Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4931 |
| ensemblid | ENSG00000143748.18 |
| hgncid | 8070 |
| symbol | NVL |
| name | nuclear VCP like |
| refseq_nuc | NM_002533.4 |
| refseq_prot | NP_002524.2 |
| ensembl_nuc | ENST00000281701.11 |
| ensembl_prot | ENSP00000281701.6 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 224227345 |
| end | 224330172 |
| strand | - |
| ver | v1.2 |
| region | chr1:224227345-224330172 |
| region5000 | chr1:224222345-224335172 |
| regionname0 | NVL_chr1_224227345_224330172 |
| regionname5000 | NVL_chr1_224222345_224335172 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 856 | 270 | 82 | 47 | 90 | 14 | 35 | 69 | NVL_chr1_224222345_224335172 | NVL | MKPRP others(851): Show |
chr1 | 224222345 | 224335172 |
| a0002 | 0/0 | 856 | 7 | 0 | 0 | 7 | 0 | 0 | 5 | NVL_chr1_224222345_224335172 | NVL | MKPRP others(851): Show |
chr1 | 224222345 | 224335172 |
| a0003 | 0/0 | 856 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | NVL_chr1_224222345_224335172 | NVL | MKPRP others(851): Show |
chr1 | 224222345 | 224335172 |
| a0004 | 0/0 | 856 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | MKPRP others(851): Show |
chr1 | 224222345 | 224335172 |
| a0005 | 0/0 | 856 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NVL_chr1_224222345_224335172 | NVL | MKPRP others(851): Show |
chr1 | 224222345 | 224335172 |
| a0006 | 0/0 | 856 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | MKPRP others(851): Show |
chr1 | 224222345 | 224335172 |
| a0007 | 0/0 | 856 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | MKPRP others(851): Show |
chr1 | 224222345 | 224335172 |
| a0008 | 0/0 | 856 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NVL_chr1_224222345_224335172 | NVL | MKPRP others(851): Show |
chr1 | 224222345 | 224335172 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2568 | 198 | 41 | 42 | 72 | 13 | 29 | NVL_chr1_224222345_224335172 | NVL | ATGAA others(2563): Show |
chr1 | 224222345 | 224335172 | ||
| a0001c0002 | 1/0 | 2568 | 45 | 21 | 2 | 14 | 1 | 6 | NVL_chr1_224222345_224335172 | NVL | ATGAA others(2563): Show |
chr1 | 224222345 | 224335172 | ||
| a0001c0003 | 0/0 | 2568 | 20 | 18 | 2 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | ATGAA others(2563): Show |
chr1 | 224222345 | 224335172 | ||
| a0001c0005 | 0/0 | 2568 | 3 | 0 | 0 | 3 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | ATGAA others(2563): Show |
chr1 | 224222345 | 224335172 | ||
| a0001c0007 | 0/0 | 2568 | 2 | 1 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | ATGAA others(2563): Show |
chr1 | 224222345 | 224335172 | ||
| a0001c0010 | 0/0 | 2568 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | ATGAA others(2563): Show |
chr1 | 224222345 | 224335172 | ||
| a0001c0012 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | ATGAA others(2563): Show |
chr1 | 224222345 | 224335172 | ||
| a0002c0004 | 0/0 | 2568 | 7 | 0 | 0 | 7 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | ATGAA others(2563): Show |
chr1 | 224222345 | 224335172 | ||
| a0003c0006 | 0/0 | 2568 | 2 | 0 | 1 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | ATGAA others(2563): Show |
chr1 | 224222345 | 224335172 | ||
| a0004c0014 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | ATGAA others(2563): Show |
chr1 | 224222345 | 224335172 | ||
| a0005c0011 | 0/0 | 2568 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | ATGAA others(2563): Show |
chr1 | 224222345 | 224335172 | ||
| a0006c0008 | 0/0 | 2568 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | ATGAA others(2563): Show |
chr1 | 224222345 | 224335172 | ||
| a0007c0013 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | ATGAA others(2563): Show |
chr1 | 224222345 | 224335172 | ||
| a0008c0009 | 0/0 | 2568 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | ATGAA others(2563): Show |
chr1 | 224222345 | 224335172 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2897 | 192 | 37 | 41 | 72 | 13 | 28 | NVL_chr1_224222345_224335172 | NVL | GACTA others(2892): Show |
chr1 | 224222345 | 224335172 |
| a0001c0001t0004 | 0/0 | 2897 | 5 | 4 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | GACTA others(2892): Show |
chr1 | 224222345 | 224335172 |
| a0001c0001t0005 | 0/0 | 2897 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | GACTA others(2892): Show |
chr1 | 224222345 | 224335172 |
| a0001c0002t0001 | 0/0 | 2897 | 6 | 6 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | GACTA others(2892): Show |
chr1 | 224222345 | 224335172 |
| a0001c0002t0002 | 1/0 | 2897 | 37 | 14 | 2 | 14 | 1 | 5 | NVL_chr1_224222345_224335172 | NVL | GACTA others(2892): Show |
chr1 | 224222345 | 224335172 |
| a0001c0002t0006 | 0/0 | 2897 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | GACTA others(2892): Show |
chr1 | 224222345 | 224335172 |
| a0001c0002t0007 | 0/0 | 2897 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | GACTA others(2892): Show |
chr1 | 224222345 | 224335172 |
| a0001c0003t0002 | 0/0 | 2897 | 12 | 11 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | GACTA others(2892): Show |
chr1 | 224222345 | 224335172 |
| a0001c0003t0003 | 0/0 | 2897 | 8 | 7 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | GACTA others(2892): Show |
chr1 | 224222345 | 224335172 |
| a0001c0005t0001 | 0/0 | 2897 | 3 | 0 | 0 | 3 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | GACTA others(2892): Show |
chr1 | 224222345 | 224335172 |
| a0001c0007t0001 | 0/0 | 2897 | 2 | 1 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | GACTA others(2892): Show |
chr1 | 224222345 | 224335172 |
| a0001c0010t0001 | 0/0 | 2897 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | GACTA others(2892): Show |
chr1 | 224222345 | 224335172 |
| a0001c0012t0001 | 0/0 | 2897 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | GACTA others(2892): Show |
chr1 | 224222345 | 224335172 |
| a0002c0004t0001 | 0/0 | 2897 | 7 | 0 | 0 | 7 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | GACTA others(2892): Show |
chr1 | 224222345 | 224335172 |
| a0003c0006t0001 | 0/0 | 2897 | 2 | 0 | 1 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | GACTA others(2892): Show |
chr1 | 224222345 | 224335172 |
| a0004c0014t0002 | 0/0 | 2897 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | GACTA others(2892): Show |
chr1 | 224222345 | 224335172 |
| a0005c0011t0001 | 0/0 | 2897 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | GACTA others(2892): Show |
chr1 | 224222345 | 224335172 |
| a0006c0008t0001 | 0/0 | 2897 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | GACTA others(2892): Show |
chr1 | 224222345 | 224335172 |
| a0007c0013t0002 | 0/0 | 2897 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | GACTA others(2892): Show |
chr1 | 224222345 | 224335172 |
| a0008c0009t0001 | 0/0 | 2897 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | GACTA others(2892): Show |
chr1 | 224222345 | 224335172 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0221 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0001t0005g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0245 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0006g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0002t0007g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0003t0002g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0003t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0003t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0003t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0003t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0003t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0003t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0003t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0003t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0003t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0003t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0003t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0003t0003g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0003t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0003t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0003t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0003t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0003t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0003t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0005t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0005t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0005t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0007t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0007t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0010t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0001c0012t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0002c0004t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0002c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0002c0004t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0002c0004t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0002c0004t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0002c0004t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0002c0004t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0003c0006t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0003c0006t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0004c0014t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0005c0011t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0006c0008t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0007c0013t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| a0008c0009t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | GBR | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | GBR | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | GBR | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0268 | EUR | GBR | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0106 | EUR | FIN | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0060 | EUR | FIN | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0231 | EUR | FIN | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | FIN | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00597 | hp1 | a0002 | c0004 | t0001 | g0128 | EAS | CHS | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00673 | hp2 | a0002 | c0004 | t0001 | g0136 | EAS | CHS | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00733 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | PUR | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0062 | AMR | PUR | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01243 | hp1 | a0001 | c0003 | t0003 | g0008 | AMR | PUR | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0273 | AMR | CLM | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0277 | AMR | CLM | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0056 | EUR | IBS | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0065 | EUR | IBS | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0166 | EUR | IBS | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | IBS | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01884 | hp1 | a0001 | c0012 | t0001 | g0017 | AFR | ACB | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01884 | hp2 | a0001 | c0003 | t0003 | g0009 | AFR | ACB | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01981 | hp2 | a0003 | c0006 | t0001 | g0088 | AMR | PEL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0266 | EAS | KHV | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0279 | AFR | ACB | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0264 | EAS | KHV | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02148 | hp2 | a0001 | c0007 | t0001 | g0086 | AMR | PEL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02257 | hp2 | a0001 | c0003 | t0003 | g0007 | AFR | ACB | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0131 | AFR | ACB | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02258 | hp2 | a0001 | c0003 | t0002 | g0240 | AFR | ACB | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02451 | hp1 | a0001 | c0003 | t0003 | g0002 | AFR | ACB | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0083 | AFR | ACB | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0255 | EAS | KHV | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | GWD | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0256 | SAS | PJL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02615 | hp2 | a0001 | c0003 | t0003 | g0004 | AFR | GWD | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02622 | hp1 | a0001 | c0003 | t0002 | g0241 | AFR | GWD | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0248 | AFR | GWD | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0270 | AFR | GWD | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02647 | hp1 | a0001 | c0003 | t0002 | g0234 | AFR | GWD | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0267 | SAS | PJL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02717 | hp2 | a0001 | c0003 | t0002 | g0001 | AFR | GWD | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0278 | AFR | GWD | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02735 | hp2 | a0005 | c0011 | t0001 | g0228 | SAS | PJL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02818 | hp2 | a0001 | c0003 | t0002 | g0237 | AFR | GWD | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0274 | AFR | ESN | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0272 | AFR | ESN | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0246 | AFR | GWD | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0249 | AFR | MSL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0012 | AFR | ESN | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03139 | hp1 | a0001 | c0003 | t0003 | g0005 | AFR | ESN | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0082 | AFR | MSL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03225 | hp1 | a0001 | c0003 | t0003 | g0006 | AFR | MSL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03225 | hp2 | a0001 | c0007 | t0001 | g0070 | AFR | MSL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03239 | hp2 | a0001 | c0002 | t0006 | g0253 | SAS | PJL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | MSL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0244 | AFR | MSL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | ESN | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0271 | AFR | GWD | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03579 | hp2 | a0001 | c0003 | t0002 | g0235 | AFR | MSL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0269 | SAS | PJL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03831 | hp2 | a0003 | c0006 | t0001 | g0073 | SAS | BEB | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0265 | SAS | BEB | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0260 | SAS | BEB | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | STU | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | STU | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | STU | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0149 | SAS | STU | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | STU | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | STU | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | STU | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0247 | AFR | YRI | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0250 | AFR | YRI | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0251 | EAS | CHB | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHB | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18747 | hp1 | a0006 | c0008 | t0001 | g0078 | EAS | CHB | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHB | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | YRI | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18906 | hp2 | a0001 | c0003 | t0003 | g0003 | AFR | YRI | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18941 | hp2 | a0001 | c0002 | t0002 | g0263 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18949 | hp1 | a0002 | c0004 | t0001 | g0099 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18959 | hp2 | a0001 | c0002 | t0002 | g0281 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18961 | hp1 | a0002 | c0004 | t0001 | g0075 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0257 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18966 | hp2 | a0001 | c0010 | t0001 | g0097 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18971 | hp1 | a0002 | c0004 | t0001 | g0076 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0254 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18992 | hp2 | a0002 | c0004 | t0001 | g0077 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18995 | hp1 | a0001 | c0005 | t0001 | g0195 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19000 | hp2 | a0001 | c0005 | t0001 | g0152 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0282 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19030 | hp1 | a0007 | c0013 | t0002 | g0243 | AFR | LWK | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19030 | hp2 | a0001 | c0003 | t0002 | g0239 | AFR | LWK | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19043 | hp1 | a0001 | c0003 | t0002 | g0238 | AFR | LWK | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19043 | hp2 | a0001 | c0002 | t0007 | g0276 | AFR | LWK | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19054 | hp2 | a0001 | c0005 | t0001 | g0184 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0252 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0258 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0261 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0259 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19085 | hp1 | a0002 | c0004 | t0001 | g0098 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0016 | AFR | YRI | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0275 | AFR | YRI | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ASW | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA20129 | hp2 | a0001 | c0003 | t0002 | g0236 | AFR | ASW | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | TSI | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0058 | EUR | TSI | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | GIH | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA20905 | hp2 | a0008 | c0009 | t0001 | g0051 | SAS | GIH | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0280 | AFR | ACB | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | ACB | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG02486 | hp2 | a0004 | c0014 | t0002 | g0283 | AFR | ACB | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG03471 | hp2 | a0001 | c0003 | t0002 | g0233 | AFR | MSL | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | USA | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | USA | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | USA | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | USA | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA21309 | hp1 | a0001 | c0003 | t0002 | g0242 | AFR | LWK | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | LWK | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0221 | REF | REF | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0245 | REF | REF | NVL_chr1_224222345_224335172 | NVL | chr1 | 224222345 | 224335172 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:224227640 | A | G | 1 | a0003 | 2 | HG01981.hp2 HG03831.hp2 |
missense_variant | MODERATE | c.2557T>C | p.Ser853Pro | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 23/23 | 2602/2897 | 2557/2571 | 853/856 | chr1 | 224227640 | |||
| chr1:224281127 | T | G | 1 | a0004 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.1958A>C | p.Asn653Thr | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/23 | 2003/2897 | 1958/2571 | 653/856 | chr1 | 224281127 | |||
| chr1:224294382 | C | T | 1 | a0005 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.1210G>A | p.Val404Ile | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/23 | 1255/2897 | 1210/2571 | 404/856 | chr1 | 224294382 | |||
| chr1:224303800 | C | T | 1 | a0002 | 7 | HG00597.hp1 HG00673.hp2 NA18949.hp1 others(4): Show |
missense_variant | MODERATE | c.883G>A | p.Val295Ile | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/23 | 928/2897 | 883/2571 | 295/856 | chr1 | 224303800 | |||
| chr1:224303829 | C | T | 1 | a0008 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.854G>A | p.Arg285His | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/23 | 899/2897 | 854/2571 | 285/856 | chr1 | 224303829 | |||
| chr1:224305042 | T | C | 1 | a0007 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.740A>G | p.Gln247Arg | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 7/23 | 785/2897 | 740/2571 | 247/856 | chr1 | 224305042 | |||
| chr1:224307996 | T | C | 1 | a0004 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.610A>G | p.Ile204Val | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/23 | 655/2897 | 610/2571 | 204/856 | chr1 | 224307996 | |||
| chr1:224308005 | T | C | 1 | a0004 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.601A>G | p.Ile201Val | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/23 | 646/2897 | 601/2571 | 201/856 | chr1 | 224308005 | |||
| chr1:224317738 | A | C | 1 | a0006 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.240T>G | p.Asp80Glu | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/23 | 285/2897 | 240/2571 | 80/856 | chr1 | 224317738 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:224300613 | T | C | 2 | a0001c0003 a0001c0007 |
22 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(19): Show |
synonymous_variant | LOW | c.1011A>G | p.Gly337Gly | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/23 | 1056/2897 | 1011/2571 | 337/856 | chr1 | 224300613 | |||
| chr1:224303822 | C | T | 1 | a0001c0010 | 1 | NA18966.hp2 | synonymous_variant | LOW | c.861G>A | p.Pro287Pro | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/23 | 906/2897 | 861/2571 | 287/856 | chr1 | 224303822 | |||
| chr1:224305044 | C | T | 9 | a0001c0001 a0001c0005 a0001c0007 others(6): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
synonymous_variant | LOW | c.738G>A | p.Leu246Leu | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 7/23 | 783/2897 | 738/2571 | 246/856 | chr1 | 224305044 | |||
| chr1:224308150 | C | T | 10 | a0001c0001 a0001c0005 a0001c0007 others(7): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
synonymous_variant | LOW | c.456G>A | p.Arg152Arg | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/23 | 501/2897 | 456/2571 | 152/856 | chr1 | 224308150 | |||
| chr1:224308243 | A | G | 1 | a0001c0005 | 3 | NA18995.hp1 NA19000.hp2 NA19054.hp2 |
synonymous_variant | LOW | c.363T>C | p.Ser121Ser | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/23 | 408/2897 | 363/2571 | 121/856 | chr1 | 224308243 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:224227414 | T | C | 2 | a0001c0001t0004 a0001c0002t0006 |
6 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*212A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 23/23 | 212 | chr1 | 224227414 | ||||||
| chr1:224227530 | G | A | 1 | a0001c0002t0007 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*96C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 23/23 | 96 | chr1 | 224227530 | ||||||
| chr1:224227585 | G | A | 1 | a0001c0001t0005 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*41C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 23/23 | 41 | chr1 | 224227585 | ||||||
| chr1:224330140 | C | T | 13 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(10): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
5_prime_UTR_variant | MODIFIER | c.-13G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/23 | 13 | chr1 | 224330140 | ||||||
| chr1:224330154 | G | T | 1 | a0001c0003t0003 | 8 | HG01243.hp1 HG01884.hp2 HG02257.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-27C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/23 | 27 | chr1 | 224330154 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:224227711 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2527-41G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224227711 | |||||||
| chr1:224227807 | A | G | 30 | a0001c0001t0001g0072 a0001c0001t0001g0081 a0001c0001t0001g0090 others(27): Show |
30 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.2527-137T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224227807 | |||||||
| chr1:224227914 | C | T | 121 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(118): Show |
121 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.2527-244G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224227914 | |||||||
| chr1:224227941 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2527-271A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224227941 | |||||||
| chr1:224227964 | G | A | 1 | a0001c0002t0002g0263 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2527-294C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224227964 | |||||||
| chr1:224228151 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2527-481A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224228151 | |||||||
| chr1:224228363 | G | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0095 |
2 | NA18906.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.2527-693C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224228363 | |||||||
| chr1:224228369 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2527-699T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224228369 | |||||||
| chr1:224228665 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2527-995G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224228665 | |||||||
| chr1:224228666 | G | A | 2 | a0004c0014t0002g0283 a0007c0013t0002g0243 |
2 | HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2527-996C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224228666 | |||||||
| chr1:224228687 | C | G | 122 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(119): Show |
122 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.2527-1017G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224228687 | |||||||
| chr1:224228894 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2527-1224C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224228894 | |||||||
| chr1:224228924 | C | CA | 74 | a0001c0001t0001g0018 a0001c0001t0001g0034 a0001c0001t0001g0035 others(71): Show |
75 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.2527-1255dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224228924 | |||||||
| chr1:224228924 | C | CAA | 172 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(169): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.2527-1256_2527-125 others(6): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224228924 | |||||||
| chr1:224228924 | C | CAAA | 22 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0032 others(19): Show |
22 | HG00642.hp2 HG00738.hp2 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.2527-1257_2527-125 others(7): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224228924 | |||||||
| chr1:224228924 | CA | C | 7 | a0001c0001t0001g0046 a0001c0001t0001g0069 a0001c0001t0001g0093 others(4): Show |
7 | HG02280.hp1 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2527-1255delT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224228924 | |||||||
| chr1:224229065 | C | T | 8 | a0001c0001t0001g0046 a0001c0001t0001g0069 a0001c0001t0001g0093 others(5): Show |
8 | HG01884.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2527-1395G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224229065 | |||||||
| chr1:224229070 | C | G | 2 | a0001c0002t0002g0250 a0001c0002t0002g0270 |
2 | HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2527-1400G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224229070 | |||||||
| chr1:224229098 | C | G | 1 | a0001c0001t0001g0034 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2527-1428G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224229098 | |||||||
| chr1:224229283 | T | C | 9 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0059 others(6): Show |
9 | HG00639.hp1 HG00741.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.2527-1613A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224229283 | |||||||
| chr1:224229296 | C | CA | 9 | a0001c0001t0001g0029 a0001c0001t0001g0039 a0001c0001t0001g0041 others(6): Show |
9 | HG01106.hp1 HG01243.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2527-1627dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224229296 | |||||||
| chr1:224229304 | T | A | 174 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(171): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.2527-1634A>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224229304 | |||||||
| chr1:224229308 | T | A | 29 | a0001c0001t0001g0033 a0001c0001t0001g0164 a0001c0001t0001g0204 others(26): Show |
29 | HG00323.hp1 HG00733.hp1 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.2527-1638A>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224229308 | |||||||
| chr1:224229363 | T | C | 2 | a0001c0001t0001g0089 a0001c0001t0001g0150 |
2 | HG00621.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.2527-1693A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224229363 | |||||||
| chr1:224229441 | A | T | 1 | a0001c0001t0001g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2527-1771T>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224229441 | |||||||
