Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23116 |
| ensemblid | ENSG00000198718.13 |
| hgncid | 19959 |
| symbol | TOGARAM1 |
| name | TOG array regulator of axonemal microtubules 1 |
| refseq_nuc | NM_001308120.2 |
| refseq_prot | NP_001295049.1 |
| ensembl_nuc | ENST00000361462.7 |
| ensembl_prot | ENSP00000354917.2 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 44962190 |
| end | 45074431 |
| strand | + |
| ver | v1.2 |
| region | chr14:44962190-45074431 |
| region5000 | chr14:44957190-45079431 |
| regionname0 | TOGARAM1_chr14_44962190_45074431 |
| regionname5000 | TOGARAM1_chr14_44957190_45079431 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1773 | 100 | 34 | 14 | 34 | 4 | 12 | 27 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | MAAAP others(1768): Show |
chr14 | 44957190 | 45079431 |
| a0002 | 0/0 | 1773 | 38 | 33 | 3 | 0 | 1 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | MAAAP others(1768): Show |
chr14 | 44957190 | 45079431 |
| a0003 | 0/0 | 1773 | 29 | 0 | 1 | 23 | 3 | 2 | 19 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | MAAAP others(1768): Show |
chr14 | 44957190 | 45079431 |
| a0004 | 0/0 | 1773 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | MAAAP others(1768): Show |
chr14 | 44957190 | 45079431 |
| a0005 | 0/0 | 1773 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | MAAAP others(1768): Show |
chr14 | 44957190 | 45079431 |
| a0006 | 0/0 | 1773 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | MAAAP others(1768): Show |
chr14 | 44957190 | 45079431 |
| a0007 | 0/0 | 1773 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | MAAAP others(1768): Show |
chr14 | 44957190 | 45079431 |
| a0008 | 0/0 | 1773 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | MAAAP others(1768): Show |
chr14 | 44957190 | 45079431 |
| a0009 | 0/0 | 1773 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | MAAAP others(1768): Show |
chr14 | 44957190 | 45079431 |
| a0010 | 0/0 | 1773 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | MAAAP others(1768): Show |
chr14 | 44957190 | 45079431 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 5319 | 94 | 30 | 14 | 32 | 4 | 12 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ATGGC others(5314): Show |
chr14 | 44957190 | 45079431 | ||
| a0001c0006 | 0/0 | 5319 | 3 | 3 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ATGGC others(5314): Show |
chr14 | 44957190 | 45079431 | ||
| a0001c0009 | 0/0 | 5319 | 2 | 0 | 0 | 2 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ATGGC others(5314): Show |
chr14 | 44957190 | 45079431 | ||
| a0001c0014 | 0/0 | 5319 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ATGGC others(5314): Show |
chr14 | 44957190 | 45079431 | ||
| a0002c0003 | 0/0 | 5319 | 21 | 18 | 2 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ATGGC others(5314): Show |
chr14 | 44957190 | 45079431 | ||
| a0002c0004 | 0/0 | 5319 | 15 | 14 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ATGGC others(5314): Show |
chr14 | 44957190 | 45079431 | ||
| a0002c0011 | 0/0 | 5319 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ATGGC others(5314): Show |
chr14 | 44957190 | 45079431 | ||
| a0002c0016 | 0/0 | 5319 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ATGGC others(5314): Show |
chr14 | 44957190 | 45079431 | ||
| a0003c0002 | 0/0 | 5319 | 29 | 0 | 1 | 23 | 3 | 2 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ATGGC others(5314): Show |
chr14 | 44957190 | 45079431 | ||
| a0004c0005 | 0/0 | 5319 | 3 | 3 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ATGGC others(5314): Show |
chr14 | 44957190 | 45079431 | ||
| a0005c0008 | 0/0 | 5319 | 2 | 2 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ATGGC others(5314): Show |
chr14 | 44957190 | 45079431 | ||
| a0006c0007 | 0/0 | 5319 | 2 | 2 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ATGGC others(5314): Show |
chr14 | 44957190 | 45079431 | ||
| a0007c0013 | 0/0 | 5319 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ATGGC others(5314): Show |
chr14 | 44957190 | 45079431 | ||
| a0008c0012 | 0/0 | 5319 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ATGGC others(5314): Show |
chr14 | 44957190 | 45079431 | ||
| a0009c0015 | 0/0 | 5319 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ATGGC others(5314): Show |
chr14 | 44957190 | 45079431 | ||
| a0010c0010 | 0/0 | 5319 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ATGGC others(5314): Show |
chr14 | 44957190 | 45079431 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 6424 | 87 | 25 | 13 | 32 | 4 | 11 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ACGTG others(6419): Show |
chr14 | 44957190 | 45079431 |
| a0001c0001t0002 | 0/0 | 6424 | 4 | 3 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ACGTG others(6419): Show |
chr14 | 44957190 | 45079431 |
| a0001c0001t0004 | 0/0 | 6424 | 2 | 2 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ACGTG others(6419): Show |
chr14 | 44957190 | 45079431 |
| a0001c0001t0007 | 0/0 | 6424 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ACGTG others(6419): Show |
chr14 | 44957190 | 45079431 |
| a0001c0006t0001 | 0/0 | 6424 | 3 | 3 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ACGTG others(6419): Show |
chr14 | 44957190 | 45079431 |
| a0001c0009t0001 | 0/0 | 6424 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ACGTG others(6419): Show |
chr14 | 44957190 | 45079431 |
| a0001c0009t0002 | 0/0 | 6424 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ACGTG others(6419): Show |
chr14 | 44957190 | 45079431 |
| a0001c0014t0001 | 0/0 | 6424 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ACGTG others(6419): Show |
chr14 | 44957190 | 45079431 |
| a0002c0003t0002 | 0/0 | 6424 | 18 | 17 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ACGTG others(6419): Show |
chr14 | 44957190 | 45079431 |
| a0002c0003t0003 | 0/0 | 6424 | 2 | 0 | 1 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ACGTG others(6419): Show |
chr14 | 44957190 | 45079431 |
| a0002c0003t0006 | 0/0 | 6424 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ACGTG others(6419): Show |
chr14 | 44957190 | 45079431 |
| a0002c0004t0001 | 0/0 | 6424 | 15 | 14 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ACGTG others(6419): Show |
chr14 | 44957190 | 45079431 |
| a0002c0011t0001 | 0/0 | 6424 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ACGTG others(6419): Show |
chr14 | 44957190 | 45079431 |
| a0002c0016t0003 | 0/0 | 6424 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ACGTG others(6419): Show |
chr14 | 44957190 | 45079431 |
| a0003c0002t0002 | 0/0 | 6424 | 28 | 0 | 1 | 23 | 3 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ACGTG others(6419): Show |
chr14 | 44957190 | 45079431 |
| a0003c0002t0008 | 0/0 | 6424 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ACGTG others(6419): Show |
chr14 | 44957190 | 45079431 |
| a0004c0005t0002 | 0/0 | 6424 | 3 | 3 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ACGTG others(6419): Show |
chr14 | 44957190 | 45079431 |
| a0005c0008t0002 | 0/0 | 6424 | 2 | 2 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ACGTG others(6419): Show |
chr14 | 44957190 | 45079431 |
| a0006c0007t0001 | 0/0 | 6424 | 2 | 2 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ACGTG others(6419): Show |
chr14 | 44957190 | 45079431 |
| a0007c0013t0005 | 0/0 | 6424 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ACGTG others(6419): Show |
chr14 | 44957190 | 45079431 |
| a0008c0012t0002 | 0/0 | 6424 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ACGTG others(6419): Show |
chr14 | 44957190 | 45079431 |
| a0009c0015t0001 | 0/0 | 6424 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ACGTG others(6419): Show |
chr14 | 44957190 | 45079431 |
| a0010c0010t0002 | 0/0 | 6424 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | ACGTG others(6419): Show |
chr14 | 44957190 | 45079431 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0124 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0157 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0007g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0006t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0006t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0006t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0009t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0009t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0014t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0003g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0006g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0011t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0016t0003g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0008g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0004c0005t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0004c0005t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0004c0005t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0005c0008t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0005c0008t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0006c0007t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0006c0007t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0007c0013t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0008c0012t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0009c0015t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0010c0010t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | FIN | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG00280 | hp2 | a0003 | c0002 | t0002 | g0005 | EUR | FIN | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG00323 | hp1 | a0003 | c0002 | t0002 | g0039 | EUR | FIN | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | FIN | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG00597 | hp2 | a0003 | c0002 | t0002 | g0045 | EAS | CHS | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG00673 | hp2 | a0003 | c0002 | t0002 | g0031 | EAS | CHS | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01106 | hp2 | a0002 | c0003 | t0003 | g0009 | AMR | PUR | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01109 | hp2 | a0002 | c0003 | t0002 | g0053 | AMR | PUR | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01358 | hp1 | a0003 | c0002 | t0002 | g0042 | AMR | CLM | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | CLM | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01496 | hp1 | a0002 | c0004 | t0001 | g0167 | AMR | CLM | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | IBS | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01516 | hp2 | a0002 | c0003 | t0003 | g0008 | EUR | IBS | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01884 | hp2 | a0002 | c0004 | t0001 | g0177 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01891 | hp1 | a0002 | c0003 | t0002 | g0003 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02055 | hp1 | a0005 | c0008 | t0002 | g0012 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02056 | hp1 | a0003 | c0002 | t0002 | g0040 | EAS | KHV | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02132 | hp1 | a0003 | c0002 | t0002 | g0041 | EAS | KHV | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02132 | hp2 | a0007 | c0013 | t0005 | g0001 | EAS | KHV | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02145 | hp2 | a0002 | c0004 | t0001 | g0161 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CDX | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CDX | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02258 | hp1 | a0002 | c0003 | t0002 | g0020 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02280 | hp2 | a0002 | c0004 | t0001 | g0173 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02451 | hp2 | a0004 | c0005 | t0002 | g0058 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02615 | hp1 | a0001 | c0006 | t0001 | g0101 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0084 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02622 | hp1 | a0002 | c0004 | t0001 | g0175 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02630 | hp1 | a0006 | c0007 | t0001 | g0165 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02647 | hp2 | a0002 | c0003 | t0002 | g0057 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02717 | hp1 | a0002 | c0011 | t0001 | g0163 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02717 | hp2 | a0004 | c0005 | t0002 | g0029 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02723 | hp1 | a0002 | c0003 | t0002 | g0049 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02723 | hp2 | a0002 | c0004 | t0001 | g0174 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02809 | hp1 | a0002 | c0004 | t0001 | g0162 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02886 | hp1 | a0008 | c0012 | t0002 | g0019 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02886 | hp2 | a0002 | c0003 | t0002 | g0013 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02896 | hp1 | a0001 | c0006 | t0001 | g0098 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02896 | hp2 | a0002 | c0003 | t0002 | g0055 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02897 | hp1 | a0002 | c0003 | t0002 | g0056 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02965 | hp1 | a0002 | c0003 | t0002 | g0050 | AFR | ESN | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02965 | hp2 | a0002 | c0004 | t0001 | g0171 | AFR | ESN | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02976 | hp1 | a0002 | c0003 | t0006 | g0002 | AFR | ESN | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03017 | hp1 | a0003 | c0002 | t0008 | g0046 | SAS | PJL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03041 | hp2 | a0006 | c0007 | t0001 | g0164 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03098 | hp1 | a0002 | c0003 | t0002 | g0021 | AFR | MSL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03098 | hp2 | a0002 | c0004 | t0001 | g0170 | AFR | MSL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | ESN | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03139 | hp2 | a0002 | c0003 | t0002 | g0052 | AFR | ESN | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03195 | hp1 | a0001 | c0006 | t0001 | g0087 | AFR | ESN | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03195 | hp2 | a0002 | c0004 | t0001 | g0168 | AFR | ESN | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03209 | hp1 | a0002 | c0004 | t0001 | g0169 | AFR | MSL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03225 | hp1 | a0002 | c0004 | t0001 | g0166 | AFR | MSL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03239 | hp1 | a0003 | c0002 | t0002 | g0034 | SAS | PJL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03453 | hp1 | a0002 | c0003 | t0002 | g0014 | AFR | MSL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0137 | AFR | MSL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03516 | hp1 | a0002 | c0004 | t0001 | g0176 | AFR | ESN | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03540 | hp2 | a0002 | c0004 | t0001 | g0172 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03579 | hp1 | a0001 | c0014 | t0001 | g0136 | AFR | MSL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03831 | hp1 | a0001 | c0001 | t0007 | g0125 | SAS | BEB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG04199 | hp1 | a0002 | c0016 | t0003 | g0007 | SAS | STU | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | STU | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG04228 | hp1 | a0009 | c0015 | t0001 | g0086 | SAS | STU | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18906 | hp1 | a0002 | c0003 | t0002 | g0015 | AFR | YRI | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18906 | hp2 | a0010 | c0010 | t0002 | g0010 | AFR | YRI | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18943 | hp1 | a0003 | c0002 | t0002 | g0023 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18952 | hp1 | a0003 | c0002 | t0002 | g0043 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18961 | hp2 | a0003 | c0002 | t0002 | g0032 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18970 | hp2 | a0003 | c0002 | t0002 | g0027 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18979 | hp2 | a0003 | c0002 | t0002 | g0037 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18982 | hp2 | a0003 | c0002 | t0002 | g0048 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18984 | hp2 | a0003 | c0002 | t0002 | g0025 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18985 | hp2 | a0003 | c0002 | t0002 | g0006 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18988 | hp1 | a0003 | c0002 | t0002 | g0011 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18990 | hp1 | a0001 | c0009 | t0001 | g0135 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18991 | hp2 | a0003 | c0002 | t0002 | g0044 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18993 | hp1 | a0003 | c0002 | t0002 | g0024 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18999 | hp2 | a0003 | c0002 | t0002 | g0033 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19007 | hp2 | a0003 | c0002 | t0002 | g0038 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19011 | hp2 | a0003 | c0002 | t0002 | g0047 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | LWK | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19030 | hp2 | a0002 | c0004 | t0001 | g0178 | AFR | LWK | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19043 | hp1 | a0005 | c0008 | t0002 | g0017 | AFR | LWK | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | LWK | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19058 | hp1 | a0003 | c0002 | t0002 | g0028 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19063 | hp1 | a0001 | c0009 | t0002 | g0145 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19066 | hp2 | a0003 | c0002 | t0002 | g0035 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19072 | hp1 | a0003 | c0002 | t0002 | g0059 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19086 | hp2 | a0003 | c0002 | t0002 | g0030 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19091 | hp2 | a0003 | c0002 | t0002 | g0026 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19240 | hp1 | a0002 | c0003 | t0002 | g0054 | AFR | YRI | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19240 | hp2 | a0004 | c0005 | t0002 | g0004 | AFR | YRI | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA20805 | hp1 | a0003 | c0002 | t0002 | g0036 | EUR | TSI | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | TSI | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02109 | hp1 | a0002 | c0003 | t0002 | g0018 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02486 | hp2 | a0002 | c0003 | t0002 | g0051 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02559 | hp2 | a0002 | c0003 | t0002 | g0022 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | MSL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | USA | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG06807 | hp2 | a0002 | c0003 | t0002 | g0016 | AFR | USA | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0124 | REF | REF | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0157 | REF | REF | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:44963535 | G | A | 1 | a0010 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.1114G>A | p.Val372Ile | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/20 | 1346/6424 | 1114/5322 | 372/1773 | chr14 | 44963535 | |||
| chr14:44963667 | G | C | 8 | a0002 a0003 a0004 others(5): Show |
77 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(74): Show |
missense_variant | MODERATE | c.1246G>C | p.Glu416Gln | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/20 | 1478/6424 | 1246/5322 | 416/1773 | chr14 | 44963667 | |||
| chr14:44963952 | C | G | 1 | a0003 | 29 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(26): Show |
missense_variant | MODERATE | c.1531C>G | p.Leu511Val | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/20 | 1763/6424 | 1531/5322 | 511/1773 | chr14 | 44963952 | |||
| chr14:45004316 | A | C | 1 | a0009 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.2594A>C | p.Gln865Pro | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/20 | 2826/6424 | 2594/5322 | 865/1773 | chr14 | 45004316 | |||
| chr14:45006126 | C | A | 1 | a0004 | 3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
missense_variant | MODERATE | c.2763C>A | p.Ser921Arg | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/20 | 2995/6424 | 2763/5322 | 921/1773 | chr14 | 45006126 | |||
| chr14:45027436 | A | G | 1 | a0008 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.3466A>G | p.Asn1156Asp | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 9/20 | 3698/6424 | 3466/5322 | 1156/1773 | chr14 | 45027436 | |||
| chr14:45046580 | A | G | 1 | a0006 | 2 | HG02630.hp1 HG03041.hp2 |
missense_variant | MODERATE | c.4190A>G | p.Gln1397Arg | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/20 | 4422/6424 | 4190/5322 | 1397/1773 | chr14 | 45046580 | |||
| chr14:45046600 | G | A | 1 | a0007 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.4210G>A | p.Glu1404Lys | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/20 | 4442/6424 | 4210/5322 | 1404/1773 | chr14 | 45046600 | |||
| chr14:45054438 | G | T | 1 | a0005 | 2 | HG02055.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.4448G>T | p.Gly1483Val | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/20 | 4680/6424 | 4448/5322 | 1483/1773 | chr14 | 45054438 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:44963123 | A | G | 1 | a0002c0016 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.702A>G | p.Thr234Thr | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/20 | 934/6424 | 702/5322 | 234/1773 | chr14 | 44963123 | |||
| chr14:44963675 | G | T | 1 | a0007c0013 | 1 | HG02132.hp2 | synonymous_variant | LOW | c.1254G>T | p.Leu418Leu | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/20 | 1486/6424 | 1254/5322 | 418/1773 | chr14 | 44963675 | |||
| chr14:44964053 | T | C | 1 | a0001c0006 | 3 | HG02615.hp1 HG02896.hp1 HG03195.hp1 |
synonymous_variant | LOW | c.1632T>C | p.Gly544Gly | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/20 | 1864/6424 | 1632/5322 | 544/1773 | chr14 | 44964053 | |||
| chr14:45004062 | G | A | 3 | a0002c0004 a0002c0011 a0006c0007 |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
splice_region_variant&synonymous_variant | LOW | c.2340G>A | p.Val780Val | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/20 | 2572/6424 | 2340/5322 | 780/1773 | chr14 | 45004062 | |||
| chr14:45006255 | G | A | 1 | a0002c0011 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.2892G>A | p.Leu964Leu | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/20 | 3124/6424 | 2892/5322 | 964/1773 | chr14 | 45006255 | |||
| chr14:45032341 | G | A | 1 | a0001c0014 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.3777G>A | p.Leu1259Leu | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/20 | 4009/6424 | 3777/5322 | 1259/1773 | chr14 | 45032341 | |||
| chr14:45046635 | A | G | 2 | a0001c0009 a0003c0002 |
31 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(28): Show |
synonymous_variant | LOW | c.4245A>G | p.Ala1415Ala | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/20 | 4477/6424 | 4245/5322 | 1415/1773 | chr14 | 45046635 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:44962225 | G | A | 1 | a0001c0001t0004 | 2 | HG02615.hp2 HG03453.hp2 |
5_prime_UTR_variant | MODIFIER | c.-197G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/20 | 197 | chr14 | 44962225 | ||||||
| chr14:44962284 | G | A | 1 | a0007c0013t0005 | 1 | HG02132.hp2 | 5_prime_UTR_variant | MODIFIER | c.-138G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/20 | 138 | chr14 | 44962284 | ||||||
| chr14:44962370 | C | A | 2 | a0002c0003t0003 a0002c0016t0003 |
3 | HG01106.hp2 HG01516.hp2 HG04199.hp1 |
5_prime_UTR_variant | MODIFIER | c.-52C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/20 | 52 | chr14 | 44962370 | ||||||
| chr14:44962409 | C | T | 1 | a0003c0002t0008 | 1 | HG03017.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-13C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/20 | chr14 | 44962409 | |||||||
| chr14:45073835 | T | C | 12 | a0001c0001t0002 a0001c0009t0002 a0002c0003t0002 others(9): Show |
63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*274T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 20/20 | 274 | chr14 | 45073835 | ||||||
| chr14:45073843 | A | G | 1 | a0001c0001t0007 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*282A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 20/20 | 282 | chr14 | 45073843 | ||||||
| chr14:45073962 | G | A | 1 | a0002c0003t0006 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*401G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 20/20 | 401 | chr14 | 45073962 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:44964494 | G | A | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2046+27G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44964494 | |||||||
| chr14:44964651 | G | A | 58 | a0002c0003t0002g0003 a0002c0003t0002g0013 a0002c0003t0002g0014 others(55): Show |
58 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.2046+184G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44964651 | |||||||
| chr14:44964687 | CAT | C | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2046+221_2046+222d others(4): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44964687 | |||||||
| chr14:44964831 | G | C | 2 | a0002c0003t0002g0003 a0002c0003t0006g0002 |
2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2046+364G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44964831 | |||||||
| chr14:44964851 | C | CTGGGAAT others(35): Show |
1 | a0001c0001t0001g0160 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2046+385_2046+426d others(44): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44964851 | ||||||
| chr14:44964951 | T | TA | 144 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0071 others(141): Show |
144 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.2046+506dupA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44964951 | ||||||
| chr14:44964951 | T | TAA | 9 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(6): Show |
9 | HG00280.hp2 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2046+505_2046+506d others(4): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44964951 | ||||||
| chr14:44965023 | T | C | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2046+556T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44965023 | |||||||
| chr14:44965036 | T | A | 4 | a0002c0003t0003g0008 a0002c0003t0003g0009 a0002c0016t0003g0007 others(1): Show |
4 | HG01106.hp2 HG01516.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.2046+569T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44965036 | |||||||
| chr14:44965494 | G | T | 3 | a0002c0003t0002g0050 a0002c0003t0002g0051 a0002c0003t0002g0052 |
3 | HG02486.hp2 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2046+1027G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44965494 | |||||||
| chr14:44965562 | A | G | 1 | a0002c0003t0002g0049 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2046+1095A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44965562 | |||||||
| chr14:44965825 | T | G | 3 | a0002c0003t0002g0050 a0002c0003t0002g0051 a0002c0003t0002g0052 |
3 | HG02486.hp2 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2046+1358T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44965825 | |||||||
| chr14:44965828 | T | C | 1 | a0003c0002t0002g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2046+1361T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44965828 | |||||||
| chr14:44965855 | G | A | 26 | a0002c0003t0002g0003 a0002c0003t0002g0013 a0002c0003t0002g0014 others(23): Show |
26 | HG01106.hp2 HG01109.hp2 HG01516.hp2 others(23): Show |
intron_variant | MODIFIER | c.2046+1388G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44965855 | |||||||
| chr14:44965869 | A | AT | 33 | a0001c0001t0001g0064 a0001c0001t0001g0141 a0001c0001t0001g0142 others(30): Show |
33 | HG00323.hp2 HG01106.hp2 HG01516.hp2 others(30): Show |
intron_variant | MODIFIER | c.2046+1425dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44965869 | ||||||
| chr14:44965869 | A | ATT | 33 | a0001c0009t0002g0145 a0002c0003t0002g0020 a0002c0003t0002g0021 others(30): Show |
33 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2046+1424_2046+142 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44965869 | ||||||
| chr14:44965873 | T | A | 1 | a0001c0001t0001g0065 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2046+1406T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44965873 | |||||||
| chr14:44965935 | C | T | 15 | a0002c0003t0002g0018 a0002c0003t0002g0020 a0002c0003t0002g0021 others(12): Show |
15 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.2046+1468C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44965935 | |||||||
| chr14:44965988 | C | T | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2046+1521C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44965988 | |||||||
| chr14:44966253 | C | A | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2046+1786C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44966253 | |||||||
| chr14:44966262 | A | G | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | NA18968.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2046+1795A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44966262 | |||||||
| chr14:44966302 | G | A | 2 | a0001c0001t0001g0066 a0002c0003t0006g0002 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2046+1835G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44966302 | |||||||
| chr14:44966353 | AT | A | 4 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(1): Show |
