Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57511 |
| ensemblid | ENSG00000133103.17 |
| hgncid | 18621 |
| symbol | COG6 |
| name | component of oligomeric golgi complex 6 |
| refseq_nuc | NM_020751.3 |
| refseq_prot | NP_065802.1 |
| ensembl_nuc | ENST00000455146.8 |
| ensembl_prot | ENSP00000397441.2 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 39655662 |
| end | 39752628 |
| strand | + |
| ver | v1.2 |
| region | chr13:39655662-39752628 |
| region5000 | chr13:39650662-39757628 |
| regionname0 | COG6_chr13_39655662_39752628 |
| regionname5000 | COG6_chr13_39650662_39757628 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 657 | 215 | 39 | 39 | 99 | 11 | 25 | 81 | COG6_chr13_39650662_39757628 | COG6 | MAEGS others(652): Show |
chr13 | 39650662 | 39757628 |
| a0002 | 0/0 | 657 | 139 | 39 | 24 | 59 | 7 | 10 | 43 | COG6_chr13_39650662_39757628 | COG6 | MAEGS others(652): Show |
chr13 | 39650662 | 39757628 |
| a0003 | 0/0 | 657 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | MAEGS others(652): Show |
chr13 | 39650662 | 39757628 |
| a0004 | 0/0 | 657 | 4 | 1 | 0 | 0 | 0 | 3 | 0 | COG6_chr13_39650662_39757628 | COG6 | MAEGS others(652): Show |
chr13 | 39650662 | 39757628 |
| a0005 | 0/0 | 657 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | MAEGS others(652): Show |
chr13 | 39650662 | 39757628 |
| a0006 | 0/0 | 657 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | MAEGS others(652): Show |
chr13 | 39650662 | 39757628 |
| a0007 | 0/0 | 657 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | MAEGS others(652): Show |
chr13 | 39650662 | 39757628 |
| a0008 | 0/0 | 657 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | MAEGS others(652): Show |
chr13 | 39650662 | 39757628 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1971 | 211 | 38 | 37 | 98 | 11 | 25 | COG6_chr13_39650662_39757628 | COG6 | ATGGC others(1966): Show |
chr13 | 39650662 | 39757628 | ||
| a0001c0006 | 0/0 | 1971 | 2 | 0 | 2 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ATGGC others(1966): Show |
chr13 | 39650662 | 39757628 | ||
| a0001c0011 | 0/0 | 1971 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ATGGC others(1966): Show |
chr13 | 39650662 | 39757628 | ||
| a0001c0012 | 0/0 | 1971 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ATGGC others(1966): Show |
chr13 | 39650662 | 39757628 | ||
| a0002c0002 | 0/0 | 1971 | 138 | 39 | 24 | 58 | 7 | 10 | COG6_chr13_39650662_39757628 | COG6 | ATGGC others(1966): Show |
chr13 | 39650662 | 39757628 | ||
| a0002c0007 | 0/0 | 1971 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ATGGC others(1966): Show |
chr13 | 39650662 | 39757628 | ||
| a0003c0003 | 0/0 | 1971 | 6 | 5 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ATGGC others(1966): Show |
chr13 | 39650662 | 39757628 | ||
| a0004c0004 | 0/0 | 1971 | 4 | 1 | 0 | 0 | 0 | 3 | COG6_chr13_39650662_39757628 | COG6 | ATGGC others(1966): Show |
chr13 | 39650662 | 39757628 | ||
| a0005c0005 | 0/0 | 1971 | 3 | 3 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ATGGC others(1966): Show |
chr13 | 39650662 | 39757628 | ||
| a0006c0010 | 0/0 | 1971 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ATGGC others(1966): Show |
chr13 | 39650662 | 39757628 | ||
| a0007c0008 | 0/0 | 1971 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ATGGC others(1966): Show |
chr13 | 39650662 | 39757628 | ||
| a0008c0009 | 0/0 | 1971 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ATGGC others(1966): Show |
chr13 | 39650662 | 39757628 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3574 | 103 | 9 | 18 | 52 | 4 | 19 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3569): Show |
chr13 | 39650662 | 39757628 |
| a0001c0001t0003 | 1/0 | 3574 | 81 | 13 | 18 | 41 | 3 | 5 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3569): Show |
chr13 | 39650662 | 39757628 |
| a0001c0001t0004 | 0/0 | 3573 | 16 | 8 | 0 | 5 | 3 | 0 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3568): Show |
chr13 | 39650662 | 39757628 |
| a0001c0001t0005 | 0/0 | 3573 | 7 | 7 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3568): Show |
chr13 | 39650662 | 39757628 |
| a0001c0001t0012 | 0/0 | 3574 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3569): Show |
chr13 | 39650662 | 39757628 |
| a0001c0001t0013 | 0/0 | 3574 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3569): Show |
chr13 | 39650662 | 39757628 |
| a0001c0001t0014 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3569): Show |
chr13 | 39650662 | 39757628 |
| a0001c0001t0015 | 0/0 | 3574 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3569): Show |
chr13 | 39650662 | 39757628 |
| a0001c0006t0003 | 0/0 | 3574 | 2 | 0 | 2 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3569): Show |
chr13 | 39650662 | 39757628 |
| a0001c0011t0003 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3569): Show |
chr13 | 39650662 | 39757628 |
| a0001c0012t0003 | 0/0 | 3574 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3569): Show |
chr13 | 39650662 | 39757628 |
| a0002c0002t0002 | 0/0 | 3574 | 102 | 17 | 21 | 47 | 7 | 10 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3569): Show |
chr13 | 39650662 | 39757628 |
| a0002c0002t0003 | 0/0 | 3574 | 4 | 4 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3569): Show |
chr13 | 39650662 | 39757628 |
| a0002c0002t0004 | 0/0 | 3573 | 6 | 4 | 0 | 2 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3568): Show |
chr13 | 39650662 | 39757628 |
| a0002c0002t0005 | 0/0 | 3573 | 4 | 4 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3568): Show |
chr13 | 39650662 | 39757628 |
| a0002c0002t0006 | 0/0 | 3575 | 8 | 2 | 2 | 4 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3570): Show |
chr13 | 39650662 | 39757628 |
| a0002c0002t0007 | 0/0 | 3575 | 4 | 2 | 0 | 2 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3570): Show |
chr13 | 39650662 | 39757628 |
| a0002c0002t0008 | 0/0 | 3574 | 4 | 3 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3569): Show |
chr13 | 39650662 | 39757628 |
| a0002c0002t0009 | 0/0 | 3574 | 3 | 0 | 0 | 3 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3569): Show |
chr13 | 39650662 | 39757628 |
| a0002c0002t0010 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3569): Show |
chr13 | 39650662 | 39757628 |
| a0002c0002t0011 | 0/0 | 3575 | 2 | 2 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3570): Show |
chr13 | 39650662 | 39757628 |
| a0002c0007t0002 | 0/0 | 3574 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3569): Show |
chr13 | 39650662 | 39757628 |
| a0003c0003t0001 | 0/0 | 3574 | 6 | 5 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3569): Show |
chr13 | 39650662 | 39757628 |
| a0004c0004t0002 | 0/0 | 3574 | 3 | 1 | 0 | 0 | 0 | 2 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3569): Show |
chr13 | 39650662 | 39757628 |
| a0004c0004t0007 | 0/0 | 3575 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3570): Show |
chr13 | 39650662 | 39757628 |
| a0005c0005t0003 | 0/0 | 3574 | 3 | 3 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3569): Show |
chr13 | 39650662 | 39757628 |
| a0006c0010t0002 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3569): Show |
chr13 | 39650662 | 39757628 |
| a0007c0008t0003 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3569): Show |
chr13 | 39650662 | 39757628 |
| a0008c0009t0010 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | ACTCG others(3569): Show |
chr13 | 39650662 | 39757628 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0191 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0187 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0005g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0005g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0012g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0013g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0014g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0001t0015g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0006t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0006t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0011t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0001c0012t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0002g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0004g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0006g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0006g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0006g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0006g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0006g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0006g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0006g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0006g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0007g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0007g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0007g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0007g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0008g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0008g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0008g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0009g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0009g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0009g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0010g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0002t0011g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0002c0007t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0003c0003t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0003c0003t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0003c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0003c0003t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0003c0003t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0003c0003t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0004c0004t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0004c0004t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0004c0004t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0004c0004t0007g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0005c0005t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0005c0005t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0005c0005t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0006c0010t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0007c0008t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| a0008c0009t0010g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0054 | EUR | GBR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0107 | EUR | GBR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0056 | EUR | GBR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0154 | EUR | GBR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | FIN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0060 | EUR | FIN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00323 | hp1 | a0001 | c0001 | t0015 | g0201 | EUR | FIN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0320 | EUR | FIN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | CHS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0300 | EAS | CHS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0284 | EAS | CHS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0337 | EAS | CHS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0308 | EAS | CHS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00609 | hp1 | a0002 | c0002 | t0006 | g0341 | EAS | CHS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0267 | EAS | CHS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0327 | EAS | CHS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00639 | hp1 | a0002 | c0002 | t0008 | g0013 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00639 | hp2 | a0001 | c0006 | t0003 | g0046 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0345 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0274 | EAS | CHS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0322 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0210 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0288 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0237 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0062 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0321 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0256 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0067 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0059 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0017 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01106 | hp2 | a0002 | c0002 | t0002 | g0291 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0241 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0238 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0211 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0239 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0343 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01192 | hp2 | a0001 | c0001 | t0012 | g0182 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01243 | hp2 | a0003 | c0003 | t0001 | g0104 | AMR | PUR | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01255 | hp1 | a0001 | c0006 | t0003 | g0045 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0296 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0058 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0289 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0053 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01261 | hp2 | a0002 | c0002 | t0006 | g0230 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0065 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0246 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0064 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0290 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01433 | hp1 | a0002 | c0002 | t0006 | g0232 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0040 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0039 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0199 | AMR | CLM | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0025 | EUR | IBS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0231 | EUR | IBS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0185 | EUR | IBS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0317 | EUR | IBS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0017 | EUR | IBS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0229 | EUR | IBS | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0096 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01884 | hp2 | a0005 | c0005 | t0003 | g0020 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01891 | hp1 | a0002 | c0002 | t0002 | g0342 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0055 | AMR | PEL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | PEL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0245 | AMR | PEL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0283 | AMR | PEL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | PEL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0247 | AMR | PEL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PEL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0277 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02055 | hp1 | a0003 | c0003 | t0001 | g0176 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0281 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02074 | hp1 | a0002 | c0007 | t0002 | g0295 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02083 | hp2 | a0002 | c0002 | t0007 | g0348 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0105 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02145 | hp1 | a0002 | c0002 | t0005 | g0218 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02145 | hp2 | a0002 | c0002 | t0002 | g0314 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CDX | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0347 | EAS | CDX | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0305 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0203 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0170 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0233 | AMR | PEL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0292 | AMR | PEL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02451 | hp1 | a0006 | c0010 | t0002 | g0244 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02451 | hp2 | a0002 | c0002 | t0007 | g0323 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02572 | hp1 | a0002 | c0002 | t0007 | g0301 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02572 | hp2 | a0002 | c0002 | t0004 | g0215 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02615 | hp1 | a0002 | c0002 | t0005 | g0216 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0126 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02630 | hp2 | a0005 | c0005 | t0003 | g0021 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0169 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02647 | hp2 | a0002 | c0002 | t0004 | g0214 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0261 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02723 | hp2 | a0003 | c0003 | t0001 | g0100 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0324 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0087 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0197 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0306 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02818 | hp2 | a0001 | c0011 | t0003 | g0209 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02886 | hp1 | a0002 | c0002 | t0003 | g0223 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0311 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02897 | hp1 | a0002 | c0002 | t0004 | g0224 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02922 | hp1 | a0005 | c0005 | t0003 | g0022 | AFR | ESN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | ESN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02965 | hp1 | a0002 | c0002 | t0005 | g0219 | AFR | ESN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0186 | AFR | ESN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02970 | hp1 | a0002 | c0002 | t0006 | g0316 | AFR | ESN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | ESN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02976 | hp1 | a0002 | c0002 | t0003 | g0226 | AFR | ESN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | ESN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03041 | hp1 | a0002 | c0002 | t0011 | g0016 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03041 | hp2 | a0002 | c0002 | t0002 | g0338 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03098 | hp1 | a0002 | c0002 | t0002 | g0307 | AFR | MSL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0188 | AFR | MSL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0312 | AFR | ESN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03139 | hp1 | a0003 | c0003 | t0001 | g0102 | AFR | ESN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03139 | hp2 | a0002 | c0002 | t0008 | g0013 | AFR | ESN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03195 | hp1 | a0001 | c0001 | t0014 | g0168 | AFR | ESN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03195 | hp2 | a0007 | c0008 | t0003 | g0225 | AFR | ESN | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0331 | AFR | MSL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03209 | hp2 | a0003 | c0003 | t0001 | g0103 | AFR | MSL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03225 | hp1 | a0004 | c0004 | t0002 | g0251 | AFR | MSL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03239 | hp1 | a0001 | c0001 | t0013 | g0134 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03453 | hp1 | a0002 | c0002 | t0008 | g0240 | AFR | MSL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03453 | hp2 | a0002 | c0002 | t0003 | g0227 | AFR | MSL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0313 | AFR | MSL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0204 | AFR | MSL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03490 | hp2 | a0002 | c0002 | t0002 | g0299 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03540 | hp1 | a0002 | c0002 | t0005 | g0217 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0303 | AFR | GWD | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03579 | hp1 | a0008 | c0009 | t0010 | g0221 | AFR | MSL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03579 | hp2 | a0002 | c0002 | t0011 | g0016 | AFR | MSL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0349 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03688 | hp1 | a0004 | c0004 | t0007 | g0250 | SAS | STU | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | STU | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0346 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0026 | SAS | PJL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0088 | SAS | BEB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03927 | hp2 | a0004 | c0004 | t0002 | g0253 | SAS | BEB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0236 | SAS | BEB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0089 | SAS | STU | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | STU | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0036 | SAS | BEB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0344 | SAS | BEB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0294 | SAS | STU | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | STU | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | STU | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0257 | SAS | STU | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0208 | AFR | YRI | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18522 | hp2 | a0002 | c0002 | t0008 | g0328 | AFR | YRI | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18612 | hp1 | a0002 | c0002 | t0002 | g0259 | EAS | CHB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CHB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0282 | EAS | CHB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | CHB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0205 | AFR | YRI | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0125 | AFR | YRI | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18939 | hp2 | a0002 | c0002 | t0004 | g0340 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0332 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0243 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18946 | hp1 | a0002 | c0002 | t0002 | g0333 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18952 | hp2 | a0002 | c0002 | t0009 | g0273 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0262 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0268 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0293 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0265 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18967 | hp1 | a0002 | c0002 | t0006 | g0297 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18971 | hp2 | a0002 | c0002 | t0007 | g0325 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0334 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0269 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0280 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0270 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0263 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18997 | hp1 | a0002 | c0002 | t0002 | g0276 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19000 | hp2 | a0002 | c0002 | t0009 | g0272 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0336 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19003 | hp2 | a0002 | c0002 | t0004 | g0260 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19007 | hp2 | a0002 | c0002 | t0006 | g0287 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19010 | hp1 | a0001 | c0012 | t0003 | g0078 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19010 | hp2 | a0002 | c0002 | t0009 | g0271 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0264 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0309 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19012 | hp2 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19030 | hp1 | a0002 | c0002 | t0006 | g0315 | AFR | LWK | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0330 | AFR | LWK | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0304 | AFR | LWK | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19043 | hp2 | a0002 | c0002 | t0003 | g0228 | AFR | LWK | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0258 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0326 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0302 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0339 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19070 | hp1 | a0002 | c0002 | t0002 | g0310 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19072 | hp2 | a0002 | c0002 | t0002 | g0279 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0255 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19075 | hp1 | a0002 | c0002 | t0002 | g0285 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19077 | hp2 | a0002 | c0002 | t0006 | g0319 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0091 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19082 | hp1 | a0002 | c0002 | t0002 | g0335 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0298 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0275 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0266 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | YRI | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0329 | AFR | YRI | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0286 | AFR | ASW | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0202 | AFR | ASW | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0278 | EUR | TSI | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0195 | EUR | TSI | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | TSI | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0235 | EUR | TSI | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0254 | SAS | GIH | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA20905 | hp2 | a0004 | c0004 | t0002 | g0252 | SAS | GIH | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0242 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02559 | hp1 | a0002 | c0002 | t0004 | g0220 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG02559 | hp2 | a0003 | c0003 | t0001 | g0101 | AFR | ACB | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03471 | hp1 | a0002 | c0002 | t0010 | g0222 | AFR | MSL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | USA | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0127 | AFR | USA | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0318 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0234 | AFR | USA | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | USA | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | LWK | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | LWK | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0191 | REF | REF | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0187 | REF | REF | COG6_chr13_39650662_39757628 | COG6 | chr13 | 39650662 | 39757628 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:39655754 | G | A | 5 | a0002 a0004 a0006 others(2): Show |
146 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(143): Show |
missense_variant | MODERATE | c.28G>A | p.Ala10Thr | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/19 | 93/3574 | 28/1974 | 10/657 | chr13 | 39655754 | |||
| chr13:39655820 | T | A | 5 | a0002 a0004 a0006 others(2): Show |
146 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(143): Show |
missense_variant | MODERATE | c.94T>A | p.Cys32Ser | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/19 | 159/3574 | 94/1974 | 32/657 | chr13 | 39655820 | |||
| chr13:39660832 | A | T | 1 | a0006 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.320A>T | p.Asp107Val | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/19 | 385/3574 | 320/1974 | 107/657 | chr13 | 39660832 | |||
| chr13:39660870 | A | G | 1 | a0005 | 3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
missense_variant | MODERATE | c.358A>G | p.Ser120Gly | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/19 | 423/3574 | 358/1974 | 120/657 | chr13 | 39660870 | |||
| chr13:39679982 | A | C | 1 | a0008 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.631A>C | p.Ile211Leu | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/19 | 696/3574 | 631/1974 | 211/657 | chr13 | 39679982 | |||
| chr13:39687612 | C | T | 1 | a0003 | 6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
missense_variant | MODERATE | c.898C>T | p.His300Tyr | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 9/19 | 963/3574 | 898/1974 | 300/657 | chr13 | 39687612 | |||
| chr13:39719291 | T | C | 1 | a0004 | 4 | HG03225.hp1 HG03688.hp1 HG03927.hp2 others(1): Show |
missense_variant | MODERATE | c.1340T>C | p.Met447Thr | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 14/19 | 1405/3574 | 1340/1974 | 447/657 | chr13 | 39719291 | |||
| chr13:39751082 | C | A | 1 | a0007 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.1963C>A | p.Leu655Ile | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 19/19 | 2028/3574 | 1963/1974 | 655/657 | chr13 | 39751082 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:39682205 | C | T | 1 | a0001c0006 | 2 | HG00639.hp2 HG01255.hp1 |
synonymous_variant | LOW | c.729C>T | p.Asp243Asp | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/19 | 794/3574 | 729/1974 | 243/657 | chr13 | 39682205 | |||
| chr13:39687729 | T | C | 1 | a0002c0007 | 1 | HG02074.hp1 | synonymous_variant | LOW | c.939T>C | p.Ala313Ala | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 10/19 | 1004/3574 | 939/1974 | 313/657 | chr13 | 39687729 | |||
| chr13:39719259 | T | G | 1 | a0001c0011 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.1308T>G | p.Leu436Leu | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 14/19 | 1373/3574 | 1308/1974 | 436/657 | chr13 | 39719259 | |||
| chr13:39719668 | A | G | 1 | a0001c0012 | 1 | NA19010.hp1 | synonymous_variant | LOW | c.1425A>G | p.Ser475Ser | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/19 | 1490/3574 | 1425/1974 | 475/657 | chr13 | 39719668 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:39655674 | T | G | 1 | a0002c0002t0009 | 3 | NA18952.hp2 NA19000.hp2 NA19010.hp2 |
5_prime_UTR_variant | MODIFIER | c.-53T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/19 | 53 | chr13 | 39655674 | ||||||
| chr13:39655705 | A | AG | 10 | a0002c0002t0002 a0002c0002t0006 a0002c0002t0007 others(7): Show |
129 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(126): Show |
5_prime_UTR_variant | MODIFIER | c.-17dupG | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/19 | 16 | INFO_REALIGN_3_PRIME | chr13 | 39655705 | |||||
| chr13:39751133 | A | G | 1 | a0001c0001t0015 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*40A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 19/19 | 40 | chr13 | 39751133 | ||||||
| chr13:39751173 | C | T | 8 | a0001c0001t0004 a0002c0002t0002 a0002c0002t0004 others(5): Show |
136 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*80C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 19/19 | 80 | chr13 | 39751173 | ||||||
| chr13:39751399 | AT | A | 2 | a0001c0001t0005 a0002c0002t0005 |
11 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*315delT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 19/19 | 315 | INFO_REALIGN_3_PRIME | chr13 | 39751399 | |||||
| chr13:39751648 | G | A | 1 | a0001c0001t0012 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*555G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 19/19 | 555 | chr13 | 39751648 | ||||||
| chr13:39751682 | C | G | 1 | a0001c0001t0014 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*589C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 19/19 | 589 | chr13 | 39751682 | ||||||
| chr13:39751854 | A | G | 1 | a0001c0001t0013 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*761A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 19/19 | 761 | chr13 | 39751854 | ||||||
| chr13:39752145 | A | G | 9 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0013 others(6): Show |
122 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*1052A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 19/19 | 1052 | chr13 | 39752145 | ||||||
| chr13:39752147 | CA | C | 8 | a0001c0001t0004 a0002c0002t0002 a0002c0002t0004 others(5): Show |
136 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*1063delA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 19/19 | 1063 | INFO_REALIGN_3_PRIME | chr13 | 39752147 | |||||
| chr13:39752186 | G | T | 1 | a0002c0002t0008 | 4 | HG00639.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1093G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 19/19 | 1093 | chr13 | 39752186 | ||||||
