): Show |
102 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.1681+1117delT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183032873 | |||||||
| chr3:183032947 | T | C | 8 | a0001c0001t0001g0044 a0001c0001t0001g0197 a0001c0001t0001g0198 others(5): Show |
8 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.1681+1044A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183032947 | |||||||
| chr3:183033145 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1681+846C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183033145 | |||||||
| chr3:183033342 | A | G | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1681+649T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183033342 | |||||||
| chr3:183033623 | T | C | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1681+368A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183033623 | |||||||
| chr3:183033628 | G | A | 61 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(58): Show |
64 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1681+363C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183033628 | |||||||
| chr3:183033890 | A | AATGTAAC others(2): Show |
3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG02717.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1681+92_1681+100du others(10): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183033890 | |||||||
| chr3:183033914 | G | A | 61 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(58): Show |
64 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1681+77C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 14/18 | chr3 | 183033914 | |||||||
| chr3:183034173 | G | A | 5 | a0001c0003t0001g0011 a0001c0003t0001g0326 a0001c0003t0001g0327 others(2): Show |
6 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1595-96C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183034173 | |||||||
| chr3:183034177 | A | G | 11 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(8): Show |
11 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.1595-100T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183034177 | |||||||
| chr3:183034179 | A | G | 11 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(8): Show |
11 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.1595-102T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183034179 | |||||||
| chr3:183034188 | T | C | 6 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(3): Show |
6 | HG02300.hp2 HG02896.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1595-111A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183034188 | |||||||
| chr3:183034255 | C | T | 4 | a0001c0001t0001g0042 a0001c0001t0001g0232 a0001c0001t0001g0233 others(1): Show |
4 | HG01074.hp1 HG02145.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595-178G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183034255 | |||||||
| chr3:183034257 | T | C | 10 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(7): Show |
10 | HG02258.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1595-180A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183034257 | |||||||
| chr3:183034258 | A | G | 23 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0022 others(20): Show |
24 | HG00639.hp1 HG00733.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.1595-181T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183034258 | |||||||
| chr3:183034278 | G | A | 3 | a0001c0001t0001g0097 a0001c0001t0001g0103 a0001c0001t0001g0157 |
3 | HG01074.hp2 NA18946.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1595-201C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183034278 | |||||||
| chr3:183034400 | A | G | 1 | a0001c0001t0001g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1595-323T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183034400 | |||||||
| chr3:183034450 | G | A | 7 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(4): Show |
7 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.1595-373C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183034450 | |||||||
| chr3:183034454 | C | CA | 132 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0022 others(129): Show |
136 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.1595-378dupT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183034454 | |||||||
| chr3:183034454 | C | CAA | 40 | a0001c0001t0001g0006 a0001c0001t0001g0037 a0001c0001t0001g0045 others(37): Show |
41 | HG00621.hp1 HG00639.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1595-379_1595-378d others(4): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183034454 | |||||||
| chr3:183034469 | AC | A | 9 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1595-393delG | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183034469 | |||||||
| chr3:183034470 | C | A | 291 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(288): Show |
299 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.1595-393G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183034470 | |||||||
| chr3:183034477 | A | C | 2 | a0002c0002t0001g0112 a0002c0002t0001g0114 |
2 | HG01167.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.1595-400T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183034477 | |||||||
| chr3:183034540 | C | A | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1595-463G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183034540 | |||||||
| chr3:183034542 | G | A | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1595-465C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183034542 | |||||||
| chr3:183034777 | C | CT | 73 | a0001c0001t0001g0030 a0002c0002t0001g0009 a0002c0002t0001g0010 others(70): Show |
75 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.1595-701dupA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183034777 | |||||||
| chr3:183034884 | T | C | 4 | a0003c0005t0001g0035 a0003c0005t0001g0036 a0003c0007t0001g0033 others(1): Show |
4 | HG02895.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595-807A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183034884 | |||||||
| chr3:183034940 | G | A | 9 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1595-863C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183034940 | |||||||
| chr3:183035068 | C | G | 2 | a0002c0002t0001g0038 a0002c0002t0001g0323 |
2 | HG02132.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1595-991G>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183035068 | |||||||
| chr3:183035093 | G | C | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1595-1016C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183035093 | |||||||
| chr3:183035218 | T | C | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1595-1141A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183035218 | |||||||
| chr3:183035370 | C | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0087 |
2 | HG01257.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1595-1293G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183035370 | |||||||
| chr3:183035399 | A | G | 1 | a0002c0002t0001g0262 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1595-1322T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183035399 | |||||||
| chr3:183035410 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1595-1333C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183035410 | |||||||
| chr3:183035504 | A | AT | 221 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(218): Show |
227 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(224): Show |
intron_variant | MODIFIER | c.1595-1428dupA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183035504 | |||||||
| chr3:183035504 | A | ATT | 7 | a0001c0001t0001g0053 a0001c0001t0001g0172 a0001c0001t0001g0210 others(4): Show |
7 | HG01993.hp2 HG02717.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1595-1429_1595-142 others(6): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183035504 | |||||||
| chr3:183035599 | T | C | 4 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0255 others(1): Show |
4 | HG01109.hp1 HG02109.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595-1522A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183035599 | |||||||
| chr3:183035600 | G | A | 8 | a0001c0001t0001g0044 a0001c0001t0001g0197 a0001c0001t0001g0198 others(5): Show |
8 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.1595-1523C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183035600 | |||||||
| chr3:183035739 | T | A | 1 | a0001c0001t0001g0238 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1594+1479A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183035739 | |||||||
| chr3:183035746 | T | A | 1 | a0002c0002t0001g0077 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1594+1472A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183035746 | |||||||
| chr3:183035758 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG00733.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1594+1460C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183035758 | |||||||
| chr3:183035874 | G | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0087 |
2 | HG01257.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1594+1344C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183035874 | |||||||
| chr3:183036070 | T | C | 1 | a0001c0001t0001g0145 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1594+1148A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183036070 | |||||||
| chr3:183036537 | C | CT | 130 | a0001c0001t0001g0045 a0001c0001t0001g0067 a0001c0001t0001g0104 others(127): Show |
135 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1594+680dupA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183036537 | |||||||
| chr3:183036537 | C | CTT | 10 | a0002c0002t0001g0119 a0002c0002t0001g0122 a0002c0002t0001g0125 others(7): Show |
10 | HG00642.hp1 HG01952.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.1594+679_1594+680d others(4): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183036537 | |||||||
| chr3:183036537 | CT | C | 11 | a0001c0001t0001g0221 a0001c0003t0001g0001 a0001c0003t0001g0007 others(8): Show |
15 | HG00323.hp2 HG01891.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1594+680delA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183036537 | |||||||
| chr3:183036786 | A | G | 307 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(304): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.1594+432T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183036786 | |||||||
| chr3:183036830 | C | G | 1 | a0002c0002t0001g0298 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1594+388G>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183036830 | |||||||
| chr3:183036906 | C | A | 317 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(314): Show |
329 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.1594+312G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183036906 | |||||||
| chr3:183037091 | C | A | 4 | a0003c0005t0001g0035 a0003c0005t0001g0036 a0003c0007t0001g0033 others(1): Show |
4 | HG02895.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1594+127G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183037091 | |||||||
| chr3:183037179 | A | G | 61 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(58): Show |
64 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1594+39T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 13/18 | chr3 | 183037179 | |||||||
| chr3:183037604 | C | CA | 4 | a0001c0001t0001g0056 a0001c0001t0001g0105 a0001c0001t0001g0274 others(1): Show |
4 | HG02559.hp2 NA18967.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1378-171dupT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 12/18 | chr3 | 183037604 | |||||||
| chr3:183037637 | C | T | 1 | a0002c0002t0001g0311 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1378-203G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 12/18 | chr3 | 183037637 | |||||||
| chr3:183037737 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1378-303C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 12/18 | chr3 | 183037737 | |||||||
| chr3:183037957 | C | T | 4 | a0003c0005t0001g0035 a0003c0005t0001g0036 a0003c0007t0001g0033 others(1): Show |
4 | HG02895.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1378-523G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 12/18 | chr3 | 183037957 | |||||||
| chr3:183038162 | G | A | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.1378-728C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 12/18 | chr3 | 183038162 | |||||||
| chr3:183038254 | A | T | 6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG02258.hp1 HG02615.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1377+772T>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 12/18 | chr3 | 183038254 | |||||||
| chr3:183038331 | C | A | 1 | a0001c0001t0001g0276 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1377+695G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 12/18 | chr3 | 183038331 | |||||||
| chr3:183038800 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1377+226G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 12/18 | chr3 | 183038800 | |||||||
| chr3:183039224 | C | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02896.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1268-89G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183039224 | |||||||
| chr3:183039225 | G | A | 1 | a0002c0002t0001g0312 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1268-90C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183039225 | |||||||
| chr3:183039296 | G | A | 72 | a0002c0002t0001g0009 a0002c0002t0001g0010 a0002c0002t0001g0029 others(69): Show |
74 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1268-161C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183039296 | |||||||
| chr3:183039390 | T | C | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1268-255A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183039390 | |||||||
| chr3:183039607 | A | G | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1268-472T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183039607 | |||||||
| chr3:183039716 | T | C | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG01109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1268-581A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183039716 | |||||||
| chr3:183039780 | C | T | 1 | a0001c0003t0001g0195 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1268-645G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183039780 | |||||||
| chr3:183039804 | A | C | 4 | a0003c0005t0001g0035 a0003c0005t0001g0036 a0003c0007t0001g0033 others(1): Show |
4 | HG02895.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1268-669T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183039804 | |||||||
| chr3:183039857 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0016 others(2): Show |
5 | HG01891.hp2 HG02055.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1268-722C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183039857 | |||||||
| chr3:183039884 | C | A | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1268-749G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183039884 | |||||||
| chr3:183040050 | C | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
4 | HG02896.hp1 HG03098.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1268-915G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183040050 | |||||||
| chr3:183040096 | C | T | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.1268-961G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183040096 | |||||||
| chr3:183040098 | G | GA | 16 | a0001c0001t0001g0212 a0001c0003t0001g0011 a0001c0003t0001g0095 others(13): Show |
17 | HG00408.hp1 HG02145.hp2 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.1268-964dupT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183040098 | |||||||
| chr3:183040098 | GA | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0017 others(161): Show |
168 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.1268-964delT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183040098 | |||||||
| chr3:183040098 | GAA | G | 51 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(48): Show |
52 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.1268-965_1268-964d others(4): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183040098 | |||||||
| chr3:183040098 | GAAAA | G | 8 | a0001c0003t0001g0001 a0001c0003t0001g0007 a0001c0003t0001g0204 others(5): Show |
12 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1268-967_1268-964d others(6): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183040098 | |||||||
| chr3:183040142 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1268-1007C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183040142 | |||||||
| chr3:183040241 | T | G | 1 | a0001c0001t0001g0049 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1268-1106A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183040241 | |||||||
| chr3:183040252 | T | C | 73 | a0002c0002t0001g0009 a0002c0002t0001g0010 a0002c0002t0001g0029 others(70): Show |
75 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.1268-1117A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183040252 | |||||||
| chr3:183040257 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1268-1122T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183040257 | |||||||
| chr3:183040435 | G | A | 1 | a0002c0002t0001g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1267+1132C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183040435 | |||||||
| chr3:183040556 | C | CAAA | 31 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0056 others(28): Show |
32 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.1267+1008_1267+101 others(7): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183040556 | |||||||
| chr3:183040556 | C | CAAAA | 26 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(23): Show |
26 | HG00558.hp1 HG00735.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.1267+1007_1267+101 others(8): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183040556 | |||||||
| chr3:183040556 | C | CAAAAA | 174 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(171): Show |
178 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.1267+1006_1267+101 others(9): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183040556 | |||||||
| chr3:183040556 | C | CAAAAAA | 76 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0058 others(73): Show |