4 | HG01358.hp2 HG01884.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2046+1887delT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44966353 | |||||||
| chr14:44966466 | G | C | 78 | a0001c0009t0002g0145 a0002c0003t0002g0003 a0002c0003t0002g0013 others(75): Show |
78 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.2046+1999G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44966466 | |||||||
| chr14:44966763 | G | T | 1 | a0001c0001t0001g0138 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2046+2296G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44966763 | |||||||
| chr14:44966937 | A | AAC | 78 | a0001c0009t0002g0145 a0002c0003t0002g0003 a0002c0003t0002g0013 others(75): Show |
78 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.2046+2471_2046+247 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44966937 | ||||||
| chr14:44967077 | G | T | 1 | a0010c0010t0002g0010 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2046+2610G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44967077 | |||||||
| chr14:44967121 | A | G | 2 | a0004c0005t0002g0004 a0004c0005t0002g0029 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2046+2654A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44967121 | |||||||
| chr14:44967481 | A | C | 1 | a0001c0001t0004g0137 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2046+3014A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44967481 | |||||||
| chr14:44967841 | G | A | 1 | a0003c0002t0002g0030 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2046+3374G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44967841 | |||||||
| chr14:44967925 | A | AT | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2046+3466dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44967925 | ||||||
| chr14:44968503 | C | T | 3 | a0003c0002t0002g0006 a0003c0002t0002g0047 a0003c0002t0002g0048 |
3 | NA18982.hp2 NA18985.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.2046+4036C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44968503 | |||||||
| chr14:44968622 | C | G | 1 | a0001c0014t0001g0136 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2046+4155C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44968622 | |||||||
| chr14:44968740 | G | T | 23 | a0002c0003t0002g0003 a0002c0003t0002g0013 a0002c0003t0002g0014 others(20): Show |
23 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.2046+4273G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44968740 | |||||||
| chr14:44969110 | T | TTTCC | 9 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(6): Show |
9 | HG02647.hp2 HG02683.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.2046+4678_2046+468 others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969110 | ||||||
| chr14:44969110 | T | TTTCCTTC others(1): Show |
14 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0141 others(11): Show |
14 | HG01109.hp2 HG01516.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.2046+4674_2046+468 others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969110 | ||||||
| chr14:44969110 | T | TTTCCTTC others(5): Show |
13 | a0002c0003t0002g0020 a0002c0004t0001g0166 a0002c0004t0001g0167 others(10): Show |
13 | HG01496.hp1 HG01884.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.2046+4670_2046+468 others(16): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969110 | ||||||
| chr14:44969110 | T | TTTCCTTC others(13): Show |
1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2046+4662_2046+468 others(24): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969110 | ||||||
| chr14:44969110 | TTTCC | T | 10 | a0001c0001t0001g0063 a0001c0001t0001g0066 a0001c0001t0001g0128 others(7): Show |
10 | HG01071.hp1 HG01109.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.2046+4678_2046+468 others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969110 | ||||||
| chr14:44969110 | TTTCCTTC others(5): Show |
T | 1 | a0001c0009t0001g0135 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2046+4670_2046+468 others(16): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969110 | ||||||
| chr14:44969134 | C | CTTCCTTC others(1): Show |
2 | a0002c0003t0002g0051 a0002c0003t0002g0052 |
2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2046+4674_2046+467 others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969134 | ||||||
| chr14:44969141 | C | CCTTT | 32 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(29): Show |
32 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.2046+4677_2046+467 others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969141 | ||||||
| chr14:44969141 | C | T | 1 | a0003c0002t0008g0046 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2046+4674C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44969141 | |||||||
| chr14:44969145 | C | CCTTCCTT others(29): Show |
1 | a0002c0016t0003g0007 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2046+4681_2046+468 others(40): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969145 | ||||||
| chr14:44969145 | C | CCTTCCTT others(17): Show |
3 | a0002c0003t0003g0008 a0002c0003t0003g0009 a0010c0010t0002g0010 |
3 | HG01106.hp2 HG01516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2046+4681_2046+468 others(28): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969145 | ||||||
| chr14:44969145 | C | CCTTCCTT others(9): Show |
2 | a0002c0003t0002g0003 a0002c0003t0006g0002 |
2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2046+4681_2046+468 others(20): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969145 | ||||||
| chr14:44969145 | C | T | 33 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(30): Show |
33 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2046+4678C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44969145 | |||||||
| chr14:44969146 | C | CTTCCTTC others(26): Show |
2 | a0002c0003t0002g0013 a0002c0003t0002g0014 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2046+4681_2046+468 others(37): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969146 | ||||||
| chr14:44969146 | C | CTTCCTTC others(22): Show |
1 | a0002c0003t0002g0015 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2046+4681_2046+468 others(33): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969146 | ||||||
| chr14:44969146 | C | CTTCCTTC others(18): Show |
2 | a0002c0003t0002g0016 a0002c0003t0002g0049 |
2 | HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2046+4681_2046+468 others(29): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969146 | ||||||
| chr14:44969149 | T | C | 34 | a0001c0001t0001g0077 a0002c0003t0002g0018 a0002c0003t0002g0020 others(31): Show |
34 | HG00673.hp1 HG01109.hp2 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.2046+4682T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44969149 | |||||||
| chr14:44969150 | C | CTTCCTTC others(26): Show |
1 | a0005c0008t0002g0012 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2046+4685_2046+468 others(37): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969150 | ||||||
| chr14:44969150 | C | CTTCCTTC others(22): Show |
3 | a0002c0004t0001g0162 a0005c0008t0002g0017 a0008c0012t0002g0019 |
3 | HG02809.hp1 HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2046+4685_2046+468 others(33): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969150 | ||||||
| chr14:44969150 | C | CTTCCTTC others(18): Show |
1 | a0002c0004t0001g0161 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2046+4685_2046+468 others(29): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969150 | ||||||
| chr14:44969150 | C | T | 5 | a0002c0003t0002g0013 a0002c0003t0002g0014 a0002c0003t0002g0015 others(2): Show |
5 | HG02723.hp1 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2046+4683C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44969150 | |||||||
| chr14:44969172 | CT | C | 11 | a0002c0003t0002g0013 a0002c0003t0002g0014 a0002c0003t0002g0015 others(8): Show |
11 | HG02055.hp1 HG02145.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.2046+4718delT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969172 | ||||||
| chr14:44969173 | T | TTTCTTTT others(1): Show |
66 | a0001c0009t0002g0145 a0002c0003t0002g0003 a0002c0003t0002g0018 others(63): Show |
66 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.2046+4708_2046+470 others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969173 | ||||||
| chr14:44969176 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2046+4709T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44969176 | |||||||
| chr14:44969178 | T | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2046+4711T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44969178 | |||||||
| chr14:44969215 | G | A | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2046+4748G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44969215 | |||||||
| chr14:44969303 | C | T | 2 | a0002c0003t0002g0051 a0002c0003t0002g0052 |
2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2046+4836C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44969303 | |||||||
| chr14:44969325 | G | C | 1 | a0001c0001t0001g0071 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2046+4858G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44969325 | |||||||
| chr14:44969381 | G | A | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2046+4914G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44969381 | |||||||
| chr14:44969742 | T | C | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG02056.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.2046+5275T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44969742 | |||||||
| chr14:44970171 | A | G | 2 | a0004c0005t0002g0004 a0004c0005t0002g0029 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2046+5704A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44970171 | |||||||
| chr14:44970313 | T | A | 3 | a0001c0001t0001g0064 a0001c0001t0001g0082 a0001c0001t0001g0083 |
3 | HG02145.hp1 HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2046+5846T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44970313 | |||||||
| chr14:44970321 | A | C | 34 | a0001c0009t0002g0145 a0002c0003t0002g0050 a0003c0002t0002g0005 others(31): Show |
34 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.2046+5854A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44970321 | |||||||
| chr14:44970466 | T | G | 1 | a0001c0001t0004g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2046+5999T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44970466 | |||||||
| chr14:44970679 | T | C | 1 | a0002c0011t0001g0163 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2046+6212T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44970679 | |||||||
| chr14:44970820 | T | A | 1 | a0001c0001t0001g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2046+6353T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44970820 | |||||||
| chr14:44970982 | T | C | 6 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0085 others(3): Show |
6 | HG02451.hp1 HG02559.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2046+6515T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44970982 | |||||||
| chr14:44971101 | T | C | 1 | a0005c0008t0002g0017 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2046+6634T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44971101 | |||||||
| chr14:44971105 | A | G | 12 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0080 others(9): Show |
12 | HG01074.hp2 HG01257.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.2046+6638A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44971105 | |||||||
| chr14:44971286 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2046+6819T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44971286 | |||||||
| chr14:44971582 | G | T | 1 | a0001c0001t0001g0119 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2046+7115G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44971582 | |||||||
| chr14:44971614 | T | C | 78 | a0001c0009t0002g0145 a0002c0003t0002g0003 a0002c0003t0002g0013 others(75): Show |
78 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.2046+7147T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44971614 | |||||||
| chr14:44971669 | A | G | 2 | a0002c0003t0002g0051 a0002c0003t0002g0052 |
2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2046+7202A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44971669 | |||||||
| chr14:44971722 | C | A | 12 | a0002c0003t0002g0018 a0002c0003t0002g0020 a0002c0003t0002g0021 others(9): Show |
12 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2046+7255C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44971722 | |||||||
| chr14:44972067 | T | G | 77 | a0001c0009t0002g0145 a0002c0003t0002g0003 a0002c0003t0002g0013 others(74): Show |
77 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.2046+7600T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44972067 | |||||||
| chr14:44972276 | T | G | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2046+7809T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44972276 | |||||||
| chr14:44972332 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2046+7865A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44972332 | |||||||
| chr14:44972338 | G | A | 1 | a0001c0006t0001g0087 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2046+7871G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44972338 | |||||||
| chr14:44972371 | A | G | 2 | a0002c0003t0002g0051 a0002c0003t0002g0052 |
2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2046+7904A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44972371 | |||||||
| chr14:44972415 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2046+7948G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44972415 | |||||||
| chr14:44972546 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2046+8079A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44972546 | |||||||
| chr14:44972631 | C | A | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2046+8164C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44972631 | |||||||
| chr14:44972729 | A | G | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2046+8262A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44972729 | |||||||
| chr14:44972784 | A | G | 3 | a0004c0005t0002g0004 a0004c0005t0002g0029 a0004c0005t0002g0058 |
3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2046+8317A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44972784 | |||||||
| chr14:44972799 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2046+8332A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44972799 | |||||||
| chr14:44972910 | G | T | 4 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(1): Show |
4 | HG01358.hp2 HG01884.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2046+8443G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44972910 | |||||||
| chr14:44973037 | A | ATC | 78 | a0001c0009t0002g0145 a0002c0003t0002g0003 a0002c0003t0002g0013 others(75): Show |
78 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.2046+8572_2046+857 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44973037 | ||||||
| chr14:44973225 | A | C | 1 | a0002c0004t0001g0161 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2046+8758A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44973225 | |||||||
| chr14:44973241 | C | CT | 14 | a0002c0004t0001g0161 a0002c0004t0001g0166 a0002c0004t0001g0167 others(11): Show |
14 | HG01496.hp1 HG02145.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.2046+8783dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44973241 | ||||||
| chr14:44973241 | C | G | 1 | a0001c0001t0001g0077 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2046+8774C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44973241 | |||||||
| chr14:44973394 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2046+8927C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44973394 | |||||||
| chr14:44973538 | G | GT | 65 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(62): Show |
65 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.2046+9081dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44973538 | ||||||
| chr14:44973578 | TTC | T | 59 | a0001c0009t0002g0145 a0002c0003t0002g0003 a0002c0003t0002g0013 others(56): Show |
59 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2046+9129_2046+913 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44973578 | ||||||
| chr14:44973590 | C | A | 26 | a0003c0002t0002g0005 a0003c0002t0002g0006 a0003c0002t0002g0023 others(23): Show |
26 | HG00280.hp2 HG00323.hp1 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.2046+9123C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44973590 | |||||||
| chr14:44973592 | C | A | 45 | a0001c0009t0002g0145 a0002c0003t0002g0018 a0002c0003t0002g0020 others(42): Show |
45 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.2046+9125C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44973592 | |||||||
| chr14:44973592 | C | CTA | 3 | a0002c0004t0001g0161 a0002c0004t0001g0177 a0002c0004t0001g0178 |
3 | HG01884.hp2 HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2046+9126_2046+912 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44973592 | ||||||
| chr14:44973594 | C | A | 62 | a0001c0001t0001g0089 a0001c0009t0002g0145 a0002c0003t0002g0003 others(59): Show |
62 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.2046+9127C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44973594 | |||||||
| chr14:44973594 | C | CTA | 15 | a0002c0004t0001g0162 a0002c0004t0001g0166 a0002c0004t0001g0167 others(12): Show |
15 | HG01496.hp1 HG02280.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.2046+9128_2046+912 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44973594 | ||||||
| chr14:44973596 | C | A | 82 | a0001c0001t0001g0064 a0001c0001t0001g0082 a0001c0001t0001g0083 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2046+9129C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44973596 | |||||||
| chr14:44973618 | C | T | 59 | a0001c0009t0002g0145 a0002c0003t0002g0003 a0002c0003t0002g0013 others(56): Show |
59 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2046+9151C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44973618 | |||||||
| chr14:44973788 | T | C | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2046+9321T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44973788 | |||||||
| chr14:44974102 | C | G | 4 | a0003c0002t0002g0025 a0003c0002t0002g0026 a0003c0002t0002g0027 others(1): Show |
4 | NA18970.hp2 NA18984.hp2 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.2046+9635C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44974102 | |||||||
| chr14:44974156 | G | C | 78 | a0001c0009t0002g0145 a0002c0003t0002g0003 a0002c0003t0002g0013 others(75): Show |
78 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.2046+9689G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44974156 | |||||||
| chr14:44974333 | G | T | 22 | a0002c0003t0002g0003 a0002c0003t0002g0013 a0002c0003t0002g0014 others(19): Show |
22 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.2046+9866G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44974333 | |||||||
| chr14:44974624 | A | G | 78 | a0001c0009t0002g0145 a0002c0003t0002g0003 a0002c0003t0002g0013 others(75): Show |
78 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.2046+10157A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44974624 | |||||||
| chr14:44974652 | G | A | 31 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(28): Show |
31 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.2046+10185G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44974652 | |||||||
| chr14:44974687 | C | T | 1 | a0002c0003t0002g0050 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2046+10220C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44974687 | |||||||
| chr14:44974688 | G | A | 3 | a0002c0003t0003g0008 a0002c0003t0003g0009 a0002c0016t0003g0007 |
3 | HG01106.hp2 HG01516.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2046+10221G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44974688 | |||||||
| chr14:44974710 | A | G | 59 | a0001c0009t0002g0145 a0002c0003t0002g0003 a0002c0003t0002g0013 others(56): Show |
59 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2046+10243A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44974710 | |||||||
| chr14:44975014 | T | A | 1 | a0001c0001t0001g0146 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2046+10547T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44975014 | |||||||
| chr14:44975054 | C | A | 2 | a0003c0002t0002g0031 a0003c0002t0002g0032 |
2 | HG00673.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.2046+10587C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44975054 | |||||||
| chr14:44975180 | G | C | 77 | a0001c0009t0002g0145 a0002c0003t0002g0003 a0002c0003t0002g0013 others(74): Show |
77 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.2046+10713G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44975180 | |||||||
| chr14:44975184 | C | G | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG01071.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.2046+10717C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44975184 | |||||||
| chr14:44975216 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2046+10749A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44975216 | |||||||
| chr14:44975256 | G | C | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2046+10789G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44975256 | |||||||
| chr14:44975284 | A | C | 12 | a0002c0003t0002g0018 a0002c0003t0002g0020 a0002c0003t0002g0021 others(9): Show |
12 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2046+10817A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44975284 | |||||||
| chr14:44975345 | T | G | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG01257.hp2 HG01943.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.2046+10878T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44975345 | |||||||
| chr14:44975554 | T | C | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2046+11087T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44975554 | |||||||
| chr14:44975844 | C | T | 1 | a0001c0009t0001g0135 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2046+11377C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44975844 | |||||||
| chr14:44976105 | G | C | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2046+11638G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44976105 | |||||||
| chr14:44976252 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2046+11785A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44976252 | |||||||
| chr14:44976265 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2046+11798C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44976265 | |||||||
| chr14:44976644 | AC | A | 2 | a0002c0003t0002g0003 a0002c0003t0006g0002 |
2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2046+12178delC | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44976644 | |||||||
| chr14:44976646 | T | A | 2 | a0002c0003t0002g0003 a0002c0003t0006g0002 |
2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2046+12179T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44976646 | |||||||
| chr14:44976647 | CTT | C | 57 | a0001c0009t0002g0145 a0002c0003t0002g0013 a0002c0003t0002g0014 others(54): Show |
57 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.2046+12181_2046+12 others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44976647 | |||||||
| chr14:44976649 | T | C | 2 | a0002c0003t0002g0003 a0002c0003t0006g0002 |
2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2046+12182T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44976649 | |||||||
| chr14:44977110 | A | G | 1 | a0010c0010t0002g0010 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2046+12643A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44977110 | |||||||
| chr14:44977157 | A | T | 31 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(28): Show |
31 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.2046+12690A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44977157 | |||||||
| chr14:44977228 | A | T | 78 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(75): Show |
78 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.2046+12761A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44977228 | |||||||
| chr14:44977231 | C | CT | 50 | a0001c0001t0001g0088 a0001c0001t0001g0115 a0001c0001t0001g0134 others(47): Show |
50 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2046+12785dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44977231 | ||||||
| chr14:44977231 | C | CTT | 15 | a0002c0003t0002g0003 a0002c0003t0002g0018 a0002c0003t0002g0020 others(12): Show |
15 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2046+12784_2046+12 others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44977231 | ||||||
| chr14:44977231 | CT | C | 14 | a0001c0001t0001g0060 a0002c0004t0001g0161 a0002c0004t0001g0162 others(11): Show |
14 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.2046+12785delT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44977231 | ||||||
| chr14:44977472 | A | G | 4 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(1): Show |
4 | HG01358.hp2 HG01884.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2046+13005A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44977472 | |||||||
| chr14:44977568 | C | T | 81 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(78): Show |
81 | HG00323.hp1 HG00597.hp2 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.2046+13101C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44977568 | |||||||
| chr14:44977595 | A | T | 12 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 others(9): Show |
12 | HG01884.hp1 HG01891.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.2046+13128A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44977595 | |||||||
| chr14:44977984 | C | T | 62 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(59): Show |
62 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.2046+13517C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44977984 | |||||||
| chr14:44978051 | A | G | 28 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(25): Show |
28 | HG01109.hp2 HG01358.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.2046+13584A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44978051 | |||||||
| chr14:44978504 | G | C | 32 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(29): Show |
32 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.2046+14037G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44978504 | |||||||
| chr14:44978556 | A | G | 81 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(78): Show |
81 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.2046+14089A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44978556 | |||||||
| chr14:44978578 | A | G | 82 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2046+14111A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44978578 | |||||||
| chr14:44978695 | G | A | 1 | a0002c0003t0002g0050 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2046+14228G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44978695 | |||||||
| chr14:44979032 | A | T | 12 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0080 others(9): Show |
12 | HG01074.hp2 HG01257.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.2046+14565A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44979032 | |||||||
| chr14:44979172 | T | TTAA | 63 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(60): Show |
63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2046+14723_2046+14 others(9): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44979172 | ||||||
| chr14:44979195 | G | A | 81 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(78): Show |
81 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.2046+14728G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44979195 | |||||||
| chr14:44979361 | A | G | 82 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2046+14894A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44979361 | |||||||
| chr14:44979469 | A | C | 1 | a0001c0001t0001g0158 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2046+15002A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44979469 | |||||||
| chr14:44980095 | A | G | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2046+15628A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44980095 | |||||||
| chr14:44980174 | G | A | 4 | a0002c0003t0003g0008 a0002c0003t0003g0009 a0002c0016t0003g0007 others(1): Show |
4 | HG01106.hp2 HG01516.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.2047-15572G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44980174 | |||||||
| chr14:44980252 | T | A | 29 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(26): Show |
29 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.2047-15494T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44980252 | |||||||
| chr14:44980393 | C | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | NA18968.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2047-15353C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44980393 | |||||||
| chr14:44980394 | G | A | 2 | a0002c0004t0001g0177 a0002c0004t0001g0178 |
2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2047-15352G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44980394 | |||||||
| chr14:44980840 | G | T | 1 | a0003c0002t0002g0032 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2047-14906G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44980840 | |||||||
| chr14:44981319 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2047-14427G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44981319 | |||||||