| chr13:39752587 | G | A | 1 | a0002c0002t0011 | 2 | HG03041.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1494G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 19/19 | 1494 | chr13 | 39752587 | ||||||
| chr13:39752601 | G | T | 2 | a0002c0002t0010 a0008c0009t0010 |
2 | HG03471.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1508G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 19/19 | 1508 | chr13 | 39752601 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:39655898 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.153+19G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39655898 | |||||||
| chr13:39655906 | C | T | 126 | a0002c0002t0002g0014 a0002c0002t0002g0015 a0002c0002t0002g0017 others(123): Show |
131 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.153+27C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39655906 | |||||||
| chr13:39655929 | C | T | 7 | a0002c0002t0002g0343 a0002c0002t0002g0344 a0002c0002t0002g0345 others(4): Show |
7 | HG00642.hp1 HG01175.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.153+50C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39655929 | |||||||
| chr13:39655985 | A | C | 141 | a0002c0002t0002g0014 a0002c0002t0002g0015 a0002c0002t0002g0017 others(138): Show |
146 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.153+106A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39655985 | |||||||
| chr13:39655997 | A | T | 1 | a0002c0002t0002g0342 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.153+118A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39655997 | |||||||
| chr13:39656079 | G | A | 142 | a0001c0001t0003g0019 a0002c0002t0002g0014 a0002c0002t0002g0015 others(139): Show |
147 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.153+200G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39656079 | |||||||
| chr13:39656092 | C | T | 144 | a0001c0001t0003g0019 a0002c0002t0002g0014 a0002c0002t0002g0015 others(141): Show |
149 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.153+213C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39656092 | |||||||
| chr13:39656157 | T | C | 144 | a0001c0001t0003g0019 a0002c0002t0002g0014 a0002c0002t0002g0015 others(141): Show |
149 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.153+278T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39656157 | |||||||
| chr13:39656228 | A | C | 1 | a0001c0001t0001g0213 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.153+349A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39656228 | |||||||
| chr13:39656408 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.153+529C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39656408 | |||||||
| chr13:39656568 | G | A | 144 | a0001c0001t0003g0019 a0002c0002t0002g0014 a0002c0002t0002g0015 others(141): Show |
149 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.153+689G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39656568 | |||||||
| chr13:39656601 | A | G | 2 | a0001c0001t0003g0210 a0001c0001t0003g0211 |
2 | HG00733.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.153+722A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39656601 | |||||||
| chr13:39656638 | A | T | 4 | a0001c0001t0003g0019 a0005c0005t0003g0020 a0005c0005t0003g0021 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+759A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39656638 | |||||||
| chr13:39656799 | C | T | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.153+920C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39656799 | |||||||
| chr13:39656803 | C | T | 2 | a0002c0002t0003g0226 a0007c0008t0003g0225 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.153+924C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39656803 | |||||||
| chr13:39656977 | C | T | 1 | a0002c0002t0004g0340 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.153+1098C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39656977 | |||||||
| chr13:39656982 | A | G | 2 | a0002c0002t0003g0223 a0002c0002t0004g0224 |
2 | HG02886.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.153+1103A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39656982 | |||||||
| chr13:39657023 | A | T | 1 | a0002c0002t0002g0339 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.153+1144A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39657023 | |||||||
| chr13:39657047 | T | C | 1 | a0007c0008t0003g0225 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.153+1168T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39657047 | |||||||
| chr13:39657092 | C | T | 3 | a0005c0005t0003g0020 a0005c0005t0003g0021 a0005c0005t0003g0022 |
3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.153+1213C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39657092 | |||||||
| chr13:39657132 | A | G | 1 | a0001c0011t0003g0209 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.153+1253A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39657132 | |||||||
| chr13:39657157 | A | G | 144 | a0001c0001t0003g0019 a0002c0002t0002g0014 a0002c0002t0002g0015 others(141): Show |
149 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.153+1278A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39657157 | |||||||
| chr13:39657354 | A | C | 1 | a0002c0002t0002g0338 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.153+1475A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39657354 | |||||||
| chr13:39657463 | T | A | 1 | a0001c0001t0001g0023 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.153+1584T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39657463 | |||||||
| chr13:39657530 | G | GT | 147 | a0001c0001t0001g0207 a0001c0001t0003g0019 a0001c0001t0003g0206 others(144): Show |
152 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.153+1661dupT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 39657530 | ||||||
| chr13:39657744 | G | A | 1 | a0001c0001t0003g0024 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.154-1620G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39657744 | |||||||
| chr13:39657778 | C | T | 119 | a0002c0002t0002g0014 a0002c0002t0002g0015 a0002c0002t0002g0017 others(116): Show |
124 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.154-1586C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39657778 | |||||||
| chr13:39657909 | A | G | 1 | a0002c0002t0002g0337 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.154-1455A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39657909 | |||||||
| chr13:39657960 | C | T | 3 | a0001c0001t0004g0205 a0002c0002t0002g0335 a0002c0002t0002g0336 |
3 | NA18906.hp1 NA19002.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.154-1404C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39657960 | |||||||
| chr13:39657970 | G | C | 16 | a0002c0002t0002g0229 a0002c0002t0002g0231 a0002c0002t0002g0233 others(13): Show |
16 | HG01261.hp2 HG01433.hp1 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.154-1394G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39657970 | |||||||
| chr13:39658063 | C | CT | 12 | a0001c0001t0001g0200 a0001c0001t0003g0199 a0001c0001t0003g0202 others(9): Show |
14 | HG00323.hp1 HG01496.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.154-1283dupT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 39658063 | ||||||
| chr13:39658063 | CTT | C | 133 | a0001c0001t0003g0019 a0002c0002t0002g0014 a0002c0002t0002g0015 others(130): Show |
138 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.154-1284_154-1283d others(4): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 39658063 | ||||||
| chr13:39658103 | A | T | 1 | a0001c0001t0003g0198 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.154-1261A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39658103 | |||||||
| chr13:39658283 | A | G | 1 | a0001c0001t0003g0197 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.154-1081A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39658283 | |||||||
| chr13:39658318 | A | AT | 7 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(4): Show |
7 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.154-1039dupT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 39658318 | ||||||
| chr13:39658331 | G | C | 1 | a0002c0002t0002g0237 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.154-1033G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39658331 | |||||||
| chr13:39658584 | A | G | 6 | a0002c0002t0002g0329 a0002c0002t0002g0330 a0002c0002t0002g0331 others(3): Show |
6 | HG03041.hp2 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.154-780A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39658584 | |||||||
| chr13:39658770 | A | C | 1 | a0002c0002t0008g0328 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.154-594A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39658770 | |||||||
| chr13:39659002 | A | G | 2 | a0002c0002t0002g0326 a0002c0002t0002g0327 |
2 | HG00621.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.154-362A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39659002 | |||||||
| chr13:39659044 | AT | A | 213 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(210): Show |
222 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.154-310delT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 39659044 | ||||||
| chr13:39659157 | T | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(107): Show |
119 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.154-207T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39659157 | |||||||
| chr13:39659267 | T | C | 214 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(211): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.154-97T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39659267 | |||||||
| chr13:39659273 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.154-91A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 1/18 | chr13 | 39659273 | |||||||
| chr13:39659554 | C | T | 214 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(211): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.297+47C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39659554 | |||||||
| chr13:39659829 | C | A | 214 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(211): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.297+322C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39659829 | |||||||
| chr13:39659845 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.297+338A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39659845 | |||||||
| chr13:39659891 | C | T | 1 | a0002c0002t0002g0324 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.297+384C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39659891 | |||||||
| chr13:39659953 | T | C | 3 | a0002c0002t0002g0343 a0002c0002t0002g0344 a0002c0002t0002g0345 |
3 | HG00642.hp1 HG01175.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.297+446T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39659953 | |||||||
| chr13:39660045 | C | T | 2 | a0002c0002t0004g0220 a0002c0002t0007g0323 |
2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.297+538C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39660045 | |||||||
| chr13:39660053 | T | A | 2 | a0002c0002t0002g0238 a0002c0002t0002g0239 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.297+546T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39660053 | |||||||
| chr13:39660168 | C | A | 223 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(220): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.298-642C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39660168 | |||||||
| chr13:39660187 | A | T | 4 | a0001c0001t0001g0184 a0005c0005t0003g0020 a0005c0005t0003g0021 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.298-623A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39660187 | |||||||
| chr13:39660195 | T | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0092 a0001c0001t0001g0093 |
4 | HG00673.hp2 HG02135.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-615T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39660195 | |||||||
| chr13:39660281 | G | A | 2 | a0001c0001t0003g0025 a0001c0001t0003g0026 |
2 | HG01515.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.298-529G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39660281 | |||||||
| chr13:39660296 | C | T | 7 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(4): Show |
7 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.298-514C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39660296 | |||||||
| chr13:39660519 | G | A | 1 | a0001c0001t0003g0199 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.298-291G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39660519 | |||||||
| chr13:39660657 | T | G | 1 | a0001c0001t0001g0094 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.298-153T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39660657 | |||||||
| chr13:39660684 | G | A | 1 | a0001c0001t0003g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.298-126G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39660684 | |||||||
| chr13:39660713 | T | G | 3 | a0002c0002t0008g0013 a0002c0002t0008g0240 a0002c0002t0008g0328 |
4 | HG00639.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-97T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39660713 | |||||||
| chr13:39660809 | G | A | 1 | a0002c0002t0002g0241 | 1 | HG01167.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.298-1G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 2/18 | chr13 | 39660809 | |||||||
| chr13:39661048 | A | G | 7 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(4): Show |
7 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.369+167A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39661048 | |||||||
| chr13:39661198 | A | G | 1 | a0002c0002t0004g0220 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.369+317A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39661198 | |||||||
| chr13:39661236 | C | T | 206 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(203): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.369+355C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39661236 | |||||||
| chr13:39661339 | A | C | 1 | a0001c0001t0001g0183 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.369+458A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39661339 | |||||||
| chr13:39661542 | A | G | 130 | a0001c0001t0004g0090 a0001c0001t0004g0091 a0001c0001t0004g0205 others(127): Show |
135 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.369+661A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39661542 | |||||||
| chr13:39661572 | T | C | 1 | a0001c0001t0003g0028 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.369+691T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39661572 | |||||||
| chr13:39661885 | T | C | 1 | a0002c0002t0002g0242 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.369+1004T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39661885 | |||||||
| chr13:39662075 | A | G | 1 | a0001c0001t0012g0182 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.369+1194A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39662075 | |||||||
| chr13:39662142 | A | AT | 9 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0003g0030 others(6): Show |
9 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.369+1279dupT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr13 | 39662142 | ||||||
| chr13:39662142 | A | ATT | 202 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(199): Show |
211 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.369+1278_369+1279d others(4): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr13 | 39662142 | ||||||
| chr13:39662142 | AT | A | 12 | a0001c0001t0001g0095 a0001c0001t0001g0189 a0001c0001t0001g0190 others(9): Show |
12 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.369+1279delT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr13 | 39662142 | ||||||
| chr13:39662168 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.369+1287A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39662168 | |||||||
| chr13:39662221 | C | G | 3 | a0001c0001t0003g0087 a0001c0001t0003g0088 a0001c0001t0003g0089 |
3 | HG02735.hp2 HG03834.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.369+1340C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39662221 | |||||||
| chr13:39662253 | A | G | 214 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(211): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.369+1372A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39662253 | |||||||
| chr13:39662368 | T | C | 214 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(211): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.369+1487T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39662368 | |||||||
| chr13:39662414 | A | T | 1 | a0002c0002t0005g0219 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.369+1533A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39662414 | |||||||
| chr13:39662459 | A | G | 2 | a0002c0002t0003g0223 a0002c0002t0004g0224 |
2 | HG02886.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.369+1578A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39662459 | |||||||
| chr13:39662464 | G | A | 214 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(211): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.369+1583G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39662464 | |||||||
| chr13:39662730 | A | G | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.369+1849A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39662730 | |||||||
| chr13:39662858 | C | T | 129 | a0001c0001t0004g0090 a0001c0001t0004g0091 a0001c0001t0004g0205 others(126): Show |
134 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.369+1977C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39662858 | |||||||
| chr13:39662872 | A | C | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | NA18940.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.369+1991A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39662872 | |||||||
| chr13:39662990 | A | T | 1 | a0001c0001t0003g0202 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.370-2106A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39662990 | |||||||
| chr13:39663053 | T | G | 1 | a0001c0001t0004g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.370-2043T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39663053 | |||||||
| chr13:39663080 | T | C | 1 | a0001c0011t0003g0209 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.370-2016T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39663080 | |||||||
| chr13:39663095 | C | CAT | 212 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(209): Show |
221 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.370-2000_370-1999d others(4): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr13 | 39663095 | ||||||
| chr13:39663140 | T | C | 1 | a0001c0001t0003g0033 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.370-1956T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39663140 | |||||||
| chr13:39663372 | G | T | 1 | a0002c0002t0002g0322 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.370-1724G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39663372 | |||||||
| chr13:39663510 | A | G | 345 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(342): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.370-1586A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39663510 | |||||||
| chr13:39663531 | G | A | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.370-1565G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39663531 | |||||||
| chr13:39663625 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.370-1471G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39663625 | |||||||
| chr13:39663758 | C | T | 1 | a0003c0003t0001g0176 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.370-1338C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39663758 | |||||||
| chr13:39663774 | G | A | 214 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(211): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.370-1322G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39663774 | |||||||
| chr13:39663890 | T | TA | 200 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(197): Show |
209 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.370-1190dupA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr13 | 39663890 | ||||||
| chr13:39663890 | T | TAA | 8 | a0001c0001t0003g0019 a0002c0002t0003g0223 a0002c0002t0003g0227 others(5): Show |
8 | HG01884.hp2 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.370-1191_370-1190d others(4): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr13 | 39663890 | ||||||
| chr13:39663890 | TA | T | 6 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(3): Show |
6 | HG01256.hp2 HG02896.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.370-1190delA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr13 | 39663890 | ||||||
| chr13:39663972 | A | G | 2 | a0002c0002t0003g0223 a0002c0002t0004g0224 |
2 | HG02886.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.370-1124A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39663972 | |||||||
| chr13:39664025 | C | G | 214 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(211): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.370-1071C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664025 | |||||||
| chr13:39664038 | C | T | 129 | a0001c0001t0004g0090 a0001c0001t0004g0091 a0001c0001t0004g0205 others(126): Show |
134 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.370-1058C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664038 | |||||||
| chr13:39664119 | G | T | 3 | a0002c0002t0002g0017 a0002c0002t0002g0317 a0002c0002t0002g0322 |
4 | HG00733.hp1 HG01099.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.370-977G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664119 | |||||||
| chr13:39664120 | T | C | 2 | a0002c0002t0002g0245 a0002c0002t0002g0246 |
2 | HG01358.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.370-976T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664120 | |||||||
| chr13:39664250 | T | C | 214 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(211): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.370-846T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664250 | |||||||
| chr13:39664344 | T | C | 214 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(211): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.370-752T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664344 | |||||||
| chr13:39664346 | G | A | 214 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(211): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.370-750G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664346 | |||||||
| chr13:39664355 | C | T | 214 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(211): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.370-741C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664355 | |||||||
| chr13:39664356 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.370-740G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664356 | |||||||
| chr13:39664484 | T | C | 1 | a0001c0001t0003g0202 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.370-612T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664484 | |||||||
| chr13:39664512 | C | T | 214 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(211): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.370-584C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664512 | |||||||
| chr13:39664598 | G | T | 7 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(4): Show |
7 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.370-498G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664598 | |||||||
| chr13:39664704 | A | G | 214 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(211): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.370-392A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664704 | |||||||
| chr13:39664762 | C | T | 214 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(211): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.370-334C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664762 | |||||||
| chr13:39664866 | A | T | 214 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(211): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.370-230A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664866 | |||||||
| chr13:39664907 | T | G | 214 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(211): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.370-189T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39664907 | |||||||
| chr13:39665002 | G | A | 214 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(211): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.370-94G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 3/18 | chr13 | 39665002 | |||||||
| chr13:39665328 | G | A | 3 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0199 |
3 | HG01496.hp2 HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.428+174G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39665328 | |||||||
| chr13:39665386 | T | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(96): Show |
107 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.428+232T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39665386 | |||||||
| chr13:39665481 | A | G | 214 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(211): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.428+327A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39665481 | |||||||
| chr13:39665514 | C | T | 8 | a0002c0002t0002g0242 a0002c0002t0002g0311 a0002c0002t0002g0312 others(5): Show |
8 | HG02109.hp1 HG02145.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.428+360C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39665514 | |||||||
| chr13:39665518 | T | C | 1 | a0001c0001t0003g0036 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.428+364T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39665518 | |||||||
| chr13:39665584 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.428+430T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39665584 | |||||||
| chr13:39665608 | G | A | 2 | a0002c0002t0010g0222 a0008c0009t0010g0221 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.428+454G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39665608 | |||||||
| chr13:39665627 | G | A | 214 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(211): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.428+473G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39665627 | |||||||
| chr13:39665648 | G | T | 214 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(211): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.428+494G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39665648 | |||||||
| chr13:39665721 | T | C | 7 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(4): Show |
7 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.428+567T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39665721 | |||||||
| chr13:39665726 | G | A | 345 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(342): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.428+572G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39665726 | |||||||
| chr13:39665797 | C | T | 1 | a0002c0002t0002g0310 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.428+643C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39665797 | |||||||
| chr13:39665896 | T | C | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.428+742T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39665896 | |||||||
| chr13:39665981 | T | C | 1 | a0001c0001t0001g0006 | 2 | NA19064.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.428+827T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39665981 | |||||||
| chr13:39666023 | C | T | 2 | a0002c0002t0002g0309 a0002c0002t0003g0223 |
2 | HG02886.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.428+869C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39666023 | |||||||
| chr13:39666244 | T | C | 135 | a0001c0001t0003g0019 a0001c0001t0004g0090 a0001c0001t0004g0091 others(132): Show |
140 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.428+1090T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39666244 | |||||||
| chr13:39666298 | G | A | 2 | a0002c0002t0003g0223 a0002c0002t0004g0224 |
2 | HG02886.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.428+1144G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39666298 | |||||||
| chr13:39666343 | G | A | 1 | a0002c0002t0003g0223 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.428+1189G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39666343 | |||||||
| chr13:39666367 | C | G | 2 | a0002c0002t0003g0226 a0007c0008t0003g0225 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.428+1213C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39666367 | |||||||
| chr13:39666543 | A | G | 1 | a0001c0001t0003g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.428+1389A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39666543 | |||||||
| chr13:39666551 | G | A | 6 | a0002c0002t0002g0229 a0002c0002t0002g0231 a0002c0002t0002g0233 others(3): Show |
6 | HG01261.hp2 HG01433.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.428+1397G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39666551 | |||||||
| chr13:39666555 | C | T | 1 | a0002c0002t0002g0308 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.428+1401C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39666555 | |||||||
| chr13:39666577 | CACTGATC others(10): Show |
C | 77 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(74): Show |
81 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.428+1424_428+1440d others(19): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39666577 | |||||||
| chr13:39666597 | T | C | 6 | a0003c0003t0001g0100 a0003c0003t0001g0101 a0003c0003t0001g0102 others(3): Show |
6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.428+1443T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39666597 | |||||||
| chr13:39666641 | A | C | 17 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0032 others(14): Show |
20 | HG00423.hp1 NA18946.hp2 NA18949.hp2 others(17): Show |
intron_variant | MODIFIER | c.428+1487A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39666641 | |||||||
| chr13:39666739 | A | G | 3 | a0005c0005t0003g0020 a0005c0005t0003g0021 a0005c0005t0003g0022 |
3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.428+1585A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39666739 | |||||||
| chr13:39666789 | T | C | 1 | a0002c0002t0002g0247 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.428+1635T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39666789 | |||||||
| chr13:39667126 | A | G | 3 | a0005c0005t0003g0020 a0005c0005t0003g0021 a0005c0005t0003g0022 |
3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.428+1972A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39667126 | |||||||
| chr13:39667527 | A | G | 1 | a0002c0002t0004g0224 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.428+2373A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39667527 | |||||||
| chr13:39667590 | C | T | 7 | a0001c0001t0004g0205 a0002c0002t0002g0303 a0002c0002t0002g0304 others(4): Show |
7 | HG01891.hp1 HG02258.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.428+2436C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39667590 | |||||||
| chr13:39667622 | A | T | 2 | a0001c0001t0005g0203 a0001c0001t0005g0204 |
2 | HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.428+2468A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39667622 | |||||||
| chr13:39667736 | G | T | 212 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(209): Show |
221 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.428+2582G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39667736 | |||||||
| chr13:39667806 | T | C | 2 | a0002c0002t0010g0222 a0008c0009t0010g0221 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.428+2652T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39667806 | |||||||
| chr13:39667831 | A | G | 345 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(342): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.428+2677A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39667831 | |||||||
| chr13:39667960 | C | T | 212 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(209): Show |
221 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.428+2806C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39667960 | |||||||
| chr13:39668018 | T | A | 1 | a0001c0001t0004g0105 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.428+2864T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668018 | |||||||
| chr13:39668051 | G | A | 75 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(72): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.428+2897G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668051 | |||||||