79 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.1267+1005_1267+101 others(10): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183040556 | |||||||
| chr3:183040574 | T | A | 1 | a0001c0001t0001g0098 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1267+993A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183040574 | |||||||
| chr3:183040575 | T | G | 4 | a0003c0005t0001g0035 a0003c0005t0001g0036 a0003c0007t0001g0033 others(1): Show |
4 | HG02895.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1267+992A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183040575 | |||||||
| chr3:183040618 | G | A | 9 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1267+949C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183040618 | |||||||
| chr3:183040728 | A | C | 14 | a0002c0002t0001g0182 a0002c0002t0001g0183 a0002c0002t0001g0247 others(11): Show |
14 | HG02071.hp1 NA18747.hp2 NA18966.hp1 others(11): Show |
intron_variant | MODIFIER | c.1267+839T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183040728 | |||||||
| chr3:183041309 | C | T | 57 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(54): Show |
58 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.1267+258G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183041309 | |||||||
| chr3:183041360 | A | G | 4 | a0003c0005t0001g0035 a0003c0005t0001g0036 a0003c0007t0001g0033 others(1): Show |
4 | HG02895.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1267+207T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183041360 | |||||||
| chr3:183041362 | G | A | 1 | a0001c0003t0001g0040 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1267+205C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 11/18 | chr3 | 183041362 | |||||||
| chr3:183041786 | G | A | 1 | a0002c0002t0001g0073 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1084-36C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183041786 | |||||||
| chr3:183041923 | T | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG02258.hp1 HG02615.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1084-173A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183041923 | |||||||
| chr3:183041967 | C | T | 72 | a0002c0002t0001g0009 a0002c0002t0001g0010 a0002c0002t0001g0029 others(69): Show |
74 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1084-217G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183041967 | |||||||
| chr3:183042118 | A | AT | 11 | a0002c0002t0001g0051 a0002c0002t0001g0052 a0002c0002t0001g0148 others(8): Show |
11 | HG00438.hp1 NA18947.hp1 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.1084-369dupA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183042118 | |||||||
| chr3:183042127 | A | T | 1 | a0001c0010t0001g0024 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1084-377T>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183042127 | |||||||
| chr3:183042146 | G | C | 1 | a0001c0001t0001g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1084-396C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183042146 | |||||||
| chr3:183042218 | A | G | 1 | a0001c0011t0001g0174 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1084-468T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183042218 | |||||||
| chr3:183042250 | G | A | 9 | a0001c0003t0001g0001 a0001c0003t0001g0007 a0001c0003t0001g0040 others(6): Show |
13 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1084-500C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183042250 | |||||||
| chr3:183042285 | T | G | 109 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0042 others(106): Show |
111 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.1084-535A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183042285 | |||||||
| chr3:183042363 | T | C | 32 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0056 others(29): Show |
33 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.1084-613A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183042363 | |||||||
| chr3:183042366 | G | A | 4 | a0003c0005t0001g0035 a0003c0005t0001g0036 a0003c0007t0001g0033 others(1): Show |
4 | HG02895.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084-616C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183042366 | |||||||
| chr3:183042654 | A | G | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1084-904T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183042654 | |||||||
| chr3:183042656 | TTA | T | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1084-908_1084-907d others(4): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183042656 | |||||||
| chr3:183042753 | A | C | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.1084-1003T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183042753 | |||||||
| chr3:183042943 | T | C | 32 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0056 others(29): Show |
33 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.1084-1193A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183042943 | |||||||
| chr3:183042989 | G | A | 32 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0056 others(29): Show |
33 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.1084-1239C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183042989 | |||||||
| chr3:183043006 | T | C | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1084-1256A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183043006 | |||||||
| chr3:183043326 | C | T | 1 | a0001c0001t0001g0275 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1084-1576G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183043326 | |||||||
| chr3:183043407 | A | C | 4 | a0003c0005t0001g0035 a0003c0005t0001g0036 a0003c0007t0001g0033 others(1): Show |
4 | HG02895.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084-1657T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183043407 | |||||||
| chr3:183043508 | C | T | 1 | a0002c0002t0001g0306 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1084-1758G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183043508 | |||||||
| chr3:183043596 | C | G | 1 | a0001c0001t0001g0215 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1083+1817G>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183043596 | |||||||
| chr3:183043627 | T | C | 1 | a0002c0002t0001g0277 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1083+1786A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183043627 | |||||||
| chr3:183043810 | T | C | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1083+1603A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183043810 | |||||||
| chr3:183043826 | T | A | 1 | a0001c0001t0001g0274 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1083+1587A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183043826 | |||||||
| chr3:183044040 | C | T | 9 | a0001c0003t0001g0001 a0001c0003t0001g0007 a0001c0003t0001g0040 others(6): Show |
13 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1083+1373G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183044040 | |||||||
| chr3:183044042 | A | G | 1 | a0002c0002t0001g0118 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1083+1371T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183044042 | |||||||
| chr3:183044229 | T | G | 1 | a0002c0002t0001g0140 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1083+1184A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183044229 | |||||||
| chr3:183044352 | C | T | 317 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(314): Show |
329 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.1083+1061G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183044352 | |||||||
| chr3:183044475 | A | G | 1 | a0002c0002t0001g0073 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1083+938T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183044475 | |||||||
| chr3:183044497 | G | A | 8 | a0002c0002t0001g0055 a0002c0002t0001g0118 a0002c0002t0001g0124 others(5): Show |
8 | HG01934.hp1 HG01952.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.1083+916C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183044497 | |||||||
| chr3:183044507 | T | C | 1 | a0002c0002t0001g0295 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1083+906A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183044507 | |||||||
| chr3:183044514 | G | A | 1 | a0002c0002t0001g0281 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1083+899C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183044514 | |||||||
| chr3:183044564 | C | A | 9 | a0001c0001t0001g0020 a0001c0001t0001g0044 a0001c0001t0001g0197 others(6): Show |
9 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1083+849G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183044564 | |||||||
| chr3:183044649 | G | A | 118 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0020 others(115): Show |
120 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.1083+764C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183044649 | |||||||
| chr3:183044729 | G | A | 32 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0056 others(29): Show |
33 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.1083+684C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183044729 | |||||||
| chr3:183044906 | T | TTTGTTG | 310 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(307): Show |
322 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(319): Show |
intron_variant | MODIFIER | c.1083+501_1083+506d others(8): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183044906 | |||||||
| chr3:183044906 | T | TTTGTTGT others(2): Show |
6 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0003c0005t0001g0035 others(3): Show |
6 | HG00733.hp2 HG02895.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1083+498_1083+506d others(11): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183044906 | |||||||
| chr3:183044927 | G | A | 2 | a0002c0002t0001g0139 a0002c0002t0001g0140 |
2 | HG00738.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1083+486C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183044927 | |||||||
| chr3:183044942 | T | C | 1 | a0001c0003t0001g0204 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1083+471A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183044942 | |||||||
| chr3:183044960 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1083+453C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183044960 | |||||||
| chr3:183045092 | C | CT | 33 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0056 others(30): Show |
34 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.1083+320dupA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183045092 | |||||||
| chr3:183045092 | CT | C | 6 | a0001c0001t0001g0181 a0001c0013t0001g0319 a0002c0002t0001g0082 others(3): Show |
6 | HG01169.hp2 HG02602.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1083+320delA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183045092 | |||||||
| chr3:183045181 | G | A | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1083+232C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183045181 | |||||||
| chr3:183045205 | G | C | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.1083+208C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183045205 | |||||||
| chr3:183045215 | G | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0251 others(5): Show |
9 | NA18941.hp2 NA18944.hp1 NA18964.hp2 others(6): Show |
intron_variant | MODIFIER | c.1083+198C>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183045215 | |||||||
| chr3:183045221 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1083+192T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183045221 | |||||||
| chr3:183045228 | C | T | 146 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0237 others(143): Show |
151 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.1083+185G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 10/18 | chr3 | 183045228 | |||||||
| chr3:183045792 | G | A | 146 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0237 others(143): Show |
151 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.956-252C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183045792 | |||||||
| chr3:183045864 | C | A | 45 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0050 others(42): Show |
47 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.956-324G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183045864 | |||||||
| chr3:183045921 | T | C | 1 | a0002c0002t0001g0041 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.956-381A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183045921 | |||||||
| chr3:183045924 | C | T | 1 | a0002c0002t0001g0318 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.956-384G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183045924 | |||||||
| chr3:183046073 | T | G | 5 | a0001c0003t0001g0011 a0001c0003t0001g0326 a0001c0003t0001g0327 others(2): Show |
6 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.956-533A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183046073 | |||||||
| chr3:183046402 | A | AT | 26 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0110 others(23): Show |
30 | HG00558.hp1 HG01081.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.956-863dupA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183046402 | |||||||
| chr3:183046402 | A | ATT | 289 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(286): Show |
297 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.956-864_956-863dup others(2): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183046402 | |||||||
| chr3:183046459 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.956-919C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183046459 | |||||||
| chr3:183046981 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.956-1441C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183046981 | |||||||
| chr3:183047107 | T | G | 1 | a0002c0002t0001g0294 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.956-1567A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183047107 | |||||||
| chr3:183047166 | T | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0042 others(90): Show |
95 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.956-1626A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183047166 | |||||||
| chr3:183047256 | G | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0145 |
2 | HG00621.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.956-1716C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183047256 | |||||||
| chr3:183047663 | G | GA | 13 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(10): Show |
13 | HG01891.hp2 HG02055.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.956-2124dupT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183047663 | |||||||
| chr3:183047799 | G | GA | 9 | a0001c0001t0001g0044 a0001c0001t0001g0197 a0001c0001t0001g0198 others(6): Show |
9 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.956-2260dupT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183047799 | |||||||
| chr3:183047942 | C | T | 3 | a0001c0003t0001g0207 a0001c0003t0001g0208 a0001c0003t0001g0209 |
3 | HG01891.hp1 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.956-2402G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183047942 | |||||||
| chr3:183048020 | T | C | 8 | a0001c0001t0001g0044 a0001c0001t0001g0197 a0001c0001t0001g0198 others(5): Show |
8 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.956-2480A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183048020 | |||||||
| chr3:183048110 | G | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
4 | HG02896.hp1 HG03098.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.956-2570C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183048110 | |||||||
| chr3:183048245 | T | C | 86 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0237 others(83): Show |
88 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.956-2705A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183048245 | |||||||
| chr3:183048381 | C | T | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.956-2841G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183048381 | |||||||
| chr3:183048550 | A | C | 2 | a0002c0002t0001g0142 a0002c0002t0001g0143 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.956-3010T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183048550 | |||||||
| chr3:183048579 | C | T | 1 | a0002c0002t0001g0073 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.956-3039G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183048579 | |||||||
| chr3:183049345 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.955+2814C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183049345 | |||||||
| chr3:183049387 | T | C | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.955+2772A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183049387 | |||||||
| chr3:183049432 | G | T | 1 | a0001c0013t0001g0319 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.955+2727C>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183049432 | |||||||
| chr3:183049440 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.955+2719C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183049440 | |||||||
| chr3:183049441 | T | C | 1 | a0001c0001t0001g0258 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.955+2718A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183049441 | |||||||
| chr3:183049464 | C | A | 61 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(58): Show |
64 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.955+2695G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183049464 | |||||||
| chr3:183049504 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.955+2655C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183049504 | |||||||
| chr3:183049520 | C | G | 1 | a0002c0002t0001g0300 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.955+2639G>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183049520 | |||||||
| chr3:183049572 | A | G | 1 | a0002c0002t0001g0183 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.955+2587T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183049572 | |||||||
| chr3:183049616 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.955+2543G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183049616 | |||||||
| chr3:183049632 | T | G | 1 | a0001c0001t0001g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.955+2527A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183049632 | |||||||