| chr14:44981427 | G | T | 13 | a0002c0004t0001g0166 a0002c0004t0001g0167 a0002c0004t0001g0168 others(10): Show |
13 | HG01496.hp1 HG02280.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.2047-14319G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44981427 | |||||||
| chr14:44981445 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2047-14301A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44981445 | |||||||
| chr14:44981652 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2047-14094A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44981652 | |||||||
| chr14:44981816 | G | A | 82 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2047-13930G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44981816 | |||||||
| chr14:44981841 | CT | C | 133 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(130): Show |
133 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.2047-13885delT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44981841 | ||||||
| chr14:44981905 | G | A | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2047-13841G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44981905 | |||||||
| chr14:44982027 | G | C | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2047-13719G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44982027 | |||||||
| chr14:44982128 | G | A | 2 | a0005c0008t0002g0012 a0005c0008t0002g0017 |
2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2047-13618G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44982128 | |||||||
| chr14:44982308 | G | A | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2047-13438G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44982308 | |||||||
| chr14:44982394 | G | T | 1 | a0001c0001t0001g0122 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2047-13352G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44982394 | |||||||
| chr14:44982543 | C | T | 1 | a0002c0003t0002g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2047-13203C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44982543 | |||||||
| chr14:44982565 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2047-13181G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44982565 | |||||||
| chr14:44982834 | A | G | 30 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(27): Show |
30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.2047-12912A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44982834 | |||||||
| chr14:44983232 | A | G | 1 | a0001c0001t0001g0149 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2047-12514A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44983232 | |||||||
| chr14:44983344 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2047-12402C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44983344 | |||||||
| chr14:44983499 | A | G | 84 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(81): Show |
84 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.2047-12247A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44983499 | |||||||
| chr14:44983897 | C | T | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2047-11849C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44983897 | |||||||
| chr14:44983899 | A | G | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2047-11847A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44983899 | |||||||
| chr14:44984134 | G | A | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2047-11612G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44984134 | |||||||
| chr14:44984140 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2047-11606T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44984140 | |||||||
| chr14:44984238 | C | T | 30 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(27): Show |
30 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.2047-11508C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44984238 | |||||||
| chr14:44984698 | C | T | 4 | a0001c0001t0001g0062 a0001c0001t0001g0109 a0001c0001t0001g0110 others(1): Show |
4 | HG02258.hp2 HG02897.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2047-11048C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44984698 | |||||||
| chr14:44984714 | G | A | 1 | a0002c0003t0002g0050 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2047-11032G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44984714 | |||||||
| chr14:44984848 | A | C | 1 | a0001c0001t0001g0108 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2047-10898A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44984848 | |||||||
| chr14:44985063 | G | C | 2 | a0001c0001t0004g0084 a0001c0001t0004g0137 |
2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2047-10683G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44985063 | |||||||
| chr14:44985456 | G | T | 1 | a0001c0001t0001g0107 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2047-10290G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44985456 | |||||||
| chr14:44985492 | C | G | 1 | a0001c0001t0001g0106 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2047-10254C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44985492 | |||||||
| chr14:44985560 | T | C | 2 | a0001c0001t0001g0091 a0001c0001t0001g0149 |
2 | HG02165.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.2047-10186T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44985560 | |||||||
| chr14:44985568 | G | T | 4 | a0002c0003t0003g0008 a0002c0003t0003g0009 a0002c0016t0003g0007 others(1): Show |
4 | HG01106.hp2 HG01516.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.2047-10178G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44985568 | |||||||
| chr14:44985622 | G | T | 1 | a0002c0003t0003g0009 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2047-10124G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44985622 | |||||||
| chr14:44985657 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2047-10089C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44985657 | |||||||
| chr14:44985660 | T | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG01257.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.2047-10086T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44985660 | |||||||
| chr14:44985689 | A | C | 26 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(23): Show |
26 | HG01109.hp2 HG01358.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.2047-10057A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44985689 | |||||||
| chr14:44985869 | A | G | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2047-9877A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44985869 | |||||||
| chr14:44985971 | A | G | 1 | a0002c0003t0002g0014 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2047-9775A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44985971 | |||||||
| chr14:44986130 | T | G | 1 | a0001c0001t0001g0129 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2047-9616T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44986130 | |||||||
| chr14:44986295 | T | G | 1 | a0003c0002t0002g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2047-9451T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44986295 | |||||||
| chr14:44986637 | C | A | 1 | a0002c0003t0002g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2047-9109C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44986637 | |||||||
| chr14:44986718 | C | G | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2047-9028C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44986718 | |||||||
| chr14:44986890 | T | C | 12 | a0002c0004t0001g0166 a0002c0004t0001g0167 a0002c0004t0001g0168 others(9): Show |
12 | HG01496.hp1 HG02280.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.2047-8856T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44986890 | |||||||
| chr14:44986965 | A | G | 3 | a0003c0002t0002g0006 a0003c0002t0002g0047 a0003c0002t0002g0048 |
3 | NA18982.hp2 NA18985.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.2047-8781A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44986965 | |||||||
| chr14:44986984 | G | A | 4 | a0002c0003t0003g0008 a0002c0003t0003g0009 a0002c0016t0003g0007 others(1): Show |
4 | HG01106.hp2 HG01516.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.2047-8762G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44986984 | |||||||
| chr14:44986991 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0146 |
2 | HG02683.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2047-8755C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44986991 | |||||||
| chr14:44987093 | C | T | 20 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(17): Show |
20 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.2047-8653C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44987093 | |||||||
| chr14:44987133 | G | A | 1 | a0002c0003t0006g0002 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2047-8613G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44987133 | |||||||
| chr14:44987313 | A | G | 1 | a0003c0002t0002g0024 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2047-8433A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44987313 | |||||||
| chr14:44987343 | T | C | 1 | a0003c0002t0002g0035 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2047-8403T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44987343 | |||||||
| chr14:44987433 | C | G | 12 | a0002c0003t0002g0018 a0002c0003t0002g0020 a0002c0003t0002g0021 others(9): Show |
12 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2047-8313C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44987433 | |||||||
| chr14:44987447 | A | C | 2 | a0002c0004t0001g0170 a0002c0004t0001g0176 |
2 | HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2047-8299A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44987447 | |||||||
| chr14:44987768 | G | T | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2047-7978G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44987768 | |||||||
| chr14:44987960 | A | T | 2 | a0002c0004t0001g0162 a0002c0011t0001g0163 |
2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2047-7786A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44987960 | |||||||
| chr14:44987990 | C | G | 1 | a0010c0010t0002g0010 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2047-7756C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44987990 | |||||||
| chr14:44988123 | G | T | 4 | a0002c0003t0003g0008 a0002c0003t0003g0009 a0002c0016t0003g0007 others(1): Show |
4 | HG01106.hp2 HG01516.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.2047-7623G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44988123 | |||||||
| chr14:44988262 | C | T | 4 | a0002c0003t0003g0008 a0002c0003t0003g0009 a0002c0016t0003g0007 others(1): Show |
4 | HG01106.hp2 HG01516.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.2047-7484C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44988262 | |||||||
| chr14:44988971 | T | A | 1 | a0001c0001t0001g0092 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2047-6775T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44988971 | |||||||
| chr14:44989074 | A | G | 81 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(78): Show |
81 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.2047-6672A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44989074 | |||||||
| chr14:44989105 | G | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2047-6641G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44989105 | |||||||
| chr14:44989121 | G | A | 98 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0071 others(95): Show |
98 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.2047-6625G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44989121 | |||||||
| chr14:44989127 | A | C | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2047-6619A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44989127 | |||||||
| chr14:44989174 | T | C | 1 | a0002c0004t0001g0161 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2047-6572T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44989174 | |||||||
| chr14:44989176 | C | T | 1 | a0002c0004t0001g0169 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2047-6570C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44989176 | |||||||
| chr14:44989550 | TA | T | 62 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(59): Show |
62 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.2047-6184delA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44989550 | ||||||
| chr14:44989908 | G | A | 1 | a0002c0004t0001g0171 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2047-5838G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44989908 | |||||||
| chr14:44989946 | C | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | NA18968.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2047-5800C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44989946 | |||||||
| chr14:44990097 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2047-5649T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44990097 | |||||||
| chr14:44990245 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2047-5501G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44990245 | |||||||
| chr14:44990328 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2047-5418C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44990328 | |||||||
| chr14:44990368 | T | C | 1 | a0002c0003t0002g0020 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2047-5378T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44990368 | |||||||
| chr14:44990693 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2047-5053A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44990693 | |||||||
| chr14:44990740 | C | T | 1 | a0002c0003t0006g0002 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2047-5006C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44990740 | |||||||
| chr14:44990915 | C | T | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2047-4831C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44990915 | |||||||
| chr14:44990916 | A | G | 84 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(81): Show |
84 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.2047-4830A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44990916 | |||||||
| chr14:44990918 | G | A | 1 | a0003c0002t0002g0036 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2047-4828G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44990918 | |||||||
| chr14:44990927 | G | T | 1 | a0002c0004t0001g0178 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2047-4819G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44990927 | |||||||
| chr14:44990930 | T | G | 1 | a0002c0004t0001g0178 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2047-4816T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44990930 | |||||||
| chr14:44990953 | C | CT | 28 | a0001c0001t0001g0060 a0001c0001t0001g0063 a0001c0001t0001g0064 others(25): Show |
28 | HG00438.hp1 HG00438.hp2 HG01516.hp1 others(25): Show |
intron_variant | MODIFIER | c.2047-4770dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44990953 | ||||||
| chr14:44990953 | C | CTTTTT | 18 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(15): Show |
18 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.2047-4774_2047-477 others(9): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44990953 | ||||||
| chr14:44990953 | C | CTTTTTT | 22 | a0002c0003t0002g0050 a0002c0003t0006g0002 a0002c0004t0001g0162 others(19): Show |
22 | HG00673.hp2 HG01358.hp1 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.2047-4775_2047-477 others(10): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44990953 | ||||||
| chr14:44990953 | C | CTTTTTTT | 21 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 others(18): Show |
21 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.2047-4776_2047-477 others(11): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44990953 | ||||||
| chr14:44990953 | C | CTTTTTTT others(1): Show |
8 | a0001c0001t0002g0067 a0002c0003t0002g0016 a0002c0003t0002g0018 others(5): Show |
8 | HG01358.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2047-4777_2047-477 others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44990953 | ||||||
| chr14:44990953 | C | CTTTTTTT others(2): Show |
8 | a0002c0003t0002g0015 a0002c0003t0002g0051 a0002c0003t0002g0052 others(5): Show |
8 | HG01106.hp2 HG01516.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.2047-4778_2047-477 others(13): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44990953 | ||||||
| chr14:44990953 | C | T | 1 | a0002c0004t0001g0178 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2047-4793C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44990953 | |||||||
| chr14:44991007 | T | C | 30 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(27): Show |
30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.2047-4739T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44991007 | |||||||
| chr14:44991061 | T | C | 82 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2047-4685T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44991061 | |||||||
| chr14:44991142 | G | C | 1 | a0001c0001t0001g0123 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2047-4604G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44991142 | |||||||
| chr14:44991274 | G | GT | 5 | a0001c0001t0002g0067 a0002c0003t0003g0008 a0002c0003t0003g0009 others(2): Show |
5 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2047-4462dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44991274 | ||||||
| chr14:44991280 | T | G | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2047-4466T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44991280 | |||||||
| chr14:44991621 | A | G | 63 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(60): Show |
63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2047-4125A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44991621 | |||||||
| chr14:44991731 | G | GT | 21 | a0001c0001t0001g0064 a0001c0001t0001g0104 a0001c0001t0001g0159 others(18): Show |
21 | HG00323.hp2 HG01496.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.2047-4005dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44991731 | ||||||
| chr14:44991867 | T | G | 29 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(26): Show |
29 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.2047-3879T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44991867 | |||||||
| chr14:44992016 | C | A | 2 | a0001c0001t0004g0084 a0001c0001t0004g0137 |
2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2047-3730C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44992016 | |||||||
| chr14:44992070 | G | C | 81 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(78): Show |
81 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.2047-3676G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44992070 | |||||||
| chr14:44992072 | T | TA | 8 | a0001c0001t0001g0151 a0002c0004t0001g0166 a0002c0004t0001g0167 others(5): Show |
8 | HG01106.hp1 HG01496.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2047-3645dupA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44992072 | ||||||
| chr14:44992072 | TA | T | 85 | a0001c0001t0001g0060 a0001c0001t0001g0063 a0001c0001t0001g0065 others(82): Show |
85 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.2047-3645delA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44992072 | ||||||
| chr14:44992072 | TAA | T | 14 | a0001c0001t0001g0100 a0001c0001t0001g0111 a0001c0001t0001g0119 others(11): Show |
14 | HG01109.hp2 HG01358.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.2047-3646_2047-364 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44992072 | ||||||
| chr14:44992072 | TAAA | T | 21 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 others(18): Show |
21 | HG01884.hp1 HG02109.hp1 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.2047-3647_2047-364 others(7): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44992072 | ||||||
| chr14:44992279 | T | A | 1 | a0003c0002t0002g0040 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2047-3467T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44992279 | |||||||
| chr14:44992299 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2047-3447G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44992299 | |||||||
| chr14:44992330 | G | C | 99 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0071 others(96): Show |
99 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.2047-3416G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44992330 | |||||||
| chr14:44992381 | A | C | 1 | a0001c0001t0001g0071 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2047-3365A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44992381 | |||||||
| chr14:44992465 | A | G | 63 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(60): Show |
63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2047-3281A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44992465 | |||||||
| chr14:44992545 | T | G | 5 | a0001c0001t0002g0067 a0002c0003t0003g0008 a0002c0003t0003g0009 others(2): Show |
5 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2047-3201T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44992545 | |||||||
| chr14:44992611 | C | CT | 8 | a0001c0001t0001g0064 a0001c0001t0001g0072 a0001c0001t0001g0080 others(5): Show |
8 | HG01071.hp1 HG01074.hp1 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.2047-3110dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44992611 | ||||||
| chr14:44992611 | CT | C | 45 | a0001c0001t0001g0073 a0001c0001t0001g0109 a0001c0001t0001g0139 others(42): Show |
45 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(42): Show |
intron_variant | MODIFIER | c.2047-3110delT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44992611 | ||||||
| chr14:44992611 | CTT | C | 40 | a0001c0001t0001g0115 a0001c0001t0002g0068 a0001c0001t0002g0069 others(37): Show |
40 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.2047-3111_2047-311 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44992611 | ||||||
| chr14:44992616 | T | C | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | NA18968.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2047-3130T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44992616 | |||||||
| chr14:44992895 | G | A | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2047-2851G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44992895 | |||||||
| chr14:44993051 | T | C | 82 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2047-2695T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44993051 | |||||||
| chr14:44993060 | C | T | 30 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(27): Show |
30 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.2047-2686C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44993060 | |||||||
| chr14:44993285 | TCAAAAA | T | 81 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(78): Show |
81 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.2047-2430_2047-242 others(10): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44993285 | ||||||
| chr14:44993603 | T | A | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2047-2143T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44993603 | |||||||
| chr14:44993605 | G | T | 1 | a0009c0015t0001g0086 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2047-2141G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44993605 | |||||||
| chr14:44993610 | G | A | 1 | a0001c0001t0004g0137 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2047-2136G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44993610 | |||||||
| chr14:44994183 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2047-1563C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44994183 | |||||||
| chr14:44994199 | T | C | 82 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2047-1547T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44994199 | |||||||
| chr14:44994428 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0126 |
2 | HG01074.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.2047-1318C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44994428 | |||||||
| chr14:44994627 | A | G | 1 | a0003c0002t0002g0006 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2047-1119A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44994627 | |||||||
| chr14:44994712 | C | T | 2 | a0002c0004t0001g0162 a0002c0011t0001g0163 |
2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2047-1034C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44994712 | |||||||
| chr14:44994839 | T | C | 5 | a0001c0001t0002g0067 a0002c0003t0003g0008 a0002c0003t0003g0009 others(2): Show |
5 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2047-907T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44994839 | |||||||
| chr14:44994909 | A | G | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2047-837A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44994909 | |||||||
| chr14:44994934 | A | G | 2 | a0002c0003t0002g0020 a0008c0012t0002g0019 |
2 | HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2047-812A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44994934 | |||||||
| chr14:44995075 | A | G | 5 | a0001c0001t0001g0088 a0001c0001t0001g0097 a0001c0001t0001g0104 others(2): Show |
5 | HG04228.hp2 NA18979.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.2047-671A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44995075 | |||||||
| chr14:44996092 | A | G | 1 | a0002c0003t0002g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2203+190A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44996092 | |||||||
| chr14:44996096 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2203+194C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44996096 | |||||||
| chr14:44996106 | T | G | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2203+204T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44996106 | |||||||
| chr14:44996137 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2203+235A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44996137 | |||||||
| chr14:44996388 | A | T | 1 | a0001c0001t0001g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2203+486A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44996388 | |||||||
| chr14:44996567 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2203+665G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44996567 | |||||||
| chr14:44996692 | G | C | 4 | a0002c0003t0003g0008 a0002c0003t0003g0009 a0002c0016t0003g0007 others(1): Show |
4 | HG01106.hp2 HG01516.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.2203+790G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44996692 | |||||||
| chr14:44996801 | A | G | 1 | a0002c0003t0002g0050 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2203+899A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44996801 | |||||||
| chr14:44996853 | G | C | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2203+951G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44996853 | |||||||
| chr14:44997009 | C | T | 3 | a0002c0003t0003g0008 a0002c0003t0003g0009 a0002c0016t0003g0007 |
3 | HG01106.hp2 HG01516.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2203+1107C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44997009 | |||||||
| chr14:44997190 | G | A | 1 | a0002c0003t0002g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2203+1288G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44997190 | |||||||
| chr14:44997404 | C | CA | 20 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0078 others(17): Show |
20 | HG01074.hp1 HG01257.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.2203+1530dupA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr14 | 44997404 | ||||||
| chr14:44997404 | C | CAAA | 12 | a0002c0004t0001g0162 a0002c0004t0001g0166 a0002c0004t0001g0168 others(9): Show |
12 | HG02280.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.2203+1528_2203+153 others(7): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr14 | 44997404 | ||||||
| chr14:44997404 | CA | C | 6 | a0001c0001t0001g0099 a0001c0001t0001g0123 a0001c0001t0001g0144 others(3): Show |
6 | HG00280.hp1 HG00323.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.2203+1530delA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr14 | 44997404 | ||||||
| chr14:44997404 | CAA | C | 6 | a0001c0001t0004g0137 a0003c0002t0002g0024 a0003c0002t0002g0037 others(3): Show |
6 | HG02055.hp1 HG02717.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.2203+1529_2203+153 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr14 | 44997404 | ||||||
| chr14:44997404 | CAAA | C | 56 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(53): Show |
56 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.2203+1528_2203+153 others(7): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr14 | 44997404 | ||||||
| chr14:44997404 | CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0153 |
3 | NA18990.hp2 NA19058.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.2203+1519_2203+153 others(16): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr14 | 44997404 | ||||||
| chr14:44997507 | A | G | 1 | a0002c0004t0001g0177 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2203+1605A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44997507 | |||||||
| chr14:44997854 | C | G | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2204-1509C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44997854 | |||||||
| chr14:44998055 | A | G | 1 | a0001c0001t0004g0137 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2204-1308A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44998055 | |||||||
| chr14:44998185 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2204-1178A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44998185 | |||||||