| chr1:224229442 | T | A | 1 | a0001c0001t0001g0061 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2527-1772A>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224229442 | |||||||
| chr1:224229473 | C | T | 3 | a0001c0001t0001g0109 a0001c0001t0001g0151 a0001c0001t0001g0156 |
3 | NA18956.hp2 NA19009.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2526+1753G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224229473 | |||||||
| chr1:224229538 | G | A | 4 | a0001c0003t0003g0002 a0001c0003t0003g0007 a0001c0003t0003g0008 others(1): Show |
4 | HG01243.hp1 HG01884.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2526+1688C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224229538 | |||||||
| chr1:224229738 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2526+1488C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224229738 | |||||||
| chr1:224229863 | G | A | 1 | a0001c0003t0002g0237 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2526+1363C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224229863 | |||||||
| chr1:224230474 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2526+752G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224230474 | |||||||
| chr1:224230526 | C | G | 1 | a0001c0002t0002g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2526+700G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224230526 | |||||||
| chr1:224230597 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2526+629G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224230597 | |||||||
| chr1:224230712 | A | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | NA18986.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2526+514T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224230712 | |||||||
| chr1:224230736 | A | G | 8 | a0001c0001t0001g0046 a0001c0001t0001g0069 a0001c0001t0001g0093 others(5): Show |
8 | HG01884.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2526+490T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224230736 | |||||||
| chr1:224230860 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2526+366C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224230860 | |||||||
| chr1:224230872 | G | A | 2 | a0001c0002t0002g0250 a0001c0002t0002g0270 |
2 | HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2526+354C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224230872 | |||||||
| chr1:224230891 | T | A | 59 | a0001c0001t0001g0018 a0001c0001t0001g0040 a0001c0001t0001g0072 others(56): Show |
60 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.2526+335A>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224230891 | |||||||
| chr1:224230903 | A | G | 13 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0069 others(10): Show |
13 | HG01884.hp1 HG02280.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.2526+323T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224230903 | |||||||
| chr1:224230909 | G | A | 9 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0059 others(6): Show |
9 | HG00639.hp1 HG00741.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.2526+317C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224230909 | |||||||
| chr1:224230990 | G | A | 2 | a0001c0002t0002g0246 a0001c0002t0002g0247 |
2 | HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2526+236C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224230990 | |||||||
| chr1:224231088 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2526+138C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224231088 | |||||||
| chr1:224231128 | G | A | 8 | a0001c0001t0001g0046 a0001c0001t0001g0069 a0001c0001t0001g0093 others(5): Show |
8 | HG01884.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2526+98C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224231128 | |||||||
| chr1:224231132 | C | CA | 14 | a0001c0001t0001g0046 a0001c0001t0001g0050 a0001c0001t0001g0069 others(11): Show |
14 | HG01192.hp1 HG01884.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.2526+93dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 22/22 | chr1 | 224231132 | |||||||
| chr1:224231386 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2456-90G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 21/22 | chr1 | 224231386 | |||||||
| chr1:224231398 | T | G | 3 | a0001c0002t0002g0246 a0001c0002t0002g0247 a0001c0003t0002g0242 |
3 | HG03041.hp2 NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2456-102A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 21/22 | chr1 | 224231398 | |||||||
| chr1:224231587 | T | C | 1 | a0001c0002t0002g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2456-291A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 21/22 | chr1 | 224231587 | |||||||
| chr1:224231635 | A | T | 1 | a0001c0001t0001g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2456-339T>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 21/22 | chr1 | 224231635 | |||||||
| chr1:224231714 | T | C | 1 | a0001c0007t0001g0070 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2456-418A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 21/22 | chr1 | 224231714 | |||||||
| chr1:224231822 | C | T | 188 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(185): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.2456-526G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 21/22 | chr1 | 224231822 | |||||||
| chr1:224231831 | C | T | 66 | a0001c0001t0001g0022 a0001c0001t0001g0031 a0001c0001t0001g0032 others(63): Show |
66 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.2456-535G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 21/22 | chr1 | 224231831 | |||||||
| chr1:224231842 | T | C | 2 | a0004c0014t0002g0283 a0007c0013t0002g0243 |
2 | HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2456-546A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 21/22 | chr1 | 224231842 | |||||||
| chr1:224231884 | T | C | 3 | a0001c0001t0001g0079 a0001c0001t0001g0100 a0001c0002t0002g0274 |
3 | HG00639.hp1 HG00741.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2456-588A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 21/22 | chr1 | 224231884 | |||||||
| chr1:224231959 | G | A | 1 | a0001c0003t0002g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2456-663C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 21/22 | chr1 | 224231959 | |||||||
| chr1:224232005 | C | T | 8 | a0001c0001t0001g0046 a0001c0001t0001g0069 a0001c0001t0001g0093 others(5): Show |
8 | HG01884.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2456-709G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 21/22 | chr1 | 224232005 | |||||||
| chr1:224232042 | A | G | 8 | a0001c0001t0001g0046 a0001c0001t0001g0069 a0001c0001t0001g0093 others(5): Show |
8 | HG01884.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2456-746T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 21/22 | chr1 | 224232042 | |||||||
| chr1:224232050 | A | AAATG | 4 | a0001c0001t0001g0121 a0001c0001t0001g0193 a0001c0001t0001g0223 others(1): Show |
4 | NA18956.hp1 NA18989.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.2456-755_2456-754i others(6): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 21/22 | chr1 | 224232050 | |||||||
| chr1:224232075 | G | A | 3 | a0001c0002t0002g0246 a0001c0002t0002g0247 a0001c0003t0002g0242 |
3 | HG03041.hp2 NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2456-779C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 21/22 | chr1 | 224232075 | |||||||
| chr1:224232222 | C | G | 1 | a0001c0001t0001g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2456-926G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 21/22 | chr1 | 224232222 | |||||||
| chr1:224232240 | C | T | 1 | a0001c0002t0002g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2456-944G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 21/22 | chr1 | 224232240 | |||||||
| chr1:224232355 | A | T | 1 | a0001c0001t0001g0074 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2455+846T>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 21/22 | chr1 | 224232355 | |||||||
| chr1:224232369 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2455+832T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 21/22 | chr1 | 224232369 | |||||||
| chr1:224232479 | C | T | 7 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0059 others(4): Show |
7 | HG00639.hp1 HG00741.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.2455+722G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 21/22 | chr1 | 224232479 | |||||||
| chr1:224232510 | C | A | 121 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(118): Show |
121 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.2455+691G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 21/22 | chr1 | 224232510 | |||||||
| chr1:224232527 | T | C | 1 | a0007c0013t0002g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2455+674A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 21/22 | chr1 | 224232527 | |||||||
| chr1:224232586 | C | T | 59 | a0001c0001t0001g0018 a0001c0001t0001g0040 a0001c0001t0001g0072 others(56): Show |
60 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.2455+615G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 21/22 | chr1 | 224232586 | |||||||
| chr1:224232609 | C | T | 15 | a0001c0001t0001g0052 a0001c0001t0001g0080 a0001c0001t0001g0096 others(12): Show |
15 | HG00099.hp1 HG01192.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.2455+592G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 21/22 | chr1 | 224232609 | |||||||
| chr1:224232729 | C | T | 1 | a0001c0007t0001g0070 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2455+472G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 21/22 | chr1 | 224232729 | |||||||
| chr1:224232766 | C | T | 2 | a0001c0001t0004g0149 a0001c0002t0006g0253 |
2 | HG03239.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2455+435G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 21/22 | chr1 | 224232766 | |||||||
| chr1:224233074 | C | T | 2 | a0001c0002t0002g0246 a0001c0002t0002g0247 |
2 | HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2455+127G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 21/22 | chr1 | 224233074 | |||||||
| chr1:224233353 | G | A | 1 | a0001c0007t0001g0070 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2367-64C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224233353 | |||||||
| chr1:224233464 | A | G | 56 | a0001c0001t0001g0018 a0001c0001t0001g0040 a0001c0001t0001g0072 others(53): Show |
56 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.2367-175T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224233464 | |||||||
| chr1:224233498 | G | A | 4 | a0001c0002t0001g0011 a0001c0002t0001g0013 a0001c0002t0001g0016 others(1): Show |
4 | HG02572.hp2 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2367-209C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224233498 | |||||||
| chr1:224233692 | G | C | 11 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0046 others(8): Show |
11 | HG01261.hp1 HG01884.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2367-403C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224233692 | |||||||
| chr1:224233738 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2367-449T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224233738 | |||||||
| chr1:224233740 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2367-451G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224233740 | |||||||
| chr1:224234166 | CA | C | 215 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(212): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.2367-878delT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224234166 | |||||||
| chr1:224234235 | A | G | 4 | a0001c0002t0001g0011 a0001c0002t0001g0013 a0001c0002t0001g0016 others(1): Show |
4 | HG02572.hp2 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2367-946T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224234235 | |||||||
| chr1:224234320 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2367-1031A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224234320 | |||||||
| chr1:224234351 | C | A | 1 | a0001c0001t0001g0027 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2367-1062G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224234351 | |||||||
| chr1:224234395 | A | T | 1 | a0001c0001t0001g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2367-1106T>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224234395 | |||||||
| chr1:224234494 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2367-1205G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224234494 | |||||||
| chr1:224234593 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2367-1304T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224234593 | |||||||
| chr1:224234639 | C | T | 4 | a0001c0002t0001g0011 a0001c0002t0001g0013 a0001c0002t0001g0016 others(1): Show |
4 | HG02572.hp2 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2367-1350G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224234639 | |||||||
| chr1:224234906 | G | A | 4 | a0001c0003t0003g0002 a0001c0003t0003g0007 a0001c0003t0003g0008 others(1): Show |
4 | HG01243.hp1 HG01884.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2366+1600C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224234906 | |||||||
| chr1:224234910 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2366+1596G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224234910 | |||||||
| chr1:224235303 | G | A | 1 | a0001c0002t0002g0279 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2366+1203C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224235303 | |||||||
| chr1:224235412 | C | A | 30 | a0001c0001t0001g0072 a0001c0001t0001g0081 a0001c0001t0001g0090 others(27): Show |
30 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.2366+1094G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224235412 | |||||||
| chr1:224235441 | A | T | 2 | a0001c0001t0001g0126 a0001c0002t0001g0015 |
2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2366+1065T>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224235441 | |||||||
| chr1:224235447 | G | A | 3 | a0001c0002t0002g0246 a0001c0002t0002g0247 a0001c0003t0002g0242 |
3 | HG03041.hp2 NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2366+1059C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224235447 | |||||||
| chr1:224235449 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2366+1057C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224235449 | |||||||
| chr1:224235583 | T | A | 1 | a0001c0007t0001g0070 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2366+923A>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224235583 | |||||||
| chr1:224235690 | T | G | 1 | a0001c0001t0001g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2366+816A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224235690 | |||||||
| chr1:224235718 | C | A | 1 | a0001c0002t0002g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2366+788G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224235718 | |||||||
| chr1:224235727 | A | G | 4 | a0001c0002t0001g0011 a0001c0002t0001g0013 a0001c0002t0001g0016 others(1): Show |
4 | HG02572.hp2 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2366+779T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224235727 | |||||||
| chr1:224235777 | A | T | 268 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(265): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.2366+729T>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224235777 | |||||||
| chr1:224235824 | C | G | 1 | a0001c0001t0001g0130 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2366+682G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224235824 | |||||||
| chr1:224235933 | G | GA | 191 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(188): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.2366+572dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224235933 | |||||||
| chr1:224235946 | G | GA | 5 | a0001c0001t0001g0066 a0001c0001t0001g0079 a0001c0001t0001g0100 others(2): Show |
5 | HG00639.hp1 HG00741.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2366+559dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224235946 | |||||||
| chr1:224235968 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2366+538G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224235968 | |||||||
| chr1:224236036 | A | G | 30 | a0001c0001t0001g0072 a0001c0001t0001g0081 a0001c0001t0001g0090 others(27): Show |
30 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.2366+470T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224236036 | |||||||
| chr1:224236293 | GA | G | 4 | a0001c0001t0001g0066 a0001c0001t0001g0079 a0001c0001t0001g0100 others(1): Show |
4 | HG00639.hp1 HG00741.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2366+212delT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 20/22 | chr1 | 224236293 | |||||||
| chr1:224236740 | A | G | 204 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(201): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.2290-158T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224236740 | |||||||
| chr1:224236771 | C | T | 122 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(119): Show |
122 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.2290-189G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224236771 | |||||||
| chr1:224236772 | G | A | 1 | a0001c0002t0002g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2290-190C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224236772 | |||||||
| chr1:224236927 | T | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0199 a0002c0004t0001g0136 |
3 | HG00597.hp2 HG00609.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.2290-345A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224236927 | |||||||
| chr1:224237112 | C | T | 2 | a0001c0001t0001g0126 a0001c0002t0001g0015 |
2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2290-530G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224237112 | |||||||
| chr1:224237248 | T | A | 1 | a0001c0001t0001g0096 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2290-666A>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224237248 | |||||||
| chr1:224237463 | T | A | 68 | a0001c0001t0001g0022 a0001c0001t0001g0031 a0001c0001t0001g0032 others(65): Show |
68 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.2290-881A>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224237463 | |||||||
| chr1:224237489 | C | A | 1 | a0001c0003t0002g0233 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2290-907G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224237489 | |||||||
| chr1:224237603 | G | A | 1 | a0001c0003t0002g0233 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2290-1021C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224237603 | |||||||
| chr1:224237658 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2290-1076G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224237658 | |||||||
| chr1:224237730 | C | CTTTTT | 6 | a0001c0002t0001g0011 a0001c0002t0001g0013 a0001c0002t0001g0016 others(3): Show |
6 | HG02572.hp2 HG02622.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2290-1153_2290-114 others(9): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224237730 | |||||||
| chr1:224237730 | C | CTTTTTTT | 178 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(175): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.2290-1155_2290-114 others(11): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224237730 | |||||||
| chr1:224237730 | C | CTTTTTTT others(1): Show |
19 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0046 others(16): Show |
19 | HG00597.hp1 HG00741.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.2290-1156_2290-114 others(12): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224237730 | |||||||
| chr1:224237811 | C | T | 2 | a0001c0002t0002g0246 a0001c0002t0002g0247 |
2 | HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2290-1229G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224237811 | |||||||
| chr1:224237878 | C | T | 3 | a0001c0001t0001g0060 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | HG00280.hp2 HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2290-1296G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224237878 | |||||||
| chr1:224237879 | G | A | 1 | a0001c0002t0002g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2290-1297C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224237879 | |||||||
| chr1:224237908 | C | T | 7 | a0001c0001t0001g0029 a0001c0001t0001g0039 a0001c0001t0001g0041 others(4): Show |
7 | HG01106.hp1 HG01243.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2290-1326G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224237908 | |||||||
| chr1:224237959 | TTCAAAAA others(2): Show |
T | 28 | a0001c0001t0001g0026 a0001c0001t0001g0081 a0001c0001t0001g0090 others(25): Show |
28 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.2290-1386_2290-137 others(13): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224237959 | |||||||
| chr1:224237961 | C | CA | 10 | a0001c0001t0001g0035 a0001c0001t0001g0059 a0001c0001t0001g0093 others(7): Show |
10 | HG01243.hp1 HG01261.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2290-1380dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224237961 | |||||||
| chr1:224237961 | CAAAAAAA others(6): Show |
C | 193 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(190): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.2290-1392_2290-138 others(17): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224237961 | |||||||
| chr1:224237983 | A | G | 1 | a0001c0003t0002g0242 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2290-1401T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224237983 | |||||||
| chr1:224238002 | A | G | 1 | a0001c0002t0002g0254 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2290-1420T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224238002 | |||||||
| chr1:224238081 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2290-1499G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224238081 | |||||||
| chr1:224238094 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2290-1512G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224238094 | |||||||
| chr1:224238115 | C | T | 3 | a0001c0001t0001g0034 a0001c0001t0001g0087 a0001c0002t0002g0267 |
3 | HG00642.hp1 HG02698.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.2290-1533G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224238115 | |||||||
| chr1:224238121 | C | T | 2 | a0001c0001t0001g0122 a0001c0002t0002g0268 |
2 | HG00140.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.2290-1539G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224238121 | |||||||
| chr1:224238130 | C | T | 3 | a0001c0002t0002g0244 a0001c0002t0002g0249 a0001c0003t0002g0235 |
3 | HG03098.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2290-1548G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224238130 | |||||||
| chr1:224238173 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2290-1591T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224238173 | |||||||
| chr1:224238180 | C | CCCA | 6 | a0001c0001t0001g0034 a0001c0001t0001g0087 a0001c0001t0001g0220 others(3): Show |
6 | HG00642.hp1 HG01106.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.2290-1601_2290-159 others(7): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224238180 | |||||||
| chr1:224238186 | A | AC | 267 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(264): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.2290-1605dupG | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224238186 | |||||||
| chr1:224238207 | A | G | 2 | a0001c0001t0001g0048 a0001c0001t0001g0126 |
2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2290-1625T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224238207 | |||||||
| chr1:224238244 | G | A | 277 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(274): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.2290-1662C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224238244 | |||||||
| chr1:224238249 | T | A | 38 | a0001c0001t0001g0024 a0001c0001t0001g0063 a0001c0001t0001g0065 others(35): Show |
38 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.2290-1667A>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224238249 | |||||||
| chr1:224238319 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2290-1737G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224238319 | |||||||
| chr1:224238349 | T | G | 1 | a0001c0001t0001g0214 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2290-1767A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224238349 | |||||||
| chr1:224238394 | G | A | 5 | a0001c0002t0001g0012 a0001c0002t0001g0014 a0001c0002t0002g0278 others(2): Show |
5 | HG02055.hp1 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2290-1812C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224238394 | |||||||
| chr1:224238527 | G | A | 23 | a0001c0001t0001g0049 a0001c0001t0001g0069 a0001c0001t0001g0158 others(20): Show |
24 | HG00733.hp2 HG00735.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.2290-1945C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224238527 | |||||||
| chr1:224238685 | T | G | 1 | a0001c0001t0001g0089 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2290-2103A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224238685 | |||||||
| chr1:224238726 | G | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0175 |
2 | HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2290-2144C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224238726 | |||||||
| chr1:224238800 | G | A | 3 | a0001c0002t0001g0012 a0001c0002t0001g0014 a0001c0002t0002g0278 |
3 | HG02723.hp2 HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2290-2218C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224238800 | |||||||
| chr1:224239021 | T | C | 1 | a0001c0001t0001g0067 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2290-2439A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224239021 | |||||||
| chr1:224239030 | A | T | 5 | a0001c0002t0001g0011 a0001c0002t0001g0013 a0001c0002t0001g0016 others(2): Show |
5 | HG02572.hp2 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2290-2448T>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224239030 | |||||||
| chr1:224239112 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2290-2530G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224239112 | |||||||
| chr1:224239123 | C | T | 221 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(218): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.2290-2541G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224239123 | |||||||
| chr1:224239193 | A | C | 9 | a0001c0001t0001g0046 a0001c0001t0001g0068 a0001c0001t0001g0205 others(6): Show |
10 | HG00733.hp2 HG02280.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2290-2611T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224239193 | |||||||
| chr1:224239209 | T | C | 131 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0029 others(128): Show |
132 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.2290-2627A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224239209 | |||||||
| chr1:224239222 | G | T | 1 | a0001c0001t0001g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2290-2640C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224239222 | |||||||
| chr1:224239244 | A | G | 3 | a0001c0002t0002g0246 a0001c0002t0002g0247 a0001c0007t0001g0070 |
3 | HG03041.hp2 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2290-2662T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224239244 | |||||||
| chr1:224239297 | AT | A | 7 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0059 others(4): Show |
7 | HG01261.hp1 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2290-2716delA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224239297 | |||||||
| chr1:224239431 | G | A | 5 | a0001c0001t0001g0066 a0001c0001t0001g0079 a0001c0001t0001g0100 others(2): Show |
5 | HG00639.hp1 HG00741.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2290-2849C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224239431 | |||||||
| chr1:224239469 | T | G | 221 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(218): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.2290-2887A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224239469 | |||||||
| chr1:224239577 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2290-2995C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224239577 | |||||||
| chr1:224239606 | T | A | 1 | a0001c0003t0003g0008 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2290-3024A>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224239606 | |||||||
| chr1:224239613 | C | T | 1 | a0001c0002t0002g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2290-3031G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224239613 | |||||||
| chr1:224239682 | C | G | 1 | a0004c0014t0002g0283 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2290-3100G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224239682 | |||||||
| chr1:224239868 | C | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0171 |
2 | NA19012.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.2290-3286G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224239868 | |||||||
| chr1:224239979 | C | T | 9 | a0001c0001t0001g0046 a0001c0001t0001g0066 a0001c0001t0001g0079 others(6): Show |
9 | HG00639.hp1 HG00741.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2290-3397G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224239979 | |||||||
