Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57533 |
| ensemblid | ENSG00000132405.19 |
| hgncid | 29246 |
| symbol | TBC1D14 |
| name | TBC1 domain family member 14 |
| refseq_nuc | NM_020773.3 |
| refseq_prot | NP_065824.2 |
| ensembl_nuc | ENST00000409757.9 |
| ensembl_prot | ENSP00000386921.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 6909826 |
| end | 7033114 |
| strand | + |
| ver | v1.2 |
| region | chr4:6909826-7033114 |
| region5000 | chr4:6904826-7038114 |
| regionname0 | TBC1D14_chr4_6909826_7033114 |
| regionname5000 | TBC1D14_chr4_6904826_7038114 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 693 | 284 | 93 | 54 | 101 | 9 | 25 | 81 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | MTDGK others(688): Show |
chr4 | 6904826 | 7038114 |
| a0002 | 0/0 | 693 | 17 | 2 | 6 | 1 | 1 | 7 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | MTDGK others(688): Show |
chr4 | 6904826 | 7038114 |
| a0003 | 0/0 | 693 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | MTDGK others(688): Show |
chr4 | 6904826 | 7038114 |
| a0004 | 0/0 | 693 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | MTDRK others(688): Show |
chr4 | 6904826 | 7038114 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2079 | 271 | 83 | 54 | 98 | 9 | 25 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ATGAC others(2074): Show |
chr4 | 6904826 | 7038114 | ||
| a0001c0003 | 0/0 | 2079 | 6 | 6 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ATGAC others(2074): Show |
chr4 | 6904826 | 7038114 | ||
| a0001c0006 | 0/0 | 2079 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ATGAC others(2074): Show |
chr4 | 6904826 | 7038114 | ||
| a0001c0007 | 0/0 | 2079 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ATGAC others(2074): Show |
chr4 | 6904826 | 7038114 | ||
| a0001c0008 | 0/0 | 2079 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ATGAC others(2074): Show |
chr4 | 6904826 | 7038114 | ||
| a0001c0009 | 0/0 | 2079 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ATGAC others(2074): Show |
chr4 | 6904826 | 7038114 | ||
| a0001c0010 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ATGAC others(2074): Show |
chr4 | 6904826 | 7038114 | ||
| a0001c0011 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ATGAC others(2074): Show |
chr4 | 6904826 | 7038114 | ||
| a0001c0012 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ATGAC others(2074): Show |
chr4 | 6904826 | 7038114 | ||
| a0002c0002 | 0/0 | 2079 | 16 | 2 | 5 | 1 | 1 | 7 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ATGAC others(2074): Show |
chr4 | 6904826 | 7038114 | ||
| a0002c0013 | 0/0 | 2079 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ATGAC others(2074): Show |
chr4 | 6904826 | 7038114 | ||
| a0003c0004 | 0/0 | 2079 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ATGAC others(2074): Show |
chr4 | 6904826 | 7038114 | ||
| a0004c0005 | 0/0 | 2079 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ATGAC others(2074): Show |
chr4 | 6904826 | 7038114 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4947 | 98 | 14 | 20 | 48 | 3 | 12 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0001t0002 | 0/0 | 4947 | 85 | 19 | 19 | 34 | 3 | 10 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0001t0003 | 0/0 | 4947 | 30 | 23 | 4 | 0 | 3 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0001t0004 | 1/0 | 4947 | 2 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0001t0005 | 0/0 | 4947 | 12 | 11 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0001t0006 | 0/0 | 4947 | 6 | 0 | 3 | 3 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0001t0007 | 0/0 | 4947 | 6 | 0 | 0 | 6 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0001t0008 | 0/0 | 4947 | 5 | 4 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0001t0009 | 0/0 | 4947 | 3 | 1 | 0 | 0 | 0 | 2 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0001t0011 | 0/0 | 4947 | 3 | 2 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0001t0012 | 0/0 | 4947 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0001t0013 | 0/0 | 4947 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0001t0014 | 0/0 | 4947 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0001t0016 | 0/0 | 4947 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0001t0017 | 0/0 | 4947 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0001t0018 | 0/0 | 4947 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0001t0019 | 0/0 | 4947 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0001t0020 | 0/0 | 4947 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0001t0021 | 0/0 | 4947 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0001t0022 | 0/0 | 4947 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0001t0023 | 0/0 | 4947 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0001t0024 | 0/0 | 4947 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0001t0025 | 0/0 | 4947 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0001t0026 | 0/0 | 4947 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0001t0027 | 0/0 | 4947 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0001t0028 | 0/0 | 4947 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0001t0029 | 0/0 | 4947 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0001t0030 | 0/0 | 4947 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0001t0031 | 0/0 | 4947 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0003t0001 | 0/0 | 4947 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0003t0002 | 0/0 | 4947 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0003t0003 | 0/0 | 4947 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0006t0001 | 0/0 | 4947 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0007t0002 | 0/0 | 4947 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0008t0003 | 0/0 | 4947 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0009t0001 | 0/0 | 4947 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0010t0002 | 0/0 | 4947 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0011t0002 | 0/0 | 4947 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0001c0012t0001 | 0/0 | 4947 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0002c0002t0002 | 0/0 | 4947 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0002c0002t0004 | 0/0 | 4947 | 11 | 2 | 4 | 0 | 1 | 4 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0002c0002t0010 | 0/0 | 4947 | 3 | 0 | 1 | 1 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0002c0002t0015 | 0/0 | 4947 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0002c0013t0004 | 0/0 | 4947 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0003c0004t0002 | 0/0 | 4947 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| a0004c0005t0005 | 0/0 | 4947 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | ACCTG others(4942): Show |
chr4 | 6904826 | 7038114 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0184 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0004g0038 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0006g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0006g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0006g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0006g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0006g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0006g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0007g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0007g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0007g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0007g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0007g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0007g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0008g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0008g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0008g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0008g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0008g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0009g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0009g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0009g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0011g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0011g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0011g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0012g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0012g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0013g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0013g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0014g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0016g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0017g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0018g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0019g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0020g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0021g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0022g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0023g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0024g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0025g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0026g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0027g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0028g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0029g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0030g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0001t0031g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0003t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0003t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0003t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0003t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0003t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0003t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0006t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0007t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0008t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0009t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0010t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0011t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0001c0012t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0002c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0002c0002t0004g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0002c0002t0004g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0002c0002t0004g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0002c0002t0004g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0002c0002t0004g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0002c0002t0004g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0002c0002t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0002c0002t0004g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0002c0002t0004g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0002c0002t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0002c0002t0004g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0002c0002t0010g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0002c0002t0010g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0002c0002t0010g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0002c0002t0015g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0002c0013t0004g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0003c0004t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0003c0004t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| a0004c0005t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0059 | EUR | FIN | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0292 | EUR | FIN | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0263 | EUR | FIN | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0001 | EUR | FIN | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | CHS | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | CHS | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG00438 | hp2 | a0001 | c0001 | t0013 | g0258 | EAS | CHS | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG00558 | hp2 | a0003 | c0004 | t0002 | g0164 | EAS | CHS | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG00609 | hp2 | a0001 | c0001 | t0007 | g0200 | EAS | CHS | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG00642 | hp1 | a0001 | c0001 | t0028 | g0161 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0086 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | CHS | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG00733 | hp1 | a0001 | c0001 | t0019 | g0288 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG00741 | hp2 | a0001 | c0001 | t0024 | g0123 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0190 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01109 | hp1 | a0001 | c0001 | t0008 | g0101 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01192 | hp1 | a0001 | c0001 | t0006 | g0171 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01255 | hp1 | a0001 | c0001 | t0023 | g0097 | AMR | CLM | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01255 | hp2 | a0001 | c0001 | t0011 | g0039 | AMR | CLM | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01258 | hp1 | a0001 | c0001 | t0031 | g0082 | AMR | CLM | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01258 | hp2 | a0001 | c0001 | t0030 | g0158 | AMR | CLM | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | CLM | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01346 | hp1 | a0002 | c0002 | t0010 | g0022 | AMR | CLM | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | CLM | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01361 | hp1 | a0002 | c0002 | t0004 | g0019 | AMR | CLM | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | CLM | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0293 | AMR | CLM | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0078 | EUR | IBS | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | IBS | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | IBS | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0199 | EUR | IBS | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0065 | AFR | ACB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | ACB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0235 | AFR | ACB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | ACB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | PEL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01934 | hp2 | a0001 | c0001 | t0006 | g0224 | AMR | PEL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | PEL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01975 | hp2 | a0002 | c0013 | t0004 | g0014 | AMR | PEL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01978 | hp1 | a0001 | c0001 | t0006 | g0170 | AMR | PEL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0069 | AMR | PEL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PEL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02004 | hp1 | a0002 | c0002 | t0004 | g0013 | AMR | PEL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02040 | hp2 | a0001 | c0001 | t0014 | g0157 | EAS | KHV | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02055 | hp1 | a0002 | c0002 | t0004 | g0030 | AFR | ACB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02055 | hp2 | a0001 | c0009 | t0001 | g0016 | AFR | ACB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | KHV | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | KHV | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02129 | hp2 | a0001 | c0001 | t0017 | g0195 | EAS | KHV | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | KHV | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02135 | hp2 | a0002 | c0002 | t0010 | g0021 | EAS | KHV | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0301 | AFR | ACB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0073 | AFR | ACB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | PEL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02257 | hp1 | a0001 | c0001 | t0012 | g0133 | AFR | ACB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0037 | AFR | ACB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02258 | hp1 | a0001 | c0001 | t0029 | g0176 | AFR | ACB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02258 | hp2 | a0001 | c0001 | t0011 | g0041 | AFR | ACB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0236 | AFR | ACB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0063 | AFR | ACB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02293 | hp2 | a0002 | c0002 | t0004 | g0012 | AMR | PEL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0071 | AFR | ACB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0273 | AFR | ACB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02572 | hp2 | a0001 | c0006 | t0001 | g0045 | AFR | GWD | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | GWD | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0276 | AFR | GWD | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0100 | AFR | GWD | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0079 | AFR | GWD | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0216 | AFR | GWD | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | GWD | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02647 | hp1 | a0001 | c0003 | t0003 | g0032 | AFR | GWD | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0066 | AFR | GWD | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02683 | hp1 | a0002 | c0002 | t0010 | g0023 | SAS | PJL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0067 | AFR | GWD | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0268 | AFR | GWD | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02723 | hp1 | a0001 | c0003 | t0002 | g0034 | AFR | GWD | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02723 | hp2 | a0001 | c0001 | t0008 | g0115 | AFR | GWD | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02735 | hp2 | a0002 | c0002 | t0015 | g0247 | SAS | PJL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02738 | hp1 | a0002 | c0002 | t0004 | g0015 | SAS | PJL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | GWD | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | GWD | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | GWD | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0250 | AFR | GWD | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02886 | hp1 | a0001 | c0001 | t0018 | g0047 | AFR | GWD | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02886 | hp2 | a0001 | c0001 | t0011 | g0040 | AFR | GWD | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0137 | AFR | GWD | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0139 | AFR | GWD | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0070 | AFR | ESN | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0249 | AFR | ESN | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0131 | AFR | ESN | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | ESN | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ESN | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02970 | hp2 | a0001 | c0001 | t0027 | g0213 | AFR | ESN | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0053 | AFR | ESN | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0076 | AFR | ESN | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0056 | AFR | MSL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03098 | hp2 | a0001 | c0001 | t0012 | g0132 | AFR | MSL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0298 | AFR | ESN | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03139 | hp2 | a0001 | c0001 | t0020 | g0265 | AFR | ESN | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | ESN | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0060 | AFR | MSL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0271 | AFR | MSL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | MSL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03453 | hp2 | a0004 | c0005 | t0005 | g0269 | AFR | MSL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0072 | AFR | MSL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0270 | AFR | MSL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0181 | SAS | PJL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ESN | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03516 | hp2 | a0001 | c0003 | t0003 | g0267 | AFR | ESN | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03540 | hp1 | a0001 | c0003 | t0003 | g0033 | AFR | GWD | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03540 | hp2 | a0001 | c0001 | t0009 | g0003 | AFR | GWD | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03579 | hp2 | a0001 | c0003 | t0003 | g0300 | AFR | MSL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03654 | hp1 | a0002 | c0002 | t0004 | g0017 | SAS | PJL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0188 | SAS | PJL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03669 | hp2 | a0002 | c0002 | t0004 | g0299 | SAS | PJL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0143 | SAS | PJL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0020 | SAS | PJL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | BEB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | BEB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03942 | hp1 | a0001 | c0001 | t0009 | g0004 | SAS | BEB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | BEB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG04115 | hp1 | a0001 | c0001 | t0016 | g0205 | SAS | STU | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0155 | SAS | STU | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG04184 | hp1 | a0001 | c0001 | t0009 | g0242 | SAS | BEB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0173 | SAS | BEB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | STU | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG04199 | hp2 | a0002 | c0002 | t0004 | g0025 | SAS | STU | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0152 | SAS | STU | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | STU | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | YRI | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | YRI | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | CHB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18747 | hp2 | a0001 | c0001 | t0007 | g0212 | EAS | CHB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18940 | hp2 | a0001 | c0001 | t0007 | g0194 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18952 | hp2 | a0001 | c0001 | t0006 | g0168 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18957 | hp2 | a0003 | c0004 | t0002 | g0163 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18973 | hp1 | a0001 | c0001 | t0005 | g0103 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18975 | hp2 | a0001 | c0001 | t0006 | g0169 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18981 | hp1 | a0001 | c0001 | t0007 | g0146 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18981 | hp2 | a0001 | c0001 | t0013 | g0256 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18985 | hp1 | a0001 | c0001 | t0006 | g0243 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18995 | hp1 | a0001 | c0012 | t0001 | g0275 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18995 | hp2 | a0001 | c0011 | t0002 | g0206 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19000 | hp2 | a0001 | c0001 | t0007 | g0210 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19030 | hp1 | a0001 | c0001 | t0008 | g0061 | AFR | LWK | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | LWK | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | LWK | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | LWK | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19054 | hp1 | a0001 | c0001 | t0007 | g0211 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19064 | hp1 | a0001 | c0001 | t0026 | g0117 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19079 | hp1 | a0001 | c0010 | t0002 | g0036 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19085 | hp1 | a0001 | c0001 | t0021 | g0234 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | YRI | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0050 | AFR | YRI | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | ASW | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ASW | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA20805 | hp1 | a0002 | c0002 | t0004 | g0026 | EUR | TSI | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0260 | EUR | TSI | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | GIH | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0294 | SAS | GIH | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01123 | hp1 | a0002 | c0002 | t0004 | g0018 | AMR | CLM | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | ACB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0272 | AFR | ACB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0246 | AFR | ACB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02486 | hp2 | a0001 | c0001 | t0025 | g0093 | AFR | ACB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | ACB | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | MSL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG03471 | hp2 | a0001 | c0001 | t0022 | g0114 | AFR | MSL | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | USA | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0262 | AFR | USA | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA20300 | hp1 | a0001 | c0007 | t0002 | g0002 | AFR | USA | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0295 | AFR | USA | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA21309 | hp1 | a0002 | c0002 | t0004 | g0024 | AFR | LWK | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| NA21309 | hp2 | a0001 | c0008 | t0003 | g0042 | AFR | LWK | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0184 | REF | REF | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0038 | REF | REF | TBC1D14_chr4_6904826_7038114 | TBC1D14 | chr4 | 6904826 | 7038114 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:6923399 | G | A | 1 | a0004 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.10G>A | p.Gly4Arg | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/14 | 153/4947 | 10/2082 | 4/693 | chr4 | 6923399 | |||
| chr4:6923510 | C | G | 1 | a0002 | 17 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(14): Show |
missense_variant | MODERATE | c.121C>G | p.Leu41Val | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/14 | 264/4947 | 121/2082 | 41/693 | chr4 | 6923510 | |||
| chr4:6924063 | A | T | 1 | a0003 | 2 | HG00558.hp2 NA18957.hp2 |
missense_variant | MODERATE | c.674A>T | p.Glu225Val | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/14 | 817/4947 | 674/2082 | 225/693 | chr4 | 6924063 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:6923617 | G | A | 1 | a0001c0006 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.228G>A | p.Pro76Pro | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/14 | 371/4947 | 228/2082 | 76/693 | chr4 | 6923617 | |||
| chr4:6923644 | C | T | 1 | a0001c0003 | 6 | HG02647.hp1 HG02723.hp1 HG02965.hp1 others(3): Show |
synonymous_variant | LOW | c.255C>T | p.His85His | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/14 | 398/4947 | 255/2082 | 85/693 | chr4 | 6923644 | |||
| chr4:6923662 | C | G | 1 | a0001c0012 | 1 | NA18995.hp1 | synonymous_variant | LOW | c.273C>G | p.Ser91Ser | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/14 | 416/4947 | 273/2082 | 91/693 | chr4 | 6923662 | |||
| chr4:6923818 | G | A | 1 | a0001c0007 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.429G>A | p.Pro143Pro | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/14 | 572/4947 | 429/2082 | 143/693 | chr4 | 6923818 | |||
| chr4:6923974 | C | T | 1 | a0003c0004 | 2 | HG00558.hp2 NA18957.hp2 |
synonymous_variant | LOW | c.585C>T | p.Asp195Asp | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/14 | 728/4947 | 585/2082 | 195/693 | chr4 | 6923974 | |||
| chr4:6999155 | C | T | 1 | a0001c0011 | 1 | NA18995.hp2 | synonymous_variant | LOW | c.1116C>T | p.Asn372Asn | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 6/14 | 1259/4947 | 1116/2082 | 372/693 | chr4 | 6999155 | |||
| chr4:7009906 | T | C | 1 | a0002c0013 | 1 | HG01975.hp2 | synonymous_variant | LOW | c.1476T>C | p.Ser492Ser | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 10/14 | 1619/4947 | 1476/2082 | 492/693 | chr4 | 7009906 | |||
| chr4:7014534 | T | C | 1 | a0001c0008 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.1734T>C | p.Thr578Thr | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/14 | 1877/4947 | 1734/2082 | 578/693 | chr4 | 7014534 | |||
| chr4:7025196 | C | T | 1 | a0001c0010 | 1 | NA19079.hp1 | synonymous_variant | LOW | c.1950C>T | p.Pro650Pro | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/14 | 2093/4947 | 1950/2082 | 650/693 | chr4 | 7025196 | |||
| chr4:7030377 | G | A | 1 | a0001c0009 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.2067G>A | p.Pro689Pro | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 14/14 | 2210/4947 | 2067/2082 | 689/693 | chr4 | 7030377 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:6909860 | C | T | 1 | a0001c0001t0031 | 1 | HG01258.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-109C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/14 | chr4 | 6909860 | |||||||
| chr4:6909869 | C | G | 1 | a0001c0001t0030 | 1 | HG01258.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-100C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/14 | chr4 | 6909869 | |||||||
| chr4:6909933 | C | T | 1 | a0001c0001t0029 | 1 | HG02258.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-36C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/14 | chr4 | 6909933 | |||||||
| chr4:6909938 | C | T | 1 | a0001c0001t0028 | 1 | HG00642.hp1 | 5_prime_UTR_variant | MODIFIER | c.-31C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/14 | 13452 | chr4 | 6909938 | ||||||
| chr4:7030453 | G | A | 4 | a0001c0001t0003 a0001c0001t0009 a0001c0003t0003 others(1): Show |
38 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*61G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 14/14 | 61 | chr4 | 7030453 | ||||||
| chr4:7030704 | A | C | 1 | a0001c0001t0027 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*312A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 14/14 | 312 | chr4 | 7030704 | ||||||
| chr4:7031022 | C | A | 1 | a0002c0002t0010 | 3 | HG01346.hp1 HG02135.hp2 HG02683.hp1 |
3_prime_UTR_variant | MODIFIER | c.*630C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 14/14 | 630 | chr4 | 7031022 | ||||||
| chr4:7031197 | A | T | 17 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0012 others(14): Show |
119 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*805A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 14/14 | 805 | chr4 | 7031197 | ||||||
| chr4:7031238 | C | T | 1 | a0001c0001t0018 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*846C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 14/14 | 846 | chr4 | 7031238 | ||||||
| chr4:7031246 | T | G | 1 | a0001c0001t0019 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*854T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 14/14 | 854 | chr4 | 7031246 | ||||||
| chr4:7031355 | C | G | 1 | a0001c0001t0026 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*963C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 14/14 | 963 | chr4 | 7031355 | ||||||
| chr4:7031458 | A | G | 1 | a0001c0001t0025 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1066A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 14/14 | 1066 | chr4 | 7031458 | ||||||
| chr4:7031476 | A | G | 2 | a0001c0001t0008 a0001c0001t0024 |
6 | HG00741.hp2 HG01109.hp1 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1084A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 14/14 | 1084 | chr4 | 7031476 | ||||||
| chr4:7031625 | G | T | 1 | a0001c0001t0017 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1233G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 14/14 | 1233 | chr4 | 7031625 | ||||||
| chr4:7031668 | G | A | 1 | a0001c0001t0014 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1276G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 14/14 | 1276 | chr4 | 7031668 | ||||||
| chr4:7031709 | C | T | 1 | a0001c0001t0013 | 2 | HG00438.hp2 NA18981.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1317C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 14/14 | 1317 | chr4 | 7031709 | ||||||
| chr4:7031936 | G | A | 1 | a0001c0001t0020 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1544G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 14/14 | 1544 | chr4 | 7031936 | ||||||
| chr4:7031944 | C | T | 17 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(14): Show |
114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*1552C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 14/14 | 1552 | chr4 | 7031944 | ||||||
| chr4:7032086 | G | A | 1 | a0001c0001t0024 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1694G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 14/14 | 1694 | chr4 | 7032086 | ||||||
| chr4:7032248 | C | T | 2 | a0001c0001t0016 a0002c0002t0015 |
2 | HG02735.hp2 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1856C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 14/14 | 1856 | chr4 | 7032248 | ||||||
| chr4:7032301 | T | A | 40 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(37): Show |
284 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(281): Show |
3_prime_UTR_variant | MODIFIER | c.*1909T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 14/14 | 1909 | chr4 | 7032301 | ||||||
| chr4:7032411 | G | C | 1 | a0001c0001t0011 | 3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2019G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 14/14 | 2019 | chr4 | 7032411 | ||||||
| chr4:7032454 | C | T | 1 | a0001c0001t0027 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2062C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 14/14 | 2062 | chr4 | 7032454 | ||||||
| chr4:7032523 | A | T | 1 | a0001c0001t0007 | 6 | HG00609.hp2 NA18747.hp2 NA18940.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2131A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 14/14 | 2131 | chr4 | 7032523 | ||||||
| chr4:7032555 | A | G | 1 | a0001c0001t0012 | 2 | HG02257.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2163A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 14/14 | 2163 | chr4 | 7032555 | ||||||
| chr4:7032904 | G | A | 1 | a0001c0001t0021 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2512G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 14/14 | 2512 | chr4 | 7032904 | ||||||
| chr4:7032949 | A | G | 1 | a0001c0001t0022 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2557A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 14/14 | 2557 | chr4 | 7032949 | ||||||
| chr4:7033007 | G | A | 1 | a0001c0001t0006 | 6 | HG01192.hp1 HG01934.hp2 HG01978.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2615G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 14/14 | 2615 | chr4 | 7033007 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:6910028 | A | G | 2 | a0001c0001t0001g0302 a0001c0001t0001g0303 |
2 | NA19010.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.-18+77A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6910028 | |||||||
| chr4:6910085 | G | A | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-18+134G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6910085 | |||||||
| chr4:6910155 | C | T | 2 | a0001c0001t0003g0301 a0001c0003t0003g0300 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-18+204C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6910155 | |||||||
| chr4:6910219 | C | G | 1 | a0002c0002t0004g0299 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-18+268C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6910219 | |||||||
| chr4:6910320 | C | T | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0002g0295 others(1): Show |
4 | HG00741.hp1 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+369C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6910320 | |||||||
| chr4:6910733 | C | T | 1 | a0001c0001t0002g0294 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-18+782C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6910733 | |||||||
| chr4:6910739 | G | A | 2 | a0001c0001t0009g0003 a0001c0001t0009g0004 |
2 | HG03540.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-18+788G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6910739 | |||||||
| chr4:6910742 | G | T | 2 | a0001c0001t0002g0292 a0001c0001t0002g0293 |
2 | HG00280.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-18+791G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6910742 | |||||||
| chr4:6910847 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-18+896G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6910847 | |||||||
| chr4:6910863 | G | T | 1 | a0001c0001t0001g0291 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-18+912G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6910863 | |||||||
| chr4:6911107 | G | T | 2 | a0001c0001t0009g0003 a0001c0001t0009g0004 |
2 | HG03540.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-18+1156G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6911107 | |||||||
| chr4:6911255 | A | G | 1 | a0001c0001t0001g0290 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-18+1304A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6911255 | |||||||
| chr4:6911469 | T | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0007 |
2 | HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-18+1518T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6911469 | |||||||
| chr4:6911594 | G | A | 1 | a0001c0001t0005g0008 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-18+1643G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6911594 | |||||||
| chr4:6911722 | T | C | 29 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(26): Show |
29 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(26): Show |
intron_variant | MODIFIER | c.-18+1771T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6911722 | |||||||
| chr4:6911844 | G | A | 22 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(19): Show |
22 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.-18+1893G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6911844 | |||||||
| chr4:6911959 | T | A | 2 | a0001c0001t0001g0035 a0001c0010t0002g0036 |
2 | NA19012.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-18+2008T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6911959 | |||||||
| chr4:6911972 | A | G | 45 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0248 others(42): Show |
45 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.-18+2021A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6911972 | |||||||
| chr4:6911980 | A | G | 119 | a0001c0001t0001g0035 a0001c0001t0001g0148 a0001c0001t0001g0150 others(116): Show |
119 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.-18+2029A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6911980 | |||||||
| chr4:6912013 | C | G | 300 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(297): Show |
301 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.-18+2062C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6912013 | |||||||
| chr4:6912281 | G | A | 4 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 others(1): Show |
4 | HG01255.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+2330G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6912281 | |||||||
| chr4:6912295 | G | A | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-18+2344G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6912295 | |||||||
| chr4:6912315 | G | A | 2 | a0001c0001t0002g0142 a0001c0001t0002g0143 |
2 | HG03704.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-18+2364G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6912315 | |||||||
| chr4:6912374 | G | C | 2 | a0001c0001t0003g0044 a0001c0006t0001g0045 |
2 | HG02572.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-18+2423G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6912374 | |||||||
| chr4:6912406 | A | T | 1 | a0001c0001t0001g0141 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-18+2455A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6912406 | |||||||
| chr4:6912412 | A | C | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-18+2461A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6912412 | |||||||
| chr4:6912412 | AT | A | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0002g0295 others(1): Show |
4 | HG00741.hp1 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+2462delT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6912412 | |||||||
| chr4:6912601 | G | T | 1 | a0001c0001t0001g0289 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-18+2650G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6912601 | |||||||
| chr4:6912608 | T | C | 1 | a0001c0001t0003g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-18+2657T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6912608 | |||||||
| chr4:6912645 | C | T | 1 | a0001c0001t0019g0288 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-18+2694C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6912645 | |||||||
| chr4:6912822 | C | T | 1 | a0002c0002t0015g0247 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-18+2871C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6912822 | |||||||
| chr4:6912877 | C | G | 1 | a0001c0001t0001g0287 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-18+2926C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6912877 | |||||||
| chr4:6913018 | C | T | 4 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(1): Show |
4 | HG01975.hp1 HG02683.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+3067C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6913018 | |||||||
| chr4:6913019 | G | A | 1 | a0001c0001t0002g0144 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-18+3068G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6913019 | |||||||
| chr4:6913037 | A | G | 11 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(8): Show |
11 | HG00558.hp1 HG00673.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18+3086A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6913037 | |||||||
| chr4:6913061 | T | C | 1 | a0001c0001t0002g0145 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-18+3110T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6913061 | |||||||
| chr4:6913313 | T | C | 1 | a0001c0001t0007g0146 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-18+3362T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6913313 | |||||||
| chr4:6913338 | T | C | 1 | a0001c0001t0003g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-18+3387T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6913338 | |||||||
| chr4:6913566 | C | G | 1 | a0001c0001t0002g0246 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-18+3615C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6913566 | |||||||
| chr4:6913615 | A | G | 29 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(26): Show |
29 | HG00639.hp2 HG01123.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.-18+3664A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6913615 | |||||||
| chr4:6913624 | C | A | 1 | a0001c0001t0002g0147 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-18+3673C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6913624 | |||||||
| chr4:6913995 | G | T | 44 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0251 others(41): Show |
44 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.-18+4044G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6913995 | |||||||
| chr4:6914105 | ACTGCAGC others(17): Show |
A | 1 | a0001c0001t0003g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-18+4156_-18+4179d others(26): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 6914105 | ||||||
| chr4:6914135 | C | CAA | 112 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(109): Show |
112 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.-18+4198_-18+4199d others(4): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 6914135 | ||||||
| chr4:6914135 | C | CAAA | 34 | a0001c0001t0001g0035 a0001c0001t0001g0148 a0001c0001t0001g0150 others(31): Show |
34 | HG00558.hp2 HG00642.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18+4197_-18+4199d others(5): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 6914135 | ||||||
| chr4:6914270 | C | T | 1 | a0001c0001t0002g0241 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-18+4319C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6914270 | |||||||
| chr4:6914437 | A | G | 1 | a0001c0001t0002g0174 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-18+4486A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6914437 | |||||||
| chr4:6914498 | G | C | 1 | a0001c0001t0003g0049 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-18+4547G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6914498 | |||||||
| chr4:6914502 | A | T | 2 | a0001c0001t0002g0239 a0001c0001t0002g0240 |
2 | HG00738.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-18+4551A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6914502 | |||||||
| chr4:6914536 | G | A | 163 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(160): Show |
164 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.-18+4585G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6914536 | |||||||
| chr4:6914589 | C | A | 1 | a0001c0001t0029g0176 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-18+4638C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6914589 | |||||||
| chr4:6914671 | C | G | 1 | a0001c0001t0001g0130 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-18+4720C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6914671 | |||||||
| chr4:6914680 | C | T | 1 | a0001c0001t0002g0238 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-18+4729C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6914680 | |||||||
| chr4:6914696 | G | C | 4 | a0001c0001t0002g0175 a0001c0001t0002g0177 a0001c0001t0002g0178 others(1): Show |
4 | HG00408.hp2 NA18942.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+4745G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6914696 | |||||||
| chr4:6914708 | C | T | 1 | a0001c0001t0009g0004 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-18+4757C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6914708 | |||||||
| chr4:6914725 | C | G | 2 | a0001c0001t0005g0043 a0001c0008t0003g0042 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-18+4774C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6914725 | |||||||
| chr4:6914744 | A | G | 1 | a0001c0001t0002g0246 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-18+4793A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6914744 | |||||||
| chr4:6914851 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-18+4900C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6914851 | |||||||
| chr4:6915018 | G | A | 2 | a0001c0001t0002g0295 a0001c0001t0004g0050 |
2 | NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-18+5067G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6915018 | |||||||
| chr4:6915359 | T | G | 147 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(144): Show |
147 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.-18+5408T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6915359 | |||||||
| chr4:6915537 | C | T | 14 | a0001c0009t0001g0016 a0002c0002t0002g0020 a0002c0002t0004g0015 others(11): Show |
14 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.-18+5586C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6915537 | |||||||
| chr4:6915538 | G | A | 1 | a0001c0001t0002g0180 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-18+5587G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6915538 | |||||||
| chr4:6915573 | G | A | 9 | a0001c0001t0005g0053 a0001c0001t0005g0139 a0001c0001t0005g0268 others(6): Show |
9 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18+5622G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6915573 | |||||||
| chr4:6915779 | C | T | 7 | a0001c0001t0001g0230 a0001c0001t0001g0233 a0001c0001t0002g0145 others(4): Show |
7 | HG01981.hp2 HG02148.hp1 NA18984.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+5828C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6915779 | |||||||
| chr4:6915784 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG01433.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.-18+5833G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6915784 | |||||||
| chr4:6915821 | G | A | 1 | a0001c0001t0004g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-18+5870G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6915821 | |||||||
| chr4:6915932 | T | A | 4 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 others(1): Show |
4 | HG03540.hp2 HG03942.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+5981T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6915932 | |||||||
| chr4:6915952 | T | TA | 9 | a0001c0001t0001g0289 a0001c0001t0001g0296 a0001c0001t0001g0297 others(6): Show |
9 | HG00741.hp1 HG01255.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18+6016dupA | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 6915952 | ||||||
| chr4:6915952 | TA | T | 14 | a0001c0009t0001g0016 a0002c0002t0002g0020 a0002c0002t0004g0015 others(11): Show |
14 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.-18+6016delA | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 6915952 | ||||||
| chr4:6916019 | G | A | 2 | a0001c0001t0002g0295 a0001c0001t0004g0050 |
2 | NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-18+6068G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6916019 | |||||||
| chr4:6916075 | G | A | 1 | a0001c0001t0001g0274 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-18+6124G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6916075 | |||||||
| chr4:6916091 | G | A | 1 | a0001c0001t0002g0181 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-18+6140G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6916091 | |||||||
