Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 154810 |
| ensemblid | ENSG00000166025.18 |
| hgncid | 17811 |
| symbol | AMOTL1 |
| name | angiomotin like 1 |
| refseq_nuc | NM_130847.3 |
| refseq_prot | NP_570899.1 |
| ensembl_nuc | ENST00000433060.3 |
| ensembl_prot | ENSP00000387739.2 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 94768356 |
| end | 94876748 |
| strand | + |
| ver | v1.2 |
| region | chr11:94768356-94876748 |
| region5000 | chr11:94763356-94881748 |
| regionname0 | AMOTL1_chr11_94768356_94876748 |
| regionname5000 | AMOTL1_chr11_94763356_94881748 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 956 | 219 | 73 | 38 | 83 | 4 | 19 | 71 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | MWRAK others(951): Show |
chr11 | 94763356 | 94881748 |
| a0002 | 0/0 | 956 | 15 | 0 | 3 | 10 | 1 | 1 | 5 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | MWRAK others(951): Show |
chr11 | 94763356 | 94881748 |
| a0003 | 0/0 | 956 | 4 | 0 | 0 | 0 | 0 | 4 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | MWRAK others(951): Show |
chr11 | 94763356 | 94881748 |
| a0004 | 0/0 | 956 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | MWRAK others(951): Show |
chr11 | 94763356 | 94881748 |
| a0005 | 0/0 | 956 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | MWRAK others(951): Show |
chr11 | 94763356 | 94881748 |
| a0006 | 0/0 | 956 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | MWRAK others(951): Show |
chr11 | 94763356 | 94881748 |
| a0007 | 0/0 | 956 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | MWRAK others(951): Show |
chr11 | 94763356 | 94881748 |
| a0008 | 0/0 | 956 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | MWRAK others(951): Show |
chr11 | 94763356 | 94881748 |
| a0009 | 0/0 | 956 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | MWRAK others(951): Show |
chr11 | 94763356 | 94881748 |
| a0010 | 0/0 | 956 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | MWRAK others(951): Show |
chr11 | 94763356 | 94881748 |
| a0011 | 0/0 | 956 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | MWRAK others(951): Show |
chr11 | 94763356 | 94881748 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2868 | 136 | 64 | 19 | 37 | 3 | 11 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | ATGTG others(2863): Show |
chr11 | 94763356 | 94881748 | ||
| a0001c0002 | 0/0 | 2868 | 72 | 3 | 16 | 44 | 1 | 8 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | ATGTG others(2863): Show |
chr11 | 94763356 | 94881748 | ||
| a0001c0005 | 0/0 | 2868 | 3 | 3 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | ATGTG others(2863): Show |
chr11 | 94763356 | 94881748 | ||
| a0001c0006 | 0/0 | 2868 | 2 | 1 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | ATGTG others(2863): Show |
chr11 | 94763356 | 94881748 | ||
| a0001c0007 | 0/0 | 2868 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | ATGTG others(2863): Show |
chr11 | 94763356 | 94881748 | ||
| a0001c0010 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | ATGTG others(2863): Show |
chr11 | 94763356 | 94881748 | ||
| a0001c0013 | 0/0 | 2868 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | ATGTG others(2863): Show |
chr11 | 94763356 | 94881748 | ||
| a0001c0016 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | ATGTG others(2863): Show |
chr11 | 94763356 | 94881748 | ||
| a0001c0018 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | ATGTG others(2863): Show |
chr11 | 94763356 | 94881748 | ||
| a0001c0020 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | ATGTG others(2863): Show |
chr11 | 94763356 | 94881748 | ||
| a0002c0003 | 0/0 | 2868 | 14 | 0 | 3 | 10 | 1 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | ATGTG others(2863): Show |
chr11 | 94763356 | 94881748 | ||
| a0002c0019 | 0/0 | 2868 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | ATGTG others(2863): Show |
chr11 | 94763356 | 94881748 | ||
| a0003c0004 | 0/0 | 2868 | 4 | 0 | 0 | 0 | 0 | 4 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | ATGTG others(2863): Show |
chr11 | 94763356 | 94881748 | ||
| a0004c0012 | 0/0 | 2868 | 1 | 0 | 0 | 0 | 1 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | ATGTG others(2863): Show |
chr11 | 94763356 | 94881748 | ||
| a0005c0015 | 0/0 | 2868 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | ATGTG others(2863): Show |
chr11 | 94763356 | 94881748 | ||
| a0006c0021 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | ATGTG others(2863): Show |
chr11 | 94763356 | 94881748 | ||
| a0007c0008 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | ATGTG others(2863): Show |
chr11 | 94763356 | 94881748 | ||
| a0008c0009 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | ATGTG others(2863): Show |
chr11 | 94763356 | 94881748 | ||
| a0009c0014 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | ATGTG others(2863): Show |
chr11 | 94763356 | 94881748 | ||
| a0010c0017 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | ATGTG others(2863): Show |
chr11 | 94763356 | 94881748 | ||
| a0011c0011 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | ATGTG others(2863): Show |
chr11 | 94763356 | 94881748 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 8980 | 44 | 13 | 7 | 17 | 2 | 4 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8975): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0002 | 0/0 | 8988 | 2 | 0 | 0 | 2 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8983): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0003 | 0/0 | 8984 | 10 | 7 | 1 | 1 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8979): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0004 | 0/0 | 8982 | 10 | 4 | 1 | 5 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8977): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0005 | 0/1 | 8980 | 8 | 1 | 3 | 0 | 1 | 2 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8975): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0007 | 0/0 | 8986 | 6 | 0 | 3 | 0 | 0 | 3 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8981): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0009 | 0/0 | 8977 | 5 | 5 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8972): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0010 | 0/0 | 8978 | 3 | 0 | 0 | 3 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8973): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0011 | 0/0 | 8981 | 5 | 5 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8976): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0012 | 0/0 | 8974 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8969): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0013 | 0/0 | 8969 | 4 | 3 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8964): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0015 | 0/0 | 8973 | 2 | 2 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8968): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0016 | 0/0 | 8990 | 3 | 3 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8985): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0017 | 0/0 | 8971 | 3 | 2 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8966): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0019 | 0/0 | 8971 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8966): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0020 | 0/0 | 8973 | 2 | 2 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8968): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0022 | 0/0 | 8986 | 2 | 2 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8981): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0025 | 0/0 | 8980 | 2 | 0 | 0 | 2 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8975): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0026 | 0/0 | 8983 | 2 | 2 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8978): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0027 | 0/0 | 8973 | 2 | 2 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8968): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0028 | 0/0 | 8979 | 2 | 2 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8974): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0029 | 0/0 | 8980 | 2 | 0 | 0 | 2 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8975): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0030 | 0/0 | 8988 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8983): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0032 | 0/0 | 8973 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8968): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0033 | 0/0 | 8971 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8966): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0034 | 0/0 | 8971 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8966): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0035 | 0/0 | 8974 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8969): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0039 | 0/0 | 8989 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8984): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0040 | 0/0 | 8985 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8980): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0042 | 0/0 | 8988 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8983): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0044 | 0/0 | 8980 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8975): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0045 | 0/0 | 8986 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8981): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0048 | 0/0 | 8980 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8975): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0050 | 0/0 | 8982 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8977): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0051 | 0/0 | 8980 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8975): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0053 | 0/0 | 8975 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8970): Show |
chr11 | 94763356 | 94881748 |
| a0001c0001t0054 | 0/0 | 8980 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8975): Show |
chr11 | 94763356 | 94881748 |
| a0001c0002t0001 | 0/0 | 8980 | 6 | 1 | 2 | 0 | 1 | 2 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8975): Show |
chr11 | 94763356 | 94881748 |
| a0001c0002t0002 | 0/0 | 8988 | 31 | 0 | 4 | 24 | 0 | 3 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8983): Show |
chr11 | 94763356 | 94881748 |
| a0001c0002t0003 | 0/0 | 8984 | 2 | 0 | 0 | 2 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8979): Show |
chr11 | 94763356 | 94881748 |
| a0001c0002t0006 | 0/0 | 8986 | 7 | 0 | 1 | 5 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8981): Show |
chr11 | 94763356 | 94881748 |
| a0001c0002t0008 | 0/0 | 8990 | 6 | 0 | 4 | 2 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8985): Show |
chr11 | 94763356 | 94881748 |
| a0001c0002t0012 | 0/0 | 8974 | 3 | 0 | 0 | 3 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8969): Show |
chr11 | 94763356 | 94881748 |
| a0001c0002t0014 | 0/0 | 8992 | 4 | 0 | 2 | 2 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8987): Show |
chr11 | 94763356 | 94881748 |
| a0001c0002t0018 | 0/0 | 8986 | 3 | 0 | 3 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8981): Show |
chr11 | 94763356 | 94881748 |
| a0001c0002t0019 | 0/0 | 8971 | 2 | 0 | 0 | 2 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8966): Show |
chr11 | 94763356 | 94881748 |
| a0001c0002t0023 | 0/0 | 8980 | 2 | 2 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8975): Show |
chr11 | 94763356 | 94881748 |
| a0001c0002t0024 | 0/0 | 8976 | 2 | 0 | 0 | 2 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8971): Show |
chr11 | 94763356 | 94881748 |
| a0001c0002t0031 | 0/0 | 8986 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8981): Show |
chr11 | 94763356 | 94881748 |
| a0001c0002t0036 | 0/0 | 8974 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8969): Show |
chr11 | 94763356 | 94881748 |
| a0001c0002t0046 | 0/0 | 8988 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8983): Show |
chr11 | 94763356 | 94881748 |
| a0001c0002t0047 | 0/0 | 8974 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8969): Show |
chr11 | 94763356 | 94881748 |
| a0001c0005t0001 | 0/0 | 8980 | 2 | 2 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8975): Show |
chr11 | 94763356 | 94881748 |
| a0001c0005t0052 | 0/0 | 8980 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8975): Show |
chr11 | 94763356 | 94881748 |
| a0001c0006t0001 | 0/0 | 8980 | 2 | 1 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8975): Show |
chr11 | 94763356 | 94881748 |
| a0001c0007t0005 | 0/0 | 8980 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8975): Show |
chr11 | 94763356 | 94881748 |
| a0001c0010t0038 | 0/0 | 8992 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8987): Show |
chr11 | 94763356 | 94881748 |
| a0001c0013t0006 | 0/0 | 8986 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8981): Show |
chr11 | 94763356 | 94881748 |
| a0001c0016t0010 | 0/0 | 8978 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8973): Show |
chr11 | 94763356 | 94881748 |
| a0001c0018t0001 | 0/0 | 8980 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8975): Show |
chr11 | 94763356 | 94881748 |
| a0001c0020t0002 | 0/0 | 8988 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8983): Show |
chr11 | 94763356 | 94881748 |
| a0002c0003t0001 | 0/0 | 8980 | 12 | 0 | 3 | 8 | 1 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8975): Show |
chr11 | 94763356 | 94881748 |
| a0002c0003t0004 | 0/0 | 8982 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8977): Show |
chr11 | 94763356 | 94881748 |
| a0002c0003t0049 | 0/0 | 8980 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8975): Show |
chr11 | 94763356 | 94881748 |
| a0002c0019t0004 | 0/0 | 8982 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8977): Show |
chr11 | 94763356 | 94881748 |
| a0003c0004t0021 | 0/0 | 8992 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8987): Show |
chr11 | 94763356 | 94881748 |
| a0003c0004t0037 | 0/0 | 8988 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8983): Show |
chr11 | 94763356 | 94881748 |
| a0003c0004t0041 | 0/0 | 8988 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8983): Show |
chr11 | 94763356 | 94881748 |
| a0003c0004t0043 | 0/0 | 8986 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8981): Show |
chr11 | 94763356 | 94881748 |
| a0004c0012t0001 | 0/0 | 8980 | 1 | 0 | 0 | 0 | 1 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8975): Show |
chr11 | 94763356 | 94881748 |
| a0005c0015t0010 | 0/0 | 8978 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8973): Show |
chr11 | 94763356 | 94881748 |
| a0006c0021t0001 | 0/0 | 8980 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8975): Show |
chr11 | 94763356 | 94881748 |
| a0007c0008t0015 | 0/0 | 8973 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8968): Show |
chr11 | 94763356 | 94881748 |
| a0008c0009t0003 | 0/0 | 8984 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8979): Show |
chr11 | 94763356 | 94881748 |
| a0009c0014t0001 | 0/0 | 8980 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8975): Show |
chr11 | 94763356 | 94881748 |
| a0010c0017t0021 | 0/0 | 8992 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8987): Show |
chr11 | 94763356 | 94881748 |
| a0011c0011t0001 | 0/0 | 8980 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | AGCGC others(8975): Show |
chr11 | 94763356 | 94881748 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0215 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0004g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0004g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0005g0017 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0005g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0007g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0007g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0007g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0007g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0007g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0007g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0009g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0009g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0009g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0009g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0010g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0010g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0010g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0011g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0011g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0011g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0011g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0011g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0012g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0013g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0013g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0013g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0013g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0015g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0015g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0016g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0016g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0016g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0017g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0017g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0017g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0019g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0020g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0020g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0022g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0022g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0025g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0025g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0026g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0026g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0027g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0027g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0028g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0028g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0029g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0029g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0030g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0032g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0033g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0034g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0035g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0039g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0040g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0042g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0044g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0045g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0048g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0050g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0051g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0053g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0001t0054g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0006g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0006g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0006g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0006g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0006g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0006g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0006g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0008g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0008g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0008g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0008g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0008g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0008g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0012g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0012g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0012g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0014g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0014g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0014g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0014g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0018g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0018g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0018g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0019g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0019g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0023g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0023g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0024g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0024g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0031g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0036g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0046g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0002t0047g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0005t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0005t0052g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0006t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0006t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0007t0005g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0010t0038g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0013t0006g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0016t0010g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0018t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0001c0020t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0002c0003t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0002c0003t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0002c0003t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0002c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0002c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0002c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0002c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0002c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0002c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0002c0003t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0002c0003t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0002c0003t0049g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0002c0019t0004g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0003c0004t0021g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0003c0004t0037g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0003c0004t0041g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0003c0004t0043g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0004c0012t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0005c0015t0010g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0006c0021t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0007c0008t0015g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0008c0009t0003g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0009c0014t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0010c0017t0021g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| a0011c0011t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0059 | EUR | FIN | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG00280 | hp2 | a0004 | c0012 | t0001 | g0087 | EUR | FIN | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG00558 | hp1 | a0001 | c0002 | t0047 | g0095 | EAS | CHS | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG00558 | hp2 | a0002 | c0003 | t0001 | g0149 | EAS | CHS | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG00735 | hp1 | a0001 | c0001 | t0005 | g0126 | AMR | PUR | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG00735 | hp2 | a0001 | c0002 | t0018 | g0088 | AMR | PUR | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG00738 | hp2 | a0001 | c0001 | t0007 | g0228 | AMR | PUR | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG00741 | hp1 | a0001 | c0006 | t0001 | g0194 | AMR | PUR | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG00741 | hp2 | a0002 | c0003 | t0001 | g0036 | AMR | PUR | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01074 | hp1 | a0005 | c0015 | t0010 | g0219 | AMR | PUR | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0041 | AMR | PUR | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01081 | hp2 | a0001 | c0002 | t0014 | g0058 | AMR | PUR | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01106 | hp1 | a0001 | c0001 | t0032 | g0068 | AMR | PUR | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01106 | hp2 | a0001 | c0007 | t0005 | g0044 | AMR | PUR | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01109 | hp1 | a0001 | c0001 | t0013 | g0209 | AMR | PUR | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01175 | hp1 | a0001 | c0002 | t0018 | g0060 | AMR | PUR | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01175 | hp2 | a0002 | c0003 | t0001 | g0007 | AMR | PUR | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01192 | hp1 | a0001 | c0002 | t0014 | g0137 | AMR | PUR | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01192 | hp2 | a0001 | c0002 | t0018 | g0139 | AMR | PUR | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01243 | hp2 | a0001 | c0001 | t0017 | g0205 | AMR | PUR | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0010 | AMR | CLM | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01257 | hp1 | a0001 | c0001 | t0030 | g0042 | AMR | CLM | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0147 | AMR | CLM | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01346 | hp1 | a0001 | c0001 | t0007 | g0094 | AMR | CLM | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | CLM | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01433 | hp2 | a0002 | c0003 | t0001 | g0150 | AMR | CLM | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01496 | hp1 | a0001 | c0002 | t0008 | g0098 | AMR | CLM | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01496 | hp2 | a0001 | c0002 | t0008 | g0162 | AMR | CLM | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01884 | hp1 | a0001 | c0001 | t0045 | g0140 | AFR | ACB | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0203 | AFR | ACB | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0138 | AMR | PEL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0169 | AMR | PEL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0161 | AMR | PEL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01943 | hp2 | a0001 | c0001 | t0007 | g0045 | AMR | PEL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01978 | hp2 | a0001 | c0002 | t0008 | g0010 | AMR | PEL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02004 | hp2 | a0001 | c0002 | t0008 | g0160 | AMR | PEL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02027 | hp2 | a0001 | c0002 | t0024 | g0037 | EAS | KHV | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02040 | hp1 | a0002 | c0003 | t0001 | g0091 | EAS | KHV | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02040 | hp2 | a0001 | c0002 | t0008 | g0185 | EAS | KHV | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02055 | hp1 | a0001 | c0016 | t0010 | g0129 | AFR | ACB | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02055 | hp2 | a0001 | c0001 | t0034 | g0127 | AFR | ACB | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02056 | hp1 | a0002 | c0003 | t0001 | g0134 | EAS | KHV | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0158 | EAS | KHV | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02080 | hp1 | a0002 | c0003 | t0001 | g0005 | EAS | KHV | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0187 | EAS | KHV | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02132 | hp1 | a0001 | c0020 | t0002 | g0175 | EAS | KHV | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0128 | AFR | ACB | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02165 | hp1 | a0001 | c0002 | t0046 | g0191 | EAS | CDX | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02165 | hp2 | a0006 | c0021 | t0001 | g0003 | EAS | CDX | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02258 | hp1 | a0001 | c0001 | t0015 | g0213 | AFR | ACB | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | ACB | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02280 | hp1 | a0001 | c0001 | t0040 | g0144 | AFR | ACB | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02280 | hp2 | a0001 | c0001 | t0020 | g0221 | AFR | ACB | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02451 | hp2 | a0001 | c0001 | t0016 | g0117 | AFR | ACB | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02523 | hp1 | a0002 | c0003 | t0004 | g0133 | EAS | KHV | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0190 | EAS | KHV | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02572 | hp1 | a0001 | c0001 | t0042 | g0008 | AFR | GWD | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0092 | SAS | PJL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02602 | hp2 | a0003 | c0004 | t0043 | g0224 | SAS | PJL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02615 | hp1 | a0001 | c0001 | t0009 | g0156 | AFR | GWD | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02615 | hp2 | a0001 | c0001 | t0026 | g0122 | AFR | GWD | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02647 | hp1 | a0001 | c0001 | t0017 | g0195 | AFR | GWD | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0009 | AFR | GWD | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0153 | SAS | PJL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02683 | hp2 | a0003 | c0004 | t0021 | g0223 | SAS | PJL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0173 | SAS | PJL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02717 | hp1 | a0001 | c0001 | t0011 | g0125 | AFR | GWD | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0110 | AFR | GWD | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02723 | hp1 | a0001 | c0001 | t0015 | g0151 | AFR | GWD | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02723 | hp2 | a0001 | c0001 | t0013 | g0207 | AFR | GWD | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0047 | SAS | PJL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02735 | hp2 | a0001 | c0001 | t0007 | g0230 | SAS | PJL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0057 | SAS | PJL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02738 | hp2 | a0003 | c0004 | t0041 | g0211 | SAS | PJL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02809 | hp1 | a0007 | c0008 | t0015 | g0225 | AFR | GWD | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0141 | AFR | GWD | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0101 | AFR | GWD | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02818 | hp2 | a0001 | c0001 | t0033 | g0199 | AFR | GWD | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0071 | AFR | GWD | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0202 | AFR | GWD | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02895 | hp1 | a0001 | c0001 | t0028 | g0196 | AFR | GWD | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02895 | hp2 | a0001 | c0001 | t0011 | g0019 | AFR | GWD | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02897 | hp2 | a0001 | c0001 | t0028 | g0197 | AFR | GWD | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02922 | hp1 | a0001 | c0001 | t0013 | g0018 | AFR | ESN | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0200 | AFR | ESN | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02965 | hp1 | a0001 | c0002 | t0023 | g0100 | AFR | ESN | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02965 | hp2 | a0001 | c0001 | t0020 | g0154 | AFR | ESN | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02970 | hp1 | a0001 | c0005 | t0001 | g0013 | AFR | ESN | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02970 | hp2 | a0001 | c0001 | t0022 | g0008 | AFR | ESN | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03017 | hp1 | a0001 | c0002 | t0036 | g0089 | SAS | PJL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03041 | hp1 | a0001 | c0001 | t0009 | g0009 | AFR | GWD | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03098 | hp1 | a0001 | c0006 | t0001 | g0214 | AFR | MSL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03098 | hp2 | a0001 | c0001 | t0039 | g0112 | AFR | MSL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03130 | hp1 | a0008 | c0009 | t0003 | g0001 | AFR | ESN | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03130 | hp2 | a0009 | c0014 | t0001 | g0201 | AFR | ESN | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03139 | hp1 | a0001 | c0001 | t0009 | g0157 | AFR | ESN | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03139 | hp2 | a0001 | c0001 | t0022 | g0152 | AFR | ESN | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03195 | hp2 | a0001 | c0001 | t0011 | g0123 | AFR | ESN | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03209 | hp1 | a0001 | c0001 | t0027 | g0217 | AFR | MSL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0072 | AFR | MSL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03225 | hp1 | a0010 | c0017 | t0021 | g0113 | AFR | MSL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03225 | hp2 | a0011 | c0011 | t0001 | g0109 | AFR | MSL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03239 | hp1 | a0002 | c0019 | t0004 | g0103 | SAS | PJL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0043 | SAS | PJL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03453 | hp2 | a0001 | c0001 | t0016 | g0146 | AFR | MSL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03491 | hp1 | a0001 | c0001 | t0054 | g0093 | SAS | PJL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03491 | hp2 | a0001 | c0002 | t0031 | g0227 | SAS | PJL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03516 | hp1 | a0001 | c0005 | t0052 | g0198 | AFR | ESN | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03516 | hp2 | a0001 | c0001 | t0013 | g0119 | AFR | ESN | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03540 | hp1 | a0001 | c0001 | t0053 | g0118 | AFR | GWD | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03579 | hp2 | a0001 | c0001 | t0009 | g0155 | AFR | MSL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03688 | hp1 | a0001 | c0001 | t0007 | g0130 | SAS | STU | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03688 | hp2 | a0001 | c0002 | t0006 | g0090 | SAS | STU | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0174 | SAS | PJL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG04204 | hp1 | a0003 | c0004 | t0037 | g0212 | SAS | STU | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | STU | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG04228 | hp1 | a0001 | c0001 | t0007 | g0229 | SAS | STU | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0069 | SAS | STU | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | YRI | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18522 | hp2 | a0001 | c0001 | t0051 | g0148 | AFR | YRI | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | CHB | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0178 | EAS | CHB | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18906 | hp2 | a0001 | c0001 | t0026 | g0124 | AFR | YRI | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18939 | hp2 | a0002 | c0003 | t0049 | g0048 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18952 | hp1 | a0002 | c0003 | t0001 | g0052 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18952 | hp2 | a0001 | c0002 | t0008 | g0012 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18953 | hp1 | a0001 | c0002 | t0006 | g0056 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18956 | hp1 | a0001 | c0002 | t0019 | g0104 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18959 | hp1 | a0001 | c0001 | t0029 | g0107 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18959 | hp2 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18962 | hp2 | a0001 | c0001 | t0048 | g0082 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0184 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18970 | hp1 | a0001 | c0002 | t0006 | g0002 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18970 | hp2 | a0001 | c0002 | t0012 | g0096 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18971 | hp1 | a0001 | c0001 | t0029 | g0172 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18972 | hp1 | a0001 | c0002 | t0003 | g0192 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18972 | hp2 | a0001 | c0001 | t0025 | g0023 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18977 | hp2 | a0001 | c0001 | t0050 | g0085 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0179 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18980 | hp2 | a0001 | c0001 | t0025 | g0121 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0181 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18985 | hp1 | a0001 | c0001 | t0035 | g0136 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18985 | hp2 | a0001 | c0002 | t0014 | g0166 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18992 | hp2 | a0001 | c0002 | t0002 | g0176 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18999 | hp1 | a0001 | c0001 | t0010 | g0028 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA18999 | hp2 | a0002 | c0003 | t0001 | g0083 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0188 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19002 | hp1 | a0001 | c0002 | t0012 | g0097 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19002 | hp2 | a0001 | c0001 | t0012 | g0078 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19003 | hp2 | a0001 | c0002 | t0006 | g0063 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19004 | hp1 | a0001 | c0002 | t0006 | g0186 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19004 | hp2 | a0001 | c0002 | t0024 | g0111 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19005 | hp1 | a0001 | c0001 | t0019 | g0064 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0177 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19062 | hp2 | a0001 | c0001 | t0010 | g0024 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19063 | hp1 | a0001 | c0001 | t0010 | g0003 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0163 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19064 | hp2 | a0001 | c0018 | t0001 | g0180 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0164 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19074 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19075 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19083 | hp1 | a0001 | c0002 | t0006 | g0061 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19084 | hp2 | a0002 | c0003 | t0001 | g0005 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19085 | hp1 | a0001 | c0002 | t0003 | g0167 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19085 | hp2 | a0001 | c0002 | t0012 | g0105 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0159 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19086 | hp2 | a0001 | c0002 | t0019 | g0102 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19090 | hp2 | a0001 | c0002 | t0014 | g0165 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19091 | hp2 | a0002 | c0003 | t0001 | g0051 | EAS | JPT | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19240 | hp1 | a0001 | c0001 | t0017 | g0204 | AFR | YRI | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA19240 | hp2 | a0001 | c0001 | t0027 | g0216 | AFR | YRI | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA20752 | hp1 | a0002 | c0003 | t0001 | g0007 | EUR | TSI | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0040 | EUR | TSI | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01123 | hp1 | a0001 | c0013 | t0006 | g0226 | AMR | CLM | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG01123 | hp2 | a0001 | c0002 | t0006 | g0011 | AMR | CLM | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02486 | hp1 | a0001 | c0005 | t0001 | g0013 | AFR | ACB | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG02559 | hp2 | a0001 | c0010 | t0038 | g0222 | AFR | ACB | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03471 | hp1 | a0001 | c0001 | t0011 | g0020 | AFR | MSL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG03471 | hp2 | a0001 | c0001 | t0016 | g0114 | AFR | MSL | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | USA | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| HG06807 | hp2 | a0001 | c0002 | t0023 | g0099 | AFR | USA | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA21309 | hp1 | a0001 | c0001 | t0011 | g0049 | AFR | LWK | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| NA21309 | hp2 | a0001 | c0001 | t0044 | g0210 | AFR | LWK | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0017 | REF | REF | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0215 | REF | REF | AMOTL1_chr11_94763356_94881748 | AMOTL1 | chr11 | 94763356 | 94881748 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:94799611 | A | G | 1 | a0006 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.421A>G | p.Thr141Ala | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/13 | 577/8980 | 421/2871 | 141/956 | chr11 | 94799611 | |||
| chr11:94799864 | G | A | 1 | a0007 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.674G>A | p.Ser225Asn | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/13 | 830/8980 | 674/2871 | 225/956 | chr11 | 94799864 | |||
| chr11:94821531 | C | T | 1 | a0010 | 1 | HG03225.hp1 | missense_variant&splice_region_variant | MODERATE | c.1123C>T | p.Arg375Cys | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/13 | 1279/8980 | 1123/2871 | 375/956 | chr11 | 94821531 | |||
| chr11:94821561 | A | G | 1 | a0003 | 4 | HG02602.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
missense_variant | MODERATE | c.1153A>G | p.Met385Val | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/13 | 1309/8980 | 1153/2871 | 385/956 | chr11 | 94821561 | |||
| chr11:94853966 | G | A | 1 | a0008 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.1828G>A | p.Glu610Lys | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/13 | 1984/8980 | 1828/2871 | 610/956 | chr11 | 94853966 | |||
| chr11:94859592 | G | A | 1 | a0011 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.2012G>A | p.Arg671Gln | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/13 | 2168/8980 | 2012/2871 | 671/956 | chr11 | 94859592 | |||
| chr11:94866021 | G | A | 1 | a0004 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.2341G>A | p.Gly781Arg | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/13 | 2497/8980 | 2341/2871 | 781/956 | chr11 | 94866021 | |||
| chr11:94869249 | C | T | 2 | a0002 a0004 |
16 | HG00280.hp2 HG00558.hp2 HG00741.hp2 others(13): Show |
missense_variant | MODERATE | c.2540C>T | p.Pro847Leu | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 12/13 | 2696/8980 | 2540/2871 | 847/956 | chr11 | 94869249 | |||
| chr11:94869401 | C | T | 1 | a0005 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.2692C>T | p.Arg898Trp | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 12/13 | 2848/8980 | 2692/2871 | 898/956 | chr11 | 94869401 | |||
| chr11:94869431 | G | A | 1 | a0009 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.2722G>A | p.Val908Ile | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 12/13 | 2878/8980 | 2722/2871 | 908/956 | chr11 | 94869431 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:94799469 | G | A | 1 | a0001c0007 | 1 | HG01106.hp2 | synonymous_variant | LOW | c.279G>A | p.Ala93Ala | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/13 | 435/8980 | 279/2871 | 93/956 | chr11 | 94799469 | |||
| chr11:94800180 | C | T | 1 | a0001c0005 | 3 | HG02486.hp1 HG02970.hp1 HG03516.hp1 |
synonymous_variant | LOW | c.990C>T | p.His330His | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/13 | 1146/8980 | 990/2871 | 330/956 | chr11 | 94800180 | |||
| chr11:94800207 | C | T | 4 | a0001c0002 a0001c0018 a0001c0020 others(1): Show |
75 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(72): Show |
synonymous_variant | LOW | c.1017C>T | p.Pro339Pro | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/13 | 1173/8980 | 1017/2871 | 339/956 | chr11 | 94800207 | |||
| chr11:94800309 | G | A | 1 | a0003c0004 | 4 | HG02602.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.1119G>A | p.Thr373Thr | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/13 | 1275/8980 | 1119/2871 | 373/956 | chr11 | 94800309 | |||
| chr11:94850226 | C | T | 1 | a0001c0020 | 1 | HG02132.hp1 | synonymous_variant | LOW | c.1761C>T | p.Asn587Asn | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/13 | 1917/8980 | 1761/2871 | 587/956 | chr11 | 94850226 | |||
| chr11:94859536 | T | C | 1 | a0001c0010 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.1956T>C | p.Asn652Asn | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/13 | 2112/8980 | 1956/2871 | 652/956 | chr11 | 94859536 | |||
| chr11:94864750 | C | T | 1 | a0001c0016 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.2151C>T | p.Ile717Ile | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 10/13 | 2307/8980 | 2151/2871 | 717/956 | chr11 | 94864750 | |||
| chr11:94869292 | G | A | 1 | a0001c0013 | 1 | HG01123.hp1 | synonymous_variant | LOW | c.2583G>A | p.Thr861Thr | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 12/13 | 2739/8980 | 2583/2871 | 861/956 | chr11 | 94869292 | |||
| chr11:94869340 | A | G | 1 | a0001c0018 | 1 | NA19064.hp2 | synonymous_variant | LOW | c.2631A>G | p.Thr877Thr | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 12/13 | 2787/8980 | 2631/2871 | 877/956 | chr11 | 94869340 | |||
| chr11:94870735 | C | G | 1 | a0001c0010 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.2811C>G | p.Val937Val | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 2967/8980 | 2811/2871 | 937/956 | chr11 | 94870735 | |||
| chr11:94870747 | G | A | 1 | a0001c0006 | 2 | HG00741.hp1 HG03098.hp1 |
synonymous_variant | LOW | c.2823G>A | p.Leu941Leu | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 2979/8980 | 2823/2871 | 941/956 | chr11 | 94870747 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:94768444 | G | A | 4 | a0001c0001t0005 a0001c0001t0030 a0001c0002t0031 others(1): Show |
10 | HG00735.hp1 HG01074.hp2 HG01106.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-68G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/13 | 68 | chr11 | 94768444 | ||||||
| chr11:94871026 | T | C | 4 | a0001c0001t0015 a0001c0001t0020 a0001c0001t0032 others(1): Show |
6 | HG01106.hp1 HG02258.hp1 HG02280.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*231T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 231 | chr11 | 94871026 | ||||||
| chr11:94871027 | G | A | 2 | a0001c0001t0033 a0001c0001t0034 |
2 | HG02055.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*232G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 232 | chr11 | 94871027 | ||||||
| chr11:94871092 | T | C | 1 | a0001c0001t0007 | 6 | HG00738.hp2 HG01346.hp1 HG01943.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*297T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 297 | chr11 | 94871092 | ||||||
| chr11:94871205 | AAGCCTCC others(11): Show |
A | 1 | a0001c0001t0035 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*413_*430delCCTCCA others(12): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 413 | INFO_REALIGN_3_PRIME | chr11 | 94871205 | |||||
| chr11:94871378 | A | G | 2 | a0001c0001t0019 a0001c0002t0019 |
3 | NA18956.hp1 NA19005.hp1 NA19086.hp2 |
3_prime_UTR_variant | MODIFIER | c.*583A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 583 | chr11 | 94871378 | ||||||
| chr11:94871379 | T | C | 1 | a0001c0002t0036 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*584T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 584 | chr11 | 94871379 | ||||||
| chr11:94871425 | A | T | 1 | a0001c0001t0054 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*630A>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 630 | chr11 | 94871425 | ||||||
| chr11:94871763 | G | A | 19 | a0001c0001t0007 a0001c0001t0016 a0001c0001t0017 others(16): Show |
30 | HG00738.hp2 HG01243.hp2 HG01346.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*968G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 968 | chr11 | 94871763 | ||||||
| chr11:94871906 | C | A | 1 | a0001c0001t0032 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1111C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 1111 | chr11 | 94871906 | ||||||
| chr11:94871955 | G | GCATA | 1 | a0001c0001t0009 | 5 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1161_*1162insATAC | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 1162 | INFO_REALIGN_3_PRIME | chr11 | 94871955 | |||||
| chr11:94871965 | A | G | 1 | a0001c0001t0007 | 6 | HG00738.hp2 HG01346.hp1 HG01943.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1170A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 1170 | chr11 | 94871965 | ||||||
| chr11:94872136 | G | A | 1 | a0001c0002t0046 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1341G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 1341 | chr11 | 94872136 | ||||||
| chr11:94872150 | G | A | 1 | a0001c0001t0007 | 6 | HG00738.hp2 HG01346.hp1 HG01943.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1355G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 1355 | chr11 | 94872150 | ||||||
| chr11:94872264 | G | A | 1 | a0003c0004t0037 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1469G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 1469 | chr11 | 94872264 | ||||||
| chr11:94872327 | A | C | 19 | a0001c0001t0007 a0001c0001t0016 a0001c0001t0017 others(16): Show |
30 | HG00738.hp2 HG01243.hp2 HG01346.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1532A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 1532 | chr11 | 94872327 | ||||||
| chr11:94872491 | G | T | 1 | a0001c0001t0029 | 2 | NA18959.hp1 NA18971.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1696G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 1696 | chr11 | 94872491 | ||||||
| chr11:94872496 | T | C | 1 | a0001c0002t0047 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1701T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 1701 | chr11 | 94872496 | ||||||
| chr11:94872655 | G | A | 1 | a0001c0001t0048 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1860G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 1860 | chr11 | 94872655 | ||||||
| chr11:94873013 | C | G | 5 | a0001c0001t0011 a0001c0001t0026 a0001c0001t0027 others(2): Show |
12 | HG02615.hp2 HG02717.hp1 HG02895.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2218C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 2218 | chr11 | 94873013 | ||||||
| chr11:94873080 | G | A | 1 | a0002c0003t0049 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2285G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 2285 | chr11 | 94873080 | ||||||
| chr11:94873222 | C | T | 18 | a0001c0001t0007 a0001c0001t0016 a0001c0001t0017 others(15): Show |
29 | HG00738.hp2 HG01243.hp2 HG01346.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2427C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 2427 | chr11 | 94873222 | ||||||
| chr11:94873292 | G | A | 19 | a0001c0001t0007 a0001c0001t0016 a0001c0001t0017 others(16): Show |
30 | HG00738.hp2 HG01243.hp2 HG01346.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2497G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 2497 | chr11 | 94873292 | ||||||
| chr11:94873484 | A | G | 2 | a0001c0001t0035 a0001c0002t0014 |
5 | HG01081.hp2 HG01192.hp1 NA18985.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2689A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 2689 | chr11 | 94873484 | ||||||
| chr11:94873523 | A | G | 30 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0011 others(27): Show |
57 | HG00738.hp2 HG01106.hp1 HG01109.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*2728A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 2728 | chr11 | 94873523 | ||||||
| chr11:94873539 | C | T | 16 | a0001c0001t0007 a0001c0001t0016 a0001c0001t0017 others(13): Show |
27 | HG00738.hp2 HG01243.hp2 HG01346.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2744C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 2744 | chr11 | 94873539 | ||||||
| chr11:94873542 | C | T | 16 | a0001c0001t0007 a0001c0001t0016 a0001c0001t0017 others(13): Show |
27 | HG00738.hp2 HG01243.hp2 HG01346.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2747C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 2747 | chr11 | 94873542 | ||||||
| chr11:94873601 | G | A | 1 | a0001c0010t0038 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2806G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 2806 | chr11 | 94873601 | ||||||
| chr11:94873718 | C | T | 1 | a0001c0001t0025 | 2 | NA18972.hp2 NA18980.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2923C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 2923 | chr11 | 94873718 | ||||||
| chr11:94873728 | T | C | 18 | a0001c0001t0007 a0001c0001t0016 a0001c0001t0017 others(15): Show |
29 | HG00738.hp2 HG01243.hp2 HG01346.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2933T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 2933 | chr11 | 94873728 | ||||||
| chr11:94873767 | A | G | 2 | a0001c0001t0007 a0001c0001t0045 |
7 | HG00738.hp2 HG01346.hp1 HG01884.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2972A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 2972 | chr11 | 94873767 | ||||||
| chr11:94873768 | C | T | 19 | a0001c0001t0007 a0001c0001t0016 a0001c0001t0017 others(16): Show |
31 | HG00738.hp2 HG01243.hp2 HG01346.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2973C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 2973 | chr11 | 94873768 | ||||||
| chr11:94873776 | T | TAC | 5 | a0001c0001t0004 a0001c0001t0028 a0001c0001t0050 others(2): Show |
15 | HG01243.hp1 HG02523.hp1 HG02622.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3017_*3018dupCA | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 3019 | INFO_REALIGN_3_PRIME | chr11 | 94873776 | |||||
| chr11:94873776 | T | TACAC | 4 | a0001c0001t0003 a0001c0001t0011 a0001c0002t0003 others(1): Show |
18 | HG01884.hp2 HG01934.hp1 HG02258.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3015_*3018dupCACA | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 3019 | INFO_REALIGN_3_PRIME | chr11 | 94873776 | |||||
| chr11:94873776 | T | TACACAC | 7 | a0001c0001t0007 a0001c0001t0022 a0001c0001t0026 others(4): Show |
20 | HG00738.hp2 HG01123.hp1 HG01123.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3013_*3018dupCACA others(2): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 3019 | INFO_REALIGN_3_PRIME | chr11 | 94873776 | |||||
| chr11:94873776 | T | TACACACA others(1): Show |
9 | a0001c0001t0002 a0001c0001t0030 a0001c0001t0040 others(6): Show |
40 | HG01256.hp1 HG01257.hp1 HG01346.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*3011_*3018dupCACA others(4): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 3019 | INFO_REALIGN_3_PRIME | chr11 | 94873776 | |||||
| chr11:94873776 | T | TACACACA others(3): Show |
2 | a0001c0001t0016 a0001c0002t0008 |
9 | HG01496.hp1 HG01496.hp2 HG01978.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3009_*3018dupCACA others(6): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 3019 | INFO_REALIGN_3_PRIME | chr11 | 94873776 | |||||
| chr11:94873776 | T | TACACACA others(5): Show |
6 | a0001c0001t0035 a0001c0001t0039 a0001c0002t0014 others(3): Show |
9 | HG01081.hp2 HG01192.hp1 HG02559.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3007_*3018dupCACA others(8): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 3019 | INFO_REALIGN_3_PRIME | chr11 | 94873776 | |||||
| chr11:94873776 | TAC | T | 4 | a0001c0001t0010 a0001c0001t0053 a0001c0016t0010 others(1): Show |
6 | HG01074.hp1 HG02055.hp1 HG03540.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3017_*3018delCA | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 3017 | INFO_REALIGN_3_PRIME | chr11 | 94873776 | |||||
| chr11:94873776 | TACAC | T | 7 | a0001c0001t0009 a0001c0001t0015 a0001c0001t0020 others(4): Show |
15 | HG01106.hp1 HG02027.hp2 HG02258.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3015_*3018delCACA | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 3015 | INFO_REALIGN_3_PRIME | chr11 | 94873776 | |||||
| chr11:94873776 | TACACAC | T | 4 | a0001c0001t0012 a0001c0002t0012 a0001c0002t0036 others(1): Show |
6 | HG00558.hp1 HG03017.hp1 NA18970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3013_*3018delCACA others(2): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 3013 | INFO_REALIGN_3_PRIME | chr11 | 94873776 | |||||
| chr11:94873776 | TACACACA others(1): Show |
T | 6 | a0001c0001t0013 a0001c0001t0017 a0001c0001t0019 others(3): Show |
12 | HG01109.hp1 HG01243.hp2 HG02055.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3011_*3018delCACA others(4): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 3011 | INFO_REALIGN_3_PRIME | chr11 | 94873776 | |||||
| chr11:94873781 | A | ACACACG | 2 | a0001c0002t0018 a0001c0002t0031 |
4 | HG00735.hp2 HG01175.hp1 HG01192.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2991_*2992insGCAC others(2): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 2992 | INFO_REALIGN_3_PRIME | chr11 | 94873781 | |||||
| chr11:94873860 | T | C | 18 | a0001c0001t0007 a0001c0001t0016 a0001c0001t0017 others(15): Show |
29 | HG00738.hp2 HG01243.hp2 HG01346.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3065T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 3065 | chr11 | 94873860 | ||||||
| chr11:94874180 | T | C | 2 | a0001c0001t0020 a0001c0001t0032 |
3 | HG01106.hp1 HG02280.hp2 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3385T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 3385 | chr11 | 94874180 | ||||||
| chr11:94874182 | G | C | 16 | a0001c0001t0007 a0001c0001t0016 a0001c0001t0017 others(13): Show |
27 | HG00738.hp2 HG01243.hp2 HG01346.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*3387G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 3387 | chr11 | 94874182 | ||||||
| chr11:94874283 | C | T | 1 | a0001c0010t0038 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3488C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 3488 | chr11 | 94874283 | ||||||
| chr11:94874583 | A | G | 1 | a0001c0005t0052 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3788A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 3788 | chr11 | 94874583 | ||||||
| chr11:94874590 | T | C | 1 | a0001c0010t0038 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3795T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 3795 | chr11 | 94874590 | ||||||
| chr11:94874604 | C | T | 2 | a0001c0001t0022 a0001c0001t0042 |
3 | HG02572.hp1 HG02970.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3809C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 3809 | chr11 | 94874604 | ||||||
| chr11:94874651 | G | A | 3 | a0001c0001t0039 a0001c0001t0040 a0001c0010t0038 |
3 | HG02280.hp1 HG02559.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3856G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 3856 | chr11 | 94874651 | ||||||
| chr11:94874684 | A | C | 1 | a0001c0001t0007 | 6 | HG00738.hp2 HG01346.hp1 HG01943.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3889A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 3889 | chr11 | 94874684 | ||||||
| chr11:94874718 | C | A | 1 | a0001c0010t0038 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3923C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 3923 | chr11 | 94874718 | ||||||
| chr11:94874867 | G | A | 1 | a0001c0002t0023 | 2 | HG02965.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4072G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 4072 | chr11 | 94874867 | ||||||
| chr11:94875250 | C | T | 1 | a0001c0001t0048 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4455C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 4455 | chr11 | 94875250 | ||||||
| chr11:94875368 | T | C | 1 | a0001c0001t0050 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4573T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 4573 | chr11 | 94875368 | ||||||
| chr11:94875478 | G | A | 1 | a0001c0001t0051 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4683G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 4683 | chr11 | 94875478 | ||||||
| chr11:94875496 | CT | C | 5 | a0001c0001t0017 a0001c0001t0019 a0001c0001t0033 others(2): Show |
8 | HG01243.hp2 HG02055.hp2 HG02647.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4705delT | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 4705 | INFO_REALIGN_3_PRIME | chr11 | 94875496 | |||||
| chr11:94875619 | ATCC | A | 13 | a0001c0001t0009 a0001c0001t0011 a0001c0001t0013 others(10): Show |
29 | HG01106.hp1 HG01109.hp1 HG02258.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*4832_*4834delCCT | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 4832 | INFO_REALIGN_3_PRIME | chr11 | 94875619 | |||||
| chr11:94875805 | G | C | 4 | a0001c0001t0015 a0001c0001t0020 a0001c0001t0032 others(1): Show |
6 | HG01106.hp1 HG02258.hp1 HG02280.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5010G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 5010 | chr11 | 94875805 | ||||||
| chr11:94875954 | G | A | 14 | a0001c0001t0009 a0001c0001t0011 a0001c0001t0013 others(11): Show |
30 | HG01106.hp1 HG01109.hp1 HG02258.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*5159G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 5159 | chr11 | 94875954 | ||||||
| chr11:94876020 | C | G | 1 | a0001c0010t0038 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5225C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 5225 | chr11 | 94876020 | ||||||
| chr11:94876193 | C | A | 15 | a0001c0001t0007 a0001c0001t0016 a0001c0001t0017 others(12): Show |
26 | HG00738.hp2 HG01243.hp2 HG01346.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*5398C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 5398 | chr11 | 94876193 | ||||||
| chr11:94876453 | A | G | 1 | a0001c0010t0038 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5658A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 5658 | chr11 | 94876453 | ||||||
| chr11:94876638 | T | C | 1 | a0001c0001t0033 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5843T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 5843 | chr11 | 94876638 | ||||||
| chr11:94876684 | G | A | 1 | a0001c0001t0045 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5889G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 5889 | chr11 | 94876684 | ||||||
| chr11:94876713 | T | A | 2 | a0001c0001t0022 a0001c0001t0042 |
3 | HG02572.hp1 HG02970.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5918T>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 13/13 | 5918 | chr11 | 94876713 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:94768585 | C | G | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.49+25C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94768585 | |||||||
| chr11:94768644 | C | T | 1 | a0001c0002t0031g0227 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.49+84C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94768644 | |||||||
| chr11:94768678 | G | T | 1 | a0001c0013t0006g0226 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.49+118G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94768678 | |||||||
| chr11:94768683 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(146): Show |
154 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.49+123G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94768683 | |||||||
| chr11:94768956 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.49+396G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94768956 | |||||||
| chr11:94769015 | G | C | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.49+455G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94769015 | |||||||
| chr11:94769018 | G | T | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.49+458G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94769018 | |||||||
| chr11:94769108 | C | T | 1 | a0007c0008t0015g0225 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.49+548C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94769108 | |||||||
| chr11:94769257 | G | GT | 4 | a0001c0001t0015g0151 a0001c0001t0022g0008 a0001c0001t0022g0152 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+703dupT | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 94769257 | ||||||
| chr11:94769337 | A | G | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.49+777A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94769337 | |||||||
| chr11:94769459 | C | T | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.49+899C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94769459 | |||||||
| chr11:94769746 | A | G | 2 | a0002c0003t0001g0007 a0002c0003t0001g0150 |
3 | HG01175.hp2 HG01433.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.49+1186A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94769746 | |||||||
| chr11:94769804 | C | A | 50 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(47): Show |
52 | HG01123.hp2 HG01256.hp1 HG01346.hp2 others(49): Show |
intron_variant | MODIFIER | c.49+1244C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94769804 | |||||||
| chr11:94770049 | T | G | 1 | a0001c0001t0001g0016 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.49+1489T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94770049 | |||||||
| chr11:94770287 | G | A | 1 | a0001c0006t0001g0194 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.49+1727G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94770287 | |||||||