| chr1:224240020 | C | T | 1 | a0001c0007t0001g0086 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2290-3438G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224240020 | |||||||
| chr1:224240061 | A | AT | 76 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0027 others(73): Show |
76 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.2290-3480dupA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224240061 | |||||||
| chr1:224240061 | A | ATT | 56 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0025 others(53): Show |
56 | HG00140.hp1 HG00642.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.2290-3481_2290-348 others(6): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224240061 | |||||||
| chr1:224240061 | A | ATTT | 56 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(53): Show |
56 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.2290-3482_2290-348 others(7): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224240061 | |||||||
| chr1:224240061 | A | ATTTT | 9 | a0001c0001t0001g0160 a0001c0001t0001g0164 a0001c0001t0001g0187 others(6): Show |
9 | HG00408.hp1 HG00597.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.2290-3483_2290-348 others(8): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224240061 | |||||||
| chr1:224240153 | C | T | 1 | a0004c0014t0002g0283 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2290-3571G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224240153 | |||||||
| chr1:224240171 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2290-3589C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224240171 | |||||||
| chr1:224240216 | C | G | 2 | a0001c0002t0002g0246 a0001c0002t0002g0247 |
2 | HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2290-3634G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224240216 | |||||||
| chr1:224240363 | C | A | 1 | a0001c0001t0001g0067 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2290-3781G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224240363 | |||||||
| chr1:224240371 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2290-3789G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224240371 | |||||||
| chr1:224240377 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2290-3795C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224240377 | |||||||
| chr1:224240463 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2290-3881G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224240463 | |||||||
| chr1:224240464 | G | A | 2 | a0001c0002t0002g0246 a0001c0002t0002g0247 |
2 | HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2290-3882C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224240464 | |||||||
| chr1:224240559 | C | T | 209 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(206): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.2290-3977G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224240559 | |||||||
| chr1:224240740 | A | G | 1 | a0001c0001t0001g0214 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2290-4158T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224240740 | |||||||
| chr1:224240746 | T | G | 1 | a0001c0012t0001g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2290-4164A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224240746 | |||||||
| chr1:224240783 | C | CT | 34 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 others(31): Show |
34 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.2290-4202dupA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224240783 | |||||||
| chr1:224240783 | CT | C | 74 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0040 others(71): Show |
75 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.2290-4202delA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224240783 | |||||||
| chr1:224240790 | T | G | 1 | a0001c0001t0001g0022 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2290-4208A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224240790 | |||||||
| chr1:224240819 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2290-4237G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224240819 | |||||||
| chr1:224240932 | A | G | 2 | a0001c0002t0002g0246 a0001c0002t0002g0247 |
2 | HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2290-4350T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224240932 | |||||||
| chr1:224240967 | T | C | 4 | a0001c0002t0002g0249 a0001c0003t0002g0001 a0001c0003t0002g0235 others(1): Show |
5 | HG00733.hp2 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2290-4385A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224240967 | |||||||
| chr1:224240970 | T | C | 1 | a0001c0003t0002g0236 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2290-4388A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224240970 | |||||||
| chr1:224240983 | G | A | 1 | a0001c0002t0002g0279 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2290-4401C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224240983 | |||||||
| chr1:224241081 | G | T | 1 | a0001c0002t0002g0278 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2290-4499C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224241081 | |||||||
| chr1:224241229 | G | A | 2 | a0001c0002t0002g0246 a0001c0002t0002g0247 |
2 | HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2290-4647C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224241229 | |||||||
| chr1:224241376 | G | A | 190 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(187): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.2290-4794C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224241376 | |||||||
| chr1:224241408 | T | G | 1 | a0001c0001t0001g0230 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2290-4826A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224241408 | |||||||
| chr1:224241492 | T | G | 1 | a0001c0001t0001g0115 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2290-4910A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224241492 | |||||||
| chr1:224241654 | G | A | 1 | a0001c0002t0002g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2290-5072C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224241654 | |||||||
| chr1:224241817 | C | T | 210 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(207): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.2290-5235G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224241817 | |||||||
| chr1:224241856 | C | CA | 204 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(201): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.2290-5275dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224241856 | |||||||
| chr1:224241859 | AAAAAAAA others(4): Show |
A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0207 |
2 | NA18747.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.2290-5288_2290-527 others(15): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224241859 | |||||||
| chr1:224241870 | T | G | 209 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(206): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.2290-5288A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224241870 | |||||||
| chr1:224241995 | G | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG00408.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.2290-5413C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224241995 | |||||||
| chr1:224242234 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2290-5652A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224242234 | |||||||
| chr1:224242351 | C | T | 2 | a0001c0001t0001g0140 a0001c0012t0001g0017 |
2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2290-5769G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224242351 | |||||||
| chr1:224242381 | G | A | 8 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(5): Show |
8 | HG02055.hp1 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2290-5799C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224242381 | |||||||
| chr1:224242417 | A | G | 2 | a0001c0001t0001g0126 a0001c0002t0001g0015 |
2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2290-5835T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224242417 | |||||||
| chr1:224242426 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2290-5844A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224242426 | |||||||
| chr1:224242487 | C | CT | 228 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0020 others(225): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.2290-5906dupA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224242487 | |||||||
| chr1:224242487 | C | CTT | 23 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0046 others(20): Show |
23 | HG01261.hp1 HG02074.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.2290-5907_2290-590 others(6): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224242487 | |||||||
| chr1:224242593 | G | C | 2 | a0001c0001t0001g0151 a0001c0001t0001g0156 |
2 | NA18956.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2290-6011C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224242593 | |||||||
| chr1:224242694 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2290-6112G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224242694 | |||||||
| chr1:224242752 | G | C | 187 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(184): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.2290-6170C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224242752 | |||||||
| chr1:224242826 | G | GT | 14 | a0001c0001t0001g0010 a0001c0001t0001g0039 a0001c0001t0001g0065 others(11): Show |
14 | HG00140.hp1 HG00735.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.2290-6245dupA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224242826 | |||||||
| chr1:224242826 | GT | G | 28 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0046 others(25): Show |
28 | HG00639.hp1 HG00741.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.2290-6245delA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224242826 | |||||||
| chr1:224242857 | G | A | 2 | a0001c0001t0001g0140 a0001c0012t0001g0017 |
2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2290-6275C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224242857 | |||||||
| chr1:224242884 | G | A | 7 | a0001c0002t0002g0271 a0001c0002t0002g0272 a0001c0002t0002g0273 others(4): Show |
7 | HG01256.hp1 HG01258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2290-6302C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224242884 | |||||||
| chr1:224242888 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2290-6306G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224242888 | |||||||
| chr1:224242922 | T | G | 1 | a0001c0002t0002g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2290-6340A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224242922 | |||||||
| chr1:224242981 | G | A | 51 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(48): Show |
51 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.2290-6399C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224242981 | |||||||
| chr1:224243183 | G | A | 1 | a0001c0001t0004g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2290-6601C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224243183 | |||||||
| chr1:224243366 | C | T | 3 | a0001c0001t0001g0140 a0001c0005t0001g0152 a0001c0012t0001g0017 |
3 | HG01884.hp1 HG03471.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.2290-6784G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224243366 | |||||||
| chr1:224243405 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2289+6807C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224243405 | |||||||
| chr1:224243456 | G | T | 1 | a0001c0001t0001g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2289+6756C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224243456 | |||||||
| chr1:224243597 | T | C | 2 | a0001c0002t0002g0250 a0001c0002t0002g0270 |
2 | HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2289+6615A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224243597 | |||||||
| chr1:224243663 | C | CTT | 203 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(200): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.2289+6547_2289+654 others(6): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224243663 | |||||||
| chr1:224243810 | G | A | 53 | a0001c0001t0001g0018 a0001c0001t0001g0040 a0001c0001t0001g0049 others(50): Show |
53 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.2289+6402C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224243810 | |||||||
| chr1:224243923 | G | C | 1 | a0001c0001t0001g0172 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2289+6289C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224243923 | |||||||
| chr1:224243941 | G | C | 2 | a0001c0001t0001g0122 a0001c0001t0001g0172 |
2 | HG00099.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.2289+6271C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224243941 | |||||||
| chr1:224244143 | G | A | 2 | a0001c0001t0001g0140 a0001c0012t0001g0017 |
2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2289+6069C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224244143 | |||||||
| chr1:224244518 | C | G | 1 | a0001c0002t0002g0279 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2289+5694G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224244518 | |||||||
| chr1:224244558 | A | G | 9 | a0001c0001t0001g0046 a0001c0001t0001g0066 a0001c0001t0001g0079 others(6): Show |
9 | HG00639.hp1 HG00741.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2289+5654T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224244558 | |||||||
| chr1:224244632 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0203 |
2 | HG03579.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2289+5580G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224244632 | |||||||
| chr1:224244633 | G | A | 1 | a0001c0002t0002g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2289+5579C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224244633 | |||||||
| chr1:224244757 | G | A | 2 | a0001c0002t0002g0246 a0001c0002t0002g0247 |
2 | HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2289+5455C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224244757 | |||||||
| chr1:224244881 | T | G | 1 | a0001c0001t0001g0182 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2289+5331A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224244881 | |||||||
| chr1:224244991 | G | A | 7 | a0001c0002t0002g0271 a0001c0002t0002g0272 a0001c0002t0002g0273 others(4): Show |
7 | HG01256.hp1 HG01258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2289+5221C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224244991 | |||||||
| chr1:224245018 | A | G | 1 | a0001c0001t0001g0034 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2289+5194T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224245018 | |||||||
| chr1:224245021 | A | C | 1 | a0004c0014t0002g0283 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2289+5191T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224245021 | |||||||
| chr1:224245320 | A | C | 215 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(212): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2289+4892T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224245320 | |||||||
| chr1:224245363 | C | G | 5 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0059 others(2): Show |
5 | HG01261.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.2289+4849G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224245363 | |||||||
| chr1:224245465 | G | A | 58 | a0001c0001t0001g0018 a0001c0001t0001g0040 a0001c0001t0001g0049 others(55): Show |
58 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.2289+4747C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224245465 | |||||||
| chr1:224245518 | C | T | 208 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(205): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.2289+4694G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224245518 | |||||||
| chr1:224245552 | G | C | 1 | a0001c0001t0001g0109 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2289+4660C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224245552 | |||||||
| chr1:224245712 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2289+4500A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224245712 | |||||||
| chr1:224245813 | C | T | 7 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0059 others(4): Show |
7 | HG01261.hp1 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2289+4399G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224245813 | |||||||
| chr1:224246033 | C | CT | 10 | a0001c0001t0001g0046 a0001c0001t0001g0066 a0001c0001t0001g0079 others(7): Show |
10 | HG00639.hp1 HG00741.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2289+4178dupA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224246033 | |||||||
| chr1:224246049 | G | C | 1 | a0001c0001t0001g0109 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2289+4163C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224246049 | |||||||
| chr1:224246145 | T | C | 219 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(216): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.2289+4067A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224246145 | |||||||
| chr1:224246272 | C | A | 1 | a0001c0001t0001g0212 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2289+3940G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224246272 | |||||||
| chr1:224246273 | A | C | 1 | a0001c0001t0001g0212 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2289+3939T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224246273 | |||||||
| chr1:224246282 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2289+3930C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224246282 | |||||||
| chr1:224246689 | T | C | 1 | a0001c0002t0002g0255 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2289+3523A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224246689 | |||||||
| chr1:224246762 | A | G | 1 | a0007c0013t0002g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2289+3450T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224246762 | |||||||
| chr1:224246763 | T | C | 1 | a0007c0013t0002g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2289+3449A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224246763 | |||||||
| chr1:224246911 | C | T | 278 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(275): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.2289+3301G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224246911 | |||||||
| chr1:224247049 | C | T | 4 | a0001c0002t0002g0278 a0001c0002t0002g0279 a0001c0012t0001g0017 others(1): Show |
4 | HG01884.hp1 HG02055.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2289+3163G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224247049 | |||||||
| chr1:224247055 | C | CA | 29 | a0001c0001t0001g0049 a0001c0001t0001g0103 a0001c0001t0001g0112 others(26): Show |
30 | HG00733.hp2 HG01256.hp1 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.2289+3156dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224247055 | |||||||
| chr1:224247067 | A | C | 158 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(155): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.2289+3145T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224247067 | |||||||
| chr1:224247087 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2289+3125T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224247087 | |||||||
| chr1:224247218 | C | A | 1 | a0001c0001t0001g0084 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2289+2994G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224247218 | |||||||
| chr1:224247332 | A | G | 1 | a0001c0002t0002g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2289+2880T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224247332 | |||||||
| chr1:224247452 | C | T | 1 | a0001c0003t0002g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2289+2760G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224247452 | |||||||
| chr1:224247541 | C | T | 1 | a0007c0013t0002g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2289+2671G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224247541 | |||||||
| chr1:224247594 | G | A | 1 | a0001c0002t0007g0276 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2289+2618C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224247594 | |||||||
| chr1:224247668 | C | CA | 89 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0031 others(86): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.2289+2543dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224247668 | |||||||
| chr1:224247723 | C | T | 1 | a0001c0002t0001g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2289+2489G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224247723 | |||||||
| chr1:224247876 | C | T | 7 | a0001c0002t0001g0015 a0001c0002t0002g0271 a0001c0002t0002g0272 others(4): Show |
7 | HG01256.hp1 HG01258.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2289+2336G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224247876 | |||||||
| chr1:224248055 | T | C | 5 | a0001c0001t0001g0046 a0001c0001t0001g0205 a0001c0001t0001g0206 others(2): Show |
5 | HG02647.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2289+2157A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224248055 | |||||||
| chr1:224248167 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2289+2045G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224248167 | |||||||
| chr1:224248212 | C | T | 27 | a0001c0001t0001g0049 a0001c0001t0001g0112 a0001c0001t0001g0140 others(24): Show |
27 | HG00140.hp2 HG02027.hp2 HG02523.hp1 others(24): Show |
intron_variant | MODIFIER | c.2289+2000G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224248212 | |||||||
| chr1:224248232 | T | C | 12 | a0001c0001t0001g0022 a0001c0001t0001g0046 a0001c0001t0001g0087 others(9): Show |
12 | HG00642.hp1 HG00735.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.2289+1980A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224248232 | |||||||
| chr1:224248271 | A | G | 7 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(4): Show |
7 | HG02055.hp1 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2289+1941T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224248271 | |||||||
| chr1:224248396 | C | T | 49 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0021 others(46): Show |
49 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.2289+1816G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224248396 | |||||||
| chr1:224248594 | A | C | 1 | a0001c0001t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2289+1618T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224248594 | |||||||
| chr1:224248681 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0137 |
2 | HG02602.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.2289+1531C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224248681 | |||||||
| chr1:224248758 | T | C | 1 | a0001c0003t0002g0242 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2289+1454A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224248758 | |||||||
| chr1:224248936 | G | C | 1 | a0001c0002t0001g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2289+1276C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224248936 | |||||||
| chr1:224249150 | A | ATT | 116 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0020 others(113): Show |
116 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.2289+1060_2289+106 others(6): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224249150 | |||||||
| chr1:224249246 | G | T | 1 | a0001c0002t0001g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2289+966C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224249246 | |||||||
| chr1:224249481 | A | G | 3 | a0001c0003t0003g0004 a0001c0003t0003g0005 a0001c0003t0003g0006 |
3 | HG02615.hp2 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2289+731T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224249481 | |||||||
| chr1:224249515 | C | T | 3 | a0001c0001t0001g0049 a0001c0002t0002g0260 a0001c0002t0006g0253 |
3 | HG03239.hp2 HG03942.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2289+697G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224249515 | |||||||
| chr1:224249706 | C | G | 1 | a0001c0001t0001g0177 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2289+506G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224249706 | |||||||
| chr1:224249735 | ACT | A | 5 | a0001c0001t0001g0046 a0001c0001t0001g0205 a0001c0001t0001g0206 others(2): Show |
5 | HG02647.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2289+475_2289+476d others(4): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224249735 | |||||||
| chr1:224249747 | A | G | 1 | a0001c0001t0001g0210 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2289+465T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224249747 | |||||||
| chr1:224250187 | A | G | 10 | a0001c0001t0001g0033 a0001c0001t0001g0053 a0001c0001t0001g0054 others(7): Show |
10 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.2289+25T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 19/22 | chr1 | 224250187 | |||||||
| chr1:224250417 | T | G | 1 | a0001c0001t0001g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2183-99A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224250417 | |||||||
| chr1:224250449 | C | T | 2 | a0001c0001t0001g0173 a0001c0001t0001g0185 |
2 | NA18944.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2183-131G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224250449 | |||||||
| chr1:224250518 | T | C | 272 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(269): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.2183-200A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224250518 | |||||||
| chr1:224250855 | C | T | 143 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0020 others(140): Show |
143 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.2183-537G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224250855 | |||||||
| chr1:224250867 | G | C | 1 | a0001c0002t0001g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2183-549C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224250867 | |||||||
| chr1:224250884 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2183-566G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224250884 | |||||||
| chr1:224250949 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2183-631C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224250949 | |||||||
| chr1:224251071 | C | G | 1 | a0001c0003t0002g0242 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2183-753G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224251071 | |||||||
| chr1:224251131 | A | G | 169 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0020 others(166): Show |
169 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.2183-813T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224251131 | |||||||
| chr1:224251255 | CAG | C | 17 | a0001c0001t0001g0026 a0001c0001t0001g0085 a0001c0001t0001g0090 others(14): Show |
17 | HG01081.hp1 HG01123.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.2183-939_2183-938d others(4): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224251255 | |||||||
| chr1:224251271 | C | CA | 97 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0020 others(94): Show |
97 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.2183-954dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224251271 | |||||||
| chr1:224251271 | C | CAA | 10 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0063 others(7): Show |
10 | HG00609.hp1 HG02074.hp1 HG03516.hp1 others(7): Show |
intron_variant | MODIFIER | c.2183-955_2183-954d others(4): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224251271 | |||||||
| chr1:224251271 | CA | C | 38 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0034 others(35): Show |
38 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.2183-954delT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224251271 | |||||||
| chr1:224251563 | C | T | 6 | a0001c0002t0002g0271 a0001c0002t0002g0272 a0001c0002t0002g0273 others(3): Show |
6 | HG01256.hp1 HG01258.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2183-1245G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224251563 | |||||||
| chr1:224251667 | T | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0071 |
2 | HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2183-1349A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224251667 | |||||||
| chr1:224251690 | C | T | 1 | a0001c0007t0001g0086 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2183-1372G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224251690 | |||||||
| chr1:224251746 | T | C | 1 | a0001c0002t0002g0279 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2183-1428A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224251746 | |||||||
| chr1:224251766 | C | G | 1 | a0001c0001t0001g0220 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2183-1448G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224251766 | |||||||
| chr1:224251791 | C | T | 2 | a0001c0002t0002g0246 a0001c0002t0002g0247 |
2 | HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2183-1473G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224251791 | |||||||