| chr4:6916107 | CAA | C | 5 | a0001c0003t0002g0034 a0001c0003t0003g0032 a0001c0003t0003g0033 others(2): Show |
5 | HG02647.hp1 HG02723.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+6157_-18+6158d others(4): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6916107 | |||||||
| chr4:6916129 | G | GA | 290 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(287): Show |
291 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(288): Show |
intron_variant | MODIFIER | c.-18+6192dupA | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 6916129 | ||||||
| chr4:6916129 | G | GAA | 6 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0002g0182 others(3): Show |
6 | HG01891.hp1 HG02738.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+6191_-18+6192d others(4): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 6916129 | ||||||
| chr4:6916144 | G | A | 1 | a0001c0001t0003g0059 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-18+6193G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6916144 | |||||||
| chr4:6916171 | A | G | 1 | a0001c0008t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18+6220A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6916171 | |||||||
| chr4:6916209 | C | T | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-18+6258C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6916209 | |||||||
| chr4:6916242 | G | A | 2 | a0001c0001t0008g0060 a0001c0001t0008g0061 |
2 | HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-18+6291G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6916242 | |||||||
| chr4:6916256 | T | C | 122 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(119): Show |
122 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.-18+6305T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6916256 | |||||||
| chr4:6916289 | G | A | 1 | a0001c0001t0002g0149 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-18+6338G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6916289 | |||||||
| chr4:6916314 | G | A | 1 | a0001c0001t0002g0183 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-18+6363G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6916314 | |||||||
| chr4:6916347 | C | T | 14 | a0001c0009t0001g0016 a0002c0002t0002g0020 a0002c0002t0004g0015 others(11): Show |
14 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.-18+6396C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6916347 | |||||||
| chr4:6916614 | A | G | 3 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0148 |
3 | NA18942.hp1 NA18947.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.-18+6663A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6916614 | |||||||
| chr4:6916671 | T | C | 3 | a0001c0001t0012g0132 a0001c0001t0012g0133 a0001c0003t0001g0131 |
3 | HG02257.hp1 HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-17-6702T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6916671 | |||||||
| chr4:6916754 | A | G | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-17-6619A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6916754 | |||||||
| chr4:6916844 | C | T | 1 | a0001c0001t0002g0173 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-17-6529C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6916844 | |||||||
| chr4:6916952 | A | G | 122 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(119): Show |
122 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.-17-6421A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6916952 | |||||||
| chr4:6917046 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-17-6327T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6917046 | |||||||
| chr4:6917087 | C | T | 1 | a0001c0008t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-17-6286C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6917087 | |||||||
| chr4:6917119 | T | C | 4 | a0001c0001t0001g0150 a0001c0001t0002g0051 a0001c0001t0002g0144 others(1): Show |
4 | NA18961.hp2 NA18994.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-6254T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6917119 | |||||||
| chr4:6917141 | C | G | 4 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 others(1): Show |
4 | HG03540.hp2 HG03942.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-6232C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6917141 | |||||||
| chr4:6917174 | A | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-17-6199A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6917174 | |||||||
| chr4:6917182 | T | C | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-17-6191T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6917182 | |||||||
| chr4:6917304 | G | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0264 others(1): Show |
4 | HG02559.hp1 HG02970.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-6069G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6917304 | |||||||
| chr4:6917371 | T | C | 1 | a0001c0001t0002g0182 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-17-6002T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6917371 | |||||||
| chr4:6917386 | A | G | 1 | a0001c0001t0002g0172 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-17-5987A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6917386 | |||||||
| chr4:6917399 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-17-5974C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6917399 | |||||||
| chr4:6917512 | C | T | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-17-5861C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6917512 | |||||||
| chr4:6917592 | G | C | 1 | a0001c0001t0002g0145 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-17-5781G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6917592 | |||||||
| chr4:6917759 | G | C | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-17-5614G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6917759 | |||||||
| chr4:6917868 | C | G | 1 | a0001c0001t0001g0290 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-17-5505C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6917868 | |||||||
| chr4:6917934 | G | A | 139 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(136): Show |
139 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.-17-5439G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6917934 | |||||||
| chr4:6917947 | C | T | 93 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(90): Show |
93 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.-17-5426C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6917947 | |||||||
| chr4:6918105 | C | G | 139 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(136): Show |
139 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.-17-5268C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6918105 | |||||||
| chr4:6918369 | G | A | 15 | a0001c0009t0001g0016 a0002c0002t0002g0020 a0002c0002t0004g0015 others(12): Show |
15 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.-17-5004G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6918369 | |||||||
| chr4:6918376 | C | T | 2 | a0001c0001t0002g0225 a0001c0001t0002g0226 |
2 | NA18943.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.-17-4997C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6918376 | |||||||
| chr4:6918446 | C | G | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-17-4927C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6918446 | |||||||
| chr4:6918507 | C | T | 1 | a0001c0001t0003g0086 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-17-4866C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6918507 | |||||||
| chr4:6918680 | G | C | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-17-4693G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6918680 | |||||||
| chr4:6918739 | G | A | 121 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(118): Show |
121 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.-17-4634G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6918739 | |||||||
| chr4:6918837 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-17-4536T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6918837 | |||||||
| chr4:6918983 | T | C | 122 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(119): Show |
122 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.-17-4390T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6918983 | |||||||
| chr4:6918999 | C | T | 111 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(108): Show |
111 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.-17-4374C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6918999 | |||||||
| chr4:6919118 | C | A | 3 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 |
3 | HG01975.hp1 HG02683.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-17-4255C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6919118 | |||||||
| chr4:6919142 | G | A | 121 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(118): Show |
121 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.-17-4231G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6919142 | |||||||
| chr4:6919170 | G | A | 1 | a0001c0003t0001g0131 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-17-4203G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6919170 | |||||||
| chr4:6919222 | C | T | 2 | a0001c0001t0003g0031 a0001c0006t0001g0045 |
2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-17-4151C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6919222 | |||||||
| chr4:6919240 | G | A | 11 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(8): Show |
11 | HG00558.hp1 HG00673.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.-17-4133G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6919240 | |||||||
| chr4:6919305 | C | T | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-17-4068C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6919305 | |||||||
| chr4:6919388 | C | T | 1 | a0001c0003t0001g0131 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-17-3985C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6919388 | |||||||
| chr4:6919397 | C | T | 15 | a0001c0009t0001g0016 a0002c0002t0002g0020 a0002c0002t0004g0015 others(12): Show |
15 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.-17-3976C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6919397 | |||||||
| chr4:6919398 | G | T | 1 | a0001c0001t0002g0143 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-17-3975G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6919398 | |||||||
| chr4:6919521 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-17-3852C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6919521 | |||||||
| chr4:6919539 | C | T | 4 | a0001c0001t0001g0150 a0001c0001t0002g0051 a0001c0001t0002g0144 others(1): Show |
4 | NA18961.hp2 NA18994.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-3834C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6919539 | |||||||
| chr4:6919631 | T | C | 6 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0002g0249 others(3): Show |
6 | HG00741.hp1 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-3742T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6919631 | |||||||
| chr4:6919652 | C | G | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-17-3721C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6919652 | |||||||
| chr4:6919697 | T | C | 254 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(251): Show |
254 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.-17-3676T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6919697 | |||||||
| chr4:6919754 | A | G | 3 | a0001c0001t0006g0170 a0001c0001t0006g0171 a0001c0001t0006g0224 |
3 | HG01192.hp1 HG01934.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.-17-3619A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6919754 | |||||||
| chr4:6919769 | C | T | 2 | a0001c0001t0006g0168 a0001c0001t0006g0169 |
2 | NA18952.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.-17-3604C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6919769 | |||||||
| chr4:6919777 | T | C | 1 | a0001c0001t0001g0186 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-17-3596T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6919777 | |||||||
| chr4:6919840 | C | T | 6 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(3): Show |
6 | NA18961.hp1 NA18983.hp1 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-3533C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6919840 | |||||||
| chr4:6919841 | A | G | 293 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(290): Show |
294 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.-17-3532A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6919841 | |||||||
| chr4:6919845 | T | C | 1 | a0001c0001t0002g0187 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-17-3528T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6919845 | |||||||
| chr4:6919852 | T | C | 1 | a0001c0001t0002g0187 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-17-3521T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6919852 | |||||||
| chr4:6919861 | T | C | 1 | a0001c0001t0002g0187 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-17-3512T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6919861 | |||||||
| chr4:6919862 | G | A | 1 | a0001c0001t0002g0187 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-17-3511G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6919862 | |||||||
| chr4:6919865 | C | T | 2 | a0001c0001t0002g0187 a0001c0001t0005g0043 |
2 | NA18983.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-17-3508C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6919865 | |||||||
| chr4:6919870 | T | C | 1 | a0001c0001t0002g0187 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-17-3503T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6919870 | |||||||
| chr4:6919899 | G | A | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-17-3474G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6919899 | |||||||
| chr4:6920198 | A | G | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-17-3175A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6920198 | |||||||
| chr4:6920296 | G | T | 14 | a0002c0002t0002g0020 a0002c0002t0004g0015 a0002c0002t0004g0017 others(11): Show |
14 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.-17-3077G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6920296 | |||||||
| chr4:6920484 | C | G | 112 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(109): Show |
112 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.-17-2889C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6920484 | |||||||
| chr4:6920516 | G | A | 285 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(282): Show |
286 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.-17-2857G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6920516 | |||||||
| chr4:6920599 | CTGTT | C | 25 | a0001c0001t0003g0001 a0001c0001t0003g0044 a0001c0001t0003g0049 others(22): Show |
26 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.-17-2771_-17-2768d others(6): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 6920599 | ||||||
| chr4:6920673 | C | T | 9 | a0001c0001t0002g0147 a0001c0001t0002g0175 a0001c0001t0002g0178 others(6): Show |
9 | HG00408.hp2 HG01109.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.-17-2700C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6920673 | |||||||
| chr4:6920893 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-17-2480C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6920893 | |||||||
| chr4:6921031 | C | T | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-17-2342C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6921031 | |||||||
| chr4:6921075 | C | T | 270 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(267): Show |
271 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.-17-2298C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6921075 | |||||||
| chr4:6921100 | A | T | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-17-2273A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6921100 | |||||||
| chr4:6921165 | C | G | 1 | a0001c0001t0008g0115 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-17-2208C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6921165 | |||||||
| chr4:6921300 | G | A | 271 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(268): Show |
272 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.-17-2073G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6921300 | |||||||
| chr4:6921353 | C | A | 146 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(143): Show |
147 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.-17-2020C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6921353 | |||||||
| chr4:6921413 | C | T | 2 | a0001c0001t0003g0079 a0001c0003t0001g0131 |
2 | HG02622.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-17-1960C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6921413 | |||||||
| chr4:6921440 | G | A | 10 | a0001c0001t0003g0044 a0001c0001t0003g0065 a0001c0001t0003g0066 others(7): Show |
10 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-1933G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6921440 | |||||||
| chr4:6921440 | G | C | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-17-1933G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6921440 | |||||||
| chr4:6921524 | T | G | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-17-1849T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6921524 | |||||||
| chr4:6921552 | G | A | 4 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(1): Show |
4 | NA18955.hp2 NA18977.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-1821G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6921552 | |||||||
| chr4:6921556 | C | T | 2 | a0001c0001t0002g0276 a0001c0008t0003g0042 |
2 | HG02615.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-17-1817C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6921556 | |||||||
| chr4:6921564 | C | T | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-17-1809C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6921564 | |||||||
| chr4:6921604 | C | T | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-17-1769C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6921604 | |||||||
| chr4:6921632 | T | G | 1 | a0002c0002t0015g0247 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-17-1741T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6921632 | |||||||
| chr4:6921693 | A | AT | 17 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(14): Show |
17 | HG01884.hp2 HG02135.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.-17-1659dupT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 6921693 | ||||||
| chr4:6921693 | AT | A | 136 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(133): Show |
136 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.-17-1659delT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 6921693 | ||||||
| chr4:6921693 | ATT | A | 27 | a0001c0001t0001g0148 a0001c0001t0003g0001 a0001c0001t0003g0044 others(24): Show |
28 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-1660_-17-1659d others(4): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 6921693 | ||||||
| chr4:6921777 | A | G | 107 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(104): Show |
107 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.-17-1596A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6921777 | |||||||
| chr4:6921817 | T | C | 288 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(285): Show |
289 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.-17-1556T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6921817 | |||||||
| chr4:6921828 | C | A | 1 | a0001c0001t0002g0155 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-17-1545C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6921828 | |||||||
| chr4:6921879 | T | C | 17 | a0002c0002t0002g0020 a0002c0002t0004g0012 a0002c0002t0004g0013 others(14): Show |
17 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-1494T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6921879 | |||||||
| chr4:6921941 | C | T | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-17-1432C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6921941 | |||||||
| chr4:6922032 | G | A | 18 | a0001c0001t0001g0237 a0002c0002t0002g0020 a0002c0002t0004g0012 others(15): Show |
18 | HG01074.hp2 HG01123.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.-17-1341G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6922032 | |||||||
| chr4:6922066 | T | G | 108 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(105): Show |
108 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.-17-1307T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6922066 | |||||||
| chr4:6922160 | C | T | 25 | a0001c0001t0003g0001 a0001c0001t0003g0044 a0001c0001t0003g0049 others(22): Show |
26 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.-17-1213C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6922160 | |||||||
| chr4:6922239 | A | G | 108 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(105): Show |
108 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.-17-1134A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6922239 | |||||||
| chr4:6922316 | T | G | 107 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(104): Show |
107 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.-17-1057T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6922316 | |||||||
| chr4:6922403 | C | T | 8 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 others(5): Show |
8 | HG01255.hp2 HG02258.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-970C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6922403 | |||||||
| chr4:6922450 | C | T | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-17-923C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6922450 | |||||||
| chr4:6922514 | G | A | 105 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(102): Show |
105 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.-17-859G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6922514 | |||||||
| chr4:6922711 | A | G | 1 | a0001c0001t0002g0294 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-17-662A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6922711 | |||||||
| chr4:6922736 | C | T | 6 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(3): Show |
6 | HG01884.hp2 HG02630.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-637C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6922736 | |||||||
| chr4:6922763 | C | G | 2 | a0001c0001t0002g0152 a0001c0001t0002g0246 |
2 | HG02486.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-17-610C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6922763 | |||||||
| chr4:6922788 | T | C | 18 | a0001c0001t0001g0237 a0002c0002t0002g0020 a0002c0002t0004g0012 others(15): Show |
18 | HG01074.hp2 HG01123.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.-17-585T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6922788 | |||||||
| chr4:6922907 | C | T | 2 | a0001c0001t0003g0001 a0001c0001t0003g0078 |
3 | HG00323.hp2 HG01123.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.-17-466C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6922907 | |||||||
| chr4:6923051 | A | G | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-17-322A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6923051 | |||||||
| chr4:6923070 | G | A | 2 | a0001c0001t0002g0152 a0001c0001t0002g0246 |
2 | HG02486.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-17-303G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6923070 | |||||||
| chr4:6923195 | C | G | 3 | a0001c0001t0001g0136 a0001c0001t0002g0064 a0001c0001t0022g0114 |
3 | HG02559.hp2 HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-17-178C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6923195 | |||||||
| chr4:6923232 | C | T | 17 | a0002c0002t0002g0020 a0002c0002t0004g0012 a0002c0002t0004g0013 others(14): Show |
17 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-141C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6923232 | |||||||
| chr4:6923239 | C | G | 1 | a0001c0001t0001g0185 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-17-134C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6923239 | |||||||
| chr4:6923282 | A | C | 109 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(106): Show |
109 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.-17-91A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6923282 | |||||||
| chr4:6923283 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-17-90G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 1/13 | chr4 | 6923283 | |||||||
| chr4:6924258 | GAATCC | G | 145 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(142): Show |
146 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.722+148_722+152del others(5): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6924258 | |||||||
| chr4:6924264 | T | G | 145 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(142): Show |
146 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.722+153T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6924264 | |||||||
| chr4:6924304 | TCGGTGTC others(2): Show |
T | 164 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(161): Show |
165 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.722+194_722+202del others(9): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6924304 | |||||||
| chr4:6924486 | A | G | 7 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(4): Show |
7 | HG01884.hp2 HG02630.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.722+375A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6924486 | |||||||
| chr4:6924548 | A | G | 8 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(5): Show |
8 | HG01884.hp2 HG02630.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.722+437A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6924548 | |||||||
| chr4:6924594 | C | T | 3 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0003g0298 |
3 | HG00741.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.722+483C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6924594 | |||||||
| chr4:6924631 | TGCACTGC others(1): Show |
T | 18 | a0001c0001t0001g0237 a0002c0002t0002g0020 a0002c0002t0004g0012 others(15): Show |
18 | HG01074.hp2 HG01123.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.722+523_722+530del others(8): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6924631 | ||||||
| chr4:6924645 | A | G | 147 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(144): Show |
148 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.722+534A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6924645 | |||||||
| chr4:6924884 | G | A | 152 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(149): Show |
153 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.722+773G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6924884 | |||||||
| chr4:6924948 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.722+837C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6924948 | |||||||
| chr4:6925150 | A | G | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.722+1039A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6925150 | |||||||
| chr4:6925223 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.722+1112C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6925223 | |||||||
| chr4:6925229 | C | T | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.722+1118C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6925229 | |||||||
| chr4:6925270 | A | C | 112 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
112 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.722+1159A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6925270 | |||||||
| chr4:6925284 | A | G | 18 | a0001c0001t0001g0237 a0002c0002t0002g0020 a0002c0002t0004g0012 others(15): Show |
18 | HG01074.hp2 HG01123.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.722+1173A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6925284 | |||||||
| chr4:6925352 | G | T | 18 | a0001c0001t0001g0237 a0002c0002t0002g0020 a0002c0002t0004g0012 others(15): Show |
18 | HG01074.hp2 HG01123.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.722+1241G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6925352 | |||||||
| chr4:6925474 | G | A | 6 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(3): Show |
6 | HG01884.hp2 HG02630.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.722+1363G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6925474 | |||||||
| chr4:6925585 | T | C | 9 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(6): Show |
9 | HG01255.hp2 HG01884.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.722+1474T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6925585 | |||||||
| chr4:6925615 | G | C | 1 | a0001c0008t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.722+1504G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6925615 | |||||||
| chr4:6925744 | T | G | 271 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(268): Show |
272 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.722+1633T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6925744 | |||||||
| chr4:6925791 | C | G | 18 | a0001c0001t0001g0237 a0002c0002t0002g0020 a0002c0002t0004g0012 others(15): Show |
18 | HG01074.hp2 HG01123.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.722+1680C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6925791 | |||||||
| chr4:6925867 | G | A | 1 | a0001c0001t0002g0219 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.722+1756G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6925867 | |||||||
| chr4:6925875 | G | C | 3 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0025g0093 |
3 | HG02486.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.722+1764G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6925875 | |||||||
| chr4:6925940 | G | C | 274 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(271): Show |
275 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.722+1829G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6925940 | |||||||
| chr4:6926051 | T | A | 1 | a0001c0001t0002g0134 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.722+1940T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6926051 | |||||||
| chr4:6926090 | G | A | 1 | a0002c0002t0004g0017 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.722+1979G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6926090 | |||||||
| chr4:6926129 | T | C | 35 | a0001c0001t0002g0244 a0001c0001t0002g0245 a0001c0001t0003g0001 others(32): Show |
36 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.722+2018T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6926129 | |||||||
| chr4:6926139 | C | T | 1 | a0001c0001t0003g0068 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.722+2028C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6926139 | |||||||
| chr4:6926319 | C | T | 2 | a0001c0001t0002g0239 a0001c0001t0002g0240 |
2 | HG00738.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.722+2208C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6926319 | |||||||
| chr4:6926353 | A | G | 1 | a0001c0001t0022g0114 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.722+2242A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6926353 | |||||||
| chr4:6926384 | T | C | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.722+2273T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6926384 | |||||||
| chr4:6926523 | G | A | 1 | a0001c0010t0002g0036 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.722+2412G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6926523 | |||||||
| chr4:6926580 | A | G | 1 | a0001c0001t0002g0177 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.722+2469A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6926580 | |||||||
| chr4:6926631 | C | A | 139 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(136): Show |
140 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.722+2520C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6926631 | |||||||
| chr4:6926655 | G | A | 3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 |
3 | HG01261.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.722+2544G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6926655 | |||||||
| chr4:6926765 | T | A | 2 | a0001c0001t0002g0156 a0001c0001t0002g0189 |
2 | HG00738.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.722+2654T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6926765 | |||||||
| chr4:6926843 | C | T | 18 | a0001c0001t0001g0237 a0002c0002t0002g0020 a0002c0002t0004g0012 others(15): Show |
18 | HG01074.hp2 HG01123.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.722+2732C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6926843 | |||||||
| chr4:6926878 | C | T | 1 | a0001c0001t0004g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.722+2767C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6926878 | |||||||
| chr4:6927009 | A | G | 1 | a0001c0001t0002g0293 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.722+2898A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6927009 | |||||||
| chr4:6927048 | T | C | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.722+2937T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6927048 | |||||||
| chr4:6927209 | C | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0020g0265 |
3 | HG02559.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.722+3098C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6927209 | |||||||
| chr4:6927218 | C | A | 285 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(282): Show |
286 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.722+3107C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6927218 | |||||||
| chr4:6927295 | T | C | 285 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(282): Show |
286 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.722+3184T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6927295 | |||||||
| chr4:6927319 | G | A | 1 | a0001c0001t0003g0190 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.722+3208G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6927319 | |||||||
| chr4:6927359 | G | A | 2 | a0001c0001t0002g0152 a0001c0001t0002g0246 |
2 | HG02486.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.722+3248G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6927359 | |||||||
| chr4:6927391 | G | C | 4 | a0001c0003t0002g0034 a0001c0003t0003g0032 a0001c0003t0003g0033 others(1): Show |
4 | HG02647.hp1 HG02723.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.722+3280G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6927391 | |||||||
| chr4:6927535 | C | T | 115 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(112): Show |
115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.722+3424C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6927535 | |||||||
| chr4:6927621 | C | T | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.722+3510C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6927621 | |||||||
| chr4:6927629 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.722+3518C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6927629 | |||||||
| chr4:6927751 | A | G | 18 | a0001c0001t0001g0237 a0002c0002t0002g0020 a0002c0002t0004g0012 others(15): Show |
18 | HG01074.hp2 HG01123.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.722+3640A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6927751 | |||||||
| chr4:6927978 | C | T | 3 | a0001c0001t0003g0066 a0001c0001t0003g0067 a0001c0001t0005g0056 |
3 | HG02647.hp2 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.722+3867C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6927978 | |||||||
| chr4:6928043 | G | A | 1 | a0001c0001t0003g0066 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.722+3932G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6928043 | |||||||
| chr4:6928048 | A | AT | 9 | a0001c0001t0001g0138 a0001c0001t0002g0009 a0001c0001t0002g0010 others(6): Show |
9 | HG01884.hp2 HG02630.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.722+3938dupT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6928048 | ||||||
| chr4:6928062 | A | G | 1 | a0001c0001t0022g0114 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.722+3951A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6928062 | |||||||
| chr4:6928174 | C | T | 105 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(102): Show |
105 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.722+4063C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6928174 | |||||||
| chr4:6928387 | T | C | 168 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(165): Show |
169 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.722+4276T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6928387 | |||||||
| chr4:6928391 | G | A | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.722+4280G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6928391 | |||||||
| chr4:6928486 | G | A | 7 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(4): Show |
7 | HG01884.hp2 HG02630.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.722+4375G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6928486 | |||||||
| chr4:6928490 | G | A | 147 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(144): Show |
148 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.722+4379G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6928490 | |||||||
| chr4:6928552 | G | C | 1 | a0001c0001t0001g0087 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.722+4441G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6928552 | |||||||
| chr4:6928689 | T | C | 18 | a0001c0001t0001g0237 a0002c0002t0002g0020 a0002c0002t0004g0012 others(15): Show |
18 | HG01074.hp2 HG01123.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.722+4578T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6928689 | |||||||
| chr4:6928751 | A | G | 18 | a0001c0001t0001g0237 a0002c0002t0002g0020 a0002c0002t0004g0012 others(15): Show |
18 | HG01074.hp2 HG01123.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.722+4640A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6928751 | |||||||
| chr4:6928784 | G | A | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG03491.hp2 HG03492.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.722+4673G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6928784 | |||||||
| chr4:6928843 | G | C | 1 | a0001c0001t0002g0154 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.722+4732G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6928843 | |||||||
| chr4:6928850 | T | TG | 8 | a0001c0001t0001g0058 a0001c0001t0001g0111 a0001c0001t0001g0118 others(5): Show |
8 | NA18961.hp1 NA18983.hp1 NA18987.hp2 others(5): Show |
intron_variant | MODIFIER | c.722+4743dupG | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6928850 | ||||||
| chr4:6928858 | A | G | 285 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(282): Show |
286 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.722+4747A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6928858 | |||||||
| chr4:6928898 | G | A | 171 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(168): Show |
172 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.722+4787G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6928898 | |||||||
| chr4:6928913 | A | G | 4 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 others(1): Show |
4 | HG03540.hp2 HG03942.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.722+4802A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6928913 | |||||||
| chr4:6929016 | A | G | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.722+4905A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6929016 | |||||||
| chr4:6929083 | G | C | 146 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(143): Show |
147 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.722+4972G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6929083 | |||||||
| chr4:6929090 | A | G | 285 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(282): Show |
286 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.722+4979A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6929090 | |||||||
| chr4:6929189 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.722+5078C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6929189 | |||||||
| chr4:6929236 | C | T | 3 | a0001c0001t0002g0156 a0001c0001t0002g0189 a0001c0001t0002g0241 |
3 | HG00738.hp1 HG01192.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.722+5125C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6929236 | |||||||
| chr4:6929241 | T | C | 146 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(143): Show |
147 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.722+5130T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6929241 | |||||||
| chr4:6929242 | G | A | 1 | a0001c0001t0002g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.722+5131G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6929242 | |||||||
| chr4:6929509 | C | T | 7 | a0001c0001t0005g0268 a0001c0001t0005g0270 a0001c0001t0005g0271 others(4): Show |
7 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.722+5398C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6929509 | |||||||
| chr4:6929609 | G | T | 6 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(3): Show |
6 | HG01884.hp2 HG02630.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.722+5498G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6929609 | |||||||
| chr4:6929720 | A | G | 15 | a0001c0001t0001g0153 a0001c0001t0001g0248 a0001c0001t0001g0251 others(12): Show |
15 | HG00323.hp1 HG00733.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.722+5609A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6929720 | |||||||
| chr4:6929987 | G | C | 5 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(2): Show |
5 | HG01099.hp2 HG01255.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.722+5876G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6929987 | |||||||
| chr4:6930040 | C | T | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.722+5929C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6930040 | |||||||
| chr4:6930054 | C | G | 1 | a0001c0001t0018g0047 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.722+5943C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6930054 | |||||||
| chr4:6930104 | G | A | 145 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(142): Show |
146 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.722+5993G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6930104 | |||||||
| chr4:6930119 | A | T | 17 | a0002c0002t0002g0020 a0002c0002t0004g0012 a0002c0002t0004g0013 others(14): Show |
17 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.722+6008A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6930119 | |||||||
| chr4:6930141 | C | T | 4 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
4 | NA18961.hp1 NA18983.hp1 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.722+6030C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6930141 | |||||||
| chr4:6930189 | C | T | 1 | a0001c0001t0029g0176 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.722+6078C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6930189 | |||||||
| chr4:6930303 | T | C | 1 | a0001c0001t0002g0241 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.722+6192T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6930303 | |||||||
| chr4:6930331 | T | A | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.722+6220T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6930331 | |||||||
| chr4:6930336 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.722+6225C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6930336 | |||||||
| chr4:6930376 | A | G | 2 | a0001c0001t0002g0167 a0001c0001t0002g0174 |
2 | NA18960.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.722+6265A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6930376 | |||||||
| chr4:6930384 | G | A | 5 | a0001c0003t0002g0034 a0001c0003t0003g0032 a0001c0003t0003g0033 others(2): Show |
5 | HG02647.hp1 HG02723.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.722+6273G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6930384 | |||||||
| chr4:6930472 | T | C | 1 | a0001c0001t0012g0132 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.722+6361T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6930472 | |||||||
| chr4:6930572 | T | C | 166 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(163): Show |
167 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.722+6461T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6930572 | |||||||
| chr4:6930682 | T | C | 1 | a0001c0001t0001g0005 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.722+6571T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6930682 | |||||||
| chr4:6930713 | G | A | 1 | a0001c0001t0020g0265 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.722+6602G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6930713 | |||||||
| chr4:6930798 | CA | C | 163 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(160): Show |
164 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.722+6701delA | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6930798 | ||||||
| chr4:6930925 | A | G | 288 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(285): Show |
289 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.722+6814A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6930925 | |||||||
| chr4:6930967 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.722+6856C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6930967 | |||||||
| chr4:6931157 | C | A | 147 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(144): Show |
148 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.722+7046C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6931157 | |||||||
| chr4:6931259 | T | C | 151 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(148): Show |
152 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.722+7148T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6931259 | |||||||
| chr4:6931357 | G | T | 6 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 others(3): Show |
6 | HG00558.hp2 NA18747.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.722+7246G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6931357 | |||||||
| chr4:6931473 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.722+7362C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6931473 | |||||||
| chr4:6931527 | T | C | 3 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | HG01070.hp1 HG01071.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.722+7416T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6931527 | |||||||
| chr4:6931570 | C | T | 149 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(146): Show |
150 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.722+7459C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6931570 | |||||||
| chr4:6931577 | T | C | 166 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(163): Show |
167 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.722+7466T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6931577 | |||||||
| chr4:6931735 | C | G | 149 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(146): Show |
150 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.722+7624C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6931735 | |||||||
| chr4:6931776 | T | TA | 17 | a0002c0002t0002g0020 a0002c0002t0004g0012 a0002c0002t0004g0013 others(14): Show |
17 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.722+7674dupA | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6931776 | ||||||
| chr4:6931825 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.722+7714G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6931825 | |||||||
| chr4:6932157 | C | G | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.722+8046C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6932157 | |||||||
| chr4:6932193 | C | G | 1 | a0001c0001t0004g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.722+8082C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6932193 | |||||||
| chr4:6932253 | G | C | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.722+8142G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6932253 | |||||||
| chr4:6932315 | C | T | 149 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(146): Show |
150 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.722+8204C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6932315 | |||||||
| chr4:6932323 | G | A | 1 | a0001c0001t0002g0191 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.722+8212G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6932323 | |||||||
| chr4:6932326 | C | T | 149 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(146): Show |
150 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.722+8215C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6932326 | |||||||
| chr4:6932376 | T | TA | 120 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(117): Show |
120 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.722+8280dupA | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6932376 | ||||||
| chr4:6932376 | TA | T | 149 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(146): Show |
150 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.722+8280delA | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6932376 | ||||||
| chr4:6932630 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.722+8519C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6932630 | |||||||
| chr4:6932635 | T | A | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.722+8524T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6932635 | |||||||
| chr4:6932720 | C | G | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.722+8609C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6932720 | |||||||
| chr4:6932813 | C | T | 13 | a0001c0001t0001g0153 a0001c0001t0001g0251 a0001c0001t0001g0252 others(10): Show |