| chr3:183049703 | C | T | 9 | a0001c0001t0001g0020 a0001c0001t0001g0044 a0001c0001t0001g0197 others(6): Show |
9 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.955+2456G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183049703 | |||||||
| chr3:183049809 | A | G | 46 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(43): Show |
47 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.955+2350T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183049809 | |||||||
| chr3:183050176 | C | T | 3 | a0002c0002t0001g0248 a0002c0002t0001g0249 a0002c0002t0001g0250 |
3 | NA18974.hp2 NA18994.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.955+1983G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183050176 | |||||||
| chr3:183050207 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.955+1952C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183050207 | |||||||
| chr3:183050262 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.955+1897T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183050262 | |||||||
| chr3:183050267 | A | T | 1 | a0001c0001t0001g0190 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.955+1892T>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183050267 | |||||||
| chr3:183050428 | C | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0042 others(89): Show |
94 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.955+1731G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183050428 | |||||||
| chr3:183050433 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.955+1726A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183050433 | |||||||
| chr3:183050477 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.955+1682G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183050477 | |||||||
| chr3:183050638 | G | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0045 a0001c0001t0001g0046 others(30): Show |
34 | HG00621.hp1 HG00642.hp2 HG01257.hp1 others(31): Show |
intron_variant | MODIFIER | c.955+1521C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183050638 | |||||||
| chr3:183050655 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.955+1504C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183050655 | |||||||
| chr3:183050657 | G | T | 9 | a0001c0003t0001g0001 a0001c0003t0001g0007 a0001c0003t0001g0040 others(6): Show |
13 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.955+1502C>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183050657 | |||||||
| chr3:183050705 | C | CA | 30 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(27): Show |
31 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.955+1453dupT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183050705 | |||||||
| chr3:183050705 | CA | C | 14 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(11): Show |
14 | HG00323.hp1 HG01891.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.955+1453delT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183050705 | |||||||
| chr3:183050705 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG02717.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.955+1444_955+1453d others(12): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183050705 | |||||||
| chr3:183050705 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.955+1441_955+1453d others(15): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183050705 | |||||||
| chr3:183050720 | A | G | 1 | a0001c0010t0001g0024 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.955+1439T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183050720 | |||||||
| chr3:183050907 | T | A | 1 | a0002c0002t0001g0264 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.955+1252A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183050907 | |||||||
| chr3:183051018 | C | T | 1 | a0002c0002t0001g0073 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.955+1141G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183051018 | |||||||
| chr3:183051087 | T | A | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.955+1072A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183051087 | |||||||
| chr3:183051091 | A | C | 36 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0056 others(33): Show |
37 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.955+1068T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183051091 | |||||||
| chr3:183051158 | C | T | 1 | a0001c0003t0001g0326 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.955+1001G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183051158 | |||||||
| chr3:183051190 | A | C | 8 | a0001c0001t0001g0044 a0001c0001t0001g0197 a0001c0001t0001g0198 others(5): Show |
8 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.955+969T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183051190 | |||||||
| chr3:183051250 | T | C | 147 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0237 others(144): Show |
152 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.955+909A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183051250 | |||||||
| chr3:183051286 | T | C | 92 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0042 others(89): Show |
94 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.955+873A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183051286 | |||||||
| chr3:183051317 | G | A | 91 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0042 others(88): Show |
93 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.955+842C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183051317 | |||||||
| chr3:183051412 | A | G | 2 | a0002c0002t0001g0091 a0002c0002t0001g0092 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.955+747T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183051412 | |||||||
| chr3:183051522 | A | G | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.955+637T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183051522 | |||||||
| chr3:183051773 | G | A | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG02717.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.955+386C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183051773 | |||||||
| chr3:183052008 | T | G | 1 | a0002c0002t0001g0305 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.955+151A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 9/18 | chr3 | 183052008 | |||||||
| chr3:183052436 | A | G | 1 | a0001c0003t0001g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.874-196T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183052436 | |||||||
| chr3:183052445 | C | T | 6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG02258.hp1 HG02615.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.874-205G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183052445 | |||||||
| chr3:183052479 | T | C | 4 | a0002c0002t0001g0278 a0002c0002t0001g0279 a0002c0002t0001g0280 others(1): Show |
4 | HG00280.hp2 HG00642.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.874-239A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183052479 | |||||||
| chr3:183052485 | C | T | 1 | a0002c0002t0001g0141 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.874-245G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183052485 | |||||||
| chr3:183052624 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.874-384G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183052624 | |||||||
| chr3:183052625 | G | A | 1 | a0002c0002t0001g0071 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.874-385C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183052625 | |||||||
| chr3:183052660 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.874-420T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183052660 | |||||||
| chr3:183052663 | AGC | A | 92 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0042 others(89): Show |
94 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.874-425_874-424del others(2): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183052663 | |||||||
| chr3:183052741 | C | T | 9 | a0001c0001t0001g0020 a0001c0001t0001g0044 a0001c0001t0001g0197 others(6): Show |
9 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.874-501G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183052741 | |||||||
| chr3:183052793 | G | C | 1 | a0002c0002t0001g0041 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.874-553C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183052793 | |||||||
| chr3:183052804 | T | C | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.874-564A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183052804 | |||||||
| chr3:183052809 | C | CA | 6 | a0001c0001t0001g0053 a0001c0001t0001g0170 a0001c0001t0001g0173 others(3): Show |
6 | HG02145.hp1 HG02145.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.874-570dupT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183052809 | |||||||
| chr3:183052809 | CA | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0021 others(91): Show |
96 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.874-570delT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183052809 | |||||||
| chr3:183052809 | CAA | C | 197 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(194): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.874-571_874-570del others(2): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183052809 | |||||||
| chr3:183052863 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.874-623T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183052863 | |||||||
| chr3:183052878 | T | C | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.874-638A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183052878 | |||||||
| chr3:183052949 | TA | T | 304 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(301): Show |
312 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.874-710delT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183052949 | |||||||
| chr3:183053171 | G | T | 1 | a0002c0002t0001g0240 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.874-931C>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183053171 | |||||||
| chr3:183053455 | T | G | 1 | a0002c0002t0001g0140 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.874-1215A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183053455 | |||||||
| chr3:183053457 | T | C | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.874-1217A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183053457 | |||||||
| chr3:183053484 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.874-1244A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183053484 | |||||||
| chr3:183053547 | C | T | 47 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0044 others(44): Show |
48 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.874-1307G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183053547 | |||||||
| chr3:183053588 | T | C | 1 | a0002c0002t0001g0041 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.874-1348A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183053588 | |||||||
| chr3:183053591 | A | G | 1 | a0002c0002t0001g0041 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.874-1351T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183053591 | |||||||
| chr3:183053596 | G | A | 9 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.874-1356C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183053596 | |||||||
| chr3:183053603 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.874-1363C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183053603 | |||||||
| chr3:183053662 | G | A | 7 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(4): Show |
7 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.874-1422C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183053662 | |||||||
| chr3:183053721 | C | T | 1 | a0001c0010t0001g0024 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.874-1481G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183053721 | |||||||
| chr3:183053804 | C | CA | 20 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(17): Show |
20 | HG01109.hp2 HG01891.hp2 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.874-1565dupT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183053804 | |||||||
| chr3:183053815 | C | A | 2 | a0001c0003t0001g0205 a0002c0002t0001g0249 |
2 | HG02257.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.874-1575G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183053815 | |||||||
| chr3:183053815 | C | CA | 25 | a0001c0001t0001g0184 a0001c0003t0001g0001 a0001c0003t0001g0007 others(22): Show |
30 | HG00323.hp2 HG00544.hp1 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.874-1576dupT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183053815 | |||||||
| chr3:183053824 | A | C | 4 | a0003c0005t0001g0035 a0003c0005t0001g0036 a0003c0007t0001g0033 others(1): Show |
4 | HG02895.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.874-1584T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183053824 | |||||||
| chr3:183053875 | G | GA | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0020 others(102): Show |
107 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(104): Show |
intron_variant | MODIFIER | c.874-1636dupT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183053875 | |||||||
| chr3:183053877 | A | AAT | 6 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0101 others(3): Show |
6 | HG00621.hp1 HG02486.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.874-1638_874-1637i others(4): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183053877 | |||||||
| chr3:183053877 | A | AT | 11 | a0002c0002t0001g0051 a0002c0002t0001g0076 a0002c0002t0001g0078 others(8): Show |
11 | HG00438.hp1 HG01433.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.874-1638dupA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183053877 | |||||||
| chr3:183053878 | T | A | 74 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(71): Show |
80 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.874-1638A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183053878 | |||||||
| chr3:183053879 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.874-1639A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183053879 | |||||||
| chr3:183053904 | G | GTCTCACT others(33): Show |
1 | a0001c0001t0002g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.874-1665_874-1664i others(42): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183053904 | |||||||
| chr3:183054040 | T | C | 248 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(245): Show |
259 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(256): Show |
intron_variant | MODIFIER | c.874-1800A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183054040 | |||||||
| chr3:183054099 | C | G | 1 | a0001c0001t0001g0192 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.874-1859G>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183054099 | |||||||
| chr3:183054188 | A | AT | 97 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0042 others(94): Show |
99 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.874-1949dupA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183054188 | |||||||
| chr3:183054188 | AT | A | 10 | a0001c0001t0001g0201 a0001c0003t0001g0001 a0001c0003t0001g0007 others(7): Show |
14 | HG01169.hp1 HG01891.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.874-1949delA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183054188 | |||||||
| chr3:183054189 | T | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0286 |
2 | NA18953.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.874-1949A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183054189 | |||||||
| chr3:183054317 | C | A | 1 | a0001c0001t0001g0013 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.874-2077G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183054317 | |||||||
| chr3:183054364 | T | G | 82 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0237 others(79): Show |
84 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.874-2124A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183054364 | |||||||
| chr3:183054398 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.874-2158C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183054398 | |||||||
| chr3:183054453 | C | CT | 9 | a0001c0003t0001g0001 a0001c0003t0001g0007 a0001c0003t0001g0040 others(6): Show |
13 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.874-2214dupA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183054453 | |||||||
| chr3:183054461 | A | G | 19 | a0001c0001t0001g0049 a0001c0001t0001g0067 a0001c0001t0001g0088 others(16): Show |
19 | HG00621.hp1 HG01346.hp2 HG01928.hp1 others(16): Show |
intron_variant | MODIFIER | c.874-2221T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183054461 | |||||||
| chr3:183054466 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.874-2226G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183054466 | |||||||
| chr3:183054477 | G | A | 1 | a0001c0010t0001g0024 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.874-2237C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183054477 | |||||||
| chr3:183054656 | C | G | 307 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(304): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.874-2416G>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183054656 | |||||||
| chr3:183055030 | G | A | 7 | a0002c0002t0001g0076 a0002c0002t0001g0077 a0002c0002t0001g0078 others(4): Show |
7 | HG01433.hp2 HG02486.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.873+2281C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183055030 | |||||||
| chr3:183055078 | A | G | 1 | a0002c0002t0001g0124 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.873+2233T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183055078 | |||||||
| chr3:183055125 | C | T | 7 | a0002c0002t0001g0076 a0002c0002t0001g0077 a0002c0002t0001g0078 others(4): Show |
7 | HG01433.hp2 HG02486.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.873+2186G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183055125 | |||||||
| chr3:183055201 | A | G | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG02717.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.873+2110T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183055201 | |||||||
| chr3:183055213 | C | A | 1 | a0001c0003t0001g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.873+2098G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183055213 | |||||||
