Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57579 |
| ensemblid | ENSG00000082269.17 |
| hgncid | 21084 |
| symbol | FAM135A |
| name | family with sequence similarity 135 member A |
| refseq_nuc | NM_001162529.3 |
| refseq_prot | NP_001156001.1 |
| ensembl_nuc | ENST00000418814.7 |
| ensembl_prot | ENSP00000410768.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 70413508 |
| end | 70561174 |
| strand | + |
| ver | v1.2 |
| region | chr6:70413508-70561174 |
| region5000 | chr6:70408508-70566174 |
| regionname0 | FAM135A_chr6_70413508_70561174 |
| regionname5000 | FAM135A_chr6_70408508_70566174 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1515 | 191 | 70 | 49 | 48 | 7 | 16 | 40 | FAM135A_chr6_70408508_70566174 | FAM135A | MTEVQ others(1510): Show |
chr6 | 70408508 | 70566174 |
| a0002 | 0/1 | 1515 | 57 | 3 | 8 | 32 | 5 | 8 | 25 | FAM135A_chr6_70408508_70566174 | FAM135A | MTEVQ others(1510): Show |
chr6 | 70408508 | 70566174 |
| a0003 | 0/0 | 1515 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | MTEVQ others(1510): Show |
chr6 | 70408508 | 70566174 |
| a0004 | 0/0 | 1515 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | MTEVQ others(1510): Show |
chr6 | 70408508 | 70566174 |
| a0005 | 0/0 | 1515 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | MTEVQ others(1510): Show |
chr6 | 70408508 | 70566174 |
| a0006 | 0/0 | 1515 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAM135A_chr6_70408508_70566174 | FAM135A | MTEVQ others(1510): Show |
chr6 | 70408508 | 70566174 |
| a0007 | 0/0 | 1515 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | MTEVQ others(1510): Show |
chr6 | 70408508 | 70566174 |
| a0008 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | MTEVQ others(1510): Show |
chr6 | 70408508 | 70566174 |
| a0009 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | MTEVQ others(1510): Show |
chr6 | 70408508 | 70566174 |
| a0010 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | MTEVQ others(1510): Show |
chr6 | 70408508 | 70566174 |
| a0011 | 0/0 | 1515 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | MTEVQ others(1510): Show |
chr6 | 70408508 | 70566174 |
| a0012 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | MTEVQ others(1510): Show |
chr6 | 70408508 | 70566174 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 4545 | 91 | 29 | 29 | 16 | 5 | 11 | FAM135A_chr6_70408508_70566174 | FAM135A | ATGAC others(4540): Show |
chr6 | 70408508 | 70566174 | ||
| a0001c0002 | 0/0 | 4545 | 65 | 10 | 16 | 32 | 2 | 5 | FAM135A_chr6_70408508_70566174 | FAM135A | ATGAC others(4540): Show |
chr6 | 70408508 | 70566174 | ||
| a0001c0004 | 0/0 | 4545 | 31 | 28 | 3 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | ATGAC others(4540): Show |
chr6 | 70408508 | 70566174 | ||
| a0001c0009 | 0/0 | 4545 | 2 | 2 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | ATGAC others(4540): Show |
chr6 | 70408508 | 70566174 | ||
| a0001c0012 | 0/0 | 4545 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | ATGAC others(4540): Show |
chr6 | 70408508 | 70566174 | ||
| a0001c0013 | 0/0 | 4545 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | ATGAC others(4540): Show |
chr6 | 70408508 | 70566174 | ||
| a0002c0003 | 0/1 | 4545 | 51 | 3 | 7 | 27 | 5 | 8 | FAM135A_chr6_70408508_70566174 | FAM135A | ATGAC others(4540): Show |
chr6 | 70408508 | 70566174 | ||
| a0002c0006 | 0/0 | 4545 | 5 | 0 | 0 | 5 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | ATGAC others(4540): Show |
chr6 | 70408508 | 70566174 | ||
| a0002c0016 | 0/0 | 4545 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | ATGAC others(4540): Show |
chr6 | 70408508 | 70566174 | ||
| a0003c0005 | 0/0 | 4545 | 8 | 7 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | ATGAC others(4540): Show |
chr6 | 70408508 | 70566174 | ||
| a0004c0008 | 0/0 | 4545 | 2 | 0 | 2 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | ATGAC others(4540): Show |
chr6 | 70408508 | 70566174 | ||
| a0005c0010 | 0/0 | 4545 | 2 | 2 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | ATGAC others(4540): Show |
chr6 | 70408508 | 70566174 | ||
| a0006c0007 | 0/0 | 4545 | 2 | 0 | 0 | 2 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | ATGAC others(4540): Show |
chr6 | 70408508 | 70566174 | ||
| a0007c0019 | 0/0 | 4545 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | ATGAC others(4540): Show |
chr6 | 70408508 | 70566174 | ||
| a0008c0017 | 0/0 | 4545 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | ATGAC others(4540): Show |
chr6 | 70408508 | 70566174 | ||
| a0009c0014 | 0/0 | 4545 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | ATGAC others(4540): Show |
chr6 | 70408508 | 70566174 | ||
| a0010c0018 | 0/0 | 4545 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | ATGAC others(4540): Show |
chr6 | 70408508 | 70566174 | ||
| a0011c0011 | 0/0 | 4545 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | ATGAC others(4540): Show |
chr6 | 70408508 | 70566174 | ||
| a0012c0015 | 0/0 | 4545 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | ATGAC others(4540): Show |
chr6 | 70408508 | 70566174 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 6215 | 91 | 29 | 29 | 16 | 5 | 11 | FAM135A_chr6_70408508_70566174 | FAM135A | GCTGG others(6210): Show |
chr6 | 70408508 | 70566174 |
| a0001c0002t0002 | 0/0 | 6215 | 65 | 10 | 16 | 32 | 2 | 5 | FAM135A_chr6_70408508_70566174 | FAM135A | GCTGG others(6210): Show |
chr6 | 70408508 | 70566174 |
| a0001c0004t0001 | 0/0 | 6215 | 4 | 3 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | GCTGG others(6210): Show |
chr6 | 70408508 | 70566174 |
| a0001c0004t0003 | 0/0 | 6215 | 24 | 23 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | GCTGG others(6210): Show |
chr6 | 70408508 | 70566174 |
| a0001c0004t0004 | 0/0 | 6215 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | GCTGG others(6210): Show |
chr6 | 70408508 | 70566174 |
| a0001c0004t0006 | 0/0 | 6215 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | GCTGG others(6210): Show |
chr6 | 70408508 | 70566174 |
| a0001c0004t0007 | 0/0 | 6215 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | GCTGG others(6210): Show |
chr6 | 70408508 | 70566174 |
| a0001c0009t0001 | 0/0 | 6215 | 2 | 2 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | GCTGG others(6210): Show |
chr6 | 70408508 | 70566174 |
| a0001c0012t0001 | 0/0 | 6215 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | GCTGG others(6210): Show |
chr6 | 70408508 | 70566174 |
| a0001c0013t0001 | 0/0 | 6215 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | GCTGG others(6210): Show |
chr6 | 70408508 | 70566174 |
| a0002c0003t0001 | 0/1 | 6215 | 50 | 3 | 7 | 26 | 5 | 8 | FAM135A_chr6_70408508_70566174 | FAM135A | GCTGG others(6210): Show |
chr6 | 70408508 | 70566174 |
| a0002c0003t0008 | 0/0 | 6215 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | GCTGG others(6210): Show |
chr6 | 70408508 | 70566174 |
| a0002c0006t0001 | 0/0 | 6215 | 5 | 0 | 0 | 5 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | GCTGG others(6210): Show |
chr6 | 70408508 | 70566174 |
| a0002c0016t0002 | 0/0 | 6215 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | GCTGG others(6210): Show |
chr6 | 70408508 | 70566174 |
| a0003c0005t0001 | 0/0 | 6215 | 8 | 7 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | GCTGG others(6210): Show |
chr6 | 70408508 | 70566174 |
| a0004c0008t0004 | 0/0 | 6215 | 2 | 0 | 2 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | GCTGG others(6210): Show |
chr6 | 70408508 | 70566174 |
| a0005c0010t0003 | 0/0 | 6215 | 2 | 2 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | GCTGG others(6210): Show |
chr6 | 70408508 | 70566174 |
| a0006c0007t0001 | 0/0 | 6215 | 2 | 0 | 0 | 2 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | GCTGG others(6210): Show |
chr6 | 70408508 | 70566174 |
| a0007c0019t0001 | 0/0 | 6215 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | GCTGG others(6210): Show |
chr6 | 70408508 | 70566174 |
| a0008c0017t0001 | 0/0 | 6215 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | GCTGG others(6210): Show |
chr6 | 70408508 | 70566174 |
| a0009c0014t0003 | 0/0 | 6215 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | GCTGG others(6210): Show |
chr6 | 70408508 | 70566174 |
| a0010c0018t0005 | 0/0 | 6215 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | GCTGG others(6210): Show |
chr6 | 70408508 | 70566174 |
| a0011c0011t0002 | 0/0 | 6215 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | GCTGG others(6210): Show |
chr6 | 70408508 | 70566174 |
| a0012c0015t0005 | 0/0 | 6215 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | GCTGG others(6210): Show |
chr6 | 70408508 | 70566174 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0032 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0006g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0004t0007g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0009t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0009t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0012t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0001c0013t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0035 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0003t0008g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0006t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0006t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0006t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0006t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0006t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0002c0016t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0003c0005t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0003c0005t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0003c0005t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0003c0005t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0003c0005t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0003c0005t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0003c0005t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0003c0005t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0004c0008t0004g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0004c0008t0004g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0005c0010t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0005c0010t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0006c0007t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0006c0007t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0007c0019t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0008c0017t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0009c0014t0003g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0010c0018t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0011c0011t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| a0012c0015t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | GBR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00140 | hp2 | a0002 | c0003 | t0001 | g0214 | EUR | GBR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0253 | EUR | FIN | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00280 | hp2 | a0002 | c0003 | t0001 | g0118 | EUR | FIN | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0202 | EAS | CHS | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00597 | hp2 | a0002 | c0006 | t0001 | g0034 | EAS | CHS | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0220 | EAS | CHS | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00609 | hp2 | a0002 | c0003 | t0001 | g0132 | EAS | CHS | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0219 | EAS | CHS | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00621 | hp2 | a0002 | c0006 | t0001 | g0138 | EAS | CHS | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0257 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0258 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0172 | EAS | CHS | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0183 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0200 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0179 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0173 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01069 | hp1 | a0001 | c0004 | t0003 | g0233 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01074 | hp2 | a0004 | c0008 | t0004 | g0003 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0201 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0177 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01109 | hp1 | a0001 | c0004 | t0001 | g0160 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0174 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01168 | hp1 | a0002 | c0003 | t0001 | g0119 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01192 | hp2 | a0001 | c0004 | t0006 | g0019 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01243 | hp1 | a0002 | c0003 | t0001 | g0131 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0263 | AMR | PUR | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0181 | AMR | CLM | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01346 | hp1 | a0004 | c0008 | t0004 | g0004 | AMR | CLM | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01358 | hp1 | a0002 | c0003 | t0001 | g0051 | AMR | CLM | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01358 | hp2 | a0002 | c0003 | t0001 | g0124 | AMR | CLM | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0169 | AMR | CLM | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0182 | AMR | CLM | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0217 | EUR | IBS | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | IBS | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0261 | EUR | IBS | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01516 | hp2 | a0002 | c0003 | t0001 | g0126 | EUR | IBS | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | IBS | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01517 | hp2 | a0002 | c0003 | t0001 | g0125 | EUR | IBS | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01975 | hp1 | a0002 | c0016 | t0002 | g0180 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0195 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01981 | hp2 | a0001 | c0013 | t0001 | g0085 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0203 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01993 | hp2 | a0002 | c0003 | t0001 | g0044 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0188 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02015 | hp1 | a0002 | c0003 | t0001 | g0123 | EAS | KHV | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02027 | hp1 | a0002 | c0006 | t0001 | g0137 | EAS | KHV | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02083 | hp1 | a0002 | c0003 | t0001 | g0120 | EAS | KHV | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02083 | hp2 | a0007 | c0019 | t0001 | g0079 | EAS | KHV | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02145 | hp1 | a0002 | c0003 | t0001 | g0122 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0262 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02280 | hp2 | a0001 | c0004 | t0003 | g0235 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02293 | hp1 | a0003 | c0005 | t0001 | g0247 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02293 | hp2 | a0002 | c0003 | t0001 | g0040 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02451 | hp2 | a0008 | c0017 | t0001 | g0018 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02523 | hp1 | a0002 | c0003 | t0001 | g0045 | EAS | KHV | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02572 | hp1 | a0001 | c0004 | t0003 | g0252 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02572 | hp2 | a0003 | c0005 | t0001 | g0244 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02602 | hp2 | a0002 | c0003 | t0001 | g0156 | SAS | PJL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02615 | hp2 | a0001 | c0004 | t0003 | g0239 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02622 | hp1 | a0001 | c0004 | t0001 | g0162 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02622 | hp2 | a0001 | c0004 | t0003 | g0232 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02647 | hp1 | a0003 | c0005 | t0001 | g0242 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02698 | hp1 | a0002 | c0003 | t0001 | g0114 | SAS | PJL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0260 | SAS | PJL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02717 | hp1 | a0001 | c0004 | t0003 | g0236 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02717 | hp2 | a0001 | c0004 | t0003 | g0013 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0208 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02735 | hp1 | a0002 | c0003 | t0001 | g0134 | SAS | PJL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0256 | SAS | PJL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02809 | hp1 | a0009 | c0014 | t0003 | g0001 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02886 | hp1 | a0010 | c0018 | t0005 | g0006 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0254 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02895 | hp2 | a0003 | c0005 | t0001 | g0246 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02896 | hp1 | a0001 | c0004 | t0003 | g0238 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0259 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02897 | hp1 | a0001 | c0004 | t0003 | g0234 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02965 | hp1 | a0001 | c0004 | t0003 | g0231 | AFR | ESN | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02970 | hp2 | a0001 | c0012 | t0001 | g0029 | AFR | ESN | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03041 | hp1 | a0001 | c0004 | t0003 | g0230 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03041 | hp2 | a0003 | c0005 | t0001 | g0248 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03130 | hp1 | a0001 | c0004 | t0001 | g0163 | AFR | ESN | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03130 | hp2 | a0005 | c0010 | t0003 | g0007 | AFR | ESN | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03195 | hp1 | a0005 | c0010 | t0003 | g0008 | AFR | ESN | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03209 | hp1 | a0001 | c0004 | t0003 | g0251 | AFR | MSL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0264 | AFR | MSL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03225 | hp1 | a0001 | c0004 | t0003 | g0014 | AFR | MSL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03453 | hp1 | a0001 | c0004 | t0003 | g0017 | AFR | MSL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03453 | hp2 | a0001 | c0009 | t0001 | g0211 | AFR | MSL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03486 | hp1 | a0001 | c0004 | t0003 | g0011 | AFR | MSL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0167 | SAS | PJL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03492 | hp2 | a0002 | c0003 | t0001 | g0121 | SAS | PJL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0175 | AFR | ESN | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0207 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03579 | hp1 | a0001 | c0004 | t0001 | g0161 | AFR | MSL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03579 | hp2 | a0003 | c0005 | t0001 | g0245 | AFR | MSL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03834 | hp1 | a0002 | c0003 | t0001 | g0116 | SAS | BEB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03942 | hp2 | a0002 | c0003 | t0001 | g0213 | SAS | BEB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG04199 | hp1 | a0002 | c0003 | t0001 | g0038 | SAS | STU | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | STU | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0266 | SAS | STU | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | STU | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0205 | AFR | YRI | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18522 | hp2 | a0001 | c0004 | t0003 | g0001 | AFR | YRI | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18906 | hp1 | a0001 | c0004 | t0003 | g0240 | AFR | YRI | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0204 | AFR | YRI | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18939 | hp1 | a0011 | c0011 | t0002 | g0170 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18939 | hp2 | a0002 | c0003 | t0001 | g0042 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18940 | hp2 | a0002 | c0003 | t0001 | g0133 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18947 | hp1 | a0002 | c0003 | t0001 | g0110 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18949 | hp1 | a0002 | c0003 | t0001 | g0033 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18950 | hp1 | a0006 | c0007 | t0001 | g0152 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0229 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18953 | hp1 | a0002 | c0003 | t0001 | g0165 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0225 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18956 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18959 | hp2 | a0006 | c0007 | t0001 | g0127 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18965 | hp1 | a0002 | c0003 | t0001 | g0135 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18971 | hp1 | a0002 | c0003 | t0001 | g0043 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0186 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0176 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18980 | hp1 | a0002 | c0006 | t0001 | g0136 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0187 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0184 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18990 | hp2 | a0002 | c0003 | t0001 | g0031 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18993 | hp1 | a0002 | c0003 | t0001 | g0130 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0190 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19006 | hp1 | a0002 | c0006 | t0001 | g0149 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19006 | hp2 | a0001 | c0002 | t0002 | g0209 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19010 | hp1 | a0002 | c0003 | t0001 | g0113 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0178 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19012 | hp2 | a0002 | c0003 | t0001 | g0041 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19030 | hp1 | a0001 | c0004 | t0003 | g0241 | AFR | LWK | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19043 | hp1 | a0001 | c0004 | t0003 | g0012 | AFR | LWK | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19043 | hp2 | a0001 | c0004 | t0003 | g0237 | AFR | LWK | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19055 | hp1 | a0002 | c0003 | t0001 | g0166 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19056 | hp1 | a0002 | c0003 | t0001 | g0022 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19060 | hp2 | a0002 | c0003 | t0001 | g0049 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19068 | hp1 | a0002 | c0003 | t0001 | g0046 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19070 | hp2 | a0002 | c0003 | t0001 | g0111 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19076 | hp1 | a0002 | c0003 | t0001 | g0030 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19076 | hp2 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19081 | hp1 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19081 | hp2 | a0002 | c0003 | t0008 | g0129 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19083 | hp1 | a0002 | c0003 | t0001 | g0112 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0191 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19091 | hp1 | a0002 | c0003 | t0001 | g0108 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19091 | hp2 | a0002 | c0003 | t0001 | g0107 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0206 | AFR | YRI | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA19240 | hp2 | a0001 | c0004 | t0003 | g0016 | AFR | YRI | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA20129 | hp1 | a0012 | c0015 | t0005 | g0005 | AFR | ASW | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ASW | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA20752 | hp1 | a0002 | c0003 | t0001 | g0216 | EUR | TSI | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | TSI | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA20905 | hp1 | a0002 | c0003 | t0001 | g0037 | SAS | GIH | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0255 | SAS | GIH | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG01123 | hp2 | a0002 | c0003 | t0001 | g0039 | AMR | CLM | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02109 | hp1 | a0003 | c0005 | t0001 | g0243 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02109 | hp2 | a0001 | c0004 | t0007 | g0265 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02486 | hp1 | a0002 | c0003 | t0001 | g0150 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02486 | hp2 | a0003 | c0005 | t0001 | g0249 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02559 | hp1 | a0001 | c0004 | t0003 | g0010 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG02559 | hp2 | a0001 | c0009 | t0001 | g0212 | AFR | ACB | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03471 | hp1 | a0001 | c0004 | t0003 | g0250 | AFR | MSL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | USA | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| HG06807 | hp2 | a0001 | c0004 | t0004 | g0015 | AFR | USA | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA18955 | hp2 | a0002 | c0003 | t0001 | g0117 | EAS | JPT | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | USA | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | USA | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA21309 | hp1 | a0002 | c0003 | t0001 | g0139 | AFR | LWK | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| NA21309 | hp2 | a0001 | c0004 | t0003 | g0009 | AFR | LWK | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| homoSapiens | chm13v2 | a0002 | c0003 | t0001 | g0035 | REF | REF | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0032 | REF | REF | FAM135A_chr6_70408508_70566174 | FAM135A | chr6 | 70408508 | 70566174 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:70452506 | G | A | 1 | a0006 | 2 | NA18950.hp1 NA18959.hp2 |
missense_variant | MODERATE | c.92G>A | p.Arg31His | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/22 | 506/6215 | 92/4548 | 31/1515 | chr6 | 70452506 | |||
| chr6:70475446 | C | G | 1 | a0007 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.194C>G | p.Ser65Cys | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 6/22 | 608/6215 | 194/4548 | 65/1515 | chr6 | 70475446 | |||
| chr6:70477227 | G | A | 1 | a0011 | 1 | NA18939.hp1 | missense_variant | MODERATE | c.437G>A | p.Arg146Lys | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/22 | 851/6215 | 437/4548 | 146/1515 | chr6 | 70477227 | |||
| chr6:70480984 | G | A | 1 | a0004 | 2 | HG01074.hp2 HG01346.hp1 |
missense_variant | MODERATE | c.626G>A | p.Ser209Asn | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 9/22 | 1040/6215 | 626/4548 | 209/1515 | chr6 | 70480984 | |||
| chr6:70522577 | A | G | 1 | a0010 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.1094A>G | p.Gln365Arg | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 13/22 | 1508/6215 | 1094/4548 | 365/1515 | chr6 | 70522577 | |||
| chr6:70524846 | C | T | 1 | a0008 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.1762C>T | p.Pro588Ser | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/22 | 2176/6215 | 1762/4548 | 588/1515 | chr6 | 70524846 | |||
| chr6:70525257 | A | G | 1 | a0003 | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
missense_variant | MODERATE | c.2173A>G | p.Ile725Val | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/22 | 2587/6215 | 2173/4548 | 725/1515 | chr6 | 70525257 | |||
| chr6:70525282 | G | A | 1 | a0009 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.2198G>A | p.Arg733Gln | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/22 | 2612/6215 | 2198/4548 | 733/1515 | chr6 | 70525282 | |||
| chr6:70525660 | T | C | 2 | a0010 a0012 |
2 | HG02886.hp1 NA20129.hp1 |
missense_variant | MODERATE | c.2576T>C | p.Val859Ala | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/22 | 2990/6215 | 2576/4548 | 859/1515 | chr6 | 70525660 | |||
| chr6:70525711 | C | T | 1 | a0005 | 2 | HG03130.hp2 HG03195.hp1 |
missense_variant | MODERATE | c.2627C>T | p.Thr876Met | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/22 | 3041/6215 | 2627/4548 | 876/1515 | chr6 | 70525711 | |||
| chr6:70525944 | C | T | 1 | a0003 | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
missense_variant | MODERATE | c.2860C>T | p.Pro954Ser | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/22 | 3274/6215 | 2860/4548 | 954/1515 | chr6 | 70525944 | |||
| chr6:70528402 | A | G | 2 | a0002 a0006 |
58 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(55): Show |
missense_variant | MODERATE | c.3725A>G | p.Asp1242Gly | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/22 | 4139/6215 | 3725/4548 | 1242/1515 | chr6 | 70528402 | |||
| chr6:70559767 | G | A | 2 | a0010 a0012 |
2 | HG02886.hp1 NA20129.hp1 |
missense_variant | MODERATE | c.4394G>A | p.Ser1465Asn | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 22/22 | 4808/6215 | 4394/4548 | 1465/1515 | chr6 | 70559767 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:70502686 | G | A | 1 | a0001c0012 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.924G>A | p.Ala308Ala | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/22 | 1338/6215 | 924/4548 | 308/1515 | chr6 | 70502686 | |||
| chr6:70502740 | G | A | 1 | a0001c0013 | 1 | HG01981.hp2 | synonymous_variant | LOW | c.978G>A | p.Thr326Thr | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/22 | 1392/6215 | 978/4548 | 326/1515 | chr6 | 70502740 | |||
| chr6:70524545 | A | G | 1 | a0002c0006 | 5 | HG00597.hp2 HG00621.hp2 HG02027.hp1 others(2): Show |
synonymous_variant | LOW | c.1461A>G | p.Ser487Ser | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/22 | 1875/6215 | 1461/4548 | 487/1515 | chr6 | 70524545 | |||
| chr6:70525514 | A | G | 1 | a0003c0005 | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
synonymous_variant | LOW | c.2430A>G | p.Lys810Lys | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/22 | 2844/6215 | 2430/4548 | 810/1515 | chr6 | 70525514 | |||
| chr6:70526513 | C | T | 10 | a0001c0002 a0001c0004 a0001c0009 others(7): Show |
107 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(104): Show |
synonymous_variant | LOW | c.3429C>T | p.Asn1143Asn | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/22 | 3843/6215 | 3429/4548 | 1143/1515 | chr6 | 70526513 | |||
| chr6:70536275 | G | A | 2 | a0001c0009 a0003c0005 |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
synonymous_variant | LOW | c.3981G>A | p.Ser1327Ser | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/22 | 4395/6215 | 3981/4548 | 1327/1515 | chr6 | 70536275 | |||
| chr6:70538343 | A | G | 1 | a0003c0005 | 8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
synonymous_variant | LOW | c.4170A>G | p.Thr1390Thr | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/22 | 4584/6215 | 4170/4548 | 1390/1515 | chr6 | 70538343 | |||
| chr6:70559756 | C | T | 3 | a0001c0002 a0002c0016 a0011c0011 |
67 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(64): Show |
synonymous_variant | LOW | c.4383C>T | p.Pro1461Pro | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 22/22 | 4797/6215 | 4383/4548 | 1461/1515 | chr6 | 70559756 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:70413617 | C | T | 1 | a0002c0003t0008 | 1 | NA19081.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-305C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/22 | chr6 | 70413617 | |||||||
| chr6:70413655 | G | A | 1 | a0001c0004t0006 | 1 | HG01192.hp2 | 5_prime_UTR_variant | MODIFIER | c.-267G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/22 | 14688 | chr6 | 70413655 | ||||||
| chr6:70559929 | G | A | 4 | a0001c0002t0002 a0001c0004t0007 a0002c0016t0002 others(1): Show |
68 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*8G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 22/22 | 8 | chr6 | 70559929 | ||||||
| chr6:70560069 | C | G | 2 | a0010c0018t0005 a0012c0015t0005 |
2 | HG02886.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*148C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 22/22 | 148 | chr6 | 70560069 | ||||||
| chr6:70560528 | A | T | 7 | a0001c0004t0003 a0001c0004t0004 a0004c0008t0004 others(4): Show |
32 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*607A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 22/22 | 607 | chr6 | 70560528 | ||||||
| chr6:70560674 | A | G | 2 | a0001c0004t0004 a0004c0008t0004 |
3 | HG01074.hp2 HG01346.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*753A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 22/22 | 753 | chr6 | 70560674 | ||||||
| chr6:70560840 | A | C | 3 | a0001c0002t0002 a0002c0016t0002 a0011c0011t0002 |
67 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*919A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 22/22 | 919 | chr6 | 70560840 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:70413763 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-220+61C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70413763 | |||||||
| chr6:70413963 | G | T | 17 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(14): Show |
17 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.-220+261G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70413963 | |||||||
| chr6:70414044 | C | T | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-220+342C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70414044 | |||||||
| chr6:70414053 | C | T | 14 | a0001c0004t0003g0001 a0001c0004t0003g0230 a0001c0004t0003g0231 others(11): Show |
14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-220+351C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70414053 | |||||||
| chr6:70414267 | C | T | 11 | a0001c0002t0002g0219 a0001c0002t0002g0220 a0001c0002t0002g0221 others(8): Show |
11 | HG00609.hp1 HG00621.hp1 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.-220+565C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70414267 | |||||||
| chr6:70414486 | A | T | 5 | a0001c0001t0001g0215 a0001c0001t0001g0217 a0001c0001t0001g0218 others(2): Show |
5 | HG00140.hp2 HG00642.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.-220+784A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70414486 | |||||||
| chr6:70414515 | TC | T | 33 | a0001c0004t0003g0001 a0001c0004t0003g0009 a0001c0004t0003g0010 others(30): Show |
33 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(30): Show |
intron_variant | MODIFIER | c.-219-767delC | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 70414515 | ||||||
| chr6:70414522 | C | G | 1 | a0002c0003t0001g0213 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-219-769C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70414522 | |||||||
| chr6:70414638 | A | G | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-219-653A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70414638 | |||||||
| chr6:70414798 | G | A | 1 | a0008c0017t0001g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-219-493G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70414798 | |||||||
| chr6:70414826 | A | T | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-219-465A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70414826 | |||||||
| chr6:70414827 | A | C | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-219-464A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70414827 | |||||||
| chr6:70414856 | A | G | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-219-435A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70414856 | |||||||
| chr6:70414869 | C | CAACAGAC others(5): Show |
1 | a0002c0003t0001g0166 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-219-420_-219-419i others(14): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 70414869 | ||||||
| chr6:70414924 | C | T | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-219-367C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70414924 | |||||||
| chr6:70415023 | C | G | 2 | a0001c0001t0001g0210 a0001c0001t0001g0267 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-219-268C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70415023 | |||||||
| chr6:70415139 | T | C | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-219-152T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 1/21 | chr6 | 70415139 | |||||||
| chr6:70415417 | T | A | 1 | a0001c0002t0002g0253 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-134+41T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70415417 | |||||||
| chr6:70415513 | A | G | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-134+137A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70415513 | |||||||
| chr6:70415757 | T | G | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-134+381T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70415757 | |||||||
| chr6:70415806 | A | G | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-134+430A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70415806 | |||||||
| chr6:70416002 | TTGAC | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0267 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-134+629_-134+632d others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr6 | 70416002 | ||||||
| chr6:70416092 | G | T | 1 | a0002c0003t0001g0165 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-134+716G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70416092 | |||||||
| chr6:70416229 | T | G | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-134+853T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70416229 | |||||||
| chr6:70416230 | C | T | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-134+854C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70416230 | |||||||
| chr6:70416231 | A | G | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-134+855A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70416231 | |||||||
| chr6:70416232 | C | A | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-134+856C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70416232 | |||||||
| chr6:70416350 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-134+974T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70416350 | |||||||
| chr6:70416353 | C | T | 1 | a0001c0002t0002g0266 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-134+977C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70416353 | |||||||
| chr6:70417191 | A | G | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.-134+1815A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70417191 | |||||||
| chr6:70417201 | A | C | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-134+1825A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70417201 | |||||||
| chr6:70417259 | CT | C | 14 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(11): Show |
14 | HG01074.hp2 HG01346.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.-134+1898delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr6 | 70417259 | ||||||
| chr6:70417307 | G | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-134+1931G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70417307 | |||||||
| chr6:70417585 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-134+2209A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70417585 | |||||||
| chr6:70417680 | T | C | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-134+2304T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70417680 | |||||||
| chr6:70417784 | A | C | 1 | a0001c0001t0001g0164 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-134+2408A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70417784 | |||||||
| chr6:70417789 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-134+2413G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70417789 | |||||||
| chr6:70417815 | T | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-134+2439T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70417815 | |||||||
| chr6:70418176 | C | T | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-134+2800C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70418176 | |||||||
| chr6:70418235 | G | A | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-134+2859G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70418235 | |||||||
| chr6:70418317 | AATTT | A | 2 | a0010c0018t0005g0006 a0012c0015t0005g0005 |
2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-134+2946_-134+294 others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr6 | 70418317 | ||||||
| chr6:70418500 | T | C | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-134+3124T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70418500 | |||||||
| chr6:70418550 | G | A | 1 | a0001c0002t0002g0169 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-134+3174G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70418550 | |||||||
| chr6:70418656 | T | C | 1 | a0001c0012t0001g0029 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-134+3280T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70418656 | |||||||
| chr6:70418952 | T | C | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-134+3576T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70418952 | |||||||
| chr6:70419054 | G | A | 2 | a0002c0003t0001g0030 a0002c0003t0001g0031 |
2 | NA18990.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.-134+3678G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70419054 | |||||||
| chr6:70419086 | G | T | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-134+3710G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70419086 | |||||||
| chr6:70419103 | C | G | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.-134+3727C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70419103 | |||||||
| chr6:70419158 | C | T | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-134+3782C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70419158 | |||||||
| chr6:70419368 | G | A | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-134+3992G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70419368 | |||||||
| chr6:70419413 | C | T | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-134+4037C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70419413 | |||||||
| chr6:70419418 | CA | C | 189 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(186): Show |
189 | HG00140.hp1 HG00280.hp2 HG00609.hp2 others(186): Show |
intron_variant | MODIFIER | c.-134+4057delA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr6 | 70419418 | ||||||
| chr6:70419418 | CAA | C | 70 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(67): Show |
70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.-134+4056_-134+405 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr6 | 70419418 | ||||||
| chr6:70419426 | A | C | 1 | a0001c0001t0001g0159 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-134+4050A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70419426 | |||||||
| chr6:70419431 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-134+4055A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70419431 | |||||||
| chr6:70419576 | T | A | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-134+4200T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70419576 | |||||||
| chr6:70419680 | T | C | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-134+4304T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70419680 | |||||||
| chr6:70419725 | T | C | 54 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(51): Show |
54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.-134+4349T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70419725 | |||||||
| chr6:70419970 | C | A | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.-134+4594C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70419970 | |||||||