| chr14:44998235 | C | A | 2 | a0004c0005t0002g0004 a0004c0005t0002g0029 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2204-1128C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44998235 | |||||||
| chr14:44998269 | A | G | 1 | a0003c0002t0002g0033 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2204-1094A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44998269 | |||||||
| chr14:44998324 | T | C | 2 | a0002c0004t0001g0177 a0002c0004t0001g0178 |
2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2204-1039T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44998324 | |||||||
| chr14:44998729 | C | G | 30 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0080 others(27): Show |
30 | HG01074.hp2 HG01257.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.2204-634C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44998729 | |||||||
| chr14:44998761 | T | A | 1 | a0001c0001t0001g0129 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2204-602T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44998761 | |||||||
| chr14:44998939 | G | A | 1 | a0003c0002t0002g0025 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2204-424G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44998939 | |||||||
| chr14:44999109 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2204-254C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44999109 | |||||||
| chr14:44999335 | A | G | 3 | a0002c0003t0002g0015 a0002c0003t0002g0016 a0002c0003t0002g0049 |
3 | HG02723.hp1 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2204-28A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44999335 | |||||||
| chr14:44999558 | C | T | 30 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0080 others(27): Show |
30 | HG01074.hp2 HG01257.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.2338+61C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 44999558 | |||||||
| chr14:44999898 | T | C | 12 | a0002c0003t0002g0018 a0002c0003t0002g0020 a0002c0003t0002g0021 others(9): Show |
12 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2338+401T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 44999898 | |||||||
| chr14:44999900 | A | G | 4 | a0002c0003t0002g0020 a0005c0008t0002g0012 a0005c0008t0002g0017 others(1): Show |
4 | HG02055.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2338+403A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 44999900 | |||||||
| chr14:44999974 | C | T | 1 | a0002c0003t0002g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2338+477C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 44999974 | |||||||
| chr14:45000084 | T | C | 94 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0080 others(91): Show |
94 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.2338+587T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45000084 | |||||||
| chr14:45000119 | C | T | 2 | a0004c0005t0002g0004 a0004c0005t0002g0029 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2338+622C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45000119 | |||||||
| chr14:45000140 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2338+643A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45000140 | |||||||
| chr14:45000185 | G | A | 1 | a0005c0008t0002g0017 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2338+688G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45000185 | |||||||
| chr14:45000287 | C | T | 9 | a0001c0001t0001g0062 a0001c0001t0001g0078 a0001c0001t0001g0079 others(6): Show |
9 | HG02258.hp2 HG02809.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.2338+790C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45000287 | |||||||
| chr14:45000436 | G | A | 1 | a0002c0003t0002g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2338+939G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45000436 | |||||||
| chr14:45000606 | A | G | 63 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(60): Show |
63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2338+1109A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45000606 | |||||||
| chr14:45000798 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2338+1301G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45000798 | |||||||
| chr14:45000930 | T | C | 81 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(78): Show |
81 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.2338+1433T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45000930 | |||||||
| chr14:45001250 | C | T | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2338+1753C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45001250 | |||||||
| chr14:45001283 | C | T | 16 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(13): Show |
16 | HG01496.hp1 HG02145.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.2338+1786C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45001283 | |||||||
| chr14:45001403 | G | A | 1 | a0001c0001t0004g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2338+1906G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45001403 | |||||||
| chr14:45001547 | A | G | 3 | a0003c0002t0002g0006 a0003c0002t0002g0047 a0003c0002t0002g0048 |
3 | NA18982.hp2 NA18985.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.2338+2050A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45001547 | |||||||
| chr14:45001650 | G | A | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2338+2153G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45001650 | |||||||
| chr14:45001657 | A | G | 5 | a0001c0001t0002g0067 a0002c0003t0003g0008 a0002c0003t0003g0009 others(2): Show |
5 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2338+2160A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45001657 | |||||||
| chr14:45001755 | C | T | 3 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 |
3 | HG01884.hp1 HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2338+2258C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45001755 | |||||||
| chr14:45001756 | G | T | 9 | a0001c0001t0001g0062 a0001c0001t0001g0078 a0001c0001t0001g0079 others(6): Show |
9 | HG02258.hp2 HG02809.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.2338+2259G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45001756 | |||||||
| chr14:45001942 | A | C | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2339-2119A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45001942 | |||||||
| chr14:45002060 | A | G | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2339-2001A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45002060 | |||||||
| chr14:45002432 | G | T | 1 | a0001c0001t0001g0062 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2339-1629G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45002432 | |||||||
| chr14:45002439 | C | T | 82 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2339-1622C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45002439 | |||||||
| chr14:45002576 | A | G | 85 | a0001c0001t0001g0085 a0001c0001t0002g0067 a0001c0001t0002g0068 others(82): Show |
85 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.2339-1485A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45002576 | |||||||
| chr14:45002706 | G | A | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2339-1355G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45002706 | |||||||
| chr14:45002842 | G | C | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2339-1219G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45002842 | |||||||
| chr14:45003263 | C | A | 2 | a0002c0004t0001g0177 a0002c0004t0001g0178 |
2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2339-798C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45003263 | |||||||
| chr14:45003286 | G | A | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2339-775G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45003286 | |||||||
| chr14:45003318 | TA | T | 63 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(60): Show |
63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2339-741delA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr14 | 45003318 | ||||||
| chr14:45003354 | A | G | 1 | a0002c0004t0001g0161 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2339-707A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45003354 | |||||||
| chr14:45003360 | G | A | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2339-701G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45003360 | |||||||
| chr14:45003470 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2339-591C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45003470 | |||||||
| chr14:45003488 | GAACTTAC | G | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2339-566_2339-560d others(9): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr14 | 45003488 | ||||||
| chr14:45003713 | G | T | 1 | a0001c0001t0001g0065 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2339-348G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45003713 | |||||||
| chr14:45003730 | A | G | 63 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(60): Show |
63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2339-331A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45003730 | |||||||
| chr14:45003766 | C | CATGCATG others(25): Show |
2 | a0002c0003t0002g0051 a0002c0003t0002g0052 |
2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2339-292_2339-291i others(34): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr14 | 45003766 | ||||||
| chr14:45003766 | C | CATGTATG others(25): Show |
28 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(25): Show |
28 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.2339-291_2339-290i others(34): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr14 | 45003766 | ||||||
| chr14:45003766 | C | CATGTATG others(57): Show |
31 | a0001c0009t0002g0145 a0003c0002t0002g0006 a0003c0002t0002g0011 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.2339-291_2339-290i others(66): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr14 | 45003766 | ||||||
| chr14:45003766 | C | CATGTATG others(89): Show |
1 | a0003c0002t0002g0005 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2339-291_2339-290i others(98): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr14 | 45003766 | ||||||
| chr14:45003766 | C | CATGTATG others(153): Show |
1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2339-291_2339-290i others(162): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr14 | 45003766 | ||||||
| chr14:45003771 | G | A | 82 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2339-290G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45003771 | |||||||
| chr14:45003884 | T | C | 5 | a0001c0001t0002g0067 a0002c0003t0003g0008 a0002c0003t0003g0009 others(2): Show |
5 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2339-177T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45003884 | |||||||
| chr14:45004017 | A | AG | 82 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2339-44_2339-43ins others(1): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45004017 | |||||||
| chr14:45004424 | A | G | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2644+58A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45004424 | |||||||
| chr14:45004780 | T | C | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2644+414T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45004780 | |||||||
| chr14:45004781 | G | A | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2644+415G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45004781 | |||||||
| chr14:45004784 | C | T | 16 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(13): Show |
16 | HG01496.hp1 HG02145.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.2644+418C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45004784 | |||||||
| chr14:45004853 | T | C | 63 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(60): Show |
63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2644+487T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45004853 | |||||||
| chr14:45004999 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2644+633G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45004999 | |||||||
| chr14:45005011 | C | T | 2 | a0002c0003t0002g0020 a0008c0012t0002g0019 |
2 | HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2644+645C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45005011 | |||||||
| chr14:45005156 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2644+790C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45005156 | |||||||
| chr14:45005347 | G | A | 7 | a0001c0009t0002g0145 a0003c0002t0002g0006 a0003c0002t0002g0031 others(4): Show |
7 | HG00597.hp2 HG00673.hp2 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.2645-661G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45005347 | |||||||
| chr14:45005408 | A | G | 3 | a0004c0005t0002g0004 a0004c0005t0002g0029 a0004c0005t0002g0058 |
3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2645-600A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45005408 | |||||||
| chr14:45005666 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2645-342G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45005666 | |||||||
| chr14:45005671 | T | A | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2645-337T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45005671 | |||||||
| chr14:45005710 | C | G | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2645-298C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45005710 | |||||||
| chr14:45005936 | G | A | 81 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(78): Show |
81 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.2645-72G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45005936 | |||||||
| chr14:45005954 | C | G | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2645-54C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45005954 | |||||||
| chr14:45006467 | C | T | 8 | a0002c0003t0002g0018 a0002c0003t0002g0021 a0002c0003t0002g0022 others(5): Show |
8 | HG01109.hp2 HG02109.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2904+200C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45006467 | |||||||
| chr14:45006519 | T | C | 1 | a0002c0004t0001g0161 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2904+252T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45006519 | |||||||
| chr14:45006641 | C | T | 63 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(60): Show |
63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2904+374C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45006641 | |||||||
| chr14:45006680 | A | T | 2 | a0004c0005t0002g0004 a0004c0005t0002g0029 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2904+413A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45006680 | |||||||
| chr14:45006725 | T | C | 1 | a0003c0002t0008g0046 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2904+458T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45006725 | |||||||
| chr14:45006822 | A | G | 13 | a0002c0004t0001g0166 a0002c0004t0001g0167 a0002c0004t0001g0168 others(10): Show |
13 | HG01496.hp1 HG02280.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.2904+555A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45006822 | |||||||
| chr14:45006850 | T | C | 82 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2904+583T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45006850 | |||||||
| chr14:45006971 | A | G | 82 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2904+704A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45006971 | |||||||
| chr14:45007104 | ATACT | A | 30 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(27): Show |
30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.2904+840_2904+843d others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr14 | 45007104 | ||||||
| chr14:45007124 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2904+857A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45007124 | |||||||
| chr14:45007867 | T | G | 1 | a0001c0001t0001g0158 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2905-1046T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45007867 | |||||||
| chr14:45008215 | A | G | 3 | a0002c0003t0002g0015 a0002c0003t0002g0016 a0002c0003t0002g0049 |
3 | HG02723.hp1 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2905-698A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45008215 | |||||||
| chr14:45008239 | CT | C | 5 | a0001c0001t0001g0109 a0002c0003t0003g0008 a0002c0003t0003g0009 others(2): Show |
5 | HG01106.hp2 HG01516.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2905-657delT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr14 | 45008239 | ||||||
| chr14:45008443 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2905-470T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45008443 | |||||||
| chr14:45008585 | C | T | 1 | a0001c0014t0001g0136 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2905-328C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45008585 | |||||||
| chr14:45008786 | T | A | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2905-127T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45008786 | |||||||
| chr14:45008803 | A | C | 1 | a0001c0001t0001g0130 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2905-110A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45008803 | |||||||
| chr14:45008852 | A | G | 1 | a0003c0002t0002g0030 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2905-61A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45008852 | |||||||
| chr14:45009280 | TG | T | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3137+137delG | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr14 | 45009280 | ||||||
| chr14:45009437 | T | C | 2 | a0002c0003t0002g0051 a0002c0003t0002g0052 |
2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3137+292T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45009437 | |||||||
| chr14:45009716 | A | T | 1 | a0001c0001t0001g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3137+571A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45009716 | |||||||
| chr14:45009880 | T | C | 1 | a0001c0006t0001g0098 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3137+735T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45009880 | |||||||
| chr14:45010177 | A | G | 2 | a0004c0005t0002g0004 a0004c0005t0002g0029 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3137+1032A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45010177 | |||||||
| chr14:45010179 | A | AATAAT | 30 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(27): Show |
30 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.3137+1034_3137+103 others(9): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45010179 | |||||||
| chr14:45010180 | G | A | 30 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(27): Show |
30 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.3137+1035G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45010180 | |||||||
| chr14:45010182 | T | TGG | 30 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(27): Show |
30 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.3137+1037_3137+103 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45010182 | |||||||
| chr14:45010183 | C | A | 30 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(27): Show |
30 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.3137+1038C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45010183 | |||||||
| chr14:45010442 | G | C | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3137+1297G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45010442 | |||||||
| chr14:45010458 | A | G | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3137+1313A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45010458 | |||||||
| chr14:45010833 | C | T | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3138-1142C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45010833 | |||||||
| chr14:45010877 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3138-1098A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45010877 | |||||||
| chr14:45011002 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3138-973A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45011002 | |||||||
| chr14:45011151 | G | A | 30 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(27): Show |
30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.3138-824G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45011151 | |||||||
| chr14:45011366 | G | A | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3138-609G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45011366 | |||||||
| chr14:45011406 | G | A | 1 | a0001c0014t0001g0136 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3138-569G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45011406 | |||||||
| chr14:45011465 | G | A | 9 | a0001c0001t0001g0062 a0001c0001t0001g0078 a0001c0001t0001g0079 others(6): Show |
9 | HG02258.hp2 HG02809.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.3138-510G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45011465 | |||||||
| chr14:45011512 | C | T | 1 | a0004c0005t0002g0029 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3138-463C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45011512 | |||||||
| chr14:45011599 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3138-376G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45011599 | |||||||
| chr14:45011785 | A | ATG | 27 | a0001c0001t0001g0064 a0001c0001t0001g0082 a0001c0001t0001g0091 others(24): Show |
27 | HG01496.hp2 HG01884.hp2 HG02132.hp1 others(24): Show |
intron_variant | MODIFIER | c.3138-164_3138-163d others(4): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr14 | 45011785 | ||||||
| chr14:45011785 | A | ATGTG | 22 | a0001c0001t0002g0068 a0001c0001t0002g0070 a0002c0003t0002g0003 others(19): Show |
22 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.3138-166_3138-163d others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr14 | 45011785 | ||||||
| chr14:45011785 | A | ATGTGTG | 10 | a0001c0001t0002g0067 a0001c0001t0002g0069 a0002c0003t0002g0020 others(7): Show |
10 | HG01358.hp2 HG01516.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.3138-168_3138-163d others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr14 | 45011785 | ||||||
| chr14:45011785 | A | ATGTGTGT others(1): Show |
21 | a0002c0003t0002g0018 a0002c0003t0002g0021 a0002c0003t0002g0022 others(18): Show |
21 | HG01106.hp2 HG01109.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.3138-170_3138-163d others(10): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr14 | 45011785 | ||||||
| chr14:45011785 | A | ATGTGTGT others(3): Show |
2 | a0002c0003t0002g0057 a0002c0004t0001g0173 |
2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.3138-172_3138-163d others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr14 | 45011785 | ||||||
| chr14:45011785 | A | G | 2 | a0004c0005t0002g0058 a0007c0013t0005g0001 |
2 | HG02132.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.3138-190A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45011785 | |||||||
| chr14:45011785 | ATG | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0114 a0001c0001t0001g0143 |
3 | HG01257.hp1 HG01891.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.3138-164_3138-163d others(4): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr14 | 45011785 | ||||||
| chr14:45011836 | GT | G | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3138-134delT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr14 | 45011836 | ||||||
| chr14:45012093 | A | T | 11 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(8): Show |
11 | HG01358.hp2 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.3238+18A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45012093 | |||||||
| chr14:45012399 | G | A | 1 | a0006c0007t0001g0164 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3238+324G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45012399 | |||||||
| chr14:45012658 | TA | T | 63 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(60): Show |
63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.3238+587delA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45012658 | ||||||
| chr14:45012831 | A | G | 2 | a0002c0004t0001g0177 a0002c0004t0001g0178 |
2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3238+756A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45012831 | |||||||
| chr14:45012917 | C | T | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3238+842C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45012917 | |||||||
| chr14:45012965 | C | A | 1 | a0002c0003t0002g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3238+890C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45012965 | |||||||
| chr14:45013122 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3238+1047G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45013122 | |||||||
| chr14:45013288 | C | G | 30 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(27): Show |
30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.3238+1213C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45013288 | |||||||
| chr14:45013496 | G | C | 1 | a0001c0001t0001g0158 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3238+1421G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45013496 | |||||||
| chr14:45013504 | A | G | 12 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0080 others(9): Show |
12 | HG01074.hp2 HG01257.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.3238+1429A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45013504 | |||||||
| chr14:45013512 | T | G | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3238+1437T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45013512 | |||||||
| chr14:45013599 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3238+1524A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45013599 | |||||||
| chr14:45013942 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3238+1867G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45013942 | |||||||
| chr14:45014043 | C | CT | 14 | a0001c0001t0001g0112 a0001c0001t0001g0133 a0001c0001t0001g0134 others(11): Show |
14 | HG01106.hp2 HG01516.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.3238+1987dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45014043 | ||||||
| chr14:45014043 | C | CTT | 69 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(66): Show |
69 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.3238+1986_3238+198 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45014043 | ||||||
| chr14:45014079 | T | G | 1 | a0001c0001t0001g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3238+2004T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45014079 | |||||||
| chr14:45014141 | G | A | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3238+2066G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45014141 | |||||||
| chr14:45014261 | G | T | 1 | a0001c0001t0001g0083 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3238+2186G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45014261 | |||||||
| chr14:45014281 | G | A | 2 | a0002c0004t0001g0177 a0002c0004t0001g0178 |
2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3238+2206G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45014281 | |||||||
| chr14:45014338 | G | A | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3238+2263G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45014338 | |||||||
| chr14:45014427 | G | A | 1 | a0001c0001t0004g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3238+2352G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45014427 | |||||||
| chr14:45014529 | G | C | 1 | a0002c0003t0002g0050 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3238+2454G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45014529 | |||||||
| chr14:45014555 | C | G | 1 | a0001c0001t0004g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3238+2480C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45014555 | |||||||
| chr14:45014601 | C | T | 1 | a0001c0014t0001g0136 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3238+2526C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45014601 | |||||||
| chr14:45014652 | A | G | 4 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(1): Show |
4 | HG01358.hp2 HG01884.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3238+2577A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45014652 | |||||||
| chr14:45015000 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3238+2925A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45015000 | |||||||
| chr14:45015058 | C | G | 4 | a0002c0003t0003g0008 a0002c0003t0003g0009 a0002c0016t0003g0007 others(1): Show |
4 | HG01106.hp2 HG01516.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.3238+2983C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45015058 | |||||||
| chr14:45015261 | T | C | 82 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.3238+3186T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45015261 | |||||||
| chr14:45015307 | A | AAAAT | 7 | a0001c0001t0001g0066 a0001c0001t0001g0073 a0001c0001t0001g0111 others(4): Show |
7 | HG02055.hp2 HG02132.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.3238+3274_3238+327 others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45015307 | ||||||
| chr14:45015307 | AAAAT | A | 34 | a0001c0001t0001g0064 a0001c0001t0001g0080 a0001c0001t0001g0081 others(31): Show |
34 | HG01358.hp2 HG01496.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.3238+3274_3238+327 others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45015307 | ||||||
| chr14:45015307 | AAAATAAA others(1): Show |
A | 31 | a0001c0009t0002g0145 a0002c0016t0003g0007 a0003c0002t0002g0005 others(28): Show |