| chr11:94770462 | G | C | 1 | a0001c0002t0002g0153 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.49+1902G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94770462 | |||||||
| chr11:94770518 | A | G | 1 | a0002c0003t0001g0149 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.49+1958A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94770518 | |||||||
| chr11:94770553 | T | C | 50 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(47): Show |
52 | HG01123.hp2 HG01256.hp1 HG01346.hp2 others(49): Show |
intron_variant | MODIFIER | c.49+1993T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94770553 | |||||||
| chr11:94771253 | C | A | 1 | a0001c0001t0020g0154 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.49+2693C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94771253 | |||||||
| chr11:94771253 | C | T | 1 | a0001c0001t0051g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.49+2693C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94771253 | |||||||
| chr11:94771256 | G | T | 45 | a0001c0001t0029g0172 a0001c0002t0002g0002 a0001c0002t0002g0010 others(42): Show |
46 | HG01123.hp2 HG01256.hp1 HG01346.hp2 others(43): Show |
intron_variant | MODIFIER | c.49+2696G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94771256 | |||||||
| chr11:94771259 | T | TG | 99 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0106 others(96): Show |
105 | HG00558.hp1 HG00642.hp1 HG00642.hp2 others(102): Show |
intron_variant | MODIFIER | c.49+2709dupG | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 94771259 | ||||||
| chr11:94771259 | T | TGG | 85 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0026 others(82): Show |
88 | HG00280.hp1 HG00280.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.49+2708_49+2709dup others(2): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 94771259 | ||||||
| chr11:94771261 | G | T | 1 | a0007c0008t0015g0225 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.49+2701G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94771261 | |||||||
| chr11:94771303 | A | G | 1 | a0001c0001t0005g0147 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.49+2743A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94771303 | |||||||
| chr11:94771714 | C | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(166): Show |
176 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(173): Show |
intron_variant | MODIFIER | c.49+3154C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94771714 | |||||||
| chr11:94771859 | G | T | 4 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0013g0207 others(1): Show |
4 | HG01109.hp1 HG02004.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+3299G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94771859 | |||||||
| chr11:94771921 | G | A | 1 | a0007c0008t0015g0225 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.49+3361G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94771921 | |||||||
| chr11:94772037 | T | C | 7 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0161 others(4): Show |
7 | HG01123.hp2 HG01256.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+3477T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94772037 | |||||||
| chr11:94772041 | G | A | 2 | a0001c0002t0002g0163 a0001c0002t0002g0164 |
2 | NA19063.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.49+3481G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94772041 | |||||||
| chr11:94772066 | G | A | 2 | a0001c0001t0028g0196 a0001c0001t0028g0197 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.49+3506G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94772066 | |||||||
| chr11:94772110 | A | G | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.49+3550A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94772110 | |||||||
| chr11:94772136 | A | G | 1 | a0001c0001t0053g0118 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.49+3576A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94772136 | |||||||
| chr11:94772287 | G | A | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.49+3727G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94772287 | |||||||
| chr11:94772779 | A | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(139): Show |
147 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.49+4219A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94772779 | |||||||
| chr11:94772806 | C | T | 6 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0016g0114 others(3): Show |
6 | HG02451.hp2 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+4246C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94772806 | |||||||
| chr11:94772827 | A | G | 6 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0013g0018 others(3): Show |
6 | HG01109.hp1 HG02004.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+4267A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94772827 | |||||||
| chr11:94772936 | T | A | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.49+4376T>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94772936 | |||||||
| chr11:94773281 | G | C | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.49+4721G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94773281 | |||||||
| chr11:94773666 | C | T | 2 | a0001c0001t0001g0116 a0001c0001t0016g0117 |
2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.49+5106C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94773666 | |||||||
| chr11:94773675 | A | G | 1 | a0001c0002t0024g0111 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.49+5115A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94773675 | |||||||
| chr11:94773924 | G | C | 2 | a0001c0001t0011g0019 a0001c0001t0011g0020 |
2 | HG02895.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+5364G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94773924 | |||||||
| chr11:94773939 | C | T | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.49+5379C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94773939 | |||||||
| chr11:94773971 | A | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(174): Show |
184 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(181): Show |
intron_variant | MODIFIER | c.49+5411A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94773971 | |||||||
| chr11:94774199 | C | T | 50 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(47): Show |
52 | HG01123.hp2 HG01256.hp1 HG01346.hp2 others(49): Show |
intron_variant | MODIFIER | c.49+5639C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94774199 | |||||||
| chr11:94774482 | A | T | 2 | a0003c0004t0037g0212 a0003c0004t0041g0211 |
2 | HG02738.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.49+5922A>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94774482 | |||||||
| chr11:94774509 | T | G | 1 | a0001c0002t0018g0088 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.49+5949T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94774509 | |||||||
| chr11:94774552 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(173): Show |
183 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(180): Show |
intron_variant | MODIFIER | c.49+5992G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94774552 | |||||||
| chr11:94774968 | C | A | 2 | a0001c0001t0004g0021 a0001c0013t0006g0226 |
2 | HG01123.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.49+6408C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94774968 | |||||||
| chr11:94775537 | G | T | 227 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
236 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(233): Show |
intron_variant | MODIFIER | c.49+6977G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94775537 | |||||||
| chr11:94775933 | G | A | 1 | a0001c0002t0036g0089 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.49+7373G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94775933 | |||||||
| chr11:94776008 | A | G | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.49+7448A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94776008 | |||||||
| chr11:94776152 | C | T | 6 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0013g0018 others(3): Show |
6 | HG01109.hp1 HG02004.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+7592C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94776152 | |||||||
| chr11:94776277 | C | T | 48 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(45): Show |
50 | HG01123.hp2 HG01256.hp1 HG01346.hp2 others(47): Show |
intron_variant | MODIFIER | c.49+7717C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94776277 | |||||||
| chr11:94776316 | C | T | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.49+7756C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94776316 | |||||||
| chr11:94776593 | A | G | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.49+8033A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94776593 | |||||||
| chr11:94776606 | C | T | 1 | a0001c0001t0016g0146 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.49+8046C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94776606 | |||||||
| chr11:94776619 | C | A | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.49+8059C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94776619 | |||||||
| chr11:94776699 | C | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(227): Show |
239 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(236): Show |
intron_variant | MODIFIER | c.49+8139C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94776699 | |||||||
| chr11:94776728 | C | G | 1 | a0001c0002t0003g0192 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.49+8168C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94776728 | |||||||
| chr11:94776749 | C | T | 4 | a0003c0004t0021g0223 a0003c0004t0037g0212 a0003c0004t0041g0211 others(1): Show |
4 | HG02602.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+8189C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94776749 | |||||||
| chr11:94777054 | A | T | 15 | a0001c0001t0003g0203 a0001c0001t0004g0014 a0001c0001t0004g0200 others(12): Show |
17 | HG00741.hp1 HG01243.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.49+8494A>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94777054 | |||||||
| chr11:94777207 | C | T | 1 | a0004c0012t0001g0087 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.49+8647C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94777207 | |||||||
| chr11:94777652 | C | T | 4 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(1): Show |
5 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+9092C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94777652 | |||||||
| chr11:94777686 | G | C | 1 | a0001c0001t0020g0154 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.49+9126G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94777686 | |||||||
| chr11:94778249 | A | G | 4 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 others(1): Show |
4 | HG00280.hp2 HG00738.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+9689A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94778249 | |||||||
| chr11:94778286 | A | C | 49 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(46): Show |
51 | HG01123.hp2 HG01256.hp1 HG01346.hp2 others(48): Show |
intron_variant | MODIFIER | c.49+9726A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94778286 | |||||||
| chr11:94778577 | G | A | 227 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
236 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(233): Show |
intron_variant | MODIFIER | c.49+10017G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94778577 | |||||||
| chr11:94778658 | A | T | 1 | a0001c0001t0020g0154 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.49+10098A>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94778658 | |||||||
| chr11:94778743 | T | C | 1 | a0001c0001t0020g0154 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.49+10183T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94778743 | |||||||
| chr11:94778761 | A | G | 2 | a0001c0001t0020g0221 a0001c0010t0038g0222 |
2 | HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.49+10201A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94778761 | |||||||
| chr11:94779012 | C | T | 230 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(227): Show |
239 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(236): Show |
intron_variant | MODIFIER | c.49+10452C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94779012 | |||||||
| chr11:94779037 | ATATAAT | A | 49 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(46): Show |
51 | HG01123.hp2 HG01256.hp1 HG01346.hp2 others(48): Show |
intron_variant | MODIFIER | c.49+10483_49+10488d others(8): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 94779037 | ||||||
| chr11:94779183 | A | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(230): Show |
242 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(239): Show |
intron_variant | MODIFIER | c.49+10623A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94779183 | |||||||
| chr11:94779372 | T | G | 2 | a0001c0002t0014g0165 a0001c0002t0014g0166 |
2 | NA18985.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.49+10812T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94779372 | |||||||
| chr11:94779536 | A | G | 1 | a0001c0010t0038g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.49+10976A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94779536 | |||||||
| chr11:94779687 | C | T | 6 | a0001c0001t0001g0001 a0001c0001t0001g0086 a0001c0001t0001g0145 others(3): Show |
7 | HG02145.hp2 HG02486.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+11127C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94779687 | |||||||
| chr11:94779860 | TA | T | 168 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(165): Show |
175 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(172): Show |
intron_variant | MODIFIER | c.49+11311delA | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 94779860 | ||||||
| chr11:94779871 | A | T | 230 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(227): Show |
239 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(236): Show |
intron_variant | MODIFIER | c.49+11311A>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94779871 | |||||||
| chr11:94779904 | T | C | 49 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(46): Show |
51 | HG01123.hp2 HG01256.hp1 HG01346.hp2 others(48): Show |
intron_variant | MODIFIER | c.49+11344T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94779904 | |||||||
| chr11:94780097 | G | A | 14 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(11): Show |
14 | HG02027.hp1 HG02165.hp2 NA18951.hp1 others(11): Show |
intron_variant | MODIFIER | c.49+11537G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94780097 | |||||||
| chr11:94780105 | A | G | 2 | a0001c0001t0001g0084 a0001c0001t0050g0085 |
2 | NA18977.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.49+11545A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94780105 | |||||||
| chr11:94780115 | G | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(164): Show |
174 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(171): Show |
intron_variant | MODIFIER | c.49+11555G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94780115 | |||||||
| chr11:94780285 | G | A | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.49+11725G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94780285 | |||||||
| chr11:94780352 | A | G | 4 | a0001c0001t0003g0022 a0003c0004t0021g0223 a0003c0004t0043g0224 others(1): Show |
4 | HG02602.hp2 HG02683.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+11792A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94780352 | |||||||
| chr11:94780557 | C | T | 6 | a0001c0001t0020g0221 a0001c0010t0038g0222 a0003c0004t0021g0223 others(3): Show |
6 | HG02280.hp2 HG02559.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+11997C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94780557 | |||||||
| chr11:94780582 | A | G | 2 | a0001c0001t0001g0108 a0001c0001t0029g0107 |
2 | NA18959.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.49+12022A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94780582 | |||||||
| chr11:94780728 | C | T | 1 | a0001c0001t0053g0118 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.49+12168C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94780728 | |||||||
| chr11:94780823 | G | A | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.49+12263G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94780823 | |||||||
| chr11:94781017 | T | G | 15 | a0001c0001t0003g0203 a0001c0001t0004g0014 a0001c0001t0004g0200 others(12): Show |
17 | HG00741.hp1 HG01243.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.49+12457T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94781017 | |||||||
| chr11:94781106 | C | T | 1 | a0001c0001t0040g0144 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.49+12546C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94781106 | |||||||
| chr11:94781148 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.49+12588G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94781148 | |||||||
| chr11:94781269 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.49+12709C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94781269 | |||||||
| chr11:94781270 | G | A | 1 | a0001c0001t0015g0213 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.49+12710G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94781270 | |||||||
| chr11:94781278 | A | G | 1 | a0001c0002t0046g0191 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.49+12718A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94781278 | |||||||
| chr11:94781517 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG01515.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.49+12957G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94781517 | |||||||
| chr11:94781588 | A | G | 1 | a0001c0001t0040g0144 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.49+13028A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94781588 | |||||||
| chr11:94781689 | C | G | 2 | a0001c0001t0002g0031 a0001c0001t0002g0032 |
2 | NA18974.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.49+13129C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94781689 | |||||||
| chr11:94781961 | C | T | 4 | a0003c0004t0021g0223 a0003c0004t0037g0212 a0003c0004t0041g0211 others(1): Show |
4 | HG02602.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-13050C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94781961 | |||||||
| chr11:94782035 | T | A | 1 | a0001c0001t0020g0154 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.50-12976T>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94782035 | |||||||
| chr11:94782080 | C | T | 23 | a0001c0001t0001g0015 a0001c0001t0001g0073 a0001c0001t0001g0074 others(20): Show |
23 | HG01433.hp1 HG02132.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.50-12931C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94782080 | |||||||
| chr11:94782091 | G | GA | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.50-12914dupA | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 94782091 | ||||||
| chr11:94782203 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(168): Show |
178 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(175): Show |
intron_variant | MODIFIER | c.50-12808T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94782203 | |||||||
| chr11:94782430 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
236 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(233): Show |
intron_variant | MODIFIER | c.50-12581T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94782430 | |||||||
| chr11:94782462 | A | G | 1 | a0001c0002t0002g0190 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.50-12549A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94782462 | |||||||
| chr11:94782641 | A | G | 1 | a0001c0001t0020g0154 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.50-12370A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94782641 | |||||||
| chr11:94782906 | T | G | 15 | a0001c0001t0003g0203 a0001c0001t0004g0014 a0001c0001t0004g0200 others(12): Show |
17 | HG00741.hp1 HG01243.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.50-12105T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94782906 | |||||||
| chr11:94782937 | T | G | 1 | a0001c0001t0053g0118 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.50-12074T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94782937 | |||||||
| chr11:94783149 | G | T | 1 | a0007c0008t0015g0225 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.50-11862G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94783149 | |||||||
| chr11:94783338 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.50-11673C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94783338 | |||||||
| chr11:94783537 | A | G | 2 | a0001c0001t0011g0019 a0001c0001t0011g0020 |
2 | HG02895.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.50-11474A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94783537 | |||||||
| chr11:94783606 | C | T | 2 | a0001c0001t0020g0221 a0001c0010t0038g0222 |
2 | HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.50-11405C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94783606 | |||||||
| chr11:94783648 | T | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(227): Show |
239 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(236): Show |
intron_variant | MODIFIER | c.50-11363T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94783648 | |||||||
| chr11:94783770 | A | G | 1 | a0001c0002t0012g0105 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.50-11241A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94783770 | |||||||
| chr11:94783926 | G | GT | 6 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0007g0228 others(3): Show |
6 | HG00738.hp2 HG02735.hp2 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-11074dupT | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 94783926 | ||||||
| chr11:94784001 | T | C | 1 | a0002c0003t0001g0036 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.50-11010T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94784001 | |||||||
| chr11:94784446 | T | G | 1 | a0001c0002t0002g0158 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.50-10565T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94784446 | |||||||
| chr11:94784910 | C | T | 1 | a0001c0001t0032g0068 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.50-10101C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94784910 | |||||||
| chr11:94784968 | CAA | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(220): Show |
232 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(229): Show |
intron_variant | MODIFIER | c.50-10031_50-10030d others(4): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 94784968 | ||||||
| chr11:94784977 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.50-10034A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94784977 | |||||||
| chr11:94785091 | A | C | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.50-9920A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94785091 | |||||||
| chr11:94785182 | C | T | 4 | a0001c0001t0015g0151 a0001c0001t0022g0008 a0001c0001t0022g0152 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-9829C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94785182 | |||||||
| chr11:94785286 | G | A | 1 | a0001c0002t0006g0090 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.50-9725G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94785286 | |||||||
| chr11:94785291 | T | C | 4 | a0001c0001t0003g0070 a0001c0001t0003g0071 a0001c0001t0003g0072 others(1): Show |
4 | HG02258.hp2 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-9720T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94785291 | |||||||
| chr11:94785310 | A | G | 7 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0016g0114 others(4): Show |
7 | HG01884.hp1 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-9701A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94785310 | |||||||
| chr11:94785423 | G | A | 2 | a0001c0001t0003g0022 a0007c0008t0015g0225 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.50-9588G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94785423 | |||||||
| chr11:94785528 | A | G | 3 | a0001c0001t0003g0081 a0001c0001t0048g0082 a0002c0003t0001g0083 |
3 | NA18962.hp2 NA18999.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.50-9483A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94785528 | |||||||
| chr11:94785577 | G | C | 15 | a0001c0001t0003g0203 a0001c0001t0004g0014 a0001c0001t0004g0200 others(12): Show |
17 | HG00741.hp1 HG01243.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.50-9434G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94785577 | |||||||
| chr11:94785673 | T | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(227): Show |
239 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(236): Show |
intron_variant | MODIFIER | c.50-9338T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94785673 | |||||||
| chr11:94785738 | G | T | 4 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0143 others(1): Show |
4 | NA18956.hp2 NA18959.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-9273G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94785738 | |||||||
| chr11:94786147 | T | C | 4 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(1): Show |
5 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-8864T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94786147 | |||||||
| chr11:94786385 | G | A | 6 | a0001c0001t0011g0019 a0001c0001t0011g0020 a0001c0001t0011g0123 others(3): Show |
6 | HG02615.hp2 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-8626G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94786385 | |||||||
| chr11:94786391 | A | C | 1 | a0001c0010t0038g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.50-8620A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94786391 | |||||||
| chr11:94786460 | T | G | 1 | a0001c0001t0005g0126 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.50-8551T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94786460 | |||||||
| chr11:94786462 | C | T | 1 | a0001c0001t0005g0126 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.50-8549C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94786462 | |||||||
| chr11:94786541 | C | G | 5 | a0001c0001t0017g0195 a0001c0001t0017g0204 a0001c0001t0017g0205 others(2): Show |
5 | HG01243.hp2 HG02647.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-8470C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94786541 | |||||||
| chr11:94786566 | CTTCTTTT | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
236 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(233): Show |
intron_variant | MODIFIER | c.50-8428_50-8422del others(7): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 94786566 | ||||||
| chr11:94786711 | C | T | 3 | a0001c0002t0002g0011 a0001c0002t0006g0011 a0001c0002t0008g0162 |
3 | HG01123.hp2 HG01346.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.50-8300C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94786711 | |||||||
| chr11:94786810 | A | G | 2 | a0001c0001t0004g0021 a0001c0013t0006g0226 |
2 | HG01123.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.50-8201A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94786810 | |||||||
| chr11:94786905 | C | T | 227 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
236 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(233): Show |
intron_variant | MODIFIER | c.50-8106C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94786905 | |||||||
| chr11:94786909 | A | G | 1 | a0001c0001t0020g0154 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.50-8102A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94786909 | |||||||
| chr11:94787076 | C | T | 227 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
236 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(233): Show |
intron_variant | MODIFIER | c.50-7935C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94787076 | |||||||
| chr11:94787456 | G | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(168): Show |
178 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(175): Show |
intron_variant | MODIFIER | c.50-7555G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94787456 | |||||||
| chr11:94787557 | G | A | 4 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0013g0207 others(1): Show |
4 | HG01109.hp1 HG02004.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-7454G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94787557 | |||||||
| chr11:94787687 | CAAAAAAA others(4): Show |
C | 1 | a0001c0006t0001g0214 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.50-7294_50-7284del others(11): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 94787687 | ||||||
| chr11:94787687 | CAAAAAAA others(5): Show |
C | 11 | a0001c0001t0009g0155 a0001c0001t0017g0195 a0001c0001t0017g0204 others(8): Show |
11 | HG01934.hp2 HG02056.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.50-7295_50-7284del others(12): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 94787687 | ||||||
| chr11:94787687 | CAAAAAAA others(6): Show |
C | 62 | a0001c0001t0001g0073 a0001c0001t0001g0086 a0001c0001t0001g0116 others(59): Show |
67 | HG00741.hp1 HG00741.hp2 HG01123.hp2 others(64): Show |
intron_variant | MODIFIER | c.50-7296_50-7284del others(13): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 94787687 | ||||||
| chr11:94787687 | CAAAAAAA others(7): Show |
C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0025 others(134): Show |
141 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.50-7297_50-7284del others(14): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 94787687 | ||||||
| chr11:94787687 | CAAAAAAA others(8): Show |
C | 13 | a0001c0001t0001g0016 a0001c0001t0001g0030 a0001c0001t0001g0035 others(10): Show |
13 | HG00642.hp2 HG01106.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.50-7298_50-7284del others(15): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 94787687 | ||||||
| chr11:94787687 | CAAAAAAA others(9): Show |
C | 3 | a0001c0001t0001g0220 a0001c0001t0020g0154 a0001c0010t0038g0222 |
3 | HG02559.hp2 HG02965.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.50-7299_50-7284del others(16): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 94787687 | ||||||
| chr11:94787687 | CAAAAAAA others(15): Show |
C | 1 | a0001c0001t0028g0197 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.50-7305_50-7284del others(22): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 94787687 | ||||||
| chr11:94788407 | A | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(132): Show |
140 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.50-6604A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94788407 | |||||||
| chr11:94788583 | A | T | 1 | a0001c0002t0002g0188 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.50-6428A>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94788583 | |||||||
| chr11:94788958 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG01515.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.50-6053G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94788958 | |||||||
| chr11:94788958 | G | T | 1 | a0001c0001t0020g0154 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.50-6053G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94788958 | |||||||
| chr11:94789202 | A | G | 2 | a0002c0003t0001g0007 a0002c0003t0001g0150 |
3 | HG01175.hp2 HG01433.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.50-5809A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94789202 | |||||||
| chr11:94789419 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.50-5592G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94789419 | |||||||
| chr11:94789454 | C | T | 6 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0013g0018 others(3): Show |
6 | HG01109.hp1 HG02004.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-5557C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94789454 | |||||||
| chr11:94789790 | G | C | 1 | a0001c0001t0004g0039 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.50-5221G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94789790 | |||||||
| chr11:94789864 | T | C | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.50-5147T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94789864 | |||||||
| chr11:94789937 | T | C | 1 | a0001c0001t0004g0039 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.50-5074T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94789937 | |||||||
| chr11:94790208 | G | A | 5 | a0001c0001t0029g0172 a0001c0002t0002g0002 a0001c0002t0002g0171 others(2): Show |
6 | NA18962.hp1 NA18970.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-4803G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94790208 | |||||||