| chr6:70420285 | TG | T | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.-134+4910delG | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70420285 | |||||||
| chr6:70420391 | A | G | 2 | a0001c0002t0002g0168 a0001c0002t0002g0209 |
2 | NA18962.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.-134+5015A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70420391 | |||||||
| chr6:70420627 | G | A | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-134+5251G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70420627 | |||||||
| chr6:70420680 | T | C | 1 | a0001c0001t0001g0036 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-134+5304T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70420680 | |||||||
| chr6:70420698 | T | A | 2 | a0002c0003t0001g0037 a0002c0003t0001g0038 |
2 | HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-134+5322T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70420698 | |||||||
| chr6:70420890 | T | G | 1 | a0001c0001t0001g0020 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-134+5514T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70420890 | |||||||
| chr6:70421021 | A | G | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.-133-5418A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70421021 | |||||||
| chr6:70421365 | C | T | 5 | a0001c0002t0002g0204 a0001c0002t0002g0205 a0001c0002t0002g0206 others(2): Show |
5 | HG02723.hp2 HG03540.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.-133-5074C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70421365 | |||||||
| chr6:70421889 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-133-4550A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70421889 | |||||||
| chr6:70421896 | G | A | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-133-4543G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70421896 | |||||||
| chr6:70421995 | G | A | 1 | a0001c0009t0001g0211 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-133-4444G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70421995 | |||||||
| chr6:70422119 | A | T | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-133-4320A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70422119 | |||||||
| chr6:70422211 | G | A | 1 | a0001c0002t0002g0254 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-133-4228G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70422211 | |||||||
| chr6:70422321 | A | G | 2 | a0001c0001t0001g0210 a0001c0001t0001g0267 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-133-4118A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70422321 | |||||||
| chr6:70422469 | G | A | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-133-3970G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70422469 | |||||||
| chr6:70422491 | A | C | 117 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(114): Show |
117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.-133-3948A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70422491 | |||||||
| chr6:70422569 | A | G | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-133-3870A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70422569 | |||||||
| chr6:70422677 | C | T | 11 | a0001c0002t0002g0219 a0001c0002t0002g0220 a0001c0002t0002g0221 others(8): Show |
11 | HG00609.hp1 HG00621.hp1 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.-133-3762C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70422677 | |||||||
| chr6:70422914 | G | C | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.-133-3525G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70422914 | |||||||
| chr6:70422965 | G | T | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-133-3474G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70422965 | |||||||
| chr6:70423014 | G | T | 1 | a0001c0002t0002g0203 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-133-3425G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70423014 | |||||||
| chr6:70423015 | T | C | 4 | a0001c0002t0002g0204 a0001c0002t0002g0205 a0001c0002t0002g0206 others(1): Show |
4 | HG03540.hp1 NA18522.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-133-3424T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70423015 | |||||||
| chr6:70423197 | G | A | 6 | a0002c0003t0001g0002 a0002c0003t0001g0039 a0002c0003t0001g0040 others(3): Show |
6 | HG01123.hp2 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.-133-3242G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70423197 | |||||||
| chr6:70423675 | T | C | 14 | a0001c0004t0003g0001 a0001c0004t0003g0230 a0001c0004t0003g0231 others(11): Show |
14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-133-2764T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70423675 | |||||||
| chr6:70423957 | T | G | 1 | a0011c0011t0002g0170 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-133-2482T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70423957 | |||||||
| chr6:70424023 | A | G | 1 | a0002c0003t0001g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-133-2416A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424023 | |||||||
| chr6:70424048 | T | A | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-133-2391T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424048 | |||||||
| chr6:70424060 | G | A | 1 | a0002c0003t0001g0044 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-133-2379G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424060 | |||||||
| chr6:70424143 | C | G | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-133-2296C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424143 | |||||||
| chr6:70424316 | A | G | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-133-2123A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424316 | |||||||
| chr6:70424320 | A | G | 11 | a0001c0004t0003g0010 a0001c0004t0003g0011 a0001c0004t0003g0012 others(8): Show |
11 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-133-2119A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424320 | |||||||
| chr6:70424329 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-133-2110C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424329 | |||||||
| chr6:70424413 | G | A | 3 | a0001c0004t0003g0250 a0001c0004t0003g0251 a0001c0004t0003g0252 |
3 | HG02572.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-133-2026G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424413 | |||||||
| chr6:70424447 | A | G | 1 | a0002c0003t0001g0044 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-133-1992A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424447 | |||||||
| chr6:70424555 | A | G | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-133-1884A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424555 | |||||||
| chr6:70424557 | C | G | 2 | a0010c0018t0005g0006 a0012c0015t0005g0005 |
2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-133-1882C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424557 | |||||||
| chr6:70424644 | G | A | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-133-1795G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424644 | |||||||
| chr6:70424736 | G | A | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-133-1703G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424736 | |||||||
| chr6:70424791 | A | G | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-133-1648A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424791 | |||||||
| chr6:70424841 | A | G | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-133-1598A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70424841 | |||||||
| chr6:70425140 | G | A | 12 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(9): Show |
12 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.-133-1299G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70425140 | |||||||
| chr6:70425153 | T | C | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-133-1286T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70425153 | |||||||
| chr6:70425557 | C | T | 4 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0004t0003g0016 others(1): Show |
4 | HG03453.hp1 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.-133-882C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70425557 | |||||||
| chr6:70425671 | A | G | 40 | a0001c0002t0002g0167 a0001c0002t0002g0176 a0001c0002t0002g0177 others(37): Show |
40 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-133-768A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70425671 | |||||||
| chr6:70425744 | C | G | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-133-695C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70425744 | |||||||
| chr6:70425749 | A | G | 46 | a0001c0002t0002g0167 a0001c0002t0002g0169 a0001c0002t0002g0176 others(43): Show |
46 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-133-690A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70425749 | |||||||
| chr6:70425778 | C | T | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-133-661C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70425778 | |||||||
| chr6:70425875 | G | A | 28 | a0001c0004t0003g0001 a0001c0004t0003g0009 a0001c0004t0003g0010 others(25): Show |
28 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.-133-564G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70425875 | |||||||
| chr6:70425930 | T | C | 117 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(114): Show |
117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.-133-509T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70425930 | |||||||
| chr6:70425933 | T | G | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-133-506T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70425933 | |||||||
| chr6:70425960 | G | A | 1 | a0001c0002t0002g0264 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-133-479G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70425960 | |||||||
| chr6:70425965 | C | T | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-133-474C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70425965 | |||||||
| chr6:70426059 | C | T | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-133-380C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70426059 | |||||||
| chr6:70426072 | C | T | 1 | a0006c0007t0001g0152 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-133-367C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70426072 | |||||||
| chr6:70426109 | C | CAAAA | 51 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(48): Show |
51 | HG00609.hp1 HG00621.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.-133-321_-133-318d others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr6 | 70426109 | ||||||
| chr6:70426119 | A | AAAAAC | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-133-318_-133-317i others(7): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr6 | 70426119 | ||||||
| chr6:70426119 | A | AAAC | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.-133-311_-133-309d others(5): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr6 | 70426119 | ||||||
| chr6:70426119 | A | C | 3 | a0001c0001t0001g0151 a0010c0018t0005g0006 a0012c0015t0005g0005 |
3 | HG02602.hp1 HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-133-320A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70426119 | |||||||
| chr6:70426131 | A | C | 3 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0004t0003g0241 |
3 | HG02818.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-133-308A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70426131 | |||||||
| chr6:70426250 | A | G | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-133-189A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 2/21 | chr6 | 70426250 | |||||||
| chr6:70426613 | T | G | 1 | a0002c0003t0001g0045 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-40+81T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70426613 | |||||||
| chr6:70426692 | T | C | 1 | a0002c0003t0001g0046 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-40+160T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70426692 | |||||||
| chr6:70426792 | A | G | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40+260A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70426792 | |||||||
| chr6:70426870 | C | T | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-40+338C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70426870 | |||||||
| chr6:70427228 | A | G | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-40+696A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70427228 | |||||||
| chr6:70427253 | C | T | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-40+721C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70427253 | |||||||
| chr6:70427463 | C | T | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-39-841C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70427463 | |||||||
| chr6:70427497 | A | G | 113 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(110): Show |
113 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.-39-807A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70427497 | |||||||
| chr6:70427533 | C | CA | 19 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0050 others(16): Show |
19 | HG01074.hp2 HG01346.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.-39-753dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr6 | 70427533 | ||||||
| chr6:70427533 | CA | C | 70 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(67): Show |
70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.-39-753delA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr6 | 70427533 | ||||||
| chr6:70427659 | TA | T | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.-39-644delA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70427659 | |||||||
| chr6:70427707 | A | C | 2 | a0010c0018t0005g0006 a0012c0015t0005g0005 |
2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-39-597A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70427707 | |||||||
| chr6:70427742 | A | G | 2 | a0001c0001t0001g0210 a0001c0001t0001g0267 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-39-562A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70427742 | |||||||
| chr6:70427948 | C | A | 1 | a0001c0001t0001g0052 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-39-356C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70427948 | |||||||
| chr6:70427988 | C | A | 81 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(78): Show |
81 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.-39-316C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70427988 | |||||||
| chr6:70428011 | A | G | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-39-293A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70428011 | |||||||
| chr6:70428139 | C | T | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-39-165C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70428139 | |||||||
| chr6:70428140 | A | G | 1 | a0001c0004t0003g0251 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-39-164A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70428140 | |||||||
| chr6:70428181 | G | A | 142 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 others(139): Show |
142 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(139): Show |
intron_variant | MODIFIER | c.-39-123G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70428181 | |||||||
| chr6:70428228 | T | A | 16 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(13): Show |
16 | HG00639.hp2 HG00735.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.-39-76T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70428228 | |||||||
| chr6:70428289 | C | T | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.-39-15C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 3/21 | chr6 | 70428289 | |||||||
| chr6:70428456 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.77+37A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70428456 | |||||||
| chr6:70428472 | A | G | 1 | a0002c0003t0001g0043 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.77+53A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70428472 | |||||||
| chr6:70428625 | C | T | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.77+206C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70428625 | |||||||
| chr6:70428680 | G | C | 1 | a0001c0004t0003g0010 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.77+261G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70428680 | |||||||
| chr6:70428840 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.77+421A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70428840 | |||||||
| chr6:70428886 | G | C | 1 | a0001c0001t0001g0053 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.77+467G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70428886 | |||||||
| chr6:70429001 | A | G | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+582A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70429001 | |||||||
| chr6:70429078 | G | C | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.77+659G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70429078 | |||||||
| chr6:70429244 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.77+825G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70429244 | |||||||
| chr6:70429464 | G | C | 1 | a0001c0001t0001g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.77+1045G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70429464 | |||||||
| chr6:70429467 | T | C | 1 | a0001c0004t0003g0011 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.77+1048T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70429467 | |||||||
| chr6:70429470 | G | A | 1 | a0001c0002t0002g0201 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.77+1051G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70429470 | |||||||
| chr6:70429481 | C | CT | 12 | a0001c0004t0003g0009 a0001c0004t0003g0010 a0001c0004t0003g0011 others(9): Show |
12 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.77+1062_77+1063ins others(1): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70429481 | |||||||
| chr6:70429539 | A | T | 1 | a0008c0017t0001g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.77+1120A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70429539 | |||||||
| chr6:70429664 | T | G | 1 | a0001c0004t0003g0230 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.77+1245T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70429664 | |||||||
| chr6:70429761 | C | T | 1 | a0002c0003t0001g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.77+1342C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70429761 | |||||||
| chr6:70429842 | T | G | 2 | a0001c0001t0001g0210 a0001c0001t0001g0267 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.77+1423T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70429842 | |||||||
| chr6:70430175 | A | G | 1 | a0002c0003t0001g0150 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.77+1756A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70430175 | |||||||
| chr6:70430209 | C | T | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.77+1790C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70430209 | |||||||
| chr6:70430213 | T | G | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.77+1794T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70430213 | |||||||
| chr6:70430316 | A | G | 219 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(216): Show |
219 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.77+1897A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70430316 | |||||||
| chr6:70430328 | C | T | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.77+1909C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70430328 | |||||||
| chr6:70430335 | T | TA | 16 | a0001c0001t0001g0036 a0001c0004t0003g0001 a0001c0004t0003g0230 others(13): Show |
16 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.77+1927dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70430335 | ||||||
| chr6:70430351 | AAAAG | A | 16 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(13): Show |
16 | HG00639.hp2 HG00735.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.77+1938_77+1941del others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70430351 | ||||||
| chr6:70430354 | A | G | 1 | a0008c0017t0001g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.77+1935A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70430354 | |||||||
| chr6:70430355 | G | A | 1 | a0002c0003t0001g0045 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.77+1936G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70430355 | |||||||
| chr6:70430528 | C | G | 1 | a0002c0003t0001g0038 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.77+2109C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70430528 | |||||||
| chr6:70430664 | A | G | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0256 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.77+2245A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70430664 | |||||||
| chr6:70430811 | A | C | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+2392A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70430811 | |||||||
| chr6:70431157 | A | G | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.77+2738A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70431157 | |||||||
| chr6:70431275 | G | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.77+2856G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70431275 | |||||||
| chr6:70431285 | A | G | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.77+2866A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70431285 | |||||||
| chr6:70431312 | G | T | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.77+2893G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70431312 | |||||||
| chr6:70431366 | G | A | 1 | a0001c0002t0002g0256 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.77+2947G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70431366 | |||||||
| chr6:70431500 | T | C | 14 | a0001c0004t0003g0001 a0001c0004t0003g0230 a0001c0004t0003g0231 others(11): Show |
14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.77+3081T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70431500 | |||||||
| chr6:70431618 | T | C | 1 | a0001c0002t0002g0254 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.77+3199T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70431618 | |||||||
| chr6:70431823 | A | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0267 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.77+3404A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70431823 | |||||||
| chr6:70431849 | C | T | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.77+3430C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70431849 | |||||||
| chr6:70431863 | G | T | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.77+3444G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70431863 | |||||||
| chr6:70431987 | C | G | 15 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(12): Show |
15 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.77+3568C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70431987 | |||||||
| chr6:70432065 | C | T | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.77+3646C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70432065 | |||||||
| chr6:70432163 | T | A | 1 | a0001c0002t0002g0254 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.77+3744T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70432163 | |||||||
| chr6:70432171 | C | A | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.77+3752C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70432171 | |||||||
| chr6:70432197 | C | T | 1 | a0002c0003t0001g0051 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.77+3778C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70432197 | |||||||
| chr6:70432405 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.77+3986T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70432405 | |||||||
| chr6:70432428 | T | G | 1 | a0001c0002t0002g0219 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.77+4009T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70432428 | |||||||
| chr6:70432510 | C | CT | 70 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(67): Show |
70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.77+4093dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70432510 | ||||||
| chr6:70432593 | T | C | 1 | a0001c0002t0002g0171 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.77+4174T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70432593 | |||||||
| chr6:70432606 | A | T | 1 | a0001c0001t0001g0106 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.77+4187A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70432606 | |||||||
| chr6:70432760 | CT | C | 18 | a0001c0004t0003g0001 a0001c0004t0003g0230 a0001c0004t0003g0231 others(15): Show |
18 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.77+4351delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70432760 | ||||||
| chr6:70432882 | A | T | 161 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(158): Show |
161 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(158): Show |
intron_variant | MODIFIER | c.77+4463A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70432882 | |||||||
| chr6:70433009 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.77+4590C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433009 | |||||||
| chr6:70433077 | CT | C | 57 | a0001c0001t0001g0091 a0001c0001t0001g0210 a0001c0001t0001g0267 others(54): Show |
57 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.77+4674delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70433077 | ||||||
| chr6:70433113 | C | T | 25 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 others(22): Show |
25 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.77+4694C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433113 | |||||||
| chr6:70433370 | G | A | 2 | a0001c0002t0002g0255 a0001c0002t0002g0257 |
2 | HG00639.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.77+4951G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433370 | |||||||
| chr6:70433373 | C | G | 9 | a0001c0002t0002g0253 a0001c0002t0002g0255 a0001c0002t0002g0256 others(6): Show |
9 | HG00280.hp1 HG00639.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.77+4954C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433373 | |||||||
| chr6:70433388 | T | C | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.77+4969T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433388 | |||||||
| chr6:70433436 | C | T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.77+5017C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433436 | |||||||
| chr6:70433465 | A | T | 136 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(133): Show |
136 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(133): Show |
intron_variant | MODIFIER | c.77+5046A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433465 | |||||||
| chr6:70433505 | C | CT | 116 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(113): Show |
116 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.77+5099dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70433505 | ||||||
| chr6:70433559 | T | TCTTTTTT others(212): Show |
2 | a0001c0002t0002g0173 a0001c0002t0002g0174 |
2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.77+5144_77+5145ins others(219): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70433559 | ||||||
| chr6:70433591 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.77+5172A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433591 | |||||||
| chr6:70433602 | G | A | 1 | a0001c0009t0001g0212 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.77+5183G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433602 | |||||||
| chr6:70433658 | C | T | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+5239C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433658 | |||||||
| chr6:70433717 | T | G | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+5298T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433717 | |||||||
| chr6:70433762 | C | T | 81 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(78): Show |
81 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.77+5343C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433762 | |||||||
| chr6:70433778 | T | G | 81 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(78): Show |
81 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.77+5359T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433778 | |||||||
| chr6:70433832 | T | C | 1 | a0001c0001t0001g0109 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.77+5413T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433832 | |||||||
| chr6:70433925 | A | C | 1 | a0001c0004t0004g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.77+5506A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70433925 | |||||||
| chr6:70433930 | AAAGAAAA others(3): Show |
A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.77+5513_77+5522del others(10): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70433930 | ||||||
| chr6:70434207 | G | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.77+5788G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70434207 | |||||||
| chr6:70434400 | A | G | 1 | a0001c0004t0003g0011 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.77+5981A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70434400 | |||||||
| chr6:70434501 | C | T | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.77+6082C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70434501 | |||||||
| chr6:70434507 | A | ACC | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.77+6088_77+6089ins others(2): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70434507 | |||||||
| chr6:70434508 | A | T | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.77+6089A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70434508 | |||||||
| chr6:70434562 | C | G | 1 | a0001c0001t0001g0074 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.77+6143C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70434562 | |||||||
| chr6:70434702 | C | T | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.77+6283C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70434702 | |||||||
| chr6:70434846 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.77+6427G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70434846 | |||||||
| chr6:70434864 | A | G | 2 | a0010c0018t0005g0006 a0012c0015t0005g0005 |
2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.77+6445A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70434864 | |||||||
| chr6:70434886 | T | C | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.77+6467T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70434886 | |||||||
| chr6:70434916 | G | A | 1 | a0001c0004t0003g0252 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.77+6497G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70434916 | |||||||
| chr6:70435026 | G | C | 14 | a0001c0004t0003g0001 a0001c0004t0003g0230 a0001c0004t0003g0231 others(11): Show |
14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.77+6607G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435026 | |||||||
| chr6:70435079 | GTGTA | G | 12 | a0001c0002t0002g0176 a0001c0002t0002g0178 a0001c0002t0002g0187 others(9): Show |
12 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.77+6662_77+6665del others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70435079 | ||||||
| chr6:70435079 | GTGTATA | G | 51 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(48): Show |
51 | HG00280.hp1 HG00597.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.77+6662_77+6667del others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70435079 | ||||||
| chr6:70435079 | GTGTATAT others(1): Show |
G | 21 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(18): Show |
21 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.77+6662_77+6669del others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70435079 | ||||||
| chr6:70435079 | GTGTATAT others(5): Show |
G | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+6662_77+6673del others(12): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70435079 | ||||||
| chr6:70435081 | G | A | 23 | a0001c0002t0002g0172 a0001c0002t0002g0183 a0001c0002t0002g0189 others(20): Show |
23 | HG00673.hp2 HG00733.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.77+6662G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435081 | |||||||
| chr6:70435081 | G | GTA | 7 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(4): Show |
7 | HG00639.hp2 HG00642.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.77+6690_77+6691dup others(2): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70435081 | ||||||
| chr6:70435081 | G | GTATA | 3 | a0001c0001t0001g0075 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG01255.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.77+6688_77+6691dup others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70435081 | ||||||
| chr6:70435081 | GTATATA | G | 45 | a0001c0001t0001g0021 a0001c0001t0001g0036 a0001c0001t0001g0053 others(42): Show |
45 | HG00140.hp1 HG00733.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.77+6686_77+6691del others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70435081 | ||||||
| chr6:70435081 | GTATATAT others(3): Show |
G | 3 | a0001c0004t0003g0230 a0010c0018t0005g0006 a0012c0015t0005g0005 |
3 | HG02886.hp1 HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.77+6682_77+6691del others(10): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70435081 | ||||||
| chr6:70435083 | A | G | 19 | a0001c0001t0001g0020 a0001c0001t0001g0095 a0001c0001t0001g0096 others(16): Show |
19 | HG01192.hp1 HG01934.hp1 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.77+6664A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435083 | |||||||
| chr6:70435085 | A | G | 4 | a0001c0004t0003g0016 a0001c0004t0003g0017 a0001c0009t0001g0211 others(1): Show |
4 | HG02559.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+6666A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435085 | |||||||
| chr6:70435088 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.77+6669T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435088 | |||||||
| chr6:70435098 | TATATATA | T | 6 | a0001c0004t0003g0010 a0001c0004t0003g0011 a0001c0004t0003g0012 others(3): Show |
6 | HG02559.hp1 HG02717.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.77+6680_77+6686del others(7): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435098 | |||||||
| chr6:70435098 | TATATATA others(4): Show |
T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.77+6680_77+6690del others(11): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435098 | |||||||
| chr6:70435101 | ATATATAT others(3): Show |
A | 12 | a0001c0004t0003g0001 a0001c0004t0003g0231 a0001c0004t0003g0232 others(9): Show |
12 | HG01069.hp1 HG02615.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.77+6684_77+6693del others(10): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70435101 | ||||||
| chr6:70435102 | TATATATA | T | 3 | a0001c0002t0002g0172 a0001c0002t0002g0183 a0001c0002t0002g0189 |
3 | HG00673.hp2 HG00733.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.77+6684_77+6690del others(7): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435102 | |||||||
| chr6:70435105 | ATATATT | A | 41 | a0001c0001t0001g0109 a0001c0001t0001g0157 a0002c0003t0001g0002 others(38): Show |
41 | HG00280.hp2 HG00597.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.77+6688_77+6693del others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70435105 | ||||||
| chr6:70435107 | A | T | 6 | a0001c0004t0003g0010 a0001c0004t0003g0011 a0001c0004t0003g0012 others(3): Show |
6 | HG02559.hp1 HG02717.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.77+6688A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435107 | |||||||
| chr6:70435109 | A | T | 21 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0103 others(18): Show |
21 | HG01074.hp2 HG01346.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.77+6690A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435109 | |||||||
| chr6:70435110 | T | TA | 7 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(4): Show |
7 | HG02109.hp1 HG02293.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+6691_77+6692ins others(1): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435110 | |||||||
| chr6:70435111 | T | A | 11 | a0001c0001t0001g0075 a0001c0001t0001g0140 a0001c0001t0001g0158 others(8): Show |
11 | HG00642.hp2 HG01109.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.77+6692T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435111 | |||||||
| chr6:70435112 | T | A | 1 | a0001c0001t0001g0092 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.77+6693T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435112 | |||||||
| chr6:70435139 | T | C | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+6720T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435139 | |||||||
| chr6:70435319 | G | T | 1 | a0002c0003t0001g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.77+6900G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435319 | |||||||
| chr6:70435322 | C | T | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.77+6903C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435322 | |||||||
| chr6:70435400 | C | T | 6 | a0002c0003t0001g0135 a0002c0006t0001g0034 a0002c0006t0001g0136 others(3): Show |
6 | HG00597.hp2 HG00621.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.77+6981C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435400 | |||||||
| chr6:70435573 | G | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0158 |
2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.77+7154G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435573 | |||||||
| chr6:70435701 | A | G | 19 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(16): Show |
19 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.77+7282A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435701 | |||||||
| chr6:70435775 | G | T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.77+7356G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435775 | |||||||
| chr6:70435844 | A | G | 12 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(9): Show |
12 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.77+7425A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70435844 | |||||||
| chr6:70436011 | C | T | 19 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(16): Show |
19 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.77+7592C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70436011 | |||||||
| chr6:70436316 | A | G | 1 | a0001c0002t0002g0207 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.77+7897A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70436316 | |||||||
| chr6:70436331 | A | G | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.77+7912A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70436331 | |||||||
| chr6:70436345 | G | A | 25 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 others(22): Show |
25 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.77+7926G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70436345 | |||||||
| chr6:70436499 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.77+8080A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70436499 | |||||||
| chr6:70436610 | C | A | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.77+8191C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70436610 | |||||||
| chr6:70436633 | G | A | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.77+8214G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70436633 | |||||||
| chr6:70436740 | T | C | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.77+8321T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70436740 | |||||||
| chr6:70436792 | T | C | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.77+8373T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70436792 | |||||||
| chr6:70437187 | G | A | 4 | a0001c0001t0001g0036 a0001c0001t0001g0090 a0001c0001t0001g0093 others(1): Show |
4 | HG02027.hp2 NA18966.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+8768G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70437187 | |||||||
| chr6:70437509 | ATTAC | A | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.77+9094_77+9097del others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70437509 | ||||||
| chr6:70437558 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.77+9139G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70437558 | |||||||
| chr6:70437574 | C | G | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.77+9155C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70437574 | |||||||
| chr6:70437937 | A | G | 28 | a0001c0004t0003g0001 a0001c0004t0003g0009 a0001c0004t0003g0010 others(25): Show |
28 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.77+9518A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70437937 | |||||||
| chr6:70438242 | C | T | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.77+9823C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70438242 | |||||||
| chr6:70438593 | C | A | 5 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(2): Show |
5 | HG00738.hp1 HG01099.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+10174C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70438593 | |||||||
| chr6:70438774 | G | A | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+10355G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70438774 | |||||||
| chr6:70438815 | A | G | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.77+10396A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70438815 | |||||||
| chr6:70438987 | C | G | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.77+10568C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70438987 | |||||||
| chr6:70439026 | G | T | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.77+10607G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70439026 | |||||||
| chr6:70439208 | A | G | 1 | a0001c0004t0003g0017 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.77+10789A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70439208 | |||||||
| chr6:70439659 | C | T | 1 | a0002c0003t0001g0033 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.77+11240C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70439659 | |||||||
| chr6:70439874 | C | T | 9 | a0002c0003t0001g0051 a0002c0003t0001g0107 a0002c0003t0001g0108 others(6): Show |
9 | HG00609.hp2 HG01243.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.77+11455C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70439874 | |||||||
| chr6:70439989 | A | G | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+11570A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70439989 | |||||||
| chr6:70440039 | A | G | 2 | a0010c0018t0005g0006 a0012c0015t0005g0005 |
2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.77+11620A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70440039 | |||||||
| chr6:70440298 | C | T | 6 | a0001c0001t0001g0036 a0001c0001t0001g0090 a0001c0001t0001g0093 others(3): Show |
6 | HG02027.hp2 NA18966.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.77+11879C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70440298 | |||||||
| chr6:70440324 | A | G | 1 | a0002c0003t0001g0134 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.77+11905A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70440324 | |||||||
| chr6:70440329 | T | C | 1 | a0001c0004t0003g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.77+11910T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70440329 | |||||||
| chr6:70440659 | A | G | 1 | a0002c0003t0001g0130 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.78-11833A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70440659 | |||||||
| chr6:70440715 | T | G | 1 | a0002c0003t0001g0039 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.78-11777T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70440715 | |||||||