| chr3:183055248 | GA | G | 150 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(147): Show |
155 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.873+2062delT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183055248 | |||||||
| chr3:183055248 | GAA | G | 7 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(4): Show |
7 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.873+2061_873+2062d others(4): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183055248 | |||||||
| chr3:183055324 | T | C | 1 | a0001c0010t0001g0024 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.873+1987A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183055324 | |||||||
| chr3:183055337 | G | C | 142 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0237 others(139): Show |
147 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.873+1974C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183055337 | |||||||
| chr3:183055381 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.873+1930C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183055381 | |||||||
| chr3:183055478 | A | C | 2 | a0002c0002t0001g0295 a0002c0002t0001g0312 |
2 | HG00735.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.873+1833T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183055478 | |||||||
| chr3:183055526 | A | G | 57 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(54): Show |
58 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.873+1785T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183055526 | |||||||
| chr3:183055633 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.873+1678C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183055633 | |||||||
| chr3:183055642 | A | G | 9 | a0001c0003t0001g0001 a0001c0003t0001g0007 a0001c0003t0001g0040 others(6): Show |
13 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.873+1669T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183055642 | |||||||
| chr3:183055684 | C | T | 6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG02258.hp1 HG02615.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.873+1627G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183055684 | |||||||
| chr3:183056176 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.873+1135A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183056176 | |||||||
| chr3:183056186 | T | C | 1 | a0001c0001t0001g0230 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.873+1125A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183056186 | |||||||
| chr3:183056818 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.873+493G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183056818 | |||||||
| chr3:183056826 | C | T | 1 | a0002c0002t0001g0123 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.873+485G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183056826 | |||||||
| chr3:183056974 | C | T | 60 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(57): Show |
63 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.873+337G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183056974 | |||||||
| chr3:183056977 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.873+334C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183056977 | |||||||
| chr3:183056979 | G | A | 1 | a0002c0002t0001g0135 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.873+332C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183056979 | |||||||
| chr3:183057055 | G | A | 1 | a0002c0002t0001g0307 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.873+256C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183057055 | |||||||
| chr3:183057233 | T | C | 12 | a0001c0001t0001g0044 a0001c0001t0001g0197 a0001c0001t0001g0198 others(9): Show |
12 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.873+78A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183057233 | |||||||
| chr3:183057275 | C | T | 2 | a0002c0002t0001g0142 a0002c0002t0001g0143 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.873+36G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 8/18 | chr3 | 183057275 | |||||||
| chr3:183057604 | T | A | 12 | a0001c0001t0001g0044 a0001c0001t0001g0197 a0001c0001t0001g0198 others(9): Show |
12 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.762-182A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183057604 | |||||||
| chr3:183057609 | C | T | 307 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(304): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.762-187G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183057609 | |||||||
| chr3:183057661 | T | A | 1 | a0001c0001t0002g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.762-239A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183057661 | |||||||
| chr3:183057777 | T | C | 2 | a0001c0001t0001g0222 a0001c0001t0001g0272 |
2 | HG02738.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.762-355A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183057777 | |||||||
| chr3:183057809 | T | C | 327 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(324): Show |
340 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(337): Show |
intron_variant | MODIFIER | c.762-387A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183057809 | |||||||
| chr3:183057833 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.762-411G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183057833 | |||||||
| chr3:183057969 | T | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0021 others(108): Show |
113 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.762-547A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183057969 | |||||||
| chr3:183058015 | G | A | 317 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(314): Show |
329 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.762-593C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183058015 | |||||||
| chr3:183058528 | A | G | 307 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(304): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.762-1106T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183058528 | |||||||
| chr3:183058647 | A | C | 1 | a0002c0008t0003g0331 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.762-1225T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183058647 | |||||||
| chr3:183058741 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.762-1319G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183058741 | |||||||
| chr3:183058822 | T | C | 307 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(304): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.762-1400A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183058822 | |||||||
| chr3:183059062 | C | T | 1 | a0002c0002t0001g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.762-1640G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183059062 | |||||||
| chr3:183059197 | A | T | 1 | a0001c0001t0001g0325 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.762-1775T>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183059197 | |||||||
| chr3:183059372 | TCCAACCT others(9): Show |
T | 12 | a0001c0001t0001g0044 a0001c0001t0001g0197 a0001c0001t0001g0198 others(9): Show |
12 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.762-1966_762-1951d others(18): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183059372 | |||||||
| chr3:183059869 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.762-2447G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183059869 | |||||||
| chr3:183059982 | G | T | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG02717.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.762-2560C>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183059982 | |||||||
| chr3:183060103 | C | T | 1 | a0001c0010t0001g0024 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.762-2681G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183060103 | |||||||
| chr3:183060201 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.762-2779A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183060201 | |||||||
| chr3:183060276 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.762-2854G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183060276 | |||||||
| chr3:183060459 | C | T | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG02717.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.762-3037G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183060459 | |||||||
| chr3:183060516 | C | T | 307 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(304): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.762-3094G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183060516 | |||||||
| chr3:183060568 | T | C | 12 | a0001c0001t0001g0044 a0001c0001t0001g0197 a0001c0001t0001g0198 others(9): Show |
12 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.762-3146A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183060568 | |||||||
| chr3:183060576 | T | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
4 | HG02896.hp1 HG03098.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.762-3154A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183060576 | |||||||
| chr3:183060578 | GTTTT | G | 31 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0056 others(28): Show |
32 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.762-3160_762-3157d others(6): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183060578 | |||||||
| chr3:183060628 | GGTTT | G | 12 | a0001c0001t0001g0044 a0001c0001t0001g0197 a0001c0001t0001g0198 others(9): Show |
12 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.762-3210_762-3207d others(6): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183060628 | |||||||
| chr3:183060652 | G | A | 2 | a0002c0002t0001g0308 a0002c0002t0001g0317 |
2 | HG00408.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.762-3230C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183060652 | |||||||
| chr3:183060664 | T | C | 43 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0044 others(40): Show |
44 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.762-3242A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183060664 | |||||||
| chr3:183060828 | C | T | 1 | a0002c0002t0001g0077 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.762-3406G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183060828 | |||||||
| chr3:183060829 | GT | G | 307 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(304): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.762-3408delA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183060829 | |||||||
| chr3:183060907 | A | T | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.762-3485T>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183060907 | |||||||
| chr3:183060922 | T | C | 1 | a0002c0002t0001g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.762-3500A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183060922 | |||||||
| chr3:183060940 | T | G | 2 | a0001c0001t0001g0220 a0001c0001t0001g0228 |
2 | HG03669.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.762-3518A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183060940 | |||||||
| chr3:183061001 | C | T | 53 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(50): Show |
56 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.762-3579G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183061001 | |||||||
| chr3:183061153 | G | A | 82 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0237 others(79): Show |
84 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.762-3731C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183061153 | |||||||
| chr3:183061159 | G | C | 4 | a0003c0005t0001g0035 a0003c0005t0001g0036 a0003c0007t0001g0033 others(1): Show |
4 | HG02895.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.762-3737C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183061159 | |||||||
| chr3:183061220 | C | T | 6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG02258.hp1 HG02615.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.762-3798G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183061220 | |||||||
| chr3:183061298 | G | C | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.762-3876C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183061298 | |||||||
| chr3:183061383 | G | T | 10 | a0001c0001t0001g0006 a0001c0001t0001g0157 a0001c0001t0001g0159 others(7): Show |
11 | HG00639.hp1 HG01074.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.762-3961C>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183061383 | |||||||
| chr3:183061384 | A | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0021 others(108): Show |
113 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.762-3962T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183061384 | |||||||
| chr3:183061451 | AT | A | 8 | a0001c0001t0001g0153 a0001c0001t0001g0171 a0001c0001t0001g0178 others(5): Show |
8 | HG00558.hp1 NA18947.hp2 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.762-4030delA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183061451 | |||||||
| chr3:183061969 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.762-4547C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183061969 | |||||||
| chr3:183062155 | A | G | 83 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0237 others(80): Show |
85 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.762-4733T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183062155 | |||||||
| chr3:183062350 | GT | G | 6 | a0001c0001t0001g0276 a0001c0003t0001g0206 a0002c0002t0001g0259 others(3): Show |
6 | HG02895.hp2 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.762-4929delA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183062350 | |||||||
| chr3:183062350 | GTT | G | 51 | a0001c0001t0001g0017 a0001c0001t0001g0044 a0001c0001t0001g0053 others(48): Show |
51 | HG00323.hp1 HG00735.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.762-4930_762-4929d others(4): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183062350 | |||||||
| chr3:183062350 | GTTT | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(183): Show |
191 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.762-4931_762-4929d others(5): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183062350 | |||||||
| chr3:183062350 | GTTTT | G | 13 | a0001c0001t0001g0023 a0001c0001t0001g0057 a0001c0001t0001g0190 others(10): Show |
13 | HG01433.hp2 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.762-4932_762-4929d others(6): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183062350 | |||||||
| chr3:183062350 | GTTTTT | G | 53 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(50): Show |
56 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.762-4933_762-4929d others(7): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183062350 | |||||||
| chr3:183062442 | C | T | 307 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(304): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.762-5020G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183062442 | |||||||
| chr3:183062503 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.762-5081G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183062503 | |||||||
| chr3:183062564 | A | G | 6 | a0001c0001t0001g0097 a0001c0001t0001g0101 a0001c0001t0001g0102 others(3): Show |
6 | NA18946.hp2 NA18964.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.762-5142T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183062564 | |||||||
| chr3:183062575 | G | A | 1 | a0002c0002t0001g0183 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.762-5153C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183062575 | |||||||
| chr3:183062647 | G | A | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG02717.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.762-5225C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183062647 | |||||||
| chr3:183062702 | T | G | 2 | a0002c0002t0001g0116 a0002c0002t0001g0120 |
2 | HG02015.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.762-5280A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183062702 | |||||||
| chr3:183062893 | C | A | 1 | a0001c0009t0001g0310 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.762-5471G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183062893 | |||||||
| chr3:183062926 | T | C | 307 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(304): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.762-5504A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183062926 | |||||||
| chr3:183063038 | C | T | 4 | a0001c0001t0001g0054 a0001c0001t0001g0085 a0001c0001t0001g0086 others(1): Show |
4 | HG01081.hp1 HG01257.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.762-5616G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183063038 | |||||||
| chr3:183063194 | A | AG | 317 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(314): Show |
329 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.762-5773dupC | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183063194 | |||||||
| chr3:183063344 | T | TTC | 307 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(304): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.762-5923_762-5922i others(4): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183063344 | |||||||
| chr3:183063367 | T | C | 3 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 |
3 | HG00280.hp1 HG01167.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.762-5945A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183063367 | |||||||
| chr3:183063577 | C | G | 1 | a0001c0001t0001g0146 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.762-6155G>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183063577 | |||||||
| chr3:183063618 | T | G | 1 | a0001c0001t0001g0220 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.762-6196A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183063618 | |||||||
| chr3:183063814 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.762-6392G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183063814 | |||||||
| chr3:183063900 | G | A | 1 | a0001c0010t0001g0024 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.762-6478C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183063900 | |||||||
| chr3:183063926 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.762-6504C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183063926 | |||||||
| chr3:183064038 | G | T | 1 | a0001c0001t0002g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.762-6616C>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183064038 | |||||||