| chr13:39668056 | A | G | 1 | a0002c0002t0002g0302 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.428+2902A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668056 | |||||||
| chr13:39668102 | TACGATTC others(8): Show |
T | 75 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(72): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.428+2951_428+2965d others(17): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 39668102 | ||||||
| chr13:39668200 | C | G | 1 | a0001c0001t0001g0165 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.428+3046C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668200 | |||||||
| chr13:39668206 | A | G | 9 | a0001c0001t0003g0202 a0001c0001t0005g0011 a0001c0001t0005g0012 others(6): Show |
11 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.428+3052A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668206 | |||||||
| chr13:39668234 | A | G | 221 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(218): Show |
230 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.428+3080A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668234 | |||||||
| chr13:39668416 | T | C | 3 | a0002c0002t0002g0248 a0002c0002t0002g0249 a0002c0002t0002g0318 |
3 | NA18942.hp2 NA18955.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.428+3262T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668416 | |||||||
| chr13:39668511 | G | A | 221 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(218): Show |
230 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.428+3357G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668511 | |||||||
| chr13:39668517 | C | T | 75 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(72): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.428+3363C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668517 | |||||||
| chr13:39668555 | G | A | 4 | a0002c0002t0002g0329 a0002c0002t0002g0330 a0002c0002t0002g0331 others(1): Show |
4 | HG03041.hp2 HG03209.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.428+3401G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668555 | |||||||
| chr13:39668577 | A | G | 221 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(218): Show |
230 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.428+3423A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668577 | |||||||
| chr13:39668584 | C | T | 221 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(218): Show |
230 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.428+3430C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668584 | |||||||
| chr13:39668603 | G | A | 2 | a0002c0002t0002g0245 a0002c0002t0002g0246 |
2 | HG01358.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.428+3449G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668603 | |||||||
| chr13:39668741 | A | T | 221 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(218): Show |
230 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.428+3587A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668741 | |||||||
| chr13:39668777 | G | A | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.428+3623G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668777 | |||||||
| chr13:39668778 | A | C | 2 | a0001c0001t0004g0071 a0001c0001t0004g0072 |
2 | NA18971.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.428+3624A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668778 | |||||||
| chr13:39668804 | A | G | 13 | a0001c0001t0003g0002 a0001c0001t0003g0032 a0001c0001t0003g0075 others(10): Show |
15 | NA18946.hp2 NA18955.hp2 NA18979.hp1 others(12): Show |
intron_variant | MODIFIER | c.428+3650A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668804 | |||||||
| chr13:39668834 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(117): Show |
131 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.428+3680G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668834 | |||||||
| chr13:39668861 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(97): Show |
108 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.428+3707G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668861 | |||||||
| chr13:39668958 | G | A | 7 | a0001c0001t0004g0205 a0002c0002t0002g0303 a0002c0002t0002g0304 others(4): Show |
7 | HG01891.hp1 HG02258.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.428+3804G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39668958 | |||||||
| chr13:39669006 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.428+3852C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39669006 | |||||||
| chr13:39669025 | TAC | T | 223 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(220): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.428+3875_428+3876d others(4): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 39669025 | ||||||
| chr13:39669063 | G | C | 2 | a0001c0001t0003g0037 a0001c0001t0003g0038 |
2 | NA18747.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.428+3909G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39669063 | |||||||
| chr13:39669068 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.428+3914A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39669068 | |||||||
| chr13:39669117 | C | T | 7 | a0001c0001t0004g0205 a0002c0002t0002g0303 a0002c0002t0002g0304 others(4): Show |
7 | HG01891.hp1 HG02258.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.428+3963C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39669117 | |||||||
| chr13:39669249 | C | T | 74 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(71): Show |
78 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.428+4095C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39669249 | |||||||
| chr13:39669283 | T | C | 223 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(220): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.428+4129T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39669283 | |||||||
| chr13:39669331 | T | G | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.428+4177T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39669331 | |||||||
| chr13:39669408 | A | C | 2 | a0002c0002t0007g0301 a0002c0002t0011g0016 |
3 | HG02572.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.428+4254A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39669408 | |||||||
| chr13:39669463 | C | T | 2 | a0003c0003t0001g0103 a0003c0003t0001g0104 |
2 | HG01243.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.428+4309C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39669463 | |||||||
| chr13:39669575 | A | G | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0175 |
3 | HG02074.hp2 NA19062.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.428+4421A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39669575 | |||||||
| chr13:39669668 | T | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.428+4514T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39669668 | |||||||
| chr13:39669691 | G | A | 54 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(51): Show |
58 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.428+4537G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39669691 | |||||||
| chr13:39669921 | G | C | 3 | a0005c0005t0003g0020 a0005c0005t0003g0021 a0005c0005t0003g0022 |
3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.428+4767G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39669921 | |||||||
| chr13:39670221 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG03704.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.428+5067C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39670221 | |||||||
| chr13:39670305 | A | G | 1 | a0002c0002t0003g0223 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.428+5151A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39670305 | |||||||
| chr13:39670367 | ATC | A | 3 | a0005c0005t0003g0020 a0005c0005t0003g0021 a0005c0005t0003g0022 |
3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.428+5217_428+5218d others(4): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 39670367 | ||||||
| chr13:39670449 | T | C | 223 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(220): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.428+5295T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39670449 | |||||||
| chr13:39670604 | G | T | 3 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0184 |
3 | HG00280.hp1 HG02683.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.428+5450G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39670604 | |||||||
| chr13:39670606 | A | T | 3 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0184 |
3 | HG00280.hp1 HG02683.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.428+5452A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39670606 | |||||||
| chr13:39670617 | G | C | 343 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(340): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.428+5463G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39670617 | |||||||
| chr13:39670793 | G | A | 9 | a0001c0001t0003g0202 a0001c0001t0005g0011 a0001c0001t0005g0012 others(6): Show |
11 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.428+5639G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39670793 | |||||||
| chr13:39670968 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.428+5814C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39670968 | |||||||
| chr13:39671020 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.428+5866A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39671020 | |||||||
| chr13:39671040 | T | C | 223 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(220): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.428+5886T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39671040 | |||||||
| chr13:39671150 | A | T | 132 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0004g0090 others(129): Show |
137 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.428+5996A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39671150 | |||||||
| chr13:39671363 | G | A | 214 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(211): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.429-6105G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39671363 | |||||||
| chr13:39671365 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.429-6103G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39671365 | |||||||
| chr13:39671388 | C | A | 1 | a0001c0001t0001g0189 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.429-6080C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39671388 | |||||||
| chr13:39671547 | T | C | 1 | a0002c0002t0002g0311 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.429-5921T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39671547 | |||||||
| chr13:39671566 | A | C | 223 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(220): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.429-5902A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39671566 | |||||||
| chr13:39671570 | T | G | 223 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(220): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.429-5898T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39671570 | |||||||
| chr13:39671649 | G | T | 1 | a0001c0001t0001g0179 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.429-5819G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39671649 | |||||||
| chr13:39671775 | C | A | 1 | a0001c0001t0003g0028 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.429-5693C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39671775 | |||||||
| chr13:39671796 | T | C | 9 | a0002c0002t0002g0017 a0002c0002t0002g0317 a0002c0002t0002g0322 others(6): Show |
11 | HG00733.hp1 HG01099.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.429-5672T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39671796 | |||||||
| chr13:39671939 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.429-5529A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39671939 | |||||||
| chr13:39671977 | G | C | 2 | a0002c0002t0010g0222 a0008c0009t0010g0221 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.429-5491G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39671977 | |||||||
| chr13:39672030 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.429-5438A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39672030 | |||||||
| chr13:39672220 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.429-5248T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39672220 | |||||||
| chr13:39672225 | A | G | 2 | a0002c0002t0007g0301 a0002c0002t0011g0016 |
3 | HG02572.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.429-5243A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39672225 | |||||||
| chr13:39672226 | T | C | 1 | a0002c0002t0002g0303 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.429-5242T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39672226 | |||||||
| chr13:39672453 | C | T | 2 | a0002c0002t0010g0222 a0008c0009t0010g0221 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.429-5015C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39672453 | |||||||
| chr13:39672538 | C | T | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.429-4930C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39672538 | |||||||
| chr13:39672549 | A | G | 1 | a0001c0001t0003g0199 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.429-4919A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39672549 | |||||||
| chr13:39672650 | A | G | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.429-4818A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39672650 | |||||||
| chr13:39673033 | TG | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(96): Show |
107 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.429-4433delG | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 39673033 | ||||||
| chr13:39673109 | G | C | 2 | a0002c0002t0004g0214 a0002c0002t0004g0215 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.429-4359G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39673109 | |||||||
| chr13:39673169 | C | A | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0175 |
3 | HG02074.hp2 NA19062.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.429-4299C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39673169 | |||||||
| chr13:39673237 | G | A | 212 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(209): Show |
221 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.429-4231G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39673237 | |||||||
| chr13:39673279 | G | A | 345 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(342): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.429-4189G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39673279 | |||||||
| chr13:39673312 | T | C | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.429-4156T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39673312 | |||||||
| chr13:39673420 | T | C | 214 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(211): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.429-4048T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39673420 | |||||||
| chr13:39673447 | G | A | 7 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(4): Show |
7 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.429-4021G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39673447 | |||||||
| chr13:39673539 | T | C | 1 | a0001c0001t0003g0028 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.429-3929T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39673539 | |||||||
| chr13:39673954 | TTCTG | T | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.429-3510_429-3507d others(6): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 39673954 | ||||||
| chr13:39673978 | A | G | 3 | a0005c0005t0003g0020 a0005c0005t0003g0021 a0005c0005t0003g0022 |
3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.429-3490A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39673978 | |||||||
| chr13:39674008 | T | C | 6 | a0003c0003t0001g0100 a0003c0003t0001g0101 a0003c0003t0001g0102 others(3): Show |
6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.429-3460T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674008 | |||||||
| chr13:39674064 | A | G | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.429-3404A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674064 | |||||||
| chr13:39674210 | C | G | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.429-3258C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674210 | |||||||
| chr13:39674280 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.429-3188C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674280 | |||||||
| chr13:39674315 | TCTTTA | T | 3 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0171 |
3 | HG02280.hp2 HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.429-3148_429-3144d others(7): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 39674315 | ||||||
| chr13:39674412 | C | T | 343 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(340): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.429-3056C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674412 | |||||||
| chr13:39674507 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.429-2961C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674507 | |||||||
| chr13:39674508 | G | A | 2 | a0002c0002t0004g0214 a0002c0002t0004g0215 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.429-2960G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674508 | |||||||
| chr13:39674536 | G | T | 2 | a0002c0002t0002g0300 a0002c0002t0002g0337 |
2 | HG00423.hp2 HG00558.hp1 |
intron_variant | MODIFIER | c.429-2932G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674536 | |||||||
| chr13:39674597 | A | G | 1 | a0002c0002t0002g0299 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.429-2871A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674597 | |||||||
| chr13:39674635 | A | T | 1 | a0001c0001t0003g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.429-2833A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674635 | |||||||
| chr13:39674640 | A | C | 1 | a0001c0001t0001g0156 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.429-2828A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674640 | |||||||
| chr13:39674665 | T | G | 1 | a0004c0004t0007g0250 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.429-2803T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674665 | |||||||
| chr13:39674852 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0005g0208 |
2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.429-2616G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674852 | |||||||
| chr13:39674867 | C | A | 8 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(5): Show |
8 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.429-2601C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674867 | |||||||
| chr13:39674869 | G | A | 3 | a0005c0005t0003g0020 a0005c0005t0003g0021 a0005c0005t0003g0022 |
3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.429-2599G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674869 | |||||||
| chr13:39674920 | A | T | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.429-2548A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39674920 | |||||||
| chr13:39675103 | A | G | 3 | a0001c0001t0001g0212 a0001c0001t0003g0010 a0001c0001t0003g0188 |
4 | HG01243.hp1 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.429-2365A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39675103 | |||||||
| chr13:39675198 | T | C | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.429-2270T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39675198 | |||||||
| chr13:39675421 | C | G | 1 | a0002c0002t0002g0298 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.429-2047C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39675421 | |||||||
| chr13:39676023 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.429-1445T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39676023 | |||||||
| chr13:39676111 | T | C | 3 | a0005c0005t0003g0020 a0005c0005t0003g0021 a0005c0005t0003g0022 |
3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.429-1357T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39676111 | |||||||
| chr13:39676268 | C | T | 2 | a0002c0002t0003g0226 a0007c0008t0003g0225 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.429-1200C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39676268 | |||||||
| chr13:39676487 | CA | C | 4 | a0001c0001t0003g0019 a0005c0005t0003g0020 a0005c0005t0003g0021 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.429-980delA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39676487 | |||||||
| chr13:39676497 | C | T | 3 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0015g0201 |
3 | HG00140.hp2 HG00323.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.429-971C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39676497 | |||||||
| chr13:39676550 | G | A | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.429-918G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39676550 | |||||||
| chr13:39676738 | A | G | 1 | a0001c0001t0003g0063 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.429-730A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39676738 | |||||||
| chr13:39676953 | G | A | 2 | a0001c0001t0003g0066 a0001c0001t0003g0085 |
2 | NA18974.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.429-515G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39676953 | |||||||
| chr13:39677121 | T | A | 1 | a0002c0002t0004g0224 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.429-347T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39677121 | |||||||
| chr13:39677142 | A | G | 1 | a0007c0008t0003g0225 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.429-326A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39677142 | |||||||
| chr13:39677188 | T | G | 4 | a0001c0001t0003g0019 a0005c0005t0003g0020 a0005c0005t0003g0021 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.429-280T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39677188 | |||||||
| chr13:39677285 | A | G | 208 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(205): Show |
217 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.429-183A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 4/18 | chr13 | 39677285 | |||||||
| chr13:39677658 | A | T | 1 | a0002c0002t0002g0338 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.540+79A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39677658 | |||||||
| chr13:39677714 | A | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(54): Show |
64 | HG00280.hp1 HG00438.hp2 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.540+135A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39677714 | |||||||
| chr13:39677874 | T | C | 2 | a0002c0002t0010g0222 a0008c0009t0010g0221 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.540+295T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39677874 | |||||||
| chr13:39677893 | A | G | 75 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(72): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.540+314A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39677893 | |||||||
| chr13:39677902 | T | C | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.540+323T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39677902 | |||||||
| chr13:39677941 | C | T | 1 | a0001c0001t0004g0127 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.540+362C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39677941 | |||||||
| chr13:39678046 | A | T | 1 | a0001c0001t0004g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.540+467A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39678046 | |||||||
| chr13:39678053 | C | T | 122 | a0001c0001t0004g0090 a0001c0001t0004g0091 a0002c0002t0002g0014 others(119): Show |
127 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.540+474C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39678053 | |||||||
| chr13:39678463 | C | T | 223 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(220): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.540+884C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39678463 | |||||||
| chr13:39678466 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.540+887G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39678466 | |||||||
| chr13:39678587 | A | C | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.541-951A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39678587 | |||||||
| chr13:39678596 | A | G | 223 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(220): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.541-942A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39678596 | |||||||
| chr13:39678723 | C | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(97): Show |
108 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.541-815C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39678723 | |||||||
| chr13:39678919 | GTTA | G | 214 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(211): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.541-601_541-599del others(3): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 39678919 | ||||||
| chr13:39679082 | A | G | 1 | a0001c0001t0003g0202 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.541-456A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39679082 | |||||||
| chr13:39679383 | C | T | 2 | a0001c0001t0003g0069 a0001c0001t0003g0198 |
2 | NA18964.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.541-155C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39679383 | |||||||
| chr13:39679384 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0004g0096 |
2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.541-154G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39679384 | |||||||
| chr13:39679431 | C | G | 1 | a0002c0002t0006g0297 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.541-107C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39679431 | |||||||
| chr13:39679458 | C | T | 2 | a0001c0001t0004g0125 a0001c0001t0004g0126 |
2 | HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.541-80C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 5/18 | chr13 | 39679458 | |||||||
| chr13:39679764 | A | G | 214 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(211): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.623+144A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 6/18 | chr13 | 39679764 | |||||||
| chr13:39679772 | A | T | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.623+152A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 6/18 | chr13 | 39679772 | |||||||
| chr13:39679805 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.624-170T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 6/18 | chr13 | 39679805 | |||||||
| chr13:39679963 | A | AT | 122 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
splice_acceptor_variant&intron_variant | HIGH | c.624-3dupT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 39679963 | ||||||
| chr13:39680144 | TCAAA | T | 74 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(71): Show |
78 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.694+102_694+105del others(4): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr13 | 39680144 | ||||||
| chr13:39680178 | A | G | 1 | a0001c0001t0003g0068 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.694+133A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39680178 | |||||||
| chr13:39680241 | A | T | 1 | a0001c0001t0001g0180 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.694+196A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39680241 | |||||||
| chr13:39680253 | C | T | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.694+208C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39680253 | |||||||
| chr13:39680388 | T | C | 3 | a0001c0001t0003g0030 a0001c0001t0003g0039 a0001c0001t0003g0040 |
3 | HG01433.hp2 HG01496.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.694+343T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39680388 | |||||||
| chr13:39680410 | T | C | 4 | a0001c0001t0003g0019 a0005c0005t0003g0020 a0005c0005t0003g0021 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+365T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39680410 | |||||||
| chr13:39680454 | G | A | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.694+409G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39680454 | |||||||
| chr13:39680717 | G | T | 7 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(4): Show |
7 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.694+672G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39680717 | |||||||
| chr13:39680880 | T | A | 2 | a0002c0002t0003g0226 a0007c0008t0003g0225 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.694+835T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39680880 | |||||||
| chr13:39680974 | T | A | 223 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(220): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.694+929T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39680974 | |||||||
| chr13:39681126 | A | G | 1 | a0001c0001t0003g0029 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.695-1045A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39681126 | |||||||
| chr13:39681150 | T | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.695-1021T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39681150 | |||||||
| chr13:39681223 | C | T | 1 | a0002c0002t0003g0223 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.695-948C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39681223 | |||||||
| chr13:39681254 | A | G | 1 | a0001c0001t0003g0062 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.695-917A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39681254 | |||||||
| chr13:39681454 | T | C | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.695-717T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39681454 | |||||||
| chr13:39681660 | T | A | 6 | a0002c0002t0007g0301 a0002c0002t0011g0016 a0004c0004t0002g0251 others(3): Show |
7 | HG02572.hp1 HG03041.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-511T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39681660 | |||||||
| chr13:39681689 | G | A | 1 | a0002c0002t0002g0304 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.695-482G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39681689 | |||||||
| chr13:39681740 | A | G | 122 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.695-431A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39681740 | |||||||
| chr13:39681996 | C | G | 1 | a0002c0002t0004g0224 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.695-175C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39681996 | |||||||
| chr13:39682093 | T | G | 1 | a0001c0001t0001g0098 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.695-78T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39682093 | |||||||
| chr13:39682115 | C | T | 7 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(4): Show |
7 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-56C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39682115 | |||||||
| chr13:39682129 | A | C | 8 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0203 others(5): Show |
10 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.695-42A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 7/18 | chr13 | 39682129 | |||||||
| chr13:39682346 | G | A | 76 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(73): Show |
80 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.788+82G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39682346 | |||||||
| chr13:39682389 | A | G | 5 | a0003c0003t0001g0100 a0003c0003t0001g0101 a0003c0003t0001g0102 others(2): Show |
5 | HG01243.hp2 HG02559.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.788+125A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39682389 | |||||||
| chr13:39682407 | A | C | 1 | a0002c0002t0002g0349 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.788+143A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39682407 | |||||||
| chr13:39682450 | A | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0166 a0001c0001t0001g0167 others(3): Show |
7 | HG01192.hp1 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.788+186A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39682450 | |||||||
| chr13:39682451 | T | C | 75 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(72): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.788+187T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39682451 | |||||||
| chr13:39682484 | C | G | 7 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(4): Show |
7 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.788+220C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39682484 | |||||||
| chr13:39682520 | T | C | 3 | a0005c0005t0003g0020 a0005c0005t0003g0021 a0005c0005t0003g0022 |