| chr6:70440983 | C | T | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-11509C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70440983 | |||||||
| chr6:70441061 | T | A | 18 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(15): Show |
18 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.78-11431T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70441061 | |||||||
| chr6:70441113 | G | T | 54 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(51): Show |
54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.78-11379G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70441113 | |||||||
| chr6:70441136 | G | T | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.78-11356G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70441136 | |||||||
| chr6:70441311 | C | G | 1 | a0002c0003t0008g0129 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.78-11181C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70441311 | |||||||
| chr6:70441399 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.78-11093A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70441399 | |||||||
| chr6:70441667 | A | G | 2 | a0001c0001t0001g0109 a0002c0003t0001g0150 |
2 | HG02486.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.78-10825A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70441667 | |||||||
| chr6:70441685 | A | AT | 31 | a0001c0001t0001g0036 a0001c0001t0001g0092 a0001c0001t0001g0102 others(28): Show |
31 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.78-10790dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70441685 | ||||||
| chr6:70441685 | A | T | 1 | a0001c0001t0001g0062 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.78-10807A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70441685 | |||||||
| chr6:70441830 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.78-10662G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70441830 | |||||||
| chr6:70442071 | A | G | 1 | a0002c0003t0001g0132 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.78-10421A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442071 | |||||||
| chr6:70442238 | G | GT | 8 | a0001c0002t0002g0195 a0001c0002t0002g0196 a0001c0002t0002g0197 others(5): Show |
8 | HG00280.hp1 HG01243.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.78-10254_78-10253i others(3): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442238 | |||||||
| chr6:70442238 | G | GTT | 13 | a0001c0004t0006g0019 a0001c0009t0001g0211 a0001c0009t0001g0212 others(10): Show |
13 | HG01192.hp2 HG02109.hp1 HG02293.hp1 others(10): Show |
intron_variant | MODIFIER | c.78-10254_78-10253i others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442238 | |||||||
| chr6:70442238 | G | GTTT | 27 | a0001c0004t0003g0001 a0001c0004t0003g0009 a0001c0004t0003g0010 others(24): Show |
27 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.78-10254_78-10253i others(5): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442238 | |||||||
| chr6:70442238 | G | GTTTT | 3 | a0001c0004t0003g0240 a0001c0004t0003g0241 a0001c0004t0003g0252 |
3 | HG02572.hp1 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.78-10254_78-10253i others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442238 | |||||||
| chr6:70442239 | G | GT | 12 | a0001c0001t0001g0036 a0001c0001t0001g0061 a0001c0001t0001g0088 others(9): Show |
12 | HG00735.hp1 HG01192.hp1 HG02300.hp1 others(9): Show |
intron_variant | MODIFIER | c.78-10235dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70442239 | ||||||
| chr6:70442239 | G | T | 111 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(108): Show |
111 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.78-10253G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442239 | |||||||
| chr6:70442260 | C | T | 2 | a0001c0002t0002g0173 a0001c0002t0002g0174 |
2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.78-10232C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442260 | |||||||
| chr6:70442273 | G | A | 72 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(69): Show |
72 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.78-10219G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442273 | |||||||
| chr6:70442339 | A | G | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-10153A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442339 | |||||||
| chr6:70442369 | T | C | 2 | a0010c0018t0005g0006 a0012c0015t0005g0005 |
2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.78-10123T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442369 | |||||||
| chr6:70442411 | T | C | 1 | a0001c0002t0002g0171 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.78-10081T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442411 | |||||||
| chr6:70442427 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.78-10065C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442427 | |||||||
| chr6:70442459 | A | G | 31 | a0001c0002t0002g0167 a0001c0002t0002g0176 a0001c0002t0002g0178 others(28): Show |
31 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.78-10033A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442459 | |||||||
| chr6:70442708 | G | A | 26 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 others(23): Show |
26 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.78-9784G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442708 | |||||||
| chr6:70442737 | C | CA | 70 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(67): Show |
70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.78-9746dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70442737 | ||||||
| chr6:70442759 | T | A | 143 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 others(140): Show |
143 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.78-9733T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442759 | |||||||
| chr6:70442772 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.78-9720T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442772 | |||||||
| chr6:70442826 | A | G | 1 | a0001c0002t0002g0258 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.78-9666A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70442826 | |||||||
| chr6:70443005 | A | G | 6 | a0001c0001t0001g0036 a0001c0001t0001g0090 a0001c0001t0001g0093 others(3): Show |
6 | HG02027.hp2 NA18966.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.78-9487A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70443005 | |||||||
| chr6:70443101 | G | T | 7 | a0001c0002t0002g0223 a0001c0002t0002g0224 a0001c0002t0002g0225 others(4): Show |
7 | NA18947.hp2 NA18950.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.78-9391G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70443101 | |||||||
| chr6:70443308 | ATGGTAGT others(5): Show |
A | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.78-9178_78-9167del others(12): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70443308 | ||||||
| chr6:70443469 | C | T | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-9023C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70443469 | |||||||
| chr6:70443516 | G | A | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-8976G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70443516 | |||||||
| chr6:70443535 | C | T | 11 | a0001c0004t0003g0010 a0001c0004t0003g0011 a0001c0004t0003g0012 others(8): Show |
11 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.78-8957C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70443535 | |||||||
| chr6:70443656 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.78-8836T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70443656 | |||||||
| chr6:70443715 | C | T | 5 | a0001c0002t0002g0204 a0001c0002t0002g0205 a0001c0002t0002g0206 others(2): Show |
5 | HG02723.hp2 HG03540.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.78-8777C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70443715 | |||||||
| chr6:70443857 | A | T | 1 | a0001c0001t0001g0099 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.78-8635A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70443857 | |||||||
| chr6:70443990 | A | C | 5 | a0001c0004t0003g0010 a0001c0004t0003g0011 a0001c0004t0003g0012 others(2): Show |
5 | HG02559.hp1 HG02717.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.78-8502A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70443990 | |||||||
| chr6:70444020 | A | G | 70 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(67): Show |
70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.78-8472A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70444020 | |||||||
| chr6:70444046 | G | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0267 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.78-8446G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70444046 | |||||||
| chr6:70444065 | C | T | 1 | a0001c0002t0002g0258 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.78-8427C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70444065 | |||||||
| chr6:70444171 | A | G | 113 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(110): Show |
113 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.78-8321A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70444171 | |||||||
| chr6:70444174 | A | G | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.78-8318A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70444174 | |||||||
| chr6:70444290 | C | T | 2 | a0002c0003t0001g0125 a0002c0003t0001g0126 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.78-8202C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70444290 | |||||||
| chr6:70444335 | A | G | 3 | a0001c0004t0004g0015 a0004c0008t0004g0003 a0004c0008t0004g0004 |
3 | HG01074.hp2 HG01346.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.78-8157A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70444335 | |||||||
| chr6:70444345 | T | C | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-8147T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70444345 | |||||||
| chr6:70444406 | AAAAT | A | 117 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(114): Show |
117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.78-8063_78-8060del others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70444406 | ||||||
| chr6:70444429 | A | C | 47 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(44): Show |
47 | HG01069.hp1 HG01074.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.78-8063A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70444429 | |||||||
| chr6:70444732 | C | T | 1 | a0002c0003t0001g0134 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.78-7760C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70444732 | |||||||
| chr6:70444760 | A | G | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.78-7732A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70444760 | |||||||
| chr6:70444791 | A | G | 1 | a0001c0004t0003g0241 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.78-7701A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70444791 | |||||||
| chr6:70444851 | A | T | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.78-7641A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70444851 | |||||||
| chr6:70445021 | A | G | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.78-7471A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445021 | |||||||
| chr6:70445102 | T | C | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.78-7390T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445102 | |||||||
| chr6:70445138 | CAG | C | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.78-7353_78-7352del others(2): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445138 | |||||||
| chr6:70445146 | G | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.78-7346G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445146 | |||||||
| chr6:70445361 | G | GAGACCA | 117 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(114): Show |
117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.78-7131_78-7130ins others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445361 | |||||||
| chr6:70445362 | T | C | 1 | a0011c0011t0002g0170 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.78-7130T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445362 | |||||||
| chr6:70445362 | T | G | 116 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(113): Show |
116 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.78-7130T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445362 | |||||||
| chr6:70445365 | T | C | 219 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(216): Show |
219 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.78-7127T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445365 | |||||||
| chr6:70445392 | G | A | 2 | a0010c0018t0005g0006 a0012c0015t0005g0005 |
2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.78-7100G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445392 | |||||||
| chr6:70445472 | A | G | 1 | a0002c0003t0001g0042 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.78-7020A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445472 | |||||||
| chr6:70445734 | C | T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.78-6758C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445734 | |||||||
| chr6:70445735 | G | A | 1 | a0001c0002t0002g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.78-6757G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445735 | |||||||
| chr6:70445852 | G | C | 6 | a0002c0003t0001g0135 a0002c0006t0001g0034 a0002c0006t0001g0136 others(3): Show |
6 | HG00597.hp2 HG00621.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.78-6640G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445852 | |||||||
| chr6:70445856 | G | A | 18 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(15): Show |
18 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.78-6636G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445856 | |||||||
| chr6:70445856 | G | C | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.78-6636G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70445856 | |||||||
| chr6:70446149 | T | C | 8 | a0001c0004t0003g0010 a0001c0004t0003g0011 a0001c0004t0003g0012 others(5): Show |
8 | HG02559.hp1 HG02572.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-6343T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446149 | |||||||
| chr6:70446155 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.78-6337A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446155 | |||||||
| chr6:70446159 | C | T | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.78-6333C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446159 | |||||||
| chr6:70446186 | C | A | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-6306C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446186 | |||||||
| chr6:70446236 | A | G | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.78-6256A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446236 | |||||||
| chr6:70446312 | C | T | 14 | a0001c0004t0003g0001 a0001c0004t0003g0230 a0001c0004t0003g0231 others(11): Show |
14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-6180C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446312 | |||||||
| chr6:70446408 | A | T | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.78-6084A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446408 | |||||||
| chr6:70446442 | C | G | 8 | a0001c0004t0003g0010 a0001c0004t0003g0011 a0001c0004t0003g0012 others(5): Show |
8 | HG02559.hp1 HG02572.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-6050C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446442 | |||||||
| chr6:70446447 | T | A | 18 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(15): Show |
18 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.78-6045T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446447 | |||||||
| chr6:70446475 | G | A | 5 | a0001c0002t0002g0204 a0001c0002t0002g0205 a0001c0002t0002g0206 others(2): Show |
5 | HG02723.hp2 HG03540.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.78-6017G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446475 | |||||||
| chr6:70446489 | G | A | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-6003G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446489 | |||||||
| chr6:70446692 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.78-5800T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446692 | |||||||
| chr6:70446693 | T | G | 1 | a0001c0002t0002g0168 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.78-5799T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446693 | |||||||
| chr6:70446882 | T | C | 1 | a0001c0009t0001g0212 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.78-5610T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446882 | |||||||
| chr6:70446924 | G | T | 1 | a0001c0001t0001g0098 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.78-5568G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70446924 | |||||||
| chr6:70447004 | C | T | 2 | a0001c0002t0002g0168 a0001c0002t0002g0209 |
2 | NA18962.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.78-5488C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70447004 | |||||||
| chr6:70447005 | G | A | 1 | a0002c0003t0001g0039 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.78-5487G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70447005 | |||||||
| chr6:70447042 | G | A | 117 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(114): Show |
117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.78-5450G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70447042 | |||||||
| chr6:70447083 | G | A | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-5409G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70447083 | |||||||
| chr6:70447099 | G | A | 2 | a0010c0018t0005g0006 a0012c0015t0005g0005 |
2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.78-5393G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70447099 | |||||||
| chr6:70447359 | A | G | 7 | a0001c0002t0002g0223 a0001c0002t0002g0224 a0001c0002t0002g0225 others(4): Show |
7 | NA18947.hp2 NA18950.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.78-5133A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70447359 | |||||||
| chr6:70447471 | C | T | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.78-5021C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70447471 | |||||||
| chr6:70447530 | A | G | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-4962A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70447530 | |||||||
| chr6:70447565 | G | A | 2 | a0001c0002t0002g0173 a0001c0002t0002g0174 |
2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.78-4927G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70447565 | |||||||
| chr6:70447759 | T | C | 2 | a0001c0001t0001g0064 a0001c0001t0001g0151 |
2 | HG01109.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.78-4733T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70447759 | |||||||
| chr6:70447791 | C | T | 1 | a0001c0004t0003g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.78-4701C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70447791 | |||||||
| chr6:70447849 | C | T | 3 | a0001c0002t0002g0254 a0001c0002t0002g0258 a0001c0002t0002g0259 |
3 | HG00642.hp2 HG02886.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.78-4643C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70447849 | |||||||
| chr6:70447876 | C | T | 14 | a0001c0004t0003g0001 a0001c0004t0003g0230 a0001c0004t0003g0231 others(11): Show |
14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-4616C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70447876 | |||||||
| chr6:70447967 | A | G | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.78-4525A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70447967 | |||||||
| chr6:70448007 | TATA | T | 26 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 others(23): Show |
26 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.78-4481_78-4479del others(3): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70448007 | ||||||
| chr6:70448194 | G | A | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-4298G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70448194 | |||||||
| chr6:70448582 | T | A | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-3910T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70448582 | |||||||
| chr6:70448600 | C | T | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.78-3892C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70448600 | |||||||
| chr6:70448641 | A | G | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.78-3851A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70448641 | |||||||
| chr6:70448671 | G | A | 32 | a0001c0004t0003g0001 a0001c0004t0003g0009 a0001c0004t0003g0010 others(29): Show |
32 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.78-3821G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70448671 | |||||||
| chr6:70448687 | G | A | 14 | a0001c0004t0003g0001 a0001c0004t0003g0230 a0001c0004t0003g0231 others(11): Show |
14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-3805G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70448687 | |||||||
| chr6:70448689 | G | A | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.78-3803G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70448689 | |||||||
| chr6:70448748 | A | C | 1 | a0001c0004t0003g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.78-3744A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70448748 | |||||||
| chr6:70448778 | G | A | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-3714G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70448778 | |||||||
| chr6:70448850 | C | T | 3 | a0001c0001t0001g0048 a0001c0001t0001g0092 a0001c0001t0001g0105 |
3 | HG01074.hp1 HG01167.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.78-3642C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70448850 | |||||||
| chr6:70448983 | A | G | 1 | a0001c0004t0003g0239 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.78-3509A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70448983 | |||||||
| chr6:70449039 | C | G | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-3453C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70449039 | |||||||
| chr6:70449107 | C | A | 14 | a0001c0004t0003g0001 a0001c0004t0003g0230 a0001c0004t0003g0231 others(11): Show |
14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-3385C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70449107 | |||||||
| chr6:70449130 | A | G | 54 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(51): Show |
54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.78-3362A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70449130 | |||||||
| chr6:70449139 | T | A | 2 | a0010c0018t0005g0006 a0012c0015t0005g0005 |
2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.78-3353T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70449139 | |||||||
| chr6:70449296 | C | T | 12 | a0001c0004t0003g0009 a0001c0004t0003g0010 a0001c0004t0003g0011 others(9): Show |
12 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.78-3196C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70449296 | |||||||
| chr6:70449586 | T | C | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-2906T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70449586 | |||||||
| chr6:70449608 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.78-2884G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70449608 | |||||||
| chr6:70449931 | C | T | 70 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(67): Show |
70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.78-2561C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70449931 | |||||||
| chr6:70449960 | C | T | 1 | a0001c0002t0002g0169 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.78-2532C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70449960 | |||||||
| chr6:70450072 | A | G | 1 | a0001c0004t0003g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.78-2420A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70450072 | |||||||
| chr6:70450215 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.78-2277G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70450215 | |||||||
| chr6:70450481 | C | A | 1 | a0001c0001t0001g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.78-2011C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70450481 | |||||||
| chr6:70450716 | G | GT | 14 | a0001c0001t0001g0073 a0001c0001t0001g0086 a0001c0001t0001g0088 others(11): Show |
14 | HG00673.hp1 HG01515.hp1 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.78-1734dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | ||||||
| chr6:70450716 | G | GTT | 8 | a0001c0001t0001g0036 a0001c0001t0001g0067 a0001c0001t0001g0087 others(5): Show |
8 | HG00738.hp1 HG01069.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.78-1735_78-1734dup others(2): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | ||||||
| chr6:70450716 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.78-1776G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70450716 | |||||||
| chr6:70450716 | GT | G | 45 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0053 others(42): Show |
45 | HG00621.hp2 HG00639.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.78-1734delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | ||||||
| chr6:70450716 | GTT | G | 19 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0057 others(16): Show |
19 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.78-1735_78-1734del others(2): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | ||||||
| chr6:70450716 | GTTT | G | 13 | a0001c0001t0001g0021 a0001c0001t0001g0054 a0001c0001t0001g0055 others(10): Show |
13 | HG00733.hp2 HG01123.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.78-1736_78-1734del others(3): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | ||||||
| chr6:70450716 | GTTTTTTT others(3): Show |
G | 11 | a0001c0004t0003g0001 a0001c0004t0003g0230 a0001c0004t0003g0232 others(8): Show |
11 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.78-1743_78-1734del others(10): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | ||||||
| chr6:70450716 | GTTTTTTT others(4): Show |
G | 5 | a0001c0001t0001g0154 a0001c0004t0004g0015 a0004c0008t0004g0003 others(2): Show |
5 | HG01074.hp2 HG01346.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.78-1744_78-1734del others(11): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | ||||||
| chr6:70450716 | GTTTTTTT others(5): Show |
G | 4 | a0001c0001t0001g0153 a0001c0004t0003g0009 a0001c0004t0003g0251 others(1): Show |
4 | HG03209.hp1 HG03491.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.78-1745_78-1734del others(12): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | ||||||
| chr6:70450716 | GTTTTTTT others(6): Show |
G | 10 | a0001c0001t0001g0104 a0001c0004t0003g0010 a0001c0004t0003g0011 others(7): Show |
10 | HG01192.hp2 HG02559.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.78-1746_78-1734del others(13): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | ||||||
| chr6:70450716 | GTTTTTTT others(7): Show |
G | 3 | a0001c0001t0001g0076 a0001c0004t0003g0012 a0001c0004t0003g0014 |
3 | HG03225.hp1 NA18979.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.78-1747_78-1734del others(14): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | ||||||
| chr6:70450716 | GTTTTTTT others(8): Show |
G | 11 | a0001c0001t0001g0063 a0001c0009t0001g0211 a0001c0009t0001g0212 others(8): Show |
11 | HG01433.hp2 HG02109.hp1 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.78-1748_78-1734del others(15): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | ||||||
| chr6:70450716 | GTTTTTTT others(9): Show |
G | 3 | a0001c0002t0002g0168 a0002c0003t0001g0111 a0002c0003t0001g0112 |
3 | NA18962.hp1 NA19070.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.78-1749_78-1734del others(16): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | ||||||
| chr6:70450716 | GTTTTTTT others(10): Show |
G | 18 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0148 others(15): Show |
18 | HG00673.hp2 HG01243.hp2 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.78-1750_78-1734del others(17): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | ||||||
| chr6:70450716 | GTTTTTTT others(11): Show |
G | 56 | a0001c0001t0001g0210 a0001c0002t0002g0167 a0001c0002t0002g0173 others(53): Show |
56 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.78-1751_78-1734del others(18): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | ||||||
| chr6:70450716 | GTTTTTTT others(17): Show |
G | 1 | a0001c0001t0001g0048 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.78-1757_78-1734del others(24): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | ||||||
| chr6:70450716 | GTTTTTTT others(19): Show |
G | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.78-1759_78-1734del others(26): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 70450716 | ||||||
| chr6:70450719 | T | G | 1 | a0002c0003t0001g0042 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.78-1773T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70450719 | |||||||
| chr6:70450732 | T | G | 2 | a0010c0018t0005g0006 a0012c0015t0005g0005 |
2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.78-1760T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70450732 | |||||||
| chr6:70450817 | C | G | 70 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(67): Show |
70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.78-1675C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70450817 | |||||||
| chr6:70451049 | C | T | 161 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(158): Show |
161 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(158): Show |
intron_variant | MODIFIER | c.78-1443C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70451049 | |||||||
| chr6:70451118 | T | G | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.78-1374T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70451118 | |||||||
| chr6:70451413 | G | A | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.78-1079G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70451413 | |||||||
| chr6:70451416 | T | C | 1 | a0002c0003t0001g0044 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.78-1076T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70451416 | |||||||
| chr6:70451451 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.78-1041C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70451451 | |||||||
| chr6:70451607 | C | G | 1 | a0001c0004t0004g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.78-885C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70451607 | |||||||
| chr6:70451613 | C | A | 113 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(110): Show |
113 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.78-879C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70451613 | |||||||
| chr6:70451677 | C | A | 1 | a0002c0003t0008g0129 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.78-815C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70451677 | |||||||
| chr6:70451719 | G | C | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.78-773G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70451719 | |||||||
| chr6:70451826 | T | A | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.78-666T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70451826 | |||||||
| chr6:70451869 | A | G | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.78-623A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70451869 | |||||||
| chr6:70451966 | G | A | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.78-526G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70451966 | |||||||
| chr6:70452115 | A | G | 1 | a0001c0002t0002g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.78-377A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70452115 | |||||||
| chr6:70452200 | C | T | 5 | a0001c0001t0001g0075 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
5 | HG00639.hp2 HG01081.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.78-292C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70452200 | |||||||
| chr6:70452285 | A | G | 1 | a0002c0003t0001g0131 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.78-207A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70452285 | |||||||
| chr6:70452427 | G | A | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.78-65G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | chr6 | 70452427 | |||||||
| chr6:70452584 | A | C | 2 | a0001c0002t0002g0258 a0001c0002t0002g0259 |
2 | HG00642.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.157+13A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70452584 | |||||||
| chr6:70452943 | A | G | 2 | a0002c0003t0001g0030 a0002c0003t0001g0031 |
2 | NA18990.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.157+372A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70452943 | |||||||
| chr6:70452989 | G | A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0267 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.157+418G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70452989 | |||||||
| chr6:70453007 | A | C | 1 | a0001c0001t0001g0076 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.157+436A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70453007 | |||||||
| chr6:70453554 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.157+983T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70453554 | |||||||
| chr6:70453576 | C | A | 1 | a0002c0003t0001g0123 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.157+1005C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70453576 | |||||||
| chr6:70453618 | A | G | 1 | a0001c0002t0002g0183 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.157+1047A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70453618 | |||||||
| chr6:70453628 | C | T | 70 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(67): Show |
70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.157+1057C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70453628 | |||||||
| chr6:70453764 | A | G | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.157+1193A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70453764 | |||||||
| chr6:70453773 | C | T | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.157+1202C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70453773 | |||||||
| chr6:70453865 | C | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0267 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.157+1294C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70453865 | |||||||
| chr6:70453922 | A | G | 1 | a0001c0004t0003g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.157+1351A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70453922 | |||||||
| chr6:70453952 | G | A | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+1381G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70453952 | |||||||
| chr6:70453969 | A | T | 1 | a0011c0011t0002g0170 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.157+1398A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70453969 | |||||||
| chr6:70454074 | T | G | 1 | a0002c0003t0001g0114 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.157+1503T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454074 | |||||||
| chr6:70454153 | C | T | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.157+1582C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454153 | |||||||
| chr6:70454184 | G | A | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.157+1613G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454184 | |||||||
| chr6:70454310 | C | T | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.157+1739C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454310 | |||||||
| chr6:70454333 | A | G | 1 | a0002c0003t0001g0118 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.157+1762A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454333 | |||||||
| chr6:70454461 | T | A | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.157+1890T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454461 | |||||||
| chr6:70454588 | G | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.157+2017G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454588 | |||||||
| chr6:70454602 | G | A | 2 | a0001c0002t0002g0258 a0001c0002t0002g0259 |
2 | HG00642.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.157+2031G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454602 | |||||||
| chr6:70454658 | A | G | 1 | a0001c0002t0002g0194 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.157+2087A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454658 | |||||||
| chr6:70454812 | A | G | 1 | a0002c0003t0001g0122 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.157+2241A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454812 | |||||||
| chr6:70454910 | C | T | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.157+2339C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454910 | |||||||
| chr6:70454911 | A | G | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.157+2340A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454911 | |||||||
| chr6:70454924 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.157+2353G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454924 | |||||||
| chr6:70454967 | A | G | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.157+2396A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454967 | |||||||
| chr6:70454979 | A | G | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.157+2408A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454979 | |||||||
| chr6:70454991 | A | G | 1 | a0002c0003t0001g0121 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.157+2420A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70454991 | |||||||
| chr6:70455020 | C | T | 1 | a0008c0017t0001g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.157+2449C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70455020 | |||||||
| chr6:70455165 | C | A | 135 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(132): Show |
135 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.157+2594C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70455165 | |||||||
| chr6:70455215 | A | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | NA19068.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.157+2644A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70455215 | |||||||
| chr6:70455275 | C | T | 9 | a0002c0003t0001g0051 a0002c0003t0001g0107 a0002c0003t0001g0108 others(6): Show |
9 | HG00609.hp2 HG01243.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.157+2704C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70455275 | |||||||
| chr6:70455311 | A | G | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.157+2740A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70455311 | |||||||
| chr6:70455381 | T | TAC | 15 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0087 others(12): Show |
15 | HG00280.hp2 HG01175.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.157+2841_157+2842d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70455381 | ||||||
| chr6:70455381 | T | TACAC | 9 | a0001c0001t0001g0102 a0001c0004t0003g0010 a0001c0004t0003g0011 others(6): Show |
9 | HG00673.hp1 HG01074.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.157+2839_157+2842d others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70455381 | ||||||
| chr6:70455381 | TAC | T | 71 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0053 others(68): Show |
71 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.157+2841_157+2842d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70455381 | ||||||
| chr6:70455381 | TACAC | T | 33 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0168 others(30): Show |
33 | HG00280.hp1 HG00621.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.157+2839_157+2842d others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70455381 | ||||||
| chr6:70455381 | TACACACA others(3): Show |
T | 1 | a0001c0002t0002g0262 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.157+2833_157+2842d others(12): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70455381 | ||||||
| chr6:70455408 | A | C | 1 | a0001c0001t0001g0128 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.157+2837A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70455408 | |||||||
| chr6:70455521 | A | G | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.157+2950A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70455521 | |||||||
| chr6:70455700 | A | T | 54 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(51): Show |
54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.157+3129A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70455700 | |||||||
| chr6:70455733 | A | G | 1 | a0002c0003t0001g0123 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.157+3162A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70455733 | |||||||
| chr6:70455813 | ATTAT | A | 32 | a0001c0004t0003g0001 a0001c0004t0003g0009 a0001c0004t0003g0010 others(29): Show |
32 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.157+3244_157+3247d others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70455813 | ||||||
| chr6:70455876 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.157+3305G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70455876 | |||||||
| chr6:70455944 | C | T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.157+3373C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70455944 | |||||||
| chr6:70455946 | G | A | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.157+3375G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70455946 | |||||||
| chr6:70455959 | C | T | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.157+3388C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70455959 | |||||||
| chr6:70456051 | C | T | 14 | a0001c0004t0003g0001 a0001c0004t0003g0230 a0001c0004t0003g0231 others(11): Show |
14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.157+3480C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70456051 | |||||||
| chr6:70456071 | C | T | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.157+3500C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70456071 | |||||||
| chr6:70456177 | A | C | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.157+3606A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70456177 | |||||||
| chr6:70456388 | A | G | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.157+3817A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70456388 | |||||||
| chr6:70456441 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.157+3870G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70456441 | |||||||
| chr6:70456472 | G | T | 1 | a0001c0001t0001g0089 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.157+3901G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70456472 | |||||||
| chr6:70456497 | A | G | 1 | a0001c0013t0001g0085 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.157+3926A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70456497 | |||||||
| chr6:70456572 | T | C | 2 | a0010c0018t0005g0006 a0012c0015t0005g0005 |
2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.157+4001T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70456572 | |||||||
| chr6:70456763 | C | A | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.157+4192C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70456763 | |||||||
| chr6:70456784 | C | T | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.157+4213C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70456784 | |||||||
| chr6:70456908 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.157+4337C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70456908 | |||||||
| chr6:70456966 | T | C | 2 | a0010c0018t0005g0006 a0012c0015t0005g0005 |
2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.157+4395T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70456966 | |||||||