13 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.722+8702C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6932813 | |||||||
| chr4:6932928 | A | G | 152 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(149): Show |
153 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.722+8817A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6932928 | |||||||
| chr4:6932935 | C | T | 5 | a0001c0001t0002g0214 a0001c0001t0002g0215 a0001c0001t0002g0218 others(2): Show |
5 | HG02135.hp1 NA18943.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.722+8824C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6932935 | |||||||
| chr4:6932948 | G | A | 1 | a0001c0008t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.722+8837G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6932948 | |||||||
| chr4:6932975 | G | C | 2 | a0001c0001t0001g0112 a0001c0001t0001g0130 |
2 | HG00639.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.722+8864G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6932975 | |||||||
| chr4:6932985 | T | C | 1 | a0001c0008t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.722+8874T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6932985 | |||||||
| chr4:6933030 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.722+8919C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6933030 | |||||||
| chr4:6933237 | A | ACCTCCCC others(8): Show |
13 | a0001c0001t0001g0048 a0001c0001t0001g0087 a0001c0001t0001g0088 others(10): Show |
13 | HG00408.hp1 HG02145.hp1 NA18940.hp1 others(10): Show |
intron_variant | MODIFIER | c.722+9143_722+9157d others(17): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933237 | ||||||
| chr4:6933237 | A | ACCTCCCC others(13): Show |
85 | a0001c0001t0001g0005 a0001c0001t0001g0054 a0001c0001t0001g0055 others(82): Show |
85 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.722+9138_722+9157d others(22): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933237 | ||||||
| chr4:6933237 | A | ACCTCCCC others(18): Show |
10 | a0001c0001t0001g0035 a0001c0001t0001g0080 a0001c0001t0001g0081 others(7): Show |
10 | HG00609.hp1 HG01952.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.722+9133_722+9157d others(27): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933237 | ||||||
| chr4:6933237 | A | ACCTCCCC others(23): Show |
3 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0020g0265 |
3 | HG02559.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.722+9128_722+9157d others(32): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933237 | ||||||
| chr4:6933237 | A | ACCTCCCC others(28): Show |
3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0274 |
3 | HG03195.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.722+9157_722+9158i others(37): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933237 | ||||||
| chr4:6933239 | CTCCCCTC others(23): Show |
C | 104 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(101): Show |
104 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.722+9139_722+9168d others(32): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933239 | ||||||
| chr4:6933244 | C | CT | 3 | a0001c0003t0003g0032 a0001c0003t0003g0033 a0001c0003t0003g0300 |
3 | HG02647.hp1 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.722+9134dupT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933244 | ||||||
| chr4:6933245 | T | TCCCCCTC others(6): Show |
1 | a0001c0003t0002g0034 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.722+9138_722+9139i others(15): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933245 | ||||||
| chr4:6933246 | CCCCTCCC others(7): Show |
C | 1 | a0001c0001t0009g0004 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.722+9139_722+9152d others(16): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933246 | ||||||
| chr4:6933246 | CCCCTCCC others(17): Show |
C | 16 | a0001c0001t0001g0138 a0001c0001t0001g0217 a0001c0001t0002g0162 others(13): Show |
16 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.722+9139_722+9162d others(26): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933246 | ||||||
| chr4:6933246 | CCCCTCCC others(29): Show |
C | 16 | a0001c0001t0003g0049 a0001c0001t0003g0059 a0001c0001t0003g0070 others(13): Show |
16 | HG00280.hp1 HG01123.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.722+9139_722+9174d others(38): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933246 | ||||||
| chr4:6933246 | CCCCTCCC others(35): Show |
C | 4 | a0001c0001t0003g0031 a0001c0001t0011g0039 a0001c0001t0011g0040 others(1): Show |
4 | HG01255.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.722+9139_722+9180d others(44): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933246 | ||||||
| chr4:6933246 | CCCCTCCC others(41): Show |
C | 1 | a0001c0001t0027g0213 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.722+9139_722+9186d others(50): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933246 | ||||||
| chr4:6933247 | CCCTCCCC others(11): Show |
C | 5 | a0001c0001t0002g0219 a0001c0001t0003g0079 a0001c0001t0021g0234 others(2): Show |
5 | HG01952.hp1 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.722+9139_722+9156d others(20): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933247 | ||||||
| chr4:6933254 | C | CCT | 4 | a0001c0003t0002g0034 a0001c0003t0003g0032 a0001c0003t0003g0033 others(1): Show |
4 | HG02647.hp1 HG02723.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.722+9143_722+9144i others(4): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6933254 | |||||||
| chr4:6933255 | T | C | 4 | a0001c0003t0002g0034 a0001c0003t0003g0032 a0001c0003t0003g0033 others(1): Show |
4 | HG02647.hp1 HG02723.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.722+9144T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6933255 | |||||||
| chr4:6933257 | CCCTCCCC others(18): Show |
C | 1 | a0001c0001t0006g0169 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.722+9149_722+9173d others(27): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933257 | ||||||
| chr4:6933259 | C | CTCCCCTC others(23): Show |
1 | a0001c0001t0001g0085 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.722+9157_722+9158i others(32): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933259 | ||||||
| chr4:6933263 | C | CCCCTCCC others(39): Show |
1 | a0001c0003t0003g0032 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.722+9153_722+9154i others(48): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933263 | ||||||
| chr4:6933263 | C | CCCTCCCC others(14): Show |
1 | a0001c0003t0003g0033 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.722+9153_722+9154i others(23): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933263 | ||||||
| chr4:6933263 | C | CCCTCCCC others(26): Show |
1 | a0001c0003t0003g0300 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.722+9153_722+9154i others(35): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933263 | ||||||
| chr4:6933265 | T | C | 4 | a0001c0003t0002g0034 a0001c0003t0003g0032 a0001c0003t0003g0033 others(1): Show |
4 | HG02647.hp1 HG02723.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.722+9154T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6933265 | |||||||
| chr4:6933269 | T | C | 33 | a0001c0001t0001g0110 a0001c0001t0001g0277 a0001c0001t0001g0278 others(30): Show |
33 | HG00741.hp1 HG01109.hp1 HG01346.hp1 others(30): Show |
intron_variant | MODIFIER | c.722+9158T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6933269 | |||||||
| chr4:6933270 | T | C | 11 | a0001c0001t0002g0219 a0001c0001t0003g0001 a0001c0001t0003g0078 others(8): Show |
12 | HG00323.hp2 HG01123.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.722+9159T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6933270 | |||||||
| chr4:6933275 | T | TCCCCTCC others(14): Show |
1 | a0001c0001t0001g0110 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.722+9168_722+9169i others(23): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933275 | ||||||
| chr4:6933276 | C | CCCCTCCC others(9): Show |
1 | a0002c0002t0004g0019 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.722+9168_722+9169i others(18): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933276 | ||||||
| chr4:6933276 | C | CCCCTCCC others(19): Show |
5 | a0002c0002t0002g0020 a0002c0002t0010g0021 a0002c0002t0010g0022 others(2): Show |
5 | HG01346.hp1 HG02135.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.722+9168_722+9169i others(28): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933276 | ||||||
| chr4:6933276 | C | CCCCTCCC others(24): Show |
7 | a0002c0002t0004g0012 a0002c0002t0004g0013 a0002c0002t0004g0017 others(4): Show |
7 | HG01975.hp2 HG02004.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.722+9168_722+9169i others(33): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933276 | ||||||
| chr4:6933276 | C | CCCCTCCC others(29): Show |
2 | a0002c0002t0004g0025 a0002c0002t0004g0026 |
2 | HG04199.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.722+9168_722+9169i others(38): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933276 | ||||||
| chr4:6933276 | C | CCCCTCCC others(34): Show |
1 | a0002c0002t0004g0015 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.722+9168_722+9169i others(43): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933276 | ||||||
| chr4:6933276 | C | CCCCTCCC others(32): Show |
3 | a0001c0001t0002g0009 a0001c0001t0005g0043 a0001c0001t0018g0047 |
3 | HG02886.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.722+9168_722+9169i others(41): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933276 | ||||||
| chr4:6933276 | C | CCCCTCCC others(27): Show |
4 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0046 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.722+9168_722+9169i others(36): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933276 | ||||||
| chr4:6933276 | C | CCCCTCCC others(12): Show |
1 | a0001c0008t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.722+9168_722+9169i others(21): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933276 | ||||||
| chr4:6933276 | C | CCCCTCCC others(7): Show |
1 | a0001c0001t0001g0290 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.722+9168_722+9169i others(16): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933276 | ||||||
| chr4:6933276 | C | CCCCTCCC others(19): Show |
3 | a0001c0001t0001g0279 a0001c0001t0001g0297 a0001c0001t0003g0298 |
3 | HG00741.hp1 HG03130.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.722+9168_722+9169i others(28): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933276 | ||||||
| chr4:6933281 | T | C | 1 | a0001c0001t0001g0286 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.722+9170T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6933281 | |||||||
| chr4:6933282 | T | C | 143 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(140): Show |
144 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.722+9171T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6933282 | |||||||
| chr4:6933283 | C | T | 1 | a0001c0001t0001g0286 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.722+9172C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6933283 | |||||||
| chr4:6933287 | T | C | 1 | a0001c0001t0002g0238 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.722+9176T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6933287 | |||||||
| chr4:6933288 | T | C | 146 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(143): Show |
147 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.722+9177T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6933288 | |||||||
| chr4:6933294 | T | C | 153 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(150): Show |
154 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.722+9183T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6933294 | |||||||
| chr4:6933300 | T | C | 152 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(149): Show |
153 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.722+9189T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6933300 | |||||||
| chr4:6933306 | T | C | 153 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(150): Show |
154 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.722+9195T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6933306 | |||||||
| chr4:6933312 | T | C | 18 | a0001c0001t0003g0001 a0001c0001t0003g0049 a0001c0001t0003g0059 others(15): Show |
19 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.722+9201T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6933312 | |||||||
| chr4:6933316 | T | C | 153 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(150): Show |
154 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.722+9205T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6933316 | |||||||
| chr4:6933344 | G | T | 1 | a0001c0001t0002g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.722+9233G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6933344 | |||||||
| chr4:6933389 | T | C | 170 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(167): Show |
171 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.722+9278T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6933389 | |||||||
| chr4:6933425 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.722+9314C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6933425 | |||||||
| chr4:6933436 | C | G | 33 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(30): Show |
34 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.722+9325C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6933436 | |||||||
| chr4:6933449 | C | T | 9 | a0001c0001t0005g0053 a0001c0001t0005g0139 a0001c0001t0005g0268 others(6): Show |
9 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.722+9338C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6933449 | |||||||
| chr4:6933453 | C | T | 7 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(4): Show |
7 | HG01884.hp2 HG02630.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.722+9342C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6933453 | |||||||
| chr4:6933495 | A | G | 4 | a0001c0001t0001g0138 a0001c0001t0011g0039 a0001c0001t0011g0040 others(1): Show |
4 | HG01255.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.722+9384A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6933495 | |||||||
| chr4:6933713 | G | GA | 7 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(4): Show |
7 | HG01884.hp2 HG02630.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.722+9604dupA | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933713 | ||||||
| chr4:6933753 | A | G | 2 | a0001c0001t0013g0256 a0001c0001t0013g0258 |
2 | HG00438.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.722+9642A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6933753 | |||||||
| chr4:6933798 | C | A | 1 | a0001c0001t0024g0123 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.722+9687C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6933798 | |||||||
| chr4:6933798 | CTG | C | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.722+9689_722+9690d others(4): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6933798 | ||||||
| chr4:6933839 | A | G | 1 | a0001c0001t0002g0209 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.722+9728A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6933839 | |||||||
| chr4:6933861 | C | A | 1 | a0001c0001t0002g0147 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.722+9750C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6933861 | |||||||
| chr4:6933920 | C | T | 16 | a0002c0002t0002g0020 a0002c0002t0004g0012 a0002c0002t0004g0013 others(13): Show |
16 | HG01346.hp1 HG01361.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.722+9809C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6933920 | |||||||
| chr4:6934022 | T | C | 169 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(166): Show |
170 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.722+9911T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6934022 | |||||||
| chr4:6934119 | G | T | 152 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(149): Show |
153 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.722+10008G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6934119 | |||||||
| chr4:6934156 | T | C | 2 | a0001c0001t0001g0266 a0001c0001t0001g0287 |
2 | HG01169.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.722+10045T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6934156 | |||||||
| chr4:6934235 | G | C | 170 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(167): Show |
171 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.722+10124G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6934235 | |||||||
| chr4:6934333 | C | T | 6 | a0001c0003t0001g0131 a0001c0003t0002g0034 a0001c0003t0003g0032 others(3): Show |
6 | HG02647.hp1 HG02723.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.722+10222C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6934333 | |||||||
| chr4:6934339 | G | T | 16 | a0002c0002t0002g0020 a0002c0002t0004g0012 a0002c0002t0004g0013 others(13): Show |
16 | HG01346.hp1 HG01361.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.722+10228G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6934339 | |||||||
| chr4:6934479 | T | G | 11 | a0001c0001t0001g0138 a0001c0001t0002g0009 a0001c0001t0002g0010 others(8): Show |
11 | HG01255.hp2 HG01884.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.722+10368T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6934479 | |||||||
| chr4:6934636 | C | T | 17 | a0001c0001t0001g0237 a0002c0002t0002g0020 a0002c0002t0004g0012 others(14): Show |
17 | HG01074.hp2 HG01346.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.722+10525C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6934636 | |||||||
| chr4:6934657 | C | CA | 8 | a0001c0001t0001g0150 a0001c0001t0002g0051 a0001c0001t0002g0144 others(5): Show |
8 | HG02135.hp1 HG02922.hp1 HG03710.hp1 others(5): Show |
intron_variant | MODIFIER | c.722+10553dupA | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6934657 | ||||||
| chr4:6934665 | C | A | 171 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(168): Show |
172 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.722+10554C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6934665 | |||||||
| chr4:6934690 | T | C | 1 | a0001c0001t0031g0082 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.722+10579T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6934690 | |||||||
| chr4:6934765 | G | A | 103 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(100): Show |
103 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.722+10654G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6934765 | |||||||
| chr4:6934914 | CA | C | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.722+10810delA | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6934914 | ||||||
| chr4:6935003 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.722+10892C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6935003 | |||||||
| chr4:6935112 | T | A | 172 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(169): Show |
173 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.722+11001T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6935112 | |||||||
| chr4:6935159 | T | A | 7 | a0001c0001t0001g0290 a0001c0001t0008g0060 a0001c0001t0008g0061 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.722+11048T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6935159 | |||||||
| chr4:6935227 | A | AT | 6 | a0001c0001t0001g0233 a0001c0001t0002g0207 a0001c0001t0009g0003 others(3): Show |
6 | HG01243.hp1 HG02258.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.722+11127dupT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6935227 | ||||||
| chr4:6935283 | G | A | 2 | a0001c0001t0001g0259 a0001c0001t0001g0263 |
2 | HG00323.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.722+11172G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6935283 | |||||||
| chr4:6935309 | A | G | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.722+11198A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6935309 | |||||||
| chr4:6935403 | A | C | 2 | a0001c0001t0005g0043 a0001c0007t0002g0002 |
2 | NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.722+11292A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6935403 | |||||||
| chr4:6935436 | G | A | 2 | a0001c0001t0001g0266 a0001c0001t0001g0287 |
2 | HG01169.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.722+11325G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6935436 | |||||||
| chr4:6935446 | C | T | 1 | a0002c0002t0004g0019 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.722+11335C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6935446 | |||||||
| chr4:6935447 | G | C | 17 | a0001c0001t0001g0237 a0002c0002t0002g0020 a0002c0002t0004g0012 others(14): Show |
17 | HG01074.hp2 HG01346.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.722+11336G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6935447 | |||||||
| chr4:6935514 | G | A | 1 | a0001c0001t0003g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.722+11403G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6935514 | |||||||
| chr4:6935557 | T | TCCTCCTC others(14): Show |
1 | a0001c0001t0002g0220 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.722+11451_722+1147 others(25): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6935557 | ||||||
| chr4:6935608 | A | G | 172 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(169): Show |
173 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.722+11497A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6935608 | |||||||
| chr4:6935648 | CT | C | 148 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(145): Show |
149 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.722+11550delT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6935648 | ||||||
| chr4:6935914 | G | A | 1 | a0001c0008t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.722+11803G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6935914 | |||||||
| chr4:6935939 | C | T | 1 | a0001c0001t0002g0209 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.722+11828C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6935939 | |||||||
| chr4:6935987 | T | C | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.722+11876T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6935987 | |||||||
| chr4:6936074 | G | A | 19 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0153 others(16): Show |
19 | HG00323.hp1 HG00438.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.722+11963G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6936074 | |||||||
| chr4:6936210 | A | G | 2 | a0001c0001t0001g0112 a0001c0001t0001g0130 |
2 | HG00639.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.722+12099A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6936210 | |||||||
| chr4:6936233 | A | G | 6 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(3): Show |
6 | NA18961.hp1 NA18983.hp1 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.722+12122A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6936233 | |||||||
| chr4:6936257 | C | T | 148 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(145): Show |
149 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.722+12146C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6936257 | |||||||
| chr4:6936268 | G | A | 167 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(164): Show |
168 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.722+12157G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6936268 | |||||||
| chr4:6936388 | A | G | 16 | a0002c0002t0002g0020 a0002c0002t0004g0012 a0002c0002t0004g0013 others(13): Show |
16 | HG01346.hp1 HG01361.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.722+12277A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6936388 | |||||||
| chr4:6936559 | T | C | 16 | a0002c0002t0002g0020 a0002c0002t0004g0012 a0002c0002t0004g0013 others(13): Show |
16 | HG01346.hp1 HG01361.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.722+12448T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6936559 | |||||||
| chr4:6936615 | A | G | 3 | a0001c0001t0003g0066 a0001c0001t0003g0067 a0001c0001t0005g0056 |
3 | HG02647.hp2 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.722+12504A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6936615 | |||||||
| chr4:6936634 | G | T | 1 | a0001c0011t0002g0206 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.722+12523G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6936634 | |||||||
| chr4:6936703 | A | T | 1 | a0001c0001t0003g0059 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.722+12592A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6936703 | |||||||
| chr4:6936779 | C | T | 1 | a0001c0001t0003g0140 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.722+12668C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6936779 | |||||||
| chr4:6936783 | G | T | 1 | a0001c0008t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.722+12672G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6936783 | |||||||
| chr4:6936824 | G | T | 17 | a0002c0002t0002g0020 a0002c0002t0004g0012 a0002c0002t0004g0013 others(14): Show |
17 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.722+12713G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6936824 | |||||||
| chr4:6936909 | T | A | 1 | a0001c0003t0001g0131 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.722+12798T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6936909 | |||||||
| chr4:6936994 | C | T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG01433.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.722+12883C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6936994 | |||||||
| chr4:6937004 | G | A | 6 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(3): Show |
6 | HG01884.hp2 HG02630.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.722+12893G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6937004 | |||||||
| chr4:6937078 | C | T | 169 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(166): Show |
170 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.722+12967C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6937078 | |||||||
| chr4:6937205 | C | T | 2 | a0001c0001t0002g0180 a0001c0001t0002g0232 |
2 | HG01981.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.722+13094C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6937205 | |||||||
| chr4:6937226 | A | T | 173 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(170): Show |
174 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.722+13115A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6937226 | |||||||
| chr4:6937298 | G | A | 1 | a0001c0001t0002g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.722+13187G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6937298 | |||||||
| chr4:6937305 | G | A | 111 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(108): Show |
111 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.722+13194G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6937305 | |||||||
| chr4:6937310 | A | G | 111 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(108): Show |
111 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.722+13199A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6937310 | |||||||
| chr4:6937316 | G | T | 19 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0237 others(16): Show |
19 | HG01074.hp2 HG01346.hp1 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.722+13205G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6937316 | |||||||
| chr4:6937435 | A | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0094 a0001c0001t0001g0095 others(2): Show |
5 | HG01099.hp2 HG01261.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.722+13324A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6937435 | |||||||
| chr4:6937484 | C | G | 6 | a0001c0001t0003g0063 a0001c0003t0002g0034 a0001c0003t0003g0032 others(3): Show |
6 | HG02280.hp2 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.722+13373C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6937484 | |||||||
| chr4:6937489 | AC | A | 120 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(117): Show |
120 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.722+13381delC | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6937489 | ||||||
| chr4:6937491 | C | G | 1 | a0001c0001t0025g0093 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.722+13380C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6937491 | |||||||
| chr4:6937512 | A | G | 14 | a0001c0001t0001g0136 a0001c0001t0003g0044 a0001c0001t0003g0063 others(11): Show |
14 | HG02109.hp2 HG02280.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.722+13401A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6937512 | |||||||
| chr4:6937584 | C | A | 23 | a0001c0001t0001g0111 a0001c0001t0001g0136 a0001c0001t0003g0044 others(20): Show |
23 | HG00280.hp1 HG00642.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.722+13473C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6937584 | |||||||
| chr4:6937608 | C | A | 1 | a0001c0001t0002g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.722+13497C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6937608 | |||||||
| chr4:6937611 | C | T | 1 | a0001c0001t0002g0134 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.722+13500C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6937611 | |||||||
| chr4:6937635 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.722+13524G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6937635 | |||||||
| chr4:6937741 | A | G | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.722+13630A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6937741 | |||||||
| chr4:6938120 | C | T | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.722+14009C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6938120 | |||||||
| chr4:6938307 | C | T | 110 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(107): Show |
110 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.722+14196C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6938307 | |||||||
| chr4:6938354 | G | C | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG03491.hp2 HG03492.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.722+14243G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6938354 | |||||||
| chr4:6938724 | G | A | 1 | a0001c0001t0003g0066 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.722+14613G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6938724 | |||||||
| chr4:6938964 | C | A | 1 | a0001c0001t0003g0066 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.722+14853C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6938964 | |||||||
| chr4:6939299 | C | T | 4 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 others(1): Show |
4 | HG01255.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.722+15188C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6939299 | |||||||
| chr4:6939433 | G | A | 28 | a0001c0001t0001g0237 a0001c0001t0003g0063 a0001c0001t0003g0301 others(25): Show |
28 | HG01074.hp2 HG01346.hp1 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.722+15322G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6939433 | |||||||
| chr4:6939542 | A | G | 1 | a0001c0001t0002g0181 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.722+15431A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6939542 | |||||||
| chr4:6939602 | G | A | 2 | a0001c0001t0002g0239 a0001c0001t0002g0240 |
2 | HG00738.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.722+15491G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6939602 | |||||||
| chr4:6939648 | C | T | 267 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(264): Show |
268 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.722+15537C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6939648 | |||||||
| chr4:6939753 | G | A | 6 | a0001c0001t0011g0040 a0001c0003t0002g0034 a0001c0003t0003g0032 others(3): Show |
6 | HG02647.hp1 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.722+15642G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6939753 | |||||||
| chr4:6939810 | G | A | 274 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(271): Show |
275 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.722+15699G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6939810 | |||||||
| chr4:6939854 | G | C | 2 | a0001c0001t0003g0063 a0001c0001t0003g0301 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.722+15743G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6939854 | |||||||
| chr4:6939966 | C | G | 118 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(115): Show |
118 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.722+15855C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6939966 | |||||||
| chr4:6940007 | G | A | 107 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(104): Show |
107 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.722+15896G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6940007 | |||||||
| chr4:6940018 | C | T | 107 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(104): Show |
107 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.722+15907C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6940018 | |||||||
| chr4:6940071 | G | A | 150 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(147): Show |
151 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.722+15960G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6940071 | |||||||
| chr4:6940075 | C | T | 150 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(147): Show |
151 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.722+15964C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6940075 | |||||||
| chr4:6940115 | G | A | 1 | a0002c0002t0002g0020 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.722+16004G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6940115 | |||||||
| chr4:6940131 | C | A | 209 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(206): Show |
209 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.722+16020C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6940131 | |||||||
| chr4:6940133 | A | G | 1 | a0001c0001t0002g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.722+16022A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6940133 | |||||||
| chr4:6940164 | C | T | 107 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(104): Show |
107 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.722+16053C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6940164 | |||||||
| chr4:6940247 | C | T | 10 | a0001c0001t0001g0291 a0001c0001t0002g0276 a0001c0001t0003g0031 others(7): Show |
10 | HG02615.hp2 HG02647.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.722+16136C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6940247 | |||||||
| chr4:6940374 | G | A | 1 | a0001c0001t0002g0174 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.722+16263G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6940374 | |||||||
| chr4:6940411 | G | T | 1 | a0001c0001t0009g0242 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.722+16300G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6940411 | |||||||
| chr4:6940805 | C | T | 1 | a0001c0001t0002g0177 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.722+16694C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6940805 | |||||||
| chr4:6940890 | G | A | 1 | a0001c0001t0002g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.722+16779G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6940890 | |||||||
| chr4:6940916 | C | G | 1 | a0001c0006t0001g0045 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.722+16805C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6940916 | |||||||
| chr4:6941028 | T | G | 1 | a0001c0001t0002g0155 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.722+16917T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6941028 | |||||||
| chr4:6941071 | C | G | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.722+16960C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6941071 | |||||||
| chr4:6941106 | A | G | 3 | a0001c0003t0003g0032 a0001c0003t0003g0033 a0001c0003t0003g0300 |
3 | HG02647.hp1 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.722+16995A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6941106 | |||||||
| chr4:6941112 | C | T | 6 | a0001c0001t0003g0044 a0001c0001t0003g0065 a0001c0001t0003g0068 others(3): Show |
6 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.722+17001C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6941112 | |||||||
| chr4:6941130 | T | G | 156 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
157 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.722+17019T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6941130 | |||||||
| chr4:6941148 | C | A | 1 | a0001c0001t0002g0155 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.722+17037C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6941148 | |||||||
| chr4:6941180 | C | CT | 71 | a0001c0001t0001g0035 a0001c0001t0001g0057 a0001c0001t0001g0084 others(68): Show |
72 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.722+17092dupT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6941180 | ||||||
| chr4:6941180 | CT | C | 25 | a0001c0001t0001g0091 a0001c0001t0001g0105 a0001c0001t0001g0106 others(22): Show |
25 | HG01346.hp1 HG01361.hp1 HG01975.hp2 others(22): Show |
intron_variant | MODIFIER | c.722+17092delT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6941180 | ||||||
| chr4:6941197 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.722+17086T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6941197 | |||||||
| chr4:6941285 | T | A | 273 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(270): Show |
274 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.722+17174T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6941285 | |||||||
| chr4:6941288 | C | T | 1 | a0001c0001t0003g0137 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.722+17177C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6941288 | |||||||
| chr4:6941320 | G | T | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.722+17209G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6941320 | |||||||
| chr4:6941335 | G | A | 5 | a0001c0003t0002g0034 a0001c0003t0003g0032 a0001c0003t0003g0033 others(2): Show |
5 | HG02647.hp1 HG02723.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.722+17224G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6941335 | |||||||
| chr4:6941365 | T | C | 1 | a0001c0001t0007g0194 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.722+17254T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6941365 | |||||||
| chr4:6941412 | C | T | 2 | a0001c0001t0002g0239 a0001c0001t0002g0240 |
2 | HG00738.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.722+17301C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6941412 | |||||||
| chr4:6941565 | A | G | 289 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(286): Show |
290 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.722+17454A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6941565 | |||||||
| chr4:6941586 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.722+17475A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6941586 | |||||||
| chr4:6941633 | C | T | 153 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(150): Show |
154 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.722+17522C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6941633 | |||||||
| chr4:6941642 | TC | T | 117 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(114): Show |
117 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.722+17533delC | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6941642 | ||||||
| chr4:6941770 | C | T | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.722+17659C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6941770 | |||||||
| chr4:6941881 | G | A | 2 | a0001c0001t0002g0064 a0001c0001t0004g0050 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.722+17770G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6941881 | |||||||
| chr4:6941935 | C | T | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.722+17824C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6941935 | |||||||
| chr4:6941936 | G | A | 6 | a0001c0001t0007g0146 a0001c0001t0007g0210 a0001c0001t0007g0211 others(3): Show |
6 | HG02129.hp2 HG04115.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.722+17825G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6941936 | |||||||
| chr4:6942044 | C | T | 102 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(99): Show |
102 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.722+17933C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6942044 | |||||||
| chr4:6942049 | G | T | 151 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(148): Show |
152 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.722+17938G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6942049 | |||||||
| chr4:6942082 | A | G | 289 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(286): Show |
290 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.722+17971A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6942082 | |||||||
| chr4:6942203 | A | AT | 4 | a0001c0001t0001g0217 a0001c0001t0001g0296 a0001c0001t0001g0297 others(1): Show |
4 | HG00741.hp1 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.722+18093dupT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6942203 | ||||||
| chr4:6942306 | A | G | 2 | a0001c0001t0012g0132 a0001c0001t0012g0133 |
2 | HG02257.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.722+18195A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6942306 | |||||||
| chr4:6942750 | A | G | 103 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(100): Show |
103 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.722+18639A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6942750 | |||||||
| chr4:6942776 | G | A | 4 | a0001c0001t0001g0217 a0001c0001t0001g0296 a0001c0001t0001g0297 others(1): Show |
4 | HG00741.hp1 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.722+18665G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6942776 | |||||||
| chr4:6942879 | G | C | 1 | a0001c0001t0012g0133 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.722+18768G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6942879 | |||||||
| chr4:6942936 | C | T | 1 | a0001c0008t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.722+18825C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6942936 | |||||||
| chr4:6943065 | G | A | 107 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(104): Show |
107 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.722+18954G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6943065 | |||||||
| chr4:6943110 | G | C | 1 | a0001c0001t0002g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.722+18999G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6943110 | |||||||
| chr4:6943136 | G | A | 3 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0003g0298 |
3 | HG00741.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.722+19025G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6943136 | |||||||
| chr4:6943166 | A | G | 272 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(269): Show |
273 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.722+19055A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6943166 | |||||||
| chr4:6943294 | A | G | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.722+19183A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6943294 | |||||||
| chr4:6943445 | C | T | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.722+19334C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6943445 | |||||||
| chr4:6943465 | A | G | 159 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(156): Show |
160 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.722+19354A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6943465 | |||||||
| chr4:6943467 | G | A | 2 | a0001c0001t0002g0064 a0001c0001t0004g0050 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.722+19356G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6943467 | |||||||
| chr4:6943506 | A | G | 232 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(229): Show |
232 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.722+19395A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6943506 | |||||||
| chr4:6943742 | G | A | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.722+19631G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6943742 | |||||||
| chr4:6943829 | T | A | 2 | a0001c0001t0002g0064 a0001c0001t0004g0050 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.722+19718T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6943829 | |||||||
| chr4:6943863 | A | G | 34 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(31): Show |
35 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.722+19752A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6943863 | |||||||
| chr4:6943865 | C | A | 34 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(31): Show |
35 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.722+19754C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6943865 | |||||||
| chr4:6943867 | TTTAAATC others(12): Show |
T | 34 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(31): Show |
35 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.722+19759_722+1977 others(23): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6943867 | ||||||
| chr4:6943888 | T | A | 34 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(31): Show |
35 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.722+19777T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6943888 | |||||||
| chr4:6943899 | T | G | 1 | a0001c0001t0002g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.722+19788T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6943899 | |||||||
| chr4:6944000 | C | T | 25 | a0001c0001t0003g0001 a0001c0001t0003g0044 a0001c0001t0003g0049 others(22): Show |
26 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.722+19889C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6944000 | |||||||
| chr4:6944028 | C | CG | 230 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(227): Show |
230 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.722+19922dupG | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6944028 | ||||||
| chr4:6944118 | A | G | 2 | a0001c0001t0002g0064 a0001c0001t0004g0050 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.722+20007A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6944118 | |||||||
| chr4:6944248 | G | A | 4 | a0001c0001t0001g0237 a0002c0002t0004g0012 a0002c0002t0004g0013 others(1): Show |
4 | HG01074.hp2 HG01975.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.722+20137G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6944248 | |||||||
| chr4:6944273 | C | T | 40 | a0001c0001t0001g0138 a0001c0001t0003g0001 a0001c0001t0003g0031 others(37): Show |
41 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.722+20162C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6944273 | |||||||
| chr4:6944365 | G | A | 227 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(224): Show |
227 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.722+20254G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6944365 | |||||||
| chr4:6944380 | G | A | 1 | a0002c0002t0004g0025 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.722+20269G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6944380 | |||||||
| chr4:6944401 | A | G | 40 | a0001c0001t0001g0138 a0001c0001t0003g0001 a0001c0001t0003g0031 others(37): Show |
41 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.722+20290A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6944401 | |||||||
| chr4:6944443 | T | C | 7 | a0001c0001t0001g0290 a0001c0001t0008g0060 a0001c0001t0008g0061 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.722+20332T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6944443 | |||||||
| chr4:6944481 | C | T | 225 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(222): Show |
225 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.722+20370C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6944481 | |||||||
| chr4:6944520 | G | C | 1 | a0001c0001t0002g0196 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.722+20409G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6944520 | |||||||
| chr4:6944677 | C | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0111 |
2 | NA19000.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.722+20566C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6944677 | |||||||
| chr4:6944684 | A | G | 40 | a0001c0001t0001g0138 a0001c0001t0003g0001 a0001c0001t0003g0031 others(37): Show |
41 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.722+20573A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6944684 | |||||||
| chr4:6944754 | C | G | 5 | a0001c0003t0002g0034 a0001c0003t0003g0032 a0001c0003t0003g0033 others(2): Show |
5 | HG02647.hp1 HG02723.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.722+20643C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6944754 | |||||||
| chr4:6944773 | G | T | 227 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(224): Show |
227 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.722+20662G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6944773 | |||||||
| chr4:6944835 | C | G | 2 | a0001c0001t0002g0064 a0001c0001t0004g0050 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.722+20724C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6944835 | |||||||
| chr4:6944843 | C | G | 1 | a0001c0001t0002g0293 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.722+20732C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6944843 | |||||||
| chr4:6944845 | G | A | 17 | a0001c0001t0001g0237 a0002c0002t0002g0020 a0002c0002t0004g0012 others(14): Show |
17 | HG01074.hp2 HG01346.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.722+20734G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6944845 | |||||||