31 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.3238+3270_3238+327 others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45015307 | ||||||
| chr14:45015307 | AAAATAAA others(5): Show |
A | 21 | a0001c0001t0001g0117 a0002c0003t0002g0018 a0002c0003t0002g0020 others(18): Show |
21 | HG01106.hp2 HG01109.hp2 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.3238+3266_3238+327 others(16): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45015307 | ||||||
| chr14:45015307 | AAAATAAA others(9): Show |
A | 1 | a0003c0002t0002g0042 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3238+3262_3238+327 others(20): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45015307 | ||||||
| chr14:45015333 | A | G | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3238+3258A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45015333 | |||||||
| chr14:45015601 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3238+3526G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45015601 | |||||||
| chr14:45015785 | C | G | 1 | a0003c0002t0002g0045 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3238+3710C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45015785 | |||||||
| chr14:45015814 | C | G | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3238+3739C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45015814 | |||||||
| chr14:45015898 | A | G | 11 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(8): Show |
11 | HG01358.hp2 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.3238+3823A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45015898 | |||||||
| chr14:45016060 | A | T | 83 | a0001c0001t0001g0085 a0001c0001t0002g0067 a0001c0001t0002g0068 others(80): Show |
83 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.3238+3985A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45016060 | |||||||
| chr14:45016445 | G | T | 11 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(8): Show |
11 | HG01358.hp2 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.3238+4370G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45016445 | |||||||
| chr14:45016734 | A | C | 2 | a0002c0004t0001g0162 a0002c0011t0001g0163 |
2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.3238+4659A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45016734 | |||||||
| chr14:45017071 | G | A | 82 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.3238+4996G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45017071 | |||||||
| chr14:45017089 | T | C | 2 | a0001c0001t0001g0090 a0001c0001t0001g0092 |
2 | HG00438.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.3238+5014T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45017089 | |||||||
| chr14:45017101 | C | A | 81 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(78): Show |
81 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.3238+5026C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45017101 | |||||||
| chr14:45017135 | A | G | 33 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(30): Show |
33 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3238+5060A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45017135 | |||||||
| chr14:45017172 | A | G | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3238+5097A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45017172 | |||||||
| chr14:45017406 | A | AAC | 15 | a0001c0001t0001g0107 a0001c0001t0001g0119 a0001c0001t0004g0137 others(12): Show |
15 | HG01106.hp2 HG01496.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.3238+5358_3238+535 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45017406 | ||||||
| chr14:45017406 | A | AACAC | 9 | a0001c0001t0001g0096 a0001c0001t0001g0100 a0001c0001t0001g0160 others(6): Show |
9 | HG01891.hp1 HG01993.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.3238+5356_3238+535 others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45017406 | ||||||
| chr14:45017406 | A | AACACAC | 19 | a0001c0001t0002g0068 a0001c0001t0002g0070 a0002c0003t0002g0015 others(16): Show |
19 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.3238+5354_3238+535 others(10): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45017406 | ||||||
| chr14:45017406 | A | AACACACA others(1): Show |
11 | a0002c0003t0002g0013 a0002c0003t0002g0014 a0002c0004t0001g0168 others(8): Show |
11 | HG01884.hp2 HG02451.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.3238+5352_3238+535 others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45017406 | ||||||
| chr14:45017406 | A | AACACACA others(3): Show |
2 | a0001c0001t0002g0067 a0001c0001t0002g0069 |
2 | HG01358.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.3238+5350_3238+535 others(14): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45017406 | ||||||
| chr14:45017406 | AACACACA others(3): Show |
A | 9 | a0001c0001t0001g0062 a0001c0001t0001g0078 a0001c0001t0001g0079 others(6): Show |
9 | HG02258.hp2 HG02809.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.3238+5350_3238+535 others(14): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45017406 | ||||||
| chr14:45017432 | C | CACACACA others(1): Show |
2 | a0003c0002t0002g0037 a0003c0002t0008g0046 |
2 | HG03017.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.3238+5359_3238+536 others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45017432 | ||||||
| chr14:45017432 | C | CACACAG | 28 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(25): Show |
28 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.3238+5359_3238+536 others(10): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45017432 | ||||||
| chr14:45017570 | A | C | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3238+5495A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45017570 | |||||||
| chr14:45017839 | G | A | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0153 |
3 | NA18990.hp2 NA19058.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.3238+5764G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45017839 | |||||||
| chr14:45017842 | G | A | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3238+5767G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45017842 | |||||||
| chr14:45017863 | A | AAG | 82 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.3238+5789_3238+579 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45017863 | ||||||
| chr14:45017878 | T | G | 1 | a0001c0006t0001g0087 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3238+5803T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45017878 | |||||||
| chr14:45017915 | TG | T | 2 | a0002c0003t0002g0051 a0002c0003t0002g0052 |
2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3238+5842delG | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45017915 | ||||||
| chr14:45017917 | G | T | 16 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(13): Show |
16 | HG01496.hp1 HG02145.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.3238+5842G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45017917 | |||||||
| chr14:45017978 | T | C | 2 | a0001c0001t0001g0091 a0001c0001t0001g0149 |
2 | HG02165.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.3238+5903T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45017978 | |||||||
| chr14:45018185 | C | T | 82 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.3238+6110C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45018185 | |||||||
| chr14:45018189 | T | A | 1 | a0002c0003t0002g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3238+6114T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45018189 | |||||||
| chr14:45018191 | A | C | 82 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.3238+6116A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45018191 | |||||||
| chr14:45018192 | A | T | 82 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.3238+6117A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45018192 | |||||||
| chr14:45018403 | G | C | 82 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.3238+6328G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45018403 | |||||||
| chr14:45018430 | G | C | 63 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(60): Show |
63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.3238+6355G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45018430 | |||||||
| chr14:45018738 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.3238+6663T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45018738 | |||||||
| chr14:45018927 | A | T | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3238+6852A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45018927 | |||||||
| chr14:45018938 | A | G | 2 | a0002c0003t0002g0051 a0002c0003t0002g0052 |
2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3239-6845A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45018938 | |||||||
| chr14:45019027 | A | G | 30 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(27): Show |
30 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.3239-6756A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45019027 | |||||||
| chr14:45019185 | A | G | 33 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(30): Show |
33 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3239-6598A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45019185 | |||||||
| chr14:45019217 | C | T | 62 | a0001c0001t0001g0116 a0001c0001t0002g0068 a0001c0001t0002g0069 others(59): Show |
62 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.3239-6566C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45019217 | |||||||
| chr14:45019396 | T | C | 10 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 others(7): Show |
10 | HG01884.hp1 HG01891.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.3239-6387T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45019396 | |||||||
| chr14:45019686 | A | G | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3239-6097A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45019686 | |||||||
| chr14:45019698 | G | T | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3239-6085G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45019698 | |||||||
| chr14:45019817 | C | T | 25 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 others(22): Show |
25 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.3239-5966C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45019817 | |||||||
| chr14:45020556 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3239-5227T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45020556 | |||||||
| chr14:45020610 | T | C | 3 | a0004c0005t0002g0004 a0004c0005t0002g0029 a0004c0005t0002g0058 |
3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3239-5173T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45020610 | |||||||
| chr14:45020741 | C | G | 3 | a0001c0001t0001g0096 a0001c0001t0001g0100 a0001c0001t0001g0160 |
3 | HG01993.hp1 HG03491.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.3239-5042C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45020741 | |||||||
| chr14:45020987 | G | A | 2 | a0002c0004t0001g0162 a0002c0011t0001g0163 |
2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.3239-4796G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45020987 | |||||||
| chr14:45021035 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3239-4748T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45021035 | |||||||
| chr14:45021126 | C | T | 82 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.3239-4657C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45021126 | |||||||
| chr14:45021295 | C | A | 2 | a0005c0008t0002g0012 a0005c0008t0002g0017 |
2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3239-4488C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45021295 | |||||||
| chr14:45021376 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3239-4407G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45021376 | |||||||
| chr14:45021557 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.3239-4226A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45021557 | |||||||
| chr14:45021636 | C | A | 2 | a0002c0004t0001g0174 a0002c0004t0001g0175 |
2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.3239-4147C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45021636 | |||||||
| chr14:45021668 | C | T | 1 | a0003c0002t0002g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.3239-4115C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45021668 | |||||||
| chr14:45021679 | C | T | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3239-4104C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45021679 | |||||||
| chr14:45021701 | C | T | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3239-4082C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45021701 | |||||||
| chr14:45021708 | C | G | 82 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.3239-4075C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45021708 | |||||||
| chr14:45021730 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.3239-4053G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45021730 | |||||||
| chr14:45021774 | C | T | 2 | a0002c0003t0002g0013 a0002c0003t0002g0014 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3239-4009C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45021774 | |||||||
| chr14:45021990 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3239-3793A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45021990 | |||||||
| chr14:45022032 | A | G | 1 | a0001c0001t0001g0131 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.3239-3751A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45022032 | |||||||
| chr14:45022118 | T | C | 1 | a0004c0005t0002g0004 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3239-3665T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45022118 | |||||||
| chr14:45022195 | G | A | 2 | a0002c0004t0001g0177 a0002c0004t0001g0178 |
2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3239-3588G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45022195 | |||||||
| chr14:45022275 | G | C | 1 | a0001c0001t0001g0062 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3239-3508G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45022275 | |||||||
| chr14:45022509 | G | A | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3239-3274G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45022509 | |||||||
| chr14:45022664 | TTTC | T | 30 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(27): Show |
30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.3239-3111_3239-310 others(7): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45022664 | ||||||
| chr14:45023568 | A | G | 12 | a0002c0004t0001g0166 a0002c0004t0001g0167 a0002c0004t0001g0168 others(9): Show |
12 | HG01496.hp1 HG02280.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.3239-2215A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45023568 | |||||||
| chr14:45023805 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3239-1978A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45023805 | |||||||
| chr14:45023903 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3239-1880G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45023903 | |||||||
| chr14:45024444 | G | GA | 81 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(78): Show |
81 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.3239-1334dupA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45024444 | ||||||
| chr14:45024573 | G | A | 30 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(27): Show |
30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.3239-1210G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45024573 | |||||||
| chr14:45024646 | T | G | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3239-1137T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45024646 | |||||||
| chr14:45024721 | T | A | 1 | a0003c0002t0002g0031 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3239-1062T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45024721 | |||||||
| chr14:45024805 | G | T | 1 | a0001c0001t0001g0103 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.3239-978G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45024805 | |||||||
| chr14:45024943 | T | C | 2 | a0002c0004t0001g0177 a0002c0004t0001g0178 |
2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3239-840T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45024943 | |||||||
| chr14:45025069 | C | A | 14 | a0002c0004t0001g0161 a0002c0004t0001g0166 a0002c0004t0001g0167 others(11): Show |
14 | HG01496.hp1 HG02145.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.3239-714C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45025069 | |||||||
| chr14:45025077 | T | G | 1 | a0001c0001t0001g0089 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3239-706T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45025077 | |||||||
| chr14:45025396 | T | G | 63 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(60): Show |
63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.3239-387T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45025396 | |||||||
| chr14:45025399 | A | G | 3 | a0004c0005t0002g0004 a0004c0005t0002g0029 a0004c0005t0002g0058 |
3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3239-384A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45025399 | |||||||
| chr14:45025479 | G | A | 5 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0139 others(2): Show |
5 | HG02451.hp2 NA18961.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.3239-304G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45025479 | |||||||
| chr14:45025484 | A | G | 1 | a0001c0006t0001g0087 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3239-299A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45025484 | |||||||
| chr14:45025563 | C | CA | 14 | a0001c0001t0001g0102 a0001c0001t0002g0067 a0002c0003t0002g0003 others(11): Show |
14 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.3239-204dupA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45025563 | ||||||
| chr14:45025614 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3239-169T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45025614 | |||||||
| chr14:45026016 | A | C | 8 | a0002c0003t0002g0018 a0002c0003t0002g0021 a0002c0003t0002g0022 others(5): Show |
8 | HG01109.hp2 HG02109.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3328+144A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | chr14 | 45026016 | |||||||
| chr14:45026051 | T | C | 33 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(30): Show |
33 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3328+179T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | chr14 | 45026051 | |||||||
| chr14:45026199 | G | A | 1 | a0003c0002t0002g0040 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3328+327G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | chr14 | 45026199 | |||||||
| chr14:45026274 | T | C | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3328+402T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | chr14 | 45026274 | |||||||
| chr14:45026418 | A | G | 63 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(60): Show |
63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.3328+546A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | chr14 | 45026418 | |||||||
| chr14:45026421 | G | A | 63 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(60): Show |
63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.3328+549G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | chr14 | 45026421 | |||||||
| chr14:45026489 | A | T | 30 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(27): Show |
30 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.3328+617A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | chr14 | 45026489 | |||||||
| chr14:45026560 | C | T | 32 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0065 others(29): Show |
32 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.3328+688C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | chr14 | 45026560 | |||||||
| chr14:45026598 | T | G | 1 | a0001c0001t0001g0143 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3329-701T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | chr14 | 45026598 | |||||||
| chr14:45026608 | C | G | 1 | a0001c0001t0001g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3329-691C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | chr14 | 45026608 | |||||||
| chr14:45026835 | C | CAAA | 20 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(17): Show |
20 | HG01496.hp1 HG01884.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.3329-452_3329-450d others(5): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr14 | 45026835 | ||||||
| chr14:45026835 | C | CAAAA | 60 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(57): Show |
60 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.3329-453_3329-450d others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr14 | 45026835 | ||||||
| chr14:45026861 | G | A | 84 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(81): Show |
84 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.3329-438G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | chr14 | 45026861 | |||||||
| chr14:45027006 | A | AAAAC | 16 | a0002c0004t0001g0161 a0002c0004t0001g0166 a0002c0004t0001g0167 others(13): Show |
16 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.3329-269_3329-266d others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr14 | 45027006 | ||||||
| chr14:45027014 | C | T | 1 | a0003c0002t0002g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3329-285C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | chr14 | 45027014 | |||||||
| chr14:45027098 | T | C | 1 | a0002c0004t0001g0166 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3329-201T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | chr14 | 45027098 | |||||||
| chr14:45027212 | G | T | 3 | a0004c0005t0002g0004 a0004c0005t0002g0029 a0004c0005t0002g0058 |
3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3329-87G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | chr14 | 45027212 | |||||||
| chr14:45027537 | T | G | 1 | a0003c0002t0008g0046 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3504+63T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 9/19 | chr14 | 45027537 | |||||||
| chr14:45027680 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3504+206C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 9/19 | chr14 | 45027680 | |||||||
| chr14:45027706 | T | C | 1 | a0003c0002t0002g0036 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3504+232T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 9/19 | chr14 | 45027706 | |||||||
| chr14:45027822 | C | T | 4 | a0002c0003t0003g0008 a0002c0003t0003g0009 a0002c0016t0003g0007 others(1): Show |
4 | HG01106.hp2 HG01516.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.3504+348C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 9/19 | chr14 | 45027822 | |||||||
| chr14:45028540 | G | T | 1 | a0001c0001t0001g0077 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3658+211G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45028540 | |||||||
| chr14:45028562 | A | G | 63 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(60): Show |
63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.3658+233A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45028562 | |||||||
| chr14:45028730 | A | G | 3 | a0004c0005t0002g0004 a0004c0005t0002g0029 a0004c0005t0002g0058 |
3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3658+401A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45028730 | |||||||
| chr14:45028819 | G | A | 16 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(13): Show |
16 | HG01496.hp1 HG02145.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.3658+490G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45028819 | |||||||
| chr14:45029159 | A | G | 1 | a0002c0003t0002g0020 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3658+830A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45029159 | |||||||
| chr14:45029223 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0152 |
2 | HG01943.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.3658+894G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45029223 | |||||||
| chr14:45029297 | A | G | 30 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(27): Show |
30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.3658+968A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45029297 | |||||||
| chr14:45029328 | G | A | 2 | a0002c0004t0001g0162 a0002c0011t0001g0163 |
2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.3658+999G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45029328 | |||||||
| chr14:45029413 | T | C | 2 | a0002c0003t0002g0051 a0002c0003t0002g0052 |
2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3658+1084T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45029413 | |||||||
| chr14:45029682 | G | C | 1 | a0005c0008t0002g0017 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3658+1353G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45029682 | |||||||
| chr14:45030006 | A | G | 81 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(78): Show |
81 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.3658+1677A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45030006 | |||||||
| chr14:45030037 | G | T | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3658+1708G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45030037 | |||||||
| chr14:45030041 | C | T | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3658+1712C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45030041 | |||||||
| chr14:45030042 | G | A | 30 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(27): Show |
30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.3658+1713G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45030042 | |||||||
| chr14:45030136 | A | T | 19 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(16): Show |
19 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.3658+1807A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45030136 | |||||||
| chr14:45030174 | T | C | 3 | a0004c0005t0002g0004 a0004c0005t0002g0029 a0004c0005t0002g0058 |
3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3658+1845T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45030174 | |||||||
| chr14:45030289 | T | C | 1 | a0002c0003t0002g0020 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3659-1934T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45030289 | |||||||
| chr14:45030324 | A | G | 82 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.3659-1899A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45030324 | |||||||
| chr14:45030326 | G | A | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3659-1897G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45030326 | |||||||
| chr14:45030649 | A | G | 3 | a0002c0003t0002g0050 a0002c0003t0002g0051 a0002c0003t0002g0052 |
3 | HG02486.hp2 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3659-1574A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45030649 | |||||||
| chr14:45030692 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3659-1531A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45030692 | |||||||
| chr14:45030877 | T | C | 5 | a0001c0001t0002g0067 a0002c0003t0003g0008 a0002c0003t0003g0009 others(2): Show |
5 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.3659-1346T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45030877 | |||||||
| chr14:45030928 | T | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0152 |
2 | HG01943.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.3659-1295T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45030928 | |||||||
| chr14:45031501 | C | T | 1 | a0002c0003t0003g0009 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3659-722C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45031501 | |||||||
| chr14:45031551 | A | G | 1 | a0003c0002t0002g0041 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3659-672A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45031551 | |||||||
| chr14:45031591 | G | A | 1 | a0002c0003t0002g0013 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3659-632G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45031591 | |||||||
| chr14:45031882 | A | G | 81 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(78): Show |
81 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.3659-341A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45031882 | |||||||
| chr14:45032021 | A | G | 81 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(78): Show |
81 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.3659-202A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45032021 | |||||||
| chr14:45032181 | A | G | 63 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(60): Show |
63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.3659-42A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45032181 | |||||||
| chr14:45032394 | A | G | 3 | a0004c0005t0002g0004 a0004c0005t0002g0029 a0004c0005t0002g0058 |
3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3812+18A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45032394 | |||||||
| chr14:45032625 | C | T | 3 | a0001c0001t0001g0064 a0001c0001t0001g0082 a0001c0001t0001g0083 |
3 | HG02145.hp1 HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3812+249C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45032625 | |||||||
| chr14:45032727 | G | A | 2 | a0005c0008t0002g0012 a0005c0008t0002g0017 |
2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3812+351G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45032727 | |||||||