| chr6:70457357 | C | T | 8 | a0001c0004t0003g0010 a0001c0004t0003g0011 a0001c0004t0003g0012 others(5): Show |
8 | HG02559.hp1 HG02572.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.157+4786C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70457357 | |||||||
| chr6:70457382 | C | T | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.157+4811C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70457382 | |||||||
| chr6:70457404 | A | T | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.157+4833A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70457404 | |||||||
| chr6:70457597 | A | T | 1 | a0001c0001t0001g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.157+5026A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70457597 | |||||||
| chr6:70457679 | T | C | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.157+5108T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70457679 | |||||||
| chr6:70457993 | T | G | 3 | a0001c0002t0002g0219 a0001c0002t0002g0220 a0001c0002t0002g0222 |
3 | HG00609.hp1 HG00621.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.157+5422T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70457993 | |||||||
| chr6:70458125 | A | G | 7 | a0001c0002t0002g0223 a0001c0002t0002g0224 a0001c0002t0002g0225 others(4): Show |
7 | NA18947.hp2 NA18950.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.157+5554A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70458125 | |||||||
| chr6:70458128 | A | ATC | 113 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(110): Show |
113 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.157+5559_157+5560d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70458128 | ||||||
| chr6:70458260 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.157+5689C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70458260 | |||||||
| chr6:70458312 | A | G | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.157+5741A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70458312 | |||||||
| chr6:70458357 | A | T | 1 | a0007c0019t0001g0079 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.157+5786A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70458357 | |||||||
| chr6:70458429 | G | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.157+5858G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70458429 | |||||||
| chr6:70458450 | G | A | 1 | a0004c0008t0004g0003 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.157+5879G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70458450 | |||||||
| chr6:70458697 | T | C | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.157+6126T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70458697 | |||||||
| chr6:70458728 | A | G | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.157+6157A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70458728 | |||||||
| chr6:70458809 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.157+6238A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70458809 | |||||||
| chr6:70458875 | C | G | 14 | a0001c0004t0003g0001 a0001c0004t0003g0230 a0001c0004t0003g0231 others(11): Show |
14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.157+6304C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70458875 | |||||||
| chr6:70458951 | A | G | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.157+6380A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70458951 | |||||||
| chr6:70458988 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.157+6417G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70458988 | |||||||
| chr6:70459531 | A | G | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.157+6960A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70459531 | |||||||
| chr6:70459827 | A | G | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.157+7256A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70459827 | |||||||
| chr6:70459946 | G | T | 1 | a0002c0003t0001g0134 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.157+7375G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70459946 | |||||||
| chr6:70459961 | G | T | 1 | a0002c0003t0001g0122 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.157+7390G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70459961 | |||||||
| chr6:70459977 | G | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.157+7406G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70459977 | |||||||
| chr6:70460088 | T | C | 1 | a0001c0002t0002g0260 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.157+7517T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70460088 | |||||||
| chr6:70460114 | G | A | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.157+7543G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70460114 | |||||||
| chr6:70460144 | G | T | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.157+7573G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70460144 | |||||||
| chr6:70460598 | G | A | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.157+8027G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70460598 | |||||||
| chr6:70460635 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.157+8064G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70460635 | |||||||
| chr6:70460788 | GATCT | G | 9 | a0002c0003t0001g0051 a0002c0003t0001g0107 a0002c0003t0001g0108 others(6): Show |
9 | HG00609.hp2 HG01243.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.157+8235_157+8238d others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70460788 | ||||||
| chr6:70460810 | G | T | 1 | a0001c0001t0001g0066 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.157+8239G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70460810 | |||||||
| chr6:70460852 | T | TTTTTTTT others(1): Show |
56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.157+8288_157+8289i others(10): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70460852 | ||||||
| chr6:70461004 | A | G | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.157+8433A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70461004 | |||||||
| chr6:70461113 | G | A | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.157+8542G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70461113 | |||||||
| chr6:70461116 | C | T | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.157+8545C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70461116 | |||||||
| chr6:70461163 | T | A | 54 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(51): Show |
54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.157+8592T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70461163 | |||||||
| chr6:70461477 | CAT | C | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+8908_157+8909d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70461477 | ||||||
| chr6:70461548 | G | A | 2 | a0001c0002t0002g0261 a0001c0002t0002g0262 |
2 | HG01516.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.157+8977G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70461548 | |||||||
| chr6:70461549 | T | G | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.157+8978T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70461549 | |||||||
| chr6:70461675 | G | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.157+9104G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70461675 | |||||||
| chr6:70461736 | A | G | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.157+9165A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70461736 | |||||||
| chr6:70462089 | C | G | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.157+9518C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70462089 | |||||||
| chr6:70462396 | G | A | 26 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 others(23): Show |
26 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.157+9825G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70462396 | |||||||
| chr6:70462404 | A | T | 40 | a0001c0002t0002g0167 a0001c0002t0002g0176 a0001c0002t0002g0177 others(37): Show |
40 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.157+9833A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70462404 | |||||||
| chr6:70462604 | C | G | 54 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(51): Show |
54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.157+10033C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70462604 | |||||||
| chr6:70462609 | A | G | 3 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0002c0003t0001g0022 |
3 | HG02027.hp2 NA19056.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.157+10038A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70462609 | |||||||
| chr6:70462686 | G | A | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.157+10115G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70462686 | |||||||
| chr6:70462887 | G | A | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.157+10316G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70462887 | |||||||
| chr6:70462930 | T | A | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+10359T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70462930 | |||||||
| chr6:70462944 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.157+10373A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70462944 | |||||||
| chr6:70462948 | G | GTTGTT | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.157+10381_157+1038 others(9): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70462948 | ||||||
| chr6:70463250 | G | C | 99 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(96): Show |
99 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.157+10679G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70463250 | |||||||
| chr6:70463252 | C | A | 1 | a0001c0002t0002g0223 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.157+10681C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70463252 | |||||||
| chr6:70463419 | T | TA | 96 | a0001c0001t0001g0028 a0001c0001t0001g0077 a0001c0001t0001g0158 others(93): Show |
96 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.157+10864dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70463419 | ||||||
| chr6:70463419 | T | TAA | 14 | a0001c0002t0002g0171 a0001c0002t0002g0253 a0001c0002t0002g0254 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.157+10863_157+1086 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70463419 | ||||||
| chr6:70463436 | T | A | 1 | a0011c0011t0002g0170 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.157+10865T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70463436 | |||||||
| chr6:70463481 | A | C | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.157+10910A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70463481 | |||||||
| chr6:70463496 | G | A | 1 | a0001c0004t0003g0013 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.157+10925G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70463496 | |||||||
| chr6:70463524 | C | T | 81 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(78): Show |
81 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.157+10953C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70463524 | |||||||
| chr6:70463525 | G | T | 1 | a0001c0001t0001g0142 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.157+10954G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70463525 | |||||||
| chr6:70463567 | T | C | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.157+10996T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70463567 | |||||||
| chr6:70463573 | A | G | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+11002A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70463573 | |||||||
| chr6:70463672 | A | C | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.157+11101A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70463672 | |||||||
| chr6:70463867 | A | G | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.157+11296A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70463867 | |||||||
| chr6:70463907 | T | G | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.157+11336T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70463907 | |||||||
| chr6:70464044 | TCTTA | T | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.158-11361_158-1135 others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464044 | ||||||
| chr6:70464360 | G | A | 2 | a0010c0018t0005g0006 a0012c0015t0005g0005 |
2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.158-11050G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70464360 | |||||||
| chr6:70464566 | C | T | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.158-10844C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70464566 | |||||||
| chr6:70464608 | G | A | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.158-10802G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70464608 | |||||||
| chr6:70464638 | ATTTC | A | 3 | a0001c0001t0001g0215 a0001c0001t0001g0217 a0002c0003t0001g0113 |
3 | HG00642.hp1 HG01515.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.158-10752_158-1074 others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464638 | ||||||
| chr6:70464654 | CTTTCTTT others(2): Show |
C | 12 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(9): Show |
12 | HG00280.hp1 HG00639.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.158-10743_158-1073 others(13): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464654 | ||||||
| chr6:70464658 | C | CT | 52 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(49): Show |
52 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.158-10744dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464658 | ||||||
| chr6:70464658 | C | CTT | 9 | a0001c0001t0001g0210 a0001c0002t0002g0191 a0003c0005t0001g0242 others(6): Show |
9 | HG02109.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.158-10745_158-1074 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464658 | ||||||
| chr6:70464658 | C | CTTTTTTT others(6): Show |
1 | a0001c0002t0002g0174 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.158-10744_158-1074 others(17): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464658 | ||||||
| chr6:70464658 | C | CTTTTTTT others(7): Show |
1 | a0001c0002t0002g0173 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.158-10744_158-1074 others(18): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464658 | ||||||
| chr6:70464658 | C | CTTTTTTT others(10): Show |
1 | a0001c0002t0002g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.158-10744_158-1074 others(21): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464658 | ||||||
| chr6:70464658 | C | CTTTTTTT others(14): Show |
1 | a0001c0001t0001g0267 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.158-10744_158-1074 others(25): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464658 | ||||||
| chr6:70464666 | TC | T | 14 | a0001c0004t0003g0001 a0001c0004t0003g0230 a0001c0004t0003g0231 others(11): Show |
14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.158-10743delC | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70464666 | |||||||
| chr6:70464667 | C | CT | 8 | a0001c0001t0001g0115 a0002c0003t0001g0044 a0002c0003t0001g0119 others(5): Show |
8 | HG00140.hp1 HG00140.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.158-10727dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464667 | ||||||
| chr6:70464667 | C | T | 85 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(82): Show |
85 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.158-10743C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70464667 | |||||||
| chr6:70464770 | G | A | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.158-10640G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70464770 | |||||||
| chr6:70464806 | A | G | 12 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0140 others(9): Show |
12 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.158-10604A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70464806 | |||||||
| chr6:70464833 | A | AT | 22 | a0001c0001t0001g0020 a0001c0001t0001g0087 a0001c0001t0001g0089 others(19): Show |
22 | HG00597.hp2 HG00735.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.158-10548dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464833 | ||||||
| chr6:70464833 | A | ATTTTT | 34 | a0001c0001t0001g0210 a0001c0002t0002g0167 a0001c0002t0002g0173 others(31): Show |
34 | HG00597.hp1 HG00733.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.158-10552_158-1054 others(9): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464833 | ||||||
| chr6:70464833 | A | ATTTTTT | 19 | a0001c0001t0001g0267 a0001c0002t0002g0168 a0001c0002t0002g0169 others(16): Show |
19 | HG00609.hp1 HG00621.hp1 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.158-10553_158-1054 others(10): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464833 | ||||||
| chr6:70464833 | AT | A | 10 | a0001c0001t0001g0028 a0001c0001t0001g0106 a0002c0003t0001g0119 others(7): Show |
10 | HG01168.hp1 HG02293.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.158-10548delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464833 | ||||||
| chr6:70464833 | ATT | A | 30 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 others(27): Show |
30 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.158-10549_158-1054 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464833 | ||||||
| chr6:70464833 | ATTTT | A | 17 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(14): Show |
17 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.158-10551_158-1054 others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464833 | ||||||
| chr6:70464833 | ATTTTT | A | 22 | a0001c0002t0002g0256 a0001c0004t0003g0001 a0001c0004t0003g0010 others(19): Show |
22 | HG01069.hp1 HG02280.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.158-10552_158-1054 others(9): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464833 | ||||||
| chr6:70464833 | ATTTTTTT others(12): Show |
A | 1 | a0001c0004t0003g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.158-10566_158-1054 others(23): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70464833 | ||||||
| chr6:70464867 | A | G | 8 | a0001c0004t0003g0010 a0001c0004t0003g0011 a0001c0004t0003g0012 others(5): Show |
8 | HG02559.hp1 HG02572.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.158-10543A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70464867 | |||||||
| chr6:70464890 | G | A | 54 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(51): Show |
54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.158-10520G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70464890 | |||||||
| chr6:70465024 | T | C | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.158-10386T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70465024 | |||||||
| chr6:70465095 | G | A | 11 | a0001c0004t0003g0010 a0001c0004t0003g0011 a0001c0004t0003g0012 others(8): Show |
11 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.158-10315G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70465095 | |||||||
| chr6:70465172 | C | T | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.158-10238C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70465172 | |||||||
| chr6:70465196 | C | G | 1 | a0001c0001t0001g0098 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.158-10214C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70465196 | |||||||
| chr6:70465206 | ATT | A | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.158-10201_158-1020 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70465206 | ||||||
| chr6:70465305 | A | G | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.158-10105A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70465305 | |||||||
| chr6:70465375 | G | T | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.158-10035G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70465375 | |||||||
| chr6:70465407 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.158-10003A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70465407 | |||||||
| chr6:70465448 | G | A | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.158-9962G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70465448 | |||||||
| chr6:70465631 | C | T | 2 | a0002c0003t0001g0051 a0002c0003t0001g0131 |
2 | HG01243.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.158-9779C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70465631 | |||||||
| chr6:70465750 | C | T | 54 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(51): Show |
54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.158-9660C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70465750 | |||||||
| chr6:70465862 | G | A | 1 | a0001c0002t0002g0266 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.158-9548G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70465862 | |||||||
| chr6:70465989 | G | A | 43 | a0001c0004t0003g0001 a0001c0004t0003g0009 a0001c0004t0003g0010 others(40): Show |
43 | HG01069.hp1 HG01074.hp2 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.158-9421G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70465989 | |||||||
| chr6:70466360 | G | T | 3 | a0001c0004t0004g0015 a0004c0008t0004g0003 a0004c0008t0004g0004 |
3 | HG01074.hp2 HG01346.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.158-9050G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70466360 | |||||||
| chr6:70466403 | A | G | 1 | a0011c0011t0002g0170 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.158-9007A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70466403 | |||||||
| chr6:70466515 | G | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.158-8895G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70466515 | |||||||
| chr6:70466586 | G | A | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.158-8824G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70466586 | |||||||
| chr6:70466739 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.158-8671G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70466739 | |||||||
| chr6:70466956 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.158-8454G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70466956 | |||||||
| chr6:70466992 | C | T | 1 | a0002c0003t0001g0150 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.158-8418C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70466992 | |||||||
| chr6:70467144 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.158-8266C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70467144 | |||||||
| chr6:70467165 | G | C | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.158-8245G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70467165 | |||||||
| chr6:70467688 | T | C | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-7722T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70467688 | |||||||
| chr6:70467736 | C | G | 54 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(51): Show |
54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.158-7674C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70467736 | |||||||
| chr6:70467776 | T | C | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.158-7634T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70467776 | |||||||
| chr6:70468270 | T | C | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.158-7140T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70468270 | |||||||
| chr6:70468325 | A | G | 1 | a0001c0002t0002g0208 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.158-7085A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70468325 | |||||||
| chr6:70468403 | T | C | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-7007T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70468403 | |||||||
| chr6:70468424 | G | A | 5 | a0001c0002t0002g0168 a0001c0002t0002g0171 a0001c0002t0002g0172 others(2): Show |
5 | HG00673.hp2 NA18939.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-6986G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70468424 | |||||||
| chr6:70468617 | A | G | 2 | a0004c0008t0004g0003 a0004c0008t0004g0004 |
2 | HG01074.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.158-6793A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70468617 | |||||||
| chr6:70468618 | T | C | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.158-6792T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70468618 | |||||||
| chr6:70468813 | T | C | 1 | a0002c0003t0008g0129 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.158-6597T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70468813 | |||||||
| chr6:70468862 | C | A | 1 | a0001c0002t0002g0254 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.158-6548C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70468862 | |||||||
| chr6:70469078 | G | A | 43 | a0001c0004t0003g0001 a0001c0004t0003g0009 a0001c0004t0003g0010 others(40): Show |
43 | HG01069.hp1 HG01074.hp2 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.158-6332G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70469078 | |||||||
| chr6:70469082 | G | A | 143 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 others(140): Show |
143 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.158-6328G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70469082 | |||||||
| chr6:70469425 | T | G | 1 | a0001c0002t0002g0266 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.158-5985T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70469425 | |||||||
| chr6:70469906 | G | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.158-5504G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70469906 | |||||||
| chr6:70469981 | ACT | A | 11 | a0001c0004t0003g0010 a0001c0004t0003g0011 a0001c0004t0003g0012 others(8): Show |
11 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.158-5426_158-5425d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70469981 | ||||||
| chr6:70470009 | A | C | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.158-5401A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70470009 | |||||||
| chr6:70470011 | AC | A | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0158 |
3 | HG02145.hp2 HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.158-5398delC | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70470011 | |||||||
| chr6:70470116 | A | G | 28 | a0001c0004t0003g0001 a0001c0004t0003g0009 a0001c0004t0003g0010 others(25): Show |
28 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.158-5294A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70470116 | |||||||
| chr6:70470362 | C | CT | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.158-5039dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70470362 | ||||||
| chr6:70470439 | C | T | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.158-4971C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70470439 | |||||||
| chr6:70470510 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.158-4900C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70470510 | |||||||
| chr6:70470593 | G | T | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.158-4817G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70470593 | |||||||
| chr6:70470679 | A | G | 18 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(15): Show |
18 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.158-4731A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70470679 | |||||||
| chr6:70470802 | C | A | 26 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 others(23): Show |
26 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.158-4608C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70470802 | |||||||
| chr6:70471168 | G | A | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.158-4242G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70471168 | |||||||
| chr6:70471177 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0104 |
2 | HG03017.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.158-4233G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70471177 | |||||||
| chr6:70471257 | G | T | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.158-4153G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70471257 | |||||||
| chr6:70471282 | G | A | 1 | a0001c0009t0001g0212 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.158-4128G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70471282 | |||||||
| chr6:70471422 | C | G | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.158-3988C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70471422 | |||||||
| chr6:70471588 | GATCA | G | 99 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(96): Show |
99 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.158-3817_158-3814d others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70471588 | ||||||
| chr6:70471614 | A | ATGCTG | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-3795_158-3791d others(7): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70471614 | ||||||
| chr6:70471699 | C | A | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-3711C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70471699 | |||||||
| chr6:70471841 | C | T | 21 | a0001c0001t0001g0021 a0001c0001t0001g0054 a0001c0001t0001g0055 others(18): Show |
21 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.158-3569C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70471841 | |||||||
| chr6:70471972 | C | A | 70 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(67): Show |
70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.158-3438C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70471972 | |||||||
| chr6:70472101 | G | A | 113 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(110): Show |
113 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.158-3309G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70472101 | |||||||
| chr6:70472221 | C | T | 117 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(114): Show |
117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.158-3189C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70472221 | |||||||
| chr6:70472310 | C | T | 135 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(132): Show |
135 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.158-3100C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70472310 | |||||||
| chr6:70472507 | T | G | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.158-2903T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70472507 | |||||||
| chr6:70472511 | C | A | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-2899C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70472511 | |||||||
| chr6:70472599 | C | T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.158-2811C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70472599 | |||||||
| chr6:70472649 | A | C | 1 | a0002c0003t0001g0122 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.158-2761A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70472649 | |||||||
| chr6:70472782 | G | C | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.158-2628G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70472782 | |||||||
| chr6:70472787 | C | G | 8 | a0002c0003t0001g0002 a0002c0003t0001g0039 a0002c0003t0001g0040 others(5): Show |
8 | HG01123.hp2 HG02293.hp2 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.158-2623C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70472787 | |||||||
| chr6:70472892 | G | A | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.158-2518G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70472892 | |||||||
| chr6:70472967 | C | T | 1 | a0002c0003t0001g0118 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.158-2443C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70472967 | |||||||
| chr6:70472968 | G | T | 1 | a0001c0001t0001g0103 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.158-2442G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70472968 | |||||||
| chr6:70472978 | T | G | 1 | a0002c0003t0001g0113 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.158-2432T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70472978 | |||||||
| chr6:70473010 | G | T | 14 | a0001c0004t0003g0001 a0001c0004t0003g0230 a0001c0004t0003g0231 others(11): Show |
14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.158-2400G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70473010 | |||||||
| chr6:70473085 | A | G | 2 | a0001c0002t0002g0258 a0001c0002t0002g0259 |
2 | HG00642.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.158-2325A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70473085 | |||||||
| chr6:70473173 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.158-2237A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70473173 | |||||||
| chr6:70473255 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.158-2155G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70473255 | |||||||
| chr6:70473382 | A | G | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.158-2028A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70473382 | |||||||
| chr6:70473425 | CTT | C | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.158-1983_158-1982d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70473425 | ||||||
| chr6:70473473 | A | G | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.158-1937A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70473473 | |||||||
| chr6:70473512 | G | A | 113 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(110): Show |
113 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.158-1898G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70473512 | |||||||
| chr6:70473706 | T | C | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.158-1704T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70473706 | |||||||
| chr6:70473810 | G | A | 70 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(67): Show |
70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.158-1600G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70473810 | |||||||
| chr6:70473880 | C | T | 2 | a0001c0002t0002g0189 a0001c0002t0002g0190 |
2 | NA18993.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.158-1530C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70473880 | |||||||
| chr6:70473917 | T | G | 70 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(67): Show |
70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.158-1493T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70473917 | |||||||
| chr6:70473975 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0074 |
2 | HG00733.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.158-1435G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70473975 | |||||||
| chr6:70474258 | GTTTCTTT others(5): Show |
G | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.158-1136_158-1125d others(14): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 70474258 | ||||||
| chr6:70474365 | A | G | 1 | a0001c0002t0002g0183 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.158-1045A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70474365 | |||||||
| chr6:70474410 | C | T | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.158-1000C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70474410 | |||||||
| chr6:70474613 | A | G | 40 | a0001c0002t0002g0167 a0001c0002t0002g0176 a0001c0002t0002g0177 others(37): Show |
40 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.158-797A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70474613 | |||||||
| chr6:70474699 | G | A | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-711G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70474699 | |||||||
| chr6:70474998 | C | G | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.158-412C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70474998 | |||||||
| chr6:70475008 | A | C | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.158-402A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70475008 | |||||||
| chr6:70475163 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.158-247C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70475163 | |||||||
| chr6:70475190 | T | G | 14 | a0001c0004t0003g0001 a0001c0004t0003g0230 a0001c0004t0003g0231 others(11): Show |
14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.158-220T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 5/21 | chr6 | 70475190 | |||||||
| chr6:70475583 | T | G | 1 | a0001c0001t0001g0164 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.297+34T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 6/21 | chr6 | 70475583 | |||||||
| chr6:70475648 | G | A | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.298-15G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 6/21 | chr6 | 70475648 | |||||||
| chr6:70475933 | C | A | 1 | a0001c0001t0001g0210 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.368+200C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 7/21 | chr6 | 70475933 | |||||||
| chr6:70476070 | G | T | 40 | a0001c0002t0002g0167 a0001c0002t0002g0176 a0001c0002t0002g0177 others(37): Show |
40 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.368+337G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 7/21 | chr6 | 70476070 | |||||||
| chr6:70476269 | T | G | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.368+536T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 7/21 | chr6 | 70476269 | |||||||
| chr6:70476315 | G | T | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.368+582G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 7/21 | chr6 | 70476315 | |||||||
| chr6:70476436 | C | T | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.368+703C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 7/21 | chr6 | 70476436 | |||||||
| chr6:70476578 | T | A | 114 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(111): Show |
114 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.369-581T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 7/21 | chr6 | 70476578 | |||||||
| chr6:70476653 | G | A | 135 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(132): Show |
135 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.369-506G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 7/21 | chr6 | 70476653 | |||||||
| chr6:70476692 | A | T | 1 | a0006c0007t0001g0127 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.369-467A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 7/21 | chr6 | 70476692 | |||||||
| chr6:70476725 | G | T | 1 | a0001c0004t0004g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.369-434G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 7/21 | chr6 | 70476725 | |||||||
| chr6:70477112 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.369-47G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 7/21 | chr6 | 70477112 | |||||||
| chr6:70477399 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.542+67G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70477399 | |||||||
| chr6:70477468 | G | A | 3 | a0002c0003t0001g0045 a0002c0003t0001g0046 a0002c0003t0001g0165 |
3 | HG02523.hp1 NA18953.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.542+136G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70477468 | |||||||
| chr6:70477618 | C | A | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0098 others(2): Show |
5 | HG01192.hp1 HG01934.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.542+286C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70477618 | |||||||
| chr6:70478110 | C | T | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.542+778C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70478110 | |||||||
| chr6:70478127 | T | C | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.542+795T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70478127 | |||||||
| chr6:70478144 | A | G | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.542+812A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70478144 | |||||||
| chr6:70478159 | A | G | 1 | a0002c0003t0001g0114 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.542+827A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70478159 | |||||||
| chr6:70478629 | A | G | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.542+1297A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70478629 | |||||||
| chr6:70478679 | C | CA | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.542+1348dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr6 | 70478679 | ||||||
| chr6:70478738 | C | A | 1 | a0001c0002t0002g0204 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.542+1406C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70478738 | |||||||
| chr6:70478825 | G | A | 2 | a0001c0002t0002g0173 a0001c0002t0002g0174 |
2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.542+1493G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70478825 | |||||||
| chr6:70478869 | T | A | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.542+1537T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70478869 | |||||||
| chr6:70478895 | ATG | A | 12 | a0001c0004t0003g0009 a0001c0004t0003g0010 a0001c0004t0003g0011 others(9): Show |
12 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.542+1568_542+1569d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr6 | 70478895 | ||||||
| chr6:70479371 | G | A | 8 | a0002c0003t0001g0051 a0002c0003t0001g0107 a0002c0003t0001g0131 others(5): Show |
8 | HG00609.hp2 HG01243.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.543-1530G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70479371 | |||||||
| chr6:70479702 | T | A | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.543-1199T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70479702 | |||||||
| chr6:70479710 | A | G | 2 | a0001c0004t0003g0010 a0001c0004t0003g0013 |
2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.543-1191A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70479710 | |||||||
| chr6:70479799 | C | T | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.543-1102C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70479799 | |||||||
| chr6:70479985 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.543-916C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70479985 | |||||||
| chr6:70480064 | C | T | 1 | a0002c0003t0001g0165 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.543-837C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70480064 | |||||||
| chr6:70480094 | G | A | 1 | a0001c0001t0001g0021 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.543-807G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70480094 | |||||||
| chr6:70480155 | A | G | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.543-746A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70480155 | |||||||
| chr6:70480339 | A | G | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.543-562A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70480339 | |||||||
| chr6:70480529 | A | G | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.543-372A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70480529 | |||||||
| chr6:70480742 | A | T | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.543-159A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70480742 | |||||||
| chr6:70480874 | A | G | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.543-27A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 8/21 | chr6 | 70480874 | |||||||
| chr6:70481364 | G | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.669+337G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 9/21 | chr6 | 70481364 | |||||||
| chr6:70481539 | A | G | 3 | a0001c0002t0002g0167 a0001c0002t0002g0188 a0001c0002t0002g0203 |
3 | HG01993.hp1 HG02004.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.670-462A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 9/21 | chr6 | 70481539 | |||||||
| chr6:70481648 | T | TA | 21 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(18): Show |
21 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.670-340dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr6 | 70481648 | ||||||
| chr6:70481648 | TA | T | 55 | a0001c0001t0001g0148 a0001c0002t0002g0167 a0001c0002t0002g0168 others(52): Show |