| chr4:6944964 | A | G | 289 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(286): Show |
290 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.722+20853A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6944964 | |||||||
| chr4:6945016 | G | T | 1 | a0001c0001t0002g0166 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.722+20905G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6945016 | |||||||
| chr4:6945133 | G | A | 227 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(224): Show |
227 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.722+21022G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6945133 | |||||||
| chr4:6945149 | T | G | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.722+21038T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6945149 | |||||||
| chr4:6945357 | G | C | 4 | a0002c0002t0002g0020 a0002c0002t0010g0021 a0002c0002t0010g0022 others(1): Show |
4 | HG01346.hp1 HG02135.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.722+21246G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6945357 | |||||||
| chr4:6945394 | C | T | 3 | a0001c0003t0003g0032 a0001c0003t0003g0033 a0001c0003t0003g0300 |
3 | HG02647.hp1 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.722+21283C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6945394 | |||||||
| chr4:6945437 | T | C | 34 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(31): Show |
35 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.722+21326T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6945437 | |||||||
| chr4:6945474 | C | T | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.722+21363C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6945474 | |||||||
| chr4:6945546 | C | T | 5 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(2): Show |
5 | HG01099.hp2 HG01255.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.722+21435C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6945546 | |||||||
| chr4:6945620 | G | A | 5 | a0001c0001t0001g0217 a0001c0001t0001g0296 a0001c0001t0001g0297 others(2): Show |
5 | HG00741.hp1 HG03041.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.722+21509G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6945620 | |||||||
| chr4:6945681 | G | A | 1 | a0001c0001t0002g0197 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.722+21570G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6945681 | |||||||
| chr4:6945706 | G | A | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.722+21595G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6945706 | |||||||
| chr4:6945742 | T | C | 1 | a0001c0011t0002g0206 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.723-21562T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6945742 | |||||||
| chr4:6945749 | C | CA | 7 | a0001c0001t0005g0008 a0001c0001t0005g0037 a0001c0001t0005g0053 others(4): Show |
7 | HG02257.hp2 HG02897.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.723-21521dupA | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6945749 | ||||||
| chr4:6945749 | C | CAAA | 6 | a0002c0002t0004g0026 a0002c0002t0004g0030 a0002c0002t0004g0299 others(3): Show |
6 | HG01346.hp1 HG02055.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.723-21523_723-2152 others(7): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6945749 | ||||||
| chr4:6945749 | C | CAAAA | 7 | a0002c0002t0002g0020 a0002c0002t0004g0012 a0002c0002t0004g0015 others(4): Show |
7 | HG01361.hp1 HG01975.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.723-21524_723-2152 others(8): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6945749 | ||||||
| chr4:6945749 | CAAAAAAA others(1): Show |
C | 16 | a0001c0001t0001g0035 a0001c0001t0001g0058 a0001c0001t0001g0126 others(13): Show |
16 | HG01109.hp1 HG02572.hp1 HG02738.hp2 others(13): Show |
intron_variant | MODIFIER | c.723-21528_723-2152 others(12): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6945749 | ||||||
| chr4:6945749 | CAAAAAAA others(2): Show |
C | 103 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(100): Show |
103 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.723-21529_723-2152 others(13): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6945749 | ||||||
| chr4:6945749 | CAAAAAAA others(3): Show |
C | 139 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(136): Show |
140 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.723-21530_723-2152 others(14): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6945749 | ||||||
| chr4:6945749 | CAAAAAAA others(4): Show |
C | 12 | a0001c0001t0001g0138 a0001c0001t0002g0011 a0001c0001t0002g0179 others(9): Show |
12 | HG01071.hp1 HG01516.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.723-21531_723-2152 others(15): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6945749 | ||||||
| chr4:6945785 | A | G | 40 | a0001c0001t0001g0138 a0001c0001t0003g0001 a0001c0001t0003g0031 others(37): Show |
41 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.723-21519A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6945785 | |||||||
| chr4:6945843 | C | T | 228 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(225): Show |
228 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.723-21461C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6945843 | |||||||
| chr4:6945928 | T | A | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.723-21376T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6945928 | |||||||
| chr4:6945958 | C | G | 271 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(268): Show |
272 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.723-21346C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6945958 | |||||||
| chr4:6946080 | T | C | 271 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(268): Show |
272 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.723-21224T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6946080 | |||||||
| chr4:6946141 | T | C | 2 | a0001c0001t0002g0064 a0001c0001t0004g0050 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.723-21163T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6946141 | |||||||
| chr4:6946184 | G | A | 230 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(227): Show |
230 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.723-21120G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6946184 | |||||||
| chr4:6946442 | C | T | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.723-20862C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6946442 | |||||||
| chr4:6946492 | G | T | 1 | a0001c0001t0003g0086 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.723-20812G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6946492 | |||||||
| chr4:6946601 | G | A | 2 | a0001c0001t0005g0053 a0001c0001t0005g0139 |
2 | HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.723-20703G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6946601 | |||||||
| chr4:6946647 | A | C | 1 | a0001c0001t0001g0087 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.723-20657A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6946647 | |||||||
| chr4:6946804 | C | T | 1 | a0001c0001t0008g0100 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.723-20500C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6946804 | |||||||
| chr4:6946881 | C | T | 1 | a0001c0001t0003g0049 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.723-20423C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6946881 | |||||||
| chr4:6947020 | T | G | 1 | a0001c0003t0002g0034 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.723-20284T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6947020 | |||||||
| chr4:6947038 | T | C | 40 | a0001c0001t0001g0138 a0001c0001t0003g0001 a0001c0001t0003g0031 others(37): Show |
41 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.723-20266T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6947038 | |||||||
| chr4:6947087 | G | A | 1 | a0001c0001t0003g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.723-20217G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6947087 | |||||||
| chr4:6947115 | C | T | 231 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(228): Show |
231 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.723-20189C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6947115 | |||||||
| chr4:6947146 | A | C | 1 | a0001c0001t0002g0165 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.723-20158A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6947146 | |||||||
| chr4:6947196 | T | A | 1 | a0001c0001t0022g0114 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.723-20108T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6947196 | |||||||
| chr4:6947223 | C | T | 230 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(227): Show |
230 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.723-20081C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6947223 | |||||||
| chr4:6947224 | G | T | 1 | a0001c0001t0003g0049 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.723-20080G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6947224 | |||||||
| chr4:6947314 | G | A | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.723-19990G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6947314 | |||||||
| chr4:6947354 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.723-19950C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6947354 | |||||||
| chr4:6947453 | G | A | 1 | a0001c0001t0024g0123 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.723-19851G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6947453 | |||||||
| chr4:6947497 | CA | C | 229 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(226): Show |
229 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.723-19792delA | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6947497 | ||||||
| chr4:6947632 | C | A | 3 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 |
3 | HG01975.hp1 HG02683.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.723-19672C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6947632 | |||||||
| chr4:6947661 | C | CA | 110 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(107): Show |
110 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.723-19625dupA | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6947661 | ||||||
| chr4:6947661 | C | CAA | 9 | a0001c0001t0002g0162 a0001c0001t0002g0177 a0001c0001t0002g0196 others(6): Show |
9 | HG00673.hp1 HG01934.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.723-19626_723-1962 others(6): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6947661 | ||||||
| chr4:6947661 | CA | C | 33 | a0001c0001t0001g0285 a0001c0001t0002g0064 a0001c0001t0002g0295 others(30): Show |
33 | HG01255.hp2 HG01346.hp1 HG01361.hp1 others(30): Show |
intron_variant | MODIFIER | c.723-19625delA | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6947661 | ||||||
| chr4:6947781 | G | C | 34 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(31): Show |
35 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.723-19523G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6947781 | |||||||
| chr4:6947783 | G | T | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.723-19521G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6947783 | |||||||
| chr4:6948128 | T | G | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.723-19176T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6948128 | |||||||
| chr4:6948201 | G | A | 267 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(264): Show |
268 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.723-19103G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6948201 | |||||||
| chr4:6948316 | C | T | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.723-18988C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6948316 | |||||||
| chr4:6948568 | TGG | T | 39 | a0001c0001t0001g0138 a0001c0001t0003g0001 a0001c0001t0003g0031 others(36): Show |
40 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.723-18731_723-1873 others(6): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6948568 | ||||||
| chr4:6948608 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.723-18696C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6948608 | |||||||
| chr4:6948609 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0005g0043 |
2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.723-18695G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6948609 | |||||||
| chr4:6948707 | G | GT | 62 | a0001c0001t0001g0096 a0001c0001t0001g0136 a0001c0001t0001g0237 others(59): Show |
63 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.723-18581dupT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6948707 | ||||||
| chr4:6948707 | G | GTT | 10 | a0001c0001t0001g0138 a0001c0001t0003g0031 a0001c0001t0003g0063 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.723-18582_723-1858 others(6): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6948707 | ||||||
| chr4:6948744 | G | T | 229 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(226): Show |
229 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.723-18560G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6948744 | |||||||
| chr4:6948802 | C | T | 1 | a0001c0001t0002g0177 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.723-18502C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6948802 | |||||||
| chr4:6948844 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.723-18460C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6948844 | |||||||
| chr4:6948968 | C | T | 2 | a0001c0001t0003g0001 a0001c0001t0003g0078 |
3 | HG00323.hp2 HG01123.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.723-18336C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6948968 | |||||||
| chr4:6949034 | C | T | 271 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(268): Show |
272 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.723-18270C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6949034 | |||||||
| chr4:6949042 | C | T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | NA18945.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.723-18262C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6949042 | |||||||
| chr4:6949132 | G | C | 272 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(269): Show |
273 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.723-18172G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6949132 | |||||||
| chr4:6949154 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.723-18150A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6949154 | |||||||
| chr4:6949203 | G | A | 39 | a0001c0001t0001g0138 a0001c0001t0003g0001 a0001c0001t0003g0031 others(36): Show |
40 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.723-18101G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6949203 | |||||||
| chr4:6949512 | A | G | 1 | a0001c0001t0002g0196 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.723-17792A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6949512 | |||||||
| chr4:6949541 | G | A | 1 | a0002c0002t0004g0019 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.723-17763G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6949541 | |||||||
| chr4:6949682 | C | CA | 51 | a0001c0001t0001g0057 a0001c0001t0001g0081 a0001c0001t0001g0084 others(48): Show |
52 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.723-17607dupA | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6949682 | ||||||
| chr4:6949682 | C | CAA | 228 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(225): Show |
228 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.723-17608_723-1760 others(6): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6949682 | ||||||
| chr4:6949724 | T | G | 1 | a0001c0001t0002g0175 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.723-17580T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6949724 | |||||||
| chr4:6949746 | C | T | 5 | a0001c0003t0002g0034 a0001c0003t0003g0032 a0001c0003t0003g0033 others(2): Show |
5 | HG02647.hp1 HG02723.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.723-17558C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6949746 | |||||||
| chr4:6949810 | C | T | 116 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(113): Show |
116 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.723-17494C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6949810 | |||||||
| chr4:6949856 | G | T | 272 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(269): Show |
273 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.723-17448G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6949856 | |||||||
| chr4:6949921 | G | T | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.723-17383G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6949921 | |||||||
| chr4:6949937 | G | A | 2 | a0001c0001t0002g0064 a0001c0001t0004g0050 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.723-17367G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6949937 | |||||||
| chr4:6950061 | C | T | 2 | a0001c0001t0003g0001 a0001c0001t0003g0078 |
3 | HG00323.hp2 HG01123.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.723-17243C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6950061 | |||||||
| chr4:6950117 | C | T | 1 | a0001c0001t0023g0097 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.723-17187C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6950117 | |||||||
| chr4:6950524 | G | A | 230 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(227): Show |
230 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.723-16780G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6950524 | |||||||
| chr4:6950589 | A | AT | 273 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(270): Show |
274 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.723-16714dupT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6950589 | ||||||
| chr4:6950614 | G | A | 2 | a0001c0001t0002g0156 a0001c0001t0002g0189 |
2 | HG00738.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.723-16690G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6950614 | |||||||
| chr4:6950619 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0005g0043 |
2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.723-16685G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6950619 | |||||||
| chr4:6950687 | AT | A | 25 | a0001c0001t0003g0001 a0001c0001t0003g0044 a0001c0001t0003g0049 others(22): Show |
26 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.723-16616delT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6950687 | |||||||
| chr4:6950703 | A | G | 7 | a0001c0001t0001g0290 a0001c0001t0008g0060 a0001c0001t0008g0061 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.723-16601A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6950703 | |||||||
| chr4:6950764 | T | A | 39 | a0001c0001t0001g0138 a0001c0001t0003g0001 a0001c0001t0003g0031 others(36): Show |
40 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.723-16540T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6950764 | |||||||
| chr4:6950857 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.723-16447T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6950857 | |||||||
| chr4:6950950 | A | G | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.723-16354A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6950950 | |||||||
| chr4:6950977 | A | T | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.723-16327A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6950977 | |||||||
| chr4:6951039 | C | T | 34 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(31): Show |
35 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.723-16265C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6951039 | |||||||
| chr4:6951051 | A | G | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.723-16253A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6951051 | |||||||
| chr4:6951222 | A | G | 1 | a0001c0001t0002g0142 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.723-16082A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6951222 | |||||||
| chr4:6951383 | C | T | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.723-15921C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6951383 | |||||||
| chr4:6951543 | A | G | 39 | a0001c0001t0001g0138 a0001c0001t0003g0001 a0001c0001t0003g0031 others(36): Show |
40 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.723-15761A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6951543 | |||||||
| chr4:6951681 | A | AT | 298 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(295): Show |
299 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.723-15623_723-1562 others(5): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6951681 | |||||||
| chr4:6951697 | T | G | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.723-15607T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6951697 | |||||||
| chr4:6951747 | G | T | 2 | a0001c0001t0002g0064 a0001c0001t0004g0050 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.723-15557G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6951747 | |||||||
| chr4:6951871 | G | T | 1 | a0001c0001t0002g0208 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.723-15433G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6951871 | |||||||
| chr4:6951889 | T | C | 1 | a0001c0001t0001g0186 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.723-15415T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6951889 | |||||||
| chr4:6951968 | G | C | 2 | a0001c0001t0001g0138 a0001c0001t0005g0043 |
2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.723-15336G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6951968 | |||||||
| chr4:6952227 | C | G | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.723-15077C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6952227 | |||||||
| chr4:6952281 | C | T | 1 | a0001c0001t0001g0285 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.723-15023C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6952281 | |||||||
| chr4:6952365 | C | G | 38 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(35): Show |
39 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.723-14939C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6952365 | |||||||
| chr4:6952542 | A | G | 1 | a0001c0001t0002g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.723-14762A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6952542 | |||||||
| chr4:6952703 | G | C | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.723-14601G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6952703 | |||||||
| chr4:6952837 | T | G | 46 | a0001c0001t0001g0138 a0001c0001t0001g0285 a0001c0001t0001g0287 others(43): Show |
47 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.723-14467T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6952837 | |||||||
| chr4:6952853 | T | C | 112 | a0001c0001t0001g0150 a0001c0001t0001g0186 a0001c0001t0001g0230 others(109): Show |
112 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.723-14451T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6952853 | |||||||
| chr4:6952899 | G | A | 1 | a0001c0001t0003g0069 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.723-14405G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6952899 | |||||||
| chr4:6952998 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.723-14306C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6952998 | |||||||
| chr4:6952999 | G | A | 2 | a0001c0001t0003g0066 a0001c0001t0003g0067 |
2 | HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.723-14305G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6952999 | |||||||
| chr4:6953010 | T | C | 1 | a0001c0001t0002g0165 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.723-14294T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6953010 | |||||||
| chr4:6953011 | ATTTTTTT others(11): Show |
A | 1 | a0001c0001t0001g0029 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.723-14285_723-1426 others(22): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6953011 | ||||||
| chr4:6953023 | C | CT | 201 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(198): Show |
201 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.723-14263dupT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6953023 | ||||||
| chr4:6953023 | C | CTT | 10 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0104 others(7): Show |
10 | HG00408.hp1 HG00609.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.723-14264_723-1426 others(6): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6953023 | ||||||
| chr4:6953023 | C | CTTT | 6 | a0001c0001t0002g0064 a0001c0001t0002g0295 a0001c0001t0004g0050 others(3): Show |
6 | HG01255.hp2 HG02258.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.723-14265_723-1426 others(7): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6953023 | ||||||
| chr4:6953026 | T | TC | 5 | a0001c0001t0001g0128 a0001c0001t0001g0138 a0001c0001t0003g0031 others(2): Show |
5 | HG02145.hp1 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.723-14278_723-1427 others(5): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6953026 | |||||||
| chr4:6953182 | G | A | 1 | a0001c0001t0002g0174 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.723-14122G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6953182 | |||||||
| chr4:6953182 | G | T | 38 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(35): Show |
39 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.723-14122G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6953182 | |||||||
| chr4:6953185 | C | T | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.723-14119C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6953185 | |||||||
| chr4:6953302 | C | T | 39 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(36): Show |
40 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.723-14002C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6953302 | |||||||
| chr4:6953343 | C | G | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.723-13961C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6953343 | |||||||
| chr4:6953359 | C | T | 111 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(108): Show |
111 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.723-13945C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6953359 | |||||||
| chr4:6953371 | C | T | 25 | a0001c0001t0003g0001 a0001c0001t0003g0044 a0001c0001t0003g0049 others(22): Show |
26 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.723-13933C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6953371 | |||||||
| chr4:6953376 | C | T | 109 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(106): Show |
109 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.723-13928C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6953376 | |||||||
| chr4:6953457 | T | TA | 14 | a0001c0001t0001g0091 a0001c0001t0001g0129 a0001c0001t0002g0294 others(11): Show |
14 | HG02280.hp2 HG02572.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.723-13832dupA | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6953457 | ||||||
| chr4:6953457 | T | TAA | 197 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0048 others(194): Show |
198 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.723-13833_723-1383 others(6): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6953457 | ||||||
| chr4:6953457 | T | TAAA | 57 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0027 others(54): Show |
57 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.723-13834_723-1383 others(7): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6953457 | ||||||
| chr4:6953473 | T | C | 112 | a0001c0001t0001g0150 a0001c0001t0001g0186 a0001c0001t0001g0230 others(109): Show |
112 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.723-13831T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6953473 | |||||||
| chr4:6953583 | G | C | 1 | a0001c0001t0002g0220 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.723-13721G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6953583 | |||||||
| chr4:6953625 | G | A | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.723-13679G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6953625 | |||||||
| chr4:6953629 | C | CA | 49 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(46): Show |
50 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.723-13653dupA | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6953629 | ||||||
| chr4:6953629 | C | CAAAA | 17 | a0001c0001t0001g0029 a0001c0001t0001g0092 a0001c0001t0001g0112 others(14): Show |
17 | HG00639.hp1 HG01070.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.723-13656_723-1365 others(8): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6953629 | ||||||
| chr4:6953629 | C | CAAAAA | 178 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0027 others(175): Show |
178 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.723-13657_723-1365 others(9): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6953629 | ||||||
| chr4:6953629 | C | CAAAAAA | 32 | a0001c0001t0001g0006 a0001c0001t0001g0085 a0001c0001t0001g0116 others(29): Show |
32 | HG00558.hp1 HG00673.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.723-13658_723-1365 others(10): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6953629 | ||||||
| chr4:6953629 | CAAAAAAA others(5): Show |
C | 1 | a0002c0002t0004g0017 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.723-13664_723-1365 others(16): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6953629 | ||||||
| chr4:6953869 | C | CGCTGTGT others(59): Show |
7 | a0001c0001t0001g0290 a0001c0001t0008g0060 a0001c0001t0008g0061 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.723-13385_723-1332 others(70): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6953869 | ||||||
| chr4:6953904 | C | T | 1 | a0001c0001t0002g0159 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.723-13400C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6953904 | |||||||
| chr4:6954045 | G | A | 39 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(36): Show |
40 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.723-13259G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6954045 | |||||||
| chr4:6954074 | G | C | 39 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(36): Show |
40 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.723-13230G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6954074 | |||||||
| chr4:6954117 | G | GC | 7 | a0001c0001t0001g0281 a0001c0001t0001g0296 a0001c0001t0002g0198 others(4): Show |
7 | HG00741.hp2 HG01934.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.723-13182dupC | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6954117 | ||||||
| chr4:6954195 | C | G | 111 | a0001c0001t0001g0150 a0001c0001t0001g0186 a0001c0001t0001g0230 others(108): Show |
111 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.723-13109C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6954195 | |||||||
| chr4:6954245 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.723-13059G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6954245 | |||||||
| chr4:6954332 | T | C | 115 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(112): Show |
115 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.723-12972T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6954332 | |||||||
| chr4:6954359 | C | T | 39 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(36): Show |
40 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.723-12945C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6954359 | |||||||
| chr4:6954407 | T | C | 232 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(229): Show |
232 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.723-12897T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6954407 | |||||||
| chr4:6954436 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.723-12868C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6954436 | |||||||
| chr4:6954525 | C | T | 2 | a0001c0001t0012g0132 a0001c0001t0012g0133 |
2 | HG02257.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.723-12779C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6954525 | |||||||
| chr4:6954548 | G | T | 1 | a0001c0001t0002g0173 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.723-12756G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6954548 | |||||||
| chr4:6954607 | G | GACTA | 274 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(271): Show |
275 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.723-12694_723-1269 others(8): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6954607 | ||||||
| chr4:6954895 | G | A | 7 | a0001c0001t0001g0290 a0001c0001t0008g0060 a0001c0001t0008g0061 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.723-12409G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6954895 | |||||||
| chr4:6954933 | C | G | 4 | a0001c0001t0001g0083 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
4 | HG01106.hp2 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.723-12371C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6954933 | |||||||
| chr4:6954942 | C | T | 1 | a0001c0001t0005g0268 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.723-12362C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6954942 | |||||||
| chr4:6955121 | G | A | 2 | a0002c0002t0004g0024 a0002c0002t0004g0030 |
2 | HG02055.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.723-12183G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6955121 | |||||||
| chr4:6955359 | C | T | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.723-11945C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6955359 | |||||||
| chr4:6955538 | C | T | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.723-11766C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6955538 | |||||||
| chr4:6955539 | T | G | 41 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(38): Show |
42 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.723-11765T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6955539 | |||||||
| chr4:6955570 | T | G | 274 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(271): Show |
275 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.723-11734T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6955570 | |||||||
| chr4:6955605 | G | A | 38 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(35): Show |
39 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.723-11699G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6955605 | |||||||
| chr4:6955660 | G | A | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.723-11644G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6955660 | |||||||
| chr4:6955771 | G | A | 1 | a0001c0001t0002g0276 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.723-11533G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6955771 | |||||||
| chr4:6955875 | G | A | 1 | a0001c0001t0002g0198 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.723-11429G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6955875 | |||||||
| chr4:6955930 | C | T | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.723-11374C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6955930 | |||||||
| chr4:6956018 | G | C | 1 | a0001c0001t0002g0142 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.723-11286G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6956018 | |||||||
| chr4:6956091 | T | A | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.723-11213T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6956091 | |||||||
| chr4:6956130 | G | T | 4 | a0001c0001t0002g0198 a0001c0001t0002g0260 a0001c0001t0002g0261 others(1): Show |
4 | HG01361.hp2 HG01934.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.723-11174G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6956130 | |||||||
| chr4:6956542 | C | G | 10 | a0001c0001t0003g0049 a0001c0001t0003g0070 a0001c0001t0003g0071 others(7): Show |
10 | HG02145.hp2 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.723-10762C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6956542 | |||||||
| chr4:6956676 | C | A | 1 | a0001c0001t0002g0276 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.723-10628C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6956676 | |||||||
| chr4:6956732 | T | C | 5 | a0001c0001t0005g0043 a0001c0001t0011g0039 a0001c0001t0011g0040 others(2): Show |
5 | HG01255.hp2 HG02258.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.723-10572T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6956732 | |||||||
| chr4:6956734 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | NA18942.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.723-10570C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6956734 | |||||||
| chr4:6956833 | G | T | 6 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 others(3): Show |
6 | HG01255.hp2 HG02258.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.723-10471G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6956833 | |||||||
| chr4:6956834 | G | T | 6 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 others(3): Show |
6 | HG01255.hp2 HG02258.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.723-10470G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6956834 | |||||||
| chr4:6956855 | C | T | 26 | a0001c0001t0003g0001 a0001c0001t0003g0044 a0001c0001t0003g0049 others(23): Show |
27 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.723-10449C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6956855 | |||||||
| chr4:6956887 | G | A | 111 | a0001c0001t0001g0058 a0001c0001t0001g0119 a0001c0001t0001g0150 others(108): Show |
111 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.723-10417G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6956887 | |||||||
| chr4:6956997 | A | G | 1 | a0001c0001t0025g0093 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.723-10307A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6956997 | |||||||
| chr4:6957029 | G | A | 1 | a0001c0001t0004g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.723-10275G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6957029 | |||||||
| chr4:6957043 | G | A | 9 | a0001c0001t0005g0053 a0001c0001t0005g0139 a0001c0001t0005g0268 others(6): Show |
9 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.723-10261G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6957043 | |||||||
| chr4:6957074 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.723-10230T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6957074 | |||||||
| chr4:6957255 | T | C | 2 | a0001c0001t0005g0043 a0001c0007t0002g0002 |
2 | NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.723-10049T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6957255 | |||||||
| chr4:6957336 | G | A | 1 | a0001c0001t0003g0086 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.723-9968G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6957336 | |||||||
| chr4:6957453 | G | A | 1 | a0001c0001t0002g0149 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.723-9851G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6957453 | |||||||
| chr4:6957469 | G | C | 1 | a0001c0001t0005g0056 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.723-9835G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6957469 | |||||||
| chr4:6957538 | G | A | 1 | a0001c0001t0002g0166 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.723-9766G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6957538 | |||||||
| chr4:6957555 | A | C | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.723-9749A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6957555 | |||||||
| chr4:6957912 | TAAATAAA others(3): Show |
T | 1 | a0001c0001t0007g0211 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.723-9378_723-9369d others(12): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6957912 | ||||||
| chr4:6957947 | C | CT | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(110): Show |
113 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.723-9345dupT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6957947 | ||||||
| chr4:6957947 | C | CTT | 120 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(117): Show |
120 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.723-9346_723-9345d others(4): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6957947 | ||||||
| chr4:6957959 | T | A | 3 | a0001c0003t0003g0032 a0001c0003t0003g0033 a0001c0003t0003g0300 |
3 | HG02647.hp1 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.723-9345T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6957959 | |||||||
| chr4:6958001 | C | G | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.723-9303C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6958001 | |||||||
| chr4:6958192 | ACT | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0274 |
3 | HG03195.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.723-9111_723-9110d others(4): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6958192 | |||||||
| chr4:6958202 | G | A | 104 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
104 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.723-9102G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6958202 | |||||||
| chr4:6958274 | T | TC | 228 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(225): Show |
228 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.723-9029dupC | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6958274 | ||||||
| chr4:6958374 | T | TACACACA others(9): Show |
1 | a0001c0003t0002g0034 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.723-8929_723-8928i others(18): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6958374 | ||||||
| chr4:6958374 | TATACAC | T | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.723-8928_723-8923d others(8): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6958374 | ||||||
| chr4:6958376 | T | C | 4 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 others(1): Show |
4 | HG02723.hp1 HG03540.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.723-8928T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6958376 | |||||||
| chr4:6958376 | T | TACAC | 21 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(18): Show |
21 | HG00280.hp2 HG00642.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.723-8904_723-8901d others(6): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6958376 | ||||||
| chr4:6958376 | T | TACACAC | 27 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0027 others(24): Show |
27 | HG00323.hp1 HG00733.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.723-8906_723-8901d others(8): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6958376 | ||||||
| chr4:6958376 | T | TACACACA others(1): Show |
143 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(140): Show |
143 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.723-8908_723-8901d others(10): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6958376 | ||||||
| chr4:6958376 | T | TACACACA others(3): Show |
33 | a0001c0001t0001g0005 a0001c0001t0001g0087 a0001c0001t0001g0088 others(30): Show |
33 | HG00639.hp2 HG00741.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.723-8910_723-8901d others(12): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6958376 | ||||||
| chr4:6958376 | T | TACACACA others(5): Show |
6 | a0001c0001t0001g0090 a0001c0001t0001g0112 a0001c0001t0002g0178 others(3): Show |
6 | HG00408.hp2 HG00639.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.723-8912_723-8901d others(14): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6958376 | ||||||
| chr4:6958376 | T | TACACACA others(7): Show |
4 | a0001c0001t0001g0035 a0001c0001t0001g0080 a0001c0001t0001g0081 others(1): Show |
4 | HG00609.hp1 NA18960.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.723-8914_723-8901d others(16): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6958376 | ||||||
| chr4:6958376 | T | TACACACA others(9): Show |
1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.723-8916_723-8901d others(18): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6958376 | ||||||
| chr4:6958376 | T | TACACACA others(13): Show |
1 | a0001c0003t0003g0300 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.723-8920_723-8901d others(22): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6958376 | ||||||
| chr4:6958376 | T | TACACACA others(15): Show |
3 | a0001c0001t0003g0140 a0001c0003t0003g0032 a0001c0003t0003g0033 |
3 | HG02647.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.723-8922_723-8901d others(24): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6958376 | ||||||
| chr4:6958376 | T | TACACACA others(17): Show |
6 | a0001c0001t0003g0070 a0001c0001t0003g0071 a0001c0001t0003g0072 others(3): Show |
6 | HG02451.hp1 HG02818.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.723-8924_723-8901d others(26): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6958376 | ||||||
| chr4:6958376 | T | TACACACA others(19): Show |
2 | a0001c0001t0003g0073 a0001c0001t0003g0074 |
2 | HG02145.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.723-8926_723-8901d others(28): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6958376 | ||||||
| chr4:6958376 | T | TACACACA others(21): Show |
1 | a0001c0001t0003g0049 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.723-8901_723-8900i others(30): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6958376 | ||||||
| chr4:6958376 | T | TATACACA others(11): Show |
3 | a0001c0001t0003g0031 a0001c0001t0003g0063 a0001c0001t0003g0069 |
3 | HG01978.hp2 HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.723-8927_723-8926i others(20): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6958376 | ||||||
| chr4:6958376 | T | TATACACA others(13): Show |
3 | a0001c0001t0003g0001 a0001c0001t0003g0059 a0001c0001t0003g0301 |
3 | HG00280.hp1 HG00323.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.723-8927_723-8926i others(22): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6958376 | ||||||
| chr4:6958376 | T | TATACACA others(15): Show |
2 | a0001c0001t0003g0079 a0001c0001t0003g0086 |
2 | HG00642.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.723-8927_723-8926i others(24): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6958376 | ||||||
| chr4:6958376 | T | TATACACA others(17): Show |
2 | a0001c0001t0003g0044 a0001c0001t0003g0078 |
2 | HG01516.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.723-8927_723-8926i others(26): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6958376 | ||||||
| chr4:6958376 | T | TATACACA others(19): Show |
7 | a0001c0001t0003g0001 a0001c0001t0003g0065 a0001c0001t0003g0066 others(4): Show |
7 | HG01123.hp2 HG01884.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.723-8927_723-8926i others(28): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6958376 | ||||||
| chr4:6958376 | T | TATACACA others(21): Show |
1 | a0001c0001t0003g0137 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.723-8927_723-8926i others(30): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6958376 | ||||||
| chr4:6958376 | TAC | T | 4 | a0001c0001t0005g0053 a0001c0001t0005g0056 a0001c0001t0005g0139 others(1): Show |
4 | HG02258.hp1 HG02897.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.723-8902_723-8901d others(4): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6958376 | ||||||
| chr4:6958413 | G | A | 2 | a0001c0001t0001g0302 a0001c0001t0001g0303 |
2 | NA19010.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.723-8891G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6958413 | |||||||
| chr4:6958432 | T | G | 6 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 others(3): Show |
6 | HG01255.hp2 HG02258.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.723-8872T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6958432 | |||||||
| chr4:6958433 | A | C | 6 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 others(3): Show |
6 | HG01255.hp2 HG02258.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.723-8871A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6958433 | |||||||
| chr4:6958548 | G | A | 289 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(286): Show |
290 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.723-8756G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6958548 | |||||||
| chr4:6958587 | G | A | 3 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0025g0093 |
3 | HG02486.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.723-8717G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6958587 | |||||||
| chr4:6958602 | A | G | 1 | a0001c0001t0009g0003 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.723-8702A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6958602 | |||||||
| chr4:6958849 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.723-8455C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6958849 | |||||||
| chr4:6958889 | A | AT | 233 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(230): Show |
233 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.723-8403dupT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6958889 | ||||||
| chr4:6959074 | G | A | 38 | a0001c0001t0002g0064 a0001c0001t0002g0295 a0001c0001t0003g0001 others(35): Show |
39 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.723-8230G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6959074 | |||||||
| chr4:6959075 | C | T | 105 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(102): Show |
105 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.723-8229C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6959075 | |||||||
| chr4:6959120 | T | C | 34 | a0001c0001t0002g0064 a0001c0001t0002g0295 a0001c0001t0003g0001 others(31): Show |
35 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.723-8184T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6959120 | |||||||
| chr4:6959184 | C | T | 1 | a0002c0002t0004g0024 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.723-8120C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6959184 | |||||||
| chr4:6959229 | A | G | 298 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(295): Show |