| chr11:94790288 | T | G | 6 | a0001c0001t0020g0221 a0001c0010t0038g0222 a0003c0004t0021g0223 others(3): Show |
6 | HG02280.hp2 HG02559.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-4723T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94790288 | |||||||
| chr11:94790513 | G | A | 2 | a0001c0001t0015g0213 a0001c0001t0020g0154 |
2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.50-4498G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94790513 | |||||||
| chr11:94790667 | A | G | 8 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0007g0228 others(5): Show |
8 | HG00738.hp2 HG01074.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.50-4344A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94790667 | |||||||
| chr11:94790671 | T | C | 64 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0007g0228 others(61): Show |
66 | HG00738.hp2 HG01074.hp1 HG01123.hp2 others(63): Show |
intron_variant | MODIFIER | c.50-4340T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94790671 | |||||||
| chr11:94790757 | C | T | 54 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0007g0228 others(51): Show |
56 | HG00738.hp2 HG01074.hp1 HG01123.hp2 others(53): Show |
intron_variant | MODIFIER | c.50-4254C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94790757 | |||||||
| chr11:94790868 | C | G | 16 | a0001c0001t0003g0203 a0001c0001t0004g0014 a0001c0001t0004g0021 others(13): Show |
18 | HG00741.hp1 HG01243.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.50-4143C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94790868 | |||||||
| chr11:94790902 | C | T | 1 | a0001c0001t0013g0209 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.50-4109C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94790902 | |||||||
| chr11:94791170 | C | G | 15 | a0001c0001t0003g0203 a0001c0001t0004g0014 a0001c0001t0004g0200 others(12): Show |
17 | HG00741.hp1 HG01243.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.50-3841C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94791170 | |||||||
| chr11:94791177 | C | A | 1 | a0002c0003t0001g0091 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.50-3834C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94791177 | |||||||
| chr11:94791388 | C | G | 1 | a0001c0001t0001g0108 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.50-3623C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94791388 | |||||||
| chr11:94791490 | G | A | 55 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0007g0228 others(52): Show |
57 | HG00738.hp2 HG01074.hp1 HG01123.hp2 others(54): Show |
intron_variant | MODIFIER | c.50-3521G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94791490 | |||||||
| chr11:94791555 | A | G | 15 | a0001c0001t0003g0203 a0001c0001t0004g0014 a0001c0001t0004g0200 others(12): Show |
17 | HG00741.hp1 HG01243.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.50-3456A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94791555 | |||||||
| chr11:94791593 | A | C | 5 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0027g0216 others(2): Show |
5 | HG01074.hp1 HG03195.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-3418A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94791593 | |||||||
| chr11:94791893 | T | G | 2 | a0001c0001t0015g0213 a0001c0001t0020g0154 |
2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.50-3118T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94791893 | |||||||
| chr11:94791950 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0050g0085 |
2 | NA18977.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.50-3061C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94791950 | |||||||
| chr11:94792046 | G | C | 2 | a0001c0001t0013g0207 a0001c0001t0013g0209 |
2 | HG01109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.50-2965G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94792046 | |||||||
| chr11:94792183 | A | G | 1 | a0002c0019t0004g0103 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.50-2828A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94792183 | |||||||
| chr11:94792213 | C | G | 1 | a0001c0001t0033g0199 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.50-2798C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94792213 | |||||||
| chr11:94792214 | G | A | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.50-2797G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94792214 | |||||||
| chr11:94792229 | C | A | 1 | a0001c0001t0019g0064 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.50-2782C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94792229 | |||||||
| chr11:94792232 | ACAC | A | 3 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0005c0015t0010g0219 |
3 | HG01074.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.50-2775_50-2773del others(3): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 94792232 | ||||||
| chr11:94792290 | A | G | 1 | a0001c0002t0002g0187 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.50-2721A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94792290 | |||||||
| chr11:94792326 | T | C | 8 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0007g0228 others(5): Show |
8 | HG00738.hp2 HG01074.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.50-2685T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94792326 | |||||||
| chr11:94792426 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.50-2585C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94792426 | |||||||
| chr11:94792455 | T | C | 91 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0001g0218 others(88): Show |
95 | HG00738.hp2 HG00741.hp1 HG01074.hp1 others(92): Show |
intron_variant | MODIFIER | c.50-2556T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94792455 | |||||||
| chr11:94792536 | C | G | 1 | a0001c0002t0018g0139 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.50-2475C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94792536 | |||||||
| chr11:94792600 | C | G | 8 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0007g0228 others(5): Show |
8 | HG00738.hp2 HG01074.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.50-2411C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94792600 | |||||||
| chr11:94792734 | C | A | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.50-2277C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94792734 | |||||||
| chr11:94792763 | T | G | 8 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0007g0228 others(5): Show |
8 | HG00738.hp2 HG01074.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.50-2248T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94792763 | |||||||
| chr11:94792780 | C | T | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.50-2231C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94792780 | |||||||
| chr11:94792805 | A | T | 5 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0027g0216 others(2): Show |
5 | HG01074.hp1 HG03195.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-2206A>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94792805 | |||||||
| chr11:94792831 | T | C | 1 | a0001c0001t0051g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.50-2180T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94792831 | |||||||
| chr11:94792838 | T | A | 6 | a0001c0001t0020g0221 a0001c0010t0038g0222 a0003c0004t0021g0223 others(3): Show |
6 | HG02280.hp2 HG02559.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-2173T>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94792838 | |||||||
| chr11:94792853 | G | C | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.50-2158G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94792853 | |||||||
| chr11:94792854 | G | T | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.50-2157G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94792854 | |||||||
| chr11:94792927 | A | G | 9 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0007g0228 others(6): Show |
9 | HG00738.hp2 HG01074.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.50-2084A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94792927 | |||||||
| chr11:94793017 | T | C | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.50-1994T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94793017 | |||||||
| chr11:94793062 | A | G | 1 | a0001c0001t0003g0138 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.50-1949A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94793062 | |||||||
| chr11:94793077 | C | T | 8 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0007g0228 others(5): Show |
8 | HG00738.hp2 HG01074.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.50-1934C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94793077 | |||||||
| chr11:94793171 | A | G | 8 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0007g0228 others(5): Show |
8 | HG00738.hp2 HG01074.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.50-1840A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94793171 | |||||||
| chr11:94793202 | T | C | 9 | a0001c0001t0005g0040 a0001c0001t0005g0041 a0001c0001t0005g0043 others(6): Show |
9 | HG00735.hp1 HG01074.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.50-1809T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94793202 | |||||||
| chr11:94793362 | G | T | 36 | a0001c0001t0001g0038 a0001c0001t0001g0054 a0001c0001t0004g0004 others(33): Show |
38 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.50-1649G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94793362 | |||||||
| chr11:94793417 | A | G | 8 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0007g0228 others(5): Show |
8 | HG00738.hp2 HG01074.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.50-1594A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94793417 | |||||||
| chr11:94793542 | T | C | 44 | a0001c0002t0002g0002 a0001c0002t0002g0010 a0001c0002t0002g0011 others(41): Show |
45 | HG01123.hp2 HG01256.hp1 HG01346.hp2 others(42): Show |
intron_variant | MODIFIER | c.50-1469T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94793542 | |||||||
| chr11:94793579 | G | A | 6 | a0001c0001t0001g0054 a0001c0001t0004g0004 a0001c0001t0004g0039 others(3): Show |
7 | NA18612.hp1 NA18945.hp2 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.50-1432G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94793579 | |||||||
| chr11:94793665 | G | A | 1 | a0001c0001t0034g0127 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.50-1346G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94793665 | |||||||
| chr11:94793675 | C | T | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.50-1336C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94793675 | |||||||
| chr11:94793730 | A | G | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.50-1281A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94793730 | |||||||
| chr11:94794081 | A | G | 2 | a0002c0003t0001g0051 a0002c0003t0001g0052 |
2 | NA18952.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.50-930A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94794081 | |||||||
| chr11:94794163 | A | T | 1 | a0001c0002t0018g0139 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.50-848A>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94794163 | |||||||
| chr11:94794278 | C | T | 1 | a0001c0001t0003g0203 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.50-733C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94794278 | |||||||
| chr11:94794296 | C | T | 3 | a0001c0001t0011g0123 a0001c0001t0011g0125 a0001c0001t0026g0124 |
3 | HG02717.hp1 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.50-715C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94794296 | |||||||
| chr11:94794717 | C | T | 44 | a0001c0002t0002g0002 a0001c0002t0002g0010 a0001c0002t0002g0011 others(41): Show |
45 | HG01123.hp2 HG01256.hp1 HG01346.hp2 others(42): Show |
intron_variant | MODIFIER | c.50-294C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94794717 | |||||||
| chr11:94794729 | T | G | 5 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0027g0216 others(2): Show |
5 | HG01074.hp1 HG03195.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-282T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94794729 | |||||||
| chr11:94794808 | T | C | 1 | a0001c0001t0005g0126 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.50-203T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94794808 | |||||||
| chr11:94794890 | A | C | 88 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0001g0218 others(85): Show |
92 | HG00738.hp2 HG00741.hp1 HG01074.hp1 others(89): Show |
intron_variant | MODIFIER | c.50-121A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94794890 | |||||||
| chr11:94794909 | T | C | 5 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0027g0216 others(2): Show |
5 | HG01074.hp1 HG03195.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-102T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 1/12 | chr11 | 94794909 | |||||||
| chr11:94795308 | C | A | 1 | a0001c0001t0032g0068 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.199+148C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94795308 | |||||||
| chr11:94795332 | A | G | 1 | a0001c0001t0001g0080 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.199+172A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94795332 | |||||||
| chr11:94795422 | A | C | 4 | a0003c0004t0021g0223 a0003c0004t0037g0212 a0003c0004t0041g0211 others(1): Show |
4 | HG02602.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+262A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94795422 | |||||||
| chr11:94795458 | C | T | 5 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0027g0216 others(2): Show |
5 | HG01074.hp1 HG03195.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.199+298C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94795458 | |||||||
| chr11:94795786 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.199+626C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94795786 | |||||||
| chr11:94795800 | T | C | 2 | a0001c0001t0027g0216 a0001c0001t0027g0217 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.199+640T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94795800 | |||||||
| chr11:94795871 | C | G | 14 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0159 others(11): Show |
14 | HG01123.hp2 HG01256.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.199+711C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94795871 | |||||||
| chr11:94796010 | C | A | 1 | a0001c0001t0053g0118 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.199+850C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94796010 | |||||||
| chr11:94796066 | A | G | 8 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0007g0228 others(5): Show |
8 | HG00738.hp2 HG01074.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.199+906A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94796066 | |||||||
| chr11:94796167 | C | T | 1 | a0001c0001t0016g0146 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.199+1007C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94796167 | |||||||
| chr11:94796179 | A | C | 8 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0007g0228 others(5): Show |
8 | HG00738.hp2 HG01074.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.199+1019A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94796179 | |||||||
| chr11:94796326 | G | A | 3 | a0001c0001t0009g0155 a0001c0001t0009g0156 a0001c0001t0009g0157 |
3 | HG02615.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.199+1166G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94796326 | |||||||
| chr11:94796615 | G | T | 63 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0007g0228 others(60): Show |
65 | HG00738.hp2 HG01074.hp1 HG01123.hp2 others(62): Show |
intron_variant | MODIFIER | c.199+1455G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94796615 | |||||||
| chr11:94796704 | G | A | 2 | a0001c0001t0003g0022 a0007c0008t0015g0225 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.199+1544G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94796704 | |||||||
| chr11:94796744 | G | A | 1 | a0001c0001t0003g0141 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.199+1584G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94796744 | |||||||
| chr11:94797014 | T | A | 1 | a0001c0016t0010g0129 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.199+1854T>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94797014 | |||||||
| chr11:94797085 | A | G | 55 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(52): Show |
57 | HG01123.hp2 HG01256.hp1 HG01346.hp2 others(54): Show |
intron_variant | MODIFIER | c.199+1925A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94797085 | |||||||
| chr11:94797187 | C | T | 1 | a0001c0001t0013g0119 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.199+2027C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94797187 | |||||||
| chr11:94797198 | T | C | 51 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(48): Show |
53 | HG01123.hp2 HG01256.hp1 HG01346.hp2 others(50): Show |
intron_variant | MODIFIER | c.199+2038T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94797198 | |||||||
| chr11:94797527 | A | G | 49 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(46): Show |
51 | HG01123.hp2 HG01256.hp1 HG01346.hp2 others(48): Show |
intron_variant | MODIFIER | c.200-1863A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94797527 | |||||||
| chr11:94797629 | C | T | 8 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0007g0228 others(5): Show |
8 | HG00738.hp2 HG01074.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.200-1761C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94797629 | |||||||
| chr11:94797670 | C | A | 1 | a0001c0001t0020g0154 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.200-1720C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94797670 | |||||||
| chr11:94797697 | C | A | 1 | a0001c0002t0002g0189 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.200-1693C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94797697 | |||||||
| chr11:94797790 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.200-1600C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94797790 | |||||||
| chr11:94797938 | T | C | 5 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0027g0216 others(2): Show |
5 | HG01074.hp1 HG03195.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.200-1452T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94797938 | |||||||
| chr11:94798189 | G | T | 55 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(52): Show |
57 | HG01123.hp2 HG01256.hp1 HG01346.hp2 others(54): Show |
intron_variant | MODIFIER | c.200-1201G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94798189 | |||||||
| chr11:94798348 | G | A | 1 | a0001c0001t0007g0228 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.200-1042G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94798348 | |||||||
| chr11:94798525 | G | A | 5 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0027g0216 others(2): Show |
5 | HG01074.hp1 HG03195.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.200-865G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94798525 | |||||||
| chr11:94798546 | A | G | 2 | a0001c0001t0001g0079 a0001c0001t0012g0078 |
2 | NA18966.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.200-844A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94798546 | |||||||
| chr11:94798565 | G | T | 1 | a0001c0013t0006g0226 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.200-825G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94798565 | |||||||
| chr11:94798639 | C | T | 2 | a0001c0001t0001g0034 a0002c0003t0001g0150 |
2 | HG01433.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.200-751C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94798639 | |||||||
| chr11:94798784 | G | A | 79 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(76): Show |
82 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.200-606G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94798784 | |||||||
| chr11:94798814 | C | A | 6 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(3): Show |
7 | HG02615.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.200-576C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | chr11 | 94798814 | |||||||
| chr11:94799297 | T | TGGGGTAG others(7): Show |
1 | a0001c0001t0025g0023 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.200-92_200-91insGG others(12): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 94799297 | ||||||
| chr11:94800315 | A | T | 1 | a0001c0001t0029g0107 | 1 | NA18959.hp1 | splice_region_variant&intron_variant | LOW | c.1121+4A>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94800315 | |||||||
| chr11:94800629 | C | T | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1121+318C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94800629 | |||||||
| chr11:94800646 | C | A | 1 | a0001c0002t0002g0190 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1121+335C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94800646 | |||||||
| chr11:94800875 | C | T | 4 | a0003c0004t0021g0223 a0003c0004t0037g0212 a0003c0004t0041g0211 others(1): Show |
4 | HG02602.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121+564C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94800875 | |||||||
| chr11:94801029 | T | C | 2 | a0001c0001t0020g0154 a0001c0001t0032g0068 |
2 | HG01106.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1121+718T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94801029 | |||||||
| chr11:94801095 | G | A | 2 | a0001c0001t0020g0221 a0001c0010t0038g0222 |
2 | HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1121+784G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94801095 | |||||||
| chr11:94801145 | T | A | 2 | a0001c0001t0027g0216 a0001c0001t0027g0217 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1121+834T>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94801145 | |||||||
| chr11:94801239 | G | A | 1 | a0001c0001t0015g0213 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1121+928G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94801239 | |||||||
| chr11:94801433 | G | A | 84 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(81): Show |
87 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.1121+1122G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94801433 | |||||||
| chr11:94801448 | G | A | 1 | a0001c0001t0005g0040 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1121+1137G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94801448 | |||||||
| chr11:94801452 | G | T | 88 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 others(85): Show |
91 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(88): Show |
intron_variant | MODIFIER | c.1121+1141G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94801452 | |||||||
| chr11:94801535 | A | G | 1 | a0001c0002t0002g0169 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1121+1224A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94801535 | |||||||
| chr11:94801566 | A | G | 73 | a0001c0002t0001g0006 a0001c0002t0001g0057 a0001c0002t0001g0059 others(70): Show |
75 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.1121+1255A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94801566 | |||||||
| chr11:94801820 | G | C | 1 | a0001c0001t0001g0074 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1121+1509G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94801820 | |||||||
| chr11:94801930 | A | T | 2 | a0001c0001t0028g0196 a0001c0001t0028g0197 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1121+1619A>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94801930 | |||||||
| chr11:94801942 | C | T | 2 | a0001c0001t0028g0196 a0001c0001t0028g0197 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1121+1631C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94801942 | |||||||
| chr11:94802088 | A | T | 4 | a0003c0004t0021g0223 a0003c0004t0037g0212 a0003c0004t0041g0211 others(1): Show |
4 | HG02602.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121+1777A>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94802088 | |||||||
| chr11:94802112 | C | A | 1 | a0001c0001t0039g0112 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1121+1801C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94802112 | |||||||
| chr11:94802209 | T | C | 85 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(82): Show |
88 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.1121+1898T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94802209 | |||||||
| chr11:94802216 | C | G | 1 | a0001c0001t0015g0213 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1121+1905C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94802216 | |||||||
| chr11:94802641 | T | G | 6 | a0001c0001t0011g0019 a0001c0001t0011g0020 a0001c0001t0011g0123 others(3): Show |
6 | HG02615.hp2 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1121+2330T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94802641 | |||||||
| chr11:94802692 | T | C | 110 | a0001c0001t0003g0022 a0001c0001t0003g0203 a0001c0001t0004g0014 others(107): Show |
115 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(112): Show |
intron_variant | MODIFIER | c.1121+2381T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94802692 | |||||||
| chr11:94803030 | A | G | 4 | a0003c0004t0021g0223 a0003c0004t0037g0212 a0003c0004t0041g0211 others(1): Show |
4 | HG02602.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121+2719A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94803030 | |||||||
| chr11:94803089 | G | C | 2 | a0001c0001t0013g0207 a0001c0001t0013g0209 |
2 | HG01109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1121+2778G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94803089 | |||||||
| chr11:94803184 | G | A | 1 | a0001c0002t0002g0153 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1121+2873G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94803184 | |||||||
| chr11:94803314 | A | G | 89 | a0001c0001t0003g0022 a0001c0001t0007g0228 a0001c0001t0007g0229 others(86): Show |
92 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.1121+3003A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94803314 | |||||||
| chr11:94803325 | T | TAAA | 3 | a0001c0001t0005g0040 a0001c0001t0005g0041 a0001c0001t0005g0092 |
3 | HG01074.hp2 HG02602.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1121+3015_1121+301 others(7): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 94803325 | ||||||
| chr11:94803687 | G | A | 4 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(1): Show |
5 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1121+3376G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94803687 | |||||||
| chr11:94803692 | C | T | 1 | a0001c0001t0010g0028 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1121+3381C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94803692 | |||||||
| chr11:94803775 | C | G | 73 | a0001c0002t0001g0006 a0001c0002t0001g0057 a0001c0002t0001g0059 others(70): Show |
75 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.1121+3464C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94803775 | |||||||
| chr11:94803803 | T | C | 4 | a0003c0004t0021g0223 a0003c0004t0037g0212 a0003c0004t0041g0211 others(1): Show |
4 | HG02602.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121+3492T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94803803 | |||||||
| chr11:94803946 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1121+3635C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94803946 | |||||||
| chr11:94803965 | T | G | 2 | a0001c0005t0001g0013 a0001c0005t0052g0198 |
3 | HG02486.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1121+3654T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94803965 | |||||||
| chr11:94804075 | C | T | 2 | a0001c0001t0020g0154 a0001c0001t0032g0068 |
2 | HG01106.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1121+3764C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94804075 | |||||||
| chr11:94804531 | G | A | 1 | a0001c0001t0004g0021 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1121+4220G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94804531 | |||||||
| chr11:94804722 | CTT | C | 7 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0046 others(4): Show |
7 | HG01346.hp1 HG01515.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.1121+4412_1121+441 others(6): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94804722 | |||||||
| chr11:94804725 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1121+4414A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94804725 | |||||||
| chr11:94804766 | T | C | 1 | a0001c0001t0004g0021 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1121+4455T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94804766 | |||||||
| chr11:94805038 | C | G | 90 | a0001c0001t0003g0022 a0001c0001t0007g0228 a0001c0001t0007g0229 others(87): Show |
93 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.1121+4727C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94805038 | |||||||
| chr11:94805056 | G | A | 4 | a0001c0001t0015g0151 a0001c0001t0022g0008 a0001c0001t0022g0152 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121+4745G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94805056 | |||||||
| chr11:94805074 | G | T | 1 | a0001c0002t0006g0063 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1121+4763G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94805074 | |||||||
| chr11:94805279 | A | G | 1 | a0003c0004t0043g0224 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1121+4968A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94805279 | |||||||
| chr11:94805323 | T | A | 86 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(83): Show |
89 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.1121+5012T>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94805323 | |||||||
| chr11:94805610 | A | G | 2 | a0001c0001t0027g0216 a0001c0001t0027g0217 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1121+5299A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94805610 | |||||||
| chr11:94805669 | A | G | 1 | a0003c0004t0021g0223 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1121+5358A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94805669 | |||||||
| chr11:94805683 | G | A | 80 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(77): Show |
83 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.1121+5372G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94805683 | |||||||
| chr11:94805691 | G | A | 1 | a0003c0004t0021g0223 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1121+5380G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94805691 | |||||||
| chr11:94805740 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1121+5429G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94805740 | |||||||
| chr11:94805879 | A | G | 116 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0003g0022 others(113): Show |
121 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(118): Show |
intron_variant | MODIFIER | c.1121+5568A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94805879 | |||||||
| chr11:94805945 | G | C | 1 | a0001c0002t0006g0056 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1121+5634G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94805945 | |||||||
| chr11:94805946 | C | T | 1 | a0001c0002t0006g0056 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1121+5635C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94805946 | |||||||
| chr11:94806181 | G | T | 86 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(83): Show |
89 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.1121+5870G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94806181 | |||||||
| chr11:94806256 | T | A | 1 | a0001c0002t0006g0056 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1121+5945T>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94806256 | |||||||
| chr11:94806551 | C | T | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG01256.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1121+6240C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94806551 | |||||||
| chr11:94806663 | C | T | 2 | a0001c0005t0001g0013 a0001c0005t0052g0198 |
3 | HG02486.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1121+6352C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94806663 | |||||||
| chr11:94806724 | A | C | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1121+6413A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94806724 | |||||||
| chr11:94806754 | T | C | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0016t0010g0129 |
3 | HG02055.hp1 HG02451.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1121+6443T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94806754 | |||||||
| chr11:94806766 | G | C | 89 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 others(86): Show |