| chr3:183064211 | G | C | 2 | a0002c0002t0001g0004 a0002c0002t0001g0083 |
3 | HG01069.hp1 HG01071.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.761+6788C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183064211 | |||||||
| chr3:183064214 | G | A | 1 | a0002c0008t0003g0331 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.761+6785C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183064214 | |||||||
| chr3:183064274 | CT | C | 306 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(303): Show |
314 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.761+6724delA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183064274 | |||||||
| chr3:183064473 | G | A | 1 | a0002c0002t0001g0136 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.761+6526C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183064473 | |||||||
| chr3:183064505 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.761+6494C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183064505 | |||||||
| chr3:183064587 | A | G | 307 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(304): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.761+6412T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183064587 | |||||||
| chr3:183064718 | T | G | 1 | a0001c0001t0001g0228 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.761+6281A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183064718 | |||||||
| chr3:183064803 | T | C | 327 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(324): Show |
340 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(337): Show |
intron_variant | MODIFIER | c.761+6196A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183064803 | |||||||
| chr3:183065148 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.761+5851T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183065148 | |||||||
| chr3:183065205 | G | T | 1 | a0001c0001t0001g0177 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.761+5794C>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183065205 | |||||||
| chr3:183065210 | T | C | 5 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0002c0002t0001g0218 others(2): Show |
5 | HG02040.hp2 NA18612.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.761+5789A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183065210 | |||||||
| chr3:183065211 | G | GA | 8 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(5): Show |
8 | HG02258.hp1 HG02615.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.761+5787dupT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183065211 | |||||||
| chr3:183065313 | A | C | 307 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(304): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.761+5686T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183065313 | |||||||
| chr3:183065362 | T | G | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG00423.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.761+5637A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183065362 | |||||||
| chr3:183065556 | C | T | 82 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0237 others(79): Show |
84 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.761+5443G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183065556 | |||||||
| chr3:183065561 | T | TTTTTG | 8 | a0001c0001t0001g0044 a0001c0001t0001g0197 a0001c0001t0001g0198 others(5): Show |
8 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.761+5433_761+5437d others(7): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183065561 | |||||||
| chr3:183065633 | A | AT | 306 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(303): Show |
314 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.761+5365dupA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183065633 | |||||||
| chr3:183065730 | A | C | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.761+5269T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183065730 | |||||||
| chr3:183065848 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.761+5151G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183065848 | |||||||
| chr3:183066167 | C | A | 47 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0044 others(44): Show |
48 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.761+4832G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183066167 | |||||||
| chr3:183066506 | T | C | 1 | a0001c0001t0001g0025 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.761+4493A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183066506 | |||||||
| chr3:183066578 | C | T | 2 | a0002c0002t0001g0003 a0002c0002t0001g0072 |
3 | HG03654.hp1 HG03831.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.761+4421G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183066578 | |||||||
| chr3:183066619 | A | G | 84 | a0001c0001t0001g0097 a0001c0001t0001g0181 a0001c0001t0001g0236 others(81): Show |
86 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.761+4380T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183066619 | |||||||
| chr3:183066636 | G | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG02258.hp1 HG02615.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.761+4363C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183066636 | |||||||
| chr3:183066719 | A | G | 1 | a0002c0002t0001g0278 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.761+4280T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183066719 | |||||||
| chr3:183066748 | A | T | 8 | a0002c0002t0001g0004 a0002c0002t0001g0070 a0002c0002t0001g0083 others(5): Show |
9 | HG01069.hp1 HG01071.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.761+4251T>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183066748 | |||||||
| chr3:183067000 | A | G | 60 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(57): Show |
63 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.761+3999T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183067000 | |||||||
| chr3:183067419 | A | G | 1 | a0002c0002t0001g0297 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.761+3580T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183067419 | |||||||
| chr3:183067629 | C | T | 2 | a0002c0002t0001g0295 a0002c0002t0001g0296 |
2 | HG01978.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.761+3370G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183067629 | |||||||
| chr3:183067674 | A | C | 1 | a0002c0008t0003g0331 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.761+3325T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183067674 | |||||||
| chr3:183067704 | C | T | 4 | a0002c0002t0001g0278 a0002c0002t0001g0279 a0002c0002t0001g0280 others(1): Show |
4 | HG00280.hp2 HG00642.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.761+3295G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183067704 | |||||||
| chr3:183067740 | C | T | 60 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(57): Show |
63 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.761+3259G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183067740 | |||||||
| chr3:183067899 | C | T | 1 | a0002c0002t0001g0266 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.761+3100G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183067899 | |||||||
| chr3:183067903 | G | T | 307 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(304): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.761+3096C>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183067903 | |||||||
| chr3:183067929 | T | C | 307 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(304): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.761+3070A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183067929 | |||||||
| chr3:183068206 | C | T | 1 | a0001c0013t0001g0319 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.761+2793G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183068206 | |||||||
| chr3:183068283 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.761+2716C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183068283 | |||||||
| chr3:183068424 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.761+2575C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183068424 | |||||||
| chr3:183068457 | G | C | 1 | a0001c0001t0001g0110 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.761+2542C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183068457 | |||||||
| chr3:183068844 | C | T | 58 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(55): Show |
59 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.761+2155G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183068844 | |||||||
| chr3:183068914 | T | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0172 |
2 | HG01074.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.761+2085A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183068914 | |||||||
| chr3:183068988 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.761+2011A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183068988 | |||||||
| chr3:183069257 | C | T | 307 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(304): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.761+1742G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183069257 | |||||||
| chr3:183069264 | T | C | 10 | a0001c0003t0001g0001 a0001c0003t0001g0007 a0001c0003t0001g0040 others(7): Show |
14 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.761+1735A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183069264 | |||||||
| chr3:183069480 | C | G | 1 | a0001c0010t0001g0024 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.761+1519G>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183069480 | |||||||
| chr3:183069678 | C | G | 5 | a0002c0002t0001g0290 a0002c0002t0001g0291 a0002c0002t0001g0293 others(2): Show |
5 | HG00738.hp1 HG01175.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.761+1321G>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183069678 | |||||||
| chr3:183069771 | T | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG00733.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.761+1228A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183069771 | |||||||
| chr3:183070227 | T | A | 1 | a0001c0013t0001g0319 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.761+772A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183070227 | |||||||
| chr3:183070235 | GAC | G | 82 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0237 others(79): Show |
84 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.761+762_761+763del others(2): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183070235 | |||||||
| chr3:183070403 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.761+596G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183070403 | |||||||
| chr3:183070575 | A | C | 1 | a0001c0001t0001g0197 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.761+424T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183070575 | |||||||
| chr3:183070602 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0251 a0001c0001t0001g0252 others(2): Show |
6 | NA18941.hp2 NA18964.hp2 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.761+397C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183070602 | |||||||
| chr3:183070733 | CA | C | 299 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(296): Show |
307 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.761+265delT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183070733 | |||||||
| chr3:183070733 | CAA | C | 7 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(4): Show |
7 | HG02258.hp1 HG02615.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.761+264_761+265del others(2): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 7/18 | chr3 | 183070733 | |||||||
| chr3:183071136 | T | C | 1 | a0002c0002t0001g0289 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.640-16A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 6/18 | chr3 | 183071136 | |||||||
| chr3:183071449 | A | T | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.492-92T>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 5/18 | chr3 | 183071449 | |||||||
| chr3:183071483 | C | T | 8 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(5): Show |
8 | HG01891.hp2 HG02055.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.492-126G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 5/18 | chr3 | 183071483 | |||||||
| chr3:183071579 | T | C | 307 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(304): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.492-222A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 5/18 | chr3 | 183071579 | |||||||
| chr3:183071687 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.492-330A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 5/18 | chr3 | 183071687 | |||||||
| chr3:183071718 | T | TAA | 223 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(220): Show |
229 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.492-362_492-361ins others(2): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 5/18 | chr3 | 183071718 | |||||||
| chr3:183071718 | T | TTAA | 84 | a0001c0001t0001g0044 a0001c0001t0001g0181 a0001c0001t0001g0236 others(81): Show |
86 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.492-362_492-361ins others(3): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 5/18 | chr3 | 183071718 | |||||||
| chr3:183071773 | T | C | 307 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(304): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.492-416A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 5/18 | chr3 | 183071773 | |||||||
| chr3:183071869 | A | AT | 139 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0237 others(136): Show |
144 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.491+496dupA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 5/18 | chr3 | 183071869 | |||||||
| chr3:183071869 | A | ATT | 48 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0014 others(45): Show |
49 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.491+495_491+496dup others(2): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 5/18 | chr3 | 183071869 | |||||||
| chr3:183071869 | A | ATTT | 113 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(110): Show |
115 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(112): Show |
intron_variant | MODIFIER | c.491+494_491+496dup others(3): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 5/18 | chr3 | 183071869 | |||||||
| chr3:183071869 | A | ATTTT | 7 | a0001c0001t0001g0027 a0001c0001t0001g0046 a0001c0001t0001g0053 others(4): Show |
7 | HG02055.hp1 HG02071.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.491+493_491+496dup others(4): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 5/18 | chr3 | 183071869 | |||||||
| chr3:183071905 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.491+461C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 5/18 | chr3 | 183071905 | |||||||
| chr3:183071950 | C | T | 3 | a0001c0001t0001g0053 a0001c0001t0001g0158 a0001c0013t0001g0319 |
3 | NA18965.hp1 NA19064.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.491+416G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 5/18 | chr3 | 183071950 | |||||||
| chr3:183072073 | G | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.491+293C>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 5/18 | chr3 | 183072073 | |||||||
| chr3:183072165 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.491+201C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 5/18 | chr3 | 183072165 | |||||||
| chr3:183072178 | T | A | 35 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0056 others(32): Show |
36 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.491+188A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 5/18 | chr3 | 183072178 | |||||||
| chr3:183072283 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.491+83T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 5/18 | chr3 | 183072283 | |||||||
| chr3:183072652 | A | G | 1 | a0002c0002t0001g0068 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.370-165T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183072652 | |||||||
| chr3:183072742 | C | A | 60 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(57): Show |
63 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.370-255G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183072742 | |||||||
| chr3:183072854 | C | T | 83 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0237 others(80): Show |
85 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.370-367G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183072854 | |||||||
| chr3:183072855 | T | G | 307 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(304): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.370-368A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183072855 | |||||||
| chr3:183072878 | G | C | 307 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(304): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.370-391C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183072878 | |||||||
| chr3:183072905 | C | G | 35 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0056 others(32): Show |
36 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.370-418G>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183072905 | |||||||
| chr3:183073125 | GAAC | G | 60 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(57): Show |
63 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.370-641_370-639del others(3): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183073125 | |||||||
| chr3:183073625 | A | G | 1 | a0001c0001t0001g0026 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.370-1138T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183073625 | |||||||
| chr3:183073657 | G | A | 1 | a0002c0002t0001g0318 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.370-1170C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183073657 | |||||||
| chr3:183073737 | A | C | 1 | a0002c0002t0001g0292 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.370-1250T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183073737 | |||||||
| chr3:183073749 | A | G | 1 | a0002c0002t0001g0076 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.370-1262T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183073749 | |||||||