55 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.670-340delA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr6 | 70481648 | ||||||
| chr6:70481873 | AT | A | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.670-122delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr6 | 70481873 | ||||||
| chr6:70481939 | A | G | 1 | a0002c0003t0001g0113 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.670-62A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 9/21 | chr6 | 70481939 | |||||||
| chr6:70482243 | C | A | 1 | a0001c0002t0002g0171 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.823+89C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70482243 | |||||||
| chr6:70482388 | TA | T | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.823+242delA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 70482388 | ||||||
| chr6:70482683 | C | G | 1 | a0002c0003t0008g0129 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.823+529C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70482683 | |||||||
| chr6:70482930 | TAA | T | 45 | a0002c0003t0001g0002 a0002c0003t0001g0022 a0002c0003t0001g0030 others(42): Show |
45 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.823+777_823+778del others(2): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70482930 | |||||||
| chr6:70482994 | C | T | 3 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0146 |
3 | HG02258.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.823+840C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70482994 | |||||||
| chr6:70483110 | G | A | 117 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(114): Show |
117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.823+956G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70483110 | |||||||
| chr6:70483394 | A | G | 1 | a0002c0006t0001g0136 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.823+1240A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70483394 | |||||||
| chr6:70483524 | C | T | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.823+1370C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70483524 | |||||||
| chr6:70483576 | A | G | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.823+1422A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70483576 | |||||||
| chr6:70483725 | C | A | 1 | a0001c0002t0002g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.823+1571C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70483725 | |||||||
| chr6:70483728 | T | C | 12 | a0001c0004t0003g0009 a0001c0004t0003g0010 a0001c0004t0003g0011 others(9): Show |
12 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.823+1574T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70483728 | |||||||
| chr6:70483751 | T | G | 70 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(67): Show |
70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.823+1597T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70483751 | |||||||
| chr6:70483834 | T | C | 54 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(51): Show |
54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.823+1680T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70483834 | |||||||
| chr6:70483846 | A | T | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.823+1692A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70483846 | |||||||
| chr6:70484097 | C | T | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.823+1943C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70484097 | |||||||
| chr6:70484622 | C | G | 4 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0083 others(1): Show |
4 | NA18961.hp2 NA18962.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.823+2468C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70484622 | |||||||
| chr6:70484653 | C | T | 1 | a0002c0003t0001g0022 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.823+2499C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70484653 | |||||||
| chr6:70484810 | A | G | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.823+2656A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70484810 | |||||||
| chr6:70484968 | T | C | 17 | a0001c0002t0002g0167 a0001c0002t0002g0176 a0001c0002t0002g0178 others(14): Show |
17 | HG00597.hp1 HG01993.hp1 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.823+2814T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70484968 | |||||||
| chr6:70485426 | G | A | 1 | a0001c0004t0003g0011 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.823+3272G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70485426 | |||||||
| chr6:70485504 | A | G | 1 | a0002c0003t0001g0045 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.823+3350A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70485504 | |||||||
| chr6:70485739 | C | T | 161 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(158): Show |
161 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(158): Show |
intron_variant | MODIFIER | c.823+3585C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70485739 | |||||||
| chr6:70486215 | A | C | 1 | a0001c0001t0001g0147 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.823+4061A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70486215 | |||||||
| chr6:70486484 | G | A | 11 | a0001c0004t0003g0010 a0001c0004t0003g0011 a0001c0004t0003g0012 others(8): Show |
11 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.823+4330G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70486484 | |||||||
| chr6:70486573 | G | A | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.823+4419G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70486573 | |||||||
| chr6:70486630 | A | G | 3 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0013t0001g0085 |
3 | HG01175.hp1 HG01981.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.824-4404A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70486630 | |||||||
| chr6:70486651 | G | T | 1 | a0001c0001t0001g0069 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.824-4383G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70486651 | |||||||
| chr6:70486727 | G | A | 1 | a0002c0003t0001g0121 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.824-4307G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70486727 | |||||||
| chr6:70486796 | C | T | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.824-4238C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70486796 | |||||||
| chr6:70486839 | A | G | 1 | a0002c0006t0001g0136 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.824-4195A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70486839 | |||||||
| chr6:70486870 | T | C | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.824-4164T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70486870 | |||||||
| chr6:70487027 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.824-4007G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70487027 | |||||||
| chr6:70487035 | A | G | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.824-3999A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70487035 | |||||||
| chr6:70487071 | G | A | 261 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(258): Show |
261 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.824-3963G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70487071 | |||||||
| chr6:70487083 | C | CA | 87 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(84): Show |
87 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.824-3926dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 70487083 | ||||||
| chr6:70487083 | C | CAA | 18 | a0001c0001t0001g0050 a0001c0001t0001g0146 a0001c0001t0001g0158 others(15): Show |
18 | HG00735.hp2 HG00738.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.824-3927_824-3926d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 70487083 | ||||||
| chr6:70487083 | CA | C | 33 | a0001c0001t0001g0155 a0001c0001t0001g0210 a0001c0001t0001g0267 others(30): Show |
33 | HG01192.hp2 HG02109.hp1 HG02280.hp2 others(30): Show |
intron_variant | MODIFIER | c.824-3926delA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 70487083 | ||||||
| chr6:70487083 | CAAA | C | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.824-3928_824-3926d others(5): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 70487083 | ||||||
| chr6:70487083 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0115 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.824-3936_824-3926d others(13): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 70487083 | ||||||
| chr6:70487398 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.824-3636T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70487398 | |||||||
| chr6:70487403 | A | C | 69 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(66): Show |
69 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.824-3631A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70487403 | |||||||
| chr6:70487403 | A | G | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.824-3631A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70487403 | |||||||
| chr6:70487404 | T | C | 1 | a0001c0002t0002g0222 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.824-3630T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70487404 | |||||||
| chr6:70487788 | T | C | 1 | a0001c0004t0003g0231 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.824-3246T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70487788 | |||||||
| chr6:70488155 | T | A | 1 | a0002c0003t0001g0133 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.824-2879T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70488155 | |||||||
| chr6:70488276 | T | G | 1 | a0002c0003t0001g0133 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.824-2758T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70488276 | |||||||
| chr6:70488403 | T | A | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.824-2631T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70488403 | |||||||
| chr6:70488445 | G | T | 55 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(52): Show |
55 | HG00597.hp1 HG00609.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.824-2589G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70488445 | |||||||
| chr6:70488452 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.824-2582T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70488452 | |||||||
| chr6:70488465 | GC | G | 178 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(175): Show |
178 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.824-2558delC | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 70488465 | ||||||
| chr6:70488480 | A | C | 1 | a0001c0002t0002g0263 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.824-2554A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70488480 | |||||||
| chr6:70488502 | T | A | 1 | a0002c0003t0001g0133 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.824-2532T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70488502 | |||||||
| chr6:70488503 | A | T | 1 | a0002c0003t0001g0133 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.824-2531A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70488503 | |||||||
| chr6:70488554 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.824-2480C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70488554 | |||||||
| chr6:70488940 | A | G | 117 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(114): Show |
117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.824-2094A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70488940 | |||||||
| chr6:70489062 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.824-1972G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489062 | |||||||
| chr6:70489129 | A | C | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.824-1905A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489129 | |||||||
| chr6:70489137 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.824-1897G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489137 | |||||||
| chr6:70489260 | G | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.824-1774G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489260 | |||||||
| chr6:70489337 | A | T | 1 | a0002c0003t0001g0133 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.824-1697A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489337 | |||||||
| chr6:70489396 | A | AT | 79 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(76): Show |
79 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.824-1635dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 70489396 | ||||||
| chr6:70489482 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.824-1552G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489482 | |||||||
| chr6:70489486 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.824-1548G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489486 | |||||||
| chr6:70489495 | C | T | 12 | a0001c0004t0003g0009 a0001c0004t0003g0010 a0001c0004t0003g0011 others(9): Show |
12 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.824-1539C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489495 | |||||||
| chr6:70489497 | T | G | 1 | a0001c0002t0002g0219 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.824-1537T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489497 | |||||||
| chr6:70489499 | C | T | 1 | a0001c0002t0002g0221 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.824-1535C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489499 | |||||||
| chr6:70489628 | A | T | 1 | a0002c0003t0001g0133 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.824-1406A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489628 | |||||||
| chr6:70489674 | C | T | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG01099.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.824-1360C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489674 | |||||||
| chr6:70489772 | T | C | 1 | a0001c0002t0002g0179 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.824-1262T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489772 | |||||||
| chr6:70489778 | C | T | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.824-1256C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489778 | |||||||
| chr6:70489984 | T | A | 1 | a0002c0003t0001g0046 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.824-1050T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70489984 | |||||||
| chr6:70490195 | A | G | 1 | a0005c0010t0003g0008 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.824-839A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70490195 | |||||||
| chr6:70490215 | G | C | 1 | a0002c0003t0001g0045 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.824-819G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70490215 | |||||||
| chr6:70490296 | G | A | 1 | a0002c0003t0001g0123 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.824-738G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70490296 | |||||||
| chr6:70490521 | C | T | 1 | a0001c0002t0002g0259 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.824-513C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70490521 | |||||||
| chr6:70491024 | C | T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.824-10C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 10/21 | chr6 | 70491024 | |||||||
| chr6:70491189 | A | G | 5 | a0002c0003t0001g0045 a0002c0003t0001g0046 a0002c0003t0001g0117 others(2): Show |
5 | HG02083.hp1 HG02523.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.873+106A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70491189 | |||||||
| chr6:70491198 | T | TA | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.873+119dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 70491198 | ||||||
| chr6:70491271 | A | C | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.873+188A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70491271 | |||||||
| chr6:70491271 | AC | A | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.873+190delC | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 70491271 | ||||||
| chr6:70491287 | A | G | 1 | a0001c0004t0003g0240 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.873+204A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70491287 | |||||||
| chr6:70491386 | A | G | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.873+303A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70491386 | |||||||
| chr6:70491417 | A | G | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.873+334A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70491417 | |||||||
| chr6:70491541 | A | G | 3 | a0003c0005t0001g0244 a0003c0005t0001g0245 a0003c0005t0001g0247 |
3 | HG02293.hp1 HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.873+458A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70491541 | |||||||
| chr6:70491760 | A | G | 1 | a0001c0004t0003g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.873+677A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70491760 | |||||||
| chr6:70491819 | A | G | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.873+736A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70491819 | |||||||
| chr6:70491930 | C | T | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.873+847C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70491930 | |||||||
| chr6:70492133 | A | C | 1 | a0002c0003t0001g0133 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.873+1050A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70492133 | |||||||
| chr6:70492137 | T | G | 1 | a0002c0003t0001g0133 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.873+1054T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70492137 | |||||||
| chr6:70492145 | A | T | 1 | a0002c0003t0001g0133 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.873+1062A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70492145 | |||||||
| chr6:70492295 | T | C | 1 | a0002c0006t0001g0136 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.873+1212T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70492295 | |||||||
| chr6:70492312 | C | T | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.873+1229C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70492312 | |||||||
| chr6:70492351 | G | A | 1 | a0001c0013t0001g0085 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.873+1268G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70492351 | |||||||
| chr6:70492385 | A | G | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.873+1302A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70492385 | |||||||
| chr6:70492478 | C | A | 54 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(51): Show |
54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.873+1395C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70492478 | |||||||
| chr6:70492489 | A | G | 5 | a0001c0002t0002g0168 a0001c0002t0002g0171 a0001c0002t0002g0172 others(2): Show |
5 | HG00673.hp2 NA18939.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.873+1406A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70492489 | |||||||
| chr6:70492547 | G | A | 21 | a0001c0001t0001g0021 a0001c0001t0001g0054 a0001c0001t0001g0055 others(18): Show |
21 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.873+1464G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70492547 | |||||||
| chr6:70492561 | G | A | 1 | a0002c0003t0001g0117 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.873+1478G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70492561 | |||||||
| chr6:70492656 | T | TA | 107 | a0001c0001t0001g0047 a0001c0001t0001g0068 a0001c0001t0001g0069 others(104): Show |
107 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.873+1589dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 70492656 | ||||||
| chr6:70492656 | TA | T | 6 | a0001c0001t0001g0060 a0001c0001t0001g0217 a0001c0004t0003g0016 others(3): Show |
6 | HG00597.hp2 HG01515.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.873+1589delA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 70492656 | ||||||
| chr6:70492681 | T | A | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.873+1598T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70492681 | |||||||
| chr6:70492861 | A | G | 1 | a0002c0006t0001g0138 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.873+1778A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70492861 | |||||||
| chr6:70492939 | CTT | C | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.873+1857_873+1858d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70492939 | |||||||
| chr6:70493081 | A | G | 8 | a0001c0004t0003g0010 a0001c0004t0003g0011 a0001c0004t0003g0012 others(5): Show |
8 | HG02559.hp1 HG02572.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.873+1998A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70493081 | |||||||
| chr6:70493145 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.873+2062C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70493145 | |||||||
| chr6:70493160 | G | A | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.873+2077G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70493160 | |||||||
| chr6:70493221 | A | G | 2 | a0010c0018t0005g0006 a0012c0015t0005g0005 |
2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.873+2138A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70493221 | |||||||
| chr6:70493385 | C | T | 113 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(110): Show |
113 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.873+2302C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70493385 | |||||||
| chr6:70493390 | G | A | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.873+2307G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70493390 | |||||||
| chr6:70493869 | A | T | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.873+2786A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70493869 | |||||||
| chr6:70494033 | G | A | 48 | a0002c0003t0001g0002 a0002c0003t0001g0022 a0002c0003t0001g0030 others(45): Show |
48 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.873+2950G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70494033 | |||||||
| chr6:70494053 | CA | C | 60 | a0001c0001t0001g0021 a0001c0001t0001g0052 a0001c0001t0001g0053 others(57): Show |
60 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.873+2991delA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 70494053 | ||||||
| chr6:70494053 | CAA | C | 79 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(76): Show |
79 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.873+2990_873+2991d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 70494053 | ||||||
| chr6:70494053 | CAAA | C | 9 | a0001c0002t0002g0177 a0003c0005t0001g0242 a0003c0005t0001g0243 others(6): Show |
9 | HG01099.hp1 HG02109.hp1 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.873+2989_873+2991d others(5): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 70494053 | ||||||
| chr6:70494125 | A | G | 2 | a0001c0002t0002g0173 a0001c0002t0002g0174 |
2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.873+3042A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70494125 | |||||||
| chr6:70494295 | G | A | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.873+3212G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70494295 | |||||||
| chr6:70494347 | T | C | 5 | a0002c0003t0001g0045 a0002c0003t0001g0046 a0002c0003t0001g0117 others(2): Show |
5 | HG02083.hp1 HG02523.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.873+3264T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70494347 | |||||||
| chr6:70494450 | T | C | 12 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(9): Show |
12 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.873+3367T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70494450 | |||||||
| chr6:70494803 | A | T | 1 | a0002c0003t0001g0040 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.873+3720A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70494803 | |||||||
| chr6:70494806 | A | G | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.873+3723A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70494806 | |||||||
| chr6:70494889 | T | C | 1 | a0002c0003t0001g0113 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.873+3806T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70494889 | |||||||
| chr6:70494898 | A | G | 5 | a0002c0003t0001g0002 a0002c0003t0001g0039 a0002c0003t0001g0040 others(2): Show |
5 | HG01123.hp2 HG02293.hp2 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.873+3815A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70494898 | |||||||
| chr6:70495149 | T | A | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.873+4066T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70495149 | |||||||
| chr6:70495559 | G | A | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.873+4476G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70495559 | |||||||
| chr6:70495707 | G | A | 117 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(114): Show |
117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.873+4624G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70495707 | |||||||
| chr6:70495747 | C | T | 1 | a0004c0008t0004g0004 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.873+4664C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70495747 | |||||||
| chr6:70495768 | A | G | 117 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(114): Show |
117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.873+4685A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70495768 | |||||||
| chr6:70495996 | C | T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0217 |
2 | HG00642.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.873+4913C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70495996 | |||||||
| chr6:70496105 | C | T | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.873+5022C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70496105 | |||||||
| chr6:70496334 | G | A | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.873+5251G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70496334 | |||||||
| chr6:70496365 | G | A | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.873+5282G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70496365 | |||||||
| chr6:70496458 | G | A | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0158 |
3 | HG02145.hp2 HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.873+5375G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70496458 | |||||||
| chr6:70496461 | C | A | 14 | a0001c0004t0003g0001 a0001c0004t0003g0230 a0001c0004t0003g0231 others(11): Show |
14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.873+5378C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70496461 | |||||||
| chr6:70496469 | T | TGA | 117 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(114): Show |
117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.873+5388_873+5389d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 70496469 | ||||||
| chr6:70496554 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.873+5471T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70496554 | |||||||
| chr6:70496572 | T | C | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.873+5489T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70496572 | |||||||
| chr6:70496609 | G | A | 1 | a0001c0004t0003g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.873+5526G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70496609 | |||||||
| chr6:70496631 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.873+5548G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70496631 | |||||||
| chr6:70496772 | AT | A | 21 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(18): Show |
21 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.873+5702delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 70496772 | ||||||
| chr6:70496790 | A | G | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.873+5707A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70496790 | |||||||
| chr6:70497081 | A | G | 22 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(19): Show |
22 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.874-5555A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70497081 | |||||||
| chr6:70497226 | A | G | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.874-5410A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70497226 | |||||||
| chr6:70497255 | C | T | 14 | a0001c0004t0003g0001 a0001c0004t0003g0230 a0001c0004t0003g0231 others(11): Show |
14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.874-5381C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70497255 | |||||||
| chr6:70497403 | C | T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.874-5233C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70497403 | |||||||
| chr6:70497473 | T | C | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.874-5163T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70497473 | |||||||
| chr6:70497504 | A | G | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.874-5132A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70497504 | |||||||
| chr6:70497589 | A | G | 1 | a0002c0003t0001g0040 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.874-5047A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70497589 | |||||||
| chr6:70497762 | C | T | 113 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(110): Show |
113 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.874-4874C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70497762 | |||||||
| chr6:70497839 | G | A | 14 | a0001c0004t0003g0001 a0001c0004t0003g0230 a0001c0004t0003g0231 others(11): Show |
14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.874-4797G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70497839 | |||||||
| chr6:70497874 | G | A | 1 | a0002c0003t0001g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.874-4762G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70497874 | |||||||
| chr6:70497877 | A | T | 1 | a0002c0003t0001g0043 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.874-4759A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70497877 | |||||||
| chr6:70498073 | A | C | 28 | a0001c0004t0003g0001 a0001c0004t0003g0009 a0001c0004t0003g0010 others(25): Show |
28 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.874-4563A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498073 | |||||||
| chr6:70498095 | G | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0267 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.874-4541G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498095 | |||||||
| chr6:70498155 | T | G | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.874-4481T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498155 | |||||||
| chr6:70498212 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.874-4424T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498212 | |||||||
| chr6:70498216 | T | C | 1 | a0001c0002t0002g0201 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.874-4420T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498216 | |||||||
| chr6:70498269 | T | A | 14 | a0001c0004t0003g0001 a0001c0004t0003g0230 a0001c0004t0003g0231 others(11): Show |
14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.874-4367T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498269 | |||||||
| chr6:70498276 | T | C | 14 | a0001c0004t0003g0001 a0001c0004t0003g0230 a0001c0004t0003g0231 others(11): Show |
14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.874-4360T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498276 | |||||||
| chr6:70498325 | T | C | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.874-4311T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498325 | |||||||
| chr6:70498460 | C | T | 1 | a0002c0003t0001g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.874-4176C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498460 | |||||||
| chr6:70498467 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.874-4169C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498467 | |||||||
| chr6:70498567 | TAC | T | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.874-4067_874-4066d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 70498567 | ||||||
| chr6:70498650 | T | C | 2 | a0001c0001t0001g0210 a0001c0001t0001g0267 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.874-3986T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498650 | |||||||
| chr6:70498726 | G | T | 1 | a0001c0002t0002g0219 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.874-3910G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498726 | |||||||
| chr6:70498748 | A | C | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0098 others(2): Show |
5 | HG01192.hp1 HG01934.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.874-3888A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498748 | |||||||
| chr6:70498752 | G | A | 7 | a0001c0002t0002g0223 a0001c0002t0002g0224 a0001c0002t0002g0225 others(4): Show |
7 | NA18947.hp2 NA18950.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.874-3884G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498752 | |||||||
| chr6:70498825 | A | G | 17 | a0001c0002t0002g0167 a0001c0002t0002g0176 a0001c0002t0002g0178 others(14): Show |
17 | HG00597.hp1 HG01993.hp1 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.874-3811A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498825 | |||||||
| chr6:70498940 | ATG | A | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.874-3694_874-3693d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 70498940 | ||||||
| chr6:70498960 | G | A | 2 | a0001c0002t0002g0253 a0001c0002t0002g0263 |
2 | HG00280.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.874-3676G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70498960 | |||||||
| chr6:70499047 | A | G | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.874-3589A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70499047 | |||||||
| chr6:70499132 | T | G | 1 | a0002c0003t0001g0118 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.874-3504T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70499132 | |||||||
| chr6:70499159 | C | T | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.874-3477C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70499159 | |||||||
| chr6:70499410 | A | G | 1 | a0001c0002t0002g0203 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.874-3226A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70499410 | |||||||
| chr6:70499613 | T | G | 5 | a0002c0003t0001g0045 a0002c0003t0001g0046 a0002c0003t0001g0117 others(2): Show |
5 | HG02083.hp1 HG02523.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.874-3023T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70499613 | |||||||
| chr6:70500151 | A | G | 1 | a0002c0006t0001g0149 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.874-2485A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70500151 | |||||||
| chr6:70500200 | A | T | 1 | a0001c0001t0001g0026 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.874-2436A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70500200 | |||||||
| chr6:70500249 | T | C | 1 | a0001c0004t0003g0252 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.874-2387T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70500249 | |||||||
| chr6:70500309 | G | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0158 |
2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.874-2327G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70500309 | |||||||
| chr6:70500327 | C | T | 1 | a0001c0004t0004g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.874-2309C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70500327 | |||||||
| chr6:70500428 | G | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.874-2208G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70500428 | |||||||
| chr6:70500457 | A | G | 11 | a0001c0004t0003g0010 a0001c0004t0003g0011 a0001c0004t0003g0012 others(8): Show |
11 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.874-2179A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70500457 | |||||||
| chr6:70500523 | G | A | 4 | a0002c0003t0001g0051 a0002c0003t0001g0107 a0002c0003t0001g0131 others(1): Show |
4 | HG01243.hp1 HG01358.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.874-2113G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70500523 | |||||||
| chr6:70500582 | A | C | 1 | a0001c0002t0002g0222 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.874-2054A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70500582 | |||||||
| chr6:70500791 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.874-1845C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70500791 | |||||||
| chr6:70500811 | G | A | 2 | a0001c0004t0003g0010 a0001c0004t0003g0013 |
2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.874-1825G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70500811 | |||||||
| chr6:70500917 | G | A | 32 | a0001c0004t0003g0001 a0001c0004t0003g0009 a0001c0004t0003g0010 others(29): Show |
32 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.874-1719G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70500917 | |||||||
| chr6:70501063 | G | A | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.874-1573G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70501063 | |||||||
| chr6:70501260 | GC | G | 26 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 others(23): Show |
26 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.874-1373delC | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 70501260 | ||||||
| chr6:70501263 | C | A | 26 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 others(23): Show |
26 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.874-1373C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70501263 | |||||||
| chr6:70501432 | C | T | 2 | a0001c0002t0002g0173 a0001c0002t0002g0174 |
2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.874-1204C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70501432 | |||||||
| chr6:70501609 | A | G | 143 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 others(140): Show |
143 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.874-1027A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70501609 | |||||||
| chr6:70501691 | G | A | 46 | a0001c0002t0002g0167 a0001c0002t0002g0169 a0001c0002t0002g0176 others(43): Show |
46 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.874-945G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70501691 | |||||||
| chr6:70501736 | C | T | 2 | a0001c0004t0003g0010 a0001c0004t0003g0013 |
2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.874-900C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70501736 | |||||||
| chr6:70501872 | T | C | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.874-764T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70501872 | |||||||
| chr6:70501971 | C | A | 1 | a0001c0001t0001g0091 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.874-665C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70501971 | |||||||
| chr6:70502117 | A | G | 1 | a0002c0003t0001g0049 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.874-519A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70502117 | |||||||
| chr6:70502142 | T | C | 32 | a0001c0004t0003g0001 a0001c0004t0003g0009 a0001c0004t0003g0010 others(29): Show |
32 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.874-494T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70502142 | |||||||
| chr6:70502275 | ACT | A | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.874-357_874-356del others(2): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 70502275 | ||||||
| chr6:70502430 | T | TAAAAATT others(309): Show |
2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.874-206_874-205ins others(316): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70502430 | |||||||
| chr6:70502431 | G | A | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.874-205G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70502431 | |||||||
| chr6:70502504 | G | GCA | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.874-129_874-128dup others(2): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 70502504 | ||||||
| chr6:70502615 | T | C | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.874-21T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 11/21 | chr6 | 70502615 | |||||||
| chr6:70502826 | A | G | 2 | a0010c0018t0005g0006 a0012c0015t0005g0005 |
2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1029+35A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70502826 | |||||||
| chr6:70502889 | A | G | 1 | a0001c0004t0003g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1029+98A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70502889 | |||||||
| chr6:70503168 | T | C | 1 | a0002c0003t0001g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1029+377T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70503168 | |||||||
| chr6:70503211 | C | A | 1 | a0001c0001t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1029+420C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70503211 | |||||||
| chr6:70503350 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0055 |
2 | HG02015.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.1029+559T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70503350 | |||||||
| chr6:70503375 | A | G | 1 | a0001c0002t0002g0179 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1029+584A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70503375 | |||||||
| chr6:70503437 | A | T | 1 | a0005c0010t0003g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1029+646A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70503437 | |||||||
| chr6:70503443 | ATTT | A | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1029+656_1029+658d others(5): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70503443 | ||||||
| chr6:70503485 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1029+694A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70503485 | |||||||
| chr6:70503532 | G | A | 1 | a0002c0003t0001g0002 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1029+741G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70503532 | |||||||
| chr6:70503765 | A | C | 4 | a0002c0003t0001g0119 a0002c0003t0001g0124 a0002c0003t0001g0125 others(1): Show |
4 | HG01168.hp1 HG01358.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1029+974A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70503765 | |||||||
| chr6:70503771 | C | T | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1029+980C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70503771 | |||||||
| chr6:70503811 | T | G | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1029+1020T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70503811 | |||||||
| chr6:70503849 | T | C | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1029+1058T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70503849 | |||||||
| chr6:70504145 | C | T | 56 | a0002c0003t0001g0002 a0002c0003t0001g0022 a0002c0003t0001g0030 others(53): Show |
56 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1029+1354C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70504145 | |||||||
| chr6:70504281 | G | C | 1 | a0001c0001t0001g0048 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1029+1490G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70504281 | |||||||
| chr6:70504352 | T | A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0267 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1029+1561T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70504352 | |||||||
| chr6:70504498 | A | G | 15 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(12): Show |
15 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1029+1707A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70504498 | |||||||
| chr6:70504547 | A | G | 1 | a0002c0006t0001g0034 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1029+1756A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70504547 | |||||||