92 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.1121+6455G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94806766 | |||||||
| chr11:94806778 | G | C | 2 | a0001c0001t0020g0221 a0001c0010t0038g0222 |
2 | HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1121+6467G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94806778 | |||||||
| chr11:94806930 | G | T | 2 | a0001c0001t0020g0221 a0001c0010t0038g0222 |
2 | HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1121+6619G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94806930 | |||||||
| chr11:94806954 | C | T | 4 | a0003c0004t0021g0223 a0003c0004t0037g0212 a0003c0004t0041g0211 others(1): Show |
4 | HG02602.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121+6643C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94806954 | |||||||
| chr11:94807071 | T | C | 6 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0013g0018 others(3): Show |
6 | HG01109.hp1 HG02004.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1121+6760T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94807071 | |||||||
| chr11:94807092 | C | T | 1 | a0001c0007t0005g0044 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1121+6781C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94807092 | |||||||
| chr11:94807162 | A | G | 1 | a0001c0001t0003g0072 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1121+6851A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94807162 | |||||||
| chr11:94807217 | C | G | 2 | a0001c0001t0020g0154 a0001c0001t0032g0068 |
2 | HG01106.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1121+6906C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94807217 | |||||||
| chr11:94807244 | G | A | 4 | a0001c0002t0012g0096 a0001c0002t0024g0037 a0001c0002t0024g0111 others(1): Show |
4 | HG00558.hp1 HG02027.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121+6933G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94807244 | |||||||
| chr11:94807300 | T | C | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1121+6989T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94807300 | |||||||
| chr11:94807391 | T | G | 87 | a0001c0001t0003g0022 a0001c0001t0009g0009 a0001c0001t0009g0155 others(84): Show |
90 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.1121+7080T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94807391 | |||||||
| chr11:94807707 | C | T | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1121+7396C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94807707 | |||||||
| chr11:94807725 | G | A | 1 | a0001c0002t0012g0097 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1121+7414G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94807725 | |||||||
| chr11:94807740 | A | G | 4 | a0003c0004t0021g0223 a0003c0004t0037g0212 a0003c0004t0041g0211 others(1): Show |
4 | HG02602.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121+7429A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94807740 | |||||||
| chr11:94807781 | G | A | 1 | a0001c0002t0018g0088 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1121+7470G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94807781 | |||||||
| chr11:94808092 | AAACAAAA others(4): Show |
A | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1121+7792_1121+780 others(15): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 94808092 | ||||||
| chr11:94808102 | AG | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(229): Show |
241 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(238): Show |
intron_variant | MODIFIER | c.1121+7792delG | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94808102 | |||||||
| chr11:94808149 | G | A | 1 | a0001c0002t0008g0098 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1121+7838G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94808149 | |||||||
| chr11:94808158 | T | A | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1121+7847T>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94808158 | |||||||
| chr11:94808282 | C | T | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1121+7971C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94808282 | |||||||
| chr11:94808299 | A | G | 2 | a0001c0001t0027g0216 a0001c0001t0027g0217 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1121+7988A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94808299 | |||||||
| chr11:94808303 | T | C | 1 | a0002c0003t0004g0133 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1121+7992T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94808303 | |||||||
| chr11:94808965 | C | CT | 31 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0038 others(28): Show |
32 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1121+8677dupT | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 94808965 | ||||||
| chr11:94808965 | CT | C | 9 | a0001c0001t0003g0081 a0001c0001t0007g0229 a0001c0001t0015g0151 others(6): Show |
9 | HG02572.hp1 HG02602.hp2 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.1121+8677delT | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 94808965 | ||||||
| chr11:94808965 | CTTTTTTT others(6): Show |
C | 81 | a0001c0001t0003g0022 a0001c0001t0009g0009 a0001c0001t0009g0155 others(78): Show |
84 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.1121+8665_1121+867 others(17): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 94808965 | ||||||
| chr11:94809184 | T | A | 87 | a0001c0001t0003g0022 a0001c0001t0009g0009 a0001c0001t0009g0155 others(84): Show |
90 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.1121+8873T>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94809184 | |||||||
| chr11:94809248 | A | G | 90 | a0001c0001t0003g0022 a0001c0001t0007g0228 a0001c0001t0007g0229 others(87): Show |
93 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.1121+8937A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94809248 | |||||||
| chr11:94809249 | G | A | 1 | a0001c0002t0002g0153 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1121+8938G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94809249 | |||||||
| chr11:94809251 | A | G | 81 | a0001c0001t0003g0022 a0001c0001t0009g0009 a0001c0001t0009g0155 others(78): Show |
84 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.1121+8940A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94809251 | |||||||
| chr11:94809501 | T | C | 90 | a0001c0001t0003g0022 a0001c0001t0007g0228 a0001c0001t0007g0229 others(87): Show |
93 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.1121+9190T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94809501 | |||||||
| chr11:94809580 | G | T | 2 | a0001c0001t0020g0221 a0001c0010t0038g0222 |
2 | HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1121+9269G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94809580 | |||||||
| chr11:94809665 | A | G | 4 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(1): Show |
5 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1121+9354A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94809665 | |||||||
| chr11:94809671 | A | G | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1121+9360A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94809671 | |||||||
| chr11:94809765 | C | T | 2 | a0001c0001t0039g0112 a0001c0001t0040g0144 |
2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1121+9454C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94809765 | |||||||
| chr11:94809852 | GT | G | 93 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0120 others(90): Show |
96 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.1121+9549delT | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 94809852 | ||||||
| chr11:94809902 | A | G | 3 | a0001c0002t0002g0159 a0001c0002t0002g0170 a0001c0002t0006g0186 |
3 | NA18951.hp2 NA19004.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1121+9591A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94809902 | |||||||
| chr11:94810128 | G | C | 87 | a0001c0001t0003g0022 a0001c0001t0009g0009 a0001c0001t0009g0155 others(84): Show |
90 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.1121+9817G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94810128 | |||||||
| chr11:94810316 | T | C | 16 | a0001c0001t0003g0203 a0001c0001t0004g0014 a0001c0001t0004g0200 others(13): Show |
18 | HG00741.hp1 HG01243.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1121+10005T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94810316 | |||||||
| chr11:94810354 | A | G | 2 | a0001c0001t0027g0216 a0001c0001t0027g0217 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1121+10043A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94810354 | |||||||
| chr11:94810449 | AC | A | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1121+10139delC | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94810449 | |||||||
| chr11:94810454 | A | T | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1121+10143A>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94810454 | |||||||
| chr11:94810458 | A | C | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1121+10147A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94810458 | |||||||
| chr11:94810496 | C | CA | 203 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(200): Show |
211 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(208): Show |
intron_variant | MODIFIER | c.1121+10201dupA | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 94810496 | ||||||
| chr11:94810496 | C | CAA | 22 | a0001c0001t0001g0038 a0001c0001t0005g0040 a0001c0001t0005g0041 others(19): Show |
22 | HG00735.hp1 HG00741.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.1121+10200_1121+10 others(8): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 94810496 | ||||||
| chr11:94810827 | A | G | 2 | a0001c0001t0039g0112 a0001c0001t0040g0144 |
2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1121+10516A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94810827 | |||||||
| chr11:94810831 | G | GAC | 3 | a0001c0001t0027g0216 a0001c0002t0001g0057 a0002c0019t0004g0103 |
3 | HG02738.hp1 HG03239.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1121+10557_1121+10 others(8): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 94810831 | ||||||
| chr11:94810831 | GAC | G | 80 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0029 others(77): Show |
82 | HG00280.hp2 HG01123.hp2 HG01175.hp1 others(79): Show |
intron_variant | MODIFIER | c.1121+10557_1121+10 others(8): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 94810831 | ||||||
| chr11:94810831 | GACAC | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0026 others(97): Show |
106 | HG00558.hp2 HG00642.hp2 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.1121+10555_1121+10 others(10): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 94810831 | ||||||
| chr11:94810831 | GACACAC | G | 18 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0003g0070 others(15): Show |
18 | HG00741.hp1 HG01074.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1121+10553_1121+10 others(12): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 94810831 | ||||||
| chr11:94810831 | GACACACA others(1): Show |
G | 6 | a0001c0001t0003g0022 a0001c0001t0007g0228 a0001c0001t0007g0229 others(3): Show |
6 | HG00738.hp2 HG02258.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1121+10551_1121+10 others(14): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 94810831 | ||||||
| chr11:94810868 | A | G | 1 | a0001c0002t0002g0062 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1121+10557A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94810868 | |||||||
| chr11:94810879 | C | T | 1 | a0001c0002t0001g0101 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1121+10568C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94810879 | |||||||
| chr11:94810880 | A | G | 2 | a0001c0001t0001g0079 a0001c0001t0012g0078 |
2 | NA18966.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1121+10569A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94810880 | |||||||
| chr11:94810941 | A | T | 90 | a0001c0001t0003g0022 a0001c0001t0007g0228 a0001c0001t0007g0229 others(87): Show |
93 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.1122-10589A>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94810941 | |||||||
| chr11:94811064 | A | G | 3 | a0001c0001t0003g0022 a0001c0001t0015g0213 a0007c0008t0015g0225 |
3 | HG02258.hp1 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1122-10466A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94811064 | |||||||
| chr11:94811265 | G | A | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1122-10265G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94811265 | |||||||
| chr11:94811368 | G | A | 2 | a0001c0001t0027g0216 a0001c0001t0027g0217 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1122-10162G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94811368 | |||||||
| chr11:94811456 | A | G | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1122-10074A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94811456 | |||||||
| chr11:94811552 | AT | A | 32 | a0001c0001t0001g0001 a0001c0001t0001g0086 a0001c0001t0001g0145 others(29): Show |
36 | HG00738.hp2 HG00741.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.1122-9967delT | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 94811552 | ||||||
| chr11:94811958 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1122-9572A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94811958 | |||||||
| chr11:94812009 | A | G | 3 | a0001c0001t0004g0004 a0001c0001t0004g0053 a0001c0001t0035g0136 |
4 | NA18612.hp1 NA18985.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122-9521A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94812009 | |||||||
| chr11:94812074 | G | T | 2 | a0001c0001t0027g0216 a0001c0001t0027g0217 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1122-9456G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94812074 | |||||||
| chr11:94812121 | T | A | 90 | a0001c0001t0003g0022 a0001c0001t0007g0228 a0001c0001t0007g0229 others(87): Show |
93 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.1122-9409T>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94812121 | |||||||
| chr11:94812151 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG01515.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1122-9379C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94812151 | |||||||
| chr11:94812338 | G | A | 90 | a0001c0001t0003g0022 a0001c0001t0007g0228 a0001c0001t0007g0229 others(87): Show |
93 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.1122-9192G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94812338 | |||||||
| chr11:94812386 | T | A | 8 | a0001c0001t0003g0022 a0001c0001t0009g0009 a0001c0001t0009g0155 others(5): Show |
9 | HG02258.hp1 HG02615.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1122-9144T>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94812386 | |||||||
| chr11:94812588 | G | T | 22 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0163 others(19): Show |
23 | HG01934.hp2 HG02080.hp2 HG02165.hp1 others(20): Show |
intron_variant | MODIFIER | c.1122-8942G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94812588 | |||||||
| chr11:94812677 | G | A | 4 | a0001c0002t0001g0069 a0001c0002t0018g0060 a0001c0002t0031g0227 others(1): Show |
4 | HG01175.hp1 HG03017.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122-8853G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94812677 | |||||||
| chr11:94813079 | T | G | 1 | a0001c0002t0047g0095 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1122-8451T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94813079 | |||||||
| chr11:94813437 | G | A | 5 | a0001c0001t0033g0199 a0001c0001t0034g0127 a0001c0006t0001g0194 others(2): Show |
5 | HG00741.hp1 HG02055.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1122-8093G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94813437 | |||||||
| chr11:94813444 | A | G | 1 | a0002c0003t0001g0052 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1122-8086A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94813444 | |||||||
| chr11:94813471 | G | A | 89 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 others(86): Show |
92 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.1122-8059G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94813471 | |||||||
| chr11:94813496 | C | T | 6 | a0001c0001t0011g0020 a0001c0001t0011g0049 a0001c0001t0011g0123 others(3): Show |
6 | HG02615.hp2 HG02717.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1122-8034C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94813496 | |||||||
| chr11:94813689 | T | A | 80 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(77): Show |
83 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.1122-7841T>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94813689 | |||||||
| chr11:94813693 | C | G | 1 | a0001c0002t0002g0062 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1122-7837C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94813693 | |||||||
| chr11:94813831 | A | T | 1 | a0002c0003t0001g0091 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1122-7699A>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94813831 | |||||||
| chr11:94814056 | G | A | 1 | a0001c0001t0039g0112 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1122-7474G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94814056 | |||||||
| chr11:94814079 | A | G | 1 | a0001c0001t0035g0136 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1122-7451A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94814079 | |||||||
| chr11:94814165 | C | A | 4 | a0003c0004t0021g0223 a0003c0004t0037g0212 a0003c0004t0041g0211 others(1): Show |
4 | HG02602.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122-7365C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94814165 | |||||||
| chr11:94814225 | C | T | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1122-7305C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94814225 | |||||||
| chr11:94814285 | G | C | 86 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(83): Show |
89 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.1122-7245G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94814285 | |||||||
| chr11:94814372 | C | T | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1122-7158C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94814372 | |||||||
| chr11:94814448 | C | G | 1 | a0001c0002t0002g0062 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1122-7082C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94814448 | |||||||
| chr11:94814481 | G | T | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1122-7049G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94814481 | |||||||
| chr11:94814513 | C | T | 1 | a0001c0002t0006g0063 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1122-7017C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94814513 | |||||||
| chr11:94814582 | C | A | 10 | a0001c0001t0001g0038 a0001c0001t0005g0040 a0001c0001t0005g0041 others(7): Show |
10 | HG00735.hp1 HG01074.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.1122-6948C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94814582 | |||||||
| chr11:94814651 | G | C | 1 | a0001c0001t0001g0075 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1122-6879G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94814651 | |||||||
| chr11:94814725 | T | C | 23 | a0001c0001t0003g0203 a0001c0001t0004g0014 a0001c0001t0004g0200 others(20): Show |
25 | HG00741.hp1 HG01243.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.1122-6805T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94814725 | |||||||
| chr11:94814784 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0002g0031 a0001c0001t0002g0032 |
3 | NA18974.hp1 NA18974.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.1122-6746G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94814784 | |||||||
| chr11:94814803 | T | A | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1122-6727T>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94814803 | |||||||
| chr11:94814937 | G | T | 1 | a0001c0010t0038g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1122-6593G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94814937 | |||||||
| chr11:94814962 | G | A | 1 | a0001c0001t0054g0093 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1122-6568G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94814962 | |||||||
| chr11:94814970 | A | C | 1 | a0002c0003t0001g0083 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1122-6560A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94814970 | |||||||
| chr11:94815218 | C | T | 2 | a0001c0001t0020g0154 a0001c0001t0032g0068 |
2 | HG01106.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1122-6312C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94815218 | |||||||
| chr11:94815355 | A | C | 1 | a0001c0001t0017g0205 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1122-6175A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94815355 | |||||||
| chr11:94815361 | A | G | 1 | a0002c0019t0004g0103 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1122-6169A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94815361 | |||||||
| chr11:94815411 | A | C | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1122-6119A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94815411 | |||||||
| chr11:94815438 | A | G | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1122-6092A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94815438 | |||||||
| chr11:94815553 | G | A | 1 | a0001c0002t0002g0169 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1122-5977G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94815553 | |||||||
| chr11:94815713 | A | G | 6 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0013g0018 others(3): Show |
6 | HG01109.hp1 HG02004.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1122-5817A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94815713 | |||||||
| chr11:94815855 | A | G | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1122-5675A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94815855 | |||||||
| chr11:94815862 | G | C | 1 | a0001c0001t0053g0118 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1122-5668G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94815862 | |||||||
| chr11:94815881 | C | T | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1122-5649C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94815881 | |||||||
| chr11:94816029 | T | A | 2 | a0001c0002t0002g0176 a0001c0010t0038g0222 |
2 | HG02559.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1122-5501T>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94816029 | |||||||
| chr11:94816073 | C | G | 2 | a0001c0001t0039g0112 a0001c0001t0040g0144 |
2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1122-5457C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94816073 | |||||||
| chr11:94816253 | CTGTT | C | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1122-5268_1122-526 others(8): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 94816253 | ||||||
| chr11:94816259 | G | T | 1 | a0001c0001t0053g0118 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1122-5271G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94816259 | |||||||
| chr11:94816348 | A | C | 73 | a0001c0002t0001g0006 a0001c0002t0001g0057 a0001c0002t0001g0059 others(70): Show |
75 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.1122-5182A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94816348 | |||||||
| chr11:94816496 | G | T | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1122-5034G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94816496 | |||||||
| chr11:94816805 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1122-4725G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94816805 | |||||||
| chr11:94817048 | A | C | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1122-4482A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94817048 | |||||||
| chr11:94817099 | A | G | 81 | a0001c0001t0003g0022 a0001c0001t0009g0009 a0001c0001t0009g0155 others(78): Show |
84 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.1122-4431A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94817099 | |||||||
| chr11:94817191 | G | A | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1122-4339G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94817191 | |||||||
| chr11:94817243 | C | G | 4 | a0001c0001t0015g0151 a0001c0001t0022g0008 a0001c0001t0022g0152 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122-4287C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94817243 | |||||||
| chr11:94817427 | A | C | 92 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0009g0009 others(89): Show |
95 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.1122-4103A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94817427 | |||||||
| chr11:94817605 | A | G | 1 | a0001c0002t0002g0164 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1122-3925A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94817605 | |||||||
| chr11:94817798 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1122-3732C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94817798 | |||||||
| chr11:94817850 | G | A | 2 | a0001c0001t0020g0221 a0001c0010t0038g0222 |
2 | HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1122-3680G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94817850 | |||||||
| chr11:94818381 | A | G | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1122-3149A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94818381 | |||||||
| chr11:94818734 | C | T | 1 | a0001c0007t0005g0044 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1122-2796C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94818734 | |||||||
| chr11:94818976 | G | A | 12 | a0001c0002t0002g0002 a0001c0002t0002g0163 a0001c0002t0002g0164 others(9): Show |
13 | HG01934.hp2 NA18612.hp2 NA18959.hp2 others(10): Show |
intron_variant | MODIFIER | c.1122-2554G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94818976 | |||||||
| chr11:94818982 | G | C | 4 | a0001c0001t0015g0151 a0001c0001t0022g0008 a0001c0001t0022g0152 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122-2548G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94818982 | |||||||
| chr11:94818994 | T | TTTTG | 94 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0003g0022 others(91): Show |
97 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.1122-2528_1122-252 others(8): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 94818994 | ||||||
| chr11:94819068 | G | T | 1 | a0001c0001t0015g0151 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1122-2462G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94819068 | |||||||
| chr11:94819182 | T | C | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1122-2348T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94819182 | |||||||
| chr11:94819241 | A | G | 1 | a0009c0014t0001g0201 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1122-2289A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94819241 | |||||||
| chr11:94819368 | A | C | 3 | a0001c0002t0002g0159 a0001c0002t0002g0170 a0001c0002t0006g0186 |
3 | NA18951.hp2 NA19004.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1122-2162A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94819368 | |||||||
| chr11:94819403 | T | C | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1122-2127T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94819403 | |||||||
| chr11:94819446 | T | G | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1122-2084T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94819446 | |||||||
| chr11:94819727 | G | C | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1122-1803G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94819727 | |||||||
| chr11:94819806 | T | A | 2 | a0001c0001t0020g0154 a0001c0001t0032g0068 |
2 | HG01106.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1122-1724T>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94819806 | |||||||
| chr11:94819854 | A | G | 1 | a0009c0014t0001g0201 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1122-1676A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94819854 | |||||||
| chr11:94819943 | G | A | 2 | a0001c0001t0020g0154 a0001c0001t0032g0068 |
2 | HG01106.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1122-1587G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94819943 | |||||||
| chr11:94819996 | T | C | 128 | a0001c0001t0001g0116 a0001c0001t0001g0206 a0001c0001t0001g0208 others(125): Show |
133 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(130): Show |
intron_variant | MODIFIER | c.1122-1534T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94819996 | |||||||
| chr11:94820005 | A | T | 1 | a0001c0002t0008g0185 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1122-1525A>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94820005 | |||||||
| chr11:94820249 | C | A | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1122-1281C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94820249 | |||||||
| chr11:94820253 | GCT | G | 73 | a0001c0002t0001g0006 a0001c0002t0001g0057 a0001c0002t0001g0059 others(70): Show |
75 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.1122-1273_1122-127 others(6): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 94820253 | ||||||
| chr11:94820261 | C | G | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1122-1269C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94820261 | |||||||
| chr11:94820448 | C | T | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1122-1082C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94820448 | |||||||
| chr11:94820559 | A | G | 91 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0003g0022 others(88): Show |
94 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.1122-971A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94820559 | |||||||
| chr11:94820913 | C | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0208 |
2 | HG02004.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1122-617C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94820913 | |||||||
| chr11:94821025 | A | G | 4 | a0001c0001t0003g0203 a0001c0001t0004g0014 a0001c0001t0004g0200 others(1): Show |
5 | HG01884.hp2 HG02622.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1122-505A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94821025 | |||||||
| chr11:94821027 | C | T | 93 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0007g0228 others(90): Show |
96 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.1122-503C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94821027 | |||||||
| chr11:94821146 | A | T | 2 | a0001c0001t0027g0216 a0001c0001t0027g0217 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1122-384A>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94821146 | |||||||
| chr11:94821180 | T | G | 1 | a0001c0001t0001g0142 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1122-350T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94821180 | |||||||
| chr11:94821192 | C | T | 6 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0013g0018 others(3): Show |
6 | HG01109.hp1 HG02004.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1122-338C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94821192 | |||||||
| chr11:94821215 | T | A | 2 | a0001c0001t0013g0207 a0001c0001t0013g0209 |
2 | HG01109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1122-315T>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94821215 | |||||||
| chr11:94821254 | C | T | 1 | a0001c0002t0006g0063 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1122-276C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94821254 | |||||||
| chr11:94821359 | A | G | 96 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0003g0022 others(93): Show |
99 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.1122-171A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94821359 | |||||||
| chr11:94821436 | A | G | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1122-94A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94821436 | |||||||
| chr11:94821450 | C | T | 2 | a0001c0001t0020g0221 a0001c0010t0038g0222 |
2 | HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1122-80C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 3/12 | chr11 | 94821450 | |||||||
| chr11:94821934 | C | T | 4 | a0001c0001t0003g0203 a0001c0001t0004g0014 a0001c0001t0004g0200 others(1): Show |
5 | HG01884.hp2 HG02622.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1413+113C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94821934 | |||||||
| chr11:94822047 | A | C | 3 | a0001c0002t0001g0101 a0001c0002t0023g0099 a0001c0002t0023g0100 |
3 | HG02818.hp1 HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1413+226A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94822047 | |||||||
| chr11:94822086 | G | A | 2 | a0001c0001t0020g0154 a0001c0001t0032g0068 |