| chr3:183073922 | A | G | 307 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(304): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.370-1435T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183073922 | |||||||
| chr3:183074060 | G | A | 307 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(304): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.370-1573C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183074060 | |||||||
| chr3:183074063 | G | A | 1 | a0001c0001t0001g0025 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.370-1576C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183074063 | |||||||
| chr3:183074313 | A | G | 9 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.370-1826T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183074313 | |||||||
| chr3:183074354 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.370-1867C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183074354 | |||||||
| chr3:183074369 | A | T | 1 | a0002c0002t0001g0259 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.370-1882T>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183074369 | |||||||
| chr3:183074407 | G | A | 307 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(304): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.370-1920C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183074407 | |||||||
| chr3:183074418 | A | C | 1 | a0002c0002t0001g0071 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.370-1931T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183074418 | |||||||
| chr3:183074579 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.370-2092T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183074579 | |||||||
| chr3:183074644 | C | T | 8 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(5): Show |
8 | HG01891.hp2 HG02055.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.370-2157G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183074644 | |||||||
| chr3:183074668 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.370-2181G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183074668 | |||||||
| chr3:183074710 | C | A | 296 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(293): Show |
304 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.370-2223G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183074710 | |||||||
| chr3:183074907 | C | T | 1 | a0002c0002t0001g0121 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.370-2420G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183074907 | |||||||
| chr3:183074911 | C | A | 4 | a0001c0003t0001g0007 a0001c0003t0001g0207 a0001c0003t0001g0208 others(1): Show |
5 | HG01891.hp1 HG02451.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.370-2424G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183074911 | |||||||
| chr3:183075545 | CT | C | 207 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(204): Show |
213 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(210): Show |
intron_variant | MODIFIER | c.370-3059delA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183075545 | |||||||
| chr3:183075545 | CTT | C | 10 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(7): Show |
10 | HG01891.hp2 HG02055.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.370-3060_370-3059d others(4): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183075545 | |||||||
| chr3:183075563 | CAG | C | 307 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(304): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.370-3078_370-3077d others(4): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183075563 | |||||||
| chr3:183075979 | T | C | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG02717.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.370-3492A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183075979 | |||||||
| chr3:183076055 | A | G | 3 | a0002c0002t0001g0278 a0002c0002t0001g0279 a0002c0002t0001g0280 |
3 | HG00280.hp2 HG00642.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.370-3568T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183076055 | |||||||
| chr3:183076134 | G | A | 8 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(5): Show |
8 | HG01891.hp2 HG02055.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.370-3647C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183076134 | |||||||
| chr3:183076316 | T | G | 1 | a0002c0002t0001g0312 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.370-3829A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183076316 | |||||||
| chr3:183076323 | A | T | 9 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.370-3836T>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183076323 | |||||||
| chr3:183076347 | A | G | 296 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(293): Show |
304 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.370-3860T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183076347 | |||||||
| chr3:183076397 | T | C | 2 | a0002c0002t0001g0091 a0002c0002t0001g0092 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.370-3910A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183076397 | |||||||
| chr3:183076408 | C | T | 2 | a0002c0002t0001g0290 a0002c0002t0001g0291 |
2 | HG01255.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.370-3921G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183076408 | |||||||
| chr3:183076728 | T | C | 95 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0042 others(92): Show |
97 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.370-4241A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183076728 | |||||||
| chr3:183076761 | T | G | 8 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(5): Show |
8 | HG01891.hp2 HG02055.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.370-4274A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183076761 | |||||||
| chr3:183076809 | C | G | 1 | a0002c0002t0001g0289 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.370-4322G>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183076809 | |||||||
| chr3:183076939 | T | C | 60 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(57): Show |
63 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.370-4452A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183076939 | |||||||
| chr3:183076950 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.370-4463T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183076950 | |||||||
| chr3:183077015 | T | C | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.370-4528A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183077015 | |||||||
| chr3:183077019 | C | T | 2 | a0002c0002t0001g0287 a0002c0002t0001g0288 |
2 | HG00639.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.370-4532G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183077019 | |||||||
| chr3:183077073 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.370-4586A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183077073 | |||||||
| chr3:183077272 | G | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
4 | HG02896.hp1 HG03098.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.370-4785C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183077272 | |||||||
| chr3:183077338 | C | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
4 | HG02896.hp1 HG03098.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.370-4851G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183077338 | |||||||
| chr3:183077433 | G | A | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.370-4946C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183077433 | |||||||
| chr3:183077575 | T | A | 8 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(5): Show |
8 | HG01891.hp2 HG02055.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.370-5088A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183077575 | |||||||
| chr3:183077607 | G | T | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.370-5120C>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183077607 | |||||||
| chr3:183077627 | AT | A | 83 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0237 others(80): Show |
85 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.370-5141delA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183077627 | |||||||
| chr3:183078001 | C | T | 12 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(9): Show |
12 | HG02258.hp1 HG02451.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.370-5514G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183078001 | |||||||
| chr3:183078027 | A | G | 35 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0056 others(32): Show |
36 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.370-5540T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183078027 | |||||||
| chr3:183078073 | G | T | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.370-5586C>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183078073 | |||||||
| chr3:183078122 | C | T | 83 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0237 others(80): Show |
85 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.370-5635G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183078122 | |||||||
| chr3:183078207 | A | G | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.370-5720T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183078207 | |||||||
| chr3:183078259 | A | G | 2 | a0002c0002t0001g0116 a0002c0002t0001g0120 |
2 | HG02015.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.370-5772T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183078259 | |||||||
| chr3:183078298 | G | C | 53 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(50): Show |
56 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.370-5811C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183078298 | |||||||
| chr3:183078524 | ATC | A | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.370-6039_370-6038d others(4): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183078524 | |||||||
| chr3:183078685 | C | A | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.370-6198G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183078685 | |||||||
| chr3:183078937 | G | C | 1 | a0001c0001t0001g0313 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.370-6450C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183078937 | |||||||
| chr3:183079052 | C | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02896.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.370-6565G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183079052 | |||||||
| chr3:183079116 | C | T | 8 | a0002c0002t0001g0004 a0002c0002t0001g0070 a0002c0002t0001g0083 others(5): Show |
9 | HG01069.hp1 HG01071.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.370-6629G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183079116 | |||||||
| chr3:183079127 | C | T | 1 | a0001c0001t0001g0276 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.370-6640G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183079127 | |||||||
| chr3:183079243 | C | T | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.370-6756G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183079243 | |||||||
| chr3:183079244 | A | G | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.370-6757T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183079244 | |||||||
| chr3:183079280 | A | G | 1 | a0003c0007t0001g0034 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.370-6793T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183079280 | |||||||
| chr3:183079329 | T | G | 317 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(314): Show |
329 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.370-6842A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183079329 | |||||||
| chr3:183079360 | T | A | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.370-6873A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183079360 | |||||||
| chr3:183079470 | G | A | 1 | a0002c0002t0001g0137 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.370-6983C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183079470 | |||||||
| chr3:183079521 | T | A | 82 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0237 others(79): Show |
84 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.370-7034A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183079521 | |||||||
| chr3:183079536 | T | G | 6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG02258.hp1 HG02615.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.370-7049A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183079536 | |||||||
| chr3:183079747 | C | G | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.369+6946G>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183079747 | |||||||
| chr3:183079832 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.369+6861C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183079832 | |||||||
| chr3:183079841 | C | A | 3 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 |
3 | NA18957.hp2 NA19057.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.369+6852G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183079841 | |||||||
| chr3:183079933 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.369+6760G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183079933 | |||||||
| chr3:183079941 | T | C | 1 | a0002c0002t0001g0218 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.369+6752A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183079941 | |||||||
| chr3:183079958 | A | G | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.369+6735T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183079958 | |||||||
| chr3:183080120 | T | C | 2 | a0002c0002t0001g0060 a0002c0002t0001g0061 |
2 | HG01069.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.369+6573A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183080120 | |||||||
| chr3:183080259 | C | T | 8 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(5): Show |
8 | HG01891.hp2 HG02055.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.369+6434G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183080259 | |||||||
| chr3:183080297 | G | A | 3 | a0002c0002t0001g0051 a0002c0002t0001g0052 a0002c0002t0001g0150 |
3 | HG00438.hp1 NA19068.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.369+6396C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183080297 | |||||||
| chr3:183080432 | A | C | 1 | a0002c0002t0001g0316 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.369+6261T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183080432 | |||||||
| chr3:183080726 | AT | A | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.369+5966delA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183080726 | |||||||
| chr3:183080744 | A | G | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.369+5949T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183080744 | |||||||
| chr3:183080883 | T | C | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.369+5810A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183080883 | |||||||
| chr3:183080977 | A | T | 1 | a0002c0002t0001g0041 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.369+5716T>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183080977 | |||||||
| chr3:183081095 | G | A | 60 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(57): Show |
63 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.369+5598C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183081095 | |||||||
| chr3:183081351 | C | T | 45 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0050 others(42): Show |
47 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.369+5342G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183081351 | |||||||
| chr3:183081359 | T | C | 4 | a0003c0005t0001g0035 a0003c0005t0001g0036 a0003c0007t0001g0033 others(1): Show |
4 | HG02895.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.369+5334A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183081359 | |||||||
| chr3:183081454 | C | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0042 others(89): Show |
94 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.369+5239G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183081454 | |||||||
| chr3:183081653 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.369+5040G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183081653 | |||||||
| chr3:183081684 | C | T | 8 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(5): Show |
8 | HG01891.hp2 HG02055.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.369+5009G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183081684 | |||||||
| chr3:183081719 | G | A | 8 | a0002c0002t0001g0004 a0002c0002t0001g0070 a0002c0002t0001g0083 others(5): Show |
9 | HG01069.hp1 HG01071.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.369+4974C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183081719 | |||||||
| chr3:183081769 | G | C | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.369+4924C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183081769 | |||||||
| chr3:183082115 | C | T | 1 | a0002c0002t0001g0061 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.369+4578G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183082115 | |||||||
| chr3:183082251 | C | T | 167 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0020 others(164): Show |
172 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.369+4442G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183082251 | |||||||
| chr3:183082463 | C | T | 1 | a0001c0001t0001g0039 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.369+4230G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183082463 | |||||||
| chr3:183082499 | G | A | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.369+4194C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183082499 | |||||||
| chr3:183082705 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.369+3988G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183082705 | |||||||
| chr3:183082715 | C | T | 7 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(4): Show |
7 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.369+3978G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183082715 | |||||||
| chr3:183082733 | G | A | 60 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(57): Show |
63 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.369+3960C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183082733 | |||||||
| chr3:183082787 | G | A | 60 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(57): Show |