3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.788+256T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39682520 | |||||||
| chr13:39682590 | A | G | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.788+326A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39682590 | |||||||
| chr13:39682619 | G | A | 2 | a0002c0002t0003g0226 a0007c0008t0003g0225 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.788+355G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39682619 | |||||||
| chr13:39682905 | G | C | 1 | a0002c0002t0002g0322 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.788+641G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39682905 | |||||||
| chr13:39682915 | A | G | 1 | a0001c0001t0004g0091 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.788+651A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39682915 | |||||||
| chr13:39683004 | A | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG00673.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.788+740A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683004 | |||||||
| chr13:39683283 | G | A | 214 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(211): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.788+1019G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683283 | |||||||
| chr13:39683290 | G | A | 3 | a0002c0002t0002g0017 a0002c0002t0002g0317 a0002c0002t0002g0322 |
4 | HG00733.hp1 HG01099.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.788+1026G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683290 | |||||||
| chr13:39683367 | C | T | 24 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0001g0099 others(21): Show |
25 | HG00609.hp1 HG00621.hp2 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.788+1103C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683367 | |||||||
| chr13:39683423 | G | A | 3 | a0002c0002t0007g0301 a0002c0002t0011g0016 a0004c0004t0002g0251 |
4 | HG02572.hp1 HG03041.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.788+1159G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683423 | |||||||
| chr13:39683425 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.788+1161A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683425 | |||||||
| chr13:39683434 | A | G | 223 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(220): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.788+1170A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683434 | |||||||
| chr13:39683437 | T | C | 1 | a0001c0001t0005g0011 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.788+1173T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683437 | |||||||
| chr13:39683708 | CA | C | 4 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
4 | HG01346.hp2 HG01361.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.788+1445delA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683708 | |||||||
| chr13:39683747 | T | TA | 220 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(217): Show |
229 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.788+1494dupA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39683747 | ||||||
| chr13:39683783 | T | C | 1 | a0001c0001t0003g0030 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.788+1519T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683783 | |||||||
| chr13:39683812 | T | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(107): Show |
119 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.788+1548T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683812 | |||||||
| chr13:39683830 | G | A | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.788+1566G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683830 | |||||||
| chr13:39683918 | G | T | 223 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(220): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.788+1654G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683918 | |||||||
| chr13:39683948 | G | A | 213 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(210): Show |
222 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.788+1684G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683948 | |||||||
| chr13:39683988 | A | G | 1 | a0002c0002t0002g0296 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.788+1724A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39683988 | |||||||
| chr13:39684117 | C | T | 223 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(220): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.788+1853C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39684117 | |||||||
| chr13:39684186 | G | T | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.788+1922G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39684186 | |||||||
| chr13:39684243 | A | AT | 90 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(87): Show |
101 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.788+2004dupT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | ||||||
| chr13:39684243 | A | ATT | 22 | a0001c0001t0001g0005 a0001c0001t0001g0097 a0001c0001t0001g0123 others(19): Show |
23 | HG01175.hp2 HG01258.hp1 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.788+2003_788+2004d others(4): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | ||||||
| chr13:39684243 | A | ATTT | 8 | a0001c0001t0001g0098 a0001c0001t0001g0124 a0001c0001t0001g0151 others(5): Show |
8 | HG01243.hp2 HG01934.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.788+2002_788+2004d others(5): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | ||||||
| chr13:39684243 | A | ATTTTTTT others(1): Show |
27 | a0001c0001t0004g0090 a0001c0001t0004g0091 a0002c0002t0002g0014 others(24): Show |
28 | HG00609.hp2 HG01169.hp2 HG02698.hp2 others(25): Show |
intron_variant | MODIFIER | c.788+1997_788+2004d others(10): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | ||||||
| chr13:39684243 | A | ATTTTTTT others(2): Show |
35 | a0002c0002t0002g0229 a0002c0002t0002g0235 a0002c0002t0002g0238 others(32): Show |
36 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.788+1996_788+2004d others(11): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | ||||||
| chr13:39684243 | A | ATTTTTTT others(3): Show |
35 | a0001c0001t0003g0070 a0001c0001t0004g0205 a0002c0002t0002g0015 others(32): Show |
36 | HG00642.hp1 HG00738.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.788+1995_788+2004d others(12): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | ||||||
| chr13:39684243 | A | ATTTTTTT others(4): Show |
38 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(35): Show |
42 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.788+1994_788+2004d others(13): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | ||||||
| chr13:39684243 | A | ATTTTTTT others(5): Show |
29 | a0001c0001t0003g0027 a0001c0001t0003g0029 a0001c0001t0003g0031 others(26): Show |
29 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.788+1993_788+2004d others(14): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | ||||||
| chr13:39684243 | A | ATTTTTTT others(6): Show |
16 | a0001c0001t0003g0028 a0001c0001t0003g0030 a0001c0001t0003g0035 others(13): Show |
16 | HG00280.hp2 HG01081.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.788+1992_788+2004d others(15): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | ||||||
| chr13:39684243 | A | ATTTTTTT others(7): Show |
1 | a0001c0001t0003g0089 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.788+1991_788+2004d others(16): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | ||||||
| chr13:39684243 | A | ATTTTTTT others(8): Show |
2 | a0001c0001t0003g0036 a0001c0001t0003g0061 |
2 | HG02040.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.788+1990_788+2004d others(17): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | ||||||
| chr13:39684243 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0004g0072 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.788+1988_788+2004d others(19): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | ||||||
| chr13:39684243 | A | ATTTTTTT others(11): Show |
1 | a0002c0002t0002g0322 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.788+1987_788+2004d others(20): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | ||||||
| chr13:39684243 | A | ATTTTTTT others(15): Show |
1 | a0002c0002t0002g0017 | 2 | HG01099.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.788+1983_788+2004d others(24): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | ||||||
| chr13:39684243 | A | ATTTTTTT others(16): Show |
1 | a0002c0002t0002g0317 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.788+1982_788+2004d others(25): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | ||||||
| chr13:39684243 | ATTTTTT | A | 12 | a0001c0001t0003g0025 a0002c0002t0002g0245 a0002c0002t0002g0246 others(9): Show |
12 | HG01070.hp1 HG01255.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.788+1999_788+2004d others(8): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | ||||||
| chr13:39684243 | ATTTTTTT others(3): Show |
A | 7 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(4): Show |
7 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.788+1995_788+2004d others(12): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | ||||||
| chr13:39684243 | ATTTTTTT others(4): Show |
A | 2 | a0002c0002t0010g0222 a0008c0009t0010g0221 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.788+1994_788+2004d others(13): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39684243 | ||||||
| chr13:39684308 | A | G | 223 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(220): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.788+2044A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39684308 | |||||||
| chr13:39684350 | C | T | 1 | a0002c0002t0002g0309 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.788+2086C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39684350 | |||||||
| chr13:39684530 | G | A | 7 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(4): Show |
7 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.788+2266G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39684530 | |||||||
| chr13:39684815 | C | T | 1 | a0002c0007t0002g0295 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.788+2551C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39684815 | |||||||
| chr13:39685286 | A | G | 4 | a0001c0001t0003g0019 a0005c0005t0003g0020 a0005c0005t0003g0021 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.789-2217A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39685286 | |||||||
| chr13:39685353 | C | A | 129 | a0001c0001t0004g0090 a0001c0001t0004g0091 a0001c0001t0004g0205 others(126): Show |
134 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.789-2150C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39685353 | |||||||
| chr13:39685419 | A | G | 1 | a0002c0002t0007g0301 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.789-2084A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39685419 | |||||||
| chr13:39685488 | C | T | 1 | a0004c0004t0002g0252 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.789-2015C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39685488 | |||||||
| chr13:39685571 | T | C | 3 | a0005c0005t0003g0020 a0005c0005t0003g0021 a0005c0005t0003g0022 |
3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.789-1932T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39685571 | |||||||
| chr13:39685589 | T | C | 223 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(220): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.789-1914T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39685589 | |||||||
| chr13:39685629 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.789-1874C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39685629 | |||||||
| chr13:39685871 | G | GTAC | 223 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(220): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.789-1630_789-1629i others(5): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 39685871 | ||||||
| chr13:39685913 | A | G | 6 | a0002c0002t0002g0241 a0002c0002t0002g0281 a0002c0002t0002g0282 others(3): Show |
6 | HG00438.hp1 HG01167.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.789-1590A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39685913 | |||||||
| chr13:39685945 | G | A | 223 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(220): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.789-1558G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39685945 | |||||||
| chr13:39685971 | A | G | 9 | a0001c0001t0003g0202 a0001c0001t0005g0011 a0001c0001t0005g0012 others(6): Show |
11 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.789-1532A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39685971 | |||||||
| chr13:39686006 | A | C | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.789-1497A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39686006 | |||||||
| chr13:39686114 | T | C | 39 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0023 others(36): Show |
40 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.789-1389T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39686114 | |||||||
| chr13:39686207 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.789-1296G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39686207 | |||||||
| chr13:39686488 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.789-1015C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39686488 | |||||||
| chr13:39686920 | G | A | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.789-583G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39686920 | |||||||
| chr13:39687083 | C | T | 343 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(340): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.789-420C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39687083 | |||||||
| chr13:39687139 | G | A | 11 | a0001c0001t0003g0002 a0001c0001t0003g0076 a0001c0001t0003g0077 others(8): Show |
13 | NA18946.hp2 NA18955.hp2 NA18979.hp1 others(10): Show |
intron_variant | MODIFIER | c.789-364G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39687139 | |||||||
| chr13:39687241 | C | G | 7 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(4): Show |
7 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.789-262C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39687241 | |||||||
| chr13:39687347 | T | C | 8 | a0002c0002t0002g0229 a0002c0002t0002g0231 a0002c0002t0002g0233 others(5): Show |
8 | HG01261.hp2 HG01433.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.789-156T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39687347 | |||||||
| chr13:39687385 | A | G | 223 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(220): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.789-118A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39687385 | |||||||
| chr13:39687426 | T | C | 1 | a0002c0002t0002g0258 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.789-77T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39687426 | |||||||
| chr13:39687446 | C | G | 1 | a0001c0001t0001g0145 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.789-57C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 8/18 | chr13 | 39687446 | |||||||
| chr13:39687658 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.917+27A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 9/18 | chr13 | 39687658 | |||||||
| chr13:39687808 | A | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(118): Show |
133 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1009+9A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 10/18 | chr13 | 39687808 | |||||||
| chr13:39688109 | C | T | 130 | a0001c0001t0004g0090 a0001c0001t0004g0091 a0001c0001t0004g0169 others(127): Show |
134 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.1009+310C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 10/18 | chr13 | 39688109 | |||||||
| chr13:39688134 | G | A | 345 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(342): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.1009+335G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 10/18 | chr13 | 39688134 | |||||||
| chr13:39688468 | A | G | 1 | a0001c0001t0012g0182 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1009+669A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 10/18 | chr13 | 39688468 | |||||||
| chr13:39688567 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1009+768C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 10/18 | chr13 | 39688567 | |||||||
| chr13:39688593 | A | G | 1 | a0002c0002t0002g0246 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1009+794A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 10/18 | chr13 | 39688593 | |||||||
| chr13:39688623 | T | C | 218 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(215): Show |
227 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.1009+824T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 10/18 | chr13 | 39688623 | |||||||
| chr13:39688798 | A | G | 2 | a0002c0002t0003g0226 a0007c0008t0003g0225 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1010-962A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 10/18 | chr13 | 39688798 | |||||||
| chr13:39689102 | A | G | 1 | a0002c0002t0008g0240 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1010-658A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 10/18 | chr13 | 39689102 | |||||||
| chr13:39689119 | A | T | 1 | a0002c0002t0002g0291 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1010-641A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 10/18 | chr13 | 39689119 | |||||||
| chr13:39689238 | T | C | 1 | a0001c0011t0003g0209 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1010-522T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 10/18 | chr13 | 39689238 | |||||||
| chr13:39689347 | T | C | 8 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0203 others(5): Show |
10 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1010-413T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 10/18 | chr13 | 39689347 | |||||||
| chr13:39689703 | A | G | 1 | a0005c0005t0003g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1010-57A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 10/18 | chr13 | 39689703 | |||||||
| chr13:39689842 | T | C | 71 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(68): Show |
75 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.1074+18T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39689842 | |||||||
| chr13:39689848 | T | C | 2 | a0002c0002t0003g0226 a0007c0008t0003g0225 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1074+24T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39689848 | |||||||
| chr13:39689929 | T | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(115): Show |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1074+105T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39689929 | |||||||
| chr13:39690099 | AT | A | 218 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(215): Show |
227 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.1074+276delT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39690099 | |||||||
| chr13:39690291 | T | C | 1 | a0002c0002t0002g0298 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1074+467T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39690291 | |||||||
| chr13:39690365 | T | C | 1 | a0002c0002t0002g0324 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1074+541T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39690365 | |||||||
| chr13:39690678 | T | C | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1074+854T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39690678 | |||||||
| chr13:39690796 | A | G | 1 | a0001c0001t0003g0060 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1074+972A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39690796 | |||||||
| chr13:39690807 | T | A | 227 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(224): Show |
236 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.1074+983T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39690807 | |||||||
| chr13:39691132 | A | G | 1 | a0002c0002t0002g0339 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1074+1308A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39691132 | |||||||
| chr13:39691212 | T | C | 1 | a0001c0011t0003g0209 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1074+1388T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39691212 | |||||||
| chr13:39691502 | A | G | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1074+1678A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39691502 | |||||||
| chr13:39691769 | T | C | 227 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(224): Show |
236 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.1074+1945T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39691769 | |||||||
| chr13:39691863 | A | G | 1 | a0002c0002t0002g0291 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1074+2039A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39691863 | |||||||
| chr13:39691927 | T | A | 212 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(209): Show |
221 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.1074+2103T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39691927 | |||||||
| chr13:39691976 | T | TAAAG | 227 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(224): Show |
236 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.1074+2155_1074+215 others(8): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr13 | 39691976 | ||||||
| chr13:39692070 | G | A | 42 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0023 others(39): Show |
43 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.1074+2246G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39692070 | |||||||
| chr13:39692353 | G | T | 1 | a0002c0002t0002g0304 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1075-2281G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39692353 | |||||||
| chr13:39692538 | C | A | 7 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(4): Show |
7 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.1075-2096C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39692538 | |||||||
| chr13:39692839 | G | A | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1075-1795G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39692839 | |||||||
| chr13:39693009 | T | C | 43 | a0001c0001t0004g0090 a0001c0001t0004g0091 a0002c0002t0002g0014 others(40): Show |
44 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1075-1625T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39693009 | |||||||
| chr13:39693099 | G | A | 3 | a0005c0005t0003g0020 a0005c0005t0003g0021 a0005c0005t0003g0022 |
3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1075-1535G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39693099 | |||||||
| chr13:39693165 | C | G | 1 | a0001c0001t0001g0184 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1075-1469C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39693165 | |||||||
| chr13:39693179 | T | G | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1075-1455T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39693179 | |||||||
| chr13:39693263 | T | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
5 | HG01192.hp1 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1075-1371T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39693263 | |||||||
| chr13:39693636 | A | G | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1075-998A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39693636 | |||||||
| chr13:39693653 | A | T | 2 | a0002c0002t0003g0226 a0007c0008t0003g0225 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1075-981A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39693653 | |||||||
| chr13:39693669 | T | C | 130 | a0001c0001t0004g0090 a0001c0001t0004g0091 a0001c0001t0004g0169 others(127): Show |
134 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.1075-965T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39693669 | |||||||
| chr13:39694085 | A | G | 227 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(224): Show |
236 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.1075-549A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39694085 | |||||||
| chr13:39694142 | A | G | 131 | a0001c0001t0004g0090 a0001c0001t0004g0091 a0001c0001t0004g0169 others(128): Show |
135 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.1075-492A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39694142 | |||||||
| chr13:39694201 | C | T | 7 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(4): Show |
7 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.1075-433C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39694201 | |||||||
| chr13:39694215 | A | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
7 | HG00438.hp2 NA18959.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.1075-419A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39694215 | |||||||
| chr13:39694419 | T | G | 13 | a0001c0001t0003g0002 a0001c0001t0003g0032 a0001c0001t0003g0075 others(10): Show |
15 | NA18946.hp2 NA18955.hp2 NA18979.hp1 others(12): Show |
intron_variant | MODIFIER | c.1075-215T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39694419 | |||||||
| chr13:39694548 | T | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(103): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.1075-86T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39694548 | |||||||
| chr13:39694586 | A | T | 2 | a0001c0001t0003g0037 a0001c0001t0003g0038 |
2 | NA18747.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.1075-48A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 11/18 | chr13 | 39694586 | |||||||
| chr13:39694793 | A | G | 78 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(75): Show |
83 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1166+68A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39694793 | |||||||
| chr13:39694954 | C | T | 1 | a0002c0002t0004g0224 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1166+229C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39694954 | |||||||
| chr13:39694955 | G | GCA | 152 | a0001c0001t0001g0094 a0001c0001t0001g0167 a0001c0001t0003g0002 others(149): Show |
160 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1166+264_1166+265d others(4): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr13 | 39694955 | ||||||
| chr13:39694955 | G | GCACA | 26 | a0001c0001t0001g0207 a0001c0001t0003g0003 a0001c0001t0003g0041 others(23): Show |
27 | HG01884.hp2 HG01891.hp1 HG02004.hp1 others(24): Show |
intron_variant | MODIFIER | c.1166+262_1166+265d others(6): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr13 | 39694955 | ||||||
| chr13:39694955 | G | GCGCA | 8 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0203 others(5): Show |
10 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1166+231_1166+232i others(6): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr13 | 39694955 | ||||||
| chr13:39694955 | GCA | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(74): Show |
84 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1166+264_1166+265d others(4): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr13 | 39694955 | ||||||
| chr13:39694955 | GCACA | G | 17 | a0001c0001t0001g0108 a0001c0001t0001g0121 a0001c0001t0001g0122 others(14): Show |
17 | HG01081.hp1 HG01106.hp1 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.1166+262_1166+265d others(6): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr13 | 39694955 | ||||||
| chr13:39694955 | GCACACA | G | 14 | a0001c0001t0001g0095 a0001c0001t0001g0123 a0001c0001t0001g0139 others(11): Show |
14 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1166+260_1166+265d others(8): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr13 | 39694955 | ||||||
| chr13:39694955 | GCACACAC others(3): Show |
G | 1 | a0002c0002t0003g0223 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1166+256_1166+265d others(12): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr13 | 39694955 | ||||||
| chr13:39694959 | A | G | 2 | a0002c0002t0010g0222 a0008c0009t0010g0221 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1166+234A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39694959 | |||||||
| chr13:39694961 | A | G | 7 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(4): Show |
7 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.1166+236A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39694961 | |||||||
| chr13:39694963 | A | G | 2 | a0002c0002t0010g0222 a0008c0009t0010g0221 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1166+238A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39694963 | |||||||
| chr13:39694965 | A | G | 7 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(4): Show |
7 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.1166+240A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39694965 | |||||||
| chr13:39694990 | C | CACA | 3 | a0001c0001t0003g0042 a0002c0002t0002g0233 a0002c0002t0009g0271 |
3 | HG02083.hp1 HG02293.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1166+265_1166+266i others(5): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39694990 | |||||||
| chr13:39694992 | C | A | 1 | a0003c0003t0001g0100 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1166+267C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39694992 | |||||||
| chr13:39695111 | G | T | 1 | a0001c0001t0001g0018 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1166+386G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39695111 | |||||||
| chr13:39695146 | G | A | 345 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(342): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.1166+421G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39695146 | |||||||
| chr13:39695228 | A | G | 3 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0199 |
3 | HG01496.hp2 HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1166+503A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39695228 | |||||||
| chr13:39695287 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1166+562G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39695287 | |||||||
| chr13:39695288 | G | C | 1 | a0002c0002t0002g0259 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1166+563G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39695288 | |||||||
| chr13:39695655 | A | G | 1 | a0002c0002t0004g0224 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1166+930A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39695655 | |||||||
| chr13:39696090 | G | GT | 5 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0199 others(2): Show |
6 | HG01496.hp2 HG02572.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1166+1372dupT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr13 | 39696090 | ||||||
| chr13:39696151 | A | G | 2 | a0002c0002t0003g0226 a0007c0008t0003g0225 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1166+1426A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39696151 | |||||||
| chr13:39696171 | A | ATTGT | 345 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(342): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.1166+1449_1166+145 others(8): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr13 | 39696171 | ||||||
| chr13:39696351 | G | T | 2 | a0002c0002t0010g0222 a0008c0009t0010g0221 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1166+1626G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39696351 | |||||||
| chr13:39696515 | A | G | 12 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(9): Show |
12 | HG00642.hp2 HG00738.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1166+1790A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39696515 | |||||||
| chr13:39696520 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1166+1795T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39696520 | |||||||
| chr13:39696690 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1166+1965A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39696690 | |||||||
| chr13:39696737 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1166+2012G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39696737 | |||||||
| chr13:39696745 | T | G | 1 | a0001c0001t0004g0205 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1166+2020T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39696745 | |||||||
| chr13:39696854 | C | T | 4 | a0002c0002t0005g0216 a0002c0002t0005g0217 a0002c0002t0005g0218 others(1): Show |
4 | HG02145.hp1 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1166+2129C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39696854 | |||||||
| chr13:39697173 | C | G | 2 | a0001c0001t0001g0192 a0001c0001t0001g0196 |
2 | HG00738.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1167-2328C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39697173 | |||||||
| chr13:39697246 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1167-2255G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39697246 | |||||||