2 | HG01106.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1413+265G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94822086 | |||||||
| chr11:94822169 | C | T | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1413+348C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94822169 | |||||||
| chr11:94822318 | C | T | 93 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0007g0228 others(90): Show |
96 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.1413+497C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94822318 | |||||||
| chr11:94822356 | A | G | 93 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0007g0228 others(90): Show |
96 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.1413+535A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94822356 | |||||||
| chr11:94822382 | G | A | 73 | a0001c0002t0001g0006 a0001c0002t0001g0057 a0001c0002t0001g0059 others(70): Show |
75 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.1413+561G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94822382 | |||||||
| chr11:94822542 | G | A | 86 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0009g0009 others(83): Show |
89 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.1413+721G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94822542 | |||||||
| chr11:94822590 | G | A | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1413+769G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94822590 | |||||||
| chr11:94822627 | A | G | 2 | a0001c0002t0006g0056 a0001c0002t0006g0061 |
2 | NA18953.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1413+806A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94822627 | |||||||
| chr11:94822732 | T | G | 86 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0009g0009 others(83): Show |
89 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.1413+911T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94822732 | |||||||
| chr11:94822797 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1413+976C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94822797 | |||||||
| chr11:94822938 | G | C | 2 | a0001c0001t0033g0199 a0001c0001t0034g0127 |
2 | HG02055.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1413+1117G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94822938 | |||||||
| chr11:94823028 | T | TG | 18 | a0001c0001t0003g0203 a0001c0001t0004g0014 a0001c0001t0004g0200 others(15): Show |
20 | HG00741.hp1 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1413+1209dupG | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 94823028 | ||||||
| chr11:94823047 | A | G | 4 | a0003c0004t0021g0223 a0003c0004t0037g0212 a0003c0004t0041g0211 others(1): Show |
4 | HG02602.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1413+1226A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94823047 | |||||||
| chr11:94823054 | G | A | 16 | a0001c0001t0003g0203 a0001c0001t0004g0014 a0001c0001t0004g0200 others(13): Show |
18 | HG00741.hp1 HG01243.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1413+1233G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94823054 | |||||||
| chr11:94823466 | T | A | 93 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0007g0228 others(90): Show |
96 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.1413+1645T>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94823466 | |||||||
| chr11:94823719 | C | CT | 85 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0003g0022 others(82): Show |
88 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.1413+1913dupT | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 94823719 | ||||||
| chr11:94823779 | G | A | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1413+1958G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94823779 | |||||||
| chr11:94823789 | C | T | 2 | a0001c0005t0001g0013 a0001c0005t0052g0198 |
3 | HG02486.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1413+1968C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94823789 | |||||||
| chr11:94823882 | A | AT | 86 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0003g0022 others(83): Show |
89 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.1413+2072dupT | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 94823882 | ||||||
| chr11:94823909 | C | T | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1413+2088C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94823909 | |||||||
| chr11:94823935 | G | A | 1 | a0001c0002t0008g0185 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1413+2114G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94823935 | |||||||
| chr11:94824327 | T | C | 87 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0003g0022 others(84): Show |
90 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.1413+2506T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94824327 | |||||||
| chr11:94824407 | A | G | 90 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0003g0022 others(87): Show |
93 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.1413+2586A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94824407 | |||||||
| chr11:94824600 | C | T | 1 | a0001c0001t0003g0110 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1413+2779C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94824600 | |||||||
| chr11:94824747 | C | T | 1 | a0001c0001t0005g0043 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1413+2926C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94824747 | |||||||
| chr11:94824801 | T | C | 94 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0003g0022 others(91): Show |
97 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.1413+2980T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94824801 | |||||||
| chr11:94824830 | T | C | 95 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0007g0228 others(92): Show |
98 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.1413+3009T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94824830 | |||||||
| chr11:94825114 | G | A | 3 | a0001c0001t0027g0216 a0001c0001t0027g0217 a0005c0015t0010g0219 |
3 | HG01074.hp1 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1413+3293G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94825114 | |||||||
| chr11:94825136 | T | C | 93 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0007g0228 others(90): Show |
96 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.1413+3315T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94825136 | |||||||
| chr11:94825162 | T | G | 1 | a0001c0002t0008g0098 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1413+3341T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94825162 | |||||||
| chr11:94825329 | G | A | 86 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0009g0009 others(83): Show |
89 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.1413+3508G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94825329 | |||||||
| chr11:94825332 | C | A | 2 | a0001c0002t0014g0058 a0001c0002t0014g0137 |
2 | HG01081.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1413+3511C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94825332 | |||||||
| chr11:94825497 | G | A | 86 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0009g0009 others(83): Show |
89 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.1413+3676G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94825497 | |||||||
| chr11:94825654 | G | C | 1 | a0009c0014t0001g0201 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1413+3833G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94825654 | |||||||
| chr11:94825842 | A | G | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1413+4021A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94825842 | |||||||
| chr11:94825847 | C | G | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1413+4026C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94825847 | |||||||
| chr11:94825916 | G | A | 6 | a0001c0001t0001g0116 a0001c0001t0016g0114 a0001c0001t0016g0117 others(3): Show |
6 | HG01884.hp1 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1413+4095G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94825916 | |||||||
| chr11:94826160 | A | C | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1414-3890A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94826160 | |||||||
| chr11:94826266 | C | T | 2 | a0001c0001t0020g0154 a0001c0001t0032g0068 |
2 | HG01106.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1414-3784C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94826266 | |||||||
| chr11:94826268 | A | G | 2 | a0001c0001t0020g0154 a0001c0001t0032g0068 |
2 | HG01106.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1414-3782A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94826268 | |||||||
| chr11:94826273 | A | G | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1414-3777A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94826273 | |||||||
| chr11:94826285 | T | G | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1414-3765T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94826285 | |||||||
| chr11:94826300 | T | A | 93 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0007g0228 others(90): Show |
96 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.1414-3750T>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94826300 | |||||||
| chr11:94826345 | C | G | 1 | a0001c0001t0009g0157 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1414-3705C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94826345 | |||||||
| chr11:94826518 | CTG | C | 5 | a0001c0001t0033g0199 a0001c0001t0034g0127 a0001c0006t0001g0194 others(2): Show |
5 | HG00741.hp1 HG02055.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1414-3528_1414-352 others(6): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 94826518 | ||||||
| chr11:94826692 | C | T | 14 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(11): Show |
14 | HG02027.hp1 HG02165.hp2 NA18951.hp1 others(11): Show |
intron_variant | MODIFIER | c.1414-3358C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94826692 | |||||||
| chr11:94826703 | A | T | 86 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0009g0009 others(83): Show |
89 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.1414-3347A>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94826703 | |||||||
| chr11:94826747 | C | T | 3 | a0001c0002t0001g0101 a0001c0002t0023g0099 a0001c0002t0023g0100 |
3 | HG02818.hp1 HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1414-3303C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94826747 | |||||||
| chr11:94826883 | GT | G | 4 | a0003c0004t0021g0223 a0003c0004t0037g0212 a0003c0004t0041g0211 others(1): Show |
4 | HG02602.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1414-3158delT | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 94826883 | ||||||
| chr11:94826884 | T | C | 2 | a0001c0002t0019g0102 a0001c0002t0019g0104 |
2 | NA18956.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1414-3166T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94826884 | |||||||
| chr11:94826896 | G | C | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1414-3154G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94826896 | |||||||
| chr11:94827116 | G | C | 1 | a0001c0001t0011g0123 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1414-2934G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94827116 | |||||||
| chr11:94827177 | C | T | 1 | a0001c0002t0014g0058 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1414-2873C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94827177 | |||||||
| chr11:94827187 | A | G | 3 | a0001c0001t0003g0022 a0001c0001t0015g0213 a0007c0008t0015g0225 |
3 | HG02258.hp1 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1414-2863A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94827187 | |||||||
| chr11:94827189 | A | G | 2 | a0001c0001t0020g0221 a0001c0010t0038g0222 |
2 | HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1414-2861A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94827189 | |||||||
| chr11:94827232 | A | G | 2 | a0001c0001t0007g0229 a0001c0001t0007g0230 |
2 | HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1414-2818A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94827232 | |||||||
| chr11:94827335 | G | A | 1 | a0001c0001t0035g0136 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1414-2715G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94827335 | |||||||
| chr11:94827551 | G | C | 2 | a0001c0002t0014g0058 a0001c0002t0014g0137 |
2 | HG01081.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1414-2499G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94827551 | |||||||
| chr11:94827740 | C | T | 1 | a0001c0001t0051g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1414-2310C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94827740 | |||||||
| chr11:94828795 | C | T | 1 | a0001c0002t0002g0182 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1414-1255C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94828795 | |||||||
| chr11:94829219 | T | TC | 11 | a0001c0001t0017g0195 a0001c0001t0017g0204 a0001c0001t0017g0205 others(8): Show |
12 | HG00741.hp1 HG01243.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1414-829dupC | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 94829219 | ||||||
| chr11:94829222 | T | C | 4 | a0001c0001t0003g0203 a0001c0001t0004g0014 a0001c0001t0004g0200 others(1): Show |
5 | HG01884.hp2 HG02622.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1414-828T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94829222 | |||||||
| chr11:94829296 | C | T | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1414-754C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94829296 | |||||||
| chr11:94829332 | T | C | 116 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0003g0022 others(113): Show |
121 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(118): Show |
intron_variant | MODIFIER | c.1414-718T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94829332 | |||||||
| chr11:94829386 | C | A | 1 | a0001c0001t0001g0038 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1414-664C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94829386 | |||||||
| chr11:94829500 | C | T | 4 | a0003c0004t0021g0223 a0003c0004t0037g0212 a0003c0004t0041g0211 others(1): Show |
4 | HG02602.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1414-550C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94829500 | |||||||
| chr11:94829631 | C | T | 2 | a0001c0001t0027g0216 a0001c0001t0027g0217 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1414-419C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94829631 | |||||||
| chr11:94829763 | A | T | 82 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0013g0018 others(79): Show |
84 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.1414-287A>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 4/12 | chr11 | 94829763 | |||||||
| chr11:94830565 | T | G | 71 | a0001c0002t0001g0006 a0001c0002t0001g0057 a0001c0002t0001g0059 others(68): Show |
73 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.1558+371T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 5/12 | chr11 | 94830565 | |||||||
| chr11:94830885 | G | C | 3 | a0001c0001t0019g0064 a0001c0002t0019g0102 a0001c0002t0019g0104 |
3 | NA18956.hp1 NA19005.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1559-567G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 5/12 | chr11 | 94830885 | |||||||
| chr11:94830902 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1559-550T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 5/12 | chr11 | 94830902 | |||||||
| chr11:94830926 | A | G | 1 | a0001c0001t0003g0138 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1559-526A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 5/12 | chr11 | 94830926 | |||||||
| chr11:94831082 | T | C | 76 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(73): Show |
79 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.1559-370T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 5/12 | chr11 | 94831082 | |||||||
| chr11:94831622 | G | C | 3 | a0001c0001t0003g0022 a0001c0001t0015g0213 a0007c0008t0015g0225 |
3 | HG02258.hp1 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1648+81G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94831622 | |||||||
| chr11:94831979 | A | G | 2 | a0001c0001t0020g0221 a0001c0010t0038g0222 |
2 | HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1648+438A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94831979 | |||||||
| chr11:94831982 | T | C | 3 | a0001c0001t0016g0114 a0001c0001t0016g0146 a0010c0017t0021g0113 |
3 | HG03225.hp1 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1648+441T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94831982 | |||||||
| chr11:94832005 | T | C | 86 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0009g0009 others(83): Show |
89 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.1648+464T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94832005 | |||||||
| chr11:94832035 | C | T | 2 | a0001c0001t0015g0213 a0007c0008t0015g0225 |
2 | HG02258.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1648+494C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94832035 | |||||||
| chr11:94832504 | A | C | 1 | a0001c0001t0048g0082 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1648+963A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94832504 | |||||||
| chr11:94833021 | A | G | 3 | a0001c0001t0003g0022 a0001c0001t0015g0213 a0007c0008t0015g0225 |
3 | HG02258.hp1 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1648+1480A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94833021 | |||||||
| chr11:94833183 | G | A | 6 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0013g0018 others(3): Show |
6 | HG01109.hp1 HG02004.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1648+1642G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94833183 | |||||||
| chr11:94833739 | T | A | 86 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0009g0009 others(83): Show |
89 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.1648+2198T>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94833739 | |||||||
| chr11:94834012 | A | G | 1 | a0001c0001t0005g0043 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1648+2471A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94834012 | |||||||
| chr11:94834305 | G | T | 6 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0013g0018 others(3): Show |
6 | HG01109.hp1 HG02004.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1648+2764G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94834305 | |||||||
| chr11:94834404 | G | A | 1 | a0010c0017t0021g0113 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1648+2863G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94834404 | |||||||
| chr11:94834490 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1648+2949G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94834490 | |||||||
| chr11:94834895 | A | T | 2 | a0001c0001t0027g0216 a0001c0001t0027g0217 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1648+3354A>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94834895 | |||||||
| chr11:94834949 | G | C | 1 | a0001c0001t0034g0127 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1648+3408G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94834949 | |||||||
| chr11:94835000 | T | C | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1648+3459T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94835000 | |||||||
| chr11:94835027 | C | T | 10 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0013g0018 others(7): Show |
10 | HG01109.hp1 HG02004.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.1648+3486C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94835027 | |||||||
| chr11:94835045 | A | G | 86 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0009g0009 others(83): Show |
89 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.1648+3504A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94835045 | |||||||
| chr11:94835383 | G | A | 76 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(73): Show |
79 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.1648+3842G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94835383 | |||||||
| chr11:94835456 | T | G | 1 | a0001c0001t0040g0144 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1648+3915T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94835456 | |||||||
| chr11:94835585 | T | G | 89 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0003g0022 others(86): Show |
92 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.1648+4044T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94835585 | |||||||
| chr11:94835610 | T | C | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1648+4069T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94835610 | |||||||
| chr11:94835648 | G | T | 4 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(1): Show |
5 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1648+4107G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94835648 | |||||||
| chr11:94835927 | A | G | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1648+4386A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94835927 | |||||||
| chr11:94836285 | C | T | 2 | a0001c0002t0002g0181 a0001c0002t0046g0191 |
2 | HG02165.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1648+4744C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94836285 | |||||||
| chr11:94836436 | A | G | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1648+4895A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94836436 | |||||||
| chr11:94836683 | A | C | 1 | a0001c0002t0002g0168 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1648+5142A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94836683 | |||||||
| chr11:94836683 | A | G | 13 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0002c0003t0001g0005 others(10): Show |
15 | HG00280.hp2 HG00558.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.1648+5142A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94836683 | |||||||
| chr11:94836701 | G | C | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1648+5160G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94836701 | |||||||
| chr11:94836732 | C | T | 1 | a0001c0002t0002g0168 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1648+5191C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94836732 | |||||||
| chr11:94836760 | CT | C | 78 | a0001c0001t0001g0084 a0001c0001t0009g0009 a0001c0001t0009g0155 others(75): Show |
81 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.1648+5234delT | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 94836760 | ||||||
| chr11:94836854 | A | G | 1 | a0001c0001t0004g0055 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1648+5313A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94836854 | |||||||
| chr11:94836868 | A | G | 113 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0003g0022 others(110): Show |
118 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(115): Show |
intron_variant | MODIFIER | c.1648+5327A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94836868 | |||||||
| chr11:94837043 | C | G | 86 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0009g0009 others(83): Show |
89 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.1648+5502C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94837043 | |||||||
| chr11:94837458 | G | A | 1 | a0011c0011t0001g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1648+5917G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94837458 | |||||||
| chr11:94837736 | A | C | 86 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0009g0009 others(83): Show |
89 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.1648+6195A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94837736 | |||||||
| chr11:94837768 | A | G | 1 | a0001c0001t0053g0118 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1648+6227A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94837768 | |||||||
| chr11:94838065 | C | T | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1648+6524C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94838065 | |||||||
| chr11:94838071 | A | G | 94 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0003g0022 others(91): Show |
97 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.1648+6530A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94838071 | |||||||
| chr11:94838367 | T | C | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1648+6826T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94838367 | |||||||
| chr11:94838567 | G | C | 1 | a0001c0002t0018g0088 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1648+7026G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94838567 | |||||||
| chr11:94838907 | G | GAT | 76 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(73): Show |
79 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.1648+7366_1648+736 others(6): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94838907 | |||||||
| chr11:94838909 | G | A | 76 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(73): Show |
79 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.1648+7368G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94838909 | |||||||
| chr11:94838910 | G | A | 76 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(73): Show |
79 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.1648+7369G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94838910 | |||||||
| chr11:94838911 | T | C | 76 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(73): Show |
79 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.1648+7370T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94838911 | |||||||
| chr11:94839075 | G | A | 3 | a0001c0001t0009g0155 a0001c0001t0009g0156 a0001c0001t0009g0157 |
3 | HG02615.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1648+7534G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94839075 | |||||||
| chr11:94839121 | C | T | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1648+7580C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94839121 | |||||||
| chr11:94839185 | A | G | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0016t0010g0129 |
3 | HG02055.hp1 HG02451.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1648+7644A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94839185 | |||||||
| chr11:94839343 | A | G | 2 | a0001c0001t0027g0216 a0001c0001t0027g0217 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1648+7802A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94839343 | |||||||
| chr11:94839511 | C | A | 1 | a0001c0001t0017g0205 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1648+7970C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94839511 | |||||||
| chr11:94839548 | T | G | 114 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0003g0022 others(111): Show |
119 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(116): Show |
intron_variant | MODIFIER | c.1648+8007T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94839548 | |||||||
| chr11:94839560 | G | A | 6 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0013g0018 others(3): Show |
6 | HG01109.hp1 HG02004.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1648+8019G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94839560 | |||||||
| chr11:94839756 | G | A | 4 | a0003c0004t0021g0223 a0003c0004t0037g0212 a0003c0004t0041g0211 others(1): Show |
4 | HG02602.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1648+8215G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94839756 | |||||||
| chr11:94839775 | G | A | 1 | a0001c0001t0015g0151 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1648+8234G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94839775 | |||||||
| chr11:94839783 | G | A | 1 | a0001c0001t0022g0152 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1648+8242G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94839783 | |||||||
| chr11:94840054 | A | C | 2 | a0001c0002t0019g0102 a0001c0002t0019g0104 |
2 | NA18956.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1648+8513A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94840054 | |||||||
| chr11:94840099 | A | G | 4 | a0003c0004t0021g0223 a0003c0004t0037g0212 a0003c0004t0041g0211 others(1): Show |
4 | HG02602.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1648+8558A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94840099 | |||||||
| chr11:94840127 | C | A | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1648+8586C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94840127 | |||||||
| chr11:94840315 | G | A | 2 | a0001c0002t0019g0102 a0001c0002t0019g0104 |
2 | NA18956.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1648+8774G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94840315 | |||||||
| chr11:94840525 | C | T | 80 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(77): Show |
83 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.1648+8984C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94840525 | |||||||
| chr11:94840564 | G | A | 2 | a0001c0001t0020g0221 a0001c0010t0038g0222 |
2 | HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1648+9023G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94840564 | |||||||
| chr11:94840571 | A | G | 3 | a0001c0001t0007g0228 a0001c0001t0007g0229 a0001c0001t0007g0230 |
3 | HG00738.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1648+9030A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94840571 | |||||||
| chr11:94840654 | G | GTA | 6 | a0001c0001t0001g0132 a0001c0001t0001g0206 a0001c0001t0001g0208 others(3): Show |
7 | HG02004.hp1 HG02055.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1648+9140_1648+914 others(6): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 94840654 | ||||||
| chr11:94840654 | G | GTATATAT others(5): Show |
4 | a0001c0001t0003g0022 a0001c0001t0028g0196 a0001c0001t0028g0197 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1648+9130_1648+914 others(16): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 94840654 | ||||||
| chr11:94840654 | G | GTATATAT others(7): Show |
2 | a0001c0001t0017g0205 a0001c0001t0020g0154 |
2 | HG01243.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1648+9128_1648+914 others(18): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 94840654 | ||||||
| chr11:94840654 | G | GTATATAT others(9): Show |
2 | a0001c0001t0017g0195 a0007c0008t0015g0225 |
2 | HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1648+9126_1648+914 others(20): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 94840654 | ||||||
| chr11:94840654 | G | GTATATAT others(11): Show |
3 | a0001c0001t0007g0228 a0001c0001t0017g0204 a0001c0001t0032g0068 |
3 | HG00738.hp2 HG01106.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1648+9124_1648+914 others(22): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 94840654 | ||||||
| chr11:94840654 | G | GTATATAT others(13): Show |
1 | a0001c0001t0015g0213 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1648+9122_1648+914 others(24): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 94840654 | ||||||
| chr11:94840654 | G | GTGTATAT others(5): Show |
1 | a0001c0006t0001g0214 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1648+9114_1648+911 others(16): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 94840654 | ||||||
| chr11:94840654 | GTA | G | 59 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0035 others(56): Show |
63 | HG00280.hp2 HG00558.hp2 HG01074.hp1 others(60): Show |
intron_variant | MODIFIER | c.1648+9140_1648+914 others(6): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 94840654 | ||||||
| chr11:94840660 | A | G | 1 | a0001c0002t0002g0173 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1648+9119A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94840660 | |||||||
| chr11:94840675 | TATATATA others(5): Show |
T | 2 | a0001c0002t0014g0165 a0001c0002t0014g0166 |
2 | NA18985.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1648+9136_1648+914 others(16): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 94840675 | ||||||
| chr11:94840679 | T | C | 6 | a0001c0001t0001g0015 a0001c0001t0001g0076 a0001c0001t0001g0077 others(3): Show |
6 | HG03225.hp1 HG03471.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.1648+9138T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94840679 | |||||||
| chr11:94840679 | TATAC | T | 4 | a0001c0001t0001g0079 a0001c0001t0012g0078 a0001c0013t0006g0226 others(1): Show |
4 | HG01123.hp1 HG02132.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.1648+9140_1648+914 others(8): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 94840679 | ||||||
| chr11:94840679 | TATACAC | T | 35 | a0001c0002t0002g0002 a0001c0002t0002g0010 a0001c0002t0002g0011 others(32): Show |
36 | HG01123.hp2 HG01256.hp1 HG01346.hp2 others(33): Show |