| chr1:224251953 | C | T | 1 | a0001c0002t0002g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2183-1635G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224251953 | |||||||
| chr1:224252079 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2183-1761G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224252079 | |||||||
| chr1:224252086 | G | A | 1 | a0001c0002t0002g0269 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2183-1768C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224252086 | |||||||
| chr1:224252101 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2183-1783C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224252101 | |||||||
| chr1:224252104 | G | C | 255 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(252): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.2183-1786C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224252104 | |||||||
| chr1:224252124 | A | T | 1 | a0001c0002t0001g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2183-1806T>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224252124 | |||||||
| chr1:224252302 | G | A | 1 | a0001c0007t0001g0086 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2183-1984C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224252302 | |||||||
| chr1:224252687 | G | A | 112 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0020 others(109): Show |
112 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.2183-2369C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224252687 | |||||||
| chr1:224252766 | A | G | 51 | a0001c0001t0001g0022 a0001c0001t0001g0030 a0001c0001t0001g0040 others(48): Show |
51 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.2183-2448T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224252766 | |||||||
| chr1:224252769 | G | A | 1 | a0001c0002t0002g0278 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2183-2451C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224252769 | |||||||
| chr1:224252851 | C | G | 8 | a0001c0002t0002g0271 a0001c0002t0002g0272 a0001c0002t0002g0273 others(5): Show |
8 | HG01256.hp1 HG01258.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2183-2533G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224252851 | |||||||
| chr1:224252880 | G | C | 3 | a0001c0001t0001g0048 a0001c0002t0002g0244 a0001c0002t0002g0280 |
3 | HG02109.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2183-2562C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224252880 | |||||||
| chr1:224252957 | T | C | 247 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(244): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.2183-2639A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224252957 | |||||||
| chr1:224253170 | A | G | 1 | a0001c0002t0002g0246 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2183-2852T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224253170 | |||||||
| chr1:224253189 | T | G | 3 | a0001c0001t0001g0126 a0001c0001t0001g0142 a0001c0003t0002g0240 |
3 | HG02258.hp2 HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2183-2871A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224253189 | |||||||
| chr1:224253212 | C | T | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG00408.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.2183-2894G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224253212 | |||||||
| chr1:224253213 | G | A | 4 | a0001c0001t0001g0071 a0001c0001t0001g0103 a0001c0001t0001g0120 others(1): Show |
4 | HG02615.hp1 HG02738.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2183-2895C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224253213 | |||||||
| chr1:224253241 | A | G | 77 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0025 others(74): Show |
77 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.2183-2923T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224253241 | |||||||
| chr1:224253338 | C | T | 29 | a0001c0001t0001g0031 a0001c0001t0001g0056 a0001c0001t0001g0058 others(26): Show |
29 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.2183-3020G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224253338 | |||||||
| chr1:224253486 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2183-3168C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224253486 | |||||||
| chr1:224253506 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2183-3188C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224253506 | |||||||
| chr1:224253593 | C | T | 2 | a0001c0002t0002g0246 a0001c0002t0002g0247 |
2 | HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2183-3275G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224253593 | |||||||
| chr1:224253616 | T | C | 262 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(259): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.2183-3298A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224253616 | |||||||
| chr1:224253682 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2183-3364C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224253682 | |||||||
| chr1:224253731 | C | CA | 68 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0034 others(65): Show |
68 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.2183-3414dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224253731 | |||||||
| chr1:224253747 | A | G | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG00323.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.2183-3429T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224253747 | |||||||
| chr1:224253748 | AG | A | 5 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(2): Show |
5 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2183-3431delC | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224253748 | |||||||
| chr1:224253749 | G | A | 226 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(223): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.2183-3431C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224253749 | |||||||
| chr1:224253785 | A | C | 1 | a0001c0001t0004g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2183-3467T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224253785 | |||||||
| chr1:224253815 | G | A | 1 | a0001c0002t0002g0279 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2183-3497C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224253815 | |||||||
| chr1:224253854 | T | G | 1 | a0002c0004t0001g0136 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2183-3536A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224253854 | |||||||
| chr1:224253934 | AGTGACTA others(12): Show |
A | 1 | a0002c0004t0001g0098 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2183-3635_2183-361 others(23): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224253934 | |||||||
| chr1:224253973 | T | G | 1 | a0002c0004t0001g0098 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2183-3655A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224253973 | |||||||
| chr1:224254011 | T | A | 1 | a0002c0004t0001g0098 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2183-3693A>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254011 | |||||||
| chr1:224254019 | T | G | 1 | a0002c0004t0001g0098 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2183-3701A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254019 | |||||||
| chr1:224254044 | A | G | 1 | a0002c0004t0001g0098 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2183-3726T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254044 | |||||||
| chr1:224254046 | T | A | 1 | a0002c0004t0001g0098 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2183-3728A>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254046 | |||||||
| chr1:224254066 | A | G | 1 | a0002c0004t0001g0098 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2183-3748T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254066 | |||||||
| chr1:224254076 | T | C | 1 | a0002c0004t0001g0098 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2183-3758A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254076 | |||||||
| chr1:224254078 | T | A | 1 | a0002c0004t0001g0098 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2183-3760A>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254078 | |||||||
| chr1:224254079 | T | G | 1 | a0002c0004t0001g0098 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2183-3761A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254079 | |||||||
| chr1:224254089 | C | G | 1 | a0002c0004t0001g0098 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2183-3771G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254089 | |||||||
| chr1:224254093 | A | AGTAGGCA others(14): Show |
1 | a0002c0004t0001g0098 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2183-3776_2183-377 others(25): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254093 | |||||||
| chr1:224254095 | G | T | 1 | a0002c0004t0001g0098 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2183-3777C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254095 | |||||||
| chr1:224254105 | G | T | 1 | a0002c0004t0001g0098 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2183-3787C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254105 | |||||||
| chr1:224254114 | T | C | 1 | a0002c0004t0001g0098 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2183-3796A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254114 | |||||||
| chr1:224254123 | A | G | 1 | a0002c0004t0001g0098 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2183-3805T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254123 | |||||||
| chr1:224254185 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | HG02922.hp2 HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2183-3867C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254185 | |||||||
| chr1:224254236 | G | A | 212 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(209): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.2183-3918C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254236 | |||||||
| chr1:224254282 | G | A | 27 | a0001c0001t0001g0140 a0001c0002t0002g0250 a0001c0002t0002g0251 others(24): Show |
27 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(24): Show |
intron_variant | MODIFIER | c.2183-3964C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254282 | |||||||
| chr1:224254327 | G | A | 19 | a0001c0003t0002g0001 a0001c0003t0002g0233 a0001c0003t0002g0234 others(16): Show |
20 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.2183-4009C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254327 | |||||||
| chr1:224254390 | A | AT | 14 | a0001c0001t0001g0140 a0001c0002t0002g0246 a0001c0002t0002g0247 others(11): Show |
14 | HG01243.hp1 HG01884.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.2183-4073dupA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254390 | |||||||
| chr1:224254390 | A | ATT | 21 | a0001c0002t0002g0251 a0001c0002t0002g0252 a0001c0002t0002g0254 others(18): Show |
21 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.2183-4074_2183-407 others(6): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254390 | |||||||
| chr1:224254390 | AT | A | 216 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2183-4073delA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254390 | |||||||
| chr1:224254390 | ATT | A | 7 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0064 others(4): Show |
7 | HG00323.hp1 HG02109.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2183-4074_2183-407 others(6): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254390 | |||||||
| chr1:224254453 | C | T | 1 | a0001c0002t0002g0256 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2183-4135G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254453 | |||||||
| chr1:224254470 | G | A | 232 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(229): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.2183-4152C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254470 | |||||||
| chr1:224254571 | T | G | 64 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0021 others(61): Show |
64 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.2183-4253A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254571 | |||||||
| chr1:224254572 | G | GT | 156 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0022 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.2183-4255dupA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254572 | |||||||
| chr1:224254572 | G | T | 66 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0021 others(63): Show |
66 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.2183-4254C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254572 | |||||||
| chr1:224254581 | T | G | 18 | a0001c0003t0002g0001 a0001c0003t0002g0233 a0001c0003t0002g0234 others(15): Show |
19 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.2183-4263A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254581 | |||||||
| chr1:224254666 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2183-4348G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254666 | |||||||
| chr1:224254700 | C | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0141 a0001c0001t0001g0194 others(1): Show |
4 | NA18949.hp1 NA18960.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.2183-4382G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254700 | |||||||
| chr1:224254764 | C | T | 1 | a0001c0002t0002g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2183-4446G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254764 | |||||||
| chr1:224254776 | G | A | 29 | a0001c0001t0001g0027 a0001c0001t0001g0034 a0001c0001t0001g0052 others(26): Show |
29 | HG00280.hp1 HG00408.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.2183-4458C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254776 | |||||||
| chr1:224254873 | T | A | 1 | a0001c0001t0001g0068 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2183-4555A>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254873 | |||||||
| chr1:224254877 | GT | G | 249 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(246): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.2183-4560delA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224254877 | |||||||
| chr1:224255092 | G | A | 27 | a0001c0001t0001g0140 a0001c0002t0002g0250 a0001c0002t0002g0251 others(24): Show |
27 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(24): Show |
intron_variant | MODIFIER | c.2183-4774C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224255092 | |||||||
| chr1:224255118 | C | T | 1 | a0001c0002t0002g0279 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2183-4800G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224255118 | |||||||
| chr1:224255182 | G | GT | 181 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.2183-4865dupA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224255182 | |||||||
| chr1:224255182 | G | GTT | 34 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0039 others(31): Show |
34 | HG00438.hp1 HG00673.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.2183-4866_2183-486 others(6): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224255182 | |||||||
| chr1:224255182 | GT | G | 17 | a0001c0002t0002g0244 a0001c0003t0002g0001 a0001c0003t0002g0233 others(14): Show |
18 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.2183-4865delA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224255182 | |||||||
| chr1:224255204 | TC | T | 5 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(2): Show |
5 | HG02055.hp1 HG02572.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2183-4887delG | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224255204 | |||||||
| chr1:224255205 | C | T | 253 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(250): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2183-4887G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224255205 | |||||||
| chr1:224255392 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2183-5074G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224255392 | |||||||
| chr1:224255435 | G | A | 1 | a0001c0003t0002g0242 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2183-5117C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224255435 | |||||||
| chr1:224255483 | C | T | 1 | a0001c0002t0002g0259 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2183-5165G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224255483 | |||||||
| chr1:224255484 | G | A | 2 | a0001c0001t0001g0026 a0001c0002t0002g0249 |
2 | HG03098.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2183-5166C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224255484 | |||||||
| chr1:224255722 | T | C | 279 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(276): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.2183-5404A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224255722 | |||||||
| chr1:224255764 | C | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0137 |
2 | HG02602.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.2183-5446G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224255764 | |||||||
| chr1:224255813 | A | T | 4 | a0001c0001t0001g0110 a0001c0001t0001g0113 a0001c0001t0001g0124 others(1): Show |
4 | HG01346.hp2 HG01943.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.2183-5495T>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224255813 | |||||||
| chr1:224256006 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2183-5688A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224256006 | |||||||
| chr1:224256074 | T | C | 231 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.2183-5756A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224256074 | |||||||
| chr1:224256108 | G | T | 1 | a0001c0001t0001g0039 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2183-5790C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224256108 | |||||||
| chr1:224256356 | C | T | 1 | a0001c0002t0002g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2183-6038G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224256356 | |||||||
| chr1:224256357 | G | A | 19 | a0001c0003t0002g0001 a0001c0003t0002g0233 a0001c0003t0002g0234 others(16): Show |
20 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.2183-6039C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224256357 | |||||||
| chr1:224256423 | T | TA | 107 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0024 others(104): Show |
107 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.2183-6106dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224256423 | |||||||
| chr1:224256423 | T | TAA | 90 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0021 others(87): Show |
90 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.2183-6107_2183-610 others(6): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224256423 | |||||||
| chr1:224256423 | T | TAAA | 26 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0043 others(23): Show |
26 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.2183-6108_2183-610 others(7): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224256423 | |||||||
| chr1:224256423 | T | TAAAAAA | 12 | a0001c0002t0002g0251 a0001c0002t0002g0252 a0001c0002t0002g0254 others(9): Show |
12 | HG02083.hp2 HG02698.hp2 HG03239.hp2 others(9): Show |
intron_variant | MODIFIER | c.2183-6111_2183-610 others(10): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224256423 | |||||||
| chr1:224256423 | T | TAAAAAAA | 11 | a0001c0001t0001g0140 a0001c0002t0002g0255 a0001c0002t0002g0257 others(8): Show |
11 | HG00140.hp2 HG02027.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.2183-6112_2183-610 others(11): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224256423 | |||||||
| chr1:224256423 | T | TTA | 4 | a0001c0001t0001g0163 a0002c0004t0001g0075 a0002c0004t0001g0076 others(1): Show |
4 | HG00673.hp2 NA18961.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.2183-6106_2183-610 others(6): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224256423 | |||||||
| chr1:224256423 | T | TTAA | 4 | a0001c0001t0001g0183 a0001c0001t0001g0199 a0001c0001t0001g0212 others(1): Show |
4 | HG00597.hp2 NA18949.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.2183-6106_2183-610 others(7): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224256423 | |||||||
| chr1:224256423 | TAAA | T | 15 | a0001c0003t0002g0001 a0001c0003t0002g0233 a0001c0003t0002g0235 others(12): Show |
16 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.2183-6108_2183-610 others(7): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224256423 | |||||||
| chr1:224256423 | TAAAAAAA others(5): Show |
T | 1 | a0001c0002t0002g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2183-6117_2183-610 others(16): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224256423 | |||||||
| chr1:224256817 | C | T | 1 | a0001c0002t0002g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2183-6499G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224256817 | |||||||
| chr1:224256926 | C | T | 258 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(255): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.2183-6608G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224256926 | |||||||
| chr1:224257167 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2183-6849G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224257167 | |||||||
| chr1:224257241 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2183-6923G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224257241 | |||||||
| chr1:224257257 | A | C | 1 | a0001c0003t0002g0233 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2183-6939T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224257257 | |||||||
| chr1:224257482 | A | G | 8 | a0001c0002t0002g0271 a0001c0002t0002g0272 a0001c0002t0002g0273 others(5): Show |
8 | HG01256.hp1 HG01258.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2183-7164T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224257482 | |||||||
| chr1:224257512 | TTGTC | T | 216 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2183-7198_2183-719 others(8): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224257512 | |||||||
| chr1:224257840 | C | T | 1 | a0001c0002t0002g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2183-7522G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224257840 | |||||||
| chr1:224258003 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2183-7685A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224258003 | |||||||
| chr1:224258123 | C | G | 1 | a0001c0001t0001g0110 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2183-7805G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224258123 | |||||||
| chr1:224258384 | G | T | 1 | a0001c0001t0001g0223 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2183-8066C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224258384 | |||||||
| chr1:224258415 | G | C | 258 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(255): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.2183-8097C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224258415 | |||||||
| chr1:224258614 | T | A | 1 | a0001c0002t0002g0279 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2183-8296A>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224258614 | |||||||
| chr1:224258697 | A | T | 1 | a0001c0001t0001g0118 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2183-8379T>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224258697 | |||||||
| chr1:224258706 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2183-8388A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224258706 | |||||||
| chr1:224258796 | T | C | 1 | a0007c0013t0002g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2183-8478A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224258796 | |||||||
| chr1:224258831 | T | C | 27 | a0001c0001t0001g0140 a0001c0002t0002g0250 a0001c0002t0002g0251 others(24): Show |
27 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(24): Show |
intron_variant | MODIFIER | c.2183-8513A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224258831 | |||||||
| chr1:224258917 | G | A | 216 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2183-8599C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224258917 | |||||||
| chr1:224258946 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2183-8628G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224258946 | |||||||
| chr1:224258977 | A | G | 1 | a0003c0006t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2183-8659T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224258977 | |||||||
| chr1:224258979 | TA | T | 227 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0020 others(224): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.2183-8662delT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224258979 | |||||||
| chr1:224259006 | A | G | 1 | a0005c0011t0001g0228 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2183-8688T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224259006 | |||||||
| chr1:224259163 | A | T | 1 | a0001c0001t0001g0210 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2183-8845T>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224259163 | |||||||
| chr1:224259164 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2183-8846G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224259164 | |||||||
| chr1:224259567 | T | C | 216 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2182+8467A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224259567 | |||||||
| chr1:224259580 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2182+8454G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224259580 | |||||||
| chr1:224259822 | C | CT | 12 | a0001c0001t0001g0048 a0001c0001t0001g0105 a0001c0001t0001g0130 others(9): Show |
12 | HG02055.hp1 HG02109.hp1 HG02300.hp1 others(9): Show |
intron_variant | MODIFIER | c.2182+8211dupA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224259822 | |||||||
| chr1:224259822 | C | CTT | 20 | a0001c0002t0002g0272 a0001c0003t0002g0001 a0001c0003t0002g0233 others(17): Show |
21 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.2182+8210_2182+821 others(6): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224259822 | |||||||
| chr1:224259822 | C | CTTT | 7 | a0001c0002t0002g0271 a0001c0002t0002g0273 a0001c0002t0002g0274 others(4): Show |
7 | HG01256.hp1 HG01258.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2182+8209_2182+821 others(7): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224259822 | |||||||
| chr1:224259824 | T | A | 1 | a0001c0002t0002g0282 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2182+8210A>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224259824 | |||||||
| chr1:224259948 | G | C | 1 | a0001c0001t0001g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2182+8086C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224259948 | |||||||
| chr1:224259970 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2182+8064C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224259970 | |||||||
| chr1:224260000 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2182+8034A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224260000 | |||||||
| chr1:224260101 | G | T | 1 | a0001c0001t0001g0172 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2182+7933C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224260101 | |||||||
| chr1:224260237 | T | C | 1 | a0001c0002t0002g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2182+7797A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224260237 | |||||||
| chr1:224260273 | C | T | 63 | a0001c0001t0001g0140 a0001c0002t0001g0011 a0001c0002t0001g0012 others(60): Show |
64 | HG00140.hp2 HG00733.hp2 HG01243.hp1 others(61): Show |
intron_variant | MODIFIER | c.2182+7761G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224260273 | |||||||
| chr1:224260357 | C | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0129 |
2 | HG01255.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.2182+7677G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224260357 | |||||||
| chr1:224260362 | G | A | 1 | a0007c0013t0002g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2182+7672C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224260362 | |||||||
| chr1:224260513 | T | TCCAAAGT others(611): Show |
1 | a0001c0001t0001g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2182+6903_2182+752 others(622): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224260513 | |||||||
| chr1:224260536 | A | T | 1 | a0001c0002t0002g0268 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2182+7498T>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224260536 | |||||||
| chr1:224260678 | G | T | 1 | a0001c0001t0001g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2182+7356C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224260678 | |||||||
| chr1:224260699 | C | CT | 38 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0047 others(35): Show |
39 | HG00733.hp2 HG01243.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.2182+7334dupA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224260699 | |||||||
| chr1:224260699 | CT | C | 32 | a0001c0001t0001g0019 a0001c0001t0001g0033 a0001c0001t0001g0035 others(29): Show |
32 | HG00140.hp2 HG01081.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.2182+7334delA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224260699 | |||||||
| chr1:224260699 | CTT | C | 7 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(4): Show |
7 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2182+7333_2182+733 others(6): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224260699 | |||||||