63 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.369+3906C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183082787 | |||||||
| chr3:183082795 | C | T | 19 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(16): Show |
19 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.369+3898G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183082795 | |||||||
| chr3:183082881 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.369+3812A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183082881 | |||||||
| chr3:183082916 | T | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.369+3777A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183082916 | |||||||
| chr3:183082989 | TA | T | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.369+3703delT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183082989 | |||||||
| chr3:183083109 | A | C | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG02717.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.369+3584T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183083109 | |||||||
| chr3:183083204 | T | G | 83 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0237 others(80): Show |
85 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.369+3489A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183083204 | |||||||
| chr3:183083356 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.369+3337G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183083356 | |||||||
| chr3:183083441 | T | C | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.369+3252A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183083441 | |||||||
| chr3:183083536 | G | T | 317 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(314): Show |
329 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.369+3157C>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183083536 | |||||||
| chr3:183083552 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.369+3141T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183083552 | |||||||
| chr3:183083567 | C | T | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.369+3126G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183083567 | |||||||
| chr3:183083685 | G | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0286 |
2 | NA18953.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.369+3008C>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183083685 | |||||||
| chr3:183084057 | T | G | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG02717.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.369+2636A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183084057 | |||||||
| chr3:183084116 | G | A | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.369+2577C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183084116 | |||||||
| chr3:183084343 | A | ATCTTATG others(6): Show |
2 | a0001c0001t0001g0067 a0001c0001t0001g0145 |
2 | HG00621.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.369+2349_369+2350i others(15): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183084343 | |||||||
| chr3:183084348 | G | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0145 |
2 | HG00621.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.369+2345C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183084348 | |||||||
| chr3:183084349 | G | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0145 |
2 | HG00621.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.369+2344C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183084349 | |||||||
| chr3:183084350 | C | G | 2 | a0001c0001t0001g0067 a0001c0001t0001g0145 |
2 | HG00621.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.369+2343G>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183084350 | |||||||
| chr3:183084354 | T | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0145 |
2 | HG00621.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.369+2339A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183084354 | |||||||
| chr3:183084376 | G | A | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.369+2317C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183084376 | |||||||
| chr3:183084446 | C | T | 2 | a0002c0002t0001g0285 a0002c0002t0001g0314 |
2 | NA18975.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.369+2247G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183084446 | |||||||
| chr3:183084746 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.369+1947C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183084746 | |||||||
| chr3:183084943 | C | T | 1 | a0002c0008t0003g0331 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.369+1750G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183084943 | |||||||
| chr3:183084957 | T | C | 1 | a0001c0003t0001g0196 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.369+1736A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183084957 | |||||||
| chr3:183085059 | A | T | 1 | a0002c0008t0003g0331 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.369+1634T>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183085059 | |||||||
| chr3:183085086 | G | T | 96 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0020 others(93): Show |
98 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.369+1607C>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183085086 | |||||||
| chr3:183085118 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.369+1575C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183085118 | |||||||
| chr3:183085144 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.369+1549T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183085144 | |||||||
| chr3:183085177 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.369+1516G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183085177 | |||||||
| chr3:183085260 | C | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02896.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.369+1433G>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183085260 | |||||||
| chr3:183085466 | C | CA | 9 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.369+1226dupT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183085466 | |||||||
| chr3:183085630 | T | TA | 9 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(6): Show |
9 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.369+1062dupT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183085630 | |||||||
| chr3:183085630 | TA | T | 262 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(259): Show |
270 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.369+1062delT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183085630 | |||||||
| chr3:183085630 | TAA | T | 22 | a0001c0001t0001g0047 a0001c0001t0001g0097 a0001c0001t0001g0098 others(19): Show |
22 | HG01169.hp1 HG01169.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.369+1061_369+1062d others(4): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183085630 | |||||||
| chr3:183085724 | A | T | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.369+969T>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183085724 | |||||||
| chr3:183085744 | T | C | 307 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(304): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.369+949A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183085744 | |||||||
| chr3:183085868 | C | T | 95 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0042 others(92): Show |
97 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.369+825G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183085868 | |||||||
| chr3:183085947 | C | T | 9 | a0001c0003t0001g0001 a0001c0003t0001g0007 a0001c0003t0001g0040 others(6): Show |
13 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.369+746G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183085947 | |||||||
| chr3:183086051 | G | A | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.369+642C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183086051 | |||||||
| chr3:183086069 | C | T | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.369+624G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183086069 | |||||||
| chr3:183086597 | G | A | 82 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0237 others(79): Show |
84 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.369+96C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 4/18 | chr3 | 183086597 | |||||||
| chr3:183087114 | T | C | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.274-326A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183087114 | |||||||
| chr3:183087273 | A | T | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.274-485T>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183087273 | |||||||
| chr3:183087288 | A | C | 1 | a0001c0001t0001g0049 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.274-500T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183087288 | |||||||
| chr3:183087301 | G | C | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.274-513C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183087301 | |||||||
| chr3:183087418 | G | A | 5 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0002c0002t0001g0218 others(2): Show |
5 | HG02040.hp2 NA18612.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-630C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183087418 | |||||||
| chr3:183087489 | C | T | 4 | a0001c0003t0001g0007 a0001c0003t0001g0207 a0001c0003t0001g0208 others(1): Show |
5 | HG01891.hp1 HG02451.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-701G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183087489 | |||||||
| chr3:183087511 | A | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.274-723T>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183087511 | |||||||
| chr3:183087564 | A | G | 1 | a0001c0001t0001g0258 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.274-776T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183087564 | |||||||
| chr3:183087869 | C | CA | 67 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0022 others(64): Show |
68 | HG00558.hp1 HG00621.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.274-1082dupT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183087869 | |||||||
| chr3:183087869 | CA | C | 12 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(9): Show |
12 | HG01069.hp2 HG01891.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.274-1082delT | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183087869 | |||||||
| chr3:183087883 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.274-1095T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183087883 | |||||||
| chr3:183087904 | T | G | 1 | a0001c0001t0001g0238 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.274-1116A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183087904 | |||||||
| chr3:183088016 | C | T | 307 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(304): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.274-1228G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183088016 | |||||||
| chr3:183088155 | G | C | 96 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0042 others(93): Show |
98 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.274-1367C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183088155 | |||||||
| chr3:183088204 | T | TTGTTG | 5 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(2): Show |
5 | HG02896.hp1 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-1417_274-1416i others(7): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183088204 | |||||||
| chr3:183088204 | T | TTGTTGTT others(4): Show |
6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG02258.hp1 HG02615.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.274-1417_274-1416i others(13): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183088204 | |||||||
| chr3:183088208 | G | GT | 3 | a0001c0001t0001g0246 a0002c0002t0001g0281 a0002c0002t0001g0282 |
3 | HG00558.hp2 HG02602.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.274-1421dupA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183088208 | |||||||
| chr3:183088209 | TG | T | 3 | a0002c0002t0001g0278 a0002c0002t0001g0279 a0002c0002t0001g0280 |
3 | HG00280.hp2 HG00642.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.274-1422delC | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183088209 | |||||||
| chr3:183088210 | G | T | 79 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0237 others(76): Show |
81 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.274-1422C>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183088210 | |||||||
| chr3:183088216 | T | C | 1 | a0002c0008t0003g0331 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.274-1428A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183088216 | |||||||
| chr3:183088245 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.274-1457G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183088245 | |||||||
| chr3:183088299 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.274-1511G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183088299 | |||||||
| chr3:183088317 | C | T | 1 | a0002c0002t0001g0116 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.274-1529G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183088317 | |||||||
| chr3:183088318 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.274-1530A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183088318 | |||||||
| chr3:183088331 | C | T | 1 | a0002c0002t0001g0239 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.274-1543G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183088331 | |||||||
| chr3:183088354 | A | G | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.274-1566T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183088354 | |||||||
| chr3:183088496 | G | A | 1 | a0002c0002t0001g0219 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.274-1708C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183088496 | |||||||
| chr3:183088656 | T | C | 4 | a0002c0002t0001g0068 a0002c0002t0001g0112 a0002c0002t0001g0113 others(1): Show |
4 | HG00280.hp1 HG01167.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-1868A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183088656 | |||||||
| chr3:183088838 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.274-2050A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183088838 | |||||||
| chr3:183088907 | G | A | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG02717.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.274-2119C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183088907 | |||||||
| chr3:183088970 | C | T | 1 | a0002c0002t0001g0277 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.274-2182G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183088970 | |||||||
| chr3:183089056 | T | C | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG02717.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.274-2268A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183089056 | |||||||
| chr3:183089422 | G | T | 12 | a0001c0001t0001g0044 a0001c0001t0001g0197 a0001c0001t0001g0198 others(9): Show |
12 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.274-2634C>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183089422 | |||||||
| chr3:183089489 | C | T | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG02717.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.274-2701G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183089489 | |||||||
| chr3:183089496 | C | A | 3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 |
3 | NA18947.hp2 NA18969.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.274-2708G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183089496 | |||||||
| chr3:183090176 | A | G | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.273+2233T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183090176 | |||||||
| chr3:183090178 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.273+2231C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183090178 | |||||||
| chr3:183090204 | G | T | 61 | a0001c0001t0001g0236 a0002c0002t0001g0003 a0002c0002t0001g0004 others(58): Show |
64 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.273+2205C>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183090204 | |||||||
| chr3:183090340 | C | A | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.273+2069G>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183090340 | |||||||
| chr3:183090386 | T | C | 1 | a0001c0001t0001g0181 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.273+2023A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183090386 | |||||||
| chr3:183090675 | C | T | 1 | a0001c0001t0001g0276 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.273+1734G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183090675 | |||||||
| chr3:183090888 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.273+1521C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183090888 | |||||||
| chr3:183091043 | T | C | 1 | a0002c0002t0001g0140 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.273+1366A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183091043 | |||||||
| chr3:183091076 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.273+1333G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183091076 | |||||||
| chr3:183091173 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.273+1236A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183091173 | |||||||
| chr3:183091226 | G | T | 35 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0056 others(32): Show |
36 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.273+1183C>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183091226 | |||||||
| chr3:183091293 | C | T | 4 | a0003c0005t0001g0035 a0003c0005t0001g0036 a0003c0007t0001g0033 others(1): Show |
4 | HG02895.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+1116G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183091293 | |||||||
| chr3:183091413 | C | T | 1 | a0002c0008t0003g0331 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.273+996G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183091413 | |||||||
| chr3:183091541 | C | T | 3 | a0001c0001t0001g0049 a0001c0001t0001g0088 a0001c0001t0001g0089 |
3 | HG01346.hp2 HG01928.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.273+868G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183091541 | |||||||
| chr3:183091573 | A | AAAAAC | 9 | a0001c0003t0001g0001 a0001c0003t0001g0007 a0001c0003t0001g0040 others(6): Show |