intron_variant | MODIFIER | c.1648+9140_1648+914 others(10): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 94840679 | ||||||
| chr11:94840681 | T | C | 24 | a0001c0001t0001g0015 a0001c0001t0001g0073 a0001c0001t0001g0074 others(21): Show |
24 | HG01884.hp1 HG02132.hp2 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.1648+9140T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94840681 | |||||||
| chr11:94840681 | T | TATATATA others(3): Show |
2 | a0001c0001t0003g0203 a0001c0001t0004g0014 |
3 | HG01884.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1648+9141_1648+914 others(14): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 94840681 | ||||||
| chr11:94840681 | T | TATATATA others(5): Show |
1 | a0001c0001t0004g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1648+9141_1648+914 others(16): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 94840681 | ||||||
| chr11:94840681 | T | TATATATA others(5): Show |
1 | a0001c0006t0001g0194 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1648+9141_1648+914 others(16): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 94840681 | ||||||
| chr11:94840681 | T | TATATATA others(9): Show |
2 | a0003c0004t0021g0223 a0003c0004t0043g0224 |
2 | HG02602.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1648+9141_1648+914 others(20): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 94840681 | ||||||
| chr11:94840681 | T | TATATATA others(13): Show |
1 | a0003c0004t0041g0211 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1648+9141_1648+914 others(24): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 94840681 | ||||||
| chr11:94840681 | T | TATATATA others(13): Show |
2 | a0001c0001t0007g0229 a0001c0001t0007g0230 |
2 | HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1648+9141_1648+914 others(24): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 94840681 | ||||||
| chr11:94840681 | T | TATATATA others(25): Show |
1 | a0001c0001t0027g0217 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1648+9141_1648+914 others(36): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 94840681 | ||||||
| chr11:94840681 | T | TATATATA others(27): Show |
1 | a0001c0001t0027g0216 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1648+9141_1648+914 others(38): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 94840681 | ||||||
| chr11:94840681 | TAC | T | 27 | a0001c0001t0001g0038 a0001c0001t0005g0041 a0001c0001t0005g0043 others(24): Show |
28 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.1648+9166_1648+916 others(6): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 94840681 | ||||||
| chr11:94840681 | TACAC | T | 13 | a0001c0001t0013g0018 a0001c0001t0013g0119 a0001c0001t0013g0207 others(10): Show |
13 | HG01109.hp1 HG01934.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.1648+9164_1648+916 others(8): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 94840681 | ||||||
| chr11:94840683 | C | T | 23 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0206 others(20): Show |
25 | HG01081.hp2 HG01192.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.1648+9142C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94840683 | |||||||
| chr11:94840685 | C | T | 28 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0003g0022 others(25): Show |
29 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.1648+9144C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94840685 | |||||||
| chr11:94840687 | C | T | 12 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0003g0022 others(9): Show |
12 | HG00735.hp2 HG01109.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.1648+9146C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94840687 | |||||||
| chr11:94840689 | C | T | 6 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0013g0018 others(3): Show |
6 | HG01109.hp1 HG02004.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1648+9148C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94840689 | |||||||
| chr11:94840707 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1648+9166C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94840707 | |||||||
| chr11:94840707 | CAT | C | 3 | a0001c0002t0006g0056 a0001c0002t0006g0061 a0001c0002t0006g0063 |
3 | NA18953.hp1 NA19003.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1648+9176_1648+917 others(6): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 94840707 | ||||||
| chr11:94840709 | T | C | 5 | a0001c0001t0027g0216 a0003c0004t0021g0223 a0003c0004t0037g0212 others(2): Show |
5 | HG02602.hp2 HG02683.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.1648+9168T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94840709 | |||||||
| chr11:94840728 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0016g0117 |
2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1648+9187G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94840728 | |||||||
| chr11:94841049 | A | C | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1649-9065A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94841049 | |||||||
| chr11:94841105 | G | A | 2 | a0001c0001t0020g0221 a0001c0010t0038g0222 |
2 | HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1649-9009G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94841105 | |||||||
| chr11:94841285 | C | G | 2 | a0001c0001t0039g0112 a0001c0001t0040g0144 |
2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1649-8829C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94841285 | |||||||
| chr11:94841432 | A | G | 1 | a0001c0001t0039g0112 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1649-8682A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94841432 | |||||||
| chr11:94841488 | A | G | 22 | a0001c0001t0001g0015 a0001c0001t0001g0073 a0001c0001t0001g0074 others(19): Show |
22 | HG01433.hp1 HG02132.hp2 HG03130.hp2 others(19): Show |
intron_variant | MODIFIER | c.1649-8626A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94841488 | |||||||
| chr11:94841599 | G | A | 4 | a0003c0004t0021g0223 a0003c0004t0037g0212 a0003c0004t0041g0211 others(1): Show |
4 | HG02602.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1649-8515G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94841599 | |||||||
| chr11:94842252 | G | A | 6 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0013g0018 others(3): Show |
6 | HG01109.hp1 HG02004.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1649-7862G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94842252 | |||||||
| chr11:94842271 | C | T | 3 | a0001c0001t0009g0155 a0001c0001t0009g0156 a0001c0001t0009g0157 |
3 | HG02615.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1649-7843C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94842271 | |||||||
| chr11:94842276 | C | T | 1 | a0001c0002t0003g0192 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1649-7838C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94842276 | |||||||
| chr11:94842392 | C | T | 1 | a0010c0017t0021g0113 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1649-7722C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94842392 | |||||||
| chr11:94842443 | A | G | 15 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(12): Show |
17 | HG00280.hp2 HG00558.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.1649-7671A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94842443 | |||||||
| chr11:94842517 | G | A | 1 | a0001c0001t0040g0144 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1649-7597G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94842517 | |||||||
| chr11:94842734 | T | A | 1 | a0001c0001t0003g0138 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1649-7380T>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94842734 | |||||||
| chr11:94842815 | A | G | 1 | a0001c0002t0003g0192 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1649-7299A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94842815 | |||||||
| chr11:94842873 | G | C | 1 | a0001c0002t0002g0174 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1649-7241G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94842873 | |||||||
| chr11:94843053 | A | G | 8 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(5): Show |
8 | HG02056.hp1 HG02132.hp2 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.1649-7061A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94843053 | |||||||
| chr11:94843190 | A | G | 2 | a0001c0001t0013g0207 a0001c0001t0013g0209 |
2 | HG01109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1649-6924A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94843190 | |||||||
| chr11:94843379 | G | T | 20 | a0001c0001t0011g0019 a0001c0001t0011g0020 a0001c0001t0011g0049 others(17): Show |
20 | HG01243.hp2 HG02055.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.1649-6735G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94843379 | |||||||
| chr11:94843407 | A | G | 4 | a0001c0001t0003g0022 a0001c0001t0015g0151 a0001c0001t0015g0213 others(1): Show |
4 | HG02258.hp1 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1649-6707A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94843407 | |||||||
| chr11:94843680 | T | C | 1 | a0001c0001t0032g0068 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1649-6434T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94843680 | |||||||
| chr11:94843876 | G | A | 8 | a0001c0001t0020g0154 a0001c0001t0032g0068 a0001c0001t0044g0210 others(5): Show |
8 | HG01106.hp1 HG02602.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.1649-6238G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94843876 | |||||||
| chr11:94843891 | C | T | 4 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(1): Show |
5 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1649-6223C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94843891 | |||||||
| chr11:94844344 | T | C | 56 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(53): Show |
57 | HG00738.hp2 HG01106.hp1 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.1649-5770T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94844344 | |||||||
| chr11:94844411 | T | C | 2 | a0001c0001t0013g0018 a0001c0001t0013g0119 |
2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1649-5703T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94844411 | |||||||
| chr11:94844518 | G | A | 2 | a0001c0001t0039g0112 a0001c0001t0040g0144 |
2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1649-5596G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94844518 | |||||||
| chr11:94844539 | A | G | 4 | a0003c0004t0021g0223 a0003c0004t0037g0212 a0003c0004t0041g0211 others(1): Show |
4 | HG02602.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1649-5575A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94844539 | |||||||
| chr11:94844750 | A | G | 3 | a0001c0001t0009g0155 a0001c0001t0009g0156 a0001c0001t0009g0157 |
3 | HG02615.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1649-5364A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94844750 | |||||||
| chr11:94844816 | A | G | 1 | a0001c0001t0009g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1649-5298A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94844816 | |||||||
| chr11:94844823 | C | G | 4 | a0001c0001t0003g0022 a0001c0001t0015g0151 a0001c0001t0015g0213 others(1): Show |
4 | HG02258.hp1 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1649-5291C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94844823 | |||||||
| chr11:94844919 | G | A | 35 | a0001c0001t0003g0022 a0001c0001t0007g0045 a0001c0001t0007g0094 others(32): Show |
35 | HG00738.hp2 HG01106.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.1649-5195G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94844919 | |||||||
| chr11:94845073 | C | T | 1 | a0001c0010t0038g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1649-5041C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94845073 | |||||||
| chr11:94845088 | C | A | 15 | a0001c0001t0017g0195 a0001c0001t0017g0204 a0001c0001t0017g0205 others(12): Show |
15 | HG01106.hp1 HG01243.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1649-5026C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94845088 | |||||||
| chr11:94845304 | T | C | 3 | a0001c0001t0022g0008 a0001c0001t0022g0152 a0001c0001t0042g0008 |
3 | HG02572.hp1 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1649-4810T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94845304 | |||||||
| chr11:94845348 | G | A | 10 | a0001c0001t0016g0114 a0001c0001t0016g0117 a0001c0001t0016g0146 others(7): Show |
10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1649-4766G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94845348 | |||||||
| chr11:94845385 | A | G | 21 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(18): Show |
22 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(19): Show |
intron_variant | MODIFIER | c.1649-4729A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94845385 | |||||||
| chr11:94845427 | A | G | 1 | a0001c0001t0026g0122 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1649-4687A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94845427 | |||||||
| chr11:94845438 | T | G | 2 | a0001c0002t0006g0056 a0001c0002t0006g0061 |
2 | NA18953.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1649-4676T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94845438 | |||||||
| chr11:94845748 | A | C | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1649-4366A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94845748 | |||||||
| chr11:94845821 | C | T | 1 | a0001c0010t0038g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1649-4293C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94845821 | |||||||
| chr11:94846094 | G | A | 2 | a0001c0001t0028g0196 a0001c0001t0028g0197 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1649-4020G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94846094 | |||||||
| chr11:94846240 | C | A | 17 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(14): Show |
18 | HG02280.hp2 HG02615.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.1649-3874C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94846240 | |||||||
| chr11:94846348 | TAAC | T | 6 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(3): Show |
6 | HG00738.hp2 HG01346.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1649-3760_1649-375 others(7): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 94846348 | ||||||
| chr11:94846653 | A | G | 2 | a0001c0001t0027g0216 a0001c0001t0027g0217 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1649-3461A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94846653 | |||||||
| chr11:94846656 | G | A | 52 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(49): Show |
53 | HG00738.hp2 HG01106.hp1 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.1649-3458G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94846656 | |||||||
| chr11:94846688 | C | G | 1 | a0001c0001t0007g0130 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1649-3426C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94846688 | |||||||
| chr11:94846817 | A | T | 1 | a0001c0001t0003g0141 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1649-3297A>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94846817 | |||||||
| chr11:94846894 | A | G | 1 | a0001c0010t0038g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1649-3220A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94846894 | |||||||
| chr11:94847020 | G | A | 38 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(35): Show |
39 | HG00738.hp2 HG01106.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.1649-3094G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94847020 | |||||||
| chr11:94847083 | T | C | 56 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(53): Show |
57 | HG00738.hp2 HG01106.hp1 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.1649-3031T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94847083 | |||||||
| chr11:94847173 | C | A | 1 | a0001c0002t0008g0098 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1649-2941C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94847173 | |||||||
| chr11:94847196 | G | A | 1 | a0001c0010t0038g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1649-2918G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94847196 | |||||||
| chr11:94847379 | C | A | 56 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(53): Show |
57 | HG00738.hp2 HG01106.hp1 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.1649-2735C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94847379 | |||||||
| chr11:94847413 | G | T | 10 | a0001c0001t0016g0114 a0001c0001t0016g0117 a0001c0001t0016g0146 others(7): Show |
10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1649-2701G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94847413 | |||||||
| chr11:94847610 | A | G | 1 | a0001c0010t0038g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1649-2504A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94847610 | |||||||
| chr11:94847876 | T | C | 1 | a0001c0001t0045g0140 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1649-2238T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94847876 | |||||||
| chr11:94847902 | T | A | 1 | a0001c0001t0003g0081 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1649-2212T>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94847902 | |||||||
| chr11:94848052 | C | T | 1 | a0005c0015t0010g0219 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1649-2062C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94848052 | |||||||
| chr11:94848194 | C | T | 4 | a0001c0001t0013g0018 a0001c0001t0013g0119 a0001c0001t0013g0207 others(1): Show |
4 | HG01109.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1649-1920C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94848194 | |||||||
| chr11:94848416 | C | T | 1 | a0001c0002t0036g0089 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1649-1698C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94848416 | |||||||
| chr11:94848493 | A | G | 1 | a0004c0012t0001g0087 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1649-1621A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94848493 | |||||||
| chr11:94848676 | A | G | 4 | a0001c0001t0003g0203 a0001c0001t0004g0014 a0001c0001t0004g0200 others(1): Show |
5 | HG01884.hp2 HG02622.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1649-1438A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94848676 | |||||||
| chr11:94848710 | T | G | 1 | a0001c0006t0001g0194 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1649-1404T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94848710 | |||||||
| chr11:94848883 | G | A | 1 | a0001c0001t0016g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1649-1231G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94848883 | |||||||
| chr11:94848933 | G | A | 1 | a0001c0001t0005g0040 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1649-1181G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94848933 | |||||||
| chr11:94849046 | G | T | 119 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0003g0081 others(116): Show |
123 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(120): Show |
intron_variant | MODIFIER | c.1649-1068G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94849046 | |||||||
| chr11:94849156 | C | T | 56 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(53): Show |
57 | HG00738.hp2 HG01106.hp1 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.1649-958C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94849156 | |||||||
| chr11:94849209 | G | A | 3 | a0001c0001t0015g0151 a0001c0001t0015g0213 a0007c0008t0015g0225 |
3 | HG02258.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1649-905G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94849209 | |||||||
| chr11:94849256 | G | A | 56 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(53): Show |
57 | HG00738.hp2 HG01106.hp1 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.1649-858G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94849256 | |||||||
| chr11:94849261 | G | C | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1649-853G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94849261 | |||||||
| chr11:94849365 | C | T | 21 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(18): Show |
22 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(19): Show |
intron_variant | MODIFIER | c.1649-749C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94849365 | |||||||
| chr11:94849539 | A | G | 35 | a0001c0001t0003g0022 a0001c0001t0007g0045 a0001c0001t0007g0094 others(32): Show |
35 | HG00738.hp2 HG01106.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.1649-575A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94849539 | |||||||
| chr11:94849756 | G | C | 1 | a0001c0001t0005g0043 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1649-358G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94849756 | |||||||
| chr11:94849813 | G | T | 6 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(3): Show |
6 | HG00738.hp2 HG01346.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1649-301G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94849813 | |||||||
| chr11:94849859 | C | T | 2 | a0001c0002t0006g0056 a0001c0002t0006g0061 |
2 | NA18953.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1649-255C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94849859 | |||||||
| chr11:94849869 | G | T | 1 | a0001c0001t0045g0140 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1649-245G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94849869 | |||||||
| chr11:94849922 | T | C | 56 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(53): Show |
57 | HG00738.hp2 HG01106.hp1 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.1649-192T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94849922 | |||||||
| chr11:94849923 | G | A | 1 | a0001c0001t0053g0118 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1649-191G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94849923 | |||||||
| chr11:94849984 | A | G | 21 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(18): Show |
22 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(19): Show |
intron_variant | MODIFIER | c.1649-130A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 6/12 | chr11 | 94849984 | |||||||
| chr11:94850307 | C | T | 3 | a0001c0001t0015g0151 a0001c0001t0015g0213 a0007c0008t0015g0225 |
3 | HG02258.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1794+48C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94850307 | |||||||
| chr11:94850446 | C | A | 1 | a0001c0010t0038g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1794+187C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94850446 | |||||||
| chr11:94850586 | G | A | 1 | a0001c0001t0003g0141 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1794+327G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94850586 | |||||||
| chr11:94850586 | G | T | 52 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(49): Show |
53 | HG00738.hp2 HG01106.hp1 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.1794+327G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94850586 | |||||||
| chr11:94850777 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1794+518C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94850777 | |||||||
| chr11:94850812 | G | A | 2 | a0001c0006t0001g0194 a0001c0006t0001g0214 |
2 | HG00741.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1794+553G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94850812 | |||||||
| chr11:94850964 | C | T | 1 | a0001c0002t0008g0098 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1794+705C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94850964 | |||||||
| chr11:94850970 | G | A | 1 | a0001c0010t0038g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1794+711G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94850970 | |||||||
| chr11:94851002 | A | G | 2 | a0001c0001t0020g0154 a0001c0001t0032g0068 |
2 | HG01106.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1794+743A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94851002 | |||||||
| chr11:94851121 | G | C | 1 | a0009c0014t0001g0201 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1794+862G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94851121 | |||||||
| chr11:94851245 | G | T | 16 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(13): Show |
17 | HG02615.hp1 HG02615.hp2 HG02647.hp2 others(14): Show |
intron_variant | MODIFIER | c.1794+986G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94851245 | |||||||
| chr11:94851368 | T | C | 2 | a0001c0001t0039g0112 a0001c0001t0040g0144 |
2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1794+1109T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94851368 | |||||||
| chr11:94851542 | T | G | 55 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(52): Show |
56 | HG00738.hp2 HG01106.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.1794+1283T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94851542 | |||||||
| chr11:94851660 | C | T | 34 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(31): Show |
34 | HG00738.hp2 HG01106.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.1794+1401C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94851660 | |||||||
| chr11:94851751 | A | G | 2 | a0001c0001t0028g0196 a0001c0001t0028g0197 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1794+1492A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94851751 | |||||||
| chr11:94851965 | C | T | 1 | a0001c0016t0010g0129 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1794+1706C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94851965 | |||||||
| chr11:94852110 | C | A | 1 | a0001c0002t0002g0177 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1795-1823C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94852110 | |||||||
| chr11:94852165 | A | G | 2 | a0001c0005t0001g0013 a0001c0005t0052g0198 |
3 | HG02486.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1795-1768A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94852165 | |||||||
| chr11:94852276 | G | T | 3 | a0001c0001t0022g0008 a0001c0001t0022g0152 a0001c0001t0042g0008 |
3 | HG02572.hp1 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1795-1657G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94852276 | |||||||
| chr11:94852342 | A | G | 1 | a0001c0010t0038g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1795-1591A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94852342 | |||||||
| chr11:94852370 | C | T | 1 | a0001c0001t0011g0049 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1795-1563C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94852370 | |||||||
| chr11:94852403 | C | T | 49 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0003g0081 others(46): Show |
50 | HG01081.hp2 HG01123.hp2 HG01192.hp1 others(47): Show |
intron_variant | MODIFIER | c.1795-1530C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94852403 | |||||||
| chr11:94852715 | A | G | 1 | a0001c0001t0029g0172 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1795-1218A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94852715 | |||||||
| chr11:94852748 | C | T | 119 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0003g0081 others(116): Show |
123 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(120): Show |
intron_variant | MODIFIER | c.1795-1185C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94852748 | |||||||
| chr11:94852760 | T | A | 2 | a0001c0001t0039g0112 a0001c0001t0040g0144 |
2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1795-1173T>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94852760 | |||||||
| chr11:94852822 | A | T | 3 | a0001c0001t0019g0064 a0001c0002t0019g0102 a0001c0002t0019g0104 |
3 | NA18956.hp1 NA19005.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1795-1111A>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94852822 | |||||||
| chr11:94852956 | T | G | 1 | a0001c0001t0009g0009 | 2 | HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1795-977T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94852956 | |||||||
| chr11:94853031 | A | C | 1 | a0002c0003t0001g0083 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1795-902A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94853031 | |||||||
| chr11:94853041 | A | G | 1 | a0001c0001t0045g0140 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1795-892A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94853041 | |||||||
| chr11:94853082 | A | G | 1 | a0001c0001t0048g0082 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1795-851A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94853082 | |||||||
| chr11:94853121 | TTCTA | T | 5 | a0001c0001t0015g0151 a0001c0001t0015g0213 a0001c0001t0020g0154 others(2): Show |
5 | HG01106.hp1 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1795-806_1795-803d others(6): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 94853121 | ||||||
| chr11:94853145 | A | G | 2 | a0001c0002t0002g0159 a0001c0002t0006g0186 |
2 | NA19004.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1795-788A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94853145 | |||||||
| chr11:94853146 | G | A | 6 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(3): Show |
6 | HG00738.hp2 HG01346.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1795-787G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94853146 | |||||||
| chr11:94853307 | G | A | 5 | a0001c0001t0015g0151 a0001c0001t0015g0213 a0001c0001t0020g0154 others(2): Show |
5 | HG01106.hp1 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1795-626G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94853307 | |||||||
| chr11:94853368 | C | T | 8 | a0001c0001t0011g0019 a0001c0001t0011g0020 a0001c0001t0011g0049 others(5): Show |
8 | HG02615.hp2 HG02717.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1795-565C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94853368 | |||||||
| chr11:94853403 | A | G | 56 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(53): Show |
57 | HG00738.hp2 HG01106.hp1 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.1795-530A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94853403 | |||||||
| chr11:94853460 | C | T | 1 | a0001c0001t0048g0082 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1795-473C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94853460 | |||||||
| chr11:94853808 | G | A | 4 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(1): Show |
5 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1795-125G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | chr11 | 94853808 | |||||||
| chr11:94853910 | CT | C | 8 | a0001c0001t0017g0195 a0001c0001t0017g0204 a0001c0001t0017g0205 others(5): Show |
8 | HG01243.hp2 HG02055.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1795-17delT | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 94853910 | ||||||
| chr11:94854204 | C | T | 1 | a0001c0010t0038g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1944+122C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94854204 | |||||||
| chr11:94854227 | A | G | 57 | a0001c0001t0003g0022 a0001c0001t0007g0045 a0001c0001t0007g0094 others(54): Show |
58 | HG00738.hp2 HG01106.hp1 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.1944+145A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94854227 | |||||||
| chr11:94854254 | C | G | 3 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0005c0015t0010g0219 |
3 | HG01074.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1944+172C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94854254 | |||||||
| chr11:94854296 | C | T | 2 | a0001c0005t0001g0013 a0001c0005t0052g0198 |
3 | HG02486.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1944+214C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94854296 | |||||||
| chr11:94854345 | A | G | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1944+263A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94854345 | |||||||
| chr11:94854406 | A | G | 2 | a0001c0005t0001g0013 a0001c0005t0052g0198 |
3 | HG02486.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1944+324A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94854406 | |||||||
| chr11:94854456 | A | G | 57 | a0001c0001t0003g0022 a0001c0001t0007g0045 a0001c0001t0007g0094 others(54): Show |
58 | HG00738.hp2 HG01106.hp1 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.1944+374A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94854456 | |||||||
| chr11:94854492 | G | T | 1 | a0001c0001t0034g0127 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1944+410G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94854492 | |||||||
| chr11:94854504 | T | A | 4 | a0001c0001t0003g0022 a0001c0001t0015g0151 a0001c0001t0015g0213 others(1): Show |
4 | HG02258.hp1 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1944+422T>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94854504 | |||||||