| chr1:224260944 | C | T | 2 | a0001c0002t0002g0250 a0001c0002t0002g0270 |
2 | HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2182+7090G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224260944 | |||||||
| chr1:224261026 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2182+7008G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224261026 | |||||||
| chr1:224261216 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2182+6818C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224261216 | |||||||
| chr1:224261704 | C | G | 1 | a0001c0001t0001g0114 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2182+6330G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224261704 | |||||||
| chr1:224261752 | G | A | 20 | a0001c0003t0002g0001 a0001c0003t0002g0233 a0001c0003t0002g0234 others(17): Show |
21 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.2182+6282C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224261752 | |||||||
| chr1:224261846 | A | G | 8 | a0001c0002t0002g0271 a0001c0002t0002g0272 a0001c0002t0002g0273 others(5): Show |
8 | HG01256.hp1 HG01258.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2182+6188T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224261846 | |||||||
| chr1:224262130 | G | A | 1 | a0001c0002t0002g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2182+5904C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224262130 | |||||||
| chr1:224262567 | T | G | 5 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(2): Show |
5 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2182+5467A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224262567 | |||||||
| chr1:224262638 | G | A | 1 | a0007c0013t0002g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2182+5396C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224262638 | |||||||
| chr1:224263268 | C | T | 20 | a0001c0003t0002g0001 a0001c0003t0002g0233 a0001c0003t0002g0234 others(17): Show |
21 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.2182+4766G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224263268 | |||||||
| chr1:224263306 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2182+4728G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224263306 | |||||||
| chr1:224263540 | A | C | 278 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(275): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.2182+4494T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224263540 | |||||||
| chr1:224263803 | GTA | G | 8 | a0001c0002t0002g0271 a0001c0002t0002g0272 a0001c0002t0002g0273 others(5): Show |
8 | HG01256.hp1 HG01258.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2182+4229_2182+423 others(6): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224263803 | |||||||
| chr1:224263936 | A | G | 2 | a0001c0002t0002g0250 a0001c0002t0002g0270 |
2 | HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2182+4098T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224263936 | |||||||
| chr1:224263969 | C | T | 1 | a0007c0013t0002g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2182+4065G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224263969 | |||||||
| chr1:224264136 | C | A | 3 | a0001c0001t0001g0079 a0001c0001t0001g0100 a0001c0001t0001g0101 |
3 | HG00099.hp2 HG00639.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.2182+3898G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224264136 | |||||||
| chr1:224264146 | G | T | 11 | a0001c0001t0001g0030 a0001c0001t0001g0143 a0001c0001t0001g0161 others(8): Show |
11 | HG00099.hp1 HG01192.hp1 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.2182+3888C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224264146 | |||||||
| chr1:224264157 | T | C | 1 | a0001c0012t0001g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2182+3877A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224264157 | |||||||
| chr1:224264291 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2182+3743A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224264291 | |||||||
| chr1:224264315 | C | T | 2 | a0001c0002t0002g0250 a0001c0002t0002g0270 |
2 | HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2182+3719G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224264315 | |||||||
| chr1:224264405 | G | C | 216 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2182+3629C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224264405 | |||||||
| chr1:224264430 | T | C | 1 | a0001c0002t0002g0279 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2182+3604A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224264430 | |||||||
| chr1:224264571 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2182+3463T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224264571 | |||||||
| chr1:224264709 | T | C | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2182+3325A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224264709 | |||||||
| chr1:224264737 | TTTA | T | 216 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2182+3294_2182+329 others(7): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224264737 | |||||||
| chr1:224264987 | C | T | 2 | a0001c0001t0001g0081 a0006c0008t0001g0078 |
2 | NA18747.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.2182+3047G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224264987 | |||||||
| chr1:224265071 | G | A | 1 | a0001c0002t0002g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2182+2963C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224265071 | |||||||
| chr1:224265180 | T | C | 2 | a0001c0002t0002g0246 a0001c0002t0002g0247 |
2 | HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2182+2854A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224265180 | |||||||
| chr1:224265241 | A | T | 28 | a0001c0002t0002g0271 a0001c0002t0002g0272 a0001c0002t0002g0273 others(25): Show |
29 | HG00733.hp2 HG01243.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.2182+2793T>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224265241 | |||||||
| chr1:224265556 | G | A | 25 | a0001c0001t0001g0140 a0001c0002t0002g0251 a0001c0002t0002g0252 others(22): Show |
25 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(22): Show |
intron_variant | MODIFIER | c.2182+2478C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224265556 | |||||||
| chr1:224265574 | T | C | 1 | a0001c0002t0001g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2182+2460A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224265574 | |||||||
| chr1:224265790 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2182+2244C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224265790 | |||||||
| chr1:224265912 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2182+2122G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224265912 | |||||||
| chr1:224265926 | C | T | 6 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(3): Show |
6 | HG02055.hp1 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2182+2108G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224265926 | |||||||
| chr1:224266001 | T | C | 1 | a0001c0003t0002g0242 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2182+2033A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224266001 | |||||||
| chr1:224266340 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0220 |
2 | HG01106.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.2182+1694G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224266340 | |||||||
| chr1:224266397 | T | C | 65 | a0001c0001t0001g0140 a0001c0002t0001g0011 a0001c0002t0001g0012 others(62): Show |
66 | HG00140.hp2 HG00733.hp2 HG01243.hp1 others(63): Show |
intron_variant | MODIFIER | c.2182+1637A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224266397 | |||||||
| chr1:224266424 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2182+1610A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224266424 | |||||||
| chr1:224266695 | C | T | 1 | a0004c0014t0002g0283 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2182+1339G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224266695 | |||||||
| chr1:224266759 | A | G | 1 | a0001c0002t0002g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2182+1275T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224266759 | |||||||
| chr1:224266849 | T | C | 1 | a0001c0001t0001g0197 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2182+1185A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224266849 | |||||||
| chr1:224267310 | A | T | 1 | a0001c0003t0002g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2182+724T>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224267310 | |||||||
| chr1:224267402 | T | C | 7 | a0001c0002t0002g0251 a0001c0002t0002g0252 a0001c0002t0002g0262 others(4): Show |
7 | HG02027.hp2 HG02083.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.2182+632A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224267402 | |||||||
| chr1:224267410 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2182+624C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224267410 | |||||||
| chr1:224267686 | C | CA | 15 | a0001c0001t0001g0025 a0001c0001t0001g0036 a0001c0001t0001g0057 others(12): Show |
15 | HG00735.hp1 HG01884.hp1 HG02148.hp1 others(12): Show |
intron_variant | MODIFIER | c.2182+347dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224267686 | |||||||
| chr1:224267723 | T | C | 1 | a0001c0002t0002g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2182+311A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224267723 | |||||||
| chr1:224267792 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2182+242G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224267792 | |||||||
| chr1:224267911 | T | C | 1 | a0001c0002t0002g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2182+123A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224267911 | |||||||
| chr1:224267979 | C | T | 1 | a0007c0013t0002g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2182+55G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 18/22 | chr1 | 224267979 | |||||||
| chr1:224268325 | C | CCA | 65 | a0001c0001t0001g0140 a0001c0002t0001g0011 a0001c0002t0001g0012 others(62): Show |
66 | HG00140.hp2 HG00733.hp2 HG01243.hp1 others(63): Show |
intron_variant | MODIFIER | c.2083-194_2083-193d others(4): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224268325 | |||||||
| chr1:224268336 | G | A | 1 | a0001c0012t0001g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2083-203C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224268336 | |||||||
| chr1:224268554 | G | A | 19 | a0001c0003t0002g0001 a0001c0003t0002g0233 a0001c0003t0002g0234 others(16): Show |
20 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.2083-421C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224268554 | |||||||
| chr1:224268570 | A | G | 1 | a0007c0013t0002g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2083-437T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224268570 | |||||||
| chr1:224268648 | TTTTG | T | 48 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0025 others(45): Show |
48 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.2083-519_2083-516d others(6): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224268648 | |||||||
| chr1:224268698 | G | T | 1 | a0007c0013t0002g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2083-565C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224268698 | |||||||
| chr1:224268723 | A | ATCTTGGC others(35): Show |
1 | a0001c0001t0001g0214 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2083-632_2083-591d others(44): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224268723 | |||||||
| chr1:224268804 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2083-671C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224268804 | |||||||
| chr1:224268813 | G | A | 3 | a0001c0002t0002g0244 a0001c0002t0002g0246 a0001c0002t0002g0247 |
3 | HG03041.hp2 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2083-680C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224268813 | |||||||
| chr1:224268976 | A | G | 3 | a0001c0002t0002g0244 a0001c0002t0002g0246 a0001c0002t0002g0247 |
3 | HG03041.hp2 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2083-843T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224268976 | |||||||
| chr1:224269037 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2083-904C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224269037 | |||||||
| chr1:224269084 | CT | C | 257 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(254): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.2083-952delA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224269084 | |||||||
| chr1:224269084 | CTT | C | 11 | a0001c0001t0001g0026 a0001c0001t0001g0103 a0001c0002t0002g0255 others(8): Show |
11 | HG01243.hp1 HG01884.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2083-953_2083-952d others(4): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224269084 | |||||||
| chr1:224269130 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2083-997C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224269130 | |||||||
| chr1:224269385 | C | T | 8 | a0001c0003t0003g0002 a0001c0003t0003g0003 a0001c0003t0003g0004 others(5): Show |
8 | HG01243.hp1 HG01884.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2083-1252G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224269385 | |||||||
| chr1:224269455 | T | A | 1 | a0001c0003t0002g0242 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2083-1322A>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224269455 | |||||||
| chr1:224269595 | G | C | 8 | a0001c0002t0002g0271 a0001c0002t0002g0272 a0001c0002t0002g0273 others(5): Show |
8 | HG01256.hp1 HG01258.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2083-1462C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224269595 | |||||||
| chr1:224269606 | C | G | 1 | a0001c0001t0001g0089 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2083-1473G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224269606 | |||||||
| chr1:224269747 | C | CTTTTTTC others(4): Show |
30 | a0001c0001t0001g0140 a0001c0002t0002g0244 a0001c0002t0002g0246 others(27): Show |
30 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(27): Show |
intron_variant | MODIFIER | c.2083-1625_2083-161 others(15): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224269747 | |||||||
| chr1:224269754 | C | CT | 13 | a0001c0001t0001g0033 a0001c0001t0001g0054 a0001c0001t0001g0055 others(10): Show |
13 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.2083-1622dupA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224269754 | |||||||
| chr1:224269936 | C | CTT | 20 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0025 others(17): Show |
20 | HG00642.hp2 HG00738.hp1 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.2083-1805_2083-180 others(6): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224269936 | |||||||
| chr1:224269936 | C | CTTT | 24 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0002t0002g0250 others(21): Show |
24 | HG01361.hp1 HG02027.hp2 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.2083-1806_2083-180 others(7): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224269936 | |||||||
| chr1:224270035 | G | T | 28 | a0001c0002t0002g0271 a0001c0002t0002g0272 a0001c0002t0002g0273 others(25): Show |
29 | HG00733.hp2 HG01243.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.2083-1902C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224270035 | |||||||
| chr1:224270089 | G | GA | 28 | a0001c0002t0002g0271 a0001c0002t0002g0272 a0001c0002t0002g0273 others(25): Show |
29 | HG00733.hp2 HG01243.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.2083-1957dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224270089 | |||||||
| chr1:224270109 | C | T | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2083-1976G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224270109 | |||||||
| chr1:224270255 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2083-2122G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224270255 | |||||||
| chr1:224270490 | G | A | 8 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0094 others(5): Show |
8 | NA18956.hp2 NA18989.hp1 NA18989.hp2 others(5): Show |
intron_variant | MODIFIER | c.2083-2357C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224270490 | |||||||
| chr1:224270536 | C | T | 1 | a0002c0004t0001g0136 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2083-2403G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224270536 | |||||||
| chr1:224270983 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2083-2850A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224270983 | |||||||
| chr1:224271070 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2083-2937G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224271070 | |||||||
| chr1:224271252 | G | T | 1 | a0001c0001t0001g0137 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2083-3119C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224271252 | |||||||
| chr1:224271272 | C | T | 2 | a0001c0001t0001g0081 a0006c0008t0001g0078 |
2 | NA18747.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.2083-3139G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224271272 | |||||||
| chr1:224271366 | G | A | 30 | a0001c0001t0001g0140 a0001c0002t0002g0244 a0001c0002t0002g0246 others(27): Show |
30 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(27): Show |
intron_variant | MODIFIER | c.2083-3233C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224271366 | |||||||
| chr1:224271501 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2083-3368C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224271501 | |||||||
| chr1:224271523 | G | A | 162 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0020 others(159): Show |
162 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.2083-3390C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224271523 | |||||||
| chr1:224271559 | T | C | 1 | a0007c0013t0002g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2083-3426A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224271559 | |||||||
| chr1:224271636 | G | A | 20 | a0001c0003t0002g0001 a0001c0003t0002g0233 a0001c0003t0002g0234 others(17): Show |
21 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.2083-3503C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224271636 | |||||||
| chr1:224271672 | T | C | 1 | a0001c0010t0001g0097 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2083-3539A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224271672 | |||||||
| chr1:224271735 | A | G | 65 | a0001c0001t0001g0140 a0001c0002t0001g0011 a0001c0002t0001g0012 others(62): Show |
66 | HG00140.hp2 HG00733.hp2 HG01243.hp1 others(63): Show |
intron_variant | MODIFIER | c.2083-3602T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224271735 | |||||||
| chr1:224271739 | G | A | 1 | a0001c0002t0001g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2082+3600C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224271739 | |||||||
| chr1:224271929 | G | A | 3 | a0001c0002t0002g0244 a0001c0002t0002g0246 a0001c0002t0002g0247 |
3 | HG03041.hp2 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2082+3410C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224271929 | |||||||
| chr1:224271968 | T | C | 30 | a0001c0001t0001g0140 a0001c0002t0002g0244 a0001c0002t0002g0246 others(27): Show |
30 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(27): Show |
intron_variant | MODIFIER | c.2082+3371A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224271968 | |||||||
| chr1:224272151 | C | A | 1 | a0001c0001t0001g0182 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2082+3188G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224272151 | |||||||
| chr1:224272173 | TA | T | 27 | a0001c0001t0001g0140 a0001c0002t0002g0250 a0001c0002t0002g0251 others(24): Show |
27 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(24): Show |
intron_variant | MODIFIER | c.2082+3165delT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224272173 | |||||||
| chr1:224272261 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | HG02922.hp2 HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2082+3078G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224272261 | |||||||
| chr1:224272300 | G | A | 216 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2082+3039C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224272300 | |||||||
| chr1:224272388 | A | C | 9 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0039 others(6): Show |
9 | HG01106.hp1 HG01243.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2082+2951T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224272388 | |||||||
| chr1:224272663 | G | A | 2 | a0001c0001t0001g0048 a0001c0012t0001g0017 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2082+2676C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224272663 | |||||||
| chr1:224272692 | G | C | 6 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(3): Show |
6 | HG02055.hp1 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2082+2647C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224272692 | |||||||
| chr1:224272711 | T | C | 1 | a0007c0013t0002g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2082+2628A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224272711 | |||||||
| chr1:224272939 | CAGG | C | 3 | a0001c0003t0002g0239 a0001c0003t0002g0240 a0001c0003t0002g0241 |
3 | HG02258.hp2 HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2082+2397_2082+239 others(7): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224272939 | |||||||
| chr1:224272951 | G | A | 1 | a0001c0002t0002g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2082+2388C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224272951 | |||||||
| chr1:224273038 | A | C | 1 | a0001c0001t0001g0040 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2082+2301T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224273038 | |||||||
| chr1:224273042 | AC | A | 4 | a0001c0002t0002g0244 a0001c0002t0002g0246 a0001c0002t0002g0247 others(1): Show |
4 | HG03041.hp2 HG03486.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2082+2296delG | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224273042 | |||||||
| chr1:224273043 | C | A | 30 | a0001c0001t0001g0140 a0001c0001t0001g0145 a0001c0001t0001g0146 others(27): Show |
30 | HG00140.hp2 HG00609.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.2082+2296G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224273043 | |||||||
| chr1:224273043 | C | CA | 154 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0020 others(151): Show |
154 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.2082+2295dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224273043 | |||||||
| chr1:224273045 | A | AC | 3 | a0001c0001t0001g0081 a0001c0001t0001g0134 a0006c0008t0001g0078 |
3 | HG01123.hp2 NA18747.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.2082+2293_2082+229 others(5): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224273045 | |||||||
| chr1:224273046 | A | C | 4 | a0001c0001t0001g0048 a0001c0002t0002g0244 a0001c0002t0002g0246 others(1): Show |
4 | HG03041.hp2 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2082+2293T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224273046 | |||||||
| chr1:224273047 | A | AC | 6 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0066 others(3): Show |
6 | HG01361.hp1 HG02148.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.2082+2291_2082+229 others(5): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224273047 | |||||||
| chr1:224273052 | C | A | 275 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(272): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.2082+2287G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224273052 | |||||||
| chr1:224273056 | C | A | 35 | a0001c0001t0001g0140 a0001c0002t0001g0011 a0001c0002t0001g0012 others(32): Show |
35 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(32): Show |
intron_variant | MODIFIER | c.2082+2283G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224273056 | |||||||
| chr1:224273057 | A | AC | 15 | a0001c0002t0002g0244 a0001c0002t0002g0246 a0001c0002t0002g0247 others(12): Show |
15 | HG02027.hp2 HG02083.hp2 HG02602.hp2 others(12): Show |
intron_variant | MODIFIER | c.2082+2281_2082+228 others(5): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224273057 | |||||||
| chr1:224273057 | A | C | 15 | a0001c0001t0001g0140 a0001c0002t0002g0251 a0001c0002t0002g0252 others(12): Show |
15 | HG00140.hp2 HG02523.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.2082+2282T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224273057 | |||||||
| chr1:224273060 | C | A | 31 | a0001c0001t0001g0140 a0001c0002t0002g0244 a0001c0002t0002g0246 others(28): Show |
31 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(28): Show |
intron_variant | MODIFIER | c.2082+2279G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224273060 | |||||||
| chr1:224273081 | C | CAA | 20 | a0001c0003t0002g0001 a0001c0003t0002g0233 a0001c0003t0002g0234 others(17): Show |
21 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.2082+2257_2082+225 others(6): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224273081 | |||||||
| chr1:224273081 | C | CGA | 8 | a0001c0002t0002g0271 a0001c0002t0002g0272 a0001c0002t0002g0273 others(5): Show |
8 | HG01256.hp1 HG01258.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2082+2257_2082+225 others(6): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224273081 | |||||||
| chr1:224273188 | G | C | 24 | a0001c0001t0001g0140 a0001c0002t0002g0251 a0001c0002t0002g0252 others(21): Show |
24 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.2082+2151C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224273188 | |||||||
| chr1:224273305 | C | T | 1 | a0001c0002t0002g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2082+2034G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224273305 | |||||||
| chr1:224273367 | A | AGCG | 6 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(3): Show |
6 | HG02055.hp1 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2082+1971_2082+197 others(7): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224273367 | |||||||
| chr1:224273369 | T | C | 65 | a0001c0001t0001g0140 a0001c0002t0001g0011 a0001c0002t0001g0012 others(62): Show |
66 | HG00140.hp2 HG00733.hp2 HG01243.hp1 others(63): Show |
intron_variant | MODIFIER | c.2082+1970A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224273369 | |||||||
| chr1:224273452 | C | G | 27 | a0001c0001t0001g0140 a0001c0002t0002g0250 a0001c0002t0002g0251 others(24): Show |
27 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(24): Show |
intron_variant | MODIFIER | c.2082+1887G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224273452 | |||||||
| chr1:224273615 | G | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0120 |
2 | HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2082+1724C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224273615 | |||||||
| chr1:224274035 | A | AACACAC | 28 | a0001c0002t0002g0271 a0001c0002t0002g0272 a0001c0002t0002g0273 others(25): Show |
29 | HG00733.hp2 HG01243.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.2082+1298_2082+130 others(10): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224274035 | |||||||
| chr1:224274035 | A | AACACACA others(1): Show |
6 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(3): Show |
6 | HG02055.hp1 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2082+1296_2082+130 others(12): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224274035 | |||||||
| chr1:224274035 | A | AACACACA others(5): Show |
127 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(124): Show |
127 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.2082+1292_2082+130 others(16): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224274035 | |||||||
| chr1:224274035 | A | AACACACA others(7): Show |
36 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0024 others(33): Show |
36 | HG00099.hp1 HG00621.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.2082+1290_2082+130 others(18): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224274035 | |||||||
| chr1:224274035 | A | AACACACA others(9): Show |
42 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0031 others(39): Show |
42 | HG00280.hp2 HG00323.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.2082+1288_2082+130 others(20): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224274035 | |||||||
| chr1:224274035 | A | AACACACA others(11): Show |
4 | a0001c0001t0001g0089 a0001c0001t0001g0132 a0001c0001t0001g0143 others(1): Show |
4 | HG00621.hp1 HG03710.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.2082+1286_2082+130 others(22): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224274035 | |||||||
| chr1:224274035 | A | AACACACA others(13): Show |
1 | a0001c0001t0001g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2082+1284_2082+130 others(24): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224274035 | |||||||
| chr1:224274035 | A | AACACACA others(15): Show |
1 | a0001c0001t0001g0205 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2082+1282_2082+130 others(26): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224274035 | |||||||
| chr1:224274058 | A | ACACACAC others(3): Show |