| chr13:39697344 | C | CAAAG | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1167-2154_1167-215 others(8): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr13 | 39697344 | ||||||
| chr13:39697388 | C | T | 1 | a0001c0001t0003g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1167-2113C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39697388 | |||||||
| chr13:39697584 | C | T | 1 | a0002c0002t0007g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1167-1917C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39697584 | |||||||
| chr13:39697591 | A | G | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1167-1910A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39697591 | |||||||
| chr13:39697662 | A | G | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1167-1839A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39697662 | |||||||
| chr13:39697716 | T | G | 2 | a0002c0002t0002g0229 a0002c0002t0002g0231 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1167-1785T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39697716 | |||||||
| chr13:39697782 | G | C | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1167-1719G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39697782 | |||||||
| chr13:39697946 | C | T | 343 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(340): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.1167-1555C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39697946 | |||||||
| chr13:39698130 | G | A | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1167-1371G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39698130 | |||||||
| chr13:39698179 | TA | T | 77 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(74): Show |
82 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1167-1311delA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr13 | 39698179 | ||||||
| chr13:39698216 | C | T | 7 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(4): Show |
7 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.1167-1285C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39698216 | |||||||
| chr13:39698439 | T | C | 3 | a0005c0005t0003g0020 a0005c0005t0003g0021 a0005c0005t0003g0022 |
3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1167-1062T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39698439 | |||||||
| chr13:39698515 | A | G | 1 | a0002c0002t0003g0223 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1167-986A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39698515 | |||||||
| chr13:39698734 | T | C | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1167-767T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39698734 | |||||||
| chr13:39698734 | T | G | 1 | a0001c0001t0001g0156 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1167-767T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39698734 | |||||||
| chr13:39698775 | T | C | 1 | a0001c0001t0001g0005 | 2 | NA18952.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1167-726T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39698775 | |||||||
| chr13:39698912 | T | C | 2 | a0002c0002t0003g0226 a0007c0008t0003g0225 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1167-589T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39698912 | |||||||
| chr13:39698928 | G | C | 8 | a0002c0002t0002g0229 a0002c0002t0002g0231 a0002c0002t0002g0233 others(5): Show |
8 | HG01261.hp2 HG01433.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1167-573G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39698928 | |||||||
| chr13:39698971 | A | G | 2 | a0002c0002t0003g0223 a0002c0002t0004g0224 |
2 | HG02886.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1167-530A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39698971 | |||||||
| chr13:39699213 | TA | T | 7 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(4): Show |
7 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.1167-287delA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 12/18 | chr13 | 39699213 | |||||||
| chr13:39699645 | A | G | 1 | a0004c0004t0002g0251 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1284+27A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39699645 | |||||||
| chr13:39699917 | G | A | 2 | a0001c0001t0003g0027 a0001c0001t0003g0070 |
2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1284+299G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39699917 | |||||||
| chr13:39699990 | C | G | 1 | a0002c0002t0002g0302 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1284+372C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39699990 | |||||||
| chr13:39700253 | T | A | 1 | a0001c0001t0003g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1284+635T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39700253 | |||||||
| chr13:39700261 | T | A | 16 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0001g0112 others(13): Show |
17 | HG00609.hp1 HG00621.hp2 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.1284+643T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39700261 | |||||||
| chr13:39700354 | G | C | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1284+736G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39700354 | |||||||
| chr13:39700435 | A | C | 3 | a0001c0001t0003g0066 a0001c0001t0003g0068 a0001c0001t0003g0085 |
3 | NA18974.hp2 NA19081.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1284+817A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39700435 | |||||||
| chr13:39700569 | T | C | 2 | a0002c0002t0002g0245 a0002c0002t0002g0246 |
2 | HG01358.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1284+951T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39700569 | |||||||
| chr13:39700627 | A | G | 3 | a0005c0005t0003g0020 a0005c0005t0003g0021 a0005c0005t0003g0022 |
3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1284+1009A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39700627 | |||||||
| chr13:39700765 | C | T | 56 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(53): Show |
60 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.1284+1147C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39700765 | |||||||
| chr13:39700777 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG03704.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1284+1159G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39700777 | |||||||
| chr13:39700815 | C | T | 1 | a0005c0005t0003g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1284+1197C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39700815 | |||||||
| chr13:39700872 | A | G | 2 | a0002c0002t0002g0279 a0002c0002t0002g0280 |
2 | NA18986.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1284+1254A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39700872 | |||||||
| chr13:39700892 | C | T | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1284+1274C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39700892 | |||||||
| chr13:39701020 | A | C | 1 | a0001c0001t0001g0164 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1284+1402A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39701020 | |||||||
| chr13:39701345 | A | T | 2 | a0002c0002t0003g0226 a0007c0008t0003g0225 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1284+1727A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39701345 | |||||||
| chr13:39701514 | G | A | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1284+1896G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39701514 | |||||||
| chr13:39701605 | C | T | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1284+1987C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39701605 | |||||||
| chr13:39701838 | C | T | 78 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(75): Show |
83 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1284+2220C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39701838 | |||||||
| chr13:39701908 | G | T | 4 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0151 others(1): Show |
4 | HG01934.hp2 HG02135.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.1284+2290G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39701908 | |||||||
| chr13:39702121 | C | T | 77 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(74): Show |
82 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1284+2503C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39702121 | |||||||
| chr13:39702228 | T | C | 23 | a0001c0001t0004g0090 a0001c0001t0004g0091 a0002c0002t0002g0014 others(20): Show |
24 | HG00323.hp2 HG00558.hp2 HG02698.hp2 others(21): Show |
intron_variant | MODIFIER | c.1284+2610T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39702228 | |||||||
| chr13:39702389 | A | C | 131 | a0001c0001t0004g0090 a0001c0001t0004g0091 a0001c0001t0004g0169 others(128): Show |
135 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.1284+2771A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39702389 | |||||||
| chr13:39702394 | C | T | 3 | a0005c0005t0003g0020 a0005c0005t0003g0021 a0005c0005t0003g0022 |
3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1284+2776C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39702394 | |||||||
| chr13:39702411 | ATATTAAA others(13): Show |
A | 1 | a0001c0001t0003g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1284+2799_1284+281 others(24): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39702411 | ||||||
| chr13:39702572 | A | G | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1284+2954A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39702572 | |||||||
| chr13:39702585 | T | G | 1 | a0001c0001t0001g0180 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1284+2967T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39702585 | |||||||
| chr13:39702663 | C | T | 1 | a0002c0002t0003g0223 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1284+3045C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39702663 | |||||||
| chr13:39702686 | C | T | 4 | a0002c0002t0006g0316 a0004c0004t0002g0251 a0004c0004t0002g0252 others(1): Show |
4 | HG02970.hp1 HG03225.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1284+3068C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39702686 | |||||||
| chr13:39702687 | G | A | 2 | a0002c0002t0010g0222 a0008c0009t0010g0221 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1284+3069G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39702687 | |||||||
| chr13:39702789 | A | G | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1284+3171A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39702789 | |||||||
| chr13:39702907 | C | T | 1 | a0002c0002t0008g0240 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1284+3289C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39702907 | |||||||
| chr13:39703021 | C | T | 2 | a0002c0002t0010g0222 a0008c0009t0010g0221 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1284+3403C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39703021 | |||||||
| chr13:39703233 | A | C | 2 | a0002c0002t0003g0226 a0007c0008t0003g0225 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1284+3615A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39703233 | |||||||
| chr13:39703340 | A | C | 78 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(75): Show |
83 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1284+3722A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39703340 | |||||||
| chr13:39703779 | C | G | 1 | a0004c0004t0002g0251 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1284+4161C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39703779 | |||||||
| chr13:39703801 | G | A | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1284+4183G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39703801 | |||||||
| chr13:39703899 | A | T | 78 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(75): Show |
83 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1284+4281A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39703899 | |||||||
| chr13:39703925 | G | A | 3 | a0002c0002t0008g0013 a0002c0002t0008g0240 a0002c0002t0008g0328 |
4 | HG00639.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1284+4307G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39703925 | |||||||
| chr13:39704219 | C | G | 2 | a0002c0002t0010g0222 a0008c0009t0010g0221 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1284+4601C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39704219 | |||||||
| chr13:39704276 | G | A | 1 | a0001c0011t0003g0209 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1284+4658G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39704276 | |||||||
| chr13:39704629 | G | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG00642.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1284+5011G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39704629 | |||||||
| chr13:39704802 | C | T | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1284+5184C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39704802 | |||||||
| chr13:39704927 | C | T | 346 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(343): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1284+5309C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39704927 | |||||||
| chr13:39704952 | A | G | 131 | a0001c0001t0004g0090 a0001c0001t0004g0091 a0001c0001t0004g0169 others(128): Show |
135 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.1284+5334A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39704952 | |||||||
| chr13:39705078 | T | C | 1 | a0002c0002t0004g0224 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1284+5460T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39705078 | |||||||
| chr13:39705195 | A | G | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1284+5577A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39705195 | |||||||
| chr13:39705231 | A | G | 2 | a0001c0001t0003g0066 a0001c0001t0003g0085 |
2 | NA18974.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1284+5613A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39705231 | |||||||
| chr13:39705312 | C | T | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1284+5694C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39705312 | |||||||
| chr13:39705484 | T | C | 2 | a0001c0001t0003g0049 a0001c0001t0003g0055 |
2 | HG01934.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1284+5866T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39705484 | |||||||
| chr13:39705507 | G | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(92): Show |
103 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.1284+5889G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39705507 | |||||||
| chr13:39705823 | C | T | 3 | a0001c0001t0001g0212 a0001c0001t0003g0010 a0001c0001t0003g0188 |
4 | HG01243.hp1 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1284+6205C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39705823 | |||||||
| chr13:39705826 | A | G | 7 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(4): Show |
7 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.1284+6208A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39705826 | |||||||
| chr13:39705972 | A | T | 1 | a0001c0001t0001g0094 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1284+6354A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39705972 | |||||||
| chr13:39706199 | T | TTATATAT others(45): Show |
2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1284+6611_1284+661 others(56): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706199 | ||||||
| chr13:39706210 | C | T | 1 | a0001c0001t0004g0071 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1284+6592C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706210 | |||||||
| chr13:39706213 | C | T | 1 | a0002c0002t0002g0264 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1284+6595C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706213 | |||||||
| chr13:39706215 | T | A | 1 | a0002c0002t0002g0264 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1284+6597T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706215 | |||||||
| chr13:39706215 | T | TTA | 320 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(317): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1284+6610_1284+661 others(6): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706215 | ||||||
| chr13:39706215 | T | TTATATAT others(37): Show |
4 | a0001c0001t0003g0076 a0001c0001t0003g0077 a0001c0001t0003g0082 others(1): Show |
4 | NA18955.hp2 NA19010.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1284+6611_1284+661 others(48): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706215 | ||||||
| chr13:39706235 | T | TTA | 8 | a0002c0002t0002g0312 a0002c0002t0002g0329 a0002c0002t0002g0330 others(5): Show |
8 | HG02970.hp1 HG03130.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1284+6630_1284+663 others(6): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706235 | ||||||
| chr13:39706235 | T | TTATA | 119 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(116): Show |
123 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.1284+6628_1284+663 others(8): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706235 | ||||||
| chr13:39706235 | T | TTATATA | 10 | a0002c0002t0002g0229 a0002c0002t0002g0231 a0002c0002t0002g0233 others(7): Show |
10 | HG01261.hp2 HG01433.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.1284+6626_1284+663 others(10): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706235 | ||||||
| chr13:39706237 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0003g0056 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1284+6632_1284+664 others(22): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706237 | ||||||
| chr13:39706255 | T | TTA | 69 | a0001c0001t0001g0008 a0001c0001t0003g0002 a0001c0001t0003g0004 others(66): Show |
73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1284+6659_1284+666 others(6): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | T | TTATA | 49 | a0001c0001t0001g0094 a0001c0001t0001g0144 a0001c0001t0001g0179 others(46): Show |
52 | HG00423.hp2 HG00741.hp1 HG01243.hp1 others(49): Show |
intron_variant | MODIFIER | c.1284+6657_1284+666 others(8): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | T | TTATATA | 78 | a0001c0001t0001g0009 a0001c0001t0001g0109 a0001c0001t0001g0110 others(75): Show |
79 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.1284+6655_1284+666 others(10): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | T | TTATATAT others(1): Show |
57 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(54): Show |
61 | HG00438.hp1 HG00673.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.1284+6653_1284+666 others(12): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | T | TTATATAT others(3): Show |
18 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0128 others(15): Show |
19 | HG01069.hp1 HG01106.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.1284+6651_1284+666 others(14): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | T | TTATATAT others(5): Show |
9 | a0001c0001t0001g0007 a0001c0001t0001g0137 a0001c0001t0001g0151 others(6): Show |
9 | HG01934.hp2 HG02559.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1284+6649_1284+666 others(16): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | T | TTATATAT others(7): Show |
3 | a0002c0002t0007g0325 a0003c0003t0001g0103 a0003c0003t0001g0104 |
3 | HG01243.hp2 HG03209.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1284+6647_1284+666 others(18): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | T | TTATATAT others(9): Show |
2 | a0001c0001t0004g0096 a0003c0003t0001g0176 |
2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1284+6645_1284+666 others(20): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | T | TTATATAT others(13): Show |
1 | a0001c0001t0001g0098 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1284+6641_1284+666 others(24): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | T | TTATATAT others(31): Show |
1 | a0001c0001t0001g0207 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1284+6660_1284+666 others(42): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | T | TTATATAT others(33): Show |
1 | a0001c0001t0005g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1284+6660_1284+666 others(44): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | T | TTATATAT others(39): Show |
2 | a0001c0001t0001g0120 a0001c0001t0004g0127 |
2 | HG06807.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1284+6660_1284+666 others(50): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | T | TTATATAT others(41): Show |
2 | a0001c0001t0001g0006 a0001c0001t0001g0117 |
2 | NA19064.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1284+6660_1284+666 others(52): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | T | TTATATAT others(43): Show |
1 | a0001c0001t0001g0116 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1284+6660_1284+666 others(54): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | T | TTATATAT others(33): Show |
1 | a0001c0001t0001g0115 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1284+6660_1284+666 others(44): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | T | TTATATAT others(37): Show |
5 | a0001c0001t0001g0114 a0001c0001t0001g0158 a0001c0001t0001g0200 others(2): Show |
5 | HG00099.hp2 HG00609.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.1284+6660_1284+666 others(48): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | T | TTATATAT others(39): Show |
2 | a0001c0001t0001g0006 a0001c0001t0001g0095 |
2 | NA18977.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1284+6660_1284+666 others(50): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | T | TTATATAT others(51): Show |
1 | a0001c0001t0001g0118 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1284+6660_1284+666 others(62): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | T | TTATATAT others(35): Show |
4 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0119 others(1): Show |
4 | NA18981.hp2 NA18984.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1284+6660_1284+666 others(46): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | T | TTATATAT others(37): Show |
2 | a0001c0001t0001g0099 a0001c0001t0001g0172 |
2 | HG02683.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1284+6660_1284+666 others(48): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | T | TTATATAT others(39): Show |
3 | a0001c0001t0001g0023 a0001c0001t0001g0155 a0001c0001t0015g0201 |
3 | HG00323.hp1 HG01069.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1284+6660_1284+666 others(50): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | T | TTATATAT others(65): Show |
1 | a0001c0001t0001g0181 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1284+6660_1284+666 others(76): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | T | TTATATAT others(29): Show |
1 | a0001c0001t0001g0018 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1284+6660_1284+666 others(40): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | T | TTATATAT others(31): Show |
3 | a0001c0001t0001g0106 a0001c0001t0001g0124 a0001c0001t0001g0161 |
3 | HG02300.hp2 HG03942.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1284+6660_1284+666 others(42): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | T | TTATATAT others(33): Show |
1 | a0001c0001t0001g0162 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1284+6660_1284+666 others(44): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | T | TTATATAT others(35): Show |
3 | a0001c0001t0001g0108 a0001c0001t0001g0123 a0001c0001t0001g0156 |
3 | HG03669.hp1 HG03927.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1284+6660_1284+666 others(46): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | T | TTATATAT others(37): Show |
1 | a0001c0001t0001g0154 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1284+6660_1284+666 others(48): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | T | TTATATAT others(31): Show |
2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1284+6660_1284+666 others(42): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | T | TTATATAT others(25): Show |
1 | a0001c0001t0001g0180 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1284+6660_1284+666 others(36): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706255 | TTA | T | 4 | a0001c0001t0003g0024 a0001c0001t0003g0080 a0001c0001t0003g0081 others(1): Show |
4 | HG02896.hp2 NA19007.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.1284+6659_1284+666 others(6): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706255 | ||||||
| chr13:39706261 | A | ATATATAT others(15): Show |
2 | a0002c0002t0010g0222 a0008c0009t0010g0221 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1284+6659_1284+666 others(26): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706261 | ||||||
| chr13:39706261 | A | ATATATAT others(21): Show |
7 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(4): Show |
7 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.1284+6660_1284+666 others(32): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706261 | ||||||
| chr13:39706290 | T | G | 1 | a0002c0002t0002g0347 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1284+6672T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706290 | |||||||
| chr13:39706292 | G | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(112): Show |
127 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1284+6674G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706292 | |||||||
| chr13:39706452 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(45): Show |
55 | HG00280.hp1 HG00438.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.1284+6834G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706452 | |||||||
| chr13:39706612 | T | TA | 78 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(75): Show |
83 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1284+7001dupA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39706612 | ||||||
| chr13:39706673 | T | A | 80 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(77): Show |
85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1284+7055T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706673 | |||||||
| chr13:39706680 | A | T | 11 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(8): Show |
11 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.1284+7062A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706680 | |||||||
| chr13:39706715 | T | C | 8 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0203 others(5): Show |
10 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1284+7097T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706715 | |||||||
| chr13:39706753 | G | T | 77 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(74): Show |
82 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1284+7135G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706753 | |||||||
| chr13:39706764 | A | G | 2 | a0002c0002t0010g0222 a0008c0009t0010g0221 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1284+7146A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706764 | |||||||
| chr13:39706771 | C | T | 79 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(76): Show |
84 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1284+7153C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706771 | |||||||
| chr13:39706798 | C | A | 1 | a0001c0001t0003g0129 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1284+7180C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706798 | |||||||
| chr13:39706874 | G | A | 7 | a0001c0001t0001g0097 a0001c0001t0001g0159 a0001c0001t0001g0160 others(4): Show |
7 | HG00280.hp1 HG01081.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1284+7256G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706874 | |||||||
| chr13:39706917 | C | A | 3 | a0005c0005t0003g0020 a0005c0005t0003g0021 a0005c0005t0003g0022 |
3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1284+7299C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39706917 | |||||||
| chr13:39707082 | A | T | 8 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0001g0193 others(5): Show |
8 | HG00738.hp2 HG02293.hp1 HG03239.hp2 others(5): Show |
intron_variant | MODIFIER | c.1284+7464A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39707082 | |||||||
| chr13:39707132 | CT | C | 6 | a0001c0001t0001g0130 a0001c0001t0001g0140 a0001c0001t0001g0200 others(3): Show |
6 | NA18612.hp2 NA18946.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.1284+7528delT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39707132 | ||||||
| chr13:39707228 | A | G | 8 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0203 others(5): Show |
10 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1284+7610A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39707228 | |||||||
| chr13:39707301 | G | A | 8 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0203 others(5): Show |
10 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1284+7683G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39707301 | |||||||
| chr13:39707373 | C | T | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1284+7755C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39707373 | |||||||
| chr13:39707379 | A | G | 2 | a0001c0001t0004g0107 a0001c0001t0004g0127 |
2 | HG00099.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1284+7761A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39707379 | |||||||
| chr13:39707389 | A | C | 3 | a0002c0002t0002g0294 a0002c0002t0002g0299 a0002c0002t0002g0321 |
3 | HG01069.hp1 HG03490.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1284+7771A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39707389 | |||||||
| chr13:39707601 | T | C | 334 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(331): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.1284+7983T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39707601 | |||||||
| chr13:39708039 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(109): Show |
123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.1284+8421C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39708039 | |||||||
| chr13:39708054 | C | G | 4 | a0002c0002t0002g0242 a0002c0002t0002g0311 a0002c0002t0002g0313 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1284+8436C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39708054 | |||||||
| chr13:39708476 | A | G | 9 | a0001c0001t0003g0202 a0001c0001t0005g0011 a0001c0001t0005g0012 others(6): Show |
11 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1284+8858A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39708476 | |||||||
| chr13:39708664 | G | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(115): Show |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1284+9046G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39708664 | |||||||
| chr13:39708921 | G | C | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1284+9303G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39708921 | |||||||
| chr13:39709169 | C | T | 1 | a0002c0002t0002g0346 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1284+9551C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39709169 | |||||||
| chr13:39709225 | G | A | 2 | a0001c0001t0004g0125 a0001c0001t0004g0126 |
2 | HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1284+9607G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39709225 | |||||||
| chr13:39709459 | C | T | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-9777C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39709459 | |||||||
| chr13:39709636 | G | A | 1 | a0002c0002t0002g0349 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1285-9600G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39709636 | |||||||
| chr13:39709814 | C | T | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1285-9422C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39709814 | |||||||
| chr13:39709868 | A | G | 1 | a0004c0004t0002g0252 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1285-9368A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39709868 | |||||||
| chr13:39709933 | T | C | 1 | a0002c0002t0002g0306 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1285-9303T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39709933 | |||||||
| chr13:39709965 | C | T | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1285-9271C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39709965 | |||||||
| chr13:39710078 | C | G | 10 | a0002c0002t0002g0229 a0002c0002t0002g0231 a0002c0002t0002g0233 others(7): Show |
10 | HG01261.hp2 HG01433.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.1285-9158C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710078 | |||||||
| chr13:39710108 | A | G | 1 | a0002c0002t0007g0348 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1285-9128A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710108 | |||||||
| chr13:39710209 | G | T | 343 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(340): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.1285-9027G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710209 | |||||||