| chr14:45032755 | G | A | 82 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.3812+379G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45032755 | |||||||
| chr14:45032989 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3812+613C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45032989 | |||||||
| chr14:45033028 | G | A | 1 | a0008c0012t0002g0019 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3812+652G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45033028 | |||||||
| chr14:45033074 | A | G | 5 | a0001c0001t0002g0067 a0002c0003t0003g0008 a0002c0003t0003g0009 others(2): Show |
5 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.3812+698A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45033074 | |||||||
| chr14:45033252 | C | CA | 13 | a0001c0001t0001g0064 a0001c0001t0001g0081 a0001c0001t0001g0107 others(10): Show |
13 | HG01109.hp2 HG01496.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.3812+894dupA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr14 | 45033252 | ||||||
| chr14:45033252 | C | CAA | 59 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(56): Show |
59 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.3812+893_3812+894d others(4): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr14 | 45033252 | ||||||
| chr14:45033252 | C | CAAA | 14 | a0002c0004t0001g0162 a0002c0004t0001g0168 a0002c0004t0001g0169 others(11): Show |
14 | HG02055.hp1 HG02280.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.3812+892_3812+894d others(5): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr14 | 45033252 | ||||||
| chr14:45033580 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3812+1204A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45033580 | |||||||
| chr14:45033821 | C | A | 5 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0085 others(2): Show |
5 | HG02451.hp1 HG02559.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3812+1445C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45033821 | |||||||
| chr14:45033936 | T | C | 1 | a0001c0001t0001g0155 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3812+1560T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45033936 | |||||||
| chr14:45034029 | C | T | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3812+1653C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45034029 | |||||||
| chr14:45034343 | G | C | 4 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(1): Show |
4 | HG01358.hp2 HG01884.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3812+1967G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45034343 | |||||||
| chr14:45034414 | C | T | 3 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 |
3 | HG01884.hp1 HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3812+2038C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45034414 | |||||||
| chr14:45034644 | T | C | 2 | a0002c0004t0001g0177 a0002c0004t0001g0178 |
2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3812+2268T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45034644 | |||||||
| chr14:45034661 | A | G | 2 | a0002c0004t0001g0162 a0002c0011t0001g0163 |
2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.3812+2285A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45034661 | |||||||
| chr14:45034689 | G | C | 2 | a0002c0004t0001g0177 a0002c0004t0001g0178 |
2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3812+2313G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45034689 | |||||||
| chr14:45034710 | A | T | 30 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(27): Show |
30 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.3812+2334A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45034710 | |||||||
| chr14:45034777 | C | T | 1 | a0003c0002t0002g0023 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.3812+2401C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45034777 | |||||||
| chr14:45035068 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3812+2692A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45035068 | |||||||
| chr14:45035908 | T | A | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3812+3532T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45035908 | |||||||
| chr14:45035948 | GA | G | 74 | a0001c0001t0001g0158 a0001c0001t0002g0067 a0001c0001t0002g0068 others(71): Show |
74 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.3812+3587delA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr14 | 45035948 | ||||||
| chr14:45035948 | GAA | G | 5 | a0002c0003t0002g0013 a0002c0003t0002g0014 a0002c0003t0002g0015 others(2): Show |
5 | HG02723.hp1 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3812+3586_3812+358 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr14 | 45035948 | ||||||
| chr14:45035976 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3812+3600A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45035976 | |||||||
| chr14:45036098 | G | A | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3812+3722G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45036098 | |||||||
| chr14:45036125 | G | C | 3 | a0001c0006t0001g0087 a0001c0006t0001g0098 a0001c0006t0001g0101 |
3 | HG02615.hp1 HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3812+3749G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45036125 | |||||||
| chr14:45036130 | T | TA | 16 | a0001c0001t0001g0063 a0001c0001t0001g0066 a0001c0001t0001g0076 others(13): Show |
16 | HG00673.hp2 HG01109.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.3812+3781dupA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr14 | 45036130 | ||||||
| chr14:45036130 | T | TC | 3 | a0002c0003t0002g0051 a0002c0003t0002g0053 a0005c0008t0002g0012 |
3 | HG01109.hp2 HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.3812+3754_3812+375 others(5): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45036130 | |||||||
| chr14:45036130 | TA | T | 7 | a0001c0001t0001g0114 a0001c0001t0001g0120 a0001c0001t0001g0148 others(4): Show |
7 | HG01257.hp1 HG01257.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.3812+3781delA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr14 | 45036130 | ||||||
| chr14:45036130 | TAAA | T | 5 | a0002c0004t0001g0162 a0002c0011t0001g0163 a0004c0005t0002g0004 others(2): Show |
5 | HG02451.hp2 HG02717.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.3812+3779_3812+378 others(7): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr14 | 45036130 | ||||||
| chr14:45036130 | TAAAA | T | 16 | a0002c0004t0001g0161 a0002c0004t0001g0166 a0002c0004t0001g0167 others(13): Show |
16 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.3812+3778_3812+378 others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr14 | 45036130 | ||||||
| chr14:45036131 | A | C | 12 | a0002c0003t0002g0018 a0002c0003t0002g0020 a0002c0003t0002g0021 others(9): Show |
12 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.3812+3755A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45036131 | |||||||
| chr14:45036131 | A | T | 3 | a0002c0003t0002g0051 a0002c0003t0002g0053 a0005c0008t0002g0012 |
3 | HG01109.hp2 HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.3812+3755A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45036131 | |||||||
| chr14:45036132 | A | T | 12 | a0002c0003t0002g0018 a0002c0003t0002g0020 a0002c0003t0002g0021 others(9): Show |
12 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.3812+3756A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45036132 | |||||||
| chr14:45036213 | A | C | 1 | a0002c0004t0001g0162 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3812+3837A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45036213 | |||||||
| chr14:45036229 | A | G | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3812+3853A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45036229 | |||||||
| chr14:45036890 | C | G | 1 | a0003c0002t0002g0036 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3812+4514C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45036890 | |||||||
| chr14:45037327 | A | AACTGATT others(18): Show |
1 | a0001c0001t0001g0153 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.3812+4952_3812+497 others(29): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr14 | 45037327 | ||||||
| chr14:45037372 | C | T | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3812+4996C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45037372 | |||||||
| chr14:45037654 | G | T | 1 | a0001c0001t0001g0129 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.3812+5278G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45037654 | |||||||
| chr14:45037804 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3812+5428G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45037804 | |||||||
| chr14:45037863 | T | TA | 30 | a0001c0001t0001g0144 a0001c0001t0002g0067 a0001c0001t0002g0068 others(27): Show |
30 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.3812+5502dupA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr14 | 45037863 | ||||||
| chr14:45038010 | T | C | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0153 |
3 | NA18990.hp2 NA19058.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.3812+5634T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45038010 | |||||||
| chr14:45038256 | A | T | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3813-5430A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45038256 | |||||||
| chr14:45038288 | C | T | 1 | a0002c0004t0001g0169 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3813-5398C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45038288 | |||||||
| chr14:45038314 | A | C | 1 | a0001c0001t0001g0091 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3813-5372A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45038314 | |||||||
| chr14:45038412 | G | A | 82 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.3813-5274G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45038412 | |||||||
| chr14:45038420 | G | A | 1 | a0002c0003t0002g0022 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3813-5266G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45038420 | |||||||
| chr14:45038442 | C | T | 2 | a0002c0004t0001g0177 a0002c0004t0001g0178 |
2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3813-5244C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45038442 | |||||||
| chr14:45038691 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3813-4995C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45038691 | |||||||
| chr14:45039077 | A | G | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3813-4609A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45039077 | |||||||
| chr14:45039399 | G | C | 10 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 others(7): Show |
10 | HG01884.hp1 HG01891.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.3813-4287G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45039399 | |||||||
| chr14:45039432 | T | A | 25 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 others(22): Show |
25 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.3813-4254T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45039432 | |||||||
| chr14:45039432 | T | G | 56 | a0001c0001t0002g0067 a0001c0009t0002g0145 a0002c0003t0003g0008 others(53): Show |
56 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.3813-4254T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45039432 | |||||||
| chr14:45039599 | A | G | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3813-4087A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45039599 | |||||||
| chr14:45039656 | C | T | 1 | a0002c0004t0001g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3813-4030C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45039656 | |||||||
| chr14:45039723 | G | C | 14 | a0002c0004t0001g0161 a0002c0004t0001g0166 a0002c0004t0001g0167 others(11): Show |
14 | HG01496.hp1 HG02145.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.3813-3963G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45039723 | |||||||
| chr14:45039911 | C | T | 2 | a0005c0008t0002g0012 a0005c0008t0002g0017 |
2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3813-3775C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45039911 | |||||||
| chr14:45040225 | A | T | 1 | a0002c0003t0002g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3813-3461A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45040225 | |||||||
| chr14:45040489 | T | A | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3813-3197T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45040489 | |||||||
| chr14:45040752 | C | G | 10 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 others(7): Show |
10 | HG01884.hp1 HG01891.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.3813-2934C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45040752 | |||||||
| chr14:45040902 | G | A | 2 | a0005c0008t0002g0012 a0005c0008t0002g0017 |
2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3813-2784G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45040902 | |||||||
| chr14:45041218 | A | G | 30 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(27): Show |
30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.3813-2468A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45041218 | |||||||
| chr14:45041262 | A | C | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3813-2424A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45041262 | |||||||
| chr14:45041312 | A | T | 3 | a0001c0006t0001g0087 a0001c0006t0001g0098 a0001c0006t0001g0101 |
3 | HG02615.hp1 HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3813-2374A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45041312 | |||||||
| chr14:45041449 | G | C | 1 | a0001c0009t0001g0135 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3813-2237G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45041449 | |||||||
| chr14:45041465 | G | A | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3813-2221G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45041465 | |||||||
| chr14:45041652 | A | G | 1 | a0002c0003t0002g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3813-2034A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45041652 | |||||||
| chr14:45041762 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3813-1924T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45041762 | |||||||
| chr14:45041847 | G | A | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3813-1839G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45041847 | |||||||
| chr14:45041944 | G | A | 1 | a0001c0009t0002g0145 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3813-1742G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45041944 | |||||||
| chr14:45042192 | G | A | 2 | a0002c0003t0002g0003 a0002c0003t0006g0002 |
2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3813-1494G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45042192 | |||||||
| chr14:45042296 | TCTCTGGA others(22): Show |
T | 63 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(60): Show |
63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.3813-1389_3813-136 others(33): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45042296 | |||||||
| chr14:45042442 | A | AAC | 76 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 others(73): Show |
76 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.3813-1228_3813-122 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr14 | 45042442 | ||||||
| chr14:45042442 | A | AACAC | 5 | a0001c0001t0002g0067 a0002c0003t0003g0008 a0002c0003t0003g0009 others(2): Show |
5 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.3813-1230_3813-122 others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr14 | 45042442 | ||||||
| chr14:45042545 | G | C | 5 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0085 others(2): Show |
5 | HG02451.hp1 HG02559.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3813-1141G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45042545 | |||||||
| chr14:45042568 | A | T | 30 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(27): Show |
30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.3813-1118A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45042568 | |||||||
| chr14:45043083 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3813-603T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45043083 | |||||||
| chr14:45043178 | A | T | 1 | a0001c0001t0001g0093 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3813-508A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45043178 | |||||||
| chr14:45043568 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3813-118C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45043568 | |||||||
| chr14:45043878 | A | G | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3918+87A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 12/19 | chr14 | 45043878 | |||||||
| chr14:45043991 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3918+200T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 12/19 | chr14 | 45043991 | |||||||
| chr14:45044305 | C | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG01257.hp2 HG01943.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.3919-330C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 12/19 | chr14 | 45044305 | |||||||
| chr14:45044897 | T | C | 1 | a0001c0001t0001g0097 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.4154+27T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45044897 | |||||||
| chr14:45044983 | A | C | 1 | a0001c0001t0001g0090 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4154+113A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45044983 | |||||||
| chr14:45045120 | A | G | 16 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(13): Show |
16 | HG01496.hp1 HG02145.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.4154+250A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045120 | |||||||
| chr14:45045144 | C | A | 2 | a0002c0004t0001g0168 a0002c0004t0001g0169 |
2 | HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.4154+274C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045144 | |||||||
| chr14:45045350 | A | G | 34 | a0001c0009t0001g0135 a0001c0009t0002g0145 a0003c0002t0002g0005 others(31): Show |
34 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.4154+480A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045350 | |||||||
| chr14:45045531 | T | C | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4154+661T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045531 | |||||||
| chr14:45045532 | G | A | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4154+662G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045532 | |||||||
| chr14:45045535 | C | CTGTGTG | 2 | a0002c0003t0002g0051 a0002c0003t0002g0052 |
2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.4154+669_4154+674d others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045535 | ||||||
| chr14:45045535 | CTG | C | 3 | a0001c0001t0001g0121 a0001c0001t0001g0130 a0001c0001t0007g0125 |
3 | HG01943.hp2 HG03239.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.4154+673_4154+674d others(4): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045535 | ||||||
| chr14:45045541 | G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0139 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.4154+672_4154+673i others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045541 | ||||||
| chr14:45045541 | GTGTA | G | 2 | a0001c0001t0001g0123 a0001c0001t0001g0134 |
2 | HG01074.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.4154+673_4154+676d others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045541 | ||||||
| chr14:45045541 | GTGTATAT others(1): Show |
G | 9 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0077 others(6): Show |
9 | HG00438.hp1 HG00673.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.4154+673_4154+680d others(10): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045541 | ||||||
| chr14:45045541 | GTGTATAT others(3): Show |
G | 15 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0092 others(12): Show |
15 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(12): Show |
intron_variant | MODIFIER | c.4154+673_4154+682d others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045541 | ||||||
| chr14:45045541 | GTGTATAT others(5): Show |
G | 4 | a0001c0001t0001g0065 a0001c0001t0001g0076 a0001c0001t0001g0103 others(1): Show |
4 | NA18990.hp2 NA18991.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.4154+673_4154+684d others(14): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045541 | ||||||
| chr14:45045541 | GTGTATAT others(7): Show |
G | 3 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0158 |
3 | HG02109.hp2 HG02165.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.4154+673_4154+686d others(16): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045541 | ||||||
| chr14:45045543 | G | A | 49 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(46): Show |
49 | HG01071.hp1 HG01071.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.4154+673G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045543 | |||||||
| chr14:45045543 | GTATATAT others(5): Show |
G | 1 | a0003c0002t0002g0041 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.4154+703_4154+714d others(14): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045543 | ||||||
| chr14:45045543 | GTATATAT others(7): Show |
G | 29 | a0001c0009t0001g0135 a0001c0009t0002g0145 a0003c0002t0002g0005 others(26): Show |
29 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.4154+701_4154+714d others(16): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045543 | ||||||
| chr14:45045545 | A | G | 50 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(47): Show |
50 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(47): Show |
intron_variant | MODIFIER | c.4154+675A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045545 | |||||||
| chr14:45045547 | A | G | 37 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(34): Show |
37 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(34): Show |
intron_variant | MODIFIER | c.4154+677A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045547 | |||||||
| chr14:45045549 | A | G | 33 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(30): Show |
33 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(30): Show |
intron_variant | MODIFIER | c.4154+679A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045549 | |||||||
| chr14:45045551 | A | G | 27 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(24): Show |
27 | HG01109.hp2 HG01358.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.4154+681A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045551 | |||||||
| chr14:45045553 | A | G | 14 | a0002c0003t0002g0013 a0002c0003t0002g0014 a0002c0003t0002g0018 others(11): Show |
14 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.4154+683A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045553 | |||||||
| chr14:45045555 | A | G | 3 | a0002c0003t0002g0020 a0002c0003t0002g0053 a0008c0012t0002g0019 |
3 | HG01109.hp2 HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.4154+685A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045555 | |||||||
| chr14:45045557 | A | G | 2 | a0003c0002t0002g0041 a0008c0012t0002g0019 |
2 | HG02132.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.4154+687A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045557 | |||||||
| chr14:45045559 | A | G | 30 | a0001c0009t0001g0135 a0001c0009t0002g0145 a0003c0002t0002g0005 others(27): Show |
30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.4154+689A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045559 | |||||||
| chr14:45045559 | ATATATAT others(33): Show |
A | 2 | a0001c0001t0004g0084 a0001c0001t0004g0137 |
2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4154+691_4154+730d others(42): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045559 | ||||||
| chr14:45045561 | A | G | 29 | a0001c0009t0001g0135 a0001c0009t0002g0145 a0003c0002t0002g0005 others(26): Show |
29 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.4154+691A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045561 | |||||||
| chr14:45045567 | ATATATAT others(15): Show |
A | 1 | a0003c0002t0002g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4154+699_4154+720d others(24): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045567 | ||||||
| chr14:45045571 | ATATATAT others(13): Show |
A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0119 |
2 | HG02056.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.4154+703_4154+722d others(22): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045571 | ||||||
| chr14:45045571 | ATATATAT others(17): Show |
A | 2 | a0004c0005t0002g0004 a0004c0005t0002g0029 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4154+703_4154+726d others(26): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045571 | ||||||
| chr14:45045573 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0001g0116 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.4154+705_4154+722d others(20): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045573 | ||||||
| chr14:45045573 | ATATATAT others(15): Show |
A | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4154+705_4154+726d others(24): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045573 | ||||||
| chr14:45045573 | ATATATAT others(23): Show |
A | 1 | a0002c0003t0006g0002 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4154+705_4154+734d others(32): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045573 | ||||||
| chr14:45045575 | ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4154+707_4154+718d others(14): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045575 | ||||||
| chr14:45045575 | ATATATAT others(9): Show |
A | 2 | a0001c0006t0001g0098 a0001c0006t0001g0101 |
2 | HG02615.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.4154+707_4154+722d others(18): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045575 | ||||||
| chr14:45045575 | ATATATAT others(21): Show |
A | 2 | a0002c0004t0001g0177 a0002c0004t0001g0178 |
2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.4154+707_4154+734d others(30): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045575 | ||||||
| chr14:45045575 | ATATATAT others(23): Show |
A | 9 | a0002c0004t0001g0162 a0002c0004t0001g0167 a0002c0004t0001g0168 others(6): Show |
9 | HG01496.hp1 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.4154+707_4154+736d others(32): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045575 | ||||||
| chr14:45045577 | ATATATAT others(3): Show |
A | 1 | a0001c0001t0001g0094 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4154+709_4154+718d others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045577 | ||||||
| chr14:45045577 | ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0071 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4154+709_4154+720d others(14): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045577 | ||||||
| chr14:45045577 | ATATATAT others(21): Show |
A | 4 | a0002c0004t0001g0161 a0002c0004t0001g0174 a0002c0004t0001g0175 others(1): Show |
4 | HG02145.hp2 HG02622.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.4154+709_4154+736d others(30): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045577 | ||||||
| chr14:45045577 | ATATATAT others(23): Show |
A | 1 | a0002c0011t0001g0163 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4154+709_4154+738d others(32): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045577 | ||||||
| chr14:45045579 | ATATATGT others(3): Show |
A | 2 | a0001c0001t0001g0093 a0001c0006t0001g0087 |
2 | HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4154+711_4154+720d others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045579 | ||||||
| chr14:45045579 | ATATATGT others(5): Show |
A | 1 | a0001c0001t0001g0074 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4154+711_4154+722d others(14): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045579 | ||||||
| chr14:45045579 | ATATATGT others(9): Show |
A | 1 | a0001c0001t0001g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4154+711_4154+726d others(18): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045579 | ||||||
| chr14:45045579 | ATATATGT others(19): Show |
A | 2 | a0002c0004t0001g0166 a0002c0004t0001g0171 |
2 | HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.4154+711_4154+736d others(28): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045579 | ||||||
| chr14:45045581 | ATATGTG | A | 3 | a0001c0001t0001g0108 a0001c0001t0001g0120 a0009c0015t0001g0086 |
3 | HG01257.hp2 HG03710.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.4154+713_4154+718d others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045581 | ||||||
| chr14:45045581 | ATATGTGT others(1): Show |
A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0144 |
2 | HG01109.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.4154+713_4154+720d others(10): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045581 | ||||||
| chr14:45045581 | ATATGTGT others(3): Show |
A | 4 | a0001c0001t0001g0062 a0001c0001t0001g0097 a0001c0001t0001g0109 others(1): Show |
4 | HG02897.hp2 HG02976.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.4154+713_4154+722d others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045581 | ||||||
| chr14:45045581 | ATATGTGT others(17): Show |
A | 1 | a0002c0003t0002g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4154+713_4154+736d others(26): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045581 | ||||||
| chr14:45045583 | ATG | A | 3 | a0001c0001t0001g0104 a0001c0001t0001g0147 a0001c0001t0001g0159 |
3 | HG00323.hp2 HG02683.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.4154+747_4154+748d others(4): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045583 | ||||||