1 | a0001c0002t0002g0258 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2082+1280_2082+128 others(14): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224274058 | |||||||
| chr1:224274058 | A | ACACACAC others(1): Show |
29 | a0001c0001t0001g0140 a0001c0002t0002g0244 a0001c0002t0002g0246 others(26): Show |
29 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(26): Show |
intron_variant | MODIFIER | c.2082+1280_2082+128 others(12): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224274058 | |||||||
| chr1:224274059 | C | CACACACA others(6): Show |
5 | a0001c0001t0001g0023 a0001c0001t0001g0147 a0001c0001t0001g0153 others(2): Show |
5 | HG01952.hp1 HG02258.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.2082+1279_2082+128 others(17): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224274059 | |||||||
| chr1:224274059 | C | CACACACA others(10): Show |
1 | a0001c0001t0005g0062 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2082+1279_2082+128 others(21): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224274059 | |||||||
| chr1:224274162 | G | A | 1 | a0001c0002t0002g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2082+1177C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224274162 | |||||||
| chr1:224274216 | G | A | 2 | a0001c0002t0002g0265 a0001c0002t0002g0266 |
2 | HG02027.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2082+1123C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224274216 | |||||||
| chr1:224274233 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0059 |
3 | HG01261.hp1 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2082+1106C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224274233 | |||||||
| chr1:224274240 | G | A | 1 | a0001c0002t0002g0279 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2082+1099C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224274240 | |||||||
| chr1:224274415 | T | A | 1 | a0001c0001t0001g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2082+924A>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224274415 | |||||||
| chr1:224274422 | A | G | 1 | a0001c0003t0003g0008 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2082+917T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224274422 | |||||||
| chr1:224274458 | G | T | 2 | a0001c0002t0001g0015 a0004c0014t0002g0283 |
2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2082+881C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224274458 | |||||||
| chr1:224274622 | G | A | 1 | a0001c0002t0002g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2082+717C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224274622 | |||||||
| chr1:224274700 | A | ATTTATTG others(6): Show |
1 | a0001c0001t0001g0021 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2082+626_2082+638d others(15): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224274700 | |||||||
| chr1:224274823 | A | G | 1 | a0007c0013t0002g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2082+516T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224274823 | |||||||
| chr1:224274905 | A | C | 216 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2082+434T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224274905 | |||||||
| chr1:224275318 | C | T | 1 | a0001c0002t0002g0282 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2082+21G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 17/22 | chr1 | 224275318 | |||||||
| chr1:224275470 | C | T | 4 | a0001c0002t0002g0251 a0001c0002t0002g0252 a0001c0002t0002g0262 others(1): Show |
4 | NA18612.hp1 NA18941.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.1963-12G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224275470 | |||||||
| chr1:224275793 | C | T | 1 | a0001c0003t0002g0241 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1963-335G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224275793 | |||||||
| chr1:224275815 | G | A | 1 | a0001c0002t0002g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1963-357C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224275815 | |||||||
| chr1:224276064 | A | G | 19 | a0001c0003t0002g0001 a0001c0003t0002g0233 a0001c0003t0002g0234 others(16): Show |
20 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1963-606T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224276064 | |||||||
| chr1:224276323 | C | T | 2 | a0001c0002t0002g0250 a0001c0002t0002g0270 |
2 | HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1963-865G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224276323 | |||||||
| chr1:224276404 | A | C | 1 | a0001c0001t0001g0052 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1963-946T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224276404 | |||||||
| chr1:224276528 | G | T | 1 | a0001c0002t0002g0260 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1963-1070C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224276528 | |||||||
| chr1:224276622 | C | T | 1 | a0001c0002t0002g0261 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1963-1164G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224276622 | |||||||
| chr1:224276911 | T | TTGACACA others(14): Show |
13 | a0001c0001t0001g0081 a0001c0001t0001g0103 a0001c0001t0001g0120 others(10): Show |
13 | HG01081.hp1 HG01168.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1963-1474_1963-145 others(25): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224276911 | |||||||
| chr1:224276911 | T | TTGACACA others(35): Show |
1 | a0001c0002t0002g0250 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1963-1495_1963-145 others(46): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224276911 | |||||||
| chr1:224276911 | T | TTGACACA others(56): Show |
2 | a0001c0002t0002g0251 a0001c0002t0002g0262 |
2 | NA18612.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1963-1516_1963-145 others(67): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224276911 | |||||||
| chr1:224276911 | TTGACACA others(14): Show |
T | 134 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0020 others(131): Show |
134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.1963-1474_1963-145 others(25): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224276911 | |||||||
| chr1:224276911 | TTGACACA others(35): Show |
T | 72 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0030 others(69): Show |
72 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.1963-1495_1963-145 others(46): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224276911 | |||||||
| chr1:224276911 | TTGACACA others(56): Show |
T | 48 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0052 others(45): Show |
49 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.1963-1516_1963-145 others(67): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224276911 | |||||||
| chr1:224277391 | A | G | 66 | a0001c0001t0001g0140 a0001c0002t0001g0011 a0001c0002t0001g0012 others(63): Show |
67 | HG00140.hp2 HG00733.hp2 HG01243.hp1 others(64): Show |
intron_variant | MODIFIER | c.1963-1933T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224277391 | |||||||
| chr1:224277466 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1963-2008C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224277466 | |||||||
| chr1:224277925 | G | A | 3 | a0001c0001t0001g0032 a0001c0002t0002g0246 a0001c0002t0002g0247 |
3 | HG02970.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1963-2467C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224277925 | |||||||
| chr1:224278078 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1963-2620A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224278078 | |||||||
| chr1:224278226 | C | CT | 50 | a0001c0001t0001g0036 a0001c0001t0001g0121 a0001c0001t0001g0138 others(47): Show |
51 | HG00140.hp2 HG00733.hp2 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.1963-2769dupA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224278226 | |||||||
| chr1:224278226 | CT | C | 27 | a0001c0001t0001g0048 a0001c0001t0001g0067 a0001c0001t0001g0084 others(24): Show |
27 | HG00735.hp1 HG01074.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.1963-2769delA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224278226 | |||||||
| chr1:224278308 | C | T | 1 | a0001c0002t0002g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1962+2815G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224278308 | |||||||
| chr1:224278504 | T | A | 1 | a0001c0002t0002g0268 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1962+2619A>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224278504 | |||||||
| chr1:224278678 | C | G | 1 | a0001c0001t0001g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1962+2445G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224278678 | |||||||
| chr1:224278680 | G | A | 2 | a0001c0002t0002g0246 a0001c0002t0002g0247 |
2 | HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1962+2443C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224278680 | |||||||
| chr1:224278818 | G | A | 30 | a0001c0001t0001g0140 a0001c0002t0002g0244 a0001c0002t0002g0246 others(27): Show |
30 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(27): Show |
intron_variant | MODIFIER | c.1962+2305C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224278818 | |||||||
| chr1:224278846 | C | G | 1 | a0001c0001t0001g0133 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1962+2277G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224278846 | |||||||
| chr1:224278907 | T | C | 1 | a0001c0002t0002g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1962+2216A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224278907 | |||||||
| chr1:224279000 | T | C | 30 | a0001c0001t0001g0140 a0001c0002t0002g0244 a0001c0002t0002g0246 others(27): Show |
30 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(27): Show |
intron_variant | MODIFIER | c.1962+2123A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224279000 | |||||||
| chr1:224279346 | G | T | 9 | a0001c0003t0002g0238 a0001c0003t0003g0002 a0001c0003t0003g0003 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1962+1777C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224279346 | |||||||
| chr1:224279415 | C | T | 211 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(208): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1962+1708G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224279415 | |||||||
| chr1:224279561 | T | C | 1 | a0001c0002t0002g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1962+1562A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224279561 | |||||||
| chr1:224279757 | T | C | 8 | a0001c0002t0002g0271 a0001c0002t0002g0272 a0001c0002t0002g0273 others(5): Show |
8 | HG01256.hp1 HG01258.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1962+1366A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224279757 | |||||||
| chr1:224279798 | C | G | 1 | a0001c0001t0005g0062 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1962+1325G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224279798 | |||||||
| chr1:224279926 | C | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0059 |
3 | HG01261.hp1 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1962+1197G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224279926 | |||||||
| chr1:224280013 | C | G | 1 | a0001c0001t0001g0071 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1962+1110G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224280013 | |||||||
| chr1:224280054 | GA | G | 3 | a0001c0002t0002g0244 a0001c0002t0002g0246 a0001c0002t0002g0247 |
3 | HG03041.hp2 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1962+1068delT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224280054 | |||||||
| chr1:224280058 | G | T | 3 | a0001c0002t0002g0244 a0001c0002t0002g0246 a0001c0002t0002g0247 |
3 | HG03041.hp2 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1962+1065C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224280058 | |||||||
| chr1:224280170 | T | G | 26 | a0001c0001t0001g0140 a0001c0002t0002g0250 a0001c0002t0002g0251 others(23): Show |
26 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(23): Show |
intron_variant | MODIFIER | c.1962+953A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224280170 | |||||||
| chr1:224280179 | G | GT | 38 | a0001c0001t0001g0010 a0001c0001t0001g0054 a0001c0001t0001g0068 others(35): Show |
39 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.1962+943dupA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224280179 | |||||||
| chr1:224280179 | G | T | 3 | a0001c0002t0001g0015 a0001c0002t0002g0244 a0004c0014t0002g0283 |
3 | HG02486.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1962+944C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224280179 | |||||||
| chr1:224280330 | C | T | 1 | a0004c0014t0002g0283 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1962+793G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224280330 | |||||||
| chr1:224280530 | CT | C | 9 | a0001c0001t0001g0033 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1962+592delA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224280530 | |||||||
| chr1:224280663 | A | G | 1 | a0001c0003t0002g0242 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1962+460T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224280663 | |||||||
| chr1:224281114 | A | G | 28 | a0001c0002t0002g0271 a0001c0002t0002g0272 a0001c0002t0002g0273 others(25): Show |
29 | HG00733.hp2 HG01243.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.1962+9T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 16/22 | chr1 | 224281114 | |||||||
| chr1:224281219 | C | T | 27 | a0001c0001t0001g0140 a0001c0002t0002g0250 a0001c0002t0002g0251 others(24): Show |
27 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(24): Show |
intron_variant | MODIFIER | c.1900-34G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224281219 | |||||||
| chr1:224281249 | G | C | 2 | a0001c0002t0002g0246 a0001c0002t0002g0247 |
2 | HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1900-64C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224281249 | |||||||
| chr1:224281277 | C | CTGTG | 4 | a0001c0001t0001g0140 a0001c0002t0002g0260 a0001c0002t0002g0264 others(1): Show |
4 | HG02083.hp2 HG02630.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1900-96_1900-93dup others(4): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224281277 | |||||||
| chr1:224281277 | C | CTGTGTG | 15 | a0001c0002t0002g0251 a0001c0002t0002g0252 a0001c0002t0002g0255 others(12): Show |
15 | HG02027.hp2 HG02523.hp1 HG02602.hp2 others(12): Show |
intron_variant | MODIFIER | c.1900-98_1900-93dup others(6): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224281277 | |||||||
| chr1:224281277 | C | CTGTGTGT others(1): Show |
5 | a0001c0002t0002g0254 a0001c0002t0002g0258 a0001c0002t0002g0259 others(2): Show |
5 | HG00140.hp2 HG02698.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.1900-93_1900-92ins others(8): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224281277 | |||||||
| chr1:224281277 | C | CTGTGTGT others(5): Show |
1 | a0001c0002t0006g0253 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1900-93_1900-92ins others(12): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224281277 | |||||||
| chr1:224281284 | C | CGT | 139 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0020 others(136): Show |
139 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1900-101_1900-100d others(4): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224281284 | |||||||
| chr1:224281284 | C | CGTGT | 60 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(57): Show |
60 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.1900-103_1900-100d others(6): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224281284 | |||||||
| chr1:224281284 | C | CGTGTGT | 5 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(2): Show |
5 | HG00438.hp2 HG02922.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1900-105_1900-100d others(8): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224281284 | |||||||
| chr1:224281284 | C | T | 27 | a0001c0001t0001g0140 a0001c0002t0002g0250 a0001c0002t0002g0251 others(24): Show |
27 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(24): Show |
intron_variant | MODIFIER | c.1900-99G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224281284 | |||||||
| chr1:224281284 | CGT | C | 30 | a0001c0001t0001g0160 a0001c0002t0002g0244 a0001c0002t0002g0271 others(27): Show |
31 | HG00733.hp2 HG01243.hp1 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.1900-101_1900-100d others(4): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224281284 | |||||||
| chr1:224281284 | CGTGT | C | 6 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(3): Show |
6 | HG02109.hp1 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1900-103_1900-100d others(6): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224281284 | |||||||
| chr1:224281288 | T | TGA | 3 | a0001c0001t0001g0079 a0001c0001t0001g0100 a0001c0001t0001g0101 |
3 | HG00099.hp2 HG00639.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.1900-104_1900-103i others(4): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224281288 | |||||||
| chr1:224281325 | G | C | 3 | a0001c0001t0001g0211 a0001c0001t0001g0216 a0001c0001t0001g0218 |
3 | HG00735.hp2 HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.1900-140C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224281325 | |||||||
| chr1:224281393 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1900-208G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224281393 | |||||||
| chr1:224281458 | G | A | 1 | a0001c0002t0002g0260 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1900-273C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224281458 | |||||||
| chr1:224281600 | C | T | 1 | a0001c0003t0002g0237 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1900-415G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224281600 | |||||||
| chr1:224281604 | T | C | 8 | a0001c0003t0003g0002 a0001c0003t0003g0003 a0001c0003t0003g0004 others(5): Show |
8 | HG01243.hp1 HG01884.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1900-419A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224281604 | |||||||
| chr1:224281810 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1900-625C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224281810 | |||||||
| chr1:224281834 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1900-649A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224281834 | |||||||
| chr1:224281877 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1900-692G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224281877 | |||||||
| chr1:224281909 | T | C | 1 | a0001c0002t0002g0255 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1900-724A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224281909 | |||||||
| chr1:224281931 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1900-746G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224281931 | |||||||
| chr1:224281940 | G | A | 1 | a0001c0002t0002g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1900-755C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224281940 | |||||||
| chr1:224281952 | C | CAAA | 6 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(3): Show |
6 | HG02055.hp1 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1900-770_1900-768d others(5): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224281952 | |||||||
| chr1:224282040 | G | A | 26 | a0001c0001t0001g0140 a0001c0002t0002g0250 a0001c0002t0002g0251 others(23): Show |
26 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(23): Show |
intron_variant | MODIFIER | c.1900-855C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224282040 | |||||||
| chr1:224282056 | T | A | 24 | a0001c0001t0001g0140 a0001c0002t0002g0251 a0001c0002t0002g0252 others(21): Show |
24 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.1900-871A>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224282056 | |||||||
| chr1:224282070 | A | AT | 19 | a0001c0002t0002g0271 a0001c0002t0002g0272 a0001c0002t0002g0273 others(16): Show |
20 | HG00733.hp2 HG01256.hp1 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.1900-886dupA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224282070 | |||||||
| chr1:224282070 | A | ATT | 9 | a0001c0003t0002g0238 a0001c0003t0003g0002 a0001c0003t0003g0003 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1900-887_1900-886d others(4): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224282070 | |||||||
| chr1:224282274 | C | T | 212 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(209): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1900-1089G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224282274 | |||||||
| chr1:224282513 | C | T | 2 | a0001c0001t0001g0048 a0001c0012t0001g0017 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1900-1328G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224282513 | |||||||
| chr1:224282722 | A | G | 8 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(5): Show |
8 | HG01074.hp2 HG01123.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1900-1537T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224282722 | |||||||
| chr1:224282944 | T | C | 1 | a0001c0003t0002g0239 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1900-1759A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224282944 | |||||||
| chr1:224282964 | T | C | 6 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(3): Show |
6 | HG02055.hp1 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1900-1779A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224282964 | |||||||
| chr1:224283149 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1900-1964A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224283149 | |||||||
| chr1:224283291 | T | C | 1 | a0001c0001t0004g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1900-2106A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224283291 | |||||||
| chr1:224283488 | AAAAG | A | 27 | a0001c0001t0001g0140 a0001c0002t0002g0250 a0001c0002t0002g0251 others(24): Show |
27 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(24): Show |
intron_variant | MODIFIER | c.1900-2307_1900-230 others(8): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224283488 | |||||||
| chr1:224283559 | G | A | 1 | a0001c0002t0002g0250 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1900-2374C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224283559 | |||||||
| chr1:224285041 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1899+985A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224285041 | |||||||
| chr1:224285086 | T | C | 2 | a0001c0001t0001g0081 a0006c0008t0001g0078 |
2 | NA18747.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.1899+940A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224285086 | |||||||
| chr1:224285113 | C | T | 26 | a0001c0001t0001g0140 a0001c0002t0002g0250 a0001c0002t0002g0251 others(23): Show |
26 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(23): Show |
intron_variant | MODIFIER | c.1899+913G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224285113 | |||||||
| chr1:224285195 | G | C | 1 | a0001c0003t0002g0242 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1899+831C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224285195 | |||||||
| chr1:224285256 | G | A | 1 | a0001c0007t0001g0086 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1899+770C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224285256 | |||||||
| chr1:224285336 | G | A | 1 | a0001c0003t0002g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1899+690C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224285336 | |||||||
| chr1:224285512 | G | T | 1 | a0001c0002t0002g0254 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1899+514C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224285512 | |||||||
| chr1:224285592 | C | T | 215 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(212): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1899+434G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 15/22 | chr1 | 224285592 | |||||||
| chr1:224286147 | A | C | 37 | a0001c0001t0001g0140 a0001c0002t0001g0011 a0001c0002t0001g0012 others(34): Show |
37 | HG00140.hp2 HG02027.hp2 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.1795-17T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 14/22 | chr1 | 224286147 | |||||||
| chr1:224286215 | G | GT | 12 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0046 others(9): Show |
12 | HG00597.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1795-86dupA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 14/22 | chr1 | 224286215 | |||||||
| chr1:224286215 | GT | G | 46 | a0001c0001t0001g0140 a0001c0002t0002g0244 a0001c0002t0002g0246 others(43): Show |
47 | HG00140.hp2 HG00733.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.1795-86delA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 14/22 | chr1 | 224286215 | |||||||
| chr1:224286328 | C | T | 1 | a0007c0013t0002g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1795-198G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 14/22 | chr1 | 224286328 | |||||||
| chr1:224286363 | G | A | 1 | a0001c0001t0004g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1795-233C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 14/22 | chr1 | 224286363 | |||||||
| chr1:224286395 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0141 |
2 | NA18983.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1795-265C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 14/22 | chr1 | 224286395 | |||||||
| chr1:224286454 | C | A | 1 | a0007c0013t0002g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1795-324G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 14/22 | chr1 | 224286454 | |||||||
| chr1:224286460 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1795-330G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 14/22 | chr1 | 224286460 | |||||||
| chr1:224286632 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1795-502A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 14/22 | chr1 | 224286632 | |||||||
| chr1:224286787 | C | T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1795-657G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 14/22 | chr1 | 224286787 | |||||||
| chr1:224286841 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1795-711G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 14/22 | chr1 | 224286841 | |||||||
| chr1:224286882 | A | G | 1 | a0001c0002t0002g0279 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1795-752T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 14/22 | chr1 | 224286882 | |||||||
| chr1:224286979 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1794+796C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 14/22 | chr1 | 224286979 | |||||||
| chr1:224287038 | C | T | 6 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(3): Show |
6 | HG02055.hp1 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1794+737G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 14/22 | chr1 | 224287038 | |||||||
| chr1:224287049 | A | T | 1 | a0001c0003t0002g0242 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1794+726T>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 14/22 | chr1 | 224287049 | |||||||
| chr1:224287108 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1794+667C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 14/22 | chr1 | 224287108 | |||||||
| chr1:224287415 | C | A | 1 | a0001c0001t0004g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1794+360G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 14/22 | chr1 | 224287415 | |||||||
| chr1:224287522 | T | C | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG00323.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1794+253A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 14/22 | chr1 | 224287522 | |||||||
| chr1:224288268 | C | T | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0162 others(4): Show |
7 | NA18949.hp2 NA18960.hp1 NA18986.hp1 others(4): Show |
intron_variant | MODIFIER | c.1576-275G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 13/22 | chr1 | 224288268 | |||||||
| chr1:224288455 | T | TA | 5 | a0001c0002t0002g0244 a0001c0002t0002g0246 a0001c0002t0002g0247 others(2): Show |
5 | HG02622.hp2 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1576-463dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 13/22 | chr1 | 224288455 | |||||||
| chr1:224288707 | C | T | 58 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0030 others(55): Show |
58 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1576-714G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 13/22 | chr1 | 224288707 | |||||||
| chr1:224288912 | T | C | 1 | a0007c0013t0002g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1575+572A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 13/22 | chr1 | 224288912 | |||||||
| chr1:224288958 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1575+526A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 13/22 | chr1 | 224288958 | |||||||
| chr1:224288978 | T | C | 5 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(2): Show |
5 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1575+506A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 13/22 | chr1 | 224288978 | |||||||
| chr1:224289087 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1575+397A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 13/22 | chr1 | 224289087 | |||||||
| chr1:224289950 | A | C | 38 | a0001c0001t0001g0140 a0001c0002t0002g0244 a0001c0002t0002g0246 others(35): Show |