| chr6:70504718 | G | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1029+1927G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70504718 | |||||||
| chr6:70504842 | G | A | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.1029+2051G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70504842 | |||||||
| chr6:70504969 | A | C | 1 | a0002c0003t0001g0132 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1029+2178A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70504969 | |||||||
| chr6:70505073 | CAT | C | 165 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0036 others(162): Show |
165 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1029+2299_1029+230 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70505073 | ||||||
| chr6:70505073 | CATAT | C | 98 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(95): Show |
98 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1029+2297_1029+230 others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70505073 | ||||||
| chr6:70505077 | T | C | 12 | a0001c0004t0003g0009 a0001c0004t0003g0010 a0001c0004t0003g0011 others(9): Show |
12 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1029+2286T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70505077 | |||||||
| chr6:70505156 | C | T | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.1029+2365C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70505156 | |||||||
| chr6:70505210 | A | G | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1029+2419A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70505210 | |||||||
| chr6:70505295 | G | A | 219 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(216): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1029+2504G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70505295 | |||||||
| chr6:70505371 | A | G | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1029+2580A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70505371 | |||||||
| chr6:70505535 | A | AT | 51 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(48): Show |
51 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.1029+2753dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70505535 | ||||||
| chr6:70505544 | T | TC | 5 | a0001c0002t0002g0168 a0001c0002t0002g0171 a0001c0002t0002g0172 others(2): Show |
5 | HG00673.hp2 NA18939.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1029+2754dupC | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70505544 | ||||||
| chr6:70505805 | T | C | 220 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(217): Show |
220 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.1029+3014T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70505805 | |||||||
| chr6:70505882 | T | C | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(3): Show |
6 | HG02615.hp1 HG02723.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1029+3091T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70505882 | |||||||
| chr6:70506064 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1029+3273G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70506064 | |||||||
| chr6:70506121 | G | T | 8 | a0002c0003t0001g0002 a0002c0003t0001g0039 a0002c0003t0001g0040 others(5): Show |
8 | HG01123.hp2 HG02293.hp2 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.1029+3330G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70506121 | |||||||
| chr6:70506201 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1029+3410C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70506201 | |||||||
| chr6:70506230 | G | C | 1 | a0001c0002t0002g0264 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1029+3439G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70506230 | |||||||
| chr6:70506479 | A | C | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1029+3688A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70506479 | |||||||
| chr6:70506834 | G | T | 1 | a0001c0002t0002g0264 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1029+4043G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70506834 | |||||||
| chr6:70506855 | T | C | 1 | a0008c0017t0001g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1029+4064T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70506855 | |||||||
| chr6:70506929 | A | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0145 |
2 | HG02451.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1029+4138A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70506929 | |||||||
| chr6:70506966 | A | C | 1 | a0002c0003t0001g0051 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1029+4175A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70506966 | |||||||
| chr6:70507095 | G | A | 1 | a0001c0004t0003g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1029+4304G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70507095 | |||||||
| chr6:70507108 | C | G | 3 | a0001c0001t0001g0048 a0001c0001t0001g0092 a0001c0001t0001g0105 |
3 | HG01074.hp1 HG01167.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1029+4317C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70507108 | |||||||
| chr6:70507120 | G | C | 1 | a0001c0001t0001g0106 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1029+4329G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70507120 | |||||||
| chr6:70507209 | C | T | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1029+4418C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70507209 | |||||||
| chr6:70507445 | T | A | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1029+4654T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70507445 | |||||||
| chr6:70507467 | A | G | 113 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(110): Show |
113 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.1029+4676A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70507467 | |||||||
| chr6:70507511 | G | A | 1 | a0008c0017t0001g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1029+4720G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70507511 | |||||||
| chr6:70507571 | T | G | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1029+4780T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70507571 | |||||||
| chr6:70507572 | T | G | 1 | a0001c0004t0003g0010 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1029+4781T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70507572 | |||||||
| chr6:70507921 | C | G | 32 | a0001c0004t0003g0001 a0001c0004t0003g0009 a0001c0004t0003g0010 others(29): Show |
32 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.1029+5130C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70507921 | |||||||
| chr6:70507969 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1029+5178A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70507969 | |||||||
| chr6:70508055 | T | C | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.1029+5264T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70508055 | |||||||
| chr6:70508085 | G | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1029+5294G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70508085 | |||||||
| chr6:70508296 | G | C | 7 | a0001c0002t0002g0223 a0001c0002t0002g0224 a0001c0002t0002g0225 others(4): Show |
7 | NA18947.hp2 NA18950.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.1029+5505G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70508296 | |||||||
| chr6:70508351 | A | G | 6 | a0001c0001t0001g0036 a0001c0001t0001g0090 a0001c0001t0001g0093 others(3): Show |
6 | HG02027.hp2 NA18966.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1029+5560A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70508351 | |||||||
| chr6:70508846 | C | G | 1 | a0001c0002t0002g0200 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1029+6055C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70508846 | |||||||
| chr6:70508878 | T | C | 70 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(67): Show |
70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1029+6087T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70508878 | |||||||
| chr6:70508880 | G | A | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1029+6089G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70508880 | |||||||
| chr6:70508938 | C | T | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1029+6147C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70508938 | |||||||
| chr6:70508996 | G | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1029+6205G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70508996 | |||||||
| chr6:70509168 | T | C | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1029+6377T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70509168 | |||||||
| chr6:70509354 | A | T | 135 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(132): Show |
135 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.1029+6563A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70509354 | |||||||
| chr6:70509374 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1029+6583G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70509374 | |||||||
| chr6:70509382 | A | T | 1 | a0002c0003t0001g0135 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1029+6591A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70509382 | |||||||
| chr6:70509544 | T | C | 14 | a0001c0004t0003g0001 a0001c0004t0003g0230 a0001c0004t0003g0231 others(11): Show |
14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1029+6753T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70509544 | |||||||
| chr6:70509662 | A | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0267 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1029+6871A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70509662 | |||||||
| chr6:70509761 | C | T | 30 | a0001c0004t0003g0001 a0001c0004t0003g0009 a0001c0004t0003g0010 others(27): Show |
30 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.1029+6970C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70509761 | |||||||
| chr6:70509817 | A | G | 1 | a0001c0002t0002g0172 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1029+7026A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70509817 | |||||||
| chr6:70509852 | C | T | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1029+7061C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70509852 | |||||||
| chr6:70509867 | G | A | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.1029+7076G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70509867 | |||||||
| chr6:70510067 | C | A | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1029+7276C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70510067 | |||||||
| chr6:70510107 | T | A | 1 | a0001c0001t0001g0020 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1029+7316T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70510107 | |||||||
| chr6:70510169 | G | A | 14 | a0001c0004t0003g0001 a0001c0004t0003g0230 a0001c0004t0003g0231 others(11): Show |
14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1029+7378G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70510169 | |||||||
| chr6:70510177 | G | A | 1 | a0001c0004t0003g0240 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1029+7386G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70510177 | |||||||
| chr6:70510304 | T | C | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.1029+7513T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70510304 | |||||||
| chr6:70510333 | A | G | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1029+7542A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70510333 | |||||||
| chr6:70510367 | T | C | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1029+7576T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70510367 | |||||||
| chr6:70510480 | G | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1029+7689G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70510480 | |||||||
| chr6:70510691 | A | G | 3 | a0002c0003t0001g0030 a0002c0003t0001g0031 a0002c0003t0001g0166 |
3 | NA18990.hp2 NA19055.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1029+7900A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70510691 | |||||||
| chr6:70510757 | G | A | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1029+7966G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70510757 | |||||||
| chr6:70510853 | C | T | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1029+8062C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70510853 | |||||||
| chr6:70510873 | A | C | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1029+8082A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70510873 | |||||||
| chr6:70510967 | G | A | 15 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(12): Show |
15 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1029+8176G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70510967 | |||||||
| chr6:70511164 | A | G | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1029+8373A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70511164 | |||||||
| chr6:70511223 | A | G | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1029+8432A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70511223 | |||||||
| chr6:70511454 | A | G | 1 | a0001c0002t0002g0182 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1029+8663A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70511454 | |||||||
| chr6:70511576 | TA | T | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.1029+8791delA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70511576 | ||||||
| chr6:70511577 | A | T | 1 | a0001c0001t0001g0097 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1029+8786A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70511577 | |||||||
| chr6:70511744 | A | G | 6 | a0002c0003t0001g0135 a0002c0006t0001g0034 a0002c0006t0001g0136 others(3): Show |
6 | HG00597.hp2 HG00621.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.1029+8953A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70511744 | |||||||
| chr6:70511971 | C | T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1029+9180C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70511971 | |||||||
| chr6:70512146 | G | C | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1029+9355G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70512146 | |||||||
| chr6:70512244 | G | A | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1029+9453G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70512244 | |||||||
| chr6:70512452 | T | C | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1029+9661T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70512452 | |||||||
| chr6:70512454 | G | A | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1029+9663G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70512454 | |||||||
| chr6:70512484 | G | A | 32 | a0001c0004t0003g0001 a0001c0004t0003g0009 a0001c0004t0003g0010 others(29): Show |
32 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.1029+9693G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70512484 | |||||||
| chr6:70512871 | T | A | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1030-9642T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70512871 | |||||||
| chr6:70512985 | C | CT | 12 | a0001c0004t0003g0009 a0001c0004t0003g0010 a0001c0004t0003g0011 others(9): Show |
12 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1030-9518dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70512985 | ||||||
| chr6:70512985 | CT | C | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1030-9518delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70512985 | ||||||
| chr6:70513218 | C | A | 26 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 others(23): Show |
26 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1030-9295C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70513218 | |||||||
| chr6:70513259 | C | T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1030-9254C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70513259 | |||||||
| chr6:70513316 | AT | A | 26 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 others(23): Show |
26 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1030-9194delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70513316 | ||||||
| chr6:70513322 | C | T | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1030-9191C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70513322 | |||||||
| chr6:70513388 | CT | C | 45 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0147 others(42): Show |
45 | HG01069.hp1 HG01074.hp2 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.1030-9107delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70513388 | ||||||
| chr6:70513388 | CTT | C | 22 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(19): Show |
22 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.1030-9108_1030-910 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70513388 | ||||||
| chr6:70513581 | C | A | 1 | a0001c0001t0001g0157 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1030-8932C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70513581 | |||||||
| chr6:70513632 | T | C | 2 | a0001c0002t0002g0171 a0001c0002t0002g0172 |
2 | HG00673.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.1030-8881T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70513632 | |||||||
| chr6:70513707 | C | G | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1030-8806C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70513707 | |||||||
| chr6:70513778 | G | A | 2 | a0002c0003t0001g0108 a0002c0003t0001g0110 |
2 | NA18947.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1030-8735G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70513778 | |||||||
| chr6:70513852 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1030-8661T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70513852 | |||||||
| chr6:70513853 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1030-8660G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70513853 | |||||||
| chr6:70513990 | GT | G | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.1030-8514delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70513990 | ||||||
| chr6:70514145 | G | A | 54 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(51): Show |
54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.1030-8368G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514145 | |||||||
| chr6:70514343 | C | T | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1030-8170C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514343 | |||||||
| chr6:70514354 | T | C | 1 | a0002c0003t0001g0133 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1030-8159T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514354 | |||||||
| chr6:70514387 | C | T | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.1030-8126C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514387 | |||||||
| chr6:70514494 | T | A | 1 | a0001c0001t0001g0106 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1030-8019T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514494 | |||||||
| chr6:70514501 | C | G | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1030-8012C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514501 | |||||||
| chr6:70514521 | T | G | 70 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(67): Show |
70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1030-7992T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514521 | |||||||
| chr6:70514528 | G | A | 1 | a0002c0003t0001g0166 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1030-7985G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514528 | |||||||
| chr6:70514593 | C | T | 2 | a0010c0018t0005g0006 a0012c0015t0005g0005 |
2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1030-7920C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514593 | |||||||
| chr6:70514602 | T | C | 1 | a0001c0004t0004g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1030-7911T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514602 | |||||||
| chr6:70514644 | G | T | 1 | a0002c0006t0001g0138 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1030-7869G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514644 | |||||||
| chr6:70514711 | G | GA | 113 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(110): Show |
113 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.1030-7801dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70514711 | ||||||
| chr6:70514821 | A | G | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1030-7692A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514821 | |||||||
| chr6:70514926 | T | C | 15 | a0001c0002t0002g0167 a0001c0002t0002g0176 a0001c0002t0002g0178 others(12): Show |
15 | HG01993.hp1 HG02004.hp1 HG03491.hp2 others(12): Show |
intron_variant | MODIFIER | c.1030-7587T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514926 | |||||||
| chr6:70514966 | C | G | 32 | a0001c0004t0003g0001 a0001c0004t0003g0009 a0001c0004t0003g0010 others(29): Show |
32 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.1030-7547C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514966 | |||||||
| chr6:70514991 | C | G | 1 | a0002c0003t0001g0213 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1030-7522C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70514991 | |||||||
| chr6:70515070 | C | G | 1 | a0001c0002t0002g0264 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1030-7443C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70515070 | |||||||
| chr6:70515070 | C | T | 112 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(109): Show |
112 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1030-7443C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70515070 | |||||||
| chr6:70515323 | T | C | 1 | a0001c0002t0002g0256 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1030-7190T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70515323 | |||||||
| chr6:70515462 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1030-7051A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70515462 | |||||||
| chr6:70515582 | C | T | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1030-6931C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70515582 | |||||||
| chr6:70515880 | G | A | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1030-6633G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70515880 | |||||||
| chr6:70515998 | T | A | 26 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 others(23): Show |
26 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1030-6515T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70515998 | |||||||
| chr6:70516021 | G | C | 143 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 others(140): Show |
143 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.1030-6492G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516021 | |||||||
| chr6:70516259 | G | C | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1030-6254G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516259 | |||||||
| chr6:70516361 | T | G | 3 | a0001c0004t0003g0250 a0001c0004t0003g0251 a0001c0004t0003g0252 |
3 | HG02572.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1030-6152T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516361 | |||||||
| chr6:70516453 | G | A | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.1030-6060G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516453 | |||||||
| chr6:70516502 | T | C | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1030-6011T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516502 | |||||||
| chr6:70516527 | TTTC | T | 7 | a0001c0009t0001g0212 a0003c0005t0001g0242 a0003c0005t0001g0243 others(4): Show |
7 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1030-5983_1030-598 others(7): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70516527 | ||||||
| chr6:70516530 | C | CT | 11 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(8): Show |
11 | HG01934.hp1 HG02027.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.1030-5960dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70516530 | ||||||
| chr6:70516530 | CT | C | 48 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 others(45): Show |
48 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.1030-5960delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70516530 | ||||||
| chr6:70516530 | CTT | C | 14 | a0001c0001t0001g0151 a0001c0004t0003g0001 a0001c0004t0003g0230 others(11): Show |
14 | HG01069.hp1 HG02280.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.1030-5961_1030-596 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70516530 | ||||||
| chr6:70516530 | CTTT | C | 5 | a0001c0002t0002g0175 a0001c0002t0002g0178 a0001c0002t0002g0207 others(2): Show |
5 | HG03516.hp2 HG03540.hp1 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.1030-5962_1030-596 others(7): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70516530 | ||||||
| chr6:70516530 | CTTTT | C | 50 | a0001c0001t0001g0267 a0001c0002t0002g0167 a0001c0002t0002g0168 others(47): Show |
50 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.1030-5963_1030-596 others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70516530 | ||||||
| chr6:70516534 | T | C | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1030-5979T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516534 | |||||||
| chr6:70516575 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1030-5938A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516575 | |||||||
| chr6:70516622 | G | A | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.1030-5891G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516622 | |||||||
| chr6:70516628 | T | C | 113 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(110): Show |
113 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.1030-5885T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516628 | |||||||
| chr6:70516634 | C | CA | 40 | a0001c0002t0002g0167 a0001c0002t0002g0176 a0001c0002t0002g0177 others(37): Show |
40 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1030-5878dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70516634 | ||||||
| chr6:70516647 | A | G | 117 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(114): Show |
117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.1030-5866A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516647 | |||||||
| chr6:70516680 | A | G | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1030-5833A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516680 | |||||||
| chr6:70516798 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0104 |
2 | HG03017.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1030-5715G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516798 | |||||||
| chr6:70516848 | T | G | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.1030-5665T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516848 | |||||||
| chr6:70516885 | G | A | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1030-5628G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516885 | |||||||
| chr6:70516932 | A | G | 12 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(9): Show |
12 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.1030-5581A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70516932 | |||||||
| chr6:70517009 | A | C | 2 | a0001c0001t0001g0210 a0001c0001t0001g0267 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1030-5504A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517009 | |||||||
| chr6:70517132 | G | A | 1 | a0001c0004t0003g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1030-5381G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517132 | |||||||
| chr6:70517147 | A | G | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1030-5366A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517147 | |||||||
| chr6:70517281 | A | T | 2 | a0001c0002t0002g0173 a0001c0002t0002g0174 |
2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1030-5232A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517281 | |||||||
| chr6:70517346 | G | T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1030-5167G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517346 | |||||||
| chr6:70517347 | A | T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1030-5166A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517347 | |||||||
| chr6:70517357 | C | T | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1030-5156C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517357 | |||||||
| chr6:70517415 | C | CT | 27 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0078 others(24): Show |
27 | HG00621.hp2 HG01069.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.1030-5077dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70517415 | ||||||
| chr6:70517415 | C | CTT | 12 | a0001c0004t0003g0009 a0001c0004t0003g0010 a0001c0004t0003g0011 others(9): Show |
12 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1030-5078_1030-507 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70517415 | ||||||
| chr6:70517415 | CT | C | 53 | a0001c0001t0001g0075 a0001c0001t0001g0153 a0001c0002t0002g0167 others(50): Show |
53 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1030-5077delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70517415 | ||||||
| chr6:70517448 | T | C | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.1030-5065T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517448 | |||||||
| chr6:70517449 | G | T | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1030-5064G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517449 | |||||||
| chr6:70517680 | T | A | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.1030-4833T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517680 | |||||||
| chr6:70517785 | A | G | 1 | a0003c0005t0001g0247 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1030-4728A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517785 | |||||||
| chr6:70517826 | A | T | 7 | a0001c0002t0002g0223 a0001c0002t0002g0224 a0001c0002t0002g0225 others(4): Show |
7 | NA18947.hp2 NA18950.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.1030-4687A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517826 | |||||||
| chr6:70517837 | A | C | 2 | a0001c0002t0002g0255 a0001c0002t0002g0257 |
2 | HG00639.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1030-4676A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517837 | |||||||
| chr6:70517944 | G | A | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1030-4569G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517944 | |||||||
| chr6:70517946 | C | T | 2 | a0002c0003t0001g0039 a0002c0003t0001g0040 |
2 | HG01123.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1030-4567C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517946 | |||||||
| chr6:70517996 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1030-4517A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70517996 | |||||||
| chr6:70518055 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1030-4458G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70518055 | |||||||
| chr6:70518093 | A | G | 1 | a0002c0003t0001g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1030-4420A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70518093 | |||||||
| chr6:70518164 | A | G | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1030-4349A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70518164 | |||||||
| chr6:70518281 | CTT | C | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1030-4229_1030-422 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70518281 | ||||||
| chr6:70518461 | T | G | 3 | a0002c0003t0001g0051 a0002c0003t0001g0121 a0002c0003t0001g0131 |
3 | HG01243.hp1 HG01358.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1030-4052T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70518461 | |||||||
| chr6:70518857 | C | A | 3 | a0001c0004t0003g0250 a0001c0004t0003g0251 a0001c0004t0003g0252 |
3 | HG02572.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1030-3656C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70518857 | |||||||
| chr6:70518912 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1030-3601C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70518912 | |||||||
| chr6:70519022 | G | T | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1030-3491G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519022 | |||||||
| chr6:70519051 | A | T | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1030-3462A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519051 | |||||||
| chr6:70519064 | T | C | 3 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0013t0001g0085 |
3 | HG01175.hp1 HG01981.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1030-3449T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519064 | |||||||
| chr6:70519167 | A | G | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.1030-3346A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519167 | |||||||
| chr6:70519176 | G | C | 70 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(67): Show |
70 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1030-3337G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519176 | |||||||
| chr6:70519271 | CATT | C | 3 | a0001c0004t0003g0234 a0001c0004t0003g0238 a0001c0004t0003g0239 |
3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1030-3239_1030-323 others(7): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70519271 | ||||||
| chr6:70519307 | A | G | 1 | a0005c0010t0003g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1030-3206A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519307 | |||||||
| chr6:70519446 | T | C | 1 | a0002c0003t0001g0132 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1030-3067T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519446 | |||||||
| chr6:70519449 | A | G | 14 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.1030-3064A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519449 | |||||||
| chr6:70519521 | G | C | 1 | a0001c0001t0001g0267 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1030-2992G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519521 | |||||||
| chr6:70519568 | T | G | 69 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(66): Show |
69 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.1030-2945T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519568 | |||||||
| chr6:70519580 | T | C | 222 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(219): Show |
222 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.1030-2933T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519580 | |||||||
| chr6:70519637 | G | C | 152 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(149): Show |
152 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(149): Show |
intron_variant | MODIFIER | c.1030-2876G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519637 | |||||||
| chr6:70519647 | G | T | 1 | a0001c0002t0002g0266 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1030-2866G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519647 | |||||||
| chr6:70519738 | TAAG | T | 14 | a0001c0004t0003g0001 a0001c0004t0003g0230 a0001c0004t0003g0231 others(11): Show |
14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1030-2773_1030-277 others(7): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70519738 | ||||||
| chr6:70519885 | C | T | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1030-2628C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519885 | |||||||
| chr6:70519909 | G | GATAT | 101 | a0001c0001t0001g0164 a0001c0001t0001g0210 a0001c0001t0001g0267 others(98): Show |
101 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1030-2599_1030-259 others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70519909 | ||||||
| chr6:70519918 | G | T | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1030-2595G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519918 | |||||||
| chr6:70519921 | A | G | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1030-2592A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519921 | |||||||
| chr6:70519956 | G | A | 118 | a0001c0001t0001g0164 a0001c0001t0001g0210 a0001c0001t0001g0267 others(115): Show |
118 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.1030-2557G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70519956 | |||||||
| chr6:70520105 | A | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0056 |
2 | HG03831.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.1030-2408A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70520105 | |||||||
| chr6:70520113 | C | G | 2 | a0010c0018t0005g0006 a0012c0015t0005g0005 |
2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1030-2400C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70520113 | |||||||
| chr6:70520169 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1030-2344C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70520169 | |||||||
| chr6:70520228 | A | G | 12 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(9): Show |
12 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.1030-2285A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70520228 | |||||||
| chr6:70520292 | GAGTT | G | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1030-2217_1030-221 others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70520292 | ||||||
| chr6:70520315 | A | G | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1030-2198A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70520315 | |||||||
| chr6:70520579 | G | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0105 |
2 | HG01074.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.1030-1934G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70520579 | |||||||
| chr6:70520654 | AATAC | A | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.1030-1851_1030-184 others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70520654 | ||||||
| chr6:70520773 | T | A | 1 | a0001c0004t0003g0236 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1030-1740T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70520773 | |||||||
| chr6:70520998 | G | C | 12 | a0001c0004t0003g0009 a0001c0004t0003g0010 a0001c0004t0003g0011 others(9): Show |
12 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1030-1515G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70520998 | |||||||
| chr6:70521060 | A | G | 1 | a0006c0007t0001g0127 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1030-1453A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70521060 | |||||||
| chr6:70521143 | G | A | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1030-1370G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70521143 | |||||||
| chr6:70521224 | A | G | 1 | a0002c0003t0001g0114 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1030-1289A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70521224 | |||||||
| chr6:70521293 | C | T | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1030-1220C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70521293 | |||||||
| chr6:70521319 | G | A | 16 | a0001c0004t0003g0001 a0001c0004t0003g0230 a0001c0004t0003g0231 others(13): Show |
16 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.1030-1194G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70521319 | |||||||
| chr6:70521319 | G | GT | 13 | a0001c0002t0002g0209 a0001c0002t0002g0253 a0001c0002t0002g0254 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.1030-1187dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70521319 | ||||||
| chr6:70521334 | T | C | 1 | a0001c0002t0002g0260 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1030-1179T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70521334 | |||||||
| chr6:70521415 | A | C | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.1030-1098A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70521415 | |||||||
| chr6:70521978 | G | A | 6 | a0001c0001t0001g0075 a0001c0001t0001g0080 a0001c0001t0001g0081 others(3): Show |
6 | HG00280.hp2 HG00639.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.1030-535G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70521978 | |||||||
| chr6:70522019 | C | T | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1030-494C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70522019 | |||||||
| chr6:70522062 | A | G | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.1030-451A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70522062 | |||||||
| chr6:70522182 | T | G | 80 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.1030-331T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70522182 | |||||||
| chr6:70522209 | G | A | 1 | a0002c0003t0001g0131 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1030-304G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70522209 | |||||||
| chr6:70522217 | C | T | 56 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(53): Show |
56 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1030-296C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70522217 | |||||||
| chr6:70522311 | GTTTATA | G | 69 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(66): Show |
69 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.1030-194_1030-189d others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 70522311 | ||||||
| chr6:70522369 | A | G | 1 | a0001c0002t0002g0264 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1030-144A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70522369 | |||||||
| chr6:70522494 | C | G | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1030-19C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 12/21 | chr6 | 70522494 | |||||||
| chr6:70522705 | T | A | 2 | a0001c0002t0002g0173 a0001c0002t0002g0174 |
2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1103+119T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 13/21 | chr6 | 70522705 | |||||||
| chr6:70523142 | A | AG | 113 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(110): Show |
113 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.1103+556_1103+557i others(3): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 13/21 | chr6 | 70523142 | |||||||
| chr6:70523358 | G | A | 3 | a0001c0001t0001g0078 a0001c0001t0001g0083 a0001c0001t0001g0086 |
3 | NA18961.hp2 NA18962.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1104-609G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 13/21 | chr6 | 70523358 | |||||||
| chr6:70523399 | A | G | 1 | a0001c0004t0003g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1104-568A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 13/21 | chr6 | 70523399 | |||||||
| chr6:70523439 | T | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(1): Show |
4 | HG02615.hp1 HG02723.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1104-528T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 13/21 | chr6 | 70523439 | |||||||
| chr6:70523468 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1104-499G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 13/21 | chr6 | 70523468 | |||||||
| chr6:70523609 | A | T | 1 | a0001c0002t0002g0254 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1104-358A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 13/21 | chr6 | 70523609 | |||||||
| chr6:70523641 | T | C | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1104-326T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 13/21 | chr6 | 70523641 | |||||||
| chr6:70523645 | T | C | 11 | a0001c0004t0007g0265 a0001c0009t0001g0211 a0001c0009t0001g0212 others(8): Show |
11 | HG02109.hp1 HG02109.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.1104-322T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 13/21 | chr6 | 70523645 | |||||||
| chr6:70523788 | A | C | 1 | a0001c0001t0001g0075 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1104-179A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 13/21 | chr6 | 70523788 | |||||||
| chr6:70523848 | G | T | 69 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(66): Show |
69 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.1104-119G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 13/21 | chr6 | 70523848 | |||||||