| chr14:45045583 | ATGTG | A | 7 | a0001c0001t0001g0085 a0001c0001t0001g0091 a0001c0001t0001g0122 others(4): Show |
7 | HG01071.hp1 HG01891.hp2 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.4154+745_4154+748d others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045583 | ||||||
| chr14:45045583 | ATGTGTG | A | 9 | a0001c0001t0001g0064 a0001c0001t0001g0072 a0001c0001t0001g0075 others(6): Show |
9 | HG01516.hp1 HG02145.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.4154+743_4154+748d others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045583 | ||||||
| chr14:45045583 | ATGTGTGT others(1): Show |
A | 4 | a0001c0001t0001g0082 a0001c0001t0001g0127 a0001c0001t0001g0141 others(1): Show |
4 | HG02132.hp2 HG02280.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.4154+741_4154+748d others(10): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045583 | ||||||
| chr14:45045583 | ATGTGTGT others(3): Show |
A | 7 | a0001c0001t0001g0110 a0001c0001t0002g0067 a0001c0001t0002g0069 others(4): Show |
7 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.4154+739_4154+748d others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045583 | ||||||
| chr14:45045583 | ATGTGTGT others(5): Show |
A | 4 | a0001c0001t0002g0070 a0002c0003t0002g0013 a0002c0003t0002g0014 others(1): Show |
4 | HG02886.hp2 HG03453.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.4154+737_4154+748d others(14): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045583 | ||||||
| chr14:45045583 | ATGTGTGT others(7): Show |
A | 1 | a0001c0001t0002g0068 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4154+735_4154+748d others(16): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045583 | ||||||
| chr14:45045583 | ATGTGTGT others(13): Show |
A | 1 | a0002c0003t0002g0049 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4154+729_4154+748d others(22): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045583 | ||||||
| chr14:45045583 | ATGTGTGT others(15): Show |
A | 1 | a0002c0003t0002g0015 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4154+727_4154+748d others(24): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045583 | ||||||
| chr14:45045585 | G | A | 27 | a0001c0001t0001g0063 a0001c0001t0001g0066 a0001c0001t0001g0078 others(24): Show |
27 | HG01074.hp2 HG01109.hp2 HG01943.hp1 others(24): Show |
intron_variant | MODIFIER | c.4154+715G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045585 | |||||||
| chr14:45045587 | G | A | 25 | a0001c0001t0001g0063 a0001c0001t0001g0066 a0001c0001t0001g0104 others(22): Show |
25 | HG00323.hp2 HG01109.hp2 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.4154+717G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045587 | |||||||
| chr14:45045589 | G | A | 24 | a0001c0001t0001g0085 a0001c0001t0001g0091 a0001c0001t0001g0104 others(21): Show |
24 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.4154+719G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045589 | |||||||
| chr14:45045591 | G | A | 20 | a0001c0001t0001g0064 a0001c0001t0001g0075 a0001c0001t0001g0080 others(17): Show |
20 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.4154+721G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045591 | |||||||
| chr14:45045593 | G | A | 12 | a0001c0001t0001g0127 a0002c0003t0002g0018 a0002c0003t0002g0021 others(9): Show |
12 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.4154+723G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045593 | |||||||
| chr14:45045595 | G | A | 12 | a0001c0001t0002g0067 a0001c0001t0002g0069 a0002c0003t0002g0003 others(9): Show |
12 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.4154+725G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045595 | |||||||
| chr14:45045597 | G | A | 14 | a0001c0001t0002g0067 a0001c0001t0002g0069 a0001c0001t0002g0070 others(11): Show |
14 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.4154+727G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045597 | |||||||
| chr14:45045599 | G | A | 13 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(10): Show |
13 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.4154+729G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045599 | |||||||
| chr14:45045601 | G | A | 11 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(8): Show |
11 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.4154+731G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045601 | |||||||
| chr14:45045603 | G | A | 11 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(8): Show |
11 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.4154+733G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045603 | |||||||
| chr14:45045603 | GTGTGTGT others(9): Show |
G | 2 | a0002c0003t0002g0055 a0002c0003t0002g0056 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.4154+735_4154+750d others(18): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045603 | ||||||
| chr14:45045605 | G | A | 7 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(4): Show |
7 | HG01358.hp2 HG01884.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.4154+735G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045605 | |||||||
| chr14:45045609 | GTGTGTGT others(3): Show |
G | 1 | a0002c0003t0002g0050 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4154+741_4154+750d others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045609 | ||||||
| chr14:45045609 | GTGTGTGT others(47): Show |
G | 27 | a0001c0009t0001g0135 a0001c0009t0002g0145 a0003c0002t0002g0005 others(24): Show |
27 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.4154+741_4154+794d others(56): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045609 | ||||||
| chr14:45045611 | GTGTGTGT others(1): Show |
G | 5 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0148 others(2): Show |
5 | HG02258.hp1 NA18990.hp2 NA19058.hp2 others(2): Show |
intron_variant | MODIFIER | c.4154+743_4154+750d others(10): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045611 | ||||||
| chr14:45045611 | GTGTGTGT others(45): Show |
G | 3 | a0003c0002t0002g0043 a0003c0002t0002g0044 a0003c0002t0008g0046 |
3 | HG03017.hp1 NA18952.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.4154+743_4154+794d others(54): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045611 | ||||||
| chr14:45045613 | GTGTGTA | G | 21 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0065 others(18): Show |
21 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.4154+745_4154+750d others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045613 | ||||||
| chr14:45045615 | GTGTA | G | 7 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0113 others(4): Show |
7 | HG00597.hp1 HG02109.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.4154+747_4154+750d others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045615 | ||||||
| chr14:45045617 | GTA | G | 3 | a0002c0003t0002g0018 a0002c0003t0002g0057 a0005c0008t0002g0012 |
3 | HG02055.hp1 HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.4154+755_4154+756d others(4): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045617 | ||||||
| chr14:45045617 | GTATA | G | 2 | a0001c0001t0001g0063 a0002c0003t0002g0052 |
2 | HG03139.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.4154+753_4154+756d others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045617 | ||||||
| chr14:45045619 | A | G | 5 | a0002c0003t0002g0021 a0002c0003t0002g0022 a0002c0003t0002g0051 others(2): Show |
5 | HG01109.hp2 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.4154+749A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045619 | |||||||
| chr14:45045621 | A | G | 1 | a0002c0003t0002g0051 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4154+751A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045621 | |||||||
| chr14:45045623 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4154+753A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045623 | |||||||
| chr14:45045623 | ATATGTAT others(39): Show |
A | 1 | a0003c0002t0002g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4154+755_4154+800d others(48): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045623 | ||||||
| chr14:45045625 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4154+755A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045625 | |||||||
| chr14:45045626 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.4154+756T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045626 | |||||||
| chr14:45045628 | TATATATA others(3): Show |
T | 1 | a0001c0001t0001g0130 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.4154+776_4154+785d others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045628 | ||||||
| chr14:45045637 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4154+767A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045637 | |||||||
| chr14:45045638 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4154+768C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045638 | |||||||
| chr14:45045646 | TACATATA others(63): Show |
T | 1 | a0001c0001t0004g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4154+790_4155-816d others(72): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045646 | ||||||
| chr14:45045656 | CACACATA others(27): Show |
C | 41 | a0001c0001t0001g0062 a0001c0001t0001g0071 a0001c0001t0001g0078 others(38): Show |
41 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.4154+833_4155-809d others(36): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045656 | ||||||
| chr14:45045669 | G | A | 30 | a0001c0009t0001g0135 a0001c0009t0002g0145 a0003c0002t0002g0005 others(27): Show |
30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.4154+799G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045669 | |||||||
| chr14:45045674 | TATATATA others(37): Show |
T | 5 | a0001c0001t0002g0067 a0002c0003t0003g0008 a0002c0003t0003g0009 others(2): Show |
5 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.4154+822_4155-810d others(46): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045674 | ||||||
| chr14:45045684 | C | T | 49 | a0001c0009t0001g0135 a0001c0009t0002g0145 a0002c0004t0001g0161 others(46): Show |
49 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.4154+814C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045684 | |||||||
| chr14:45045684 | CATATATA others(17): Show |
C | 1 | a0001c0001t0001g0153 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4154+832_4155-820d others(26): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045684 | ||||||
| chr14:45045690 | T | C | 47 | a0001c0009t0001g0135 a0001c0009t0002g0145 a0002c0004t0001g0161 others(44): Show |
47 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.4154+820T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045690 | |||||||
| chr14:45045721 | A | T | 1 | a0002c0004t0001g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4155-824A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045721 | |||||||
| chr14:45045722 | T | A | 1 | a0002c0004t0001g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4155-823T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045722 | |||||||
| chr14:45045904 | T | C | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4155-641T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045904 | |||||||
| chr14:45046149 | C | CT | 83 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(80): Show |
83 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.4155-394dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45046149 | ||||||
| chr14:45046472 | C | A | 1 | a0001c0014t0001g0136 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4155-73C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45046472 | |||||||
| chr14:45046505 | A | G | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4155-40A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45046505 | |||||||
| chr14:45046761 | A | C | 2 | a0001c0001t0004g0084 a0001c0001t0004g0137 |
2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4313+58A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45046761 | |||||||
| chr14:45047093 | G | T | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4313+390G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45047093 | |||||||
| chr14:45047117 | C | T | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4313+414C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45047117 | |||||||
| chr14:45047391 | C | CA | 21 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(18): Show |
21 | HG01496.hp1 HG01884.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.4313+702dupA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45047391 | ||||||
| chr14:45047406 | G | A | 51 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(48): Show |
51 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(48): Show |
intron_variant | MODIFIER | c.4313+703G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45047406 | |||||||
| chr14:45047497 | T | C | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4313+794T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45047497 | |||||||
| chr14:45047603 | A | G | 21 | a0001c0001t0004g0084 a0001c0001t0004g0137 a0002c0004t0001g0161 others(18): Show |
21 | HG01496.hp1 HG01884.hp2 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.4313+900A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45047603 | |||||||
| chr14:45047604 | A | G | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4313+901A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45047604 | |||||||
| chr14:45048055 | C | CA | 32 | a0001c0001t0001g0081 a0001c0001t0001g0091 a0001c0001t0001g0149 others(29): Show |
32 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.4313+1368dupA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45048055 | ||||||
| chr14:45048055 | CA | C | 21 | a0002c0003t0003g0008 a0002c0003t0003g0009 a0002c0004t0001g0162 others(18): Show |
21 | HG01106.hp2 HG01496.hp1 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.4313+1368delA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45048055 | ||||||
| chr14:45048245 | G | T | 4 | a0002c0003t0003g0008 a0002c0003t0003g0009 a0002c0016t0003g0007 others(1): Show |
4 | HG01106.hp2 HG01516.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.4313+1542G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45048245 | |||||||
| chr14:45048314 | C | CA | 13 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0090 others(10): Show |
13 | HG00438.hp1 HG01884.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.4313+1633dupA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45048314 | ||||||
| chr14:45048314 | C | CAA | 8 | a0001c0001t0001g0064 a0001c0001t0002g0067 a0001c0001t0002g0068 others(5): Show |
8 | HG01358.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.4313+1632_4313+163 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45048314 | ||||||
| chr14:45048314 | CA | C | 19 | a0001c0001t0001g0100 a0001c0001t0001g0153 a0001c0001t0004g0084 others(16): Show |
19 | HG01496.hp1 HG02132.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.4313+1633delA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45048314 | ||||||
| chr14:45048395 | G | A | 2 | a0005c0008t0002g0012 a0005c0008t0002g0017 |
2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4313+1692G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45048395 | |||||||
| chr14:45048465 | C | T | 2 | a0003c0002t0002g0036 a0003c0002t0008g0046 |
2 | HG03017.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.4313+1762C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45048465 | |||||||
| chr14:45048519 | T | A | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4313+1816T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45048519 | |||||||
| chr14:45048845 | C | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4313+2142C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45048845 | |||||||
| chr14:45048892 | G | A | 2 | a0002c0004t0001g0166 a0002c0004t0001g0167 |
2 | HG01496.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4313+2189G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45048892 | |||||||
| chr14:45049057 | C | CA | 21 | a0001c0001t0001g0062 a0001c0001t0001g0078 a0001c0001t0001g0079 others(18): Show |
21 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.4313+2383dupA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45049057 | ||||||
| chr14:45049057 | C | CAA | 10 | a0001c0001t0002g0067 a0001c0001t0002g0069 a0001c0001t0002g0070 others(7): Show |
10 | HG01109.hp2 HG01358.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.4313+2382_4313+238 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45049057 | ||||||
| chr14:45049057 | CA | C | 82 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0001c0001t0001g0071 others(79): Show |
82 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.4313+2383delA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45049057 | ||||||
| chr14:45049057 | CAA | C | 18 | a0001c0001t0001g0073 a0001c0001t0001g0080 a0001c0001t0001g0100 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.4313+2382_4313+238 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45049057 | ||||||
| chr14:45049057 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0004g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4313+2374_4313+238 others(14): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45049057 | ||||||
| chr14:45049073 | A | C | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4313+2370A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45049073 | |||||||
| chr14:45049171 | C | G | 1 | a0001c0001t0007g0125 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4313+2468C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45049171 | |||||||
| chr14:45049327 | A | G | 1 | a0002c0003t0002g0013 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4313+2624A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45049327 | |||||||
| chr14:45049382 | C | T | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4313+2679C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45049382 | |||||||
| chr14:45049489 | G | C | 1 | a0001c0014t0001g0136 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4313+2786G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45049489 | |||||||
| chr14:45049520 | A | G | 30 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(27): Show |
30 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.4313+2817A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45049520 | |||||||
| chr14:45049585 | G | A | 3 | a0004c0005t0002g0004 a0004c0005t0002g0029 a0004c0005t0002g0058 |
3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4314-2851G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45049585 | |||||||
| chr14:45049736 | A | G | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4314-2700A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45049736 | |||||||
| chr14:45049855 | A | T | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4314-2581A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45049855 | |||||||
| chr14:45049916 | C | A | 1 | a0002c0004t0001g0168 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4314-2520C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45049916 | |||||||
| chr14:45049984 | G | A | 1 | a0003c0002t0002g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.4314-2452G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45049984 | |||||||
| chr14:45050073 | ACCTAGAG others(22): Show |
A | 30 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(27): Show |
30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.4314-2362_4314-233 others(33): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45050073 | |||||||
| chr14:45050200 | A | G | 1 | a0002c0004t0001g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4314-2236A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45050200 | |||||||
| chr14:45050717 | C | T | 1 | a0002c0003t0002g0050 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4314-1719C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45050717 | |||||||
| chr14:45051124 | T | G | 1 | a0001c0001t0001g0118 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.4314-1312T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45051124 | |||||||
| chr14:45051167 | T | C | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4314-1269T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45051167 | |||||||
| chr14:45051229 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.4314-1207T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45051229 | |||||||
| chr14:45051239 | T | C | 4 | a0001c0001t0001g0088 a0001c0001t0001g0097 a0001c0001t0001g0144 others(1): Show |
4 | NA18979.hp1 NA18982.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.4314-1197T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45051239 | |||||||
| chr14:45051502 | A | AT | 30 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(27): Show |
30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.4314-931dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45051502 | ||||||
| chr14:45051553 | C | CT | 33 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(30): Show |
33 | HG00438.hp2 HG01496.hp1 HG01516.hp2 others(30): Show |
intron_variant | MODIFIER | c.4314-859dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45051553 | ||||||
| chr14:45051553 | C | CTT | 15 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(12): Show |
15 | HG01106.hp2 HG01358.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.4314-860_4314-859d others(4): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45051553 | ||||||
| chr14:45051553 | CTTT | C | 10 | a0002c0003t0002g0018 a0002c0003t0002g0020 a0002c0003t0002g0021 others(7): Show |
10 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.4314-861_4314-859d others(5): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45051553 | ||||||
| chr14:45051590 | C | T | 2 | a0002c0004t0001g0162 a0002c0011t0001g0163 |
2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.4314-846C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45051590 | |||||||
| chr14:45052019 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0126 |
2 | HG01074.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.4314-417C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45052019 | |||||||
| chr14:45052024 | A | G | 82 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.4314-412A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45052024 | |||||||
| chr14:45052091 | G | A | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4314-345G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45052091 | |||||||
| chr14:45052141 | C | T | 33 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(30): Show |
33 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.4314-295C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45052141 | |||||||
| chr14:45052207 | A | G | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4314-229A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45052207 | |||||||
| chr14:45052328 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.4314-108T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45052328 | |||||||
| chr14:45052380 | C | A | 82 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.4314-56C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45052380 | |||||||
| chr14:45052733 | A | G | 2 | a0002c0004t0001g0177 a0002c0004t0001g0178 |
2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.4440+171A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | chr14 | 45052733 | |||||||
| chr14:45052817 | A | G | 8 | a0002c0003t0002g0018 a0002c0003t0002g0021 a0002c0003t0002g0022 others(5): Show |
8 | HG01109.hp2 HG02109.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.4440+255A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | chr14 | 45052817 | |||||||
| chr14:45053032 | CT | C | 21 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0002g0067 others(18): Show |
21 | HG00323.hp2 HG01106.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.4440+490delT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr14 | 45053032 | ||||||
| chr14:45053032 | CTT | C | 13 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 others(10): Show |
13 | HG01516.hp2 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.4440+489_4440+490d others(4): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr14 | 45053032 | ||||||
| chr14:45053142 | G | A | 10 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 others(7): Show |
10 | HG01884.hp1 HG01891.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.4440+580G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | chr14 | 45053142 | |||||||
| chr14:45053190 | C | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0160 |
2 | HG01993.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.4440+628C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | chr14 | 45053190 | |||||||
| chr14:45053195 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4440+633C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | chr14 | 45053195 | |||||||
| chr14:45053202 | C | A | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4440+640C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | chr14 | 45053202 | |||||||
| chr14:45053293 | G | A | 2 | a0001c0001t0004g0084 a0001c0001t0004g0137 |
2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4440+731G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | chr14 | 45053293 | |||||||
| chr14:45053456 | A | T | 82 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.4440+894A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | chr14 | 45053456 | |||||||
| chr14:45053460 | A | T | 1 | a0002c0003t0002g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4440+898A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | chr14 | 45053460 | |||||||
| chr14:45053463 | AAT | A | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4440+904_4440+905d others(4): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr14 | 45053463 | ||||||
| chr14:45053609 | C | T | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4441-822C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | chr14 | 45053609 | |||||||
| chr14:45053624 | T | C | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4441-807T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | chr14 | 45053624 | |||||||
| chr14:45053843 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4441-588T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | chr14 | 45053843 | |||||||
| chr14:45053870 | A | ATATTAT | 11 | a0002c0003t0002g0018 a0002c0003t0002g0020 a0002c0003t0002g0021 others(8): Show |
11 | HG02055.hp1 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.4441-541_4441-536d others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr14 | 45053870 | ||||||
| chr14:45053870 | A | ATATTATT others(2): Show |
4 | a0002c0003t0002g0053 a0002c0003t0002g0054 a0002c0003t0002g0055 others(1): Show |
4 | HG01109.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.4441-544_4441-536d others(11): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr14 | 45053870 | ||||||
| chr14:45053918 | C | T | 3 | a0004c0005t0002g0004 a0004c0005t0002g0029 a0004c0005t0002g0058 |
3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4441-513C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | chr14 | 45053918 | |||||||
| chr14:45054715 | A | G | 1 | a0003c0002t0002g0037 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.4559+166A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45054715 | |||||||
| chr14:45054751 | G | A | 4 | a0002c0003t0003g0008 a0002c0003t0003g0009 a0002c0016t0003g0007 others(1): Show |
4 | HG01106.hp2 HG01516.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.4559+202G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45054751 | |||||||
| chr14:45054994 | T | C | 33 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(30): Show |
33 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.4559+445T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45054994 | |||||||
| chr14:45055305 | C | T | 3 | a0002c0003t0002g0050 a0002c0003t0002g0051 a0002c0003t0002g0052 |
3 | HG02486.hp2 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4559+756C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45055305 | |||||||
| chr14:45055575 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.4559+1026C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45055575 | |||||||
| chr14:45055586 | C | T | 1 | a0009c0015t0001g0086 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4559+1037C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45055586 | |||||||
| chr14:45055736 | G | A | 63 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(60): Show |
63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.4559+1187G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45055736 | |||||||
| chr14:45055785 | A | T | 2 | a0001c0001t0001g0089 a0001c0001t0001g0114 |
2 | HG01257.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.4559+1236A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45055785 | |||||||
| chr14:45055800 | C | CA | 5 | a0001c0001t0001g0081 a0001c0001t0001g0096 a0001c0001t0001g0160 others(2): Show |
5 | HG01993.hp1 HG02056.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.4559+1270dupA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45055800 | ||||||
| chr14:45055800 | C | CAA | 58 | a0001c0001t0001g0113 a0001c0001t0002g0067 a0001c0001t0002g0068 others(55): Show |
58 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.4559+1269_4559+127 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45055800 | ||||||
| chr14:45055800 | C | CAAA | 19 | a0001c0001t0002g0069 a0002c0003t0002g0021 a0002c0003t0002g0051 others(16): Show |