299 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.723-8075A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6959229 | |||||||
| chr4:6959247 | T | A | 3 | a0001c0001t0002g0064 a0001c0001t0002g0295 a0001c0001t0004g0050 |
3 | HG02559.hp2 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.723-8057T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6959247 | |||||||
| chr4:6959376 | C | A | 1 | a0001c0001t0030g0158 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.723-7928C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6959376 | |||||||
| chr4:6959380 | G | T | 38 | a0001c0001t0002g0064 a0001c0001t0002g0295 a0001c0001t0003g0001 others(35): Show |
39 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.723-7924G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6959380 | |||||||
| chr4:6959410 | A | C | 10 | a0001c0001t0003g0049 a0001c0001t0003g0070 a0001c0001t0003g0071 others(7): Show |
10 | HG02145.hp2 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.723-7894A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6959410 | |||||||
| chr4:6959675 | C | T | 4 | a0001c0001t0001g0035 a0001c0001t0001g0080 a0001c0001t0001g0081 others(1): Show |
4 | HG00609.hp1 HG01952.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.723-7629C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6959675 | |||||||
| chr4:6959862 | C | T | 235 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(232): Show |
235 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.723-7442C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6959862 | |||||||
| chr4:6959876 | G | C | 6 | a0001c0001t0005g0268 a0001c0001t0005g0270 a0001c0001t0005g0271 others(3): Show |
6 | HG02109.hp2 HG02451.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.723-7428G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6959876 | |||||||
| chr4:6959946 | C | T | 110 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(107): Show |
110 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.723-7358C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6959946 | |||||||
| chr4:6960021 | C | T | 35 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(32): Show |
36 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.723-7283C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6960021 | |||||||
| chr4:6960041 | A | C | 1 | a0002c0002t0004g0025 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.723-7263A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6960041 | |||||||
| chr4:6960074 | T | A | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.723-7230T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6960074 | |||||||
| chr4:6960081 | C | CTT | 108 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(105): Show |
108 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.723-7206_723-7205d others(4): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6960081 | ||||||
| chr4:6960081 | C | CTTT | 12 | a0001c0001t0002g0051 a0001c0001t0002g0149 a0001c0001t0002g0172 others(9): Show |
12 | HG00642.hp1 HG00733.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.723-7207_723-7205d others(5): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6960081 | ||||||
| chr4:6960081 | CT | C | 64 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(61): Show |
65 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.723-7205delT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6960081 | ||||||
| chr4:6960082 | T | C | 1 | a0002c0002t0004g0017 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.723-7222T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6960082 | |||||||
| chr4:6960083 | T | C | 1 | a0001c0001t0003g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.723-7221T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6960083 | |||||||
| chr4:6960090 | T | A | 1 | a0001c0001t0001g0135 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.723-7214T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6960090 | |||||||
| chr4:6960247 | A | AT | 11 | a0001c0001t0001g0058 a0001c0001t0002g0174 a0001c0001t0002g0182 others(8): Show |
11 | HG01934.hp2 HG02818.hp2 HG03540.hp2 others(8): Show |
intron_variant | MODIFIER | c.723-7041dupT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6960247 | ||||||
| chr4:6960334 | C | T | 37 | a0001c0001t0002g0064 a0001c0001t0002g0295 a0001c0001t0003g0001 others(34): Show |
38 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.723-6970C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6960334 | |||||||
| chr4:6960348 | T | A | 2 | a0002c0002t0002g0020 a0002c0002t0010g0021 |
2 | HG02135.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.723-6956T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6960348 | |||||||
| chr4:6960363 | A | G | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.723-6941A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6960363 | |||||||
| chr4:6960507 | A | G | 1 | a0001c0001t0002g0231 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.723-6797A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6960507 | |||||||
| chr4:6960576 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.723-6728A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6960576 | |||||||
| chr4:6960816 | C | T | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.723-6488C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6960816 | |||||||
| chr4:6960883 | C | T | 3 | a0002c0002t0004g0015 a0002c0002t0004g0018 a0002c0002t0004g0026 |
3 | HG01123.hp1 HG02738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.723-6421C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6960883 | |||||||
| chr4:6961001 | T | C | 298 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(295): Show |
299 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.723-6303T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6961001 | |||||||
| chr4:6961009 | C | G | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.723-6295C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6961009 | |||||||
| chr4:6961210 | A | AG | 230 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(227): Show |
230 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.723-6092dupG | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6961210 | ||||||
| chr4:6961230 | C | T | 1 | a0001c0001t0002g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.723-6074C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6961230 | |||||||
| chr4:6961246 | C | G | 252 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(249): Show |
252 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.723-6058C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6961246 | |||||||
| chr4:6961311 | G | T | 286 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(283): Show |
287 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.723-5993G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6961311 | |||||||
| chr4:6961340 | C | T | 1 | a0001c0001t0009g0004 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.723-5964C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6961340 | |||||||
| chr4:6961391 | C | G | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.723-5913C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6961391 | |||||||
| chr4:6961396 | ATCTC | A | 34 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(31): Show |
35 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.723-5904_723-5901d others(6): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6961396 | ||||||
| chr4:6961431 | GC | G | 3 | a0001c0001t0002g0192 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02818.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.723-5872delC | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6961431 | |||||||
| chr4:6961916 | G | A | 1 | a0001c0001t0003g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.723-5388G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6961916 | |||||||
| chr4:6961971 | A | C | 1 | a0001c0001t0003g0068 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.723-5333A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6961971 | |||||||
| chr4:6962092 | G | A | 1 | a0001c0001t0019g0288 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.723-5212G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6962092 | |||||||
| chr4:6962166 | G | A | 33 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(30): Show |
34 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.723-5138G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6962166 | |||||||
| chr4:6962263 | G | A | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.723-5041G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6962263 | |||||||
| chr4:6962321 | G | A | 34 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(31): Show |
35 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.723-4983G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6962321 | |||||||
| chr4:6962527 | T | C | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.723-4777T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6962527 | |||||||
| chr4:6962813 | G | A | 39 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(36): Show |
40 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.723-4491G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6962813 | |||||||
| chr4:6962907 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.723-4397A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6962907 | |||||||
| chr4:6962967 | T | A | 1 | a0002c0002t0004g0025 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.723-4337T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6962967 | |||||||
| chr4:6962974 | G | A | 2 | a0002c0002t0004g0024 a0002c0002t0004g0030 |
2 | HG02055.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.723-4330G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6962974 | |||||||
| chr4:6963016 | G | A | 2 | a0001c0001t0002g0295 a0001c0003t0003g0032 |
2 | HG02647.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.723-4288G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6963016 | |||||||
| chr4:6963155 | C | T | 4 | a0001c0001t0007g0146 a0001c0001t0007g0211 a0001c0001t0007g0212 others(1): Show |
4 | NA18747.hp2 NA18981.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.723-4149C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6963155 | |||||||
| chr4:6963183 | C | G | 34 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(31): Show |
35 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.723-4121C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6963183 | |||||||
| chr4:6963421 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.723-3883A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6963421 | |||||||
| chr4:6963498 | G | A | 1 | a0001c0001t0029g0176 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.723-3806G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6963498 | |||||||
| chr4:6963503 | C | T | 1 | a0001c0011t0002g0206 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.723-3801C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6963503 | |||||||
| chr4:6963555 | C | G | 3 | a0001c0001t0003g0031 a0001c0001t0003g0063 a0001c0001t0003g0301 |
3 | HG02145.hp1 HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.723-3749C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6963555 | |||||||
| chr4:6963568 | G | T | 1 | a0001c0001t0001g0128 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.723-3736G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6963568 | |||||||
| chr4:6963701 | A | T | 34 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(31): Show |
35 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.723-3603A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6963701 | |||||||
| chr4:6963764 | T | C | 119 | a0001c0001t0001g0150 a0001c0001t0001g0186 a0001c0001t0001g0230 others(116): Show |
119 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.723-3540T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6963764 | |||||||
| chr4:6963946 | C | T | 34 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(31): Show |
35 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.723-3358C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6963946 | |||||||
| chr4:6964150 | TA | T | 272 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(269): Show |
273 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.723-3152delA | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6964150 | ||||||
| chr4:6964203 | C | T | 34 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(31): Show |
35 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.723-3101C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6964203 | |||||||
| chr4:6964365 | C | T | 4 | a0001c0001t0002g0204 a0001c0001t0002g0207 a0001c0001t0002g0209 others(1): Show |
4 | HG01243.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.723-2939C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6964365 | |||||||
| chr4:6964444 | A | C | 1 | a0002c0002t0004g0015 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.723-2860A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6964444 | |||||||
| chr4:6964466 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.723-2838A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6964466 | |||||||
| chr4:6964505 | T | G | 1 | a0001c0001t0001g0279 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.723-2799T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6964505 | |||||||
| chr4:6964564 | G | A | 4 | a0002c0002t0002g0020 a0002c0002t0010g0021 a0002c0002t0010g0022 others(1): Show |
4 | HG01346.hp1 HG02135.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.723-2740G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6964564 | |||||||
| chr4:6964575 | T | C | 233 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(230): Show |
233 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.723-2729T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6964575 | |||||||
| chr4:6964975 | T | G | 3 | a0001c0001t0003g0031 a0001c0001t0003g0063 a0001c0001t0003g0301 |
3 | HG02145.hp1 HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.723-2329T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6964975 | |||||||
| chr4:6965171 | TTG | T | 255 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(252): Show |
256 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.723-2132_723-2131d others(4): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6965171 | |||||||
| chr4:6965172 | TG | T | 31 | a0001c0001t0001g0237 a0001c0001t0003g0031 a0001c0001t0003g0063 others(28): Show |
31 | HG01074.hp2 HG01123.hp1 HG01346.hp1 others(28): Show |
intron_variant | MODIFIER | c.723-2130delG | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 6965172 | ||||||
| chr4:6965176 | G | T | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.723-2128G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6965176 | |||||||
| chr4:6965345 | G | A | 1 | a0001c0001t0002g0011 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.723-1959G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6965345 | |||||||
| chr4:6965515 | A | G | 299 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(296): Show |
300 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.723-1789A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6965515 | |||||||
| chr4:6965717 | T | G | 1 | a0001c0003t0003g0267 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.723-1587T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6965717 | |||||||
| chr4:6965756 | G | A | 1 | a0001c0006t0001g0045 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.723-1548G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6965756 | |||||||
| chr4:6966020 | G | C | 34 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(31): Show |
35 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.723-1284G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6966020 | |||||||
| chr4:6966124 | C | A | 1 | a0001c0001t0001g0027 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.723-1180C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6966124 | |||||||
| chr4:6966463 | A | G | 233 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(230): Show |
233 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.723-841A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6966463 | |||||||
| chr4:6966471 | T | C | 1 | a0003c0004t0002g0163 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.723-833T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6966471 | |||||||
| chr4:6966896 | G | A | 1 | a0002c0002t0002g0020 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.723-408G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6966896 | |||||||
| chr4:6966932 | C | G | 1 | a0001c0001t0002g0159 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.723-372C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6966932 | |||||||
| chr4:6967080 | A | T | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.723-224A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6967080 | |||||||
| chr4:6967149 | G | A | 1 | a0001c0001t0030g0158 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.723-155G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6967149 | |||||||
| chr4:6967215 | C | A | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.723-89C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6967215 | |||||||
| chr4:6967215 | C | T | 266 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(263): Show |
267 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.723-89C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6967215 | |||||||
| chr4:6967230 | T | G | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.723-74T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 2/13 | chr4 | 6967230 | |||||||
| chr4:6967436 | A | G | 16 | a0002c0002t0002g0020 a0002c0002t0004g0012 a0002c0002t0004g0013 others(13): Show |
16 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.843+12A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6967436 | |||||||
| chr4:6967568 | G | C | 1 | a0001c0001t0002g0202 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.843+144G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6967568 | |||||||
| chr4:6967578 | T | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0237 |
2 | HG01074.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.843+154T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6967578 | |||||||
| chr4:6967856 | TCTG | T | 9 | a0001c0001t0003g0044 a0001c0001t0003g0065 a0001c0001t0003g0066 others(6): Show |
9 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.843+436_843+438del others(3): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6967856 | ||||||
| chr4:6967861 | T | C | 9 | a0001c0001t0003g0044 a0001c0001t0003g0065 a0001c0001t0003g0066 others(6): Show |
9 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.843+437T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6967861 | |||||||
| chr4:6967862 | G | C | 9 | a0001c0001t0003g0044 a0001c0001t0003g0065 a0001c0001t0003g0066 others(6): Show |
9 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.843+438G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6967862 | |||||||
| chr4:6967863 | G | A | 9 | a0001c0001t0003g0044 a0001c0001t0003g0065 a0001c0001t0003g0066 others(6): Show |
9 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.843+439G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6967863 | |||||||
| chr4:6967886 | T | C | 233 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(230): Show |
233 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.843+462T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6967886 | |||||||
| chr4:6968000 | G | C | 119 | a0001c0001t0001g0150 a0001c0001t0001g0186 a0001c0001t0001g0230 others(116): Show |
119 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.843+576G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6968000 | |||||||
| chr4:6968045 | G | A | 1 | a0001c0001t0003g0086 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.843+621G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6968045 | |||||||
| chr4:6968122 | G | A | 1 | a0001c0011t0002g0206 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.843+698G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6968122 | |||||||
| chr4:6968127 | A | G | 3 | a0001c0001t0002g0064 a0001c0001t0002g0295 a0001c0001t0004g0050 |
3 | HG02559.hp2 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.843+703A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6968127 | |||||||
| chr4:6968156 | T | C | 299 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(296): Show |
300 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.843+732T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6968156 | |||||||
| chr4:6968192 | A | G | 152 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(149): Show |
153 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.843+768A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6968192 | |||||||
| chr4:6968201 | G | T | 24 | a0001c0001t0003g0001 a0001c0001t0003g0044 a0001c0001t0003g0049 others(21): Show |
25 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.843+777G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6968201 | |||||||
| chr4:6968212 | C | T | 1 | a0001c0001t0002g0276 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.843+788C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6968212 | |||||||
| chr4:6968215 | C | T | 33 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(30): Show |
34 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.843+791C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6968215 | |||||||
| chr4:6968479 | G | C | 1 | a0001c0008t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.843+1055G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6968479 | |||||||
| chr4:6968511 | G | A | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.843+1087G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6968511 | |||||||
| chr4:6968563 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.843+1139C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6968563 | |||||||
| chr4:6968658 | C | CAGGAGGC others(11): Show |
22 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(19): Show |
23 | HG00323.hp2 HG01123.hp2 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.843+1251_843+1268d others(20): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6968658 | ||||||
| chr4:6968658 | C | CAGGAGGC others(29): Show |
1 | a0001c0001t0003g0086 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.843+1268_843+1269i others(38): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6968658 | ||||||
| chr4:6968670 | C | CGCCGGGA others(11): Show |
1 | a0001c0001t0006g0171 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.843+1263_843+1264i others(20): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6968670 | ||||||
| chr4:6968673 | C | CGGGAGGA others(11): Show |
109 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0138 others(106): Show |
109 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.843+1263_843+1264i others(20): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6968673 | ||||||
| chr4:6968675 | GGAGGAGG others(11): Show |
G | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 |
3 | NA18955.hp2 NA18977.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.843+1264_843+1281d others(20): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6968675 | ||||||
| chr4:6968680 | A | C | 1 | a0001c0001t0002g0145 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.843+1256A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6968680 | |||||||
| chr4:6968688 | C | CGCCGGGA others(11): Show |
20 | a0001c0001t0002g0244 a0001c0001t0009g0003 a0001c0001t0009g0004 others(17): Show |
20 | HG00639.hp2 HG01123.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.843+1268_843+1269i others(20): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6968688 | ||||||
| chr4:6968688 | C | T | 232 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(229): Show |
232 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.843+1264C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6968688 | |||||||
| chr4:6968691 | C | T | 108 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(105): Show |
108 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.843+1267C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6968691 | |||||||
| chr4:6968693 | A | G | 283 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(280): Show |
284 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.843+1269A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6968693 | |||||||
| chr4:6968706 | T | C | 24 | a0001c0001t0003g0001 a0001c0001t0003g0044 a0001c0001t0003g0049 others(21): Show |
25 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.843+1282T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6968706 | |||||||
| chr4:6968726 | T | C | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.843+1302T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6968726 | |||||||
| chr4:6968733 | T | C | 1 | a0001c0001t0002g0238 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.843+1309T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6968733 | |||||||
| chr4:6968746 | C | G | 1 | a0001c0001t0003g0069 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.843+1322C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6968746 | |||||||
| chr4:6968797 | G | T | 285 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(282): Show |
286 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.843+1373G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6968797 | |||||||
| chr4:6968802 | T | C | 36 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(33): Show |
37 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.843+1378T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6968802 | |||||||
| chr4:6968884 | G | A | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.843+1460G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6968884 | |||||||
| chr4:6968886 | G | A | 1 | a0001c0001t0006g0171 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.843+1462G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6968886 | |||||||
| chr4:6969074 | G | A | 1 | a0001c0008t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.843+1650G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6969074 | |||||||
| chr4:6969081 | C | T | 19 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0029 others(16): Show |
19 | HG00323.hp1 HG00438.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.843+1657C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6969081 | |||||||
| chr4:6969249 | A | G | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.843+1825A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6969249 | |||||||
| chr4:6969250 | T | A | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.843+1826T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6969250 | |||||||
| chr4:6969414 | T | C | 2 | a0001c0001t0002g0064 a0001c0001t0004g0050 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.843+1990T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6969414 | |||||||
| chr4:6969429 | G | A | 110 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(107): Show |
110 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.843+2005G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6969429 | |||||||
| chr4:6969515 | C | T | 1 | a0001c0001t0002g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.843+2091C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6969515 | |||||||
| chr4:6969654 | C | T | 1 | a0001c0001t0002g0188 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.843+2230C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6969654 | |||||||
| chr4:6969878 | G | A | 55 | a0001c0001t0002g0064 a0001c0001t0002g0295 a0001c0001t0003g0001 others(52): Show |
56 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.843+2454G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6969878 | |||||||
| chr4:6969906 | T | G | 2 | a0001c0003t0003g0032 a0001c0003t0003g0033 |
2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.843+2482T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6969906 | |||||||
| chr4:6969929 | C | T | 3 | a0001c0001t0002g0064 a0001c0001t0002g0295 a0001c0001t0004g0050 |
3 | HG02559.hp2 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.843+2505C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6969929 | |||||||
| chr4:6969938 | C | T | 3 | a0002c0002t0004g0012 a0002c0002t0004g0013 a0002c0013t0004g0014 |
3 | HG01975.hp2 HG02004.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.843+2514C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6969938 | |||||||
| chr4:6969952 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0130 |
2 | HG00639.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.843+2528C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6969952 | |||||||
| chr4:6970129 | C | A | 8 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(5): Show |
8 | HG00558.hp1 HG00673.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.843+2705C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6970129 | |||||||
| chr4:6970141 | G | A | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.843+2717G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6970141 | |||||||
| chr4:6970272 | G | A | 1 | a0001c0001t0002g0177 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.843+2848G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6970272 | |||||||
| chr4:6970545 | A | G | 286 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(283): Show |
287 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.843+3121A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6970545 | |||||||
| chr4:6970683 | C | T | 1 | a0001c0001t0003g0059 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.843+3259C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6970683 | |||||||
| chr4:6970776 | C | T | 1 | a0001c0001t0027g0213 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.843+3352C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6970776 | |||||||
| chr4:6970974 | A | G | 1 | a0001c0001t0002g0009 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.843+3550A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6970974 | |||||||
| chr4:6971096 | G | A | 16 | a0002c0002t0002g0020 a0002c0002t0004g0012 a0002c0002t0004g0013 others(13): Show |
16 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.843+3672G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6971096 | |||||||
| chr4:6971293 | T | G | 1 | a0001c0001t0027g0213 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.843+3869T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6971293 | |||||||
| chr4:6971322 | G | T | 24 | a0001c0001t0003g0001 a0001c0001t0003g0044 a0001c0001t0003g0049 others(21): Show |
25 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.843+3898G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6971322 | |||||||
| chr4:6971452 | C | T | 1 | a0001c0001t0001g0007 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.843+4028C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6971452 | |||||||
| chr4:6971457 | G | C | 32 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(29): Show |
33 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.843+4033G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6971457 | |||||||
| chr4:6971564 | A | G | 111 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(108): Show |
111 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.843+4140A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6971564 | |||||||
| chr4:6971641 | A | T | 1 | a0001c0008t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.843+4217A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6971641 | |||||||
| chr4:6971648 | C | T | 1 | a0001c0001t0002g0196 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.843+4224C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6971648 | |||||||
| chr4:6971693 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.843+4269G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6971693 | |||||||
| chr4:6971722 | C | T | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.843+4298C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6971722 | |||||||
| chr4:6971904 | A | G | 2 | a0001c0001t0003g0063 a0001c0001t0003g0301 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.843+4480A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6971904 | |||||||
| chr4:6972105 | C | A | 36 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(33): Show |
37 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.843+4681C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6972105 | |||||||
| chr4:6972380 | C | T | 10 | a0001c0001t0003g0049 a0001c0001t0003g0070 a0001c0001t0003g0071 others(7): Show |
10 | HG02145.hp2 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.843+4956C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6972380 | |||||||
| chr4:6972428 | G | A | 4 | a0001c0001t0002g0149 a0001c0001t0002g0172 a0001c0001t0002g0294 others(1): Show |
4 | HG00642.hp1 HG00733.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.843+5004G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6972428 | |||||||
| chr4:6972517 | A | G | 2 | a0001c0001t0003g0063 a0001c0001t0003g0301 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.843+5093A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6972517 | |||||||
| chr4:6972592 | G | A | 37 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(34): Show |
38 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.843+5168G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6972592 | |||||||
| chr4:6972805 | G | A | 286 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(283): Show |
287 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.843+5381G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6972805 | |||||||
| chr4:6972843 | T | C | 6 | a0001c0001t0001g0217 a0001c0001t0001g0296 a0001c0001t0001g0297 others(3): Show |
6 | HG00741.hp1 HG02559.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.843+5419T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6972843 | |||||||
| chr4:6972961 | G | A | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.843+5537G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6972961 | |||||||
| chr4:6972991 | T | C | 2 | a0001c0001t0002g0244 a0001c0001t0002g0245 |
2 | HG00639.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.843+5567T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6972991 | |||||||
| chr4:6973079 | T | C | 5 | a0001c0001t0003g0298 a0001c0003t0003g0032 a0001c0003t0003g0033 others(2): Show |
5 | HG02647.hp1 HG03130.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.843+5655T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6973079 | |||||||
| chr4:6973281 | A | G | 256 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(253): Show |
257 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.843+5857A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6973281 | |||||||
| chr4:6973298 | A | G | 12 | a0001c0001t0001g0085 a0001c0001t0001g0266 a0001c0001t0001g0277 others(9): Show |
12 | HG00558.hp1 HG00673.hp2 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.843+5874A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6973298 | |||||||
| chr4:6973430 | C | T | 1 | a0001c0001t0026g0117 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.843+6006C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6973430 | |||||||
| chr4:6973884 | C | T | 114 | a0001c0001t0001g0150 a0001c0001t0001g0186 a0001c0001t0001g0230 others(111): Show |
114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.843+6460C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6973884 | |||||||
| chr4:6974083 | C | T | 1 | a0001c0001t0001g0005 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.843+6659C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6974083 | |||||||
| chr4:6974326 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.843+6902C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6974326 | |||||||
| chr4:6974387 | G | C | 2 | a0001c0001t0002g0064 a0001c0001t0004g0050 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.843+6963G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6974387 | |||||||
| chr4:6974414 | A | C | 2 | a0001c0001t0002g0219 a0001c0001t0002g0222 |
2 | HG01109.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.843+6990A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6974414 | |||||||
| chr4:6974583 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0026g0117 |
2 | NA19007.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.843+7159C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6974583 | |||||||
| chr4:6974823 | T | TA | 17 | a0002c0002t0002g0020 a0002c0002t0004g0012 a0002c0002t0004g0013 others(14): Show |
17 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.843+7411dupA | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6974823 | ||||||
| chr4:6974962 | AG | A | 17 | a0002c0002t0002g0020 a0002c0002t0004g0012 a0002c0002t0004g0013 others(14): Show |
17 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.843+7539delG | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6974962 | |||||||
| chr4:6974963 | G | A | 1 | a0001c0001t0003g0067 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.843+7539G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6974963 | |||||||
| chr4:6975140 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.843+7716C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6975140 | |||||||
| chr4:6975156 | C | T | 1 | a0001c0001t0013g0256 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.843+7732C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6975156 | |||||||
| chr4:6975341 | C | T | 1 | a0001c0001t0002g0241 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.843+7917C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6975341 | |||||||
| chr4:6975356 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.843+7932G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6975356 | |||||||
| chr4:6975382 | A | G | 120 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(117): Show |
120 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.843+7958A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6975382 | |||||||
| chr4:6975384 | A | G | 21 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0153 others(18): Show |
21 | HG00323.hp1 HG00438.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.843+7960A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6975384 | |||||||
| chr4:6975441 | T | A | 4 | a0001c0001t0002g0198 a0001c0001t0002g0260 a0001c0001t0002g0261 others(1): Show |
4 | HG01361.hp2 HG01934.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.843+8017T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6975441 | |||||||
| chr4:6975503 | G | A | 1 | a0001c0001t0002g0046 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.843+8079G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6975503 | |||||||
| chr4:6975617 | G | A | 3 | a0001c0001t0002g0064 a0001c0001t0002g0295 a0001c0001t0004g0050 |
3 | HG02559.hp2 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.843+8193G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6975617 | |||||||
| chr4:6975743 | A | G | 1 | a0001c0001t0002g0196 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.843+8319A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6975743 | |||||||
| chr4:6975903 | G | A | 3 | a0001c0001t0001g0217 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG00741.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.843+8479G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6975903 | |||||||
| chr4:6976025 | G | A | 1 | a0001c0001t0002g0199 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.843+8601G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6976025 | |||||||
| chr4:6976308 | A | G | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.843+8884A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6976308 | |||||||
| chr4:6976379 | A | G | 2 | a0001c0001t0001g0099 a0001c0001t0005g0103 |
2 | NA18973.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.843+8955A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6976379 | |||||||
| chr4:6976394 | C | T | 1 | a0001c0001t0031g0082 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.843+8970C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6976394 | |||||||
| chr4:6976455 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.843+9031G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6976455 | |||||||
| chr4:6976470 | A | G | 2 | a0001c0001t0001g0259 a0001c0001t0001g0263 |
2 | HG00323.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.843+9046A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6976470 | |||||||
| chr4:6976525 | G | A | 3 | a0001c0001t0001g0282 a0001c0001t0001g0285 a0001c0001t0001g0289 |
3 | HG00673.hp2 HG02071.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.843+9101G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6976525 | |||||||
| chr4:6976730 | G | A | 1 | a0001c0001t0002g0182 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.843+9306G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6976730 | |||||||
| chr4:6976849 | A | G | 1 | a0001c0001t0001g0281 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.843+9425A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6976849 | |||||||
| chr4:6976900 | A | G | 2 | a0001c0001t0001g0057 a0001c0001t0001g0084 |
2 | NA18975.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.843+9476A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6976900 | |||||||
| chr4:6976947 | T | C | 1 | a0001c0001t0003g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.843+9523T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6976947 | |||||||
| chr4:6977000 | A | G | 118 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(115): Show |
118 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.843+9576A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6977000 | |||||||
| chr4:6977002 | C | A | 37 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(34): Show |
38 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.843+9578C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6977002 | |||||||
| chr4:6977040 | C | T | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.843+9616C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6977040 | |||||||
| chr4:6977063 | T | TCCTCTCC others(14): Show |
1 | a0001c0001t0001g0055 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.843+9655_843+9656i others(23): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977063 | ||||||
| chr4:6977063 | T | TCCTCTCC others(29): Show |
1 | a0001c0001t0001g0148 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.843+9655_843+9656i others(38): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977063 | ||||||
| chr4:6977077 | C | CTCCTCTC others(30): Show |
1 | a0001c0001t0003g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.843+9655_843+9656i others(39): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(47): Show |
2 | a0001c0001t0003g0063 a0001c0001t0003g0301 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.843+9655_843+9656i others(56): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(62): Show |
5 | a0001c0001t0003g0001 a0001c0001t0003g0044 a0001c0001t0003g0066 others(2): Show |
6 | HG00323.hp2 HG01123.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.843+9655_843+9656i others(71): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(79): Show |
17 | a0001c0001t0003g0049 a0001c0001t0003g0065 a0001c0001t0003g0067 others(14): Show |
17 | HG00642.hp2 HG01884.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.843+9655_843+9656i others(88): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(96): Show |
2 | a0001c0001t0003g0059 a0001c0001t0003g0137 |
2 | HG00280.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.843+9655_843+9656i others(105): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(144): Show |
2 | a0001c0001t0002g0052 a0001c0001t0018g0047 |
2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.843+9655_843+9656i others(153): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(129): Show |
7 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0046 others(4): Show |
7 | HG02615.hp2 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.843+9655_843+9656i others(138): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(129): Show |
4 | a0001c0001t0007g0210 a0001c0001t0007g0211 a0001c0001t0007g0212 others(1): Show |
4 | HG02129.hp2 NA18747.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.843+9655_843+9656i others(138): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(97): Show |
1 | a0001c0001t0002g0196 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.843+9655_843+9656i others(106): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(114): Show |
44 | a0001c0001t0002g0009 a0001c0001t0002g0051 a0001c0001t0002g0142 others(41): Show |
44 | HG00438.hp1 HG00558.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.843+9655_843+9656i others(123): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(131): Show |
1 | a0001c0001t0002g0162 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.843+9655_843+9656i others(140): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(120): Show |
1 | a0001c0001t0030g0158 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.843+9655_843+9656i others(129): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(83): Show |
1 | a0001c0008t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.843+9655_843+9656i others(92): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(101): Show |
1 | a0001c0001t0002g0188 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.843+9655_843+9656i others(110): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(114): Show |
3 | a0001c0001t0007g0146 a0001c0001t0007g0200 a0001c0001t0016g0205 |
3 | HG00609.hp2 HG04115.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.843+9655_843+9656i others(123): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(93): Show |
2 | a0001c0001t0002g0193 a0001c0001t0002g0208 |
2 | HG02109.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.843+9655_843+9656i others(102): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(82): Show |
2 | a0001c0001t0002g0214 a0001c0001t0002g0215 |
2 | NA18955.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.843+9655_843+9656i others(91): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(99): Show |
42 | a0001c0001t0001g0150 a0001c0001t0001g0186 a0001c0001t0001g0230 others(39): Show |
42 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.843+9655_843+9656i others(108): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(72): Show |
4 | a0001c0001t0003g0298 a0001c0003t0003g0032 a0001c0003t0003g0033 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.843+9655_843+9656i others(81): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(89): Show |
1 | a0001c0003t0003g0267 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.843+9655_843+9656i others(98): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(61): Show |
1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.843+9655_843+9656i others(70): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(78): Show |
3 | a0001c0001t0001g0217 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG00741.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.843+9655_843+9656i others(87): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(84): Show |
2 | a0001c0001t0002g0295 a0001c0001t0004g0050 |
2 | NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.843+9655_843+9656i others(93): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(34): Show |
1 | a0001c0001t0001g0090 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.843+9655_843+9656i others(43): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(51): Show |
3 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 |
3 | NA18955.hp2 NA18994.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.843+9655_843+9656i others(60): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(84): Show |
2 | a0001c0001t0002g0218 a0001c0001t0002g0220 |
2 | HG02135.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.843+9655_843+9656i others(93): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(57): Show |
1 | a0001c0001t0024g0123 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.843+9655_843+9656i others(66): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(46): Show |
44 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0048 others(41): Show |
44 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.843+9655_843+9656i others(55): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(63): Show |
22 | a0001c0001t0001g0128 a0001c0001t0001g0136 a0001c0001t0001g0263 others(19): Show |
22 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.843+9655_843+9656i others(72): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(69): Show |
1 | a0001c0001t0002g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.843+9655_843+9656i others(78): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(42): Show |
1 | a0002c0002t0004g0013 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.843+9655_843+9656i others(51): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(31): Show |
21 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0062 others(18): Show |
21 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.843+9655_843+9656i others(40): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(48): Show |
33 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0153 others(30): Show |
33 | HG00438.hp2 HG00733.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.843+9655_843+9656i others(57): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCCTCTC others(65): Show |
5 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(2): Show |
5 | HG01169.hp1 HG01975.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.843+9655_843+9656i others(74): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | C | CTCTCCCC others(4): Show |
1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.843+9659_843+9660i others(13): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977077 | CTCTCCCT others(10): Show |