| chr6:70523860 | A | G | 1 | a0001c0002t0002g0220 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1104-107A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 13/21 | chr6 | 70523860 | |||||||
| chr6:70523942 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1104-25A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 13/21 | chr6 | 70523942 | |||||||
| chr6:70524133 | C | T | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1258+12C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 14/21 | chr6 | 70524133 | |||||||
| chr6:70526748 | TATACACA others(5): Show |
T | 1 | a0001c0002t0002g0224 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3614+52_3614+63del others(12): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526748 | ||||||
| chr6:70526748 | TATACACA others(13): Show |
T | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.3614+52_3614+71del others(20): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526748 | ||||||
| chr6:70526750 | T | TACACACA others(13): Show |
1 | a0001c0004t0003g0250 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3614+67_3614+68ins others(20): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526750 | ||||||
| chr6:70526750 | TACACACA others(7): Show |
T | 3 | a0001c0002t0002g0204 a0001c0002t0002g0205 a0001c0002t0002g0206 |
3 | NA18522.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3614+54_3614+67del others(14): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526750 | ||||||
| chr6:70526752 | C | CACACACA others(9): Show |
1 | a0001c0004t0003g0251 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3614+67_3614+68ins others(16): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526752 | ||||||
| chr6:70526752 | C | T | 43 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(40): Show |
43 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.3614+54C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70526752 | |||||||
| chr6:70526754 | C | CACACACA others(7): Show |
1 | a0001c0004t0003g0252 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3614+67_3614+68ins others(14): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526754 | ||||||
| chr6:70526754 | CACACACA others(5): Show |
C | 46 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(43): Show |
46 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.3614+68_3614+79del others(12): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526754 | ||||||
| chr6:70526756 | CACACACA others(3): Show |
C | 3 | a0001c0002t0002g0173 a0001c0002t0002g0174 a0001c0002t0002g0189 |
3 | HG00741.hp2 HG01167.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.3614+68_3614+77del others(10): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526756 | ||||||
| chr6:70526762 | CACAT | C | 4 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0142 others(1): Show |
4 | HG02258.hp1 HG02647.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3614+68_3614+71del others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526762 | ||||||
| chr6:70526766 | T | C | 4 | a0001c0002t0002g0224 a0001c0004t0003g0250 a0001c0004t0003g0251 others(1): Show |
4 | HG02572.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3614+68T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70526766 | |||||||
| chr6:70526766 | T | TAC | 12 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0002c0003t0001g0030 others(9): Show |
12 | HG00280.hp2 HG00597.hp2 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.3614+104_3614+105d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526766 | ||||||
| chr6:70526766 | T | TACAC | 4 | a0001c0001t0001g0104 a0001c0004t0004g0015 a0004c0008t0004g0003 others(1): Show |
4 | HG01074.hp2 HG01346.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.3614+102_3614+105d others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526766 | ||||||
| chr6:70526766 | T | TACACACA others(3): Show |
1 | a0001c0004t0003g0011 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3614+96_3614+105du others(11): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526766 | ||||||
| chr6:70526766 | T | TACACACA others(7): Show |
1 | a0001c0004t0003g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3614+92_3614+105du others(15): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526766 | ||||||
| chr6:70526766 | TAC | T | 32 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(29): Show |
32 | HG01069.hp1 HG01168.hp1 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.3614+104_3614+105d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526766 | ||||||
| chr6:70526766 | TACAC | T | 3 | a0001c0001t0001g0147 a0001c0009t0001g0211 a0001c0009t0001g0212 |
3 | HG02258.hp2 HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3614+102_3614+105d others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526766 | ||||||
| chr6:70526766 | TACACACA others(3): Show |
T | 2 | a0001c0001t0001g0053 a0001c0004t0003g0009 |
2 | HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3614+96_3614+105de others(11): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526766 | ||||||
| chr6:70526768 | C | T | 4 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0142 others(1): Show |
4 | HG02258.hp1 HG02647.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3614+70C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70526768 | |||||||
| chr6:70526770 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3614+72C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70526770 | |||||||
| chr6:70526792 | CACACACA others(7): Show |
C | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.3614+96_3614+109de others(15): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr6 | 70526792 | ||||||
| chr6:70526794 | C | T | 1 | a0001c0002t0002g0254 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3614+96C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70526794 | |||||||
| chr6:70526796 | C | T | 71 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(68): Show |
71 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.3614+98C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70526796 | |||||||
| chr6:70526798 | C | T | 78 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(75): Show |
78 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.3614+100C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70526798 | |||||||
| chr6:70526800 | C | T | 78 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(75): Show |
78 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.3614+102C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70526800 | |||||||
| chr6:70526802 | C | T | 92 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(89): Show |
92 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.3614+104C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70526802 | |||||||
| chr6:70526804 | T | C | 4 | a0001c0004t0004g0015 a0001c0004t0006g0019 a0004c0008t0004g0003 others(1): Show |
4 | HG01074.hp2 HG01192.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.3614+106T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70526804 | |||||||
| chr6:70527040 | C | T | 117 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(114): Show |
117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.3614+342C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70527040 | |||||||
| chr6:70527073 | A | G | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3614+375A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70527073 | |||||||
| chr6:70527133 | G | A | 1 | a0002c0003t0001g0123 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3614+435G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70527133 | |||||||
| chr6:70527372 | T | G | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3614+674T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70527372 | |||||||
| chr6:70527431 | A | G | 67 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(64): Show |
67 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.3614+733A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70527431 | |||||||
| chr6:70527518 | G | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3615-774G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70527518 | |||||||
| chr6:70527835 | G | A | 1 | a0002c0006t0001g0138 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3615-457G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70527835 | |||||||
| chr6:70527857 | A | G | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3615-435A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70527857 | |||||||
| chr6:70527862 | G | A | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.3615-430G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70527862 | |||||||
| chr6:70528024 | T | C | 2 | a0001c0001t0001g0210 a0001c0001t0001g0267 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3615-268T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70528024 | |||||||
| chr6:70528039 | G | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3615-253G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70528039 | |||||||
| chr6:70528114 | A | G | 3 | a0002c0003t0001g0124 a0002c0003t0001g0125 a0002c0003t0001g0126 |
3 | HG01358.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.3615-178A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70528114 | |||||||
| chr6:70528136 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3615-156C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 15/21 | chr6 | 70528136 | |||||||
| chr6:70528548 | G | T | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.3775+96G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70528548 | |||||||
| chr6:70528666 | C | T | 1 | a0001c0002t0002g0264 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3775+214C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70528666 | |||||||
| chr6:70528674 | C | T | 135 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(132): Show |
135 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.3775+222C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70528674 | |||||||
| chr6:70528702 | A | AT | 218 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(215): Show |
218 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.3775+260dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr6 | 70528702 | ||||||
| chr6:70528813 | T | G | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3775+361T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70528813 | |||||||
| chr6:70528850 | T | C | 111 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(108): Show |
111 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.3775+398T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70528850 | |||||||
| chr6:70528851 | G | A | 2 | a0001c0002t0002g0173 a0001c0002t0002g0174 |
2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.3775+399G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70528851 | |||||||
| chr6:70529002 | G | T | 3 | a0001c0001t0001g0077 a0001c0001t0001g0155 a0007c0019t0001g0079 |
3 | HG02083.hp2 HG02523.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.3775+550G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70529002 | |||||||
| chr6:70529438 | T | TA | 6 | a0001c0001t0001g0058 a0001c0001t0001g0210 a0001c0002t0002g0171 others(3): Show |
6 | HG02300.hp2 HG02572.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.3775+1002dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr6 | 70529438 | ||||||
| chr6:70529669 | C | T | 1 | a0002c0003t0001g0214 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3775+1217C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70529669 | |||||||
| chr6:70529789 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3775+1337G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70529789 | |||||||
| chr6:70529866 | T | G | 1 | a0001c0002t0002g0208 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3775+1414T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70529866 | |||||||
| chr6:70529889 | C | T | 1 | a0002c0003t0001g0134 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3775+1437C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70529889 | |||||||
| chr6:70530030 | C | G | 54 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(51): Show |
54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.3775+1578C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70530030 | |||||||
| chr6:70530063 | CA | C | 12 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(9): Show |
12 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.3775+1622delA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr6 | 70530063 | ||||||
| chr6:70530070 | A | G | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3775+1618A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70530070 | |||||||
| chr6:70530072 | A | T | 4 | a0001c0004t0003g0250 a0001c0004t0003g0251 a0001c0004t0003g0252 others(1): Show |
4 | HG02572.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3775+1620A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70530072 | |||||||
| chr6:70530195 | G | C | 1 | a0002c0003t0001g0150 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3775+1743G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70530195 | |||||||
| chr6:70530244 | C | T | 1 | a0005c0010t0003g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3775+1792C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70530244 | |||||||
| chr6:70530331 | A | G | 1 | a0001c0002t0002g0258 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3775+1879A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70530331 | |||||||
| chr6:70530363 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3775+1911T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70530363 | |||||||
| chr6:70530389 | A | T | 1 | a0001c0002t0002g0262 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3775+1937A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70530389 | |||||||
| chr6:70530390 | A | C | 111 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(108): Show |
111 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.3775+1938A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70530390 | |||||||
| chr6:70530397 | A | C | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3775+1945A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70530397 | |||||||
| chr6:70530493 | G | A | 5 | a0001c0002t0002g0204 a0001c0002t0002g0205 a0001c0002t0002g0206 others(2): Show |
5 | HG02723.hp2 HG03540.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.3775+2041G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70530493 | |||||||
| chr6:70530606 | G | T | 1 | a0001c0002t0002g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3775+2154G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70530606 | |||||||
| chr6:70531145 | G | A | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.3776-2015G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70531145 | |||||||
| chr6:70531186 | A | G | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3776-1974A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70531186 | |||||||
| chr6:70531497 | A | G | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3776-1663A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70531497 | |||||||
| chr6:70531502 | G | A | 5 | a0001c0002t0002g0204 a0001c0002t0002g0205 a0001c0002t0002g0206 others(2): Show |
5 | HG02723.hp2 HG03540.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.3776-1658G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70531502 | |||||||
| chr6:70531531 | A | G | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3776-1629A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70531531 | |||||||
| chr6:70531731 | C | T | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.3776-1429C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70531731 | |||||||
| chr6:70531800 | C | T | 15 | a0001c0004t0003g0001 a0001c0004t0003g0230 a0001c0004t0003g0231 others(12): Show |
15 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.3776-1360C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70531800 | |||||||
| chr6:70531888 | C | CT | 15 | a0001c0001t0001g0063 a0001c0001t0001g0069 a0001c0001t0001g0084 others(12): Show |
15 | HG00621.hp2 HG00735.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.3776-1247dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr6 | 70531888 | ||||||
| chr6:70531888 | CT | C | 18 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(15): Show |
18 | HG01099.hp2 HG01168.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.3776-1247delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr6 | 70531888 | ||||||
| chr6:70531888 | CTT | C | 14 | a0001c0001t0001g0210 a0001c0004t0001g0160 a0001c0004t0001g0161 others(11): Show |
14 | HG01109.hp1 HG02109.hp1 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.3776-1248_3776-124 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr6 | 70531888 | ||||||
| chr6:70531888 | CTTT | C | 9 | a0001c0002t0002g0173 a0001c0002t0002g0174 a0001c0002t0002g0175 others(6): Show |
9 | HG00741.hp2 HG01167.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3776-1249_3776-124 others(7): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr6 | 70531888 | ||||||
| chr6:70531888 | CTTTT | C | 48 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(45): Show |
48 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.3776-1250_3776-124 others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr6 | 70531888 | ||||||
| chr6:70531888 | CTTTTT | C | 14 | a0001c0002t0002g0220 a0001c0002t0002g0253 a0001c0002t0002g0255 others(11): Show |
14 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.3776-1251_3776-124 others(9): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr6 | 70531888 | ||||||
| chr6:70531888 | CTTTTTTT others(1): Show |
C | 14 | a0001c0004t0003g0001 a0001c0004t0003g0230 a0001c0004t0003g0231 others(11): Show |
14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.3776-1254_3776-124 others(12): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr6 | 70531888 | ||||||
| chr6:70532233 | A | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(1): Show |
4 | HG02615.hp1 HG02723.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3776-927A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70532233 | |||||||
| chr6:70532242 | T | C | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3776-918T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70532242 | |||||||
| chr6:70532246 | A | G | 1 | a0001c0002t0002g0197 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.3776-914A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70532246 | |||||||
| chr6:70532298 | A | G | 1 | a0001c0002t0002g0258 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3776-862A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70532298 | |||||||
| chr6:70532378 | A | G | 7 | a0001c0001t0001g0027 a0001c0001t0001g0140 a0001c0001t0001g0141 others(4): Show |
7 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3776-782A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70532378 | |||||||
| chr6:70532708 | G | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3776-452G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70532708 | |||||||
| chr6:70532748 | C | T | 7 | a0001c0002t0002g0223 a0001c0002t0002g0224 a0001c0002t0002g0225 others(4): Show |
7 | NA18947.hp2 NA18950.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.3776-412C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70532748 | |||||||
| chr6:70532844 | A | G | 3 | a0001c0004t0003g0250 a0001c0004t0003g0251 a0001c0004t0003g0252 |
3 | HG02572.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3776-316A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 16/21 | chr6 | 70532844 | |||||||
| chr6:70533382 | GTA | G | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.3867+135_3867+136d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr6 | 70533382 | ||||||
| chr6:70533403 | A | T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3867+152A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 17/21 | chr6 | 70533403 | |||||||
| chr6:70533408 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3867+157T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 17/21 | chr6 | 70533408 | |||||||
| chr6:70533432 | C | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3867+181C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 17/21 | chr6 | 70533432 | |||||||
| chr6:70533566 | C | T | 1 | a0001c0002t0002g0171 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3868-191C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 17/21 | chr6 | 70533566 | |||||||
| chr6:70533649 | A | G | 111 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(108): Show |
111 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.3868-108A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 17/21 | chr6 | 70533649 | |||||||
| chr6:70533681 | A | G | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3868-76A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 17/21 | chr6 | 70533681 | |||||||
| chr6:70534062 | G | A | 1 | a0002c0003t0001g0108 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.3965+208G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70534062 | |||||||
| chr6:70534227 | G | A | 2 | a0002c0003t0001g0108 a0002c0003t0001g0110 |
2 | NA18947.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.3965+373G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70534227 | |||||||
| chr6:70534241 | CATATATG others(6): Show |
C | 144 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 others(141): Show |
144 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.3965+415_3965+427d others(15): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70534241 | ||||||
| chr6:70534312 | C | CT | 30 | a0001c0001t0001g0025 a0001c0001t0001g0059 a0001c0001t0001g0060 others(27): Show |
30 | HG00621.hp2 HG00735.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.3965+483dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70534312 | ||||||
| chr6:70534312 | C | CTTTTT | 7 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(4): Show |
7 | HG00280.hp1 HG00639.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.3965+479_3965+483d others(7): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70534312 | ||||||
| chr6:70534312 | C | CTTTTTT | 5 | a0001c0002t0002g0258 a0001c0002t0002g0262 a0001c0002t0002g0263 others(2): Show |
5 | HG00642.hp2 HG01243.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.3965+478_3965+483d others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70534312 | ||||||
| chr6:70534312 | C | CTTTTTTT others(3): Show |
1 | a0001c0002t0002g0222 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.3965+474_3965+483d others(12): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70534312 | ||||||
| chr6:70534312 | C | CTTTTTTT others(4): Show |
10 | a0001c0002t0002g0168 a0001c0002t0002g0186 a0001c0002t0002g0188 others(7): Show |
10 | HG01975.hp1 HG01993.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.3965+473_3965+483d others(13): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70534312 | ||||||
| chr6:70534312 | C | CTTTTTTT others(5): Show |
20 | a0001c0002t0002g0169 a0001c0002t0002g0171 a0001c0002t0002g0172 others(17): Show |
20 | HG00597.hp1 HG00609.hp1 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.3965+472_3965+483d others(14): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70534312 | ||||||
| chr6:70534312 | C | CTTTTTTT others(6): Show |
23 | a0001c0002t0002g0167 a0001c0002t0002g0173 a0001c0002t0002g0174 others(20): Show |
23 | HG00621.hp1 HG00735.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.3965+471_3965+483d others(15): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70534312 | ||||||
| chr6:70534312 | C | CTTTTTTT others(7): Show |
3 | a0001c0002t0002g0181 a0001c0002t0002g0208 a0003c0005t0001g0249 |
3 | HG01255.hp2 HG02486.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.3965+470_3965+483d others(16): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70534312 | ||||||
| chr6:70534312 | C | CTTTTTTT others(8): Show |
1 | a0001c0002t0002g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3965+469_3965+483d others(17): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70534312 | ||||||
| chr6:70534312 | C | CTTTTTTT others(25): Show |
1 | a0003c0005t0001g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3965+483_3965+484i others(34): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70534312 | ||||||
| chr6:70534312 | C | CTTTTTTT others(26): Show |
2 | a0003c0005t0001g0245 a0003c0005t0001g0247 |
2 | HG02293.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3965+483_3965+484i others(35): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70534312 | ||||||
| chr6:70534312 | C | CTTTTTTT others(30): Show |
1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3965+483_3965+484i others(39): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70534312 | ||||||
| chr6:70534312 | CT | C | 11 | a0001c0001t0001g0073 a0001c0001t0001g0075 a0001c0001t0001g0080 others(8): Show |
11 | HG00639.hp2 HG01081.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.3965+483delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70534312 | ||||||
| chr6:70534426 | C | T | 12 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(9): Show |
12 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.3965+572C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70534426 | |||||||
| chr6:70534444 | C | A | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3965+590C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70534444 | |||||||
| chr6:70534582 | G | C | 67 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(64): Show |
67 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.3965+728G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70534582 | |||||||
| chr6:70534626 | C | A | 1 | a0002c0006t0001g0034 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3965+772C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70534626 | |||||||
| chr6:70535220 | C | T | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3966-1040C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70535220 | |||||||
| chr6:70535317 | A | G | 12 | a0001c0004t0003g0009 a0001c0004t0003g0010 a0001c0004t0003g0011 others(9): Show |
12 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.3966-943A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70535317 | |||||||
| chr6:70535423 | G | A | 23 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(20): Show |
23 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.3966-837G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70535423 | |||||||
| chr6:70535571 | G | T | 1 | a0001c0001t0001g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3966-689G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70535571 | |||||||
| chr6:70535614 | G | A | 1 | a0001c0002t0002g0254 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3966-646G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70535614 | |||||||
| chr6:70535684 | A | G | 54 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(51): Show |
54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.3966-576A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70535684 | |||||||
| chr6:70535729 | A | G | 1 | a0002c0003t0001g0046 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3966-531A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70535729 | |||||||
| chr6:70535762 | A | T | 12 | a0001c0004t0003g0009 a0001c0004t0003g0010 a0001c0004t0003g0011 others(9): Show |
12 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.3966-498A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70535762 | |||||||
| chr6:70535805 | A | G | 23 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(20): Show |
23 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.3966-455A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70535805 | |||||||
| chr6:70535833 | A | G | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3966-427A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70535833 | |||||||
| chr6:70535864 | G | A | 6 | a0002c0003t0001g0119 a0002c0003t0001g0122 a0002c0003t0001g0124 others(3): Show |
6 | HG00140.hp2 HG01168.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.3966-396G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70535864 | |||||||
| chr6:70535981 | C | T | 2 | a0010c0018t0005g0006 a0012c0015t0005g0005 |
2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3966-279C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70535981 | |||||||
| chr6:70535982 | G | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3966-278G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70535982 | |||||||
| chr6:70536033 | ATGT | A | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3966-222_3966-220d others(5): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 70536033 | ||||||
| chr6:70536072 | G | C | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3966-188G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70536072 | |||||||
| chr6:70536090 | ACATTTTT others(6): Show |
A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0267 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3966-169_3966-157d others(15): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 18/21 | chr6 | 70536090 | |||||||
| chr6:70536503 | G | A | 26 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 others(23): Show |
26 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.4117+92G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70536503 | |||||||
| chr6:70536797 | G | T | 1 | a0002c0003t0001g0045 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4117+386G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70536797 | |||||||
| chr6:70536802 | A | G | 1 | a0001c0002t0002g0197 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.4117+391A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70536802 | |||||||
| chr6:70536837 | G | A | 1 | a0001c0009t0001g0212 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4117+426G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70536837 | |||||||
| chr6:70536932 | T | A | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4117+521T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70536932 | |||||||
| chr6:70536934 | A | AT | 60 | a0001c0001t0001g0093 a0001c0001t0001g0102 a0001c0001t0001g0267 others(57): Show |
60 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.4117+543dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr6 | 70536934 | ||||||
| chr6:70536934 | A | ATT | 7 | a0001c0002t0002g0169 a0001c0002t0002g0173 a0001c0002t0002g0175 others(4): Show |
7 | HG00741.hp2 HG01433.hp1 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.4117+542_4117+543d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr6 | 70536934 | ||||||
| chr6:70536934 | AT | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0095 a0001c0002t0002g0255 others(2): Show |
5 | HG02004.hp2 NA19055.hp1 NA19055.hp2 others(2): Show |
intron_variant | MODIFIER | c.4117+543delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr6 | 70536934 | ||||||
| chr6:70537060 | G | A | 11 | a0001c0002t0002g0219 a0001c0002t0002g0220 a0001c0002t0002g0221 others(8): Show |
11 | HG00609.hp1 HG00621.hp1 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.4117+649G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70537060 | |||||||
| chr6:70537238 | T | C | 54 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(51): Show |
54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.4117+827T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70537238 | |||||||
| chr6:70537346 | T | G | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4117+935T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70537346 | |||||||
| chr6:70537488 | G | C | 1 | a0001c0004t0003g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4118-803G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70537488 | |||||||
| chr6:70537602 | A | C | 2 | a0001c0001t0001g0210 a0001c0001t0001g0267 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4118-689A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70537602 | |||||||
| chr6:70537628 | T | C | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4118-663T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70537628 | |||||||
| chr6:70537637 | A | C | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4118-654A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70537637 | |||||||
| chr6:70537671 | G | C | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4118-620G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70537671 | |||||||
| chr6:70537682 | A | G | 78 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(75): Show |
78 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.4118-609A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70537682 | |||||||
| chr6:70537684 | A | G | 1 | a0001c0004t0003g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4118-607A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70537684 | |||||||
| chr6:70537737 | C | T | 23 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(20): Show |
23 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.4118-554C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70537737 | |||||||
| chr6:70537869 | A | G | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.4118-422A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70537869 | |||||||
| chr6:70537960 | ATCT | A | 23 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(20): Show |
23 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.4118-323_4118-321d others(5): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr6 | 70537960 | ||||||
| chr6:70538036 | G | C | 1 | a0011c0011t0002g0170 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.4118-255G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70538036 | |||||||
| chr6:70538084 | A | G | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4118-207A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70538084 | |||||||
| chr6:70538126 | A | T | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4118-165A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70538126 | |||||||
| chr6:70538129 | G | A | 1 | a0001c0004t0003g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4118-162G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70538129 | |||||||
| chr6:70538160 | T | C | 23 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(20): Show |
23 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.4118-131T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 19/21 | chr6 | 70538160 | |||||||
| chr6:70538448 | TA | T | 55 | a0001c0001t0001g0071 a0001c0002t0002g0167 a0001c0002t0002g0168 others(52): Show |
55 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.4228+53delA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538448 | ||||||
| chr6:70538603 | G | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4228+202G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70538603 | |||||||
| chr6:70538660 | T | C | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4228+259T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70538660 | |||||||
| chr6:70538667 | C | T | 55 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(52): Show |
55 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.4228+266C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70538667 | |||||||
| chr6:70538690 | A | G | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4228+289A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70538690 | |||||||
| chr6:70538762 | T | G | 1 | a0007c0019t0001g0079 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.4228+361T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70538762 | |||||||
| chr6:70538787 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4228+386A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70538787 | |||||||
| chr6:70538795 | ATTATG | A | 11 | a0001c0001t0001g0028 a0001c0001t0001g0142 a0001c0002t0002g0255 others(8): Show |
11 | HG00642.hp2 HG01109.hp1 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.4228+404_4228+408d others(7): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538795 | ||||||
| chr6:70538800 | G | GTTATA | 2 | a0001c0002t0002g0254 a0001c0002t0002g0263 |
2 | HG01243.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.4228+403_4228+404i others(7): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538800 | ||||||
| chr6:70538800 | G | GTTATATT others(3): Show |
2 | a0001c0002t0002g0253 a0001c0002t0002g0257 |
2 | HG00280.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.4228+403_4228+404i others(12): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538800 | ||||||
| chr6:70538800 | G | GTTATATT others(8): Show |
1 | a0001c0002t0002g0259 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.4228+403_4228+404i others(17): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538800 | ||||||
| chr6:70538800 | GTTATGTT others(3): Show |
G | 29 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0050 others(26): Show |
29 | HG01069.hp1 HG01074.hp2 HG02258.hp1 others(26): Show |
intron_variant | MODIFIER | c.4228+404_4228+413d others(12): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538800 | ||||||
| chr6:70538800 | GTTATGTT others(8): Show |
G | 7 | a0001c0001t0001g0148 a0001c0004t0003g0237 a0001c0004t0003g0250 others(4): Show |
7 | HG01192.hp2 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.4228+404_4228+418d others(17): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538800 | ||||||
| chr6:70538800 | GTTATGTT others(13): Show |
G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0004t0003g0232 |
3 | HG02622.hp2 HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4228+404_4228+423d others(22): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538800 | ||||||
| chr6:70538800 | GTTATGTT others(28): Show |
G | 1 | a0001c0004t0003g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4228+404_4228+438d others(37): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538800 | ||||||
| chr6:70538805 | G | A | 23 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0253 others(20): Show |
23 | HG00280.hp1 HG00639.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.4228+404G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70538805 | |||||||
| chr6:70538805 | G | GTTATA | 18 | a0001c0001t0001g0058 a0001c0001t0001g0073 a0001c0001t0001g0094 others(15): Show |
18 | HG00280.hp2 HG00621.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.4228+456_4228+460d others(7): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538805 | ||||||
| chr6:70538805 | G | GTTATATT others(3): Show |
7 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0002t0002g0208 others(4): Show |
7 | HG02723.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.4228+451_4228+460d others(12): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538805 | ||||||
| chr6:70538805 | GTTATA | G | 44 | a0001c0001t0001g0021 a0001c0001t0001g0047 a0001c0001t0001g0055 others(41): Show |
44 | HG00597.hp1 HG00609.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.4228+456_4228+460d others(7): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538805 | ||||||
| chr6:70538805 | GTTATATT others(3): Show |
G | 14 | a0001c0001t0001g0036 a0001c0001t0001g0056 a0001c0001t0001g0102 others(11): Show |
14 | HG00673.hp1 HG01123.hp2 HG02293.hp2 others(11): Show |
intron_variant | MODIFIER | c.4228+451_4228+460d others(12): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538805 | ||||||
| chr6:70538805 | GTTATATT others(8): Show |
G | 5 | a0001c0001t0001g0091 a0001c0002t0002g0184 a0001c0002t0002g0185 others(2): Show |
5 | HG03195.hp2 NA18953.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.4228+446_4228+460d others(17): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538805 | ||||||
| chr6:70538805 | GTTATATT others(13): Show |
G | 1 | a0001c0002t0002g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4228+441_4228+460d others(22): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538805 | ||||||
| chr6:70538835 | A | ATTATATT others(8): Show |
6 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(3): Show |
6 | HG02109.hp1 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.4228+448_4228+449i others(17): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538835 | ||||||
| chr6:70538835 | A | ATTATATT others(3): Show |
2 | a0003c0005t0001g0247 a0003c0005t0001g0249 |
2 | HG02293.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.4228+443_4228+444i others(12): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538835 | ||||||
| chr6:70538842 | TATATTAT others(4): Show |
T | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4228+442_4228+452d others(13): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70538842 | |||||||
| chr6:70538851 | TTA | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0267 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4228+454_4228+455d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538851 | ||||||
| chr6:70538917 | C | CTTTTTTT others(176): Show |
1 | a0001c0002t0002g0257 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.4228+517_4228+518i others(185): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538917 | ||||||
| chr6:70538917 | C | CTTTTTTT others(177): Show |
8 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(5): Show |
8 | HG00280.hp1 HG00642.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.4228+517_4228+518i others(186): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538917 | ||||||
| chr6:70538917 | C | CTTTTTTT others(178): Show |
4 | a0001c0002t0002g0256 a0001c0002t0002g0260 a0001c0002t0002g0262 others(1): Show |
4 | HG02257.hp2 HG02698.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.4228+517_4228+518i others(187): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70538917 | ||||||
| chr6:70538919 | A | T | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.4228+518A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70538919 | |||||||
| chr6:70538920 | C | G | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.4228+519C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70538920 | |||||||
| chr6:70538921 | A | T | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.4228+520A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70538921 | |||||||
| chr6:70539298 | C | G | 32 | a0001c0004t0003g0001 a0001c0004t0003g0009 a0001c0004t0003g0010 others(29): Show |
32 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.4228+897C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70539298 | |||||||
| chr6:70539485 | A | G | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.4228+1084A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70539485 | |||||||
| chr6:70539596 | C | T | 1 | a0001c0004t0003g0252 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4228+1195C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70539596 | |||||||
| chr6:70539718 | G | A | 5 | a0001c0002t0002g0254 a0001c0002t0002g0258 a0001c0002t0002g0259 others(2): Show |
5 | HG00642.hp2 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.4228+1317G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70539718 | |||||||
| chr6:70539797 | C | A | 26 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 others(23): Show |
26 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.4228+1396C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70539797 | |||||||
| chr6:70539853 | A | G | 219 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(216): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.4228+1452A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70539853 | |||||||
| chr6:70539920 | T | C | 1 | a0001c0002t0002g0220 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.4228+1519T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70539920 | |||||||
| chr6:70539945 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.4228+1544G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70539945 | |||||||
| chr6:70539991 | G | A | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4228+1590G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70539991 | |||||||