| chr11:94855027 | C | T | 1 | a0001c0001t0009g0156 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1944+945C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94855027 | |||||||
| chr11:94855131 | G | A | 1 | a0001c0010t0038g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1944+1049G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94855131 | |||||||
| chr11:94855202 | G | A | 1 | a0003c0004t0043g0224 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1944+1120G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94855202 | |||||||
| chr11:94855205 | C | T | 7 | a0001c0001t0011g0019 a0001c0001t0011g0020 a0001c0001t0011g0049 others(4): Show |
7 | HG02615.hp2 HG02717.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1944+1123C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94855205 | |||||||
| chr11:94855300 | A | G | 61 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0003g0081 others(58): Show |
63 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.1944+1218A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94855300 | |||||||
| chr11:94855539 | A | G | 1 | a0001c0002t0031g0227 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1944+1457A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94855539 | |||||||
| chr11:94855618 | G | A | 8 | a0001c0001t0011g0019 a0001c0001t0011g0020 a0001c0001t0011g0049 others(5): Show |
8 | HG02615.hp2 HG02717.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1944+1536G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94855618 | |||||||
| chr11:94855644 | C | T | 1 | a0001c0002t0006g0056 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1944+1562C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94855644 | |||||||
| chr11:94855784 | C | T | 26 | a0001c0001t0015g0151 a0001c0001t0015g0213 a0001c0001t0016g0114 others(23): Show |
26 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1944+1702C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94855784 | |||||||
| chr11:94855785 | C | A | 3 | a0001c0001t0001g0079 a0001c0001t0012g0078 a0001c0018t0001g0180 |
3 | NA18966.hp1 NA19002.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1944+1703C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94855785 | |||||||
| chr11:94856225 | G | A | 3 | a0001c0001t0001g0079 a0001c0001t0012g0078 a0001c0018t0001g0180 |
3 | NA18966.hp1 NA19002.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1944+2143G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94856225 | |||||||
| chr11:94856289 | T | C | 1 | a0001c0001t0011g0020 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1944+2207T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94856289 | |||||||
| chr11:94856452 | GGTC | G | 17 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(14): Show |
18 | HG02280.hp2 HG02615.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.1944+2371_1944+237 others(7): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94856452 | |||||||
| chr11:94856457 | G | T | 17 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(14): Show |
18 | HG02280.hp2 HG02615.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.1944+2375G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94856457 | |||||||
| chr11:94856539 | C | T | 1 | a0001c0001t0011g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1944+2457C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94856539 | |||||||
| chr11:94856781 | G | A | 2 | a0001c0001t0039g0112 a0001c0001t0040g0144 |
2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1944+2699G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94856781 | |||||||
| chr11:94857032 | C | T | 8 | a0001c0001t0017g0195 a0001c0001t0017g0204 a0001c0001t0017g0205 others(5): Show |
8 | HG01243.hp2 HG02055.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1945-2493C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94857032 | |||||||
| chr11:94857169 | A | T | 35 | a0001c0001t0003g0022 a0001c0001t0007g0045 a0001c0001t0007g0094 others(32): Show |
35 | HG00738.hp2 HG01106.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.1945-2356A>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94857169 | |||||||
| chr11:94857232 | C | T | 1 | a0001c0002t0002g0181 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1945-2293C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94857232 | |||||||
| chr11:94857298 | A | G | 57 | a0001c0001t0003g0022 a0001c0001t0007g0045 a0001c0001t0007g0094 others(54): Show |
58 | HG00738.hp2 HG01106.hp1 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.1945-2227A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94857298 | |||||||
| chr11:94857328 | A | T | 56 | a0001c0001t0003g0022 a0001c0001t0007g0045 a0001c0001t0007g0094 others(53): Show |
57 | HG00738.hp2 HG01106.hp1 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.1945-2197A>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94857328 | |||||||
| chr11:94857410 | G | A | 1 | a0001c0001t0054g0093 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1945-2115G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94857410 | |||||||
| chr11:94857507 | A | G | 1 | a0001c0001t0013g0207 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1945-2018A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94857507 | |||||||
| chr11:94857531 | C | T | 1 | a0001c0001t0033g0199 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1945-1994C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94857531 | |||||||
| chr11:94857571 | TAAAAG | T | 3 | a0001c0001t0022g0008 a0001c0001t0022g0152 a0001c0001t0042g0008 |
3 | HG02572.hp1 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1945-1952_1945-194 others(9): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 94857571 | ||||||
| chr11:94857765 | C | T | 1 | a0001c0010t0038g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1945-1760C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94857765 | |||||||
| chr11:94857807 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1945-1718G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94857807 | |||||||
| chr11:94857954 | A | G | 21 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(18): Show |
22 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(19): Show |
intron_variant | MODIFIER | c.1945-1571A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94857954 | |||||||
| chr11:94857957 | C | G | 6 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(3): Show |
6 | HG00738.hp2 HG01346.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1945-1568C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94857957 | |||||||
| chr11:94857974 | A | G | 1 | a0001c0002t0024g0037 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1945-1551A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94857974 | |||||||
| chr11:94858043 | G | A | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1945-1482G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94858043 | |||||||
| chr11:94858124 | T | C | 61 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0003g0081 others(58): Show |
63 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.1945-1401T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94858124 | |||||||
| chr11:94858310 | A | G | 3 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 |
3 | HG01346.hp1 HG01943.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1945-1215A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94858310 | |||||||
| chr11:94858316 | G | C | 2 | a0001c0001t0001g0079 a0001c0001t0012g0078 |
2 | NA18966.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1945-1209G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94858316 | |||||||
| chr11:94858338 | C | T | 1 | a0002c0003t0004g0133 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1945-1187C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94858338 | |||||||
| chr11:94858610 | G | T | 56 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(53): Show |
57 | HG00738.hp2 HG01106.hp1 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.1945-915G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94858610 | |||||||
| chr11:94858670 | T | C | 6 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(3): Show |
6 | HG00738.hp2 HG01346.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1945-855T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94858670 | |||||||
| chr11:94858714 | A | G | 56 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(53): Show |
57 | HG00738.hp2 HG01106.hp1 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.1945-811A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94858714 | |||||||
| chr11:94858732 | C | G | 1 | a0003c0004t0021g0223 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1945-793C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94858732 | |||||||
| chr11:94858757 | C | T | 3 | a0001c0002t0006g0056 a0001c0002t0006g0061 a0001c0002t0006g0063 |
3 | NA18953.hp1 NA19003.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1945-768C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94858757 | |||||||
| chr11:94858890 | T | C | 1 | a0001c0001t0027g0216 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1945-635T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94858890 | |||||||
| chr11:94858897 | G | A | 2 | a0001c0001t0005g0128 a0001c0001t0054g0093 |
2 | HG02145.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.1945-628G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94858897 | |||||||
| chr11:94858941 | T | C | 1 | a0001c0001t0017g0204 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1945-584T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94858941 | |||||||
| chr11:94858984 | G | A | 34 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(31): Show |
34 | HG00738.hp2 HG01106.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.1945-541G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94858984 | |||||||
| chr11:94859087 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1945-438G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94859087 | |||||||
| chr11:94859135 | T | A | 3 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 |
3 | HG01346.hp1 HG01943.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1945-390T>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94859135 | |||||||
| chr11:94859247 | C | G | 2 | a0001c0001t0039g0112 a0001c0001t0040g0144 |
2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1945-278C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 8/12 | chr11 | 94859247 | |||||||
| chr11:94860171 | A | G | 2 | a0001c0001t0003g0070 a0001c0001t0003g0071 |
2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2135+456A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94860171 | |||||||
| chr11:94860283 | A | G | 2 | a0001c0005t0001g0013 a0001c0005t0052g0198 |
3 | HG02486.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2135+568A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94860283 | |||||||
| chr11:94860290 | A | G | 29 | a0001c0001t0003g0022 a0001c0001t0009g0009 a0001c0001t0009g0155 others(26): Show |
30 | HG01106.hp1 HG01109.hp1 HG02258.hp1 others(27): Show |
intron_variant | MODIFIER | c.2135+575A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94860290 | |||||||
| chr11:94860345 | A | C | 2 | a0001c0002t0002g0181 a0001c0002t0046g0191 |
2 | HG02165.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.2135+630A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94860345 | |||||||
| chr11:94860455 | T | C | 1 | a0002c0003t0001g0051 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2135+740T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94860455 | |||||||
| chr11:94860467 | C | G | 1 | a0001c0010t0038g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2135+752C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94860467 | |||||||
| chr11:94860511 | A | C | 1 | a0001c0001t0001g0015 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2135+796A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94860511 | |||||||
| chr11:94860721 | C | T | 1 | a0001c0002t0006g0090 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2135+1006C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94860721 | |||||||
| chr11:94860825 | T | G | 1 | a0001c0001t0003g0138 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2135+1110T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94860825 | |||||||
| chr11:94860861 | G | A | 4 | a0001c0001t0013g0018 a0001c0001t0013g0119 a0001c0001t0013g0207 others(1): Show |
4 | HG01109.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2135+1146G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94860861 | |||||||
| chr11:94860931 | G | A | 6 | a0001c0001t0015g0151 a0001c0001t0015g0213 a0001c0001t0020g0154 others(3): Show |
6 | HG01106.hp1 HG02258.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2135+1216G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94860931 | |||||||
| chr11:94861001 | G | T | 1 | a0001c0010t0038g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2135+1286G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94861001 | |||||||
| chr11:94861043 | G | A | 2 | a0001c0001t0039g0112 a0001c0001t0040g0144 |
2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2135+1328G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94861043 | |||||||
| chr11:94861261 | C | A | 3 | a0001c0001t0015g0151 a0001c0001t0015g0213 a0007c0008t0015g0225 |
3 | HG02258.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2135+1546C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94861261 | |||||||
| chr11:94861284 | G | A | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2135+1569G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94861284 | |||||||
| chr11:94861512 | T | C | 7 | a0001c0001t0003g0022 a0001c0001t0015g0151 a0001c0001t0015g0213 others(4): Show |
7 | HG01106.hp1 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.2135+1797T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94861512 | |||||||
| chr11:94861755 | C | G | 7 | a0001c0001t0003g0022 a0001c0001t0015g0151 a0001c0001t0015g0213 others(4): Show |
7 | HG01106.hp1 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.2135+2040C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94861755 | |||||||
| chr11:94861920 | G | T | 30 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(27): Show |
30 | HG00738.hp2 HG01243.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.2135+2205G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94861920 | |||||||
| chr11:94862176 | C | A | 29 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(26): Show |
29 | HG00738.hp2 HG01243.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.2135+2461C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94862176 | |||||||
| chr11:94862252 | C | CT | 6 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(3): Show |
6 | HG00738.hp2 HG01346.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.2136-2479dupT | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 94862252 | ||||||
| chr11:94862386 | A | G | 16 | a0001c0001t0011g0019 a0001c0001t0011g0020 a0001c0001t0011g0049 others(13): Show |
16 | HG01109.hp1 HG02615.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136-2349A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94862386 | |||||||
| chr11:94862451 | A | G | 3 | a0001c0001t0009g0155 a0001c0001t0009g0156 a0001c0001t0009g0157 |
3 | HG02615.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2136-2284A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94862451 | |||||||
| chr11:94862523 | A | G | 1 | a0001c0001t0027g0216 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2136-2212A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94862523 | |||||||
| chr11:94862713 | G | C | 7 | a0001c0001t0003g0022 a0001c0001t0015g0151 a0001c0001t0015g0213 others(4): Show |
7 | HG01106.hp1 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.2136-2022G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94862713 | |||||||
| chr11:94862878 | G | A | 30 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(27): Show |
30 | HG00738.hp2 HG01243.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.2136-1857G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94862878 | |||||||
| chr11:94862955 | T | A | 1 | a0001c0001t0011g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2136-1780T>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94862955 | |||||||
| chr11:94863279 | T | TA | 25 | a0001c0001t0001g0033 a0001c0001t0003g0022 a0001c0001t0004g0021 others(22): Show |
26 | HG01081.hp1 HG01106.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.2136-1440dupA | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 94863279 | ||||||
| chr11:94863279 | TA | T | 25 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0016g0114 others(22): Show |
25 | HG00741.hp2 HG01243.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.2136-1440delA | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 94863279 | ||||||
| chr11:94863301 | A | G | 1 | a0001c0010t0038g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2136-1434A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94863301 | |||||||
| chr11:94863314 | G | A | 1 | a0001c0001t0009g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2136-1421G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94863314 | |||||||
| chr11:94863330 | C | T | 8 | a0001c0001t0016g0114 a0001c0001t0016g0117 a0001c0001t0016g0146 others(5): Show |
8 | HG01884.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2136-1405C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94863330 | |||||||
| chr11:94863409 | G | A | 30 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(27): Show |
30 | HG00738.hp2 HG01243.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.2136-1326G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94863409 | |||||||
| chr11:94863520 | A | G | 1 | a0001c0001t0007g0228 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2136-1215A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94863520 | |||||||
| chr11:94863592 | CA | C | 11 | a0001c0001t0004g0004 a0001c0001t0004g0053 a0001c0001t0004g0055 others(8): Show |
12 | HG00558.hp1 HG03017.hp1 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.2136-1131delA | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 94863592 | ||||||
| chr11:94863603 | A | AG | 6 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(3): Show |
6 | HG02132.hp2 NA18939.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.2136-1132_2136-113 others(5): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94863603 | |||||||
| chr11:94863956 | C | T | 2 | a0001c0001t0039g0112 a0001c0001t0040g0144 |
2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2136-779C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94863956 | |||||||
| chr11:94864054 | C | T | 1 | a0001c0010t0038g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2136-681C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94864054 | |||||||
| chr11:94864098 | G | A | 4 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(1): Show |
5 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2136-637G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94864098 | |||||||
| chr11:94864182 | A | G | 1 | a0001c0001t0044g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2136-553A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94864182 | |||||||
| chr11:94864250 | C | CAAT | 4 | a0001c0001t0001g0038 a0001c0002t0002g0168 a0001c0007t0005g0044 others(1): Show |
4 | HG00558.hp2 HG01106.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.2136-459_2136-457d others(5): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 94864250 | ||||||
| chr11:94864250 | C | CAATAAT | 2 | a0001c0001t0039g0112 a0001c0001t0040g0144 |
2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2136-462_2136-457d others(8): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 94864250 | ||||||
| chr11:94864250 | CAAT | C | 62 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0046 others(59): Show |
65 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.2136-459_2136-457d others(5): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 94864250 | ||||||
| chr11:94864285 | A | G | 1 | a0001c0001t0039g0112 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2136-450A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94864285 | |||||||
| chr11:94864352 | C | T | 1 | a0001c0002t0002g0161 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2136-383C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94864352 | |||||||
| chr11:94864502 | G | T | 1 | a0001c0001t0020g0221 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2136-233G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94864502 | |||||||
| chr11:94864513 | A | G | 30 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(27): Show |
30 | HG00738.hp2 HG01243.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.2136-222A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94864513 | |||||||
| chr11:94864723 | T | C | 3 | a0001c0001t0017g0195 a0001c0001t0017g0204 a0001c0001t0017g0205 |
3 | HG01243.hp2 HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2136-12T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 9/12 | chr11 | 94864723 | |||||||
| chr11:94864893 | C | T | 14 | a0001c0001t0011g0019 a0001c0001t0011g0020 a0001c0001t0011g0049 others(11): Show |
14 | HG02280.hp1 HG02615.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.2261+33C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 10/12 | chr11 | 94864893 | |||||||
| chr11:94865035 | G | T | 1 | a0001c0001t0045g0140 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2261+175G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 10/12 | chr11 | 94865035 | |||||||
| chr11:94865040 | A | G | 4 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(1): Show |
5 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2261+180A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 10/12 | chr11 | 94865040 | |||||||
| chr11:94865263 | T | G | 2 | a0001c0001t0001g0038 a0001c0007t0005g0044 |
2 | HG01106.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.2261+403T>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 10/12 | chr11 | 94865263 | |||||||
| chr11:94865323 | A | C | 1 | a0001c0002t0002g0174 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2261+463A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 10/12 | chr11 | 94865323 | |||||||
| chr11:94865529 | C | A | 61 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0003g0081 others(58): Show |
63 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.2262-413C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 10/12 | chr11 | 94865529 | |||||||
| chr11:94865563 | C | T | 30 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(27): Show |
30 | HG00738.hp2 HG01243.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.2262-379C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 10/12 | chr11 | 94865563 | |||||||
| chr11:94865819 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2262-123G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 10/12 | chr11 | 94865819 | |||||||
| chr11:94866208 | A | C | 1 | a0001c0001t0001g0076 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2488+40A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/12 | chr11 | 94866208 | |||||||
| chr11:94866397 | C | G | 8 | a0001c0001t0016g0114 a0001c0001t0016g0117 a0001c0001t0016g0146 others(5): Show |
8 | HG01884.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2488+229C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/12 | chr11 | 94866397 | |||||||
| chr11:94866440 | C | T | 1 | a0001c0002t0002g0187 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2488+272C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/12 | chr11 | 94866440 | |||||||
| chr11:94866580 | A | C | 59 | a0001c0001t0003g0022 a0001c0001t0007g0045 a0001c0001t0007g0094 others(56): Show |
61 | HG00738.hp2 HG01106.hp1 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.2488+412A>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/12 | chr11 | 94866580 | |||||||
| chr11:94866636 | A | G | 5 | a0001c0001t0016g0114 a0001c0001t0016g0117 a0001c0001t0016g0146 others(2): Show |
5 | HG01884.hp1 HG02451.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2488+468A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/12 | chr11 | 94866636 | |||||||
| chr11:94866699 | T | C | 61 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0003g0081 others(58): Show |
63 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.2488+531T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/12 | chr11 | 94866699 | |||||||
| chr11:94866766 | C | T | 3 | a0001c0001t0015g0151 a0001c0001t0015g0213 a0007c0008t0015g0225 |
3 | HG02258.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2488+598C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/12 | chr11 | 94866766 | |||||||
| chr11:94867048 | C | T | 1 | a0001c0002t0008g0160 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2488+880C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/12 | chr11 | 94867048 | |||||||
| chr11:94867096 | G | T | 8 | a0001c0001t0011g0019 a0001c0001t0011g0020 a0001c0001t0011g0049 others(5): Show |
8 | HG02615.hp2 HG02717.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.2488+928G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/12 | chr11 | 94867096 | |||||||
| chr11:94867141 | A | G | 1 | a0001c0001t0005g0092 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2488+973A>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/12 | chr11 | 94867141 | |||||||
| chr11:94867277 | G | C | 29 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(26): Show |
29 | HG00738.hp2 HG01243.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.2488+1109G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/12 | chr11 | 94867277 | |||||||
| chr11:94867409 | C | A | 58 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(55): Show |
60 | HG00738.hp2 HG01106.hp1 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.2488+1241C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/12 | chr11 | 94867409 | |||||||
| chr11:94867474 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2488+1306G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/12 | chr11 | 94867474 | |||||||
| chr11:94867605 | C | CAGGG | 30 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(27): Show |
30 | HG00738.hp2 HG01243.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.2488+1439_2488+144 others(8): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr11 | 94867605 | ||||||
| chr11:94867613 | C | G | 6 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(3): Show |
6 | HG00738.hp2 HG01346.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.2488+1445C>G | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/12 | chr11 | 94867613 | |||||||
| chr11:94867638 | G | C | 1 | a0001c0010t0038g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2488+1470G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/12 | chr11 | 94867638 | |||||||
| chr11:94867731 | C | T | 4 | a0001c0001t0009g0009 a0001c0001t0009g0155 a0001c0001t0009g0156 others(1): Show |
5 | HG02615.hp1 HG02647.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2489-1467C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/12 | chr11 | 94867731 | |||||||
| chr11:94867965 | CTGTCTCG others(7): Show |
C | 1 | a0001c0002t0002g0062 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2489-1232_2489-121 others(18): Show |
AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/12 | chr11 | 94867965 | |||||||
| chr11:94868114 | G | A | 1 | a0001c0001t0011g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2489-1084G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/12 | chr11 | 94868114 | |||||||
| chr11:94868242 | G | T | 2 | a0001c0001t0003g0070 a0001c0001t0003g0071 |
2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2489-956G>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/12 | chr11 | 94868242 | |||||||
| chr11:94868348 | G | A | 2 | a0001c0001t0004g0021 a0001c0013t0006g0226 |
2 | HG01123.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.2489-850G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/12 | chr11 | 94868348 | |||||||
| chr11:94868444 | C | T | 1 | a0001c0001t0004g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2489-754C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/12 | chr11 | 94868444 | |||||||
| chr11:94868618 | C | T | 1 | a0001c0001t0003g0047 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2489-580C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/12 | chr11 | 94868618 | |||||||
| chr11:94868677 | G | A | 1 | a0001c0001t0003g0047 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2489-521G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/12 | chr11 | 94868677 | |||||||
| chr11:94868745 | G | A | 1 | a0001c0002t0002g0179 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2489-453G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/12 | chr11 | 94868745 | |||||||
| chr11:94868770 | C | T | 29 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(26): Show |
29 | HG00738.hp2 HG01243.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.2489-428C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/12 | chr11 | 94868770 | |||||||
| chr11:94868877 | T | A | 2 | a0001c0001t0001g0038 a0001c0007t0005g0044 |
2 | HG01106.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.2489-321T>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/12 | chr11 | 94868877 | |||||||
| chr11:94868944 | C | CA | 39 | a0001c0001t0003g0022 a0001c0001t0007g0045 a0001c0001t0007g0094 others(36): Show |
39 | HG00738.hp2 HG01106.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2489-242dupA | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr11 | 94868944 | ||||||
| chr11:94869635 | C | T | 2 | a0001c0005t0001g0013 a0001c0005t0052g0198 |
3 | HG02486.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2764+162C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 12/12 | chr11 | 94869635 | |||||||
| chr11:94869636 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2764+163G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 12/12 | chr11 | 94869636 | |||||||
| chr11:94869717 | T | C | 1 | a0010c0017t0021g0113 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2764+244T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 12/12 | chr11 | 94869717 | |||||||
| chr11:94869839 | T | C | 1 | a0001c0002t0012g0097 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2764+366T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 12/12 | chr11 | 94869839 | |||||||
| chr11:94869896 | G | A | 29 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(26): Show |
29 | HG00738.hp2 HG01243.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.2764+423G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 12/12 | chr11 | 94869896 | |||||||
| chr11:94869933 | C | T | 1 | a0001c0001t0003g0072 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2764+460C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 12/12 | chr11 | 94869933 | |||||||
| chr11:94869983 | C | T | 1 | a0001c0010t0038g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2764+510C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 12/12 | chr11 | 94869983 | |||||||
| chr11:94870109 | C | T | 1 | a0001c0001t0013g0119 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2765-580C>T | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 12/12 | chr11 | 94870109 | |||||||
| chr11:94870304 | T | C | 1 | a0001c0010t0038g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2765-385T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 12/12 | chr11 | 94870304 | |||||||
| chr11:94870373 | G | A | 6 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(3): Show |
6 | HG00738.hp2 HG01346.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.2765-316G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 12/12 | chr11 | 94870373 | |||||||
| chr11:94870377 | C | A | 30 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(27): Show |
30 | HG00738.hp2 HG01243.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.2765-312C>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 12/12 | chr11 | 94870377 | |||||||
| chr11:94870470 | T | C | 30 | a0001c0001t0007g0045 a0001c0001t0007g0094 a0001c0001t0007g0130 others(27): Show |
30 | HG00738.hp2 HG01243.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.2765-219T>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 12/12 | chr11 | 94870470 | |||||||
| chr11:94870548 | G | A | 3 | a0001c0001t0015g0151 a0001c0001t0015g0213 a0007c0008t0015g0225 |
3 | HG02258.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2765-141G>A | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 12/12 | chr11 | 94870548 | |||||||
| chr11:94870600 | G | C | 2 | a0001c0001t0039g0112 a0001c0001t0040g0144 |
2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2765-89G>C | AMOTL1 | ENSG00000166025.18 | transcript | ENST00000433060.3 | protein_coding | 12/12 | chr11 | 94870600 |