13 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.273+831_273+835dup others(5): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183091573 | |||||||
| chr3:183091573 | AAAAAC | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0210 a0001c0001t0001g0211 others(5): Show |
9 | HG02717.hp1 HG02922.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.273+831_273+835del others(5): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183091573 | |||||||
| chr3:183091660 | A | C | 4 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(1): Show |
4 | HG02559.hp2 HG02647.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+749T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183091660 | |||||||
| chr3:183091724 | CCAGT | C | 78 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0237 others(75): Show |
80 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.273+681_273+684del others(4): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183091724 | |||||||
| chr3:183091764 | T | C | 1 | a0002c0002t0001g0060 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.273+645A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183091764 | |||||||
| chr3:183091769 | A | G | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(4): Show |
7 | HG02109.hp2 HG02258.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+640T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183091769 | |||||||
| chr3:183091770 | C | T | 1 | a0002c0002t0001g0060 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.273+639G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183091770 | |||||||
| chr3:183091773 | T | G | 1 | a0001c0001t0001g0025 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.273+636A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183091773 | |||||||
| chr3:183091805 | A | G | 70 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0027 others(67): Show |
76 | HG00408.hp1 HG00544.hp1 HG01069.hp1 others(73): Show |
intron_variant | MODIFIER | c.273+604T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183091805 | |||||||
| chr3:183091806 | A | G | 64 | a0001c0001t0001g0006 a0001c0001t0001g0042 a0001c0001t0001g0043 others(61): Show |
65 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.273+603T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183091806 | |||||||
| chr3:183091821 | G | A | 5 | a0002c0008t0003g0331 a0003c0005t0001g0035 a0003c0005t0001g0036 others(2): Show |
5 | HG02280.hp1 HG02895.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.273+588C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183091821 | |||||||
| chr3:183091834 | T | C | 3 | a0003c0005t0001g0035 a0003c0007t0001g0033 a0003c0007t0001g0034 |
3 | HG02895.hp1 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.273+575A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183091834 | |||||||
| chr3:183091859 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.273+550T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183091859 | |||||||
| chr3:183091862 | A | C | 76 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0042 others(73): Show |
78 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.273+547T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183091862 | |||||||
| chr3:183091936 | GTCGAGGC others(7): Show |
G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG00733.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.273+459_273+472del others(14): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183091936 | |||||||
| chr3:183091946 | G | C | 2 | a0001c0001t0001g0085 a0001c0001t0001g0087 |
2 | HG01257.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.273+463C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183091946 | |||||||
| chr3:183091983 | C | T | 1 | a0001c0001t0001g0025 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.273+426G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183091983 | |||||||
| chr3:183092027 | G | C | 1 | a0001c0001t0001g0235 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.273+382C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183092027 | |||||||
| chr3:183092139 | G | A | 27 | a0002c0002t0001g0005 a0002c0002t0001g0050 a0002c0002t0001g0055 others(24): Show |
28 | HG00408.hp1 HG00544.hp1 HG01934.hp1 others(25): Show |
intron_variant | MODIFIER | c.273+270C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183092139 | |||||||
| chr3:183092340 | T | C | 1 | a0002c0008t0003g0331 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.273+69A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183092340 | |||||||
| chr3:183092356 | T | G | 92 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0192 others(89): Show |
95 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.273+53A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183092356 | |||||||
| chr3:183092393 | A | G | 1 | a0002c0002t0001g0055 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.273+16T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 3/18 | chr3 | 183092393 | |||||||
| chr3:183092697 | T | A | 2 | a0003c0007t0001g0033 a0003c0007t0001g0034 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.137-152A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 2/18 | chr3 | 183092697 | |||||||
| chr3:183092879 | GTATT | G | 4 | a0002c0002t0001g0141 a0002c0002t0001g0142 a0002c0002t0001g0143 others(1): Show |
4 | HG02258.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-338_137-335del others(4): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 2/18 | chr3 | 183092879 | |||||||
| chr3:183092976 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.137-431G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 2/18 | chr3 | 183092976 | |||||||
| chr3:183093160 | C | G | 1 | a0001c0001t0001g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.137-615G>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 2/18 | chr3 | 183093160 | |||||||
| chr3:183093348 | T | C | 1 | a0002c0008t0003g0331 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.137-803A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 2/18 | chr3 | 183093348 | |||||||
| chr3:183093420 | T | A | 1 | a0001c0001t0001g0145 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.137-875A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 2/18 | chr3 | 183093420 | |||||||
| chr3:183093501 | T | C | 19 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(16): Show |
19 | HG00544.hp2 HG01255.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.137-956A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 2/18 | chr3 | 183093501 | |||||||
| chr3:183093517 | G | C | 1 | a0002c0002t0001g0320 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.137-972C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 2/18 | chr3 | 183093517 | |||||||
| chr3:183093520 | TGGC | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0251 a0001c0001t0001g0252 others(2): Show |
6 | NA18941.hp2 NA18964.hp2 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.137-978_137-976del others(3): Show |
MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 2/18 | chr3 | 183093520 | |||||||
| chr3:183093621 | T | C | 1 | a0002c0002t0001g0321 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.136+938A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 2/18 | chr3 | 183093621 | |||||||
| chr3:183093634 | C | T | 3 | a0002c0002t0001g0248 a0002c0002t0001g0249 a0002c0002t0001g0250 |
3 | NA18974.hp2 NA18994.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.136+925G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 2/18 | chr3 | 183093634 | |||||||
| chr3:183093702 | G | C | 59 | a0001c0001t0001g0006 a0001c0001t0001g0042 a0001c0001t0001g0043 others(56): Show |
60 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.136+857C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 2/18 | chr3 | 183093702 | |||||||
| chr3:183093889 | GT | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
4 | HG02896.hp1 HG03098.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+669delA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 2/18 | chr3 | 183093889 | |||||||
| chr3:183094048 | C | CT | 12 | a0001c0001t0001g0045 a0001c0001t0001g0053 a0001c0001t0001g0246 others(9): Show |
13 | HG00438.hp1 HG02080.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.136+510dupA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 2/18 | chr3 | 183094048 | |||||||
| chr3:183094088 | G | A | 1 | a0001c0001t0001g0325 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.136+471C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 2/18 | chr3 | 183094088 | |||||||
| chr3:183094161 | G | C | 1 | a0002c0002t0001g0323 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.136+398C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 2/18 | chr3 | 183094161 | |||||||
| chr3:183094196 | C | G | 4 | a0003c0005t0001g0035 a0003c0005t0001g0036 a0003c0007t0001g0033 others(1): Show |
4 | HG02895.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+363G>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 2/18 | chr3 | 183094196 | |||||||
| chr3:183094198 | G | A | 1 | a0001c0003t0001g0209 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.136+361C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 2/18 | chr3 | 183094198 | |||||||
| chr3:183094269 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.136+290G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 2/18 | chr3 | 183094269 | |||||||
| chr3:183094318 | G | A | 1 | a0003c0005t0001g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.136+241C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 2/18 | chr3 | 183094318 | |||||||
| chr3:183094697 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.90-92G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183094697 | |||||||
| chr3:183094708 | C | T | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG01109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.90-103G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183094708 | |||||||
| chr3:183095040 | T | C | 1 | a0001c0010t0001g0024 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.90-435A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183095040 | |||||||
| chr3:183095503 | A | C | 1 | a0001c0001t0001g0232 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.90-898T>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183095503 | |||||||
| chr3:183095553 | T | A | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.90-948A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183095553 | |||||||
| chr3:183095573 | T | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
4 | HG02896.hp1 HG03098.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.90-968A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183095573 | |||||||
| chr3:183095814 | C | T | 19 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(16): Show |
19 | HG00544.hp2 HG01255.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.90-1209G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183095814 | |||||||
| chr3:183096064 | A | G | 327 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(324): Show |
340 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(337): Show |
intron_variant | MODIFIER | c.90-1459T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183096064 | |||||||
| chr3:183096095 | A | G | 1 | a0002c0008t0003g0331 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.90-1490T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183096095 | |||||||
| chr3:183096305 | C | T | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02071.hp2 HG02080.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.90-1700G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183096305 | |||||||
| chr3:183096323 | G | A | 1 | a0002c0008t0003g0331 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.90-1718C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183096323 | |||||||
| chr3:183096343 | A | T | 109 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(106): Show |
112 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.90-1738T>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183096343 | |||||||
| chr3:183096346 | AT | A | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG02717.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.90-1742delA | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183096346 | |||||||
| chr3:183096347 | T | A | 29 | a0001c0001t0001g0006 a0001c0001t0001g0037 a0001c0001t0001g0054 others(26): Show |
35 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.90-1742A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183096347 | |||||||
| chr3:183096370 | T | G | 1 | a0002c0008t0003g0331 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.90-1765A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183096370 | |||||||
| chr3:183096620 | G | A | 7 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(4): Show |
7 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.90-2015C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183096620 | |||||||
| chr3:183096712 | G | A | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 |
3 | HG01167.hp2 HG01169.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.90-2107C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183096712 | |||||||
| chr3:183096866 | T | G | 12 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 others(9): Show |
16 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.90-2261A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183096866 | |||||||
| chr3:183097036 | G | C | 96 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0236 others(93): Show |
99 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.89+2316C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183097036 | |||||||
| chr3:183097188 | C | T | 5 | a0002c0002t0001g0239 a0002c0002t0001g0240 a0002c0002t0001g0241 others(2): Show |
5 | NA18947.hp1 NA18951.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.89+2164G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183097188 | |||||||
| chr3:183097209 | C | T | 3 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 |
3 | NA18957.hp2 NA19057.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.89+2143G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183097209 | |||||||
| chr3:183097302 | T | G | 96 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0236 others(93): Show |
99 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.89+2050A>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183097302 | |||||||
| chr3:183097555 | T | A | 19 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(16): Show |
19 | HG00544.hp2 HG01255.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.89+1797A>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183097555 | |||||||
| chr3:183097591 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.89+1761G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183097591 | |||||||
| chr3:183097752 | G | A | 4 | a0001c0001t0001g0042 a0001c0001t0001g0232 a0001c0001t0001g0233 others(1): Show |
4 | HG01074.hp1 HG02145.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.89+1600C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183097752 | |||||||
| chr3:183097768 | T | C | 100 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0236 others(97): Show |
103 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.89+1584A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183097768 | |||||||
| chr3:183098123 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.89+1229C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183098123 | |||||||
| chr3:183098130 | C | G | 1 | a0001c0001t0001g0042 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.89+1222G>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183098130 | |||||||
| chr3:183098141 | G | A | 96 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0236 others(93): Show |
99 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.89+1211C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183098141 | |||||||
| chr3:183098316 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.89+1036T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183098316 | |||||||
| chr3:183098389 | A | G | 1 | a0002c0002t0001g0041 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.89+963T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183098389 | |||||||
| chr3:183098439 | T | C | 5 | a0001c0003t0001g0011 a0001c0003t0001g0326 a0001c0003t0001g0327 others(2): Show |
6 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.89+913A>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183098439 | |||||||
| chr3:183098541 | A | G | 1 | a0001c0003t0001g0040 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.89+811T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183098541 | |||||||
| chr3:183098570 | A | G | 1 | a0001c0001t0001g0039 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.89+782T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183098570 | |||||||
| chr3:183098617 | A | T | 1 | a0002c0002t0001g0038 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.89+735T>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183098617 | |||||||
| chr3:183098658 | G | A | 4 | a0003c0005t0001g0035 a0003c0005t0001g0036 a0003c0007t0001g0033 others(1): Show |
4 | HG02895.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.89+694C>T | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183098658 | |||||||
| chr3:183098848 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.89+504T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183098848 | |||||||
| chr3:183098987 | A | G | 7 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(4): Show |
7 | HG02258.hp1 HG02615.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.89+365T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183098987 | |||||||
| chr3:183098998 | A | G | 1 | a0002c0002t0001g0029 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.89+354T>C | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183098998 | |||||||
| chr3:183099300 | G | C | 1 | a0002c0002t0001g0330 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.89+52C>G | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183099300 | |||||||
| chr3:183099310 | C | T | 17 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(14): Show |
17 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.89+42G>A | MCCC1 | ENSG00000078070.14 | transcript | ENST00000265594.9 | protein_coding | 1/18 | chr3 | 183099310 |