19 | HG01496.hp1 HG01884.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.4559+1268_4559+127 others(7): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45055800 | ||||||
| chr14:45055842 | C | CT | 10 | a0001c0001t0001g0063 a0001c0001t0001g0160 a0002c0003t0002g0050 others(7): Show |
10 | HG02451.hp2 HG02717.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.4559+1311dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45055842 | ||||||
| chr14:45055842 | C | CTT | 17 | a0002c0004t0001g0162 a0002c0004t0001g0166 a0002c0004t0001g0167 others(14): Show |
17 | HG01496.hp1 HG01884.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.4559+1310_4559+131 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45055842 | ||||||
| chr14:45055999 | C | G | 4 | a0002c0003t0003g0008 a0002c0003t0003g0009 a0002c0016t0003g0007 others(1): Show |
4 | HG01106.hp2 HG01516.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.4559+1450C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45055999 | |||||||
| chr14:45056296 | A | C | 1 | a0001c0001t0001g0062 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4559+1747A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45056296 | |||||||
| chr14:45056297 | G | T | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4559+1748G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45056297 | |||||||
| chr14:45056396 | T | C | 2 | a0005c0008t0002g0012 a0005c0008t0002g0017 |
2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4559+1847T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45056396 | |||||||
| chr14:45056411 | T | C | 33 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(30): Show |
33 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.4559+1862T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45056411 | |||||||
| chr14:45056770 | T | G | 3 | a0004c0005t0002g0004 a0004c0005t0002g0029 a0004c0005t0002g0058 |
3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4559+2221T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45056770 | |||||||
| chr14:45056838 | C | T | 1 | a0002c0004t0001g0161 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4559+2289C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45056838 | |||||||
| chr14:45056942 | TTTTA | T | 15 | a0002c0003t0002g0018 a0002c0003t0002g0020 a0002c0003t0002g0021 others(12): Show |
15 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.4559+2413_4559+241 others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45056942 | ||||||
| chr14:45056962 | A | G | 3 | a0001c0001t0001g0077 a0002c0004t0001g0174 a0002c0004t0001g0175 |
3 | HG00673.hp1 HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.4559+2413A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45056962 | |||||||
| chr14:45056962 | ATTTG | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0129 |
2 | HG01071.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.4559+2425_4559+242 others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45056962 | ||||||
| chr14:45056966 | G | A | 2 | a0002c0004t0001g0177 a0002c0004t0001g0178 |
2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.4559+2417G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45056966 | |||||||
| chr14:45057070 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.4559+2521C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45057070 | |||||||
| chr14:45057285 | C | G | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4559+2736C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45057285 | |||||||
| chr14:45057603 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4559+3054C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45057603 | |||||||
| chr14:45057737 | T | C | 1 | a0006c0007t0001g0164 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4559+3188T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45057737 | |||||||
| chr14:45057846 | T | C | 1 | a0001c0001t0004g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4559+3297T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45057846 | |||||||
| chr14:45057869 | G | A | 1 | a0001c0001t0007g0125 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4559+3320G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45057869 | |||||||
| chr14:45058142 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4559+3593T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45058142 | |||||||
| chr14:45058273 | T | C | 1 | a0002c0003t0002g0014 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4559+3724T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45058273 | |||||||
| chr14:45058297 | C | CT | 7 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0009t0002g0145 others(4): Show |
7 | HG02055.hp1 HG02132.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.4559+3763dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45058297 | ||||||
| chr14:45058311 | T | C | 1 | a0002c0003t0002g0052 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4559+3762T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45058311 | |||||||
| chr14:45058331 | A | G | 64 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(61): Show |
64 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.4559+3782A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45058331 | |||||||
| chr14:45058417 | C | T | 2 | a0002c0004t0001g0162 a0002c0011t0001g0163 |
2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.4559+3868C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45058417 | |||||||
| chr14:45059523 | C | T | 1 | a0005c0008t0002g0017 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4559+4974C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45059523 | |||||||
| chr14:45059544 | G | A | 25 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 others(22): Show |
25 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.4559+4995G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45059544 | |||||||
| chr14:45059634 | C | T | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4559+5085C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45059634 | |||||||
| chr14:45059659 | A | AAAAAC | 6 | a0001c0001t0001g0113 a0001c0001t0002g0067 a0002c0003t0003g0008 others(3): Show |
6 | HG00597.hp1 HG01106.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.4559+5135_4559+513 others(9): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45059659 | ||||||
| chr14:45059659 | A | C | 1 | a0001c0001t0001g0152 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.4559+5110A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45059659 | |||||||
| chr14:45059659 | AAAAACAA others(3): Show |
A | 13 | a0002c0004t0001g0166 a0002c0004t0001g0167 a0002c0004t0001g0168 others(10): Show |
13 | HG01496.hp1 HG02280.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.4559+5130_4559+513 others(14): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45059659 | ||||||
| chr14:45059742 | G | T | 5 | a0001c0001t0002g0067 a0002c0003t0003g0008 a0002c0003t0003g0009 others(2): Show |
5 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.4559+5193G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45059742 | |||||||
| chr14:45059817 | C | A | 81 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(78): Show |
81 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.4559+5268C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45059817 | |||||||
| chr14:45059842 | G | A | 8 | a0002c0003t0002g0018 a0002c0003t0002g0021 a0002c0003t0002g0022 others(5): Show |
8 | HG01109.hp2 HG02109.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.4559+5293G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45059842 | |||||||
| chr14:45059913 | A | AT | 9 | a0001c0001t0001g0062 a0001c0001t0001g0078 a0001c0001t0001g0079 others(6): Show |
9 | HG02258.hp2 HG02809.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.4559+5381dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45059913 | ||||||
| chr14:45059913 | AT | A | 21 | a0001c0001t0001g0130 a0002c0004t0001g0161 a0002c0004t0001g0162 others(18): Show |
21 | HG01496.hp1 HG01884.hp2 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.4559+5381delT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45059913 | ||||||
| chr14:45059934 | A | G | 2 | a0002c0004t0001g0172 a0002c0004t0001g0173 |
2 | HG02280.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.4559+5385A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45059934 | |||||||
| chr14:45059983 | G | T | 1 | a0002c0004t0001g0161 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4559+5434G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45059983 | |||||||
| chr14:45060119 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4559+5570C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45060119 | |||||||
| chr14:45060217 | C | CT | 31 | a0001c0001t0001g0095 a0001c0001t0001g0102 a0001c0001t0001g0103 others(28): Show |
31 | HG01106.hp2 HG01358.hp2 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.4559+5684dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45060217 | ||||||
| chr14:45060683 | T | C | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4560-5895T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45060683 | |||||||
| chr14:45060882 | G | T | 15 | a0002c0003t0002g0018 a0002c0003t0002g0020 a0002c0003t0002g0021 others(12): Show |
15 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.4560-5696G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45060882 | |||||||
| chr14:45060907 | A | G | 1 | a0009c0015t0001g0086 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4560-5671A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45060907 | |||||||
| chr14:45060986 | C | T | 5 | a0001c0001t0002g0067 a0002c0003t0003g0008 a0002c0003t0003g0009 others(2): Show |
5 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.4560-5592C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45060986 | |||||||
| chr14:45061049 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4560-5529A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45061049 | |||||||
| chr14:45061087 | G | C | 1 | a0001c0001t0001g0147 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4560-5491G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45061087 | |||||||
| chr14:45061392 | T | G | 1 | a0001c0001t0001g0088 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.4560-5186T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45061392 | |||||||
| chr14:45061734 | G | C | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4560-4844G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45061734 | |||||||
| chr14:45062124 | T | C | 1 | a0002c0004t0001g0161 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4560-4454T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45062124 | |||||||
| chr14:45062447 | C | T | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4560-4131C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45062447 | |||||||
| chr14:45062690 | T | C | 1 | a0002c0003t0006g0002 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4560-3888T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45062690 | |||||||
| chr14:45062694 | T | G | 1 | a0003c0002t0002g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4560-3884T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45062694 | |||||||
| chr14:45062781 | G | T | 30 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(27): Show |
30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.4560-3797G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45062781 | |||||||
| chr14:45062835 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4560-3743C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45062835 | |||||||
| chr14:45063070 | T | C | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG01257.hp2 HG01943.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.4560-3508T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45063070 | |||||||
| chr14:45063479 | G | GT | 14 | a0001c0001t0001g0060 a0001c0001t0001g0064 a0001c0001t0001g0066 others(11): Show |
14 | HG01106.hp2 HG02055.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.4560-3077dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45063479 | ||||||
| chr14:45063479 | G | GTTT | 18 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0002c0003t0002g0003 others(15): Show |
18 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.4560-3079_4560-307 others(7): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45063479 | ||||||
| chr14:45063479 | G | GTTTT | 11 | a0001c0001t0002g0070 a0002c0003t0002g0013 a0002c0003t0002g0015 others(8): Show |
11 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.4560-3080_4560-307 others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45063479 | ||||||
| chr14:45063479 | G | GTTTTT | 7 | a0002c0004t0001g0166 a0002c0004t0001g0167 a0002c0004t0001g0171 others(4): Show |
7 | HG01496.hp1 HG02723.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.4560-3081_4560-307 others(9): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45063479 | ||||||
| chr14:45063479 | G | GTTTTTT | 6 | a0002c0004t0001g0162 a0002c0004t0001g0170 a0002c0004t0001g0173 others(3): Show |
6 | HG02280.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.4560-3082_4560-307 others(10): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45063479 | ||||||
| chr14:45063479 | G | GTTTTTTT others(10): Show |
2 | a0001c0001t0002g0067 a0010c0010t0002g0010 |
2 | HG01358.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4560-3093_4560-307 others(21): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45063479 | ||||||
| chr14:45063479 | G | GTTTTTTT others(14): Show |
1 | a0002c0016t0003g0007 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4560-3097_4560-307 others(25): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45063479 | ||||||
| chr14:45063479 | G | GTTTTTTT others(16): Show |
1 | a0002c0003t0003g0008 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.4560-3077_4560-307 others(27): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45063479 | ||||||
| chr14:45063479 | GTTTTT | G | 31 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(28): Show |
31 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.4560-3081_4560-307 others(9): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45063479 | ||||||
| chr14:45063545 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.4560-3033C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45063545 | |||||||
| chr14:45063629 | G | T | 3 | a0004c0005t0002g0004 a0004c0005t0002g0029 a0004c0005t0002g0058 |
3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4560-2949G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45063629 | |||||||
| chr14:45063630 | C | T | 3 | a0004c0005t0002g0004 a0004c0005t0002g0029 a0004c0005t0002g0058 |
3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4560-2948C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45063630 | |||||||
| chr14:45063656 | T | A | 2 | a0003c0002t0002g0031 a0003c0002t0002g0032 |
2 | HG00673.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.4560-2922T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45063656 | |||||||
| chr14:45063745 | T | C | 2 | a0002c0003t0002g0003 a0002c0003t0006g0002 |
2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.4560-2833T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45063745 | |||||||
| chr14:45063804 | T | C | 6 | a0001c0001t0002g0067 a0002c0003t0003g0008 a0002c0003t0003g0009 others(3): Show |
6 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.4560-2774T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45063804 | |||||||
| chr14:45063921 | A | T | 1 | a0001c0001t0001g0062 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4560-2657A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45063921 | |||||||
| chr14:45063929 | T | G | 2 | a0002c0004t0001g0168 a0002c0004t0001g0169 |
2 | HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.4560-2649T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45063929 | |||||||
| chr14:45064128 | T | C | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | NA18968.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.4560-2450T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45064128 | |||||||
| chr14:45064134 | C | T | 1 | a0002c0004t0001g0162 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4560-2444C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45064134 | |||||||
| chr14:45064289 | A | T | 1 | a0002c0004t0001g0174 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4560-2289A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45064289 | |||||||
| chr14:45064291 | A | T | 1 | a0002c0004t0001g0174 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4560-2287A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45064291 | |||||||
| chr14:45064532 | G | T | 1 | a0002c0004t0001g0173 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4560-2046G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45064532 | |||||||
| chr14:45064690 | A | G | 1 | a0002c0003t0002g0050 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4560-1888A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45064690 | |||||||
| chr14:45064882 | TA | T | 4 | a0002c0003t0003g0008 a0002c0003t0003g0009 a0002c0016t0003g0007 others(1): Show |
4 | HG01106.hp2 HG01516.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.4560-1695delA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45064882 | |||||||
| chr14:45064908 | A | G | 26 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(23): Show |
26 | HG01109.hp2 HG01358.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.4560-1670A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45064908 | |||||||
| chr14:45064948 | TTTG | T | 29 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(26): Show |
29 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.4560-1627_4560-162 others(7): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45064948 | ||||||
| chr14:45065184 | TAGATAGA others(1): Show |
T | 32 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(29): Show |
32 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.4560-1386_4560-137 others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45065184 | ||||||
| chr14:45065655 | G | A | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4560-923G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45065655 | |||||||
| chr14:45065691 | C | G | 2 | a0001c0001t0001g0091 a0001c0001t0001g0149 |
2 | HG02165.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.4560-887C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45065691 | |||||||
| chr14:45066373 | T | TAG | 2 | a0003c0002t0002g0031 a0003c0002t0002g0032 |
2 | HG00673.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.4560-204_4560-203i others(4): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45066373 | ||||||
| chr14:45066470 | T | C | 30 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(27): Show |
30 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.4560-108T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45066470 | |||||||
| chr14:45066553 | T | C | 1 | a0002c0016t0003g0007 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4560-25T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45066553 | |||||||
| chr14:45066782 | G | A | 83 | a0001c0001t0001g0105 a0001c0001t0002g0067 a0001c0001t0002g0068 others(80): Show |
83 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.4749+15G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 17/19 | chr14 | 45066782 | |||||||
| chr14:45066862 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.4749+95G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 17/19 | chr14 | 45066862 | |||||||
| chr14:45067157 | T | G | 82 | a0001c0001t0001g0105 a0001c0001t0002g0067 a0001c0001t0002g0068 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.4749+390T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 17/19 | chr14 | 45067157 | |||||||
| chr14:45067312 | G | A | 29 | a0001c0009t0002g0145 a0003c0002t0002g0005 a0003c0002t0002g0006 others(26): Show |
29 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.4749+545G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 17/19 | chr14 | 45067312 | |||||||
| chr14:45067393 | A | G | 1 | a0001c0014t0001g0136 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4749+626A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 17/19 | chr14 | 45067393 | |||||||
| chr14:45067428 | G | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0130 |
2 | HG03239.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.4749+661G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 17/19 | chr14 | 45067428 | |||||||
| chr14:45067583 | A | G | 1 | a0003c0002t0002g0031 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.4749+816A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 17/19 | chr14 | 45067583 | |||||||
| chr14:45068014 | T | C | 63 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(60): Show |
63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.4750-410T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 17/19 | chr14 | 45068014 | |||||||
| chr14:45068099 | A | G | 1 | a0004c0005t0002g0029 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4750-325A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 17/19 | chr14 | 45068099 | |||||||
| chr14:45068366 | T | C | 4 | a0002c0004t0001g0168 a0002c0004t0001g0169 a0006c0007t0001g0164 others(1): Show |
4 | HG02630.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.4750-58T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 17/19 | chr14 | 45068366 | |||||||
| chr14:45068394 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.4750-30A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 17/19 | chr14 | 45068394 | |||||||
| chr14:45068661 | G | A | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4969+18G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45068661 | |||||||
| chr14:45069198 | A | G | 82 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(79): Show |
82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.4969+555A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45069198 | |||||||
| chr14:45069229 | T | C | 5 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0152 others(2): Show |
5 | HG00323.hp2 HG01106.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.4969+586T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45069229 | |||||||
| chr14:45069283 | C | T | 3 | a0004c0005t0002g0004 a0004c0005t0002g0029 a0004c0005t0002g0058 |
3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4969+640C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45069283 | |||||||
| chr14:45069335 | C | G | 1 | a0003c0002t0002g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4969+692C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45069335 | |||||||
| chr14:45069466 | T | TTG | 3 | a0004c0005t0002g0004 a0004c0005t0002g0029 a0004c0005t0002g0058 |
3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4969+823_4969+824i others(4): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45069466 | |||||||
| chr14:45069467 | A | G | 3 | a0004c0005t0002g0004 a0004c0005t0002g0029 a0004c0005t0002g0058 |
3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4969+824A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45069467 | |||||||
| chr14:45069630 | T | G | 11 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(8): Show |
11 | HG01358.hp2 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.4969+987T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45069630 | |||||||
| chr14:45069765 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4969+1122G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45069765 | |||||||
| chr14:45070296 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4970-1416C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45070296 | |||||||
| chr14:45070311 | A | C | 63 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(60): Show |
63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.4970-1401A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45070311 | |||||||
| chr14:45070600 | A | G | 2 | a0003c0002t0002g0011 a0003c0002t0002g0040 |
2 | HG02056.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.4970-1112A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45070600 | |||||||
| chr14:45070835 | C | A | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4970-877C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45070835 | |||||||
| chr14:45070910 | C | CTGT | 24 | a0001c0001t0001g0080 a0001c0001t0001g0083 a0001c0001t0001g0151 others(21): Show |
24 | HG01106.hp1 HG01106.hp2 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.4970-776_4970-774d others(5): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr14 | 45070910 | ||||||
| chr14:45070910 | C | CTGTTGT | 2 | a0002c0004t0001g0174 a0002c0004t0001g0175 |
2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.4970-779_4970-774d others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr14 | 45070910 | ||||||
| chr14:45070910 | CTGTTGTT others(5): Show |
C | 1 | a0001c0001t0001g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4970-785_4970-774d others(14): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr14 | 45070910 | ||||||
| chr14:45071078 | C | T | 10 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 others(7): Show |
10 | HG01884.hp1 HG01891.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.4970-634C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45071078 | |||||||
| chr14:45071216 | G | A | 2 | a0001c0001t0004g0084 a0001c0001t0004g0137 |
2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4970-496G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45071216 | |||||||
| chr14:45071250 | A | G | 10 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 others(7): Show |
10 | HG01884.hp1 HG01891.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.4970-462A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45071250 | |||||||
| chr14:45071285 | GT | G | 117 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(114): Show |
117 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.4970-408delT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr14 | 45071285 | ||||||
| chr14:45071285 | GTT | G | 55 | a0001c0001t0001g0071 a0001c0001t0001g0088 a0001c0001t0001g0097 others(52): Show |
55 | HG00323.hp1 HG00597.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.4970-409_4970-408d others(4): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr14 | 45071285 | ||||||
| chr14:45071404 | T | C | 18 | a0002c0004t0001g0161 a0002c0004t0001g0162 a0002c0004t0001g0166 others(15): Show |
18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4970-308T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45071404 | |||||||
| chr14:45071452 | C | A | 33 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(30): Show |
33 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(30): Show |
intron_variant | MODIFIER | c.4970-260C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45071452 | |||||||
| chr14:45071582 | G | A | 2 | a0002c0004t0001g0177 a0002c0004t0001g0178 |
2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.4970-130G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45071582 | |||||||
| chr14:45071640 | A | G | 2 | a0005c0008t0002g0012 a0005c0008t0002g0017 |
2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4970-72A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45071640 | |||||||
| chr14:45071647 | G | A | 1 | a0007c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4970-65G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45071647 | |||||||
| chr14:45071663 | A | G | 26 | a0002c0003t0002g0018 a0002c0003t0002g0021 a0002c0003t0002g0022 others(23): Show |
26 | HG01109.hp2 HG01496.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.4970-49A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45071663 | |||||||
| chr14:45071677 | C | T | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4970-35C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45071677 | |||||||
| chr14:45071964 | T | G | 1 | a0003c0002t0002g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5056+166T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 19/19 | chr14 | 45071964 | |||||||
| chr14:45072458 | G | A | 2 | a0001c0001t0001g0071 a0002c0003t0002g0050 |
2 | HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.5056+660G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 19/19 | chr14 | 45072458 | |||||||
| chr14:45072542 | A | G | 2 | a0002c0003t0002g0003 a0002c0003t0006g0002 |
2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.5056+744A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 19/19 | chr14 | 45072542 | |||||||
| chr14:45072761 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0092 |
2 | HG00438.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.5057-535G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 19/19 | chr14 | 45072761 | |||||||
| chr14:45072828 | C | T | 30 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(27): Show |
30 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.5057-468C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 19/19 | chr14 | 45072828 | |||||||
| chr14:45072896 | G | A | 3 | a0001c0001t0001g0064 a0001c0001t0001g0082 a0001c0001t0001g0083 |
3 | HG02145.hp1 HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.5057-400G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 19/19 | chr14 | 45072896 | |||||||
| chr14:45073179 | T | C | 15 | a0002c0003t0002g0018 a0002c0003t0002g0020 a0002c0003t0002g0021 others(12): Show |
15 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.5057-117T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 19/19 | chr14 | 45073179 | |||||||
| chr14:45073269 | C | A | 1 | a0001c0001t0001g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5057-27C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 19/19 | chr14 | 45073269 |