C | 1 | a0001c0001t0009g0242 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.843+9669_843+9685d others(19): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977077 | ||||||
| chr4:6977089 | C | T | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.843+9665C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6977089 | |||||||
| chr4:6977092 | C | T | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.843+9668C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6977092 | |||||||
| chr4:6977093 | T | G | 271 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(268): Show |
272 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.843+9669T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6977093 | |||||||
| chr4:6977135 | T | G | 1 | a0001c0003t0001g0131 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.843+9711T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6977135 | |||||||
| chr4:6977136 | C | T | 1 | a0001c0001t0002g0292 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.843+9712C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6977136 | |||||||
| chr4:6977160 | C | T | 252 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(249): Show |
252 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.843+9736C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6977160 | |||||||
| chr4:6977187 | A | G | 1 | a0001c0008t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.843+9763A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6977187 | |||||||
| chr4:6977198 | C | G | 1 | a0001c0008t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.843+9774C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6977198 | |||||||
| chr4:6977245 | C | G | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.843+9821C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6977245 | |||||||
| chr4:6977269 | C | T | 33 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(30): Show |
34 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.843+9845C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6977269 | |||||||
| chr4:6977356 | C | T | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.843+9932C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6977356 | |||||||
| chr4:6977374 | C | T | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.843+9950C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6977374 | |||||||
| chr4:6977409 | G | A | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.843+9985G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6977409 | |||||||
| chr4:6977415 | G | A | 253 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(250): Show |
253 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.843+9991G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6977415 | |||||||
| chr4:6977430 | G | T | 1 | a0001c0001t0002g0238 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.843+10006G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6977430 | |||||||
| chr4:6977441 | G | A | 2 | a0001c0001t0012g0132 a0001c0001t0012g0133 |
2 | HG02257.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.843+10017G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6977441 | |||||||
| chr4:6977516 | A | G | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0274 |
3 | HG03195.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.843+10092A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6977516 | |||||||
| chr4:6977541 | A | AC | 9 | a0001c0001t0001g0088 a0001c0001t0001g0279 a0001c0001t0001g0282 others(6): Show |
9 | HG00438.hp2 HG00673.hp1 HG00673.hp2 others(6): Show |
intron_variant | MODIFIER | c.843+10121dupC | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977541 | ||||||
| chr4:6977573 | T | G | 1 | a0001c0001t0001g0141 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.843+10149T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6977573 | |||||||
| chr4:6977610 | C | T | 48 | a0001c0001t0001g0186 a0001c0001t0002g0051 a0001c0001t0002g0142 others(45): Show |
48 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.843+10186C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6977610 | |||||||
| chr4:6977628 | A | AAAGTGAG others(73): Show |
33 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(30): Show |
34 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.843+10225_843+1030 others(84): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977628 | ||||||
| chr4:6977649 | CGGCCGCC others(33): Show |
C | 1 | a0001c0001t0001g0107 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.843+10385_843+1042 others(44): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977649 | ||||||
| chr4:6977649 | CGGCCGCC others(73): Show |
C | 255 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(252): Show |
255 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(252): Show |
intron_variant | MODIFIER | c.843+10345_843+1042 others(84): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977649 | ||||||
| chr4:6977831 | G | A | 1 | a0001c0001t0003g0074 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.843+10407G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6977831 | |||||||
| chr4:6977877 | G | A | 17 | a0002c0002t0002g0020 a0002c0002t0004g0012 a0002c0002t0004g0013 others(14): Show |
17 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.843+10453G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6977877 | |||||||
| chr4:6977879 | G | A | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.843+10455G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6977879 | |||||||
| chr4:6977911 | G | A | 22 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0027 others(19): Show |
22 | HG00323.hp1 HG00438.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.843+10487G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6977911 | |||||||
| chr4:6977925 | CGGCCGCC others(30): Show |
C | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.843+10505_843+1054 others(41): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6977925 | ||||||
| chr4:6977962 | T | C | 294 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(291): Show |
295 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.843+10538T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6977962 | |||||||
| chr4:6977998 | C | T | 2 | a0001c0001t0001g0302 a0001c0001t0001g0303 |
2 | NA19010.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.843+10574C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6977998 | |||||||
| chr4:6978003 | G | A | 1 | a0001c0001t0006g0170 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.843+10579G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978003 | |||||||
| chr4:6978007 | GCCACTCC others(206): Show |
G | 1 | a0001c0001t0004g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.843+10588_843+1080 others(4): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6978007 | ||||||
| chr4:6978023 | C | T | 2 | a0001c0001t0002g0197 a0001c0001t0002g0201 |
2 | HG02523.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.843+10599C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978023 | |||||||
| chr4:6978042 | C | T | 1 | a0001c0001t0002g0196 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.843+10618C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978042 | |||||||
| chr4:6978052 | C | T | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.843+10628C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978052 | |||||||
| chr4:6978054 | C | G | 2 | a0001c0001t0002g0187 a0001c0001t0002g0191 |
2 | HG00438.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.843+10630C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978054 | |||||||
| chr4:6978062 | A | AC | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.843+10638_843+1063 others(5): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978062 | |||||||
| chr4:6978064 | G | T | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.843+10640G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978064 | |||||||
| chr4:6978069 | T | A | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.843+10645T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978069 | |||||||
| chr4:6978071 | G | C | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.843+10647G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978071 | |||||||
| chr4:6978073 | G | A | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.843+10649G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978073 | |||||||
| chr4:6978074 | G | C | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.843+10650G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978074 | |||||||
| chr4:6978077 | A | C | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.843+10653A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978077 | |||||||
| chr4:6978088 | T | C | 35 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(32): Show |
36 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.843+10664T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978088 | |||||||
| chr4:6978091 | C | G | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.843+10667C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978091 | |||||||
| chr4:6978097 | G | A | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.843+10673G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978097 | |||||||
| chr4:6978102 | A | G | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.843+10678A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978102 | |||||||
| chr4:6978105 | C | T | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.843+10681C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978105 | |||||||
| chr4:6978141 | T | C | 37 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(34): Show |
38 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.843+10717T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978141 | |||||||
| chr4:6978147 | C | G | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.843+10723C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978147 | |||||||
| chr4:6978150 | C | T | 2 | a0002c0002t0004g0024 a0002c0002t0004g0030 |
2 | HG02055.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.843+10726C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978150 | |||||||
| chr4:6978157 | G | A | 10 | a0001c0001t0003g0049 a0001c0001t0003g0070 a0001c0001t0003g0071 others(7): Show |
10 | HG02145.hp2 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.843+10733G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978157 | |||||||
| chr4:6978182 | C | T | 2 | a0001c0001t0003g0063 a0001c0001t0003g0301 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.843+10758C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978182 | |||||||
| chr4:6978228 | G | C | 1 | a0001c0001t0001g0296 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.843+10804G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978228 | |||||||
| chr4:6978243 | T | C | 1 | a0001c0001t0001g0135 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.843+10819T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978243 | |||||||
| chr4:6978247 | C | G | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.843+10823C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978247 | |||||||
| chr4:6978255 | T | C | 115 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(112): Show |
115 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.843+10831T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978255 | |||||||
| chr4:6978263 | G | C | 1 | a0001c0001t0002g0173 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.843+10839G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978263 | |||||||
| chr4:6978341 | T | C | 298 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(295): Show |
299 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.843+10917T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978341 | |||||||
| chr4:6978342 | G | A | 298 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(295): Show |
299 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.843+10918G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978342 | |||||||
| chr4:6978348 | G | T | 17 | a0002c0002t0002g0020 a0002c0002t0004g0012 a0002c0002t0004g0013 others(14): Show |
17 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.843+10924G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978348 | |||||||
| chr4:6978391 | T | C | 37 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(34): Show |
38 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.843+10967T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978391 | |||||||
| chr4:6978405 | C | A | 2 | a0001c0001t0003g0063 a0001c0001t0003g0301 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.843+10981C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978405 | |||||||
| chr4:6978544 | A | G | 18 | a0001c0001t0001g0279 a0002c0002t0002g0020 a0002c0002t0004g0012 others(15): Show |
18 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.843+11120A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978544 | |||||||
| chr4:6978626 | A | C | 36 | a0001c0001t0002g0229 a0001c0001t0003g0001 a0001c0001t0003g0031 others(33): Show |
37 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.843+11202A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978626 | |||||||
| chr4:6978688 | C | T | 266 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(263): Show |
267 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.843+11264C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978688 | |||||||
| chr4:6978693 | T | C | 37 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(34): Show |
38 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.843+11269T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978693 | |||||||
| chr4:6978738 | T | TA | 22 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(19): Show |
22 | HG00323.hp1 HG00733.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.843+11332dupA | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6978738 | ||||||
| chr4:6978738 | T | TAA | 21 | a0001c0001t0001g0266 a0001c0001t0001g0277 a0001c0001t0001g0279 others(18): Show |
21 | HG00438.hp2 HG01123.hp1 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.843+11331_843+1133 others(6): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6978738 | ||||||
| chr4:6978738 | TA | T | 11 | a0001c0001t0001g0088 a0001c0001t0001g0285 a0001c0001t0002g0177 others(8): Show |
11 | HG00738.hp2 HG02257.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.843+11332delA | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6978738 | ||||||
| chr4:6978738 | TAAA | T | 33 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(30): Show |
34 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.843+11330_843+1133 others(7): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6978738 | ||||||
| chr4:6978739 | A | T | 1 | a0001c0001t0002g0173 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.843+11315A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978739 | |||||||
| chr4:6978752 | A | G | 1 | a0001c0001t0002g0154 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.843+11328A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978752 | |||||||
| chr4:6978871 | CAGT | C | 111 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(108): Show |
111 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.843+11450_843+1145 others(7): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6978871 | ||||||
| chr4:6978989 | G | C | 1 | a0001c0001t0002g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.843+11565G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6978989 | |||||||
| chr4:6979209 | AAAG | A | 8 | a0001c0001t0001g0058 a0001c0001t0001g0111 a0001c0001t0001g0118 others(5): Show |
8 | NA18961.hp1 NA18983.hp1 NA18987.hp2 others(5): Show |
intron_variant | MODIFIER | c.843+11787_843+1178 others(7): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6979209 | ||||||
| chr4:6979392 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.843+11968C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6979392 | |||||||
| chr4:6979481 | C | G | 1 | a0001c0001t0018g0047 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.843+12057C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6979481 | |||||||
| chr4:6979495 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.843+12071C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6979495 | |||||||
| chr4:6979580 | C | G | 1 | a0001c0001t0029g0176 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.843+12156C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6979580 | |||||||
| chr4:6979675 | C | A | 1 | a0001c0001t0002g0165 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.843+12251C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6979675 | |||||||
| chr4:6979675 | C | T | 1 | a0001c0001t0005g0268 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.843+12251C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6979675 | |||||||
| chr4:6979754 | A | C | 1 | a0001c0001t0002g0196 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.843+12330A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6979754 | |||||||
| chr4:6979862 | A | G | 1 | a0001c0001t0003g0059 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.843+12438A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6979862 | |||||||
| chr4:6980070 | G | C | 1 | a0001c0001t0007g0212 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.843+12646G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6980070 | |||||||
| chr4:6980195 | C | T | 3 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0025g0093 |
3 | HG02486.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.843+12771C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6980195 | |||||||
| chr4:6980213 | G | A | 7 | a0001c0001t0007g0146 a0001c0001t0007g0200 a0001c0001t0007g0210 others(4): Show |
7 | HG00609.hp2 HG02129.hp2 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.843+12789G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6980213 | |||||||
| chr4:6980295 | A | C | 1 | a0001c0001t0003g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.843+12871A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6980295 | |||||||
| chr4:6980542 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0104 |
2 | HG02004.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.843+13118G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6980542 | |||||||
| chr4:6980666 | A | G | 1 | a0001c0001t0019g0288 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.843+13242A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6980666 | |||||||
| chr4:6980738 | C | T | 1 | a0001c0001t0002g0191 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.843+13314C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6980738 | |||||||
| chr4:6980888 | T | G | 1 | a0001c0001t0008g0115 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.844-13296T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6980888 | |||||||
| chr4:6980916 | C | T | 1 | a0001c0001t0029g0176 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.844-13268C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6980916 | |||||||
| chr4:6980917 | G | A | 1 | a0001c0001t0002g0201 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.844-13267G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6980917 | |||||||
| chr4:6980936 | C | T | 1 | a0002c0002t0004g0015 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.844-13248C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6980936 | |||||||
| chr4:6981006 | C | T | 1 | a0001c0001t0002g0228 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.844-13178C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6981006 | |||||||
| chr4:6981022 | C | CT | 44 | a0001c0001t0001g0058 a0001c0001t0001g0111 a0001c0001t0001g0118 others(41): Show |
44 | HG01106.hp1 HG01123.hp1 HG01261.hp1 others(41): Show |
intron_variant | MODIFIER | c.844-13143dupT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6981022 | ||||||
| chr4:6981022 | CT | C | 13 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0124 others(10): Show |
13 | HG01074.hp1 HG01099.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.844-13143delT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6981022 | ||||||
| chr4:6981042 | A | T | 35 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(32): Show |
36 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.844-13142A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6981042 | |||||||
| chr4:6981071 | C | T | 3 | a0002c0002t0004g0012 a0002c0002t0004g0013 a0002c0013t0004g0014 |
3 | HG01975.hp2 HG02004.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.844-13113C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6981071 | |||||||
| chr4:6981088 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.844-13096G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6981088 | |||||||
| chr4:6981313 | C | G | 37 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(34): Show |
38 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.844-12871C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6981313 | |||||||
| chr4:6981408 | C | A | 1 | a0002c0002t0004g0024 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.844-12776C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6981408 | |||||||
| chr4:6981503 | C | T | 1 | a0001c0001t0028g0161 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.844-12681C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6981503 | |||||||
| chr4:6981549 | C | A | 36 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(33): Show |
37 | HG00280.hp1 HG00323.hp2 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.844-12635C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6981549 | |||||||
| chr4:6981774 | G | A | 2 | a0001c0001t0002g0064 a0001c0001t0004g0050 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.844-12410G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6981774 | |||||||
| chr4:6981794 | C | G | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.844-12390C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6981794 | |||||||
| chr4:6981941 | C | T | 9 | a0001c0001t0005g0053 a0001c0001t0005g0139 a0001c0001t0005g0268 others(6): Show |
9 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.844-12243C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6981941 | |||||||
| chr4:6981950 | T | C | 117 | a0001c0001t0001g0150 a0001c0001t0001g0186 a0001c0001t0001g0230 others(114): Show |
117 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.844-12234T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6981950 | |||||||
| chr4:6982014 | C | G | 1 | a0001c0001t0002g0220 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.844-12170C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6982014 | |||||||
| chr4:6982015 | T | C | 1 | a0001c0008t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.844-12169T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6982015 | |||||||
| chr4:6982221 | C | T | 1 | a0001c0001t0003g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.844-11963C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6982221 | |||||||
| chr4:6982282 | A | C | 117 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(114): Show |
117 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.844-11902A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6982282 | |||||||
| chr4:6982317 | G | A | 1 | a0001c0001t0003g0069 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.844-11867G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6982317 | |||||||
| chr4:6982424 | A | G | 1 | a0001c0001t0003g0140 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.844-11760A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6982424 | |||||||
| chr4:6982454 | C | T | 33 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(30): Show |
34 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.844-11730C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6982454 | |||||||
| chr4:6982478 | T | G | 1 | a0001c0001t0002g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.844-11706T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6982478 | |||||||
| chr4:6982499 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.844-11685A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6982499 | |||||||
| chr4:6982503 | C | G | 4 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0003c0004t0002g0163 others(1): Show |
4 | HG00558.hp2 NA18747.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.844-11681C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6982503 | |||||||
| chr4:6982614 | A | T | 33 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(30): Show |
34 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.844-11570A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6982614 | |||||||
| chr4:6982713 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.844-11471G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6982713 | |||||||
| chr4:6982737 | C | G | 33 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(30): Show |
34 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.844-11447C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6982737 | |||||||
| chr4:6982826 | G | C | 37 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(34): Show |
38 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.844-11358G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6982826 | |||||||
| chr4:6983404 | A | G | 1 | a0001c0003t0002g0034 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.844-10780A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6983404 | |||||||
| chr4:6983442 | C | G | 1 | a0001c0001t0002g0167 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.844-10742C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6983442 | |||||||
| chr4:6983527 | G | A | 9 | a0001c0001t0001g0035 a0001c0001t0001g0080 a0001c0001t0001g0081 others(6): Show |
9 | HG00609.hp1 HG01258.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.844-10657G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6983527 | |||||||
| chr4:6983576 | G | C | 1 | a0001c0001t0001g0111 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.844-10608G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6983576 | |||||||
| chr4:6983887 | G | A | 37 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(34): Show |
38 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.844-10297G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6983887 | |||||||
| chr4:6984162 | T | C | 289 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(286): Show |
290 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.844-10022T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6984162 | |||||||
| chr4:6984257 | A | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0020g0265 |
3 | HG02559.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.844-9927A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6984257 | |||||||
| chr4:6984330 | C | A | 33 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(30): Show |
34 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.844-9854C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6984330 | |||||||
| chr4:6984334 | C | T | 1 | a0001c0008t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.844-9850C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6984334 | |||||||
| chr4:6984355 | C | T | 1 | a0001c0001t0003g0086 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.844-9829C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6984355 | |||||||
| chr4:6984367 | C | T | 33 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(30): Show |
34 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.844-9817C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6984367 | |||||||
| chr4:6984459 | A | G | 1 | a0001c0001t0003g0069 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.844-9725A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6984459 | |||||||
| chr4:6984481 | T | TAGC | 37 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(34): Show |
38 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.844-9701_844-9700i others(5): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6984481 | ||||||
| chr4:6984509 | T | A | 24 | a0001c0001t0003g0001 a0001c0001t0003g0044 a0001c0001t0003g0049 others(21): Show |
25 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.844-9675T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6984509 | |||||||
| chr4:6984800 | A | G | 1 | a0001c0001t0019g0288 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.844-9384A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6984800 | |||||||
| chr4:6984901 | C | T | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.844-9283C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6984901 | |||||||
| chr4:6984933 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.844-9251G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6984933 | |||||||
| chr4:6984944 | G | T | 6 | a0001c0001t0001g0083 a0001c0001t0001g0124 a0001c0001t0001g0125 others(3): Show |
6 | HG00738.hp1 HG01106.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.844-9240G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6984944 | |||||||
| chr4:6984950 | C | T | 37 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(34): Show |
38 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.844-9234C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6984950 | |||||||
| chr4:6985131 | A | G | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.844-9053A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6985131 | |||||||
| chr4:6985276 | C | T | 17 | a0002c0002t0002g0020 a0002c0002t0004g0012 a0002c0002t0004g0013 others(14): Show |
17 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.844-8908C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6985276 | |||||||
| chr4:6985442 | T | C | 1 | a0002c0002t0015g0247 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.844-8742T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6985442 | |||||||
| chr4:6985526 | G | A | 36 | a0001c0001t0002g0147 a0001c0001t0002g0175 a0001c0001t0002g0177 others(33): Show |
36 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.844-8658G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6985526 | |||||||
| chr4:6985667 | G | T | 289 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(286): Show |
290 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.844-8517G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6985667 | |||||||
| chr4:6985685 | C | T | 37 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(34): Show |
38 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.844-8499C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6985685 | |||||||
| chr4:6985701 | A | G | 107 | a0001c0001t0001g0186 a0001c0001t0002g0009 a0001c0001t0002g0010 others(104): Show |
107 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.844-8483A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6985701 | |||||||
| chr4:6985715 | T | TTAAA | 286 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(283): Show |
287 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.844-8466_844-8465i others(6): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6985715 | ||||||
| chr4:6985736 | T | C | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 |
3 | NA18955.hp2 NA18977.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.844-8448T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6985736 | |||||||
| chr4:6985769 | C | A | 2 | a0001c0001t0003g0063 a0001c0001t0003g0301 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.844-8415C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6985769 | |||||||
| chr4:6985948 | T | G | 3 | a0001c0001t0003g0031 a0001c0001t0003g0063 a0001c0001t0003g0301 |
3 | HG02145.hp1 HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.844-8236T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6985948 | |||||||
| chr4:6985998 | A | T | 6 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(3): Show |
6 | HG01884.hp2 HG02630.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.844-8186A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6985998 | |||||||
| chr4:6986183 | T | C | 37 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(34): Show |
38 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.844-8001T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6986183 | |||||||
| chr4:6986511 | C | T | 106 | a0001c0001t0001g0186 a0001c0001t0002g0009 a0001c0001t0002g0010 others(103): Show |
106 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.844-7673C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6986511 | |||||||
| chr4:6986514 | G | A | 1 | a0001c0003t0002g0034 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.844-7670G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6986514 | |||||||
| chr4:6986550 | ATCTGCGG others(8): Show |
A | 1 | a0001c0001t0001g0127 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.844-7632_844-7618d others(17): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6986550 | ||||||
| chr4:6986797 | G | C | 1 | a0001c0008t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.844-7387G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6986797 | |||||||
| chr4:6986910 | A | G | 2 | a0001c0001t0005g0008 a0001c0001t0005g0037 |
2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.844-7274A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6986910 | |||||||
| chr4:6986950 | G | A | 48 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(45): Show |
49 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.844-7234G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6986950 | |||||||
| chr4:6986987 | G | T | 1 | a0001c0001t0001g0263 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.844-7197G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6986987 | |||||||
| chr4:6987008 | T | G | 2 | a0003c0004t0002g0163 a0003c0004t0002g0164 |
2 | HG00558.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.844-7176T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6987008 | |||||||
| chr4:6987018 | C | A | 36 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(33): Show |
37 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.844-7166C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6987018 | |||||||
| chr4:6987036 | C | G | 3 | a0001c0001t0001g0217 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG00741.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.844-7148C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6987036 | |||||||
| chr4:6987239 | C | A | 1 | a0002c0002t0004g0030 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.844-6945C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6987239 | |||||||
| chr4:6987324 | G | C | 3 | a0001c0001t0006g0170 a0001c0001t0006g0171 a0001c0001t0006g0224 |
3 | HG01192.hp1 HG01934.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.844-6860G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6987324 | |||||||
| chr4:6987396 | C | G | 1 | a0004c0005t0005g0269 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.844-6788C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6987396 | |||||||
| chr4:6987526 | A | G | 1 | a0001c0001t0021g0234 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.844-6658A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6987526 | |||||||
| chr4:6987623 | C | T | 1 | a0001c0001t0021g0234 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.844-6561C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6987623 | |||||||
| chr4:6987894 | T | G | 12 | a0001c0001t0005g0008 a0001c0001t0005g0037 a0001c0001t0005g0053 others(9): Show |
12 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.844-6290T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6987894 | |||||||
| chr4:6987936 | A | T | 1 | a0001c0001t0003g0059 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.844-6248A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6987936 | |||||||
| chr4:6987939 | C | T | 1 | a0001c0001t0005g0056 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.844-6245C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6987939 | |||||||
| chr4:6987951 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.844-6233G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6987951 | |||||||
| chr4:6987970 | G | A | 1 | a0001c0001t0014g0157 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.844-6214G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6987970 | |||||||
| chr4:6987991 | C | T | 36 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(33): Show |
37 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.844-6193C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6987991 | |||||||
| chr4:6988189 | C | T | 1 | a0001c0001t0003g0190 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.844-5995C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6988189 | |||||||
| chr4:6988224 | G | A | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.844-5960G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6988224 | |||||||
| chr4:6988411 | A | G | 1 | a0001c0001t0001g0281 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.844-5773A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6988411 | |||||||
| chr4:6988633 | G | A | 1 | a0001c0001t0002g0228 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.844-5551G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6988633 | |||||||
| chr4:6988647 | C | T | 38 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(35): Show |
39 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.844-5537C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6988647 | |||||||
| chr4:6988766 | G | C | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.844-5418G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6988766 | |||||||
| chr4:6988770 | C | T | 1 | a0001c0001t0002g0276 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.844-5414C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6988770 | |||||||
| chr4:6988842 | C | G | 36 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(33): Show |
37 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.844-5342C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6988842 | |||||||
| chr4:6988885 | C | CT | 90 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0057 others(87): Show |
90 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.844-5276dupT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6988885 | ||||||
| chr4:6988885 | C | CTT | 56 | a0001c0001t0001g0083 a0001c0001t0001g0186 a0001c0001t0001g0266 others(53): Show |
56 | HG00609.hp2 HG01106.hp1 HG01106.hp2 others(53): Show |
intron_variant | MODIFIER | c.844-5277_844-5276d others(4): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6988885 | ||||||
| chr4:6988885 | CT | C | 13 | a0001c0001t0001g0092 a0001c0001t0001g0126 a0001c0001t0003g0298 others(10): Show |
13 | HG01255.hp2 HG02258.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.844-5276delT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6988885 | ||||||
| chr4:6988885 | CTTTT | C | 22 | a0001c0001t0003g0001 a0001c0001t0003g0044 a0001c0001t0003g0049 others(19): Show |
22 | HG00280.hp1 HG00642.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.844-5279_844-5276d others(6): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6988885 | ||||||
| chr4:6988889 | T | C | 1 | a0001c0001t0009g0004 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.844-5295T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6988889 | |||||||
| chr4:6988890 | T | C | 2 | a0001c0001t0009g0003 a0001c0001t0009g0242 |
2 | HG03540.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.844-5294T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6988890 | |||||||
| chr4:6988899 | T | TC | 4 | a0001c0001t0002g0214 a0001c0001t0002g0215 a0001c0001t0002g0225 others(1): Show |
4 | NA18943.hp2 NA18955.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.844-5285_844-5284i others(3): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6988899 | |||||||
| chr4:6989029 | C | T | 1 | a0001c0001t0001g0281 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.844-5155C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6989029 | |||||||
| chr4:6989081 | T | C | 2 | a0001c0001t0003g0063 a0001c0001t0003g0301 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.844-5103T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6989081 | |||||||
| chr4:6989086 | G | C | 39 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(36): Show |
40 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.844-5098G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6989086 | |||||||
| chr4:6989112 | C | T | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.844-5072C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6989112 | |||||||
| chr4:6989216 | C | A | 9 | a0001c0001t0005g0053 a0001c0001t0005g0139 a0001c0001t0005g0268 others(6): Show |
9 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.844-4968C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6989216 | |||||||
| chr4:6989220 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.844-4964G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6989220 | |||||||
| chr4:6989233 | T | G | 39 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(36): Show |
40 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.844-4951T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6989233 | |||||||
| chr4:6989573 | C | T | 1 | a0001c0001t0012g0132 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.844-4611C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6989573 | |||||||
| chr4:6989625 | G | C | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.844-4559G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6989625 | |||||||
| chr4:6989717 | C | T | 1 | a0001c0001t0022g0114 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.844-4467C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6989717 | |||||||
| chr4:6989789 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.844-4395A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6989789 | |||||||
| chr4:6989914 | A | G | 1 | a0001c0001t0002g0159 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.844-4270A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6989914 | |||||||
| chr4:6990067 | C | T | 2 | a0001c0001t0001g0282 a0001c0001t0001g0289 |
2 | HG00673.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.844-4117C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6990067 | |||||||
| chr4:6990304 | C | T | 1 | a0001c0001t0022g0114 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.844-3880C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6990304 | |||||||
| chr4:6990374 | G | A | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.844-3810G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6990374 | |||||||
| chr4:6990435 | C | T | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.844-3749C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6990435 | |||||||
| chr4:6990518 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.844-3666A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6990518 | |||||||
| chr4:6990604 | C | G | 1 | a0001c0001t0002g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.844-3580C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6990604 | |||||||
| chr4:6990651 | G | A | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.844-3533G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6990651 | |||||||
| chr4:6990861 | C | T | 4 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0003c0004t0002g0163 others(1): Show |
4 | HG00558.hp2 NA18747.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.844-3323C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6990861 | |||||||
| chr4:6990903 | A | AG | 72 | a0001c0001t0001g0266 a0001c0001t0001g0277 a0001c0001t0001g0279 others(69): Show |
73 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.844-3280dupG | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6990903 | ||||||
| chr4:6991167 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0020g0265 |
3 | HG02559.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.844-3017C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6991167 | |||||||
| chr4:6991208 | G | A | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.844-2976G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6991208 | |||||||
| chr4:6991244 | G | A | 110 | a0001c0001t0001g0057 a0001c0001t0001g0084 a0001c0001t0001g0186 others(107): Show |
110 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.844-2940G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6991244 | |||||||
| chr4:6991249 | C | T | 34 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(31): Show |
34 | HG00408.hp1 HG01074.hp2 HG01433.hp2 others(31): Show |
intron_variant | MODIFIER | c.844-2935C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6991249 | |||||||
| chr4:6991550 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.844-2634A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6991550 | |||||||
| chr4:6991590 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.844-2594C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6991590 | |||||||
| chr4:6991727 | T | TA | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.844-2456dupA | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 6991727 | ||||||
| chr4:6991760 | G | A | 12 | a0001c0001t0005g0008 a0001c0001t0005g0037 a0001c0001t0005g0053 others(9): Show |
12 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.844-2424G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6991760 | |||||||
| chr4:6992109 | C | T | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.844-2075C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6992109 | |||||||
| chr4:6992210 | G | A | 61 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(58): Show |
62 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.844-1974G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6992210 | |||||||
| chr4:6992284 | G | T | 30 | a0001c0001t0004g0050 a0001c0001t0005g0008 a0001c0001t0005g0037 others(27): Show |
30 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.844-1900G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6992284 | |||||||
| chr4:6992351 | T | C | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.844-1833T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6992351 | |||||||
| chr4:6992354 | G | A | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 |
3 | HG00408.hp1 NA18940.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.844-1830G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6992354 | |||||||
| chr4:6992357 | C | T | 112 | a0001c0001t0001g0150 a0001c0001t0001g0186 a0001c0001t0001g0230 others(109): Show |
112 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.844-1827C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6992357 | |||||||
| chr4:6992451 | C | G | 1 | a0001c0001t0002g0229 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.844-1733C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6992451 | |||||||
| chr4:6992480 | A | G | 2 | a0001c0001t0002g0167 a0001c0001t0002g0174 |
2 | NA18960.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.844-1704A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6992480 | |||||||
| chr4:6992541 | A | G | 1 | a0001c0001t0002g0181 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.844-1643A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6992541 | |||||||
| chr4:6992626 | T | C | 1 | a0001c0001t0002g0183 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.844-1558T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6992626 | |||||||
| chr4:6992762 | C | G | 73 | a0001c0001t0001g0266 a0001c0001t0001g0277 a0001c0001t0001g0279 others(70): Show |
74 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.844-1422C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6992762 | |||||||
| chr4:6992905 | G | A | 1 | a0004c0005t0005g0269 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.844-1279G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6992905 | |||||||
| chr4:6992935 | G | A | 1 | a0001c0001t0002g0226 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.844-1249G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6992935 | |||||||
| chr4:6992939 | A | G | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.844-1245A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6992939 | |||||||
| chr4:6993084 | G | A | 33 | a0001c0001t0001g0266 a0001c0001t0001g0277 a0001c0001t0001g0279 others(30): Show |
33 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(30): Show |
intron_variant | MODIFIER | c.844-1100G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6993084 | |||||||
| chr4:6993114 | A | G | 3 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | HG01070.hp1 HG01071.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.844-1070A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6993114 | |||||||
| chr4:6993150 | A | C | 6 | a0001c0001t0005g0268 a0001c0001t0005g0270 a0001c0001t0005g0271 others(3): Show |
6 | HG02109.hp2 HG02451.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.844-1034A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6993150 | |||||||
| chr4:6993371 | A | G | 2 | a0001c0001t0002g0244 a0001c0001t0002g0245 |
2 | HG00639.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.844-813A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6993371 | |||||||
| chr4:6993383 | G | A | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.844-801G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6993383 | |||||||
| chr4:6993415 | C | T | 1 | a0001c0001t0002g0172 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.844-769C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6993415 | |||||||
| chr4:6993712 | C | T | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.844-472C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6993712 | |||||||
| chr4:6993780 | C | T | 1 | a0001c0001t0002g0196 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.844-404C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6993780 | |||||||