38 | HG00140.hp2 HG01256.hp1 HG01258.hp2 others(35): Show |
intron_variant | MODIFIER | c.1326-217T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224289950 | |||||||
| chr1:224289953 | T | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0130 |
2 | HG02683.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1326-220A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224289953 | |||||||
| chr1:224290246 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1326-513G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224290246 | |||||||
| chr1:224290330 | A | G | 5 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(2): Show |
5 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1326-597T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224290330 | |||||||
| chr1:224290385 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1326-652C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224290385 | |||||||
| chr1:224290396 | C | A | 22 | a0001c0001t0001g0140 a0001c0002t0002g0251 a0001c0002t0002g0252 others(19): Show |
22 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(19): Show |
intron_variant | MODIFIER | c.1326-663G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224290396 | |||||||
| chr1:224290432 | A | C | 33 | a0001c0001t0001g0140 a0001c0002t0002g0250 a0001c0002t0002g0251 others(30): Show |
33 | HG00140.hp2 HG01256.hp1 HG01258.hp2 others(30): Show |
intron_variant | MODIFIER | c.1326-699T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224290432 | |||||||
| chr1:224290486 | G | A | 2 | a0001c0002t0002g0246 a0001c0002t0002g0247 |
2 | HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1326-753C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224290486 | |||||||
| chr1:224290797 | G | A | 5 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(2): Show |
5 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1326-1064C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224290797 | |||||||
| chr1:224290801 | C | CA | 45 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0109 others(42): Show |
45 | HG00140.hp2 HG00597.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.1326-1069dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224290801 | |||||||
| chr1:224290863 | G | A | 1 | a0001c0002t0002g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1326-1130C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224290863 | |||||||
| chr1:224290943 | C | T | 44 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0024 others(41): Show |
44 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.1326-1210G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224290943 | |||||||
| chr1:224290947 | C | T | 6 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0079 others(3): Show |
6 | HG00099.hp2 HG00639.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.1326-1214G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224290947 | |||||||
| chr1:224291283 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0138 |
2 | HG02572.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1326-1550C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224291283 | |||||||
| chr1:224291317 | T | C | 37 | a0001c0001t0001g0140 a0001c0002t0002g0244 a0001c0002t0002g0246 others(34): Show |
37 | HG00140.hp2 HG01256.hp1 HG01258.hp2 others(34): Show |
intron_variant | MODIFIER | c.1326-1584A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224291317 | |||||||
| chr1:224291355 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1326-1622C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224291355 | |||||||
| chr1:224291380 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1326-1647G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224291380 | |||||||
| chr1:224291511 | A | G | 2 | a0001c0003t0003g0005 a0001c0003t0003g0006 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1326-1778T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224291511 | |||||||
| chr1:224291539 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1326-1806G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224291539 | |||||||
| chr1:224291817 | A | T | 5 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(2): Show |
5 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1326-2084T>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224291817 | |||||||
| chr1:224291958 | C | T | 38 | a0001c0001t0001g0140 a0001c0002t0002g0244 a0001c0002t0002g0246 others(35): Show |
38 | HG00140.hp2 HG01256.hp1 HG01258.hp2 others(35): Show |
intron_variant | MODIFIER | c.1326-2225G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224291958 | |||||||
| chr1:224292267 | C | T | 1 | a0008c0009t0001g0051 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1325+2000G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224292267 | |||||||
| chr1:224292284 | C | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG00642.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1325+1983G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224292284 | |||||||
| chr1:224292753 | C | T | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG01516.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1325+1514G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224292753 | |||||||
| chr1:224292806 | A | C | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | NA19070.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1325+1461T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224292806 | |||||||
| chr1:224292896 | A | G | 40 | a0001c0001t0001g0140 a0001c0002t0002g0244 a0001c0002t0002g0246 others(37): Show |
40 | HG00140.hp2 HG01256.hp1 HG01258.hp2 others(37): Show |
intron_variant | MODIFIER | c.1325+1371T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224292896 | |||||||
| chr1:224293070 | AT | A | 6 | a0001c0001t0001g0092 a0001c0002t0002g0244 a0001c0002t0002g0246 others(3): Show |
6 | HG02622.hp2 HG03041.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1325+1196delA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224293070 | |||||||
| chr1:224293272 | T | C | 5 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(2): Show |
5 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1325+995A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224293272 | |||||||
| chr1:224293348 | C | T | 1 | a0001c0002t0002g0282 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1325+919G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224293348 | |||||||
| chr1:224293551 | C | T | 2 | a0001c0002t0002g0279 a0001c0002t0002g0280 |
2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1325+716G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224293551 | |||||||
| chr1:224293614 | G | A | 5 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(2): Show |
5 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1325+653C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224293614 | |||||||
| chr1:224293673 | A | T | 2 | a0001c0002t0002g0279 a0001c0002t0002g0280 |
2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1325+594T>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224293673 | |||||||
| chr1:224293946 | A | G | 68 | a0001c0001t0001g0140 a0001c0002t0001g0011 a0001c0002t0001g0012 others(65): Show |
69 | HG00140.hp2 HG00733.hp2 HG01243.hp1 others(66): Show |
intron_variant | MODIFIER | c.1325+321T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 12/22 | chr1 | 224293946 | |||||||
| chr1:224294514 | T | C | 213 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(210): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1181-103A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 11/22 | chr1 | 224294514 | |||||||
| chr1:224294718 | A | C | 32 | a0001c0001t0001g0140 a0001c0002t0002g0250 a0001c0002t0002g0251 others(29): Show |
32 | HG00140.hp2 HG01256.hp1 HG01258.hp2 others(29): Show |
intron_variant | MODIFIER | c.1181-307T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 11/22 | chr1 | 224294718 | |||||||
| chr1:224294725 | C | A | 33 | a0001c0001t0001g0140 a0001c0002t0002g0250 a0001c0002t0002g0251 others(30): Show |
33 | HG00140.hp2 HG01256.hp1 HG01258.hp2 others(30): Show |
intron_variant | MODIFIER | c.1181-314G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 11/22 | chr1 | 224294725 | |||||||
| chr1:224294753 | G | C | 1 | a0001c0003t0002g0242 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1181-342C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 11/22 | chr1 | 224294753 | |||||||
| chr1:224294791 | G | A | 33 | a0001c0001t0001g0140 a0001c0002t0002g0250 a0001c0002t0002g0251 others(30): Show |
33 | HG00140.hp2 HG01256.hp1 HG01258.hp2 others(30): Show |
intron_variant | MODIFIER | c.1181-380C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 11/22 | chr1 | 224294791 | |||||||
| chr1:224294814 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1181-403T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 11/22 | chr1 | 224294814 | |||||||
| chr1:224294951 | A | G | 2 | a0001c0002t0002g0246 a0001c0002t0002g0247 |
2 | HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1181-540T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 11/22 | chr1 | 224294951 | |||||||
| chr1:224295106 | A | G | 1 | a0001c0001t0001g0040 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1181-695T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 11/22 | chr1 | 224295106 | |||||||
| chr1:224295148 | G | A | 19 | a0001c0003t0002g0001 a0001c0003t0002g0233 a0001c0003t0002g0234 others(16): Show |
20 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1181-737C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 11/22 | chr1 | 224295148 | |||||||
| chr1:224295197 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1181-786G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 11/22 | chr1 | 224295197 | |||||||
| chr1:224295207 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1181-796A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 11/22 | chr1 | 224295207 | |||||||
| chr1:224295216 | G | A | 4 | a0001c0002t0002g0251 a0001c0002t0002g0252 a0001c0002t0002g0262 others(1): Show |
4 | NA18612.hp1 NA18941.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.1181-805C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 11/22 | chr1 | 224295216 | |||||||
| chr1:224295354 | G | A | 2 | a0001c0002t0002g0279 a0001c0002t0002g0280 |
2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1181-943C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 11/22 | chr1 | 224295354 | |||||||
| chr1:224295807 | G | A | 1 | a0004c0014t0002g0283 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1180+694C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 11/22 | chr1 | 224295807 | |||||||
| chr1:224295865 | C | T | 1 | a0005c0011t0001g0228 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1180+636G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 11/22 | chr1 | 224295865 | |||||||
| chr1:224295960 | C | CA | 60 | a0001c0001t0001g0025 a0001c0001t0001g0035 a0001c0001t0001g0036 others(57): Show |
60 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1180+540dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 11/22 | chr1 | 224295960 | |||||||
| chr1:224295960 | CA | C | 20 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0162 others(17): Show |
20 | HG01256.hp1 HG01258.hp2 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.1180+540delT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 11/22 | chr1 | 224295960 | |||||||
| chr1:224295960 | CAA | C | 20 | a0001c0001t0001g0140 a0001c0002t0002g0251 a0001c0002t0002g0252 others(17): Show |
20 | HG00140.hp2 HG02083.hp2 HG02523.hp1 others(17): Show |
intron_variant | MODIFIER | c.1180+539_1180+540d others(4): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 11/22 | chr1 | 224295960 | |||||||
| chr1:224296028 | G | A | 33 | a0001c0001t0001g0140 a0001c0002t0002g0250 a0001c0002t0002g0251 others(30): Show |
33 | HG00140.hp2 HG01256.hp1 HG01258.hp2 others(30): Show |
intron_variant | MODIFIER | c.1180+473C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 11/22 | chr1 | 224296028 | |||||||
| chr1:224296276 | C | T | 6 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(3): Show |
6 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1180+225G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 11/22 | chr1 | 224296276 | |||||||
| chr1:224296287 | C | G | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1180+214G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 11/22 | chr1 | 224296287 | |||||||
| chr1:224296360 | A | G | 2 | a0001c0001t0001g0159 a0001c0001t0001g0197 |
2 | HG01081.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.1180+141T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 11/22 | chr1 | 224296360 | |||||||
| chr1:224296406 | T | C | 1 | a0001c0012t0001g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1180+95A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 11/22 | chr1 | 224296406 | |||||||
| chr1:224296421 | T | C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0137 |
2 | HG02602.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1180+80A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 11/22 | chr1 | 224296421 | |||||||
| chr1:224296648 | T | C | 20 | a0001c0003t0002g0001 a0001c0003t0002g0233 a0001c0003t0002g0234 others(17): Show |
21 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1063-30A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224296648 | |||||||
| chr1:224296695 | T | A | 1 | a0001c0002t0002g0268 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1063-77A>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224296695 | |||||||
| chr1:224296708 | C | A | 67 | a0001c0001t0001g0140 a0001c0002t0001g0011 a0001c0002t0001g0012 others(64): Show |
68 | HG00140.hp2 HG00733.hp2 HG01243.hp1 others(65): Show |
intron_variant | MODIFIER | c.1063-90G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224296708 | |||||||
| chr1:224296897 | T | C | 22 | a0001c0001t0001g0140 a0001c0002t0002g0251 a0001c0002t0002g0252 others(19): Show |
22 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(19): Show |
intron_variant | MODIFIER | c.1063-279A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224296897 | |||||||
| chr1:224297265 | C | T | 2 | a0001c0002t0002g0279 a0001c0002t0002g0280 |
2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1063-647G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224297265 | |||||||
| chr1:224297310 | A | G | 6 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(3): Show |
6 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1063-692T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224297310 | |||||||
| chr1:224297377 | T | C | 1 | a0001c0002t0002g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1063-759A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224297377 | |||||||
| chr1:224297414 | C | T | 1 | a0001c0012t0001g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1063-796G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224297414 | |||||||
| chr1:224297578 | T | C | 1 | a0001c0003t0002g0240 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1063-960A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224297578 | |||||||
| chr1:224297808 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1063-1190C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224297808 | |||||||
| chr1:224297914 | G | A | 13 | a0001c0001t0001g0028 a0001c0001t0001g0039 a0001c0001t0001g0041 others(10): Show |
13 | HG01106.hp1 HG01243.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1063-1296C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224297914 | |||||||
| chr1:224298003 | T | C | 68 | a0001c0001t0001g0140 a0001c0002t0001g0011 a0001c0002t0001g0012 others(65): Show |
69 | HG00140.hp2 HG00733.hp2 HG01243.hp1 others(66): Show |
intron_variant | MODIFIER | c.1063-1385A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224298003 | |||||||
| chr1:224298036 | C | CA | 41 | a0001c0001t0001g0030 a0001c0001t0001g0040 a0001c0001t0001g0092 others(38): Show |
41 | HG00140.hp2 HG01256.hp1 HG01258.hp2 others(38): Show |
intron_variant | MODIFIER | c.1063-1419dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224298036 | |||||||
| chr1:224298076 | T | G | 1 | a0004c0014t0002g0283 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1063-1458A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224298076 | |||||||
| chr1:224298133 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1063-1515C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224298133 | |||||||
| chr1:224298140 | G | A | 2 | a0001c0002t0002g0250 a0001c0002t0002g0270 |
2 | HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1063-1522C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224298140 | |||||||
| chr1:224298603 | G | C | 22 | a0001c0001t0001g0140 a0001c0002t0002g0251 a0001c0002t0002g0252 others(19): Show |
22 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(19): Show |
intron_variant | MODIFIER | c.1062+1959C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224298603 | |||||||
| chr1:224298704 | G | A | 1 | a0001c0003t0002g0242 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1062+1858C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224298704 | |||||||
| chr1:224298769 | T | C | 33 | a0001c0001t0001g0140 a0001c0002t0002g0250 a0001c0002t0002g0251 others(30): Show |
33 | HG00140.hp2 HG01256.hp1 HG01258.hp2 others(30): Show |
intron_variant | MODIFIER | c.1062+1793A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224298769 | |||||||
| chr1:224298976 | T | C | 1 | a0001c0001t0001g0092 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1062+1586A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224298976 | |||||||
| chr1:224299088 | C | T | 1 | a0001c0003t0003g0004 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1062+1474G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224299088 | |||||||
| chr1:224299187 | T | C | 20 | a0001c0003t0002g0001 a0001c0003t0002g0233 a0001c0003t0002g0234 others(17): Show |
21 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1062+1375A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224299187 | |||||||
| chr1:224299275 | C | A | 1 | a0001c0003t0002g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1062+1287G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224299275 | |||||||
| chr1:224299318 | A | G | 2 | a0001c0002t0002g0248 a0001c0002t0002g0249 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1062+1244T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224299318 | |||||||
| chr1:224299346 | T | G | 1 | a0001c0001t0001g0033 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1062+1216A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224299346 | |||||||
| chr1:224299364 | T | C | 59 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0030 others(56): Show |
59 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.1062+1198A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224299364 | |||||||
| chr1:224299588 | T | C | 213 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(210): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1062+974A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224299588 | |||||||
| chr1:224299822 | G | T | 243 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(240): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1062+740C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224299822 | |||||||
| chr1:224299834 | GT | G | 36 | a0001c0001t0001g0140 a0001c0002t0002g0246 a0001c0002t0002g0247 others(33): Show |
36 | HG00140.hp2 HG01256.hp1 HG01258.hp2 others(33): Show |
intron_variant | MODIFIER | c.1062+727delA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224299834 | |||||||
| chr1:224300037 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG00609.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1062+525C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224300037 | |||||||
| chr1:224300126 | G | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0120 |
2 | HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1062+436C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224300126 | |||||||
| chr1:224300368 | G | A | 8 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(5): Show |
8 | HG01074.hp2 HG01123.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1062+194C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224300368 | |||||||
| chr1:224300539 | G | T | 1 | a0001c0001t0001g0202 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1062+23C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 10/22 | chr1 | 224300539 | |||||||
| chr1:224300843 | G | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0183 a0001c0001t0001g0194 others(1): Show |
4 | NA18949.hp2 NA18960.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.961-180C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/22 | chr1 | 224300843 | |||||||
| chr1:224300892 | G | T | 4 | a0001c0001t0001g0052 a0001c0001t0001g0057 a0001c0001t0001g0061 others(1): Show |
4 | HG03704.hp2 HG04199.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.961-229C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/22 | chr1 | 224300892 | |||||||
| chr1:224301093 | C | CA | 32 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0034 others(29): Show |
32 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.961-431dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/22 | chr1 | 224301093 | |||||||
| chr1:224301106 | C | CA | 23 | a0001c0001t0001g0039 a0001c0002t0002g0251 a0001c0002t0002g0252 others(20): Show |
23 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(20): Show |
intron_variant | MODIFIER | c.961-444dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/22 | chr1 | 224301106 | |||||||
| chr1:224301203 | C | A | 10 | a0001c0002t0002g0250 a0001c0002t0002g0270 a0001c0002t0002g0271 others(7): Show |
10 | HG01256.hp1 HG01258.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.961-540G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/22 | chr1 | 224301203 | |||||||
| chr1:224301376 | G | A | 2 | a0001c0002t0002g0248 a0001c0002t0002g0249 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.961-713C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/22 | chr1 | 224301376 | |||||||
| chr1:224301508 | T | C | 19 | a0001c0002t0002g0251 a0001c0002t0002g0252 a0001c0002t0002g0254 others(16): Show |
19 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.961-845A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/22 | chr1 | 224301508 | |||||||
| chr1:224301562 | C | A | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG00323.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.961-899G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/22 | chr1 | 224301562 | |||||||
| chr1:224301562 | C | T | 2 | a0001c0002t0002g0248 a0001c0002t0002g0249 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.961-899G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/22 | chr1 | 224301562 | |||||||
| chr1:224301662 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.961-999A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/22 | chr1 | 224301662 | |||||||
| chr1:224301709 | A | G | 31 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 others(28): Show |
31 | HG00140.hp2 HG01256.hp1 HG01258.hp2 others(28): Show |
intron_variant | MODIFIER | c.961-1046T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/22 | chr1 | 224301709 | |||||||
| chr1:224301798 | CA | C | 193 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(190): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.961-1136delT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/22 | chr1 | 224301798 | |||||||
| chr1:224301798 | CAA | C | 39 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0053 others(36): Show |
40 | HG00733.hp2 HG01243.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.961-1137_961-1136d others(4): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/22 | chr1 | 224301798 | |||||||
| chr1:224301800 | A | C | 1 | a0001c0001t0005g0062 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.961-1137T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/22 | chr1 | 224301800 | |||||||
| chr1:224301820 | A | G | 29 | a0001c0001t0001g0021 a0001c0002t0001g0011 a0001c0002t0001g0012 others(26): Show |
30 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.961-1157T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/22 | chr1 | 224301820 | |||||||
| chr1:224302164 | C | T | 21 | a0001c0003t0002g0001 a0001c0003t0002g0233 a0001c0003t0002g0234 others(18): Show |
22 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.961-1501G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/22 | chr1 | 224302164 | |||||||
| chr1:224302282 | G | A | 6 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(3): Show |
6 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.960+1441C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/22 | chr1 | 224302282 | |||||||
| chr1:224302345 | C | A | 32 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 others(29): Show |
32 | HG00140.hp2 HG01256.hp1 HG01258.hp2 others(29): Show |
intron_variant | MODIFIER | c.960+1378G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/22 | chr1 | 224302345 | |||||||
| chr1:224302569 | A | G | 1 | a0001c0003t0003g0004 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.960+1154T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/22 | chr1 | 224302569 | |||||||
| chr1:224302579 | G | A | 6 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(3): Show |
6 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.960+1144C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/22 | chr1 | 224302579 | |||||||
| chr1:224302602 | T | C | 2 | a0001c0002t0002g0248 a0001c0002t0002g0249 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.960+1121A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/22 | chr1 | 224302602 | |||||||
| chr1:224303142 | C | T | 1 | a0001c0012t0001g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.960+581G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/22 | chr1 | 224303142 | |||||||
| chr1:224303318 | C | T | 1 | a0004c0014t0002g0283 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.960+405G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/22 | chr1 | 224303318 | |||||||
| chr1:224303435 | C | CA | 10 | a0001c0002t0002g0250 a0001c0002t0002g0270 a0001c0002t0002g0271 others(7): Show |
10 | HG01256.hp1 HG01258.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.960+287dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/22 | chr1 | 224303435 | |||||||
| chr1:224303502 | T | TA | 31 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(28): Show |
32 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.960+220dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/22 | chr1 | 224303502 | |||||||
| chr1:224303528 | C | T | 1 | a0001c0002t0002g0272 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.960+195G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/22 | chr1 | 224303528 | |||||||
| chr1:224303529 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.960+194C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/22 | chr1 | 224303529 | |||||||
| chr1:224303562 | T | A | 276 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(273): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.960+161A>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 9/22 | chr1 | 224303562 | |||||||
| chr1:224304151 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.826-294C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 8/22 | chr1 | 224304151 | |||||||
| chr1:224304152 | C | T | 223 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(220): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.826-295G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 8/22 | chr1 | 224304152 | |||||||
| chr1:224304154 | T | C | 1 | a0006c0008t0001g0078 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.826-297A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 8/22 | chr1 | 224304154 | |||||||
| chr1:224304165 | G | A | 1 | a0001c0002t0002g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.826-308C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 8/22 | chr1 | 224304165 | |||||||
| chr1:224304237 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.826-380G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 8/22 | chr1 | 224304237 | |||||||
| chr1:224304253 | T | C | 2 | a0001c0002t0002g0248 a0001c0002t0002g0249 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.826-396A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 8/22 | chr1 | 224304253 | |||||||
| chr1:224304349 | T | C | 10 | a0001c0002t0002g0250 a0001c0002t0002g0270 a0001c0002t0002g0271 others(7): Show |
10 | HG01256.hp1 HG01258.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.825+387A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 8/22 | chr1 | 224304349 | |||||||
| chr1:224304512 | C | G | 1 | a0001c0001t0001g0030 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.825+224G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 8/22 | chr1 | 224304512 | |||||||
| chr1:224304641 | C | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | HG02615.hp1 HG02630.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.825+95G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 8/22 | chr1 | 224304641 | |||||||
| chr1:224304679 | C | T | 276 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(273): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.825+57G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 8/22 | chr1 | 224304679 | |||||||