| chr6:70540063 | G | A | 111 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(108): Show |
111 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.4228+1662G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540063 | |||||||
| chr6:70540130 | T | G | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.4228+1729T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540130 | |||||||
| chr6:70540217 | A | C | 1 | a0001c0001t0001g0047 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.4228+1816A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540217 | |||||||
| chr6:70540228 | A | G | 12 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(9): Show |
12 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.4228+1827A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540228 | |||||||
| chr6:70540230 | G | A | 143 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 others(140): Show |
143 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.4228+1829G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540230 | |||||||
| chr6:70540257 | T | C | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.4228+1856T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540257 | |||||||
| chr6:70540318 | C | CT | 111 | a0001c0001t0001g0020 a0001c0001t0001g0027 a0001c0001t0001g0047 others(108): Show |
111 | HG00140.hp1 HG00597.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.4228+1941dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70540318 | ||||||
| chr6:70540318 | C | CTT | 20 | a0001c0001t0001g0036 a0001c0001t0001g0048 a0001c0001t0001g0084 others(17): Show |
20 | HG00735.hp1 HG00735.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.4228+1940_4228+194 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70540318 | ||||||
| chr6:70540318 | C | CTTTTT | 6 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0245 others(3): Show |
6 | HG02109.hp1 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.4228+1937_4228+194 others(9): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70540318 | ||||||
| chr6:70540318 | CT | C | 11 | a0001c0002t0002g0254 a0001c0002t0002g0255 a0001c0002t0002g0256 others(8): Show |
11 | HG00639.hp1 HG00642.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.4228+1941delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70540318 | ||||||
| chr6:70540386 | A | G | 111 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(108): Show |
111 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.4228+1985A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540386 | |||||||
| chr6:70540406 | G | A | 2 | a0010c0018t0005g0006 a0012c0015t0005g0005 |
2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.4228+2005G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540406 | |||||||
| chr6:70540474 | G | A | 1 | a0002c0003t0001g0134 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4228+2073G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540474 | |||||||
| chr6:70540546 | C | T | 1 | a0001c0002t0002g0169 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.4228+2145C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540546 | |||||||
| chr6:70540568 | G | A | 1 | a0001c0002t0002g0264 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4228+2167G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540568 | |||||||
| chr6:70540635 | A | G | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.4228+2234A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540635 | |||||||
| chr6:70540749 | T | A | 1 | a0002c0003t0001g0039 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4228+2348T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540749 | |||||||
| chr6:70540951 | C | T | 3 | a0001c0001t0001g0028 a0005c0010t0003g0007 a0005c0010t0003g0008 |
3 | HG02976.hp1 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4228+2550C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540951 | |||||||
| chr6:70540952 | A | T | 1 | a0001c0004t0003g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4228+2551A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70540952 | |||||||
| chr6:70541017 | A | G | 5 | a0001c0002t0002g0204 a0001c0002t0002g0205 a0001c0002t0002g0206 others(2): Show |
5 | HG02723.hp2 HG03540.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.4228+2616A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70541017 | |||||||
| chr6:70541226 | T | C | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4228+2825T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70541226 | |||||||
| chr6:70541718 | T | C | 111 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(108): Show |
111 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.4228+3317T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70541718 | |||||||
| chr6:70541840 | G | T | 1 | a0001c0004t0003g0231 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4228+3439G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70541840 | |||||||
| chr6:70542018 | A | G | 1 | a0002c0003t0001g0038 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4228+3617A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70542018 | |||||||
| chr6:70542130 | C | G | 11 | a0001c0004t0003g0010 a0001c0004t0003g0011 a0001c0004t0003g0012 others(8): Show |
11 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.4228+3729C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70542130 | |||||||
| chr6:70542248 | G | GCA | 61 | a0001c0001t0001g0047 a0001c0001t0001g0105 a0001c0001t0001g0128 others(58): Show |
61 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.4228+3875_4228+387 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542248 | ||||||
| chr6:70542248 | G | GCACA | 13 | a0001c0002t0002g0173 a0001c0002t0002g0174 a0001c0002t0002g0175 others(10): Show |
13 | HG00741.hp2 HG01167.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.4228+3873_4228+387 others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542248 | ||||||
| chr6:70542248 | G | GCACACA | 9 | a0001c0002t0002g0169 a0001c0002t0002g0204 a0001c0002t0002g0205 others(6): Show |
9 | HG01192.hp2 HG01433.hp1 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.4228+3871_4228+387 others(10): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542248 | ||||||
| chr6:70542248 | G | GCACACAC others(3): Show |
3 | a0001c0002t0002g0256 a0001c0002t0002g0258 a0001c0002t0002g0264 |
3 | HG00642.hp2 HG02735.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.4228+3867_4228+387 others(14): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542248 | ||||||
| chr6:70542248 | G | GCACACAC others(5): Show |
8 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(5): Show |
8 | HG00280.hp1 HG00639.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.4228+3865_4228+387 others(16): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542248 | ||||||
| chr6:70542248 | G | GCACACAC others(7): Show |
2 | a0001c0002t0002g0262 a0001c0004t0003g0233 |
2 | HG01069.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.4228+3863_4228+387 others(18): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542248 | ||||||
| chr6:70542248 | G | GCACACAC others(9): Show |
13 | a0001c0004t0003g0230 a0001c0004t0003g0232 a0001c0004t0003g0234 others(10): Show |
13 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.4228+3861_4228+387 others(20): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542248 | ||||||
| chr6:70542248 | G | GCACACAC others(11): Show |
6 | a0001c0004t0003g0231 a0001c0004t0003g0241 a0003c0005t0001g0244 others(3): Show |
6 | HG02293.hp1 HG02572.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.4228+3859_4228+387 others(22): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542248 | ||||||
| chr6:70542248 | G | GCACACAC others(13): Show |
2 | a0001c0004t0003g0001 a0009c0014t0003g0001 |
2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4228+3857_4228+387 others(24): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542248 | ||||||
| chr6:70542248 | GCA | G | 18 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(15): Show |
18 | HG00639.hp2 HG00735.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.4228+3875_4228+387 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542248 | ||||||
| chr6:70542276 | A | ACACACAC others(19): Show |
1 | a0001c0004t0003g0010 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4228+3876_4228+387 others(30): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542276 | ||||||
| chr6:70542276 | A | ACACACAC others(15): Show |
1 | a0001c0004t0003g0013 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4228+3876_4228+387 others(26): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542276 | ||||||
| chr6:70542276 | A | ACACACAC others(11): Show |
5 | a0001c0004t0003g0011 a0001c0004t0003g0012 a0001c0004t0003g0250 others(2): Show |
5 | HG02572.hp1 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.4228+3876_4228+387 others(22): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542276 | ||||||
| chr6:70542276 | A | ACACACAC others(7): Show |
1 | a0001c0004t0003g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4228+3876_4228+387 others(18): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542276 | ||||||
| chr6:70542276 | A | ACACACAC others(3): Show |
1 | a0001c0004t0003g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4228+3876_4228+387 others(14): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542276 | ||||||
| chr6:70542277 | C | CACACACA others(10): Show |
1 | a0001c0004t0003g0235 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4228+3876_4228+387 others(21): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70542277 | |||||||
| chr6:70542278 | C | A | 10 | a0001c0004t0003g0016 a0001c0004t0003g0017 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4228+3877C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70542278 | |||||||
| chr6:70542331 | C | CTTTTTGT others(98): Show |
1 | a0001c0004t0003g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4228+3989_4228+399 others(109): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542331 | ||||||
| chr6:70542333 | T | C | 1 | a0005c0010t0003g0008 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4228+3932T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70542333 | |||||||
| chr6:70542344 | CTCATGTG others(8): Show |
C | 3 | a0001c0002t0002g0171 a0001c0009t0001g0211 a0001c0009t0001g0212 |
3 | HG02559.hp2 HG03453.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.4228+3962_4228+397 others(19): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70542344 | ||||||
| chr6:70542374 | A | G | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4228+3973A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70542374 | |||||||
| chr6:70542661 | A | G | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4228+4260A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70542661 | |||||||
| chr6:70542762 | G | A | 2 | a0004c0008t0004g0003 a0004c0008t0004g0004 |
2 | HG01074.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.4228+4361G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70542762 | |||||||
| chr6:70542972 | A | C | 3 | a0001c0001t0001g0048 a0001c0001t0001g0092 a0001c0001t0001g0105 |
3 | HG01074.hp1 HG01167.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.4228+4571A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70542972 | |||||||
| chr6:70543057 | T | C | 80 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(77): Show |
80 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.4228+4656T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70543057 | |||||||
| chr6:70543093 | G | A | 1 | a0001c0002t0002g0266 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.4228+4692G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70543093 | |||||||
| chr6:70543323 | G | A | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4228+4922G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70543323 | |||||||
| chr6:70543579 | TTACAAAA others(6): Show |
T | 1 | a0001c0001t0001g0047 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.4228+5187_4228+519 others(17): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70543579 | ||||||
| chr6:70543615 | G | A | 128 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(125): Show |
128 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.4228+5214G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70543615 | |||||||
| chr6:70543681 | T | C | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4228+5280T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70543681 | |||||||
| chr6:70543769 | C | A | 111 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(108): Show |
111 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.4228+5368C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70543769 | |||||||
| chr6:70543825 | T | G | 1 | a0001c0004t0004g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4228+5424T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70543825 | |||||||
| chr6:70543887 | T | G | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4228+5486T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70543887 | |||||||
| chr6:70543998 | C | T | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4228+5597C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70543998 | |||||||
| chr6:70544108 | T | TA | 68 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(65): Show |
68 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.4228+5720dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70544108 | ||||||
| chr6:70544118 | A | G | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4228+5717A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70544118 | |||||||
| chr6:70544150 | C | G | 1 | a0002c0003t0001g0108 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.4228+5749C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70544150 | |||||||
| chr6:70544150 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4228+5749C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70544150 | |||||||
| chr6:70544169 | G | A | 1 | a0001c0002t0002g0219 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4228+5768G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70544169 | |||||||
| chr6:70544183 | A | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.4228+5782A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70544183 | |||||||
| chr6:70544220 | G | A | 1 | a0002c0003t0001g0130 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.4228+5819G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70544220 | |||||||
| chr6:70544373 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4228+5972A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70544373 | |||||||
| chr6:70544529 | A | C | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.4228+6128A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70544529 | |||||||
| chr6:70544530 | A | G | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.4228+6129A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70544530 | |||||||
| chr6:70544724 | G | A | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4228+6323G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70544724 | |||||||
| chr6:70544746 | T | TA | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.4228+6354dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70544746 | ||||||
| chr6:70544799 | C | G | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4228+6398C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70544799 | |||||||
| chr6:70544819 | G | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4228+6418G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70544819 | |||||||
| chr6:70544868 | TG | T | 6 | a0002c0003t0001g0135 a0002c0006t0001g0034 a0002c0006t0001g0136 others(3): Show |
6 | HG00597.hp2 HG00621.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.4228+6469delG | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70544868 | ||||||
| chr6:70545017 | C | A | 67 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(64): Show |
67 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.4228+6616C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70545017 | |||||||
| chr6:70545038 | T | G | 1 | a0001c0001t0001g0267 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4228+6637T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70545038 | |||||||
| chr6:70545080 | C | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4228+6679C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70545080 | |||||||
| chr6:70545721 | G | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4228+7320G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70545721 | |||||||
| chr6:70545730 | G | A | 68 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(65): Show |
68 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.4228+7329G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70545730 | |||||||
| chr6:70545733 | A | G | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.4228+7332A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70545733 | |||||||
| chr6:70545763 | C | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0267 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4228+7362C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70545763 | |||||||
| chr6:70545992 | C | A | 1 | a0001c0001t0001g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4228+7591C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70545992 | |||||||
| chr6:70545992 | C | G | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4228+7591C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70545992 | |||||||
| chr6:70546009 | C | T | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4228+7608C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70546009 | |||||||
| chr6:70546051 | G | T | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4228+7650G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70546051 | |||||||
| chr6:70546062 | G | A | 2 | a0002c0003t0001g0111 a0002c0003t0001g0113 |
2 | NA19010.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.4228+7661G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70546062 | |||||||
| chr6:70546108 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.4228+7707A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70546108 | |||||||
| chr6:70546125 | G | T | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4228+7724G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70546125 | |||||||
| chr6:70546445 | A | G | 1 | a0001c0004t0003g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4228+8044A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70546445 | |||||||
| chr6:70546502 | C | T | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4228+8101C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70546502 | |||||||
| chr6:70546651 | A | T | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.4228+8250A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70546651 | |||||||
| chr6:70546857 | T | C | 8 | a0001c0001t0001g0075 a0001c0001t0001g0080 a0001c0001t0001g0081 others(5): Show |
8 | HG00639.hp2 HG01081.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.4228+8456T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70546857 | |||||||
| chr6:70546901 | G | T | 1 | a0001c0001t0001g0072 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.4228+8500G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70546901 | |||||||
| chr6:70546935 | G | C | 1 | a0002c0006t0001g0034 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.4228+8534G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70546935 | |||||||
| chr6:70547019 | G | T | 54 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(51): Show |
54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.4228+8618G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70547019 | |||||||
| chr6:70547473 | A | G | 3 | a0001c0002t0002g0189 a0001c0002t0002g0190 a0001c0002t0002g0194 |
3 | NA18993.hp2 NA19070.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.4228+9072A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70547473 | |||||||
| chr6:70547698 | A | T | 5 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(2): Show |
5 | HG00738.hp1 HG01099.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.4229-9052A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70547698 | |||||||
| chr6:70547733 | A | G | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4229-9017A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70547733 | |||||||
| chr6:70547921 | C | T | 54 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(51): Show |
54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.4229-8829C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70547921 | |||||||
| chr6:70548023 | G | T | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4229-8727G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70548023 | |||||||
| chr6:70548439 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4229-8311A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70548439 | |||||||
| chr6:70548442 | A | G | 1 | a0002c0006t0001g0138 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.4229-8308A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70548442 | |||||||
| chr6:70548520 | C | T | 1 | a0002c0003t0001g0049 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.4229-8230C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70548520 | |||||||
| chr6:70548538 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4229-8212T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70548538 | |||||||
| chr6:70548604 | A | G | 2 | a0001c0002t0002g0173 a0001c0002t0002g0174 |
2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.4229-8146A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70548604 | |||||||
| chr6:70548701 | A | T | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4229-8049A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70548701 | |||||||
| chr6:70548727 | GA | G | 67 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(64): Show |
67 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.4229-8020delA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70548727 | ||||||
| chr6:70549055 | A | G | 12 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0052 others(9): Show |
12 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.4229-7695A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70549055 | |||||||
| chr6:70549286 | C | T | 12 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(9): Show |
12 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.4229-7464C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70549286 | |||||||
| chr6:70549387 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4229-7363A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70549387 | |||||||
| chr6:70549432 | T | A | 1 | a0002c0003t0001g0043 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4229-7318T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70549432 | |||||||
| chr6:70549712 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4229-7038G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70549712 | |||||||
| chr6:70549730 | T | C | 1 | a0002c0003t0001g0134 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4229-7020T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70549730 | |||||||
| chr6:70549764 | A | C | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.4229-6986A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70549764 | |||||||
| chr6:70549800 | A | C | 1 | a0002c0006t0001g0136 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.4229-6950A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70549800 | |||||||
| chr6:70550554 | T | A | 67 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(64): Show |
67 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.4229-6196T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70550554 | |||||||
| chr6:70550578 | A | G | 1 | a0002c0003t0001g0117 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.4229-6172A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70550578 | |||||||
| chr6:70550717 | G | A | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4229-6033G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70550717 | |||||||
| chr6:70550759 | G | C | 27 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 others(24): Show |
27 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.4229-5991G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70550759 | |||||||
| chr6:70550761 | A | G | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4229-5989A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70550761 | |||||||
| chr6:70550863 | T | C | 1 | a0001c0004t0003g0011 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4229-5887T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70550863 | |||||||
| chr6:70550929 | C | T | 1 | a0002c0003t0001g0133 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4229-5821C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70550929 | |||||||
| chr6:70550931 | C | T | 1 | a0002c0003t0001g0133 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4229-5819C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70550931 | |||||||
| chr6:70550932 | T | A | 1 | a0002c0003t0001g0133 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4229-5818T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70550932 | |||||||
| chr6:70550933 | T | C | 1 | a0002c0003t0001g0133 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4229-5817T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70550933 | |||||||
| chr6:70550934 | T | A | 1 | a0002c0003t0001g0133 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4229-5816T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70550934 | |||||||
| chr6:70550940 | T | G | 1 | a0002c0003t0001g0133 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4229-5810T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70550940 | |||||||
| chr6:70550944 | G | T | 1 | a0002c0003t0001g0133 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4229-5806G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70550944 | |||||||
| chr6:70550945 | A | T | 1 | a0002c0003t0001g0133 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4229-5805A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70550945 | |||||||
| chr6:70551446 | A | C | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.4229-5304A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70551446 | |||||||
| chr6:70551497 | G | C | 1 | a0001c0001t0001g0146 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4229-5253G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70551497 | |||||||
| chr6:70551518 | G | C | 1 | a0001c0001t0001g0147 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4229-5232G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70551518 | |||||||
| chr6:70551701 | C | A | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4229-5049C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70551701 | |||||||
| chr6:70552033 | A | G | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4229-4717A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70552033 | |||||||
| chr6:70552073 | G | C | 1 | a0001c0001t0001g0157 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.4229-4677G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70552073 | |||||||
| chr6:70552218 | G | C | 1 | a0002c0006t0001g0137 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.4229-4532G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70552218 | |||||||
| chr6:70552290 | GCTTTATA others(6): Show |
G | 1 | a0001c0004t0003g0011 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4229-4433_4229-442 others(17): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70552290 | ||||||
| chr6:70552387 | C | T | 14 | a0001c0004t0003g0001 a0001c0004t0003g0230 a0001c0004t0003g0231 others(11): Show |
14 | HG01069.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.4229-4363C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70552387 | |||||||
| chr6:70552418 | G | A | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4229-4332G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70552418 | |||||||
| chr6:70552465 | C | CT | 8 | a0001c0001t0001g0064 a0001c0001t0001g0098 a0001c0001t0001g0102 others(5): Show |
8 | HG00673.hp1 HG01109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.4229-4264dupT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70552465 | ||||||
| chr6:70552465 | CT | C | 117 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(114): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.4229-4264delT | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70552465 | ||||||
| chr6:70552465 | CTT | C | 88 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(85): Show |
88 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.4229-4265_4229-426 others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70552465 | ||||||
| chr6:70552465 | CTTTTTTT others(6): Show |
C | 1 | a0002c0003t0001g0130 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.4229-4276_4229-426 others(17): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70552465 | ||||||
| chr6:70552491 | C | T | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4229-4259C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70552491 | |||||||
| chr6:70552555 | G | A | 1 | a0006c0007t0001g0127 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.4229-4195G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70552555 | |||||||
| chr6:70552571 | C | T | 2 | a0001c0009t0001g0211 a0001c0009t0001g0212 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4229-4179C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70552571 | |||||||
| chr6:70552759 | C | T | 1 | a0002c0003t0001g0113 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.4229-3991C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70552759 | |||||||
| chr6:70553155 | C | A | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4229-3595C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70553155 | |||||||
| chr6:70553193 | T | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0104 |
2 | HG03017.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.4229-3557T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70553193 | |||||||
| chr6:70553303 | G | A | 1 | a0001c0002t0002g0193 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.4229-3447G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70553303 | |||||||
| chr6:70553339 | A | G | 54 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(51): Show |
54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.4229-3411A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70553339 | |||||||
| chr6:70553695 | T | A | 11 | a0001c0004t0007g0265 a0001c0009t0001g0211 a0001c0009t0001g0212 others(8): Show |
11 | HG02109.hp1 HG02109.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.4229-3055T>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70553695 | |||||||
| chr6:70553695 | T | TTAAA | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.4229-3055_4229-305 others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70553695 | |||||||
| chr6:70553696 | A | T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4229-3054A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70553696 | |||||||
| chr6:70553700 | A | AAAAG | 65 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(62): Show |
65 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.4229-3050_4229-304 others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70553700 | |||||||
| chr6:70553700 | A | G | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.4229-3050A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70553700 | |||||||
| chr6:70553727 | C | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4229-3023C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70553727 | |||||||
| chr6:70553813 | C | T | 67 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(64): Show |
67 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.4229-2937C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70553813 | |||||||
| chr6:70553931 | C | A | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.4229-2819C>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70553931 | |||||||
| chr6:70554045 | G | A | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4229-2705G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70554045 | |||||||
| chr6:70554087 | G | A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0267 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4229-2663G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70554087 | |||||||
| chr6:70554146 | G | C | 2 | a0006c0007t0001g0127 a0006c0007t0001g0152 |
2 | NA18950.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.4229-2604G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70554146 | |||||||
| chr6:70554157 | C | T | 28 | a0001c0004t0003g0001 a0001c0004t0003g0009 a0001c0004t0003g0010 others(25): Show |
28 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.4229-2593C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70554157 | |||||||
| chr6:70554168 | G | A | 1 | a0002c0003t0001g0108 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.4229-2582G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70554168 | |||||||
| chr6:70554174 | AAAGT | A | 8 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(5): Show |
8 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.4229-2571_4229-256 others(8): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70554174 | ||||||
| chr6:70554299 | T | G | 1 | a0002c0003t0001g0123 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.4229-2451T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70554299 | |||||||
| chr6:70554458 | G | A | 1 | a0001c0002t0002g0266 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.4229-2292G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70554458 | |||||||
| chr6:70554590 | G | A | 4 | a0001c0004t0001g0160 a0001c0004t0001g0161 a0001c0004t0001g0162 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.4229-2160G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70554590 | |||||||
| chr6:70554631 | T | C | 5 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0142 others(2): Show |
5 | HG02258.hp1 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.4229-2119T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70554631 | |||||||
| chr6:70554667 | G | A | 54 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(51): Show |
54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.4229-2083G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70554667 | |||||||
| chr6:70554713 | C | T | 5 | a0001c0002t0002g0204 a0001c0002t0002g0205 a0001c0002t0002g0206 others(2): Show |
5 | HG02723.hp2 HG03540.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.4229-2037C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70554713 | |||||||
| chr6:70554740 | G | T | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.4229-2010G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70554740 | |||||||
| chr6:70554847 | G | A | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4229-1903G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70554847 | |||||||
| chr6:70554978 | G | A | 1 | a0002c0003t0001g0043 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4229-1772G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70554978 | |||||||
| chr6:70555028 | C | T | 1 | a0008c0017t0001g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4229-1722C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70555028 | |||||||
| chr6:70555043 | C | T | 5 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(2): Show |
5 | HG02615.hp1 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.4229-1707C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70555043 | |||||||
| chr6:70555331 | C | T | 1 | a0001c0004t0006g0019 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4229-1419C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70555331 | |||||||
| chr6:70555408 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.4229-1342T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70555408 | |||||||
| chr6:70555488 | G | A | 1 | a0001c0004t0003g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4229-1262G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70555488 | |||||||
| chr6:70555696 | G | C | 2 | a0005c0010t0003g0007 a0005c0010t0003g0008 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4229-1054G>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70555696 | |||||||
| chr6:70555728 | AG | A | 10 | a0003c0005t0001g0242 a0003c0005t0001g0243 a0003c0005t0001g0244 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4229-1014delG | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70555728 | ||||||
| chr6:70556000 | T | G | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4229-750T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70556000 | |||||||
| chr6:70556226 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4229-524G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70556226 | |||||||
| chr6:70556239 | A | T | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4229-511A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70556239 | |||||||
| chr6:70556349 | G | A | 1 | a0001c0002t0002g0253 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.4229-401G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70556349 | |||||||
| chr6:70556355 | T | C | 1 | a0002c0016t0002g0180 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.4229-395T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70556355 | |||||||
| chr6:70556519 | C | T | 7 | a0001c0002t0002g0223 a0001c0002t0002g0224 a0001c0002t0002g0225 others(4): Show |
7 | NA18947.hp2 NA18950.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.4229-231C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | chr6 | 70556519 | |||||||
| chr6:70556681 | TATG | T | 10 | a0001c0009t0001g0211 a0001c0009t0001g0212 a0003c0005t0001g0242 others(7): Show |
10 | HG02109.hp1 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4229-66_4229-64del others(3): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 70556681 | ||||||
| chr6:70556922 | T | G | 4 | a0002c0003t0001g0119 a0002c0003t0001g0124 a0002c0003t0001g0125 others(1): Show |
4 | HG01168.hp1 HG01358.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.4342+59T>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70556922 | |||||||
| chr6:70557275 | A | C | 54 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(51): Show |
54 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.4342+412A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70557275 | |||||||
| chr6:70557379 | C | G | 1 | a0002c0003t0001g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4342+516C>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70557379 | |||||||
| chr6:70557551 | G | A | 8 | a0001c0004t0003g0010 a0001c0004t0003g0011 a0001c0004t0003g0012 others(5): Show |
8 | HG02559.hp1 HG02572.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.4342+688G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70557551 | |||||||
| chr6:70557601 | C | T | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4342+738C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70557601 | |||||||
| chr6:70557626 | A | G | 117 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(114): Show |
117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.4342+763A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70557626 | |||||||
| chr6:70557694 | C | CA | 63 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0026 others(60): Show |
63 | HG00642.hp1 HG00673.hp1 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.4342+855dupA | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr6 | 70557694 | ||||||
| chr6:70557694 | C | CAA | 69 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(66): Show |
69 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.4342+854_4342+855d others(4): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr6 | 70557694 | ||||||
| chr6:70557694 | C | CAAA | 31 | a0001c0002t0002g0172 a0001c0002t0002g0175 a0001c0002t0002g0176 others(28): Show |
31 | HG00280.hp1 HG00621.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.4342+853_4342+855d others(5): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr6 | 70557694 | ||||||
| chr6:70557694 | C | CAAAA | 6 | a0001c0002t0002g0199 a0001c0002t0002g0258 a0001c0002t0002g0259 others(3): Show |
6 | HG00642.hp2 HG01243.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.4342+852_4342+855d others(6): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr6 | 70557694 | ||||||
| chr6:70557702 | A | C | 6 | a0001c0001t0001g0036 a0001c0001t0001g0090 a0001c0001t0001g0093 others(3): Show |
6 | HG02027.hp2 NA18966.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.4342+839A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70557702 | |||||||
| chr6:70557707 | A | C | 1 | a0001c0001t0001g0089 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.4342+844A>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70557707 | |||||||
| chr6:70557812 | G | A | 1 | a0002c0003t0001g0134 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4342+949G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70557812 | |||||||
| chr6:70557863 | G | A | 117 | a0001c0001t0001g0210 a0001c0001t0001g0267 a0001c0002t0002g0167 others(114): Show |
117 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.4342+1000G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70557863 | |||||||
| chr6:70557963 | G | A | 13 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0255 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.4342+1100G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70557963 | |||||||
| chr6:70557972 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4342+1109A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70557972 | |||||||
| chr6:70558066 | A | G | 78 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(75): Show |
78 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.4342+1203A>G | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70558066 | |||||||
| chr6:70558536 | G | A | 12 | a0001c0004t0003g0009 a0001c0004t0003g0010 a0001c0004t0003g0011 others(9): Show |
12 | HG01074.hp2 HG01346.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.4343-1180G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70558536 | |||||||
| chr6:70558708 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0055 |
2 | HG02015.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.4343-1008C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70558708 | |||||||
| chr6:70558710 | T | C | 78 | a0001c0002t0002g0167 a0001c0002t0002g0168 a0001c0002t0002g0169 others(75): Show |
78 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.4343-1006T>C | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70558710 | |||||||
| chr6:70558778 | C | T | 2 | a0001c0004t0003g0016 a0001c0004t0003g0017 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4343-938C>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70558778 | |||||||
| chr6:70559138 | G | A | 30 | a0001c0004t0003g0001 a0001c0004t0003g0009 a0001c0004t0003g0010 others(27): Show |
30 | HG01069.hp1 HG01074.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.4343-578G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70559138 | |||||||
| chr6:70559212 | G | A | 8 | a0001c0002t0002g0221 a0001c0002t0002g0223 a0001c0002t0002g0224 others(5): Show |
8 | NA18947.hp2 NA18950.hp2 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.4343-504G>A | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70559212 | |||||||
| chr6:70559260 | G | T | 1 | a0001c0004t0007g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4343-456G>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70559260 | |||||||
| chr6:70559452 | A | T | 1 | a0002c0016t0002g0180 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.4343-264A>T | FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 21/21 | chr6 | 70559452 |