| chr13:39710236 | G | C | 1 | a0001c0001t0003g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1285-9000G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710236 | |||||||
| chr13:39710248 | G | A | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-8988G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710248 | |||||||
| chr13:39710535 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1285-8701G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710535 | |||||||
| chr13:39710555 | C | A | 1 | a0001c0001t0003g0055 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1285-8681C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710555 | |||||||
| chr13:39710685 | T | C | 11 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(8): Show |
11 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.1285-8551T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710685 | |||||||
| chr13:39710714 | A | G | 1 | a0007c0008t0003g0225 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1285-8522A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710714 | |||||||
| chr13:39710783 | A | G | 8 | a0002c0002t0002g0229 a0002c0002t0002g0231 a0002c0002t0002g0233 others(5): Show |
8 | HG01261.hp2 HG01433.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1285-8453A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710783 | |||||||
| chr13:39710840 | T | TTTC | 11 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(8): Show |
11 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.1285-8394_1285-839 others(7): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39710840 | ||||||
| chr13:39710844 | C | T | 11 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(8): Show |
11 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.1285-8392C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710844 | |||||||
| chr13:39710844 | CT | C | 326 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(323): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1285-8381delT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39710844 | ||||||
| chr13:39710845 | T | C | 11 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(8): Show |
11 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.1285-8391T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710845 | |||||||
| chr13:39710847 | T | C | 3 | a0001c0001t0003g0024 a0001c0001t0004g0125 a0001c0001t0004g0126 |
3 | HG02630.hp1 HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1285-8389T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710847 | |||||||
| chr13:39710890 | T | A | 70 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(67): Show |
74 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.1285-8346T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710890 | |||||||
| chr13:39710949 | C | T | 345 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(342): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.1285-8287C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39710949 | |||||||
| chr13:39711042 | C | CT | 7 | a0001c0001t0003g0031 a0001c0001t0003g0053 a0001c0001t0003g0058 others(4): Show |
7 | HG00099.hp1 HG00741.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.1285-8184dupT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39711042 | ||||||
| chr13:39711222 | G | A | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-8014G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39711222 | |||||||
| chr13:39711301 | C | T | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-7935C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39711301 | |||||||
| chr13:39711490 | G | C | 2 | a0002c0002t0010g0222 a0008c0009t0010g0221 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1285-7746G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39711490 | |||||||
| chr13:39711508 | TTCTAAGA others(20): Show |
T | 214 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(211): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.1285-7726_1285-770 others(31): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39711508 | ||||||
| chr13:39711591 | T | C | 6 | a0001c0001t0001g0009 a0001c0001t0001g0166 a0001c0001t0001g0167 others(3): Show |
7 | HG01192.hp1 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1285-7645T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39711591 | |||||||
| chr13:39711686 | A | G | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-7550A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39711686 | |||||||
| chr13:39711834 | T | C | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1285-7402T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39711834 | |||||||
| chr13:39711844 | A | C | 1 | a0001c0001t0003g0047 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1285-7392A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39711844 | |||||||
| chr13:39711888 | C | T | 1 | a0001c0001t0004g0054 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1285-7348C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39711888 | |||||||
| chr13:39711943 | T | A | 130 | a0001c0001t0004g0090 a0001c0001t0004g0091 a0001c0001t0004g0169 others(127): Show |
134 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.1285-7293T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39711943 | |||||||
| chr13:39711977 | A | T | 130 | a0001c0001t0004g0090 a0001c0001t0004g0091 a0001c0001t0004g0169 others(127): Show |
134 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.1285-7259A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39711977 | |||||||
| chr13:39712000 | C | T | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-7236C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39712000 | |||||||
| chr13:39712056 | C | T | 1 | a0001c0001t0014g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1285-7180C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39712056 | |||||||
| chr13:39712091 | C | T | 2 | a0002c0002t0002g0229 a0002c0002t0002g0231 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1285-7145C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39712091 | |||||||
| chr13:39712236 | T | C | 1 | a0002c0002t0002g0237 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1285-7000T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39712236 | |||||||
| chr13:39712267 | C | T | 6 | a0001c0001t0001g0009 a0001c0001t0001g0166 a0001c0001t0001g0167 others(3): Show |
7 | HG01192.hp1 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1285-6969C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39712267 | |||||||
| chr13:39712321 | G | A | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-6915G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39712321 | |||||||
| chr13:39712406 | T | TAGTCCCT others(332): Show |
2 | a0001c0001t0005g0203 a0001c0001t0005g0204 |
2 | HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1285-6814_1285-681 others(343): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39712406 | ||||||
| chr13:39712462 | T | C | 1 | a0002c0002t0002g0349 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1285-6774T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39712462 | |||||||
| chr13:39712476 | A | G | 3 | a0001c0001t0003g0024 a0001c0001t0004g0125 a0001c0001t0004g0126 |
3 | HG02630.hp1 HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1285-6760A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39712476 | |||||||
| chr13:39712864 | C | T | 2 | a0002c0002t0002g0289 a0002c0002t0002g0290 |
2 | HG01257.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1285-6372C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39712864 | |||||||
| chr13:39712865 | G | A | 3 | a0005c0005t0003g0020 a0005c0005t0003g0021 a0005c0005t0003g0022 |
3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1285-6371G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39712865 | |||||||
| chr13:39713220 | T | C | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1285-6016T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39713220 | |||||||
| chr13:39713263 | T | A | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1285-5973T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39713263 | |||||||
| chr13:39713382 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(109): Show |
123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.1285-5854T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39713382 | |||||||
| chr13:39713399 | A | G | 1 | a0002c0002t0002g0278 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1285-5837A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39713399 | |||||||
| chr13:39713633 | G | A | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1285-5603G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39713633 | |||||||
| chr13:39713637 | A | G | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-5599A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39713637 | |||||||
| chr13:39713651 | G | T | 1 | a0002c0002t0002g0299 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1285-5585G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39713651 | |||||||
| chr13:39713678 | G | A | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1285-5558G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39713678 | |||||||
| chr13:39713707 | G | A | 134 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(131): Show |
138 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.1285-5529G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39713707 | |||||||
| chr13:39713898 | A | G | 3 | a0005c0005t0003g0020 a0005c0005t0003g0021 a0005c0005t0003g0022 |
3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1285-5338A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39713898 | |||||||
| chr13:39713988 | T | A | 1 | a0002c0002t0002g0248 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1285-5248T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39713988 | |||||||
| chr13:39714224 | G | GT | 219 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(216): Show |
228 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.1285-5001dupT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39714224 | ||||||
| chr13:39714224 | GT | G | 36 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0023 others(33): Show |
38 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.1285-5001delT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39714224 | ||||||
| chr13:39714394 | T | C | 1 | a0001c0011t0003g0209 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1285-4842T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39714394 | |||||||
| chr13:39714434 | A | C | 1 | a0002c0002t0002g0233 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1285-4802A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39714434 | |||||||
| chr13:39714549 | G | T | 1 | a0001c0001t0001g0140 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1285-4687G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39714549 | |||||||
| chr13:39714622 | C | A | 10 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(7): Show |
10 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1285-4614C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39714622 | |||||||
| chr13:39714784 | A | G | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-4452A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39714784 | |||||||
| chr13:39714786 | T | A | 227 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(224): Show |
236 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.1285-4450T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39714786 | |||||||
| chr13:39714897 | A | C | 1 | a0002c0002t0002g0290 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1285-4339A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39714897 | |||||||
| chr13:39714933 | T | G | 127 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(124): Show |
131 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1285-4303T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39714933 | |||||||
| chr13:39714981 | A | T | 135 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(132): Show |
139 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.1285-4255A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39714981 | |||||||
| chr13:39715198 | G | A | 11 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(8): Show |
11 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.1285-4038G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715198 | |||||||
| chr13:39715208 | A | C | 1 | a0002c0002t0002g0299 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1285-4028A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715208 | |||||||
| chr13:39715216 | A | T | 11 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(8): Show |
11 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.1285-4020A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715216 | |||||||
| chr13:39715256 | C | CCTCT | 162 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(159): Show |
178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.1285-3967_1285-396 others(8): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39715256 | ||||||
| chr13:39715271 | C | CTCTCTA | 167 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0023 others(164): Show |
172 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.1285-3964_1285-396 others(10): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39715271 | ||||||
| chr13:39715271 | C | CTCTG | 7 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(4): Show |
7 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.1285-3964_1285-396 others(8): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39715271 | ||||||
| chr13:39715271 | C | G | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-3965C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715271 | |||||||
| chr13:39715273 | A | C | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1285-3963A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715273 | |||||||
| chr13:39715274 | T | C | 169 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0023 others(166): Show |
174 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.1285-3962T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715274 | |||||||
| chr13:39715283 | A | C | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1285-3953A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715283 | |||||||
| chr13:39715284 | C | T | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1285-3952C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715284 | |||||||
| chr13:39715286 | C | T | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1285-3950C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715286 | |||||||
| chr13:39715310 | A | G | 1 | a0001c0001t0003g0044 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1285-3926A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715310 | |||||||
| chr13:39715386 | C | A | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1285-3850C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715386 | |||||||
| chr13:39715386 | C | T | 2 | a0002c0002t0010g0222 a0008c0009t0010g0221 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1285-3850C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715386 | |||||||
| chr13:39715587 | G | T | 1 | a0002c0002t0004g0224 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1285-3649G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715587 | |||||||
| chr13:39715591 | C | A | 1 | a0001c0001t0003g0037 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1285-3645C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715591 | |||||||
| chr13:39715904 | T | G | 7 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(4): Show |
7 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.1285-3332T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39715904 | |||||||
| chr13:39716052 | A | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(115): Show |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1285-3184A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39716052 | |||||||
| chr13:39716059 | G | A | 1 | a0004c0004t0007g0250 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1285-3177G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39716059 | |||||||
| chr13:39716196 | T | A | 1 | a0002c0002t0004g0220 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1285-3040T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39716196 | |||||||
| chr13:39716342 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1285-2894C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39716342 | |||||||
| chr13:39716359 | C | G | 1 | a0001c0001t0003g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1285-2877C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39716359 | |||||||
| chr13:39716390 | A | T | 1 | a0001c0001t0003g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1285-2846A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39716390 | |||||||
| chr13:39716560 | G | A | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-2676G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39716560 | |||||||
| chr13:39716582 | C | G | 5 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0199 others(2): Show |
6 | HG01496.hp2 HG02572.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1285-2654C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39716582 | |||||||
| chr13:39716936 | T | A | 1 | a0001c0001t0003g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1285-2300T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39716936 | |||||||
| chr13:39717008 | G | T | 130 | a0001c0001t0004g0090 a0001c0001t0004g0091 a0001c0001t0004g0169 others(127): Show |
134 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.1285-2228G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39717008 | |||||||
| chr13:39717149 | G | A | 1 | a0002c0002t0003g0223 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1285-2087G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39717149 | |||||||
| chr13:39717266 | A | T | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1285-1970A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39717266 | |||||||
| chr13:39717282 | G | A | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-1954G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39717282 | |||||||
| chr13:39717488 | C | CA | 345 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(342): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.1285-1746dupA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39717488 | ||||||
| chr13:39717548 | G | A | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-1688G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39717548 | |||||||
| chr13:39717760 | A | G | 7 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(4): Show |
7 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.1285-1476A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39717760 | |||||||
| chr13:39717812 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1285-1424G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39717812 | |||||||
| chr13:39717869 | A | G | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1285-1367A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39717869 | |||||||
| chr13:39717883 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1285-1353A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39717883 | |||||||
| chr13:39717980 | T | C | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-1256T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39717980 | |||||||
| chr13:39717997 | GT | G | 3 | a0002c0002t0008g0013 a0002c0002t0008g0240 a0002c0002t0008g0328 |
4 | HG00639.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1285-1235delT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39717997 | ||||||
| chr13:39718180 | A | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0157 |
2 | HG01346.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1285-1056A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39718180 | |||||||
| chr13:39718257 | C | T | 1 | a0002c0002t0002g0309 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1285-979C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39718257 | |||||||
| chr13:39718261 | T | C | 1 | a0002c0002t0002g0312 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1285-975T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39718261 | |||||||
| chr13:39718360 | A | G | 4 | a0002c0002t0002g0238 a0002c0002t0002g0239 a0002c0002t0002g0288 others(1): Show |
4 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1285-876A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39718360 | |||||||
| chr13:39718372 | G | A | 2 | a0002c0002t0003g0226 a0007c0008t0003g0225 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1285-864G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39718372 | |||||||
| chr13:39718399 | G | A | 3 | a0005c0005t0003g0020 a0005c0005t0003g0021 a0005c0005t0003g0022 |
3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1285-837G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39718399 | |||||||
| chr13:39718511 | T | C | 2 | a0002c0002t0004g0214 a0002c0002t0004g0215 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1285-725T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39718511 | |||||||
| chr13:39718790 | A | G | 35 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0023 others(32): Show |
36 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.1285-446A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39718790 | |||||||
| chr13:39718804 | C | T | 2 | a0001c0001t0004g0125 a0001c0001t0004g0126 |
2 | HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1285-432C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39718804 | |||||||
| chr13:39718841 | G | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(109): Show |
123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.1285-395G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39718841 | |||||||
| chr13:39718847 | G | A | 1 | a0001c0011t0003g0209 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1285-389G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39718847 | |||||||
| chr13:39718850 | G | A | 1 | a0002c0002t0003g0223 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1285-386G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39718850 | |||||||
| chr13:39718925 | A | G | 2 | a0002c0002t0003g0226 a0007c0008t0003g0225 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1285-311A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39718925 | |||||||
| chr13:39719006 | G | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0128 a0001c0001t0001g0131 others(3): Show |
7 | HG01106.hp1 HG02074.hp2 NA19056.hp2 others(4): Show |
intron_variant | MODIFIER | c.1285-230G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39719006 | |||||||
| chr13:39719065 | C | G | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1285-171C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39719065 | |||||||
| chr13:39719085 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1285-151G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39719085 | |||||||
| chr13:39719151 | AT | A | 339 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(336): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1285-76delT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr13 | 39719151 | ||||||
| chr13:39719178 | A | G | 1 | a0001c0001t0003g0036 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1285-58A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 13/18 | chr13 | 39719178 | |||||||
| chr13:39719428 | AATTCTGG others(13): Show |
A | 8 | a0002c0002t0002g0242 a0002c0002t0002g0311 a0002c0002t0002g0312 others(5): Show |
8 | HG02109.hp1 HG02145.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1416+64_1416+83del others(20): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr13 | 39719428 | ||||||
| chr13:39719464 | CTCTT | C | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1416+102_1416+105d others(6): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr13 | 39719464 | ||||||
| chr13:39719549 | C | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(53): Show |
63 | HG00280.hp1 HG00438.hp2 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.1417-111C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 14/18 | chr13 | 39719549 | |||||||
| chr13:39719994 | A | AAC | 60 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(57): Show |
65 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.1584+199_1584+200d others(4): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr13 | 39719994 | ||||||
| chr13:39719994 | A | AACAC | 120 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(117): Show |
123 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(120): Show |
intron_variant | MODIFIER | c.1584+197_1584+200d others(6): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr13 | 39719994 | ||||||
| chr13:39719994 | A | AACACAC | 27 | a0001c0001t0004g0205 a0002c0002t0002g0236 a0002c0002t0002g0238 others(24): Show |
28 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1584+195_1584+200d others(8): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr13 | 39719994 | ||||||
| chr13:39719994 | AAC | A | 14 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(11): Show |
14 | HG00642.hp2 HG00738.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1584+199_1584+200d others(4): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr13 | 39719994 | ||||||
| chr13:39719994 | AACACAC | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(106): Show |
120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1584+195_1584+200d others(8): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr13 | 39719994 | ||||||
| chr13:39720297 | C | T | 345 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(342): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.1584+470C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39720297 | |||||||
| chr13:39720402 | G | A | 11 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(8): Show |
11 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.1584+575G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39720402 | |||||||
| chr13:39720418 | A | G | 4 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
4 | HG01346.hp2 HG01361.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1584+591A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39720418 | |||||||
| chr13:39720613 | C | T | 1 | a0001c0001t0003g0061 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1584+786C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39720613 | |||||||
| chr13:39720657 | C | T | 1 | a0002c0002t0002g0335 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1584+830C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39720657 | |||||||
| chr13:39720732 | A | G | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1584+905A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39720732 | |||||||
| chr13:39720830 | A | C | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1584+1003A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39720830 | |||||||
| chr13:39720931 | T | C | 135 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(132): Show |
139 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.1584+1104T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39720931 | |||||||
| chr13:39720992 | A | G | 56 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(53): Show |
60 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.1584+1165A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39720992 | |||||||
| chr13:39721126 | C | G | 1 | a0002c0002t0002g0312 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1584+1299C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39721126 | |||||||
| chr13:39721143 | T | C | 1 | a0002c0002t0002g0337 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1584+1316T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39721143 | |||||||
| chr13:39721243 | G | A | 2 | a0002c0002t0003g0226 a0007c0008t0003g0225 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1584+1416G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39721243 | |||||||
| chr13:39721303 | A | G | 3 | a0002c0002t0002g0234 a0002c0002t0006g0230 a0002c0002t0006g0232 |
3 | HG01261.hp2 HG01433.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1584+1476A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39721303 | |||||||
| chr13:39721351 | A | G | 1 | a0001c0001t0003g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1584+1524A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39721351 | |||||||
| chr13:39721422 | T | C | 1 | a0002c0002t0002g0281 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1584+1595T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39721422 | |||||||
| chr13:39721452 | C | G | 1 | a0001c0001t0001g0018 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1584+1625C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39721452 | |||||||
| chr13:39721474 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1584+1647A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39721474 | |||||||
| chr13:39721502 | T | A | 1 | a0001c0001t0001g0124 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1584+1675T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39721502 | |||||||
| chr13:39721540 | C | A | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1584+1713C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39721540 | |||||||
| chr13:39721646 | A | G | 4 | a0001c0001t0001g0139 a0001c0001t0001g0149 a0001c0001t0001g0152 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1585-1687A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39721646 | |||||||
| chr13:39721879 | A | T | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1585-1454A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39721879 | |||||||
| chr13:39721887 | T | G | 2 | a0002c0002t0002g0335 a0002c0002t0002g0336 |
2 | NA19002.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1585-1446T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39721887 | |||||||
| chr13:39721950 | T | C | 1 | a0001c0001t0013g0134 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1585-1383T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39721950 | |||||||
| chr13:39722084 | G | A | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1585-1249G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722084 | |||||||
| chr13:39722092 | A | G | 1 | a0002c0002t0002g0283 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1585-1241A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722092 | |||||||
| chr13:39722177 | C | T | 11 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(8): Show |
11 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.1585-1156C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722177 | |||||||
| chr13:39722178 | C | G | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1585-1155C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722178 | |||||||
| chr13:39722194 | T | C | 11 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(8): Show |
11 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.1585-1139T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722194 | |||||||
| chr13:39722229 | C | T | 1 | a0001c0001t0003g0069 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1585-1104C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722229 | |||||||
| chr13:39722236 | G | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(112): Show |
126 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.1585-1097G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722236 | |||||||
| chr13:39722310 | TA | T | 10 | a0001c0001t0001g0190 a0001c0001t0001g0192 a0001c0001t0001g0193 others(7): Show |
10 | HG00642.hp2 HG00738.hp2 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.1585-1009delA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr13 | 39722310 | ||||||
| chr13:39722331 | T | C | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1585-1002T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722331 | |||||||
| chr13:39722395 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1585-938G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722395 | |||||||
| chr13:39722452 | C | T | 1 | a0002c0002t0002g0309 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1585-881C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722452 | |||||||
| chr13:39722617 | C | CA | 21 | a0001c0001t0001g0106 a0001c0001t0001g0123 a0001c0001t0003g0033 others(18): Show |
21 | HG01081.hp2 HG01884.hp1 HG02004.hp2 others(18): Show |
intron_variant | MODIFIER | c.1585-699dupA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr13 | 39722617 | ||||||
| chr13:39722617 | CA | C | 119 | a0001c0001t0001g0130 a0001c0001t0004g0090 a0001c0001t0004g0091 others(116): Show |
122 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.1585-699delA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr13 | 39722617 | ||||||