| chr4:6993965 | A | G | 184 | a0001c0001t0001g0138 a0001c0001t0001g0150 a0001c0001t0001g0186 others(181): Show |
185 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.844-219A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6993965 | |||||||
| chr4:6993996 | C | T | 2 | a0001c0001t0003g0001 a0001c0001t0003g0078 |
3 | HG00323.hp2 HG01123.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.844-188C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6993996 | |||||||
| chr4:6994017 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.844-167A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6994017 | |||||||
| chr4:6994130 | G | A | 1 | a0001c0001t0006g0168 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.844-54G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 3/13 | chr4 | 6994130 | |||||||
| chr4:6994329 | G | A | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.962+27G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 4/13 | chr4 | 6994329 | |||||||
| chr4:6994402 | G | A | 74 | a0001c0001t0001g0266 a0001c0001t0001g0277 a0001c0001t0001g0279 others(71): Show |
75 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.962+100G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 4/13 | chr4 | 6994402 | |||||||
| chr4:6994564 | G | A | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.962+262G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 4/13 | chr4 | 6994564 | |||||||
| chr4:6994660 | C | T | 34 | a0001c0001t0002g0009 a0001c0001t0003g0001 a0001c0001t0003g0031 others(31): Show |
35 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.962+358C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 4/13 | chr4 | 6994660 | |||||||
| chr4:6994737 | G | A | 1 | a0001c0001t0003g0086 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.962+435G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 4/13 | chr4 | 6994737 | |||||||
| chr4:6994864 | CA | C | 23 | a0001c0001t0001g0266 a0001c0001t0001g0277 a0001c0001t0001g0279 others(20): Show |
23 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.962+579delA | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 6994864 | ||||||
| chr4:6994864 | CAA | C | 49 | a0001c0001t0002g0009 a0001c0001t0003g0001 a0001c0001t0003g0044 others(46): Show |
50 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.962+578_962+579del others(2): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 6994864 | ||||||
| chr4:6994998 | C | T | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.962+696C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 4/13 | chr4 | 6994998 | |||||||
| chr4:6995012 | G | A | 1 | a0001c0008t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.962+710G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 4/13 | chr4 | 6995012 | |||||||
| chr4:6995027 | G | A | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.962+725G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 4/13 | chr4 | 6995027 | |||||||
| chr4:6995153 | G | A | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.962+851G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 4/13 | chr4 | 6995153 | |||||||
| chr4:6995154 | C | T | 58 | a0001c0001t0002g0009 a0001c0001t0003g0001 a0001c0001t0003g0044 others(55): Show |
59 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.962+852C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 4/13 | chr4 | 6995154 | |||||||
| chr4:6995238 | G | C | 3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 |
3 | HG01261.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.962+936G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 4/13 | chr4 | 6995238 | |||||||
| chr4:6995517 | CT | C | 62 | a0001c0001t0001g0266 a0001c0001t0001g0277 a0001c0001t0001g0279 others(59): Show |
63 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.963-795delT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 6995517 | ||||||
| chr4:6995574 | G | A | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.963-751G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 4/13 | chr4 | 6995574 | |||||||
| chr4:6995669 | T | C | 74 | a0001c0001t0001g0266 a0001c0001t0001g0277 a0001c0001t0001g0279 others(71): Show |
75 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.963-656T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 4/13 | chr4 | 6995669 | |||||||
| chr4:6995763 | C | T | 5 | a0001c0001t0003g0298 a0001c0003t0003g0032 a0001c0003t0003g0033 others(2): Show |
5 | HG02647.hp1 HG03130.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.963-562C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 4/13 | chr4 | 6995763 | |||||||
| chr4:6995843 | T | A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0233 |
2 | NA18984.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.963-482T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 4/13 | chr4 | 6995843 | |||||||
| chr4:6995875 | C | T | 12 | a0001c0001t0005g0008 a0001c0001t0005g0037 a0001c0001t0005g0053 others(9): Show |
12 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.963-450C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 4/13 | chr4 | 6995875 | |||||||
| chr4:6996102 | C | G | 1 | a0001c0001t0001g0099 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.963-223C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 4/13 | chr4 | 6996102 | |||||||
| chr4:6996115 | C | T | 33 | a0001c0001t0004g0050 a0001c0001t0005g0008 a0001c0001t0005g0037 others(30): Show |
33 | HG01123.hp1 HG01255.hp2 HG01346.hp1 others(30): Show |
intron_variant | MODIFIER | c.963-210C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 4/13 | chr4 | 6996115 | |||||||
| chr4:6996123 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.963-202A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 4/13 | chr4 | 6996123 | |||||||
| chr4:6996154 | T | C | 2 | a0001c0001t0001g0280 a0001c0001t0001g0283 |
2 | NA18957.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.963-171T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 4/13 | chr4 | 6996154 | |||||||
| chr4:6996535 | T | TA | 23 | a0001c0001t0001g0263 a0001c0001t0001g0266 a0001c0001t0001g0277 others(20): Show |
23 | HG00323.hp1 HG01123.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.1045+142dupA | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr4 | 6996535 | ||||||
| chr4:6996745 | G | T | 109 | a0001c0001t0001g0186 a0001c0001t0001g0257 a0001c0001t0002g0010 others(106): Show |
109 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1045+338G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 5/13 | chr4 | 6996745 | |||||||
| chr4:6996857 | T | C | 1 | a0001c0001t0022g0114 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1045+450T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 5/13 | chr4 | 6996857 | |||||||
| chr4:6996964 | T | C | 1 | a0001c0001t0026g0117 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1045+557T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 5/13 | chr4 | 6996964 | |||||||
| chr4:6997234 | C | G | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1045+827C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 5/13 | chr4 | 6997234 | |||||||
| chr4:6997364 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1045+957C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 5/13 | chr4 | 6997364 | |||||||
| chr4:6997392 | C | T | 1 | a0001c0008t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1045+985C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 5/13 | chr4 | 6997392 | |||||||
| chr4:6997424 | C | T | 2 | a0001c0001t0002g0207 a0001c0001t0002g0209 |
2 | HG01243.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.1045+1017C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 5/13 | chr4 | 6997424 | |||||||
| chr4:6997480 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1045+1073G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 5/13 | chr4 | 6997480 | |||||||
| chr4:6997574 | C | T | 25 | a0001c0001t0002g0009 a0001c0001t0003g0001 a0001c0001t0003g0044 others(22): Show |
26 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.1045+1167C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 5/13 | chr4 | 6997574 | |||||||
| chr4:6997785 | A | G | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1046-1300A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 5/13 | chr4 | 6997785 | |||||||
| chr4:6997803 | G | A | 1 | a0001c0001t0003g0190 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1046-1282G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 5/13 | chr4 | 6997803 | |||||||
| chr4:6997843 | G | A | 35 | a0001c0001t0001g0266 a0001c0001t0001g0277 a0001c0001t0001g0279 others(32): Show |
35 | HG01123.hp1 HG01255.hp2 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.1046-1242G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 5/13 | chr4 | 6997843 | |||||||
| chr4:6997852 | T | C | 195 | a0001c0001t0001g0138 a0001c0001t0001g0150 a0001c0001t0001g0186 others(192): Show |
196 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.1046-1233T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 5/13 | chr4 | 6997852 | |||||||
| chr4:6998044 | G | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0274 |
3 | HG03195.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1046-1041G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 5/13 | chr4 | 6998044 | |||||||
| chr4:6998150 | A | C | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1046-935A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 5/13 | chr4 | 6998150 | |||||||
| chr4:6998259 | C | G | 1 | a0001c0001t0004g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1046-826C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 5/13 | chr4 | 6998259 | |||||||
| chr4:6998358 | T | TA | 24 | a0001c0001t0001g0084 a0001c0001t0001g0279 a0001c0001t0001g0281 others(21): Show |
24 | HG01255.hp2 HG02109.hp2 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.1046-710dupA | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr4 | 6998358 | ||||||
| chr4:6998546 | C | CT | 39 | a0001c0001t0002g0009 a0001c0001t0002g0225 a0001c0001t0002g0226 others(36): Show |
40 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1046-529dupT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr4 | 6998546 | ||||||
| chr4:6998653 | C | T | 2 | a0001c0001t0001g0266 a0001c0001t0001g0277 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1046-432C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 5/13 | chr4 | 6998653 | |||||||
| chr4:6998655 | T | C | 3 | a0001c0001t0008g0060 a0001c0001t0008g0061 a0001c0001t0008g0100 |
3 | HG02622.hp1 HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1046-430T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 5/13 | chr4 | 6998655 | |||||||
| chr4:6998694 | A | C | 2 | a0001c0001t0002g0064 a0001c0001t0002g0295 |
2 | HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1046-391A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 5/13 | chr4 | 6998694 | |||||||
| chr4:6998757 | T | C | 9 | a0001c0001t0005g0053 a0001c0001t0005g0139 a0001c0001t0005g0268 others(6): Show |
9 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1046-328T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 5/13 | chr4 | 6998757 | |||||||
| chr4:6998953 | G | A | 29 | a0001c0001t0004g0050 a0001c0001t0005g0008 a0001c0001t0005g0037 others(26): Show |
29 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(26): Show |
intron_variant | MODIFIER | c.1046-132G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 5/13 | chr4 | 6998953 | |||||||
| chr4:6999333 | C | T | 3 | a0001c0001t0002g0219 a0001c0001t0002g0221 a0001c0001t0002g0222 |
3 | HG01109.hp2 HG01952.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1163+131C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 6/13 | chr4 | 6999333 | |||||||
| chr4:6999408 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1163+206C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 6/13 | chr4 | 6999408 | |||||||
| chr4:6999553 | C | T | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1163+351C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 6/13 | chr4 | 6999553 | |||||||
| chr4:6999787 | A | C | 1 | a0001c0001t0001g0029 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1163+585A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 6/13 | chr4 | 6999787 | |||||||
| chr4:6999936 | C | T | 2 | a0001c0001t0001g0259 a0001c0001t0001g0263 |
2 | HG00323.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1163+734C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 6/13 | chr4 | 6999936 | |||||||
| chr4:7000054 | G | A | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1163+852G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 6/13 | chr4 | 7000054 | |||||||
| chr4:7000055 | G | A | 1 | a0001c0001t0003g0190 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1163+853G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 6/13 | chr4 | 7000055 | |||||||
| chr4:7000112 | A | G | 1 | a0001c0001t0002g0223 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1163+910A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 6/13 | chr4 | 7000112 | |||||||
| chr4:7000247 | G | A | 1 | a0001c0008t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1164-898G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 6/13 | chr4 | 7000247 | |||||||
| chr4:7000283 | C | T | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1164-862C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 6/13 | chr4 | 7000283 | |||||||
| chr4:7000311 | G | A | 105 | a0001c0001t0001g0186 a0001c0001t0002g0009 a0001c0001t0002g0010 others(102): Show |
105 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1164-834G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 6/13 | chr4 | 7000311 | |||||||
| chr4:7000393 | C | T | 24 | a0001c0001t0003g0001 a0001c0001t0003g0044 a0001c0001t0003g0049 others(21): Show |
25 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.1164-752C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 6/13 | chr4 | 7000393 | |||||||
| chr4:7000455 | CA | C | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0274 |
3 | HG03195.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1164-689delA | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 6/13 | chr4 | 7000455 | |||||||
| chr4:7000552 | G | T | 1 | a0001c0001t0002g0221 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1164-593G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 6/13 | chr4 | 7000552 | |||||||
| chr4:7000617 | A | G | 108 | a0001c0001t0001g0186 a0001c0001t0002g0009 a0001c0001t0002g0010 others(105): Show |
108 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.1164-528A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 6/13 | chr4 | 7000617 | |||||||
| chr4:7000650 | G | C | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1164-495G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 6/13 | chr4 | 7000650 | |||||||
| chr4:7000701 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1164-444C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 6/13 | chr4 | 7000701 | |||||||
| chr4:7000749 | G | A | 4 | a0001c0001t0002g0204 a0001c0001t0002g0207 a0001c0001t0002g0209 others(1): Show |
4 | HG01243.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1164-396G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 6/13 | chr4 | 7000749 | |||||||
| chr4:7000851 | C | T | 1 | a0001c0001t0002g0209 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1164-294C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 6/13 | chr4 | 7000851 | |||||||
| chr4:7000879 | A | T | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1164-266A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 6/13 | chr4 | 7000879 | |||||||
| chr4:7000880 | A | T | 2 | a0001c0001t0002g0064 a0001c0001t0002g0295 |
2 | HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1164-265A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 6/13 | chr4 | 7000880 | |||||||
| chr4:7000962 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1164-183G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 6/13 | chr4 | 7000962 | |||||||
| chr4:7001047 | G | A | 7 | a0001c0001t0001g0290 a0001c0001t0008g0060 a0001c0001t0008g0061 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1164-98G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 6/13 | chr4 | 7001047 | |||||||
| chr4:7001076 | C | T | 261 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(258): Show |
262 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.1164-69C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 6/13 | chr4 | 7001076 | |||||||
| chr4:7001453 | C | T | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1270+202C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7001453 | |||||||
| chr4:7001544 | C | A | 1 | a0001c0001t0001g0186 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1270+293C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7001544 | |||||||
| chr4:7001545 | A | G | 1 | a0001c0001t0002g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1270+294A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7001545 | |||||||
| chr4:7001600 | G | T | 1 | a0002c0002t0004g0017 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1270+349G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7001600 | |||||||
| chr4:7001610 | C | T | 12 | a0001c0001t0005g0008 a0001c0001t0005g0037 a0001c0001t0005g0053 others(9): Show |
12 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1270+359C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7001610 | |||||||
| chr4:7001639 | T | A | 108 | a0001c0001t0001g0186 a0001c0001t0002g0009 a0001c0001t0002g0010 others(105): Show |
108 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.1270+388T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7001639 | |||||||
| chr4:7001737 | G | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0274 |
3 | HG03195.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1270+486G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7001737 | |||||||
| chr4:7001832 | G | A | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1270+581G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7001832 | |||||||
| chr4:7001925 | G | A | 1 | a0002c0002t0010g0022 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1270+674G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7001925 | |||||||
| chr4:7001979 | C | T | 16 | a0001c0001t0005g0008 a0001c0001t0005g0037 a0001c0001t0005g0053 others(13): Show |
16 | HG01255.hp2 HG02109.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1270+728C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7001979 | |||||||
| chr4:7002280 | C | T | 16 | a0001c0001t0005g0008 a0001c0001t0005g0037 a0001c0001t0005g0043 others(13): Show |
16 | HG01255.hp2 HG02109.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1270+1029C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7002280 | |||||||
| chr4:7002501 | G | A | 1 | a0001c0001t0002g0218 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1270+1250G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7002501 | |||||||
| chr4:7002511 | C | T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | NA18945.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1270+1260C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7002511 | |||||||
| chr4:7002533 | A | G | 1 | a0001c0001t0001g0281 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1270+1282A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7002533 | |||||||
| chr4:7002768 | G | A | 226 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(223): Show |
226 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.1270+1517G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7002768 | |||||||
| chr4:7002773 | T | A | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1270+1522T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7002773 | |||||||
| chr4:7002779 | G | A | 225 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(222): Show |
225 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.1270+1528G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7002779 | |||||||
| chr4:7003186 | T | C | 5 | a0001c0001t0003g0298 a0001c0003t0003g0032 a0001c0003t0003g0033 others(2): Show |
5 | HG02647.hp1 HG03130.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1271-1658T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7003186 | |||||||
| chr4:7003310 | G | T | 76 | a0001c0001t0001g0266 a0001c0001t0001g0277 a0001c0001t0001g0279 others(73): Show |
77 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.1271-1534G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7003310 | |||||||
| chr4:7003336 | A | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG00609.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1271-1508A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7003336 | |||||||
| chr4:7003389 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1271-1455G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7003389 | |||||||
| chr4:7003410 | T | A | 1 | a0001c0001t0002g0220 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1271-1434T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7003410 | |||||||
| chr4:7003469 | G | A | 225 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(222): Show |
225 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.1271-1375G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7003469 | |||||||
| chr4:7003472 | C | G | 110 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(107): Show |
110 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.1271-1372C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7003472 | |||||||
| chr4:7003700 | A | C | 1 | a0001c0001t0001g0141 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1271-1144A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7003700 | |||||||
| chr4:7003800 | G | C | 1 | a0001c0001t0002g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1271-1044G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7003800 | |||||||
| chr4:7003861 | A | G | 55 | a0001c0001t0002g0009 a0001c0001t0002g0064 a0001c0001t0002g0276 others(52): Show |
56 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.1271-983A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7003861 | |||||||
| chr4:7003867 | G | A | 25 | a0001c0001t0002g0276 a0001c0001t0003g0001 a0001c0001t0003g0044 others(22): Show |
26 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.1271-977G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7003867 | |||||||
| chr4:7003918 | TGA | T | 17 | a0001c0001t0002g0064 a0001c0001t0005g0008 a0001c0001t0005g0037 others(14): Show |
17 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1271-923_1271-922d others(4): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr4 | 7003918 | ||||||
| chr4:7003958 | A | G | 2 | a0001c0001t0012g0132 a0001c0001t0012g0133 |
2 | HG02257.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1271-886A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7003958 | |||||||
| chr4:7004026 | C | T | 225 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(222): Show |
225 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.1271-818C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7004026 | |||||||
| chr4:7004060 | G | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0237 |
2 | HG01074.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1271-784G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7004060 | |||||||
| chr4:7004112 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1271-732G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7004112 | |||||||
| chr4:7004257 | A | T | 1 | a0001c0001t0007g0194 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1271-587A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7004257 | |||||||
| chr4:7004299 | C | T | 1 | a0001c0001t0002g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1271-545C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7004299 | |||||||
| chr4:7004364 | G | A | 2 | a0001c0001t0003g0063 a0001c0001t0003g0301 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1271-480G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7004364 | |||||||
| chr4:7004529 | C | T | 17 | a0001c0001t0002g0064 a0001c0001t0005g0008 a0001c0001t0005g0037 others(14): Show |
17 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1271-315C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7004529 | |||||||
| chr4:7004536 | A | T | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1271-308A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7004536 | |||||||
| chr4:7004542 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1271-302C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7004542 | |||||||
| chr4:7004605 | G | A | 1 | a0001c0001t0027g0213 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1271-239G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7004605 | |||||||
| chr4:7004624 | C | G | 4 | a0001c0001t0002g0198 a0001c0001t0002g0260 a0001c0001t0002g0261 others(1): Show |
4 | HG01361.hp2 HG01934.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1271-220C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7004624 | |||||||
| chr4:7004671 | A | G | 20 | a0001c0001t0001g0266 a0001c0001t0001g0277 a0001c0001t0001g0279 others(17): Show |
20 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.1271-173A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7004671 | |||||||
| chr4:7004696 | G | C | 1 | a0001c0001t0027g0213 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1271-148G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7004696 | |||||||
| chr4:7004741 | A | G | 1 | a0001c0001t0002g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1271-103A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7004741 | |||||||
| chr4:7004814 | G | A | 40 | a0001c0001t0001g0266 a0001c0001t0001g0277 a0001c0001t0001g0279 others(37): Show |
40 | HG01123.hp1 HG01255.hp2 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.1271-30G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 7/13 | chr4 | 7004814 | |||||||
| chr4:7005012 | A | T | 1 | a0001c0001t0022g0114 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1351+88A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 8/13 | chr4 | 7005012 | |||||||
| chr4:7005072 | G | GT | 16 | a0001c0001t0005g0008 a0001c0001t0005g0037 a0001c0001t0005g0053 others(13): Show |
16 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1351+156dupT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr4 | 7005072 | ||||||
| chr4:7005139 | C | T | 1 | a0001c0001t0003g0190 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1351+215C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 8/13 | chr4 | 7005139 | |||||||
| chr4:7005187 | G | A | 20 | a0001c0001t0002g0064 a0001c0001t0005g0008 a0001c0001t0005g0037 others(17): Show |
20 | HG01255.hp2 HG02109.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1351+263G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 8/13 | chr4 | 7005187 | |||||||
| chr4:7005274 | G | A | 1 | a0001c0001t0005g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1351+350G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 8/13 | chr4 | 7005274 | |||||||
| chr4:7005734 | C | A | 20 | a0001c0001t0002g0064 a0001c0001t0005g0008 a0001c0001t0005g0037 others(17): Show |
20 | HG01255.hp2 HG02109.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1351+810C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 8/13 | chr4 | 7005734 | |||||||
| chr4:7005765 | C | G | 1 | a0001c0001t0002g0166 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1351+841C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 8/13 | chr4 | 7005765 | |||||||
| chr4:7005990 | G | A | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1352-642G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 8/13 | chr4 | 7005990 | |||||||
| chr4:7006150 | CAAAG | C | 17 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(14): Show |
17 | HG00323.hp1 HG00438.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.1352-476_1352-473d others(6): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr4 | 7006150 | ||||||
| chr4:7006222 | T | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0278 |
2 | HG03491.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1352-410T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 8/13 | chr4 | 7006222 | |||||||
| chr4:7006273 | A | AATATG | 14 | a0001c0001t0002g0064 a0001c0001t0005g0008 a0001c0001t0005g0037 others(11): Show |
14 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1352-359_1352-358i others(7): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 8/13 | chr4 | 7006273 | |||||||
| chr4:7006273 | A | AATATGTG | 6 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 others(3): Show |
6 | HG01255.hp2 HG02258.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1352-359_1352-358i others(9): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 8/13 | chr4 | 7006273 | |||||||
| chr4:7006275 | A | ATG | 6 | a0001c0001t0002g0177 a0001c0001t0002g0187 a0001c0001t0002g0191 others(3): Show |
6 | HG00438.hp1 HG00673.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.1352-339_1352-338d others(4): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr4 | 7006275 | ||||||
| chr4:7006275 | A | G | 20 | a0001c0001t0002g0064 a0001c0001t0005g0008 a0001c0001t0005g0037 others(17): Show |
20 | HG01255.hp2 HG02109.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1352-357A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 8/13 | chr4 | 7006275 | |||||||
| chr4:7006351 | T | A | 2 | a0001c0001t0001g0302 a0001c0001t0001g0303 |
2 | NA19010.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1352-281T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 8/13 | chr4 | 7006351 | |||||||
| chr4:7006351 | T | G | 118 | a0001c0001t0001g0085 a0001c0001t0001g0150 a0001c0001t0001g0186 others(115): Show |
118 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.1352-281T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 8/13 | chr4 | 7006351 | |||||||
| chr4:7006734 | G | T | 1 | a0001c0001t0003g0063 | 1 | HG02280.hp2 | splice_region_variant&intron_variant | LOW | c.1446+8G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7006734 | |||||||
| chr4:7006787 | C | A | 1 | a0001c0001t0001g0291 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1446+61C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7006787 | |||||||
| chr4:7006870 | A | G | 1 | a0004c0005t0005g0269 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1446+144A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7006870 | |||||||
| chr4:7006972 | A | G | 1 | a0001c0001t0014g0157 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1446+246A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7006972 | |||||||
| chr4:7007063 | G | A | 16 | a0001c0001t0005g0008 a0001c0001t0005g0037 a0001c0001t0005g0043 others(13): Show |
16 | HG01255.hp2 HG02109.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1446+337G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7007063 | |||||||
| chr4:7007155 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1446+429G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7007155 | |||||||
| chr4:7007261 | G | A | 1 | a0001c0001t0022g0114 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1446+535G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7007261 | |||||||
| chr4:7007456 | C | T | 1 | a0001c0001t0003g0059 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1446+730C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7007456 | |||||||
| chr4:7007460 | G | A | 1 | a0001c0008t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1446+734G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7007460 | |||||||
| chr4:7007546 | G | A | 3 | a0001c0001t0003g0031 a0001c0001t0003g0063 a0001c0001t0003g0301 |
3 | HG02145.hp1 HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1446+820G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7007546 | |||||||
| chr4:7007604 | G | T | 1 | a0001c0001t0002g0155 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1446+878G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7007604 | |||||||
| chr4:7007640 | C | T | 2 | a0001c0001t0003g0001 a0001c0001t0003g0078 |
3 | HG00323.hp2 HG01123.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1446+914C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7007640 | |||||||
| chr4:7007644 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0005g0103 |
2 | NA18973.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1446+918C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7007644 | |||||||
| chr4:7007746 | C | A | 1 | a0001c0001t0001g0127 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1446+1020C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7007746 | |||||||
| chr4:7007764 | C | T | 6 | a0001c0001t0002g0155 a0001c0001t0007g0146 a0001c0001t0007g0200 others(3): Show |
6 | HG00609.hp2 HG04115.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.1446+1038C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7007764 | |||||||
| chr4:7007813 | G | T | 1 | a0001c0001t0007g0210 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1446+1087G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7007813 | |||||||
| chr4:7007848 | T | G | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1446+1122T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7007848 | |||||||
| chr4:7007866 | G | A | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1446+1140G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7007866 | |||||||
| chr4:7007897 | G | A | 6 | a0001c0001t0001g0083 a0001c0001t0001g0124 a0001c0001t0001g0125 others(3): Show |
6 | HG00738.hp1 HG01106.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.1446+1171G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7007897 | |||||||
| chr4:7007949 | A | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0104 |
2 | HG02004.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1446+1223A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7007949 | |||||||
| chr4:7008036 | C | A | 12 | a0001c0001t0005g0008 a0001c0001t0005g0037 a0001c0001t0005g0053 others(9): Show |
12 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1446+1310C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7008036 | |||||||
| chr4:7008079 | C | T | 109 | a0001c0001t0001g0085 a0001c0001t0001g0186 a0001c0001t0002g0010 others(106): Show |
109 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1446+1353C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7008079 | |||||||
| chr4:7008094 | T | C | 1 | a0001c0001t0002g0166 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1446+1368T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7008094 | |||||||
| chr4:7008138 | C | T | 1 | a0001c0001t0013g0258 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1446+1412C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7008138 | |||||||
| chr4:7008139 | G | C | 19 | a0001c0001t0005g0008 a0001c0001t0005g0037 a0001c0001t0005g0043 others(16): Show |
19 | HG01255.hp2 HG02109.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1446+1413G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7008139 | |||||||
| chr4:7008537 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1447-1340C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7008537 | |||||||
| chr4:7008538 | G | A | 1 | a0001c0001t0002g0179 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1447-1339G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7008538 | |||||||
| chr4:7008562 | A | G | 1 | a0001c0010t0002g0036 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1447-1315A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7008562 | |||||||
| chr4:7008586 | C | T | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
281 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.1447-1291C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7008586 | |||||||
| chr4:7008777 | G | A | 106 | a0001c0001t0001g0186 a0001c0001t0002g0010 a0001c0001t0002g0011 others(103): Show |
106 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1447-1100G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7008777 | |||||||
| chr4:7008963 | A | G | 1 | a0001c0003t0003g0267 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1447-914A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7008963 | |||||||
| chr4:7009026 | T | C | 2 | a0001c0001t0012g0132 a0001c0001t0012g0133 |
2 | HG02257.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1447-851T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7009026 | |||||||
| chr4:7009277 | G | A | 1 | a0001c0001t0002g0187 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1447-600G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7009277 | |||||||
| chr4:7009300 | T | C | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1447-577T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7009300 | |||||||
| chr4:7009306 | A | G | 1 | a0001c0001t0001g0290 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1447-571A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7009306 | |||||||
| chr4:7009395 | A | G | 1 | a0001c0001t0004g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1447-482A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7009395 | |||||||
| chr4:7009459 | G | A | 278 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(275): Show |
279 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.1447-418G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7009459 | |||||||
| chr4:7009671 | A | G | 1 | a0001c0008t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1447-206A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7009671 | |||||||
| chr4:7009813 | G | T | 1 | a0001c0007t0002g0002 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1447-64G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 9/13 | chr4 | 7009813 | |||||||
| chr4:7010047 | C | T | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1518+99C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 10/13 | chr4 | 7010047 | |||||||
| chr4:7010131 | C | G | 110 | a0001c0001t0001g0186 a0001c0001t0002g0009 a0001c0001t0002g0010 others(107): Show |
110 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1518+183C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 10/13 | chr4 | 7010131 | |||||||
| chr4:7010165 | C | A | 109 | a0001c0001t0001g0186 a0001c0001t0002g0009 a0001c0001t0002g0010 others(106): Show |
109 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1518+217C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 10/13 | chr4 | 7010165 | |||||||
| chr4:7010329 | A | G | 1 | a0001c0003t0003g0267 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1519-324A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 10/13 | chr4 | 7010329 | |||||||
| chr4:7010611 | G | T | 24 | a0001c0001t0003g0001 a0001c0001t0003g0044 a0001c0001t0003g0049 others(21): Show |
25 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.1519-42G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 10/13 | chr4 | 7010611 | |||||||
| chr4:7011002 | G | A | 116 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.1647+221G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7011002 | |||||||
| chr4:7011086 | A | T | 2 | a0001c0001t0012g0132 a0001c0001t0012g0133 |
2 | HG02257.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1647+305A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7011086 | |||||||
| chr4:7011127 | C | T | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1647+346C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7011127 | |||||||
| chr4:7011260 | G | C | 3 | a0001c0001t0003g0031 a0001c0001t0003g0063 a0001c0001t0003g0301 |
3 | HG02145.hp1 HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1647+479G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7011260 | |||||||
| chr4:7011294 | T | C | 2 | a0001c0001t0002g0156 a0001c0001t0002g0189 |
2 | HG00738.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1647+513T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7011294 | |||||||
| chr4:7011305 | G | T | 116 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.1647+524G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7011305 | |||||||
| chr4:7011317 | CGGTGACA others(9): Show |
C | 6 | a0001c0001t0003g0298 a0001c0003t0003g0032 a0001c0003t0003g0033 others(3): Show |
6 | HG02647.hp1 HG03130.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1647+553_1647+568d others(18): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr4 | 7011317 | ||||||
| chr4:7011387 | T | C | 1 | a0001c0001t0003g0079 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1647+606T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7011387 | |||||||
| chr4:7011545 | G | GT | 12 | a0001c0001t0002g0147 a0001c0001t0002g0182 a0001c0001t0002g0220 others(9): Show |
12 | HG01255.hp2 HG02258.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.1647+772dupT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr4 | 7011545 | ||||||
| chr4:7011665 | T | C | 232 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(229): Show |
232 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.1647+884T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7011665 | |||||||
| chr4:7011770 | C | G | 1 | a0001c0001t0003g0190 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1647+989C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7011770 | |||||||
| chr4:7011792 | A | G | 1 | a0001c0001t0016g0205 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1647+1011A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7011792 | |||||||
| chr4:7011824 | C | T | 1 | a0001c0008t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1647+1043C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7011824 | |||||||
| chr4:7011825 | T | C | 4 | a0001c0001t0002g0051 a0001c0001t0002g0144 a0001c0001t0002g0145 others(1): Show |
4 | NA18961.hp2 NA18994.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.1647+1044T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7011825 | |||||||
| chr4:7011898 | A | G | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1647+1117A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7011898 | |||||||
| chr4:7011959 | G | A | 1 | a0001c0001t0017g0195 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1647+1178G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7011959 | |||||||
| chr4:7012032 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1647+1251G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7012032 | |||||||
| chr4:7012117 | C | A | 1 | a0001c0001t0002g0165 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1647+1336C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7012117 | |||||||
| chr4:7012249 | C | T | 113 | a0001c0001t0001g0138 a0001c0001t0001g0186 a0001c0001t0002g0009 others(110): Show |
113 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1647+1468C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7012249 | |||||||
| chr4:7012267 | A | G | 33 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(30): Show |
34 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1647+1486A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7012267 | |||||||
| chr4:7012301 | CA | C | 38 | a0001c0001t0001g0091 a0001c0001t0001g0138 a0001c0001t0001g0217 others(35): Show |
39 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1647+1539delA | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr4 | 7012301 | ||||||
| chr4:7012301 | CAA | C | 115 | a0001c0001t0001g0186 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1647+1538_1647+153 others(6): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr4 | 7012301 | ||||||
| chr4:7012304 | A | C | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1647+1523A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7012304 | |||||||
| chr4:7012326 | T | C | 16 | a0001c0001t0005g0008 a0001c0001t0005g0037 a0001c0001t0005g0043 others(13): Show |
16 | HG01255.hp2 HG02109.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1647+1545T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7012326 | |||||||
| chr4:7012411 | A | T | 3 | a0001c0001t0001g0217 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG00741.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1647+1630A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7012411 | |||||||
| chr4:7012425 | G | A | 1 | a0001c0001t0002g0159 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1647+1644G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7012425 | |||||||
| chr4:7012511 | T | C | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1647+1730T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7012511 | |||||||
| chr4:7012554 | T | C | 2 | a0001c0001t0001g0255 a0001c0001t0001g0257 |
2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1647+1773T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7012554 | |||||||
| chr4:7012745 | A | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0104 |
2 | HG02004.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1648-1703A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7012745 | |||||||
| chr4:7012802 | T | C | 1 | a0001c0001t0001g0028 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1648-1646T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7012802 | |||||||
| chr4:7012921 | T | G | 1 | a0001c0001t0002g0223 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1648-1527T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7012921 | |||||||
| chr4:7012922 | A | G | 1 | a0001c0001t0002g0223 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1648-1526A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7012922 | |||||||
| chr4:7013098 | G | T | 7 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(4): Show |
7 | HG01884.hp2 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1648-1350G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7013098 | |||||||
| chr4:7013162 | T | C | 298 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(295): Show |
299 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.1648-1286T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7013162 | |||||||
| chr4:7013215 | C | T | 7 | a0001c0001t0001g0290 a0001c0001t0008g0060 a0001c0001t0008g0061 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1648-1233C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7013215 | |||||||
| chr4:7013312 | G | A | 15 | a0001c0001t0005g0008 a0001c0001t0005g0037 a0001c0001t0005g0053 others(12): Show |
15 | HG01255.hp2 HG02109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1648-1136G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7013312 | |||||||
| chr4:7013415 | G | A | 12 | a0001c0001t0005g0008 a0001c0001t0005g0037 a0001c0001t0005g0053 others(9): Show |
12 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1648-1033G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7013415 | |||||||
| chr4:7013451 | T | C | 284 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(281): Show |
285 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.1648-997T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7013451 | |||||||
| chr4:7013492 | T | C | 2 | a0001c0001t0003g0066 a0001c0001t0003g0067 |
2 | HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1648-956T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7013492 | |||||||
| chr4:7013516 | T | A | 1 | a0001c0001t0001g0148 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1648-932T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7013516 | |||||||
| chr4:7013585 | C | T | 3 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0025g0093 |
3 | HG02486.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1648-863C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7013585 | |||||||
| chr4:7013743 | CT | C | 274 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(271): Show |
275 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.1648-689delT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr4 | 7013743 | ||||||
| chr4:7013783 | G | A | 33 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(30): Show |
34 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1648-665G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7013783 | |||||||
| chr4:7013933 | T | C | 1 | a0001c0001t0017g0195 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1648-515T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7013933 | |||||||
| chr4:7013979 | G | C | 24 | a0001c0001t0003g0001 a0001c0001t0003g0044 a0001c0001t0003g0049 others(21): Show |
25 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.1648-469G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7013979 | |||||||
| chr4:7014012 | G | A | 1 | a0001c0001t0002g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1648-436G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7014012 | |||||||
| chr4:7014038 | C | T | 1 | a0001c0001t0002g0188 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1648-410C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7014038 | |||||||
| chr4:7014144 | T | A | 1 | a0001c0001t0003g0070 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1648-304T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7014144 | |||||||
| chr4:7014224 | T | C | 12 | a0001c0001t0005g0008 a0001c0001t0005g0037 a0001c0001t0005g0053 others(9): Show |
12 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1648-224T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 11/13 | chr4 | 7014224 | |||||||
| chr4:7014805 | A | G | 1 | a0001c0001t0002g0182 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1757+248A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7014805 | |||||||
| chr4:7014809 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1757+252G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7014809 | |||||||
| chr4:7014924 | A | G | 284 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(281): Show |
285 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.1757+367A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7014924 | |||||||
| chr4:7014925 | C | A | 110 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0048 others(107): Show |
110 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.1757+368C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7014925 | |||||||
| chr4:7014939 | G | A | 1 | a0001c0001t0002g0180 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1757+382G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7014939 | |||||||