| chr13:39722632 | A | G | 2 | a0001c0001t0003g0010 a0001c0001t0003g0188 |
3 | HG01243.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1585-701A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722632 | |||||||
| chr13:39722704 | C | A | 9 | a0001c0001t0003g0202 a0001c0001t0005g0011 a0001c0001t0005g0012 others(6): Show |
11 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1585-629C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722704 | |||||||
| chr13:39722711 | C | A | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0192 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1585-622C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722711 | |||||||
| chr13:39722804 | A | G | 2 | a0002c0002t0003g0226 a0007c0008t0003g0225 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1585-529A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722804 | |||||||
| chr13:39722824 | A | G | 3 | a0001c0001t0001g0179 a0002c0002t0002g0238 a0002c0002t0002g0239 |
3 | HG01168.hp1 HG01169.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1585-509A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722824 | |||||||
| chr13:39722839 | C | G | 2 | a0001c0001t0003g0010 a0001c0001t0003g0188 |
3 | HG01243.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1585-494C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722839 | |||||||
| chr13:39722846 | A | G | 1 | a0001c0001t0003g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1585-487A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722846 | |||||||
| chr13:39722892 | C | T | 2 | a0002c0002t0003g0226 a0007c0008t0003g0225 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1585-441C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722892 | |||||||
| chr13:39722895 | T | A | 130 | a0001c0001t0003g0069 a0001c0001t0003g0198 a0001c0001t0004g0090 others(127): Show |
134 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.1585-438T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722895 | |||||||
| chr13:39722917 | C | G | 1 | a0001c0001t0001g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1585-416C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722917 | |||||||
| chr13:39722918 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1585-415T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722918 | |||||||
| chr13:39722966 | G | A | 1 | a0001c0001t0004g0170 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1585-367G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722966 | |||||||
| chr13:39722971 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1585-362G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39722971 | |||||||
| chr13:39723080 | G | C | 2 | a0002c0002t0003g0227 a0002c0002t0003g0228 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1585-253G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39723080 | |||||||
| chr13:39723084 | C | T | 1 | a0002c0002t0002g0334 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1585-249C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39723084 | |||||||
| chr13:39723176 | C | A | 1 | a0001c0001t0001g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1585-157C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39723176 | |||||||
| chr13:39723230 | A | G | 3 | a0001c0001t0003g0087 a0001c0001t0003g0088 a0001c0001t0003g0089 |
3 | HG02735.hp2 HG03834.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1585-103A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39723230 | |||||||
| chr13:39723244 | C | T | 3 | a0005c0005t0003g0020 a0005c0005t0003g0021 a0005c0005t0003g0022 |
3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1585-89C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 15/18 | chr13 | 39723244 | |||||||
| chr13:39723477 | A | G | 9 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0199 others(6): Show |
10 | HG01496.hp2 HG02280.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1692+37A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39723477 | |||||||
| chr13:39723501 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1692+61A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39723501 | |||||||
| chr13:39723547 | C | T | 230 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(227): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1692+107C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39723547 | |||||||
| chr13:39723619 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0185 |
2 | HG01175.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1692+179G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39723619 | |||||||
| chr13:39723660 | T | C | 64 | a0001c0001t0001g0094 a0001c0001t0001g0099 a0001c0001t0001g0139 others(61): Show |
69 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1692+220T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39723660 | |||||||
| chr13:39723696 | G | T | 1 | a0002c0002t0002g0330 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1692+256G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39723696 | |||||||
| chr13:39723702 | A | G | 10 | a0001c0001t0005g0203 a0001c0001t0005g0204 a0002c0002t0002g0312 others(7): Show |
10 | HG01884.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1692+262A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39723702 | |||||||
| chr13:39723724 | GT | G | 3 | a0001c0001t0001g0094 a0002c0002t0010g0222 a0008c0009t0010g0221 |
3 | HG03471.hp1 HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1692+289delT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr13 | 39723724 | ||||||
| chr13:39723942 | A | G | 1 | a0002c0002t0002g0256 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1692+502A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39723942 | |||||||
| chr13:39723948 | A | G | 2 | a0001c0001t0003g0010 a0001c0001t0003g0188 |
3 | HG01243.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1692+508A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39723948 | |||||||
| chr13:39724039 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1693-469A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39724039 | |||||||
| chr13:39724084 | C | G | 1 | a0003c0003t0001g0102 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1693-424C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39724084 | |||||||
| chr13:39724087 | T | C | 3 | a0005c0005t0003g0020 a0005c0005t0003g0021 a0005c0005t0003g0022 |
3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1693-421T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39724087 | |||||||
| chr13:39724325 | A | G | 1 | a0002c0002t0002g0293 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1693-183A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39724325 | |||||||
| chr13:39724410 | G | A | 2 | a0002c0002t0010g0222 a0008c0009t0010g0221 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1693-98G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39724410 | |||||||
| chr13:39724451 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1693-57A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39724451 | |||||||
| chr13:39724483 | CT | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(199): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
splice_region_variant&intron_variant | LOW | c.1693-7delT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr13 | 39724483 | ||||||
| chr13:39724484 | T | C | 1 | a0001c0001t0003g0056 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1693-24T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39724484 | |||||||
| chr13:39724485 | T | C | 88 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(85): Show |
95 | HG00280.hp2 HG00423.hp1 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.1693-23T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39724485 | |||||||
| chr13:39724486 | T | C | 2 | a0001c0001t0003g0030 a0001c0001t0003g0058 |
2 | HG01256.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.1693-22T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39724486 | |||||||
| chr13:39724501 | TA | T | 135 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(132): Show |
138 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(135): Show |
splice_region_variant&intron_variant | LOW | c.1693-4delA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr13 | 39724501 | ||||||
| chr13:39724502 | A | T | 1 | a0002c0002t0002g0235 | 1 | NA20805.hp2 | splice_region_variant&intron_variant | LOW | c.1693-6A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 16/18 | chr13 | 39724502 | |||||||
| chr13:39724668 | C | T | 345 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(342): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.1746+107C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39724668 | |||||||
| chr13:39724810 | C | G | 1 | a0001c0001t0003g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1746+249C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39724810 | |||||||
| chr13:39725062 | C | T | 5 | a0001c0001t0004g0105 a0002c0002t0002g0345 a0002c0002t0002g0346 others(2): Show |
5 | HG00642.hp1 HG02135.hp1 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.1746+501C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39725062 | |||||||
| chr13:39725115 | T | C | 139 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(136): Show |
143 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.1746+554T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39725115 | |||||||
| chr13:39725132 | T | C | 2 | a0002c0002t0003g0226 a0007c0008t0003g0225 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1746+571T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39725132 | |||||||
| chr13:39725292 | CTT | C | 4 | a0001c0001t0003g0010 a0001c0001t0003g0188 a0002c0002t0003g0226 others(1): Show |
5 | HG01243.hp1 HG02976.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1746+733_1746+734d others(4): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr13 | 39725292 | ||||||
| chr13:39725585 | A | C | 70 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(67): Show |
74 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1746+1024A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39725585 | |||||||
| chr13:39725633 | A | G | 1 | a0002c0002t0003g0223 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1746+1072A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39725633 | |||||||
| chr13:39725686 | CTA | C | 136 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(133): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1746+1131_1746+113 others(6): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr13 | 39725686 | ||||||
| chr13:39725705 | ATAG | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(106): Show |
118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1746+1148_1746+115 others(7): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr13 | 39725705 | ||||||
| chr13:39725743 | T | C | 6 | a0003c0003t0001g0100 a0003c0003t0001g0101 a0003c0003t0001g0102 others(3): Show |
6 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1746+1182T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39725743 | |||||||
| chr13:39725815 | A | G | 1 | a0003c0003t0001g0176 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1746+1254A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39725815 | |||||||
| chr13:39726012 | T | G | 2 | a0001c0001t0004g0195 a0002c0002t0002g0237 |
2 | HG00741.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1746+1451T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39726012 | |||||||
| chr13:39726159 | G | A | 1 | a0002c0002t0002g0332 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1747-1310G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39726159 | |||||||
| chr13:39726191 | T | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(96): Show |
107 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1747-1278T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39726191 | |||||||
| chr13:39726408 | A | G | 172 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0023 others(169): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1747-1061A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39726408 | |||||||
| chr13:39726413 | G | A | 2 | a0002c0002t0002g0289 a0002c0002t0002g0290 |
2 | HG01257.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1747-1056G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39726413 | |||||||
| chr13:39726437 | A | G | 1 | a0001c0001t0003g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1747-1032A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39726437 | |||||||
| chr13:39726548 | G | A | 6 | a0002c0002t0002g0245 a0002c0002t0002g0246 a0002c0002t0002g0247 others(3): Show |
6 | HG01070.hp1 HG01255.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1747-921G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39726548 | |||||||
| chr13:39726615 | C | G | 1 | a0002c0002t0003g0226 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1747-854C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39726615 | |||||||
| chr13:39726710 | G | C | 1 | a0004c0004t0002g0253 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1747-759G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39726710 | |||||||
| chr13:39726763 | C | A | 3 | a0001c0001t0003g0087 a0001c0001t0003g0088 a0001c0001t0003g0089 |
3 | HG02735.hp2 HG03834.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1747-706C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39726763 | |||||||
| chr13:39726866 | G | A | 1 | a0001c0001t0003g0087 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1747-603G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39726866 | |||||||
| chr13:39727166 | C | A | 9 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0203 others(6): Show |
11 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1747-303C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39727166 | |||||||
| chr13:39727319 | T | A | 1 | a0001c0001t0001g0094 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1747-150T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | chr13 | 39727319 | |||||||
| chr13:39727319 | T | TAGAAAAT others(161): Show |
1 | a0002c0002t0003g0223 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1747-133_1747-132i others(170): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr13 | 39727319 | ||||||
| chr13:39727572 | G | C | 1 | a0001c0001t0003g0079 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1826+24G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39727572 | |||||||
| chr13:39727626 | T | A | 92 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(89): Show |
99 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1826+78T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39727626 | |||||||
| chr13:39727765 | G | C | 1 | a0001c0001t0001g0115 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1826+217G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39727765 | |||||||
| chr13:39728212 | G | A | 1 | a0002c0002t0002g0258 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1826+664G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39728212 | |||||||
| chr13:39728224 | C | T | 2 | a0002c0002t0010g0222 a0008c0009t0010g0221 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1826+676C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39728224 | |||||||
| chr13:39728260 | A | G | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1826+712A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39728260 | |||||||
| chr13:39728273 | A | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(74): Show |
85 | HG00280.hp1 HG00438.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.1826+725A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39728273 | |||||||
| chr13:39728471 | CT | C | 130 | a0001c0001t0004g0054 a0001c0001t0004g0071 a0001c0001t0004g0072 others(127): Show |
134 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.1826+936delT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39728471 | ||||||
| chr13:39728553 | TG | T | 2 | a0001c0001t0003g0010 a0001c0001t0003g0188 |
3 | HG01243.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1826+1006delG | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39728553 | |||||||
| chr13:39728674 | T | G | 92 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(89): Show |
99 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1826+1126T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39728674 | |||||||
| chr13:39728708 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1826+1160C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39728708 | |||||||
| chr13:39728716 | C | A | 1 | a0001c0001t0001g0112 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1826+1168C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39728716 | |||||||
| chr13:39728807 | G | A | 7 | a0001c0001t0003g0033 a0001c0001t0003g0036 a0001c0001t0003g0069 others(4): Show |
7 | HG02004.hp2 HG02735.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.1826+1259G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39728807 | |||||||
| chr13:39728926 | G | A | 1 | a0001c0001t0003g0024 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1826+1378G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39728926 | |||||||
| chr13:39728989 | T | G | 1 | a0001c0001t0003g0039 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1826+1441T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39728989 | |||||||
| chr13:39729023 | T | C | 138 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(135): Show |
142 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.1826+1475T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39729023 | |||||||
| chr13:39729057 | C | T | 131 | a0001c0001t0004g0054 a0001c0001t0004g0071 a0001c0001t0004g0072 others(128): Show |
135 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.1826+1509C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39729057 | |||||||
| chr13:39729069 | A | G | 1 | a0002c0002t0002g0331 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1826+1521A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39729069 | |||||||
| chr13:39729141 | C | T | 1 | a0001c0001t0001g0005 | 2 | NA18952.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1826+1593C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39729141 | |||||||
| chr13:39729256 | A | G | 345 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(342): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.1826+1708A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39729256 | |||||||
| chr13:39729396 | G | A | 1 | a0004c0004t0002g0252 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1826+1848G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39729396 | |||||||
| chr13:39729527 | A | C | 1 | a0001c0001t0003g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1826+1979A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39729527 | |||||||
| chr13:39729576 | A | T | 91 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(88): Show |
98 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1826+2028A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39729576 | |||||||
| chr13:39729636 | A | G | 88 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(85): Show |
94 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.1826+2088A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39729636 | |||||||
| chr13:39729666 | A | G | 88 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(85): Show |
94 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.1826+2118A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39729666 | |||||||
| chr13:39729668 | G | A | 1 | a0001c0001t0003g0043 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1826+2120G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39729668 | |||||||
| chr13:39729768 | G | A | 1 | a0002c0002t0010g0222 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1826+2220G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39729768 | |||||||
| chr13:39729890 | A | G | 1 | a0002c0002t0002g0299 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1826+2342A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39729890 | |||||||
| chr13:39730103 | C | A | 1 | a0002c0002t0002g0274 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1826+2555C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39730103 | |||||||
| chr13:39730492 | C | T | 2 | a0001c0001t0004g0125 a0001c0001t0004g0126 |
2 | HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1826+2944C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39730492 | |||||||
| chr13:39730558 | G | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0166 a0001c0001t0001g0167 others(2): Show |
6 | HG01192.hp1 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1826+3010G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39730558 | |||||||
| chr13:39730654 | T | G | 171 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0023 others(168): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.1826+3106T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39730654 | |||||||
| chr13:39730750 | G | C | 1 | a0002c0002t0002g0294 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1826+3202G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39730750 | |||||||
| chr13:39730757 | G | A | 1 | a0002c0002t0002g0288 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1826+3209G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39730757 | |||||||
| chr13:39730760 | C | A | 1 | a0004c0004t0002g0253 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1826+3212C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39730760 | |||||||
| chr13:39730773 | C | CA | 7 | a0001c0001t0001g0177 a0003c0003t0001g0100 a0003c0003t0001g0101 others(4): Show |
7 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1826+3251dupA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | ||||||
| chr13:39730773 | C | CAA | 13 | a0001c0001t0001g0183 a0001c0001t0003g0027 a0001c0001t0003g0037 others(10): Show |
15 | HG00639.hp2 HG01256.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1826+3250_1826+325 others(6): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | ||||||
| chr13:39730773 | C | CAAA | 61 | a0001c0001t0001g0167 a0001c0001t0003g0002 a0001c0001t0003g0003 others(58): Show |
65 | HG00140.hp1 HG00280.hp2 HG01081.hp2 others(62): Show |
intron_variant | MODIFIER | c.1826+3249_1826+325 others(7): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | ||||||
| chr13:39730773 | C | CAAAA | 15 | a0001c0001t0003g0004 a0001c0001t0003g0029 a0001c0001t0003g0033 others(12): Show |
16 | HG00741.hp2 HG01934.hp1 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.1826+3248_1826+325 others(8): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | ||||||
| chr13:39730773 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG00642.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1826+3241_1826+325 others(15): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | ||||||
| chr13:39730773 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1826+3238_1826+325 others(18): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | ||||||
| chr13:39730773 | C | CAAAAAAA others(8): Show |
10 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0131 others(7): Show |
15 | HG00738.hp2 HG02040.hp2 HG03239.hp2 others(12): Show |
intron_variant | MODIFIER | c.1826+3237_1826+325 others(19): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | ||||||
| chr13:39730773 | C | CAAAAAAA others(9): Show |
18 | a0001c0001t0001g0007 a0001c0001t0001g0094 a0001c0001t0001g0098 others(15): Show |
19 | HG01106.hp1 HG01516.hp1 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.1826+3236_1826+325 others(20): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | ||||||
| chr13:39730773 | C | CAAAAAAA others(10): Show |
15 | a0001c0001t0001g0018 a0001c0001t0001g0097 a0001c0001t0001g0109 others(12): Show |
15 | HG00280.hp1 HG00323.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.1826+3235_1826+325 others(21): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | ||||||
| chr13:39730773 | C | CAAAAAAA others(11): Show |
11 | a0001c0001t0001g0023 a0001c0001t0001g0099 a0001c0001t0001g0106 others(8): Show |
11 | HG01169.hp1 HG01258.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.1826+3234_1826+325 others(22): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | ||||||
| chr13:39730773 | C | CAAAAAAA others(12): Show |
7 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0117 others(4): Show |
7 | HG01081.hp1 HG01361.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1826+3233_1826+325 others(23): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | ||||||
| chr13:39730773 | C | CAAAAAAA others(13): Show |
8 | a0001c0001t0001g0006 a0001c0001t0001g0115 a0001c0001t0001g0116 others(5): Show |
9 | HG00621.hp2 HG03239.hp1 NA18979.hp2 others(6): Show |
intron_variant | MODIFIER | c.1826+3232_1826+325 others(24): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | ||||||
| chr13:39730773 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0178 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1826+3231_1826+325 others(25): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | ||||||
| chr13:39730773 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0164 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1826+3229_1826+325 others(27): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | ||||||
| chr13:39730773 | C | CAAAAAAA others(18): Show |
1 | a0001c0001t0001g0114 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1826+3227_1826+325 others(29): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | ||||||
| chr13:39730773 | C | CAAAAAAA others(20): Show |
1 | a0001c0001t0001g0123 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1826+3251_1826+325 others(31): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | ||||||
| chr13:39730773 | C | CAAAAAAA others(29): Show |
1 | a0001c0001t0014g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1826+3251_1826+325 others(40): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | ||||||
| chr13:39730773 | CA | C | 118 | a0001c0001t0001g0095 a0001c0001t0001g0121 a0001c0001t0001g0122 others(115): Show |
122 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1826+3251delA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | ||||||
| chr13:39730773 | CAA | C | 8 | a0002c0002t0002g0242 a0002c0002t0002g0268 a0002c0002t0002g0311 others(5): Show |
8 | HG02109.hp1 HG02145.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1826+3250_1826+325 others(6): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | ||||||
| chr13:39730773 | CAAAAAAA others(3): Show |
C | 4 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0002c0002t0006g0315 others(1): Show |
4 | HG02056.hp2 HG02970.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1826+3242_1826+325 others(14): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730773 | ||||||
| chr13:39730790 | A | AAAAAAAA others(9): Show |
2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | NA18959.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1826+3251_1826+325 others(20): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730790 | ||||||
| chr13:39730790 | A | AAAAAAAA others(8): Show |
4 | a0001c0001t0001g0008 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
5 | HG00438.hp2 NA18967.hp2 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826+3251_1826+325 others(19): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39730790 | ||||||
| chr13:39730800 | G | A | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0175 |
3 | HG02074.hp2 NA19062.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1826+3252G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39730800 | |||||||
| chr13:39730861 | A | T | 2 | a0001c0001t0003g0010 a0001c0001t0003g0188 |
3 | HG01243.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1826+3313A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39730861 | |||||||
| chr13:39730866 | G | A | 2 | a0002c0002t0006g0315 a0002c0002t0006g0316 |
2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1826+3318G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39730866 | |||||||
| chr13:39730911 | T | A | 3 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0083 |
3 | NA19007.hp1 NA19066.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1826+3363T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39730911 | |||||||
| chr13:39730929 | C | T | 1 | a0002c0002t0002g0303 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1826+3381C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39730929 | |||||||
| chr13:39730979 | T | C | 2 | a0001c0001t0003g0010 a0001c0001t0003g0188 |
3 | HG01243.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1826+3431T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39730979 | |||||||
| chr13:39731059 | A | G | 1 | a0001c0001t0004g0054 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1826+3511A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39731059 | |||||||
| chr13:39731087 | T | C | 2 | a0002c0002t0003g0226 a0007c0008t0003g0225 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1826+3539T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39731087 | |||||||
| chr13:39731320 | T | C | 2 | a0002c0002t0004g0214 a0002c0002t0004g0215 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1826+3772T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39731320 | |||||||
| chr13:39731381 | A | G | 1 | a0001c0011t0003g0209 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1826+3833A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39731381 | |||||||
| chr13:39731454 | C | A | 91 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(88): Show |
98 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1826+3906C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39731454 | |||||||
| chr13:39731469 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1826+3921T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39731469 | |||||||
| chr13:39731995 | G | C | 1 | a0002c0002t0002g0258 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1826+4447G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39731995 | |||||||
| chr13:39732078 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1826+4530A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39732078 | |||||||
| chr13:39732119 | A | G | 171 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0023 others(168): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.1826+4571A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39732119 | |||||||
| chr13:39732551 | T | G | 338 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(335): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1826+5003T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39732551 | |||||||
| chr13:39732982 | T | C | 171 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0023 others(168): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.1826+5434T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39732982 | |||||||
| chr13:39733123 | C | T | 91 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(88): Show |
98 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1826+5575C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39733123 | |||||||
| chr13:39733189 | C | CT | 7 | a0001c0001t0001g0147 a0001c0001t0001g0150 a0001c0001t0001g0156 others(4): Show |
7 | HG03927.hp1 HG04115.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.1826+5659dupT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39733189 | ||||||
| chr13:39733213 | C | T | 1 | a0002c0002t0003g0226 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1826+5665C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39733213 | |||||||
| chr13:39733227 | G | T | 8 | a0002c0002t0002g0265 a0002c0002t0002g0266 a0002c0002t0002g0267 others(5): Show |
8 | HG00609.hp2 HG02027.hp1 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.1826+5679G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39733227 | |||||||
| chr13:39733288 | G | T | 168 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0023 others(165): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1826+5740G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39733288 | |||||||
| chr13:39733308 | G | A | 1 | a0001c0001t0013g0134 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1826+5760G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39733308 | |||||||
| chr13:39733380 | G | A | 1 | a0001c0001t0003g0069 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1826+5832G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39733380 | |||||||
| chr13:39733400 | C | T | 135 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(132): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1826+5852C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39733400 | |||||||
| chr13:39733419 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1826+5871G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39733419 | |||||||