| chr4:7015227 | G | A | 1 | a0001c0001t0003g0074 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1757+670G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7015227 | |||||||
| chr4:7015316 | C | T | 16 | a0001c0001t0005g0008 a0001c0001t0005g0037 a0001c0001t0005g0043 others(13): Show |
16 | HG01255.hp2 HG02109.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1757+759C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7015316 | |||||||
| chr4:7015436 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1757+879G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7015436 | |||||||
| chr4:7015456 | A | T | 141 | a0001c0001t0001g0186 a0001c0001t0002g0009 a0001c0001t0002g0010 others(138): Show |
142 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.1757+899A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7015456 | |||||||
| chr4:7015532 | A | G | 1 | a0001c0001t0002g0216 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1757+975A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7015532 | |||||||
| chr4:7015637 | A | G | 4 | a0001c0001t0002g0192 a0001c0001t0002g0202 a0001c0001t0002g0249 others(1): Show |
4 | HG02818.hp2 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1757+1080A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7015637 | |||||||
| chr4:7015685 | C | T | 127 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(124): Show |
127 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1757+1128C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7015685 | |||||||
| chr4:7015707 | C | T | 108 | a0001c0001t0001g0186 a0001c0001t0002g0009 a0001c0001t0002g0010 others(105): Show |
108 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.1757+1150C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7015707 | |||||||
| chr4:7015741 | T | C | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1757+1184T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7015741 | |||||||
| chr4:7015746 | T | A | 2 | a0001c0001t0009g0003 a0001c0001t0009g0004 |
2 | HG03540.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1757+1189T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7015746 | |||||||
| chr4:7015763 | T | C | 4 | a0001c0001t0002g0198 a0001c0001t0002g0260 a0001c0001t0002g0261 others(1): Show |
4 | HG01361.hp2 HG01934.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1757+1206T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7015763 | |||||||
| chr4:7015782 | C | T | 33 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(30): Show |
34 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1757+1225C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7015782 | |||||||
| chr4:7015787 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1757+1230G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7015787 | |||||||
| chr4:7015814 | A | G | 1 | a0001c0001t0003g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1757+1257A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7015814 | |||||||
| chr4:7015864 | G | A | 33 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(30): Show |
34 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1757+1307G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7015864 | |||||||
| chr4:7015909 | C | G | 3 | a0001c0001t0003g0031 a0001c0001t0003g0063 a0001c0001t0003g0301 |
3 | HG02145.hp1 HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1757+1352C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7015909 | |||||||
| chr4:7016007 | A | C | 4 | a0001c0001t0003g0298 a0001c0003t0003g0032 a0001c0003t0003g0033 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1757+1450A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7016007 | |||||||
| chr4:7016036 | A | G | 1 | a0001c0001t0007g0146 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1757+1479A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7016036 | |||||||
| chr4:7016041 | A | G | 1 | a0001c0001t0002g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1757+1484A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7016041 | |||||||
| chr4:7016060 | C | G | 1 | a0001c0001t0027g0213 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1757+1503C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7016060 | |||||||
| chr4:7016137 | G | C | 284 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(281): Show |
285 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.1757+1580G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7016137 | |||||||
| chr4:7016458 | G | A | 20 | a0001c0001t0001g0138 a0001c0001t0005g0008 a0001c0001t0005g0037 others(17): Show |
20 | HG01255.hp2 HG02109.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1757+1901G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7016458 | |||||||
| chr4:7016468 | G | A | 137 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(134): Show |
137 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.1757+1911G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7016468 | |||||||
| chr4:7016604 | A | G | 2 | a0001c0001t0008g0060 a0001c0001t0008g0061 |
2 | HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1757+2047A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7016604 | |||||||
| chr4:7016608 | T | C | 284 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(281): Show |
285 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.1757+2051T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7016608 | |||||||
| chr4:7016732 | A | G | 1 | a0001c0001t0004g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1757+2175A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7016732 | |||||||
| chr4:7016752 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1757+2195G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7016752 | |||||||
| chr4:7016779 | G | C | 4 | a0001c0001t0003g0059 a0001c0001t0003g0069 a0001c0001t0003g0086 others(1): Show |
4 | HG00280.hp1 HG00642.hp2 HG01070.hp2 others(1): Show |
intron_variant | MODIFIER | c.1757+2222G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7016779 | |||||||
| chr4:7016790 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1757+2233T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7016790 | |||||||
| chr4:7016865 | G | A | 104 | a0001c0001t0001g0186 a0001c0001t0002g0009 a0001c0001t0002g0010 others(101): Show |
104 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.1757+2308G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7016865 | |||||||
| chr4:7016910 | C | T | 1 | a0001c0001t0002g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1757+2353C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7016910 | |||||||
| chr4:7016911 | G | A | 1 | a0001c0001t0002g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1757+2354G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7016911 | |||||||
| chr4:7016923 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1757+2366G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7016923 | |||||||
| chr4:7016965 | C | G | 32 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(29): Show |
33 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1757+2408C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7016965 | |||||||
| chr4:7017438 | G | C | 1 | a0001c0001t0003g0070 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1757+2881G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7017438 | |||||||
| chr4:7017441 | C | G | 3 | a0001c0001t0002g0064 a0001c0001t0002g0295 a0001c0001t0003g0059 |
3 | HG00280.hp1 HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1757+2884C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7017441 | |||||||
| chr4:7017535 | C | A | 178 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
179 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.1757+2978C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7017535 | |||||||
| chr4:7017535 | C | G | 105 | a0001c0001t0001g0186 a0001c0001t0002g0009 a0001c0001t0002g0010 others(102): Show |
105 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1757+2978C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7017535 | |||||||
| chr4:7017539 | G | A | 6 | a0001c0001t0006g0168 a0001c0001t0006g0169 a0001c0001t0006g0170 others(3): Show |
6 | HG01192.hp1 HG01934.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1757+2982G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7017539 | |||||||
| chr4:7017857 | T | A | 1 | a0002c0002t0010g0021 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1757+3300T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7017857 | |||||||
| chr4:7017870 | G | A | 1 | a0002c0002t0010g0022 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1757+3313G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7017870 | |||||||
| chr4:7018263 | C | T | 9 | a0001c0001t0003g0044 a0001c0001t0003g0065 a0001c0001t0003g0066 others(6): Show |
9 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1757+3706C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7018263 | |||||||
| chr4:7018511 | T | G | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1757+3954T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7018511 | |||||||
| chr4:7018720 | G | A | 10 | a0001c0001t0001g0058 a0001c0001t0001g0111 a0001c0001t0001g0118 others(7): Show |
10 | HG02257.hp1 HG03098.hp2 NA18961.hp1 others(7): Show |
intron_variant | MODIFIER | c.1757+4163G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7018720 | |||||||
| chr4:7018959 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1757+4402C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7018959 | |||||||
| chr4:7018979 | A | G | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0274 |
3 | HG03195.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1757+4422A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7018979 | |||||||
| chr4:7019026 | G | T | 104 | a0001c0001t0001g0186 a0001c0001t0002g0009 a0001c0001t0002g0010 others(101): Show |
104 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.1757+4469G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019026 | |||||||
| chr4:7019071 | T | G | 14 | a0001c0001t0002g0156 a0001c0001t0002g0183 a0001c0001t0002g0189 others(11): Show |
14 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1757+4514T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019071 | |||||||
| chr4:7019089 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1757+4532T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019089 | |||||||
| chr4:7019108 | G | A | 1 | a0001c0001t0002g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1757+4551G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019108 | |||||||
| chr4:7019126 | A | G | 105 | a0001c0001t0001g0186 a0001c0001t0002g0009 a0001c0001t0002g0010 others(102): Show |
105 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1757+4569A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019126 | |||||||
| chr4:7019166 | C | T | 2 | a0002c0002t0004g0024 a0002c0002t0004g0030 |
2 | HG02055.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1757+4609C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019166 | |||||||
| chr4:7019375 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1757+4818G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019375 | |||||||
| chr4:7019376 | T | C | 8 | a0001c0001t0003g0049 a0001c0001t0003g0070 a0001c0001t0003g0071 others(5): Show |
8 | HG02145.hp2 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1757+4819T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019376 | |||||||
| chr4:7019380 | T | C | 116 | a0001c0001t0001g0186 a0001c0001t0002g0009 a0001c0001t0002g0010 others(113): Show |
116 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.1757+4823T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019380 | |||||||
| chr4:7019390 | T | TG | 9 | a0001c0001t0003g0044 a0001c0001t0003g0065 a0001c0001t0003g0066 others(6): Show |
9 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1757+4834dupG | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 7019390 | ||||||
| chr4:7019394 | C | T | 1 | a0002c0002t0004g0012 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1757+4837C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019394 | |||||||
| chr4:7019443 | G | T | 110 | a0001c0001t0001g0186 a0001c0001t0002g0009 a0001c0001t0002g0010 others(107): Show |
110 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1757+4886G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019443 | |||||||
| chr4:7019457 | G | C | 16 | a0001c0001t0005g0008 a0001c0001t0005g0037 a0001c0001t0005g0043 others(13): Show |
16 | HG01255.hp2 HG02109.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1757+4900G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019457 | |||||||
| chr4:7019484 | T | G | 113 | a0001c0001t0001g0186 a0001c0001t0002g0009 a0001c0001t0002g0010 others(110): Show |
113 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1757+4927T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019484 | |||||||
| chr4:7019489 | T | C | 284 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(281): Show |
285 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.1757+4932T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019489 | |||||||
| chr4:7019524 | G | A | 5 | a0001c0001t0003g0298 a0001c0003t0003g0032 a0001c0003t0003g0033 others(2): Show |
5 | HG02647.hp1 HG03130.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1757+4967G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019524 | |||||||
| chr4:7019638 | G | A | 111 | a0001c0001t0001g0186 a0001c0001t0002g0009 a0001c0001t0002g0010 others(108): Show |
111 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1757+5081G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019638 | |||||||
| chr4:7019695 | TGCTGGGC others(47): Show |
T | 2 | a0001c0001t0003g0063 a0001c0001t0003g0301 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1757+5152_1757+520 others(58): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 7019695 | ||||||
| chr4:7019709 | TAGGGAGG others(47): Show |
T | 1 | a0001c0001t0001g0080 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1757+5192_1758-520 others(58): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 7019709 | ||||||
| chr4:7019724 | G | GGCACAGA others(47): Show |
16 | a0001c0001t0005g0008 a0001c0001t0005g0037 a0001c0001t0005g0043 others(13): Show |
16 | HG01255.hp2 HG02109.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1757+5205_1757+520 others(58): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 7019724 | ||||||
| chr4:7019725 | GCACAGAG others(155): Show |
G | 7 | a0001c0001t0003g0298 a0001c0001t0009g0003 a0001c0001t0009g0242 others(4): Show |
7 | HG02647.hp1 HG03130.hp2 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.1757+5206_1758-508 others(4): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 7019725 | ||||||
| chr4:7019749 | CGCTGGGC others(47): Show |
C | 258 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(255): Show |
259 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.1757+5206_1758-518 others(58): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 7019749 | ||||||
| chr4:7019803 | T | C | 18 | a0001c0001t0003g0063 a0001c0001t0003g0301 a0001c0001t0005g0008 others(15): Show |
18 | HG01255.hp2 HG02109.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1758-5201T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019803 | |||||||
| chr4:7019826 | C | A | 1 | a0001c0001t0001g0028 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1758-5178C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019826 | |||||||
| chr4:7019832 | G | T | 261 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(258): Show |
262 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.1758-5172G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019832 | |||||||
| chr4:7019887 | A | G | 277 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(274): Show |
278 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.1758-5117A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019887 | |||||||
| chr4:7019911 | C | CGCTGGGC others(47): Show |
3 | a0001c0001t0005g0037 a0001c0001t0011g0041 a0001c0001t0029g0176 |
3 | HG02257.hp2 HG02258.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1758-5080_1758-507 others(58): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 7019911 | ||||||
| chr4:7019911 | C | T | 107 | a0001c0001t0001g0186 a0001c0001t0002g0009 a0001c0001t0002g0010 others(104): Show |
107 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.1758-5093C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019911 | |||||||
| chr4:7019925 | T | C | 13 | a0001c0001t0005g0008 a0001c0001t0005g0043 a0001c0001t0005g0053 others(10): Show |
13 | HG01255.hp2 HG02109.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1758-5079T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019925 | |||||||
| chr4:7019926 | A | G | 13 | a0001c0001t0005g0008 a0001c0001t0005g0043 a0001c0001t0005g0053 others(10): Show |
13 | HG01255.hp2 HG02109.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1758-5078A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019926 | |||||||
| chr4:7019928 | G | A | 13 | a0001c0001t0005g0008 a0001c0001t0005g0043 a0001c0001t0005g0053 others(10): Show |
13 | HG01255.hp2 HG02109.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1758-5076G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019928 | |||||||
| chr4:7019935 | C | T | 16 | a0001c0001t0005g0008 a0001c0001t0005g0037 a0001c0001t0005g0043 others(13): Show |
16 | HG01255.hp2 HG02109.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1758-5069C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019935 | |||||||
| chr4:7019940 | G | T | 7 | a0001c0001t0003g0298 a0001c0001t0009g0003 a0001c0001t0009g0242 others(4): Show |
7 | HG02647.hp1 HG03130.hp2 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.1758-5064G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019940 | |||||||
| chr4:7019941 | G | A | 13 | a0001c0001t0005g0008 a0001c0001t0005g0043 a0001c0001t0005g0053 others(10): Show |
13 | HG01255.hp2 HG02109.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1758-5063G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019941 | |||||||
| chr4:7019949 | G | A | 1 | a0001c0001t0001g0290 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1758-5055G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019949 | |||||||
| chr4:7019951 | G | T | 3 | a0001c0001t0005g0037 a0001c0001t0011g0041 a0001c0001t0029g0176 |
3 | HG02257.hp2 HG02258.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1758-5053G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019951 | |||||||
| chr4:7019959 | G | A | 13 | a0001c0001t0005g0008 a0001c0001t0005g0043 a0001c0001t0005g0053 others(10): Show |
13 | HG01255.hp2 HG02109.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1758-5045G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019959 | |||||||
| chr4:7019963 | C | T | 3 | a0001c0001t0005g0037 a0001c0001t0011g0041 a0001c0001t0029g0176 |
3 | HG02257.hp2 HG02258.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1758-5041C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019963 | |||||||
| chr4:7019965 | C | T | 13 | a0001c0001t0005g0008 a0001c0001t0005g0043 a0001c0001t0005g0053 others(10): Show |
13 | HG01255.hp2 HG02109.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1758-5039C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019965 | |||||||
| chr4:7019966 | G | T | 3 | a0001c0001t0005g0037 a0001c0001t0011g0041 a0001c0001t0029g0176 |
3 | HG02257.hp2 HG02258.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1758-5038G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019966 | |||||||
| chr4:7019971 | G | C | 3 | a0001c0001t0005g0037 a0001c0001t0011g0041 a0001c0001t0029g0176 |
3 | HG02257.hp2 HG02258.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1758-5033G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019971 | |||||||
| chr4:7019974 | C | T | 3 | a0001c0001t0005g0037 a0001c0001t0011g0041 a0001c0001t0029g0176 |
3 | HG02257.hp2 HG02258.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1758-5030C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019974 | |||||||
| chr4:7019979 | C | T | 16 | a0001c0001t0005g0008 a0001c0001t0005g0037 a0001c0001t0005g0043 others(13): Show |
16 | HG01255.hp2 HG02109.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1758-5025C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019979 | |||||||
| chr4:7019980 | A | AGGGAGGA others(47): Show |
13 | a0001c0001t0005g0008 a0001c0001t0005g0043 a0001c0001t0005g0053 others(10): Show |
13 | HG01255.hp2 HG02109.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1758-5000_1758-499 others(58): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 7019980 | ||||||
| chr4:7019980 | A | G | 3 | a0001c0001t0005g0037 a0001c0001t0011g0041 a0001c0001t0029g0176 |
3 | HG02257.hp2 HG02258.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1758-5024A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7019980 | |||||||
| chr4:7020022 | T | TG | 112 | a0001c0001t0001g0186 a0001c0001t0002g0009 a0001c0001t0002g0010 others(109): Show |
112 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.1758-4979dupG | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 7020022 | ||||||
| chr4:7020025 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1758-4979G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7020025 | |||||||
| chr4:7020087 | T | C | 2 | a0001c0001t0009g0003 a0001c0001t0009g0242 |
2 | HG03540.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1758-4917T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7020087 | |||||||
| chr4:7020126 | C | T | 1 | a0001c0001t0014g0157 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1758-4878C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7020126 | |||||||
| chr4:7020180 | C | G | 1 | a0001c0001t0001g0296 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1758-4824C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7020180 | |||||||
| chr4:7020558 | T | C | 3 | a0001c0001t0001g0217 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG00741.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1758-4446T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7020558 | |||||||
| chr4:7020587 | T | A | 1 | a0001c0001t0003g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1758-4417T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7020587 | |||||||
| chr4:7020588 | T | A | 1 | a0001c0001t0003g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1758-4416T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7020588 | |||||||
| chr4:7020588 | T | C | 283 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(280): Show |
284 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.1758-4416T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7020588 | |||||||
| chr4:7020589 | G | A | 1 | a0001c0001t0002g0218 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1758-4415G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7020589 | |||||||
| chr4:7020613 | G | C | 112 | a0001c0001t0001g0186 a0001c0001t0002g0009 a0001c0001t0002g0010 others(109): Show |
112 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.1758-4391G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7020613 | |||||||
| chr4:7020648 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1758-4356T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7020648 | |||||||
| chr4:7020769 | T | C | 284 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(281): Show |
285 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.1758-4235T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7020769 | |||||||
| chr4:7020781 | G | A | 5 | a0001c0001t0003g0298 a0001c0003t0003g0032 a0001c0003t0003g0033 others(2): Show |
5 | HG02647.hp1 HG03130.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1758-4223G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7020781 | |||||||
| chr4:7021015 | T | G | 1 | a0001c0001t0001g0153 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1758-3989T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7021015 | |||||||
| chr4:7021427 | A | G | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1758-3577A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7021427 | |||||||
| chr4:7021457 | T | A | 1 | a0001c0001t0002g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1758-3547T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7021457 | |||||||
| chr4:7021539 | G | T | 14 | a0001c0001t0005g0043 a0001c0001t0005g0053 a0001c0001t0005g0056 others(11): Show |
14 | HG01255.hp2 HG02109.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1758-3465G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7021539 | |||||||
| chr4:7021658 | CT | C | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
281 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.1758-3332delT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 7021658 | ||||||
| chr4:7021706 | A | T | 32 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(29): Show |
33 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1758-3298A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7021706 | |||||||
| chr4:7021752 | G | A | 278 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(275): Show |
279 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.1758-3252G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7021752 | |||||||
| chr4:7021813 | G | T | 1 | a0001c0001t0002g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1758-3191G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7021813 | |||||||
| chr4:7021903 | T | C | 2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1758-3101T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7021903 | |||||||
| chr4:7021925 | C | T | 1 | a0001c0001t0004g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1758-3079C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7021925 | |||||||
| chr4:7022247 | G | C | 1 | a0001c0001t0029g0176 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1758-2757G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7022247 | |||||||
| chr4:7022350 | A | G | 284 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(281): Show |
285 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.1758-2654A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7022350 | |||||||
| chr4:7022517 | A | G | 29 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(26): Show |
30 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.1758-2487A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7022517 | |||||||
| chr4:7022622 | G | A | 106 | a0001c0001t0001g0186 a0001c0001t0002g0009 a0001c0001t0002g0010 others(103): Show |
106 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1758-2382G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7022622 | |||||||
| chr4:7022634 | A | G | 5 | a0001c0001t0003g0298 a0001c0003t0003g0032 a0001c0003t0003g0033 others(2): Show |
5 | HG02647.hp1 HG03130.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1758-2370A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7022634 | |||||||
| chr4:7022671 | A | G | 264 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
265 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.1758-2333A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7022671 | |||||||
| chr4:7022856 | T | C | 1 | a0001c0001t0001g0303 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1758-2148T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7022856 | |||||||
| chr4:7022869 | G | C | 1 | a0001c0001t0002g0159 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1758-2135G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7022869 | |||||||
| chr4:7022989 | C | T | 1 | a0001c0001t0002g0149 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1758-2015C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7022989 | |||||||
| chr4:7023110 | C | T | 11 | a0001c0001t0005g0043 a0001c0001t0005g0053 a0001c0001t0005g0056 others(8): Show |
11 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1758-1894C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7023110 | |||||||
| chr4:7023215 | T | C | 1 | a0001c0001t0002g0178 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1758-1789T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7023215 | |||||||
| chr4:7023251 | G | A | 6 | a0001c0001t0003g0044 a0001c0001t0003g0065 a0001c0001t0003g0068 others(3): Show |
6 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1758-1753G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7023251 | |||||||
| chr4:7023323 | G | T | 6 | a0001c0001t0005g0268 a0001c0001t0005g0270 a0001c0001t0005g0271 others(3): Show |
6 | HG02109.hp2 HG02451.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1758-1681G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7023323 | |||||||
| chr4:7023344 | G | A | 1 | a0001c0011t0002g0206 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1758-1660G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7023344 | |||||||
| chr4:7023488 | T | C | 1 | a0001c0001t0001g0186 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1758-1516T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7023488 | |||||||
| chr4:7023593 | C | G | 1 | a0001c0001t0001g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1758-1411C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7023593 | |||||||
| chr4:7023758 | A | G | 14 | a0001c0001t0005g0043 a0001c0001t0005g0053 a0001c0001t0005g0056 others(11): Show |
14 | HG01255.hp2 HG02109.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1758-1246A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7023758 | |||||||
| chr4:7023775 | C | T | 4 | a0001c0001t0003g0059 a0001c0001t0003g0069 a0001c0001t0003g0086 others(1): Show |
4 | HG00280.hp1 HG00642.hp2 HG01070.hp2 others(1): Show |
intron_variant | MODIFIER | c.1758-1229C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7023775 | |||||||
| chr4:7023796 | T | C | 113 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(110): Show |
113 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1758-1208T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7023796 | |||||||
| chr4:7023843 | G | A | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1758-1161G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7023843 | |||||||
| chr4:7024103 | G | A | 126 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(123): Show |
126 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.1758-901G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7024103 | |||||||
| chr4:7024162 | G | A | 1 | a0001c0001t0002g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1758-842G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7024162 | |||||||
| chr4:7024182 | T | C | 121 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(118): Show |
121 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.1758-822T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7024182 | |||||||
| chr4:7024182 | T | G | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1758-822T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7024182 | |||||||
| chr4:7024406 | T | C | 4 | a0001c0001t0002g0204 a0001c0001t0002g0207 a0001c0001t0002g0209 others(1): Show |
4 | HG01243.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1758-598T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7024406 | |||||||
| chr4:7024483 | G | A | 1 | a0001c0001t0017g0195 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1758-521G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7024483 | |||||||
| chr4:7024594 | G | C | 1 | a0001c0001t0003g0298 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1758-410G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7024594 | |||||||
| chr4:7024652 | C | T | 104 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(101): Show |
104 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.1758-352C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7024652 | |||||||
| chr4:7024676 | C | T | 14 | a0001c0001t0005g0043 a0001c0001t0005g0053 a0001c0001t0005g0056 others(11): Show |
14 | HG01255.hp2 HG02109.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1758-328C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7024676 | |||||||
| chr4:7024706 | C | G | 1 | a0001c0001t0002g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1758-298C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7024706 | |||||||
| chr4:7024713 | C | A | 1 | a0001c0001t0002g0221 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1758-291C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7024713 | |||||||
| chr4:7024719 | G | A | 1 | a0001c0001t0023g0097 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1758-285G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7024719 | |||||||
| chr4:7024806 | C | G | 1 | a0001c0001t0025g0093 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1758-198C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 12/13 | chr4 | 7024806 | |||||||
| chr4:7025302 | C | T | 4 | a0001c0001t0002g0192 a0001c0001t0002g0202 a0001c0001t0002g0249 others(1): Show |
4 | HG02818.hp2 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2016+40C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7025302 | |||||||
| chr4:7025314 | C | T | 270 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(267): Show |
271 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.2016+52C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7025314 | |||||||
| chr4:7025433 | C | T | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2016+171C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7025433 | |||||||
| chr4:7025442 | T | G | 1 | a0001c0001t0002g0221 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2016+180T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7025442 | |||||||
| chr4:7025525 | G | C | 1 | a0001c0001t0002g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2016+263G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7025525 | |||||||
| chr4:7025585 | C | T | 1 | a0002c0002t0004g0026 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2016+323C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7025585 | |||||||
| chr4:7025659 | G | C | 1 | a0001c0001t0002g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2016+397G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7025659 | |||||||
| chr4:7026091 | C | G | 1 | a0001c0001t0009g0004 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2016+829C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7026091 | |||||||
| chr4:7026101 | G | T | 123 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(120): Show |
123 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.2016+839G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7026101 | |||||||
| chr4:7026154 | CT | C | 283 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(280): Show |
284 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.2016+905delT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 7026154 | ||||||
| chr4:7026255 | A | G | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2016+993A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7026255 | |||||||
| chr4:7026550 | C | T | 1 | a0001c0001t0002g0174 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2016+1288C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7026550 | |||||||
| chr4:7026687 | A | G | 1 | a0001c0001t0020g0265 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2016+1425A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7026687 | |||||||
| chr4:7026744 | A | C | 1 | a0001c0001t0001g0274 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2016+1482A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7026744 | |||||||
| chr4:7026896 | TAAAAAAA others(14): Show |
T | 1 | a0001c0001t0002g0142 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2016+1644_2016+166 others(25): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 7026896 | ||||||
| chr4:7026916 | C | A | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2016+1654C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7026916 | |||||||
| chr4:7026952 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2016+1690C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7026952 | |||||||
| chr4:7026964 | A | G | 25 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0027 others(22): Show |
25 | HG00323.hp1 HG00438.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.2016+1702A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7026964 | |||||||
| chr4:7026976 | G | C | 1 | a0001c0001t0007g0212 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2016+1714G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7026976 | |||||||
| chr4:7027036 | A | C | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2016+1774A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7027036 | |||||||
| chr4:7027040 | A | T | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2016+1778A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7027040 | |||||||
| chr4:7027043 | T | A | 121 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(118): Show |
121 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.2016+1781T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7027043 | |||||||
| chr4:7027064 | A | G | 270 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(267): Show |
271 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.2016+1802A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7027064 | |||||||
| chr4:7027202 | C | T | 1 | a0002c0002t0015g0247 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2016+1940C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7027202 | |||||||
| chr4:7027204 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2016+1942C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7027204 | |||||||
| chr4:7027206 | A | G | 1 | a0002c0002t0010g0021 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2016+1944A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7027206 | |||||||
| chr4:7027228 | G | A | 284 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(281): Show |
285 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.2016+1966G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7027228 | |||||||
| chr4:7027290 | AC | A | 267 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(264): Show |
268 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.2016+2036delC | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 7027290 | ||||||
| chr4:7027333 | CCACA | C | 3 | a0001c0001t0001g0217 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG00741.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2016+2078_2016+208 others(8): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 7027333 | ||||||
| chr4:7027379 | C | A | 121 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(118): Show |
121 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.2016+2117C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7027379 | |||||||
| chr4:7027382 | C | T | 14 | a0001c0001t0005g0043 a0001c0001t0005g0053 a0001c0001t0005g0056 others(11): Show |
14 | HG01255.hp2 HG02109.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.2016+2120C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7027382 | |||||||
| chr4:7027466 | C | G | 2 | a0001c0001t0013g0256 a0001c0001t0013g0258 |
2 | HG00438.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.2016+2204C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7027466 | |||||||
| chr4:7027486 | CCA | C | 3 | a0001c0001t0002g0064 a0001c0001t0002g0208 a0001c0001t0002g0295 |
3 | HG02559.hp2 HG02735.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2016+2227_2016+222 others(6): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 7027486 | ||||||
| chr4:7027500 | C | T | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2016+2238C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7027500 | |||||||
| chr4:7027501 | TAC | T | 5 | a0001c0001t0003g0298 a0001c0003t0003g0032 a0001c0003t0003g0033 others(2): Show |
5 | HG02647.hp1 HG03130.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2016+2242_2016+224 others(6): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 7027501 | ||||||
| chr4:7027514 | C | T | 5 | a0001c0001t0003g0298 a0001c0003t0003g0032 a0001c0003t0003g0033 others(2): Show |
5 | HG02647.hp1 HG03130.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2016+2252C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7027514 | |||||||
| chr4:7027533 | T | C | 1 | a0001c0001t0012g0132 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2016+2271T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7027533 | |||||||
| chr4:7027593 | G | A | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2016+2331G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7027593 | |||||||
| chr4:7027620 | CCA | C | 111 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(108): Show |
111 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.2016+2365_2016+236 others(6): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 7027620 | ||||||
| chr4:7027627 | C | T | 1 | a0002c0002t0004g0017 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2016+2365C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7027627 | |||||||
| chr4:7027665 | CCACA | C | 111 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(108): Show |
111 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.2016+2406_2016+240 others(8): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 7027665 | ||||||
| chr4:7027703 | C | G | 270 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(267): Show |
271 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.2016+2441C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7027703 | |||||||
| chr4:7027769 | CATCACAC others(27): Show |
C | 2 | a0001c0001t0001g0302 a0001c0001t0001g0303 |
2 | NA19010.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2016+2516_2017-251 others(38): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 7027769 | ||||||
| chr4:7027871 | G | C | 2 | a0001c0001t0002g0064 a0001c0001t0002g0295 |
2 | HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2017-2456G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7027871 | |||||||
| chr4:7027955 | C | A | 4 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
4 | NA18961.hp1 NA18983.hp1 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.2017-2372C>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7027955 | |||||||
| chr4:7027957 | A | C | 3 | a0001c0001t0001g0217 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG00741.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2017-2370A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7027957 | |||||||
| chr4:7027988 | A | G | 1 | a0001c0001t0005g0008 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2017-2339A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7027988 | |||||||
| chr4:7028116 | C | T | 3 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0001c0001t0011g0041 |
3 | HG01255.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2017-2211C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7028116 | |||||||
| chr4:7028131 | C | T | 2 | a0001c0001t0013g0256 a0001c0001t0013g0258 |
2 | HG00438.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.2017-2196C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7028131 | |||||||
| chr4:7028152 | C | T | 1 | a0001c0001t0003g0059 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2017-2175C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7028152 | |||||||
| chr4:7028212 | G | A | 121 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(118): Show |
121 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.2017-2115G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7028212 | |||||||
| chr4:7028429 | G | GT | 13 | a0001c0001t0001g0136 a0001c0001t0002g0064 a0001c0001t0002g0144 others(10): Show |
13 | HG00741.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2017-1895dupT | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 7028429 | ||||||
| chr4:7028433 | G | T | 282 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(279): Show |
283 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.2017-1894G>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7028433 | |||||||
| chr4:7028540 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2017-1787C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7028540 | |||||||
| chr4:7028555 | T | C | 1 | a0001c0001t0005g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2017-1772T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7028555 | |||||||
| chr4:7028593 | A | C | 1 | a0002c0002t0010g0021 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2017-1734A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7028593 | |||||||
| chr4:7028628 | C | T | 284 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(281): Show |
285 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.2017-1699C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7028628 | |||||||
| chr4:7028720 | T | C | 284 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(281): Show |
285 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.2017-1607T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7028720 | |||||||
| chr4:7028825 | T | C | 1 | a0001c0001t0003g0079 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2017-1502T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7028825 | |||||||
| chr4:7028899 | G | GCGATC | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2017-1427_2017-142 others(9): Show |
TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 7028899 | ||||||
| chr4:7028929 | C | T | 1 | a0001c0001t0002g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2017-1398C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7028929 | |||||||
| chr4:7028955 | A | C | 3 | a0001c0001t0009g0003 a0001c0001t0009g0004 a0001c0001t0009g0242 |
3 | HG03540.hp2 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2017-1372A>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7028955 | |||||||
| chr4:7028962 | C | G | 25 | a0001c0001t0003g0001 a0001c0001t0003g0044 a0001c0001t0003g0049 others(22): Show |
26 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.2017-1365C>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7028962 | |||||||
| chr4:7028977 | G | A | 34 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(31): Show |
35 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.2017-1350G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7028977 | |||||||
| chr4:7029011 | T | G | 1 | a0001c0001t0001g0035 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2017-1316T>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7029011 | |||||||
| chr4:7029081 | C | T | 9 | a0001c0001t0005g0053 a0001c0001t0005g0056 a0001c0001t0005g0139 others(6): Show |
9 | HG02109.hp2 HG02451.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.2017-1246C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7029081 | |||||||
| chr4:7029109 | G | A | 14 | a0001c0001t0005g0043 a0001c0001t0005g0053 a0001c0001t0005g0056 others(11): Show |
14 | HG01255.hp2 HG02109.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.2017-1218G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7029109 | |||||||
| chr4:7029115 | C | T | 1 | a0001c0001t0002g0201 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2017-1212C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7029115 | |||||||
| chr4:7029271 | A | T | 1 | a0001c0001t0007g0210 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2017-1056A>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7029271 | |||||||
| chr4:7029337 | T | C | 284 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(281): Show |
285 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.2017-990T>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7029337 | |||||||
| chr4:7029346 | C | T | 4 | a0001c0001t0005g0043 a0001c0001t0011g0039 a0001c0001t0011g0040 others(1): Show |
4 | HG01255.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2017-981C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7029346 | |||||||
| chr4:7029359 | A | G | 2 | a0001c0001t0003g0063 a0001c0001t0003g0301 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2017-968A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7029359 | |||||||
| chr4:7029455 | C | T | 3 | a0001c0001t0003g0070 a0001c0001t0003g0075 a0001c0001t0003g0076 |
3 | HG02922.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2017-872C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7029455 | |||||||
| chr4:7029476 | T | A | 1 | a0001c0001t0012g0132 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2017-851T>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7029476 | |||||||
| chr4:7029529 | C | T | 1 | a0002c0002t0002g0020 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2017-798C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7029529 | |||||||
| chr4:7029765 | C | T | 1 | a0002c0002t0004g0018 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2017-562C>T | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7029765 | |||||||
| chr4:7029800 | G | A | 1 | a0004c0005t0005g0269 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2017-527G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7029800 | |||||||
| chr4:7029977 | G | A | 33 | a0001c0001t0003g0001 a0001c0001t0003g0031 a0001c0001t0003g0044 others(30): Show |
34 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.2017-350G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7029977 | |||||||
| chr4:7029980 | G | A | 1 | a0002c0013t0004g0014 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2017-347G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7029980 | |||||||
| chr4:7030019 | G | A | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG00741.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2017-308G>A | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7030019 | |||||||
| chr4:7030115 | A | G | 1 | a0001c0001t0026g0117 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2017-212A>G | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7030115 | |||||||
| chr4:7030230 | G | C | 2 | a0001c0001t0001g0254 a0001c0012t0001g0275 |
2 | HG02129.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.2017-97G>C | TBC1D14 | ENSG00000132405.19 | transcript | ENST00000409757.9 | protein_coding | 13/13 | chr4 | 7030230 |