| chr13:39733459 | G | A | 1 | a0002c0002t0002g0333 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1826+5911G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39733459 | |||||||
| chr13:39733476 | A | C | 1 | a0001c0001t0003g0061 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1826+5928A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39733476 | |||||||
| chr13:39733477 | C | A | 1 | a0001c0001t0003g0061 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1826+5929C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39733477 | |||||||
| chr13:39733595 | G | GT | 6 | a0001c0001t0004g0096 a0002c0002t0002g0329 a0002c0002t0002g0330 others(3): Show |
6 | HG01884.hp1 HG01891.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1826+6058dupT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39733595 | ||||||
| chr13:39733939 | C | A | 2 | a0002c0002t0003g0226 a0007c0008t0003g0225 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1826+6391C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39733939 | |||||||
| chr13:39733968 | T | C | 4 | a0002c0002t0002g0229 a0002c0002t0002g0231 a0002c0002t0002g0233 others(1): Show |
4 | HG01515.hp2 HG01517.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.1826+6420T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39733968 | |||||||
| chr13:39733980 | C | T | 135 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(132): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1826+6432C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39733980 | |||||||
| chr13:39734060 | A | G | 2 | a0002c0002t0003g0226 a0007c0008t0003g0225 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1826+6512A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39734060 | |||||||
| chr13:39734067 | T | G | 1 | a0002c0002t0002g0345 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1826+6519T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39734067 | |||||||
| chr13:39734170 | T | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(108): Show |
120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.1826+6622T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39734170 | |||||||
| chr13:39734289 | G | A | 1 | a0004c0004t0002g0252 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1826+6741G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39734289 | |||||||
| chr13:39734426 | T | C | 7 | a0001c0001t0003g0010 a0001c0001t0003g0188 a0002c0002t0003g0226 others(4): Show |
8 | HG01243.hp1 HG01884.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1826+6878T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39734426 | |||||||
| chr13:39734553 | C | G | 171 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0023 others(168): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.1826+7005C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39734553 | |||||||
| chr13:39734613 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1826+7065C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39734613 | |||||||
| chr13:39734625 | A | C | 1 | a0001c0001t0015g0201 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1826+7077A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39734625 | |||||||
| chr13:39734684 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1826+7136C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39734684 | |||||||
| chr13:39734924 | A | G | 168 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0023 others(165): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1826+7376A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39734924 | |||||||
| chr13:39734978 | T | C | 1 | a0002c0002t0002g0276 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1826+7430T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39734978 | |||||||
| chr13:39734985 | A | G | 5 | a0001c0001t0003g0010 a0001c0001t0003g0188 a0005c0005t0003g0020 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1826+7437A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39734985 | |||||||
| chr13:39735250 | T | G | 2 | a0002c0002t0003g0226 a0007c0008t0003g0225 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1826+7702T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39735250 | |||||||
| chr13:39735418 | G | GCTTT | 338 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(335): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1826+7872_1826+787 others(8): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39735418 | ||||||
| chr13:39735657 | G | A | 1 | a0002c0002t0002g0349 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1826+8109G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39735657 | |||||||
| chr13:39735706 | C | CT | 16 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0124 others(13): Show |
16 | HG01255.hp1 HG02056.hp2 HG03490.hp1 others(13): Show |
intron_variant | MODIFIER | c.1826+8177dupT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39735706 | ||||||
| chr13:39735721 | TTTTTG | T | 127 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(124): Show |
131 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.1826+8174_1826+817 others(9): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39735721 | |||||||
| chr13:39735722 | TTTTG | T | 7 | a0001c0001t0004g0205 a0002c0002t0002g0303 a0002c0002t0002g0304 others(4): Show |
7 | HG01891.hp1 HG02258.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1826+8175_1826+817 others(8): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39735722 | |||||||
| chr13:39735808 | T | A | 1 | a0001c0001t0004g0105 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1826+8260T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39735808 | |||||||
| chr13:39736009 | G | A | 1 | a0001c0001t0003g0198 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1826+8461G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39736009 | |||||||
| chr13:39736198 | C | T | 2 | a0001c0001t0003g0010 a0001c0001t0003g0188 |
3 | HG01243.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1826+8650C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39736198 | |||||||
| chr13:39736362 | G | A | 3 | a0001c0001t0003g0024 a0002c0002t0007g0301 a0002c0002t0011g0016 |
4 | HG02572.hp1 HG02896.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1826+8814G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39736362 | |||||||
| chr13:39736373 | G | A | 1 | a0002c0002t0002g0288 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1826+8825G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39736373 | |||||||
| chr13:39736398 | G | T | 1 | a0001c0001t0004g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1826+8850G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39736398 | |||||||
| chr13:39736596 | C | G | 4 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
4 | HG01346.hp2 HG01361.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1826+9048C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39736596 | |||||||
| chr13:39736875 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1826+9327A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39736875 | |||||||
| chr13:39737127 | G | C | 4 | a0001c0001t0003g0004 a0001c0001t0003g0073 a0001c0001t0003g0074 others(1): Show |
5 | HG00423.hp1 NA18949.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.1826+9579G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737127 | |||||||
| chr13:39737148 | C | T | 2 | a0001c0001t0001g0163 a0001c0001t0001g0175 |
2 | NA19062.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1826+9600C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737148 | |||||||
| chr13:39737163 | G | A | 134 | a0001c0001t0004g0054 a0001c0001t0004g0071 a0001c0001t0004g0072 others(131): Show |
138 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.1826+9615G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737163 | |||||||
| chr13:39737222 | A | G | 2 | a0001c0001t0001g0116 a0001c0001t0003g0068 |
2 | NA18979.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1826+9674A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737222 | |||||||
| chr13:39737231 | C | T | 2 | a0001c0001t0003g0210 a0001c0001t0003g0211 |
2 | HG00733.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1826+9683C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737231 | |||||||
| chr13:39737232 | G | A | 1 | a0007c0008t0003g0225 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1826+9684G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737232 | |||||||
| chr13:39737253 | C | T | 1 | a0002c0002t0002g0321 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1826+9705C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737253 | |||||||
| chr13:39737362 | C | T | 5 | a0001c0001t0004g0096 a0002c0002t0002g0329 a0002c0002t0002g0330 others(2): Show |
5 | HG01884.hp1 HG03041.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826+9814C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737362 | |||||||
| chr13:39737468 | C | G | 1 | a0002c0002t0002g0289 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1826+9920C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737468 | |||||||
| chr13:39737485 | T | C | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | NA18940.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1826+9937T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737485 | |||||||
| chr13:39737619 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1826+10071C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737619 | |||||||
| chr13:39737621 | G | A | 21 | a0001c0001t0004g0090 a0001c0001t0004g0091 a0002c0002t0002g0014 others(18): Show |
22 | HG00323.hp2 HG00558.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1826+10073G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737621 | |||||||
| chr13:39737682 | C | T | 1 | a0001c0011t0003g0209 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1826+10134C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737682 | |||||||
| chr13:39737770 | T | A | 1 | a0001c0001t0001g0130 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1826+10222T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737770 | |||||||
| chr13:39737789 | C | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0166 a0001c0001t0001g0167 others(2): Show |
6 | HG01192.hp1 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1826+10241C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737789 | |||||||
| chr13:39737834 | G | A | 9 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0203 others(6): Show |
11 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1826+10286G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39737834 | |||||||
| chr13:39738009 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1826+10461G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39738009 | |||||||
| chr13:39738010 | C | T | 3 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0004c0004t0007g0250 |
3 | HG01515.hp1 HG03688.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1826+10462C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39738010 | |||||||
| chr13:39738207 | T | C | 3 | a0001c0001t0003g0066 a0001c0001t0003g0068 a0001c0001t0003g0085 |
3 | NA18974.hp2 NA19081.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1826+10659T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39738207 | |||||||
| chr13:39738367 | T | A | 2 | a0002c0002t0002g0262 a0002c0002t0002g0335 |
2 | NA18954.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1826+10819T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39738367 | |||||||
| chr13:39738911 | G | A | 171 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0023 others(168): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.1826+11363G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39738911 | |||||||
| chr13:39738959 | G | A | 2 | a0005c0005t0003g0020 a0005c0005t0003g0022 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1826+11411G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39738959 | |||||||
| chr13:39739089 | G | A | 92 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(89): Show |
99 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1826+11541G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39739089 | |||||||
| chr13:39739321 | AT | A | 8 | a0002c0002t0002g0265 a0002c0002t0002g0266 a0002c0002t0002g0267 others(5): Show |
8 | HG00609.hp2 HG02027.hp1 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.1827-11622delT | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39739321 | ||||||
| chr13:39739325 | C | A | 337 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(334): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1827-11621C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39739325 | |||||||
| chr13:39739325 | C | T | 1 | a0001c0001t0003g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1827-11621C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39739325 | |||||||
| chr13:39739726 | C | A | 345 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(342): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.1827-11220C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39739726 | |||||||
| chr13:39739846 | G | A | 3 | a0001c0001t0003g0087 a0001c0001t0003g0088 a0001c0001t0003g0089 |
3 | HG02735.hp2 HG03834.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1827-11100G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39739846 | |||||||
| chr13:39739851 | T | C | 1 | a0001c0011t0003g0209 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1827-11095T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39739851 | |||||||
| chr13:39740032 | A | G | 1 | a0001c0001t0004g0205 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1827-10914A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39740032 | |||||||
| chr13:39740119 | A | C | 6 | a0001c0001t0003g0029 a0001c0001t0003g0042 a0001c0001t0003g0051 others(3): Show |
6 | HG02040.hp1 HG02071.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.1827-10827A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39740119 | |||||||
| chr13:39740223 | T | G | 1 | a0002c0002t0003g0223 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1827-10723T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39740223 | |||||||
| chr13:39740272 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1827-10674G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39740272 | |||||||
| chr13:39740630 | G | A | 337 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(334): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1827-10316G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39740630 | |||||||
| chr13:39741038 | A | C | 4 | a0001c0001t0003g0024 a0002c0002t0003g0226 a0002c0002t0007g0301 others(1): Show |
4 | HG02572.hp1 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1827-9908A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39741038 | |||||||
| chr13:39741132 | A | G | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0161 others(1): Show |
4 | HG03490.hp1 HG03492.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1827-9814A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39741132 | |||||||
| chr13:39741143 | A | G | 169 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0023 others(166): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1827-9803A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39741143 | |||||||
| chr13:39741288 | G | C | 2 | a0002c0002t0004g0214 a0002c0002t0004g0215 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1827-9658G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39741288 | |||||||
| chr13:39741443 | G | A | 92 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(89): Show |
99 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1827-9503G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39741443 | |||||||
| chr13:39741457 | G | T | 1 | a0004c0004t0002g0253 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1827-9489G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39741457 | |||||||
| chr13:39741468 | C | T | 6 | a0002c0002t0002g0245 a0002c0002t0002g0246 a0002c0002t0002g0247 others(3): Show |
6 | HG01070.hp1 HG01255.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1827-9478C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39741468 | |||||||
| chr13:39741473 | A | G | 2 | a0001c0001t0003g0010 a0001c0001t0003g0188 |
3 | HG01243.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1827-9473A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39741473 | |||||||
| chr13:39741546 | T | C | 6 | a0002c0002t0002g0242 a0002c0002t0002g0311 a0002c0002t0002g0312 others(3): Show |
6 | HG02109.hp1 HG02145.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1827-9400T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39741546 | |||||||
| chr13:39742452 | T | A | 1 | a0002c0002t0002g0345 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1827-8494T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39742452 | |||||||
| chr13:39742467 | G | A | 136 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0161 others(133): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1827-8479G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39742467 | |||||||
| chr13:39742745 | C | T | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1827-8201C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39742745 | |||||||
| chr13:39742781 | C | A | 9 | a0002c0002t0002g0229 a0002c0002t0002g0231 a0002c0002t0002g0233 others(6): Show |
9 | HG01106.hp2 HG01515.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1827-8165C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39742781 | |||||||
| chr13:39742797 | A | G | 1 | a0002c0002t0005g0219 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1827-8149A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39742797 | |||||||
| chr13:39742860 | C | G | 7 | a0001c0001t0003g0033 a0001c0001t0003g0036 a0001c0001t0003g0069 others(4): Show |
7 | HG02004.hp2 HG02735.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.1827-8086C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39742860 | |||||||
| chr13:39743212 | A | G | 1 | a0002c0002t0002g0299 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1827-7734A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39743212 | |||||||
| chr13:39743244 | G | A | 345 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(342): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.1827-7702G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39743244 | |||||||
| chr13:39743350 | C | T | 1 | a0001c0001t0003g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1827-7596C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39743350 | |||||||
| chr13:39743396 | A | G | 1 | a0002c0002t0009g0273 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1827-7550A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39743396 | |||||||
| chr13:39743434 | A | C | 345 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(342): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.1827-7512A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39743434 | |||||||
| chr13:39743838 | G | A | 1 | a0001c0001t0005g0204 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1827-7108G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39743838 | |||||||
| chr13:39743945 | T | C | 169 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0023 others(166): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1827-7001T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39743945 | |||||||
| chr13:39744155 | C | G | 1 | a0001c0001t0001g0165 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1827-6791C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39744155 | |||||||
| chr13:39744156 | A | G | 169 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0023 others(166): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1827-6790A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39744156 | |||||||
| chr13:39744280 | A | G | 169 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0023 others(166): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1827-6666A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39744280 | |||||||
| chr13:39744317 | C | T | 3 | a0005c0005t0003g0020 a0005c0005t0003g0021 a0005c0005t0003g0022 |
3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1827-6629C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39744317 | |||||||
| chr13:39744371 | A | G | 2 | a0002c0002t0002g0262 a0002c0002t0002g0335 |
2 | NA18954.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1827-6575A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39744371 | |||||||
| chr13:39744451 | A | G | 169 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0023 others(166): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1827-6495A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39744451 | |||||||
| chr13:39744514 | A | G | 1 | a0002c0002t0003g0223 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1827-6432A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39744514 | |||||||
| chr13:39744671 | C | G | 1 | a0002c0002t0003g0223 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1827-6275C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39744671 | |||||||
| chr13:39744682 | A | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(107): Show |
119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.1827-6264A>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39744682 | |||||||
| chr13:39744822 | G | A | 1 | a0001c0001t0004g0054 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1827-6124G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39744822 | |||||||
| chr13:39744856 | A | G | 1 | a0002c0002t0002g0349 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1827-6090A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39744856 | |||||||
| chr13:39744960 | C | T | 90 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(87): Show |
97 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1827-5986C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39744960 | |||||||
| chr13:39744999 | C | A | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1827-5947C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39744999 | |||||||
| chr13:39745088 | T | A | 227 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0161 others(224): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1827-5858T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39745088 | |||||||
| chr13:39745107 | C | T | 1 | a0001c0001t0003g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1827-5839C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39745107 | |||||||
| chr13:39745120 | C | G | 136 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0161 others(133): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1827-5826C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39745120 | |||||||
| chr13:39745206 | A | G | 1 | a0001c0001t0003g0199 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1827-5740A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39745206 | |||||||
| chr13:39745784 | G | C | 1 | a0002c0002t0007g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1827-5162G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39745784 | |||||||
| chr13:39745817 | A | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
106 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.1827-5129A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39745817 | |||||||
| chr13:39746013 | C | T | 1 | a0002c0002t0002g0291 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1827-4933C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39746013 | |||||||
| chr13:39746026 | T | C | 1 | a0002c0002t0002g0286 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1827-4920T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39746026 | |||||||
| chr13:39746335 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1827-4611G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39746335 | |||||||
| chr13:39746346 | A | G | 345 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(342): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.1827-4600A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39746346 | |||||||
| chr13:39746401 | C | T | 3 | a0001c0001t0003g0024 a0002c0002t0007g0301 a0002c0002t0011g0016 |
4 | HG02572.hp1 HG02896.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1827-4545C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39746401 | |||||||
| chr13:39746440 | C | A | 4 | a0002c0002t0002g0238 a0002c0002t0002g0239 a0002c0002t0002g0288 others(1): Show |
4 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1827-4506C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39746440 | |||||||
| chr13:39746543 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1827-4403C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39746543 | |||||||
| chr13:39746738 | A | G | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1827-4208A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39746738 | |||||||
| chr13:39746793 | T | C | 1 | a0001c0001t0003g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1827-4153T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39746793 | |||||||
| chr13:39746847 | T | A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1827-4099T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39746847 | |||||||
| chr13:39746970 | C | T | 3 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0208 |
5 | HG01891.hp2 HG02109.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1827-3976C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39746970 | |||||||
| chr13:39747093 | C | T | 1 | a0001c0001t0003g0068 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1827-3853C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39747093 | |||||||
| chr13:39747161 | G | C | 338 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(335): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1827-3785G>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39747161 | |||||||
| chr13:39747215 | A | G | 72 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(69): Show |
76 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1827-3731A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39747215 | |||||||
| chr13:39747272 | T | A | 2 | a0001c0001t0003g0010 a0001c0001t0003g0188 |
3 | HG01243.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1827-3674T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39747272 | |||||||
| chr13:39747340 | G | A | 345 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(342): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.1827-3606G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39747340 | |||||||
| chr13:39747419 | C | A | 3 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0002c0002t0004g0220 |
3 | HG02280.hp2 HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1827-3527C>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39747419 | |||||||
| chr13:39747485 | G | A | 4 | a0002c0002t0002g0303 a0002c0002t0002g0305 a0002c0002t0002g0306 others(1): Show |
4 | HG02258.hp1 HG02818.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1827-3461G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39747485 | |||||||
| chr13:39747626 | C | G | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1827-3320C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39747626 | |||||||
| chr13:39747657 | T | C | 2 | a0002c0002t0010g0222 a0008c0009t0010g0221 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1827-3289T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39747657 | |||||||
| chr13:39747691 | T | C | 1 | a0001c0001t0003g0029 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1827-3255T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39747691 | |||||||
| chr13:39747709 | A | G | 1 | a0002c0002t0002g0298 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1827-3237A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39747709 | |||||||
| chr13:39747863 | G | A | 1 | a0001c0011t0003g0209 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1827-3083G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39747863 | |||||||
| chr13:39747890 | G | GTTAAATA others(12): Show |
1 | a0001c0001t0001g0006 | 2 | NA19064.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1827-3055_1827-303 others(23): Show |
COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39747890 | ||||||
| chr13:39747958 | T | C | 140 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(137): Show |
144 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.1827-2988T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39747958 | |||||||
| chr13:39748002 | T | A | 3 | a0005c0005t0003g0020 a0005c0005t0003g0021 a0005c0005t0003g0022 |
3 | HG01884.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1827-2944T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39748002 | |||||||
| chr13:39748353 | G | A | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1827-2593G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39748353 | |||||||
| chr13:39748424 | T | G | 170 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0023 others(167): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.1827-2522T>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39748424 | |||||||
| chr13:39748560 | A | G | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1827-2386A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39748560 | |||||||
| chr13:39748569 | C | G | 2 | a0002c0002t0010g0222 a0008c0009t0010g0221 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1827-2377C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39748569 | |||||||
| chr13:39748590 | G | T | 1 | a0003c0003t0001g0102 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1827-2356G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39748590 | |||||||
| chr13:39748622 | G | GA | 7 | a0001c0001t0003g0053 a0001c0001t0003g0057 a0001c0001t0003g0058 others(4): Show |
7 | HG01256.hp1 HG01258.hp2 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.1827-2312dupA | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 39748622 | ||||||
| chr13:39749049 | T | C | 91 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(88): Show |
98 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1827-1897T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39749049 | |||||||
| chr13:39749070 | C | T | 1 | a0001c0001t0004g0170 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1827-1876C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39749070 | |||||||
| chr13:39749072 | C | T | 1 | a0001c0001t0004g0170 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1827-1874C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39749072 | |||||||
| chr13:39749073 | A | T | 1 | a0001c0001t0004g0170 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1827-1873A>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39749073 | |||||||
| chr13:39749074 | A | G | 1 | a0001c0001t0004g0170 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1827-1872A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39749074 | |||||||
| chr13:39749101 | C | T | 136 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(133): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1827-1845C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39749101 | |||||||
| chr13:39749306 | C | T | 136 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(133): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1827-1640C>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39749306 | |||||||
| chr13:39749314 | T | A | 136 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(133): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1827-1632T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39749314 | |||||||
| chr13:39749399 | T | C | 1 | a0001c0001t0003g0202 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1827-1547T>C | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39749399 | |||||||
| chr13:39749751 | A | G | 1 | a0002c0007t0002g0295 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1827-1195A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39749751 | |||||||
| chr13:39749796 | G | T | 1 | a0001c0001t0001g0124 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1827-1150G>T | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39749796 | |||||||
| chr13:39750081 | A | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0172 |
2 | HG03491.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1827-865A>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39750081 | |||||||
| chr13:39750614 | G | A | 1 | a0002c0002t0003g0223 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1827-332G>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39750614 | |||||||
| chr13:39750659 | T | A | 1 | a0001c0001t0001g0180 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1827-287T>A | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39750659 | |||||||
| chr13:39750782 | C | G | 1 | a0002c0002t0002g0342 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1827-164C>G | COG6 | ENSG00000133103.17 | transcript | ENST00000455146.8 | protein_coding | 18/18 | chr13 | 39750782 |