| chr1:224304841 | G | T | 1 | a0001c0001t0001g0055 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.749-29C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 7/22 | chr1 | 224304841 | |||||||
| chr1:224304853 | A | T | 1 | a0001c0003t0002g0242 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.749-41T>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 7/22 | chr1 | 224304853 | |||||||
| chr1:224304968 | T | C | 1 | a0001c0002t0002g0246 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.748+66A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 7/22 | chr1 | 224304968 | |||||||
| chr1:224305232 | T | A | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 |
3 | HG02055.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.616-66A>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224305232 | |||||||
| chr1:224305374 | C | T | 2 | a0001c0002t0002g0248 a0001c0002t0002g0249 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.616-208G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224305374 | |||||||
| chr1:224305480 | G | A | 1 | a0004c0014t0002g0283 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.616-314C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224305480 | |||||||
| chr1:224305483 | GA | G | 10 | a0001c0002t0002g0250 a0001c0002t0002g0270 a0001c0002t0002g0271 others(7): Show |
10 | HG01256.hp1 HG01258.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.616-318delT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224305483 | |||||||
| chr1:224305526 | G | A | 1 | a0004c0014t0002g0283 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.616-360C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224305526 | |||||||
| chr1:224305589 | G | C | 244 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(241): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.616-423C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224305589 | |||||||
| chr1:224305620 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.616-454G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224305620 | |||||||
| chr1:224305665 | C | A | 1 | a0004c0014t0002g0283 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.616-499G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224305665 | |||||||
| chr1:224305763 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.616-597C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224305763 | |||||||
| chr1:224305822 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.616-656G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224305822 | |||||||
| chr1:224305999 | TTTTA | T | 243 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(240): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.616-837_616-834del others(4): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224305999 | |||||||
| chr1:224306320 | G | A | 31 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 others(28): Show |
31 | HG00140.hp2 HG01256.hp1 HG01258.hp2 others(28): Show |
intron_variant | MODIFIER | c.616-1154C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224306320 | |||||||
| chr1:224306359 | C | T | 32 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 others(29): Show |
32 | HG00140.hp2 HG01256.hp1 HG01258.hp2 others(29): Show |
intron_variant | MODIFIER | c.616-1193G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224306359 | |||||||
| chr1:224306437 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.616-1271A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224306437 | |||||||
| chr1:224306562 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.616-1396C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224306562 | |||||||
| chr1:224306571 | A | T | 1 | a0001c0001t0001g0056 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.616-1405T>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224306571 | |||||||
| chr1:224306840 | A | G | 4 | a0001c0001t0001g0087 a0001c0001t0001g0132 a0003c0006t0001g0073 others(1): Show |
4 | HG00642.hp1 HG01981.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.615+1151T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224306840 | |||||||
| chr1:224306968 | G | T | 101 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(98): Show |
101 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.615+1023C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224306968 | |||||||
| chr1:224306970 | T | C | 1 | a0004c0014t0002g0283 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.615+1021A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224306970 | |||||||
| chr1:224307018 | T | TG | 10 | a0001c0002t0002g0250 a0001c0002t0002g0270 a0001c0002t0002g0271 others(7): Show |
10 | HG01256.hp1 HG01258.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.615+972dupC | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224307018 | |||||||
| chr1:224307148 | A | G | 4 | a0001c0003t0002g0001 a0001c0003t0002g0235 a0001c0003t0002g0236 others(1): Show |
5 | HG00733.hp2 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.615+843T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224307148 | |||||||
| chr1:224307308 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.615+683T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224307308 | |||||||
| chr1:224307349 | C | T | 243 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(240): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.615+642G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224307349 | |||||||
| chr1:224307367 | G | A | 1 | a0001c0012t0001g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.615+624C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224307367 | |||||||
| chr1:224307373 | G | T | 1 | a0001c0001t0001g0121 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.615+618C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224307373 | |||||||
| chr1:224307532 | T | C | 2 | a0001c0001t0001g0044 a0001c0003t0002g0242 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.615+459A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224307532 | |||||||
| chr1:224307617 | T | C | 276 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(273): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.615+374A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224307617 | |||||||
| chr1:224307698 | CA | C | 229 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0020 others(226): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.615+292delT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224307698 | |||||||
| chr1:224307698 | CAA | C | 15 | a0001c0001t0001g0030 a0001c0001t0001g0095 a0001c0001t0001g0142 others(12): Show |
15 | HG01081.hp2 HG01258.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.615+291_615+292del others(2): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224307698 | |||||||
| chr1:224307698 | CAAA | C | 16 | a0001c0002t0002g0273 a0001c0002t0002g0279 a0001c0002t0002g0280 others(13): Show |
16 | HG01243.hp1 HG01256.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.615+290_615+292del others(3): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224307698 | |||||||
| chr1:224307698 | CAAAA | C | 7 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(4): Show |
7 | HG02486.hp2 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.615+289_615+292del others(4): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224307698 | |||||||
| chr1:224307698 | CAAAAAAA others(4): Show |
C | 6 | a0001c0003t0002g0001 a0001c0003t0002g0233 a0001c0003t0002g0234 others(3): Show |
7 | HG00733.hp2 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.615+282_615+292del others(11): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224307698 | |||||||
| chr1:224307725 | A | C | 1 | a0001c0001t0001g0155 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.615+266T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224307725 | |||||||
| chr1:224307922 | T | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | HG02922.hp2 HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.615+69A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224307922 | |||||||
| chr1:224307927 | T | C | 18 | a0001c0003t0002g0001 a0001c0003t0002g0233 a0001c0003t0002g0234 others(15): Show |
19 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.615+64A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 6/22 | chr1 | 224307927 | |||||||
| chr1:224308483 | G | A | 7 | a0001c0001t0001g0028 a0001c0001t0001g0041 a0001c0001t0001g0042 others(4): Show |
7 | HG01106.hp1 HG01243.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.343-220C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224308483 | |||||||
| chr1:224308548 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0138 |
2 | HG02572.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.343-285C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224308548 | |||||||
| chr1:224308584 | G | A | 216 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.343-321C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224308584 | |||||||
| chr1:224308587 | A | C | 22 | a0001c0001t0001g0022 a0001c0001t0001g0030 a0001c0001t0001g0035 others(19): Show |
22 | HG00438.hp1 HG00735.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.343-324T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224308587 | |||||||
| chr1:224308623 | G | A | 19 | a0001c0003t0002g0001 a0001c0003t0002g0233 a0001c0003t0002g0234 others(16): Show |
20 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.343-360C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224308623 | |||||||
| chr1:224308690 | C | CA | 27 | a0001c0001t0001g0033 a0001c0002t0002g0251 a0001c0002t0002g0252 others(24): Show |
28 | HG00733.hp2 HG01168.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.343-428dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224308690 | |||||||
| chr1:224308799 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.343-536G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224308799 | |||||||
| chr1:224308838 | G | A | 19 | a0001c0003t0002g0001 a0001c0003t0002g0233 a0001c0003t0002g0234 others(16): Show |
20 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.343-575C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224308838 | |||||||
| chr1:224308889 | G | A | 1 | a0001c0001t0001g0023 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.343-626C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224308889 | |||||||
| chr1:224308934 | G | A | 6 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(3): Show |
6 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.343-671C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224308934 | |||||||
| chr1:224309043 | A | G | 32 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 others(29): Show |
32 | HG00140.hp2 HG01256.hp1 HG01258.hp2 others(29): Show |
intron_variant | MODIFIER | c.343-780T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224309043 | |||||||
| chr1:224309068 | A | C | 1 | a0004c0014t0002g0283 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.343-805T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224309068 | |||||||
| chr1:224309069 | A | C | 15 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0094 others(12): Show |
15 | HG01884.hp1 HG02572.hp2 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.343-806T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224309069 | |||||||
| chr1:224309071 | A | C | 1 | a0004c0014t0002g0283 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.343-808T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224309071 | |||||||
| chr1:224309074 | A | C | 1 | a0004c0014t0002g0283 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.343-811T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224309074 | |||||||
| chr1:224309237 | A | G | 1 | a0001c0001t0001g0026 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.343-974T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224309237 | |||||||
| chr1:224309265 | T | C | 1 | a0001c0001t0004g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.343-1002A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224309265 | |||||||
| chr1:224309340 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.343-1077C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224309340 | |||||||
| chr1:224309426 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.343-1163C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224309426 | |||||||
| chr1:224309475 | T | C | 276 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(273): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.343-1212A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224309475 | |||||||
| chr1:224309582 | A | G | 4 | a0001c0002t0002g0246 a0001c0002t0002g0247 a0001c0002t0002g0248 others(1): Show |
4 | HG02622.hp2 HG03041.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-1319T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224309582 | |||||||
| chr1:224309943 | C | G | 1 | a0001c0001t0001g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.343-1680G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224309943 | |||||||
| chr1:224310086 | G | A | 1 | a0001c0002t0002g0256 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.342+1714C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224310086 | |||||||
| chr1:224310113 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.342+1687A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224310113 | |||||||
| chr1:224310125 | TCGGTGAT others(5): Show |
T | 21 | a0001c0002t0002g0251 a0001c0002t0002g0252 a0001c0002t0002g0254 others(18): Show |
21 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.342+1663_342+1674d others(14): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224310125 | |||||||
| chr1:224310158 | G | A | 4 | a0001c0002t0002g0246 a0001c0002t0002g0247 a0001c0002t0002g0248 others(1): Show |
4 | HG02622.hp2 HG03041.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.342+1642C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224310158 | |||||||
| chr1:224310178 | C | CA | 24 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0045 others(21): Show |
24 | HG00609.hp1 HG00609.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.342+1621dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224310178 | |||||||
| chr1:224310194 | A | AG | 6 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(3): Show |
6 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.342+1605_342+1606i others(3): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224310194 | |||||||
| chr1:224310231 | C | T | 276 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(273): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.342+1569G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224310231 | |||||||
| chr1:224310238 | A | G | 241 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(238): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.342+1562T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224310238 | |||||||
| chr1:224310290 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.342+1510T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224310290 | |||||||
| chr1:224310318 | A | G | 4 | a0001c0003t0002g0001 a0001c0003t0002g0235 a0001c0003t0002g0236 others(1): Show |
5 | HG00733.hp2 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.342+1482T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224310318 | |||||||
| chr1:224310344 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.342+1456C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224310344 | |||||||
| chr1:224310468 | T | C | 2 | a0001c0002t0002g0250 a0001c0002t0002g0270 |
2 | HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.342+1332A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224310468 | |||||||
| chr1:224310486 | T | C | 6 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(3): Show |
6 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.342+1314A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224310486 | |||||||
| chr1:224310820 | TC | T | 4 | a0001c0002t0002g0246 a0001c0002t0002g0247 a0001c0002t0002g0248 others(1): Show |
4 | HG02622.hp2 HG03041.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.342+979delG | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224310820 | |||||||
| chr1:224311010 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.342+790C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224311010 | |||||||
| chr1:224311012 | C | T | 1 | a0001c0003t0002g0242 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.342+788G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224311012 | |||||||
| chr1:224311510 | A | G | 255 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(252): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.342+290T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224311510 | |||||||
| chr1:224311541 | G | GTA | 18 | a0001c0003t0002g0001 a0001c0003t0002g0233 a0001c0003t0002g0234 others(15): Show |
19 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.342+257_342+258dup others(2): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224311541 | |||||||
| chr1:224311544 | T | TATTTTTT others(46): Show |
1 | a0001c0003t0002g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.342+255_342+256ins others(53): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224311544 | |||||||
| chr1:224311550 | G | A | 1 | a0001c0003t0002g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.342+250C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 5/22 | chr1 | 224311550 | |||||||
| chr1:224311918 | C | A | 1 | a0001c0002t0002g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.285-61G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224311918 | |||||||
| chr1:224312001 | A | G | 6 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(3): Show |
6 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.285-144T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224312001 | |||||||
| chr1:224312590 | T | C | 276 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(273): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.285-733A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224312590 | |||||||
| chr1:224312684 | G | A | 1 | a0004c0014t0002g0283 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.285-827C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224312684 | |||||||
| chr1:224312819 | T | A | 1 | a0001c0001t0001g0063 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.285-962A>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224312819 | |||||||
| chr1:224312819 | T | TA | 43 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0046 others(40): Show |
43 | HG00408.hp2 HG00438.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.285-963dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224312819 | |||||||
| chr1:224312880 | A | T | 1 | a0001c0001t0001g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.285-1023T>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224312880 | |||||||
| chr1:224313089 | G | A | 6 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(3): Show |
6 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.285-1232C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224313089 | |||||||
| chr1:224313172 | A | AAC | 18 | a0001c0003t0002g0001 a0001c0003t0002g0233 a0001c0003t0002g0234 others(15): Show |
19 | HG00733.hp2 HG01884.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.285-1316_285-1315i others(4): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224313172 | |||||||
| chr1:224313172 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.285-1315T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224313172 | |||||||
| chr1:224313179 | A | AG | 12 | a0001c0001t0001g0036 a0001c0001t0001g0130 a0001c0001t0001g0142 others(9): Show |
12 | HG00438.hp2 HG00597.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.285-1323_285-1322i others(3): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224313179 | |||||||
| chr1:224313179 | A | G | 243 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(240): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.285-1322T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224313179 | |||||||
| chr1:224313267 | T | G | 1 | a0001c0002t0002g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.285-1410A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224313267 | |||||||
| chr1:224313269 | G | GA | 10 | a0001c0002t0002g0250 a0001c0002t0002g0270 a0001c0002t0002g0271 others(7): Show |
10 | HG01256.hp1 HG01258.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.285-1413dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224313269 | |||||||
| chr1:224313405 | T | G | 19 | a0001c0003t0002g0001 a0001c0003t0002g0233 a0001c0003t0002g0234 others(16): Show |
20 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.285-1548A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224313405 | |||||||
| chr1:224313502 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0129 |
2 | HG01255.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.285-1645C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224313502 | |||||||
| chr1:224313555 | G | C | 1 | a0001c0001t0001g0055 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.285-1698C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224313555 | |||||||
| chr1:224313578 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.285-1721G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224313578 | |||||||
| chr1:224313835 | T | C | 19 | a0001c0003t0002g0001 a0001c0003t0002g0233 a0001c0003t0002g0234 others(16): Show |
20 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.285-1978A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224313835 | |||||||
| chr1:224313958 | G | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | NA19070.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.285-2101C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224313958 | |||||||
| chr1:224313967 | G | T | 97 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(94): Show |
97 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.285-2110C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224313967 | |||||||
| chr1:224314132 | T | C | 4 | a0001c0002t0002g0246 a0001c0002t0002g0247 a0001c0002t0002g0248 others(1): Show |
4 | HG02622.hp2 HG03041.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-2275A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224314132 | |||||||
| chr1:224314264 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02148.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.285-2407G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224314264 | |||||||
| chr1:224314268 | A | G | 1 | a0001c0002t0002g0279 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.285-2411T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224314268 | |||||||
| chr1:224314289 | T | C | 18 | a0001c0003t0002g0001 a0001c0003t0002g0233 a0001c0003t0002g0234 others(15): Show |
19 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.285-2432A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224314289 | |||||||
| chr1:224314290 | A | C | 242 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.285-2433T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224314290 | |||||||
| chr1:224314452 | C | A | 276 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(273): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.285-2595G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224314452 | |||||||
| chr1:224314546 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.285-2689G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224314546 | |||||||
| chr1:224314601 | T | C | 216 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.285-2744A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224314601 | |||||||
| chr1:224314730 | C | T | 32 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 others(29): Show |
32 | HG00140.hp2 HG01256.hp1 HG01258.hp2 others(29): Show |
intron_variant | MODIFIER | c.285-2873G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224314730 | |||||||
| chr1:224314850 | T | G | 1 | a0004c0014t0002g0283 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.284+2844A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224314850 | |||||||
| chr1:224314990 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.284+2704C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224314990 | |||||||
| chr1:224315022 | C | T | 1 | a0004c0014t0002g0283 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.284+2672G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224315022 | |||||||
| chr1:224315057 | CT | C | 276 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(273): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.284+2636delA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224315057 | |||||||
| chr1:224315205 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.284+2489G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224315205 | |||||||
| chr1:224315235 | T | C | 18 | a0001c0003t0002g0001 a0001c0003t0002g0233 a0001c0003t0002g0234 others(15): Show |
19 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.284+2459A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224315235 | |||||||
| chr1:224315369 | T | C | 242 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.284+2325A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224315369 | |||||||
| chr1:224315483 | G | T | 8 | a0001c0001t0001g0030 a0001c0001t0001g0081 a0001c0001t0004g0038 others(5): Show |
8 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.284+2211C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224315483 | |||||||
| chr1:224315522 | C | A | 2 | a0001c0002t0002g0250 a0001c0002t0002g0270 |
2 | HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.284+2172G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224315522 | |||||||
| chr1:224315575 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.284+2119G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224315575 | |||||||
| chr1:224315881 | A | C | 1 | a0001c0001t0001g0081 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.284+1813T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224315881 | |||||||
| chr1:224315897 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.284+1797T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224315897 | |||||||
| chr1:224316076 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.284+1618C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224316076 | |||||||
| chr1:224316156 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.284+1538T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224316156 | |||||||
| chr1:224316187 | A | C | 1 | a0001c0001t0001g0080 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.284+1507T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224316187 | |||||||
| chr1:224316228 | T | C | 1 | a0001c0002t0002g0279 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.284+1466A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224316228 | |||||||
| chr1:224316233 | A | T | 1 | a0001c0002t0002g0262 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.284+1461T>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224316233 | |||||||
| chr1:224316362 | A | G | 223 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(220): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.284+1332T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224316362 | |||||||
| chr1:224316423 | C | T | 1 | a0001c0003t0003g0002 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.284+1271G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224316423 | |||||||
| chr1:224316521 | A | G | 1 | a0007c0013t0002g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.284+1173T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224316521 | |||||||
| chr1:224316574 | AAGG | A | 242 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.284+1117_284+1119d others(5): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224316574 | |||||||
| chr1:224316655 | C | T | 32 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 others(29): Show |
32 | HG00140.hp2 HG01256.hp1 HG01258.hp2 others(29): Show |
intron_variant | MODIFIER | c.284+1039G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224316655 | |||||||
| chr1:224316662 | C | CA | 242 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.284+1031dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224316662 | |||||||
| chr1:224316945 | C | A | 223 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(220): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.284+749G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224316945 | |||||||
| chr1:224316995 | C | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | NA18986.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.284+699G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224316995 | |||||||
| chr1:224317143 | GA | G | 8 | a0001c0001t0001g0020 a0001c0001t0001g0157 a0001c0002t0001g0011 others(5): Show |
8 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.284+550delT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224317143 | |||||||
| chr1:224317213 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.284+481T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224317213 | |||||||
| chr1:224317481 | A | C | 1 | a0001c0001t0001g0155 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.284+213T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224317481 | |||||||
| chr1:224317569 | G | A | 3 | a0001c0003t0002g0239 a0001c0003t0002g0240 a0001c0003t0002g0241 |
3 | HG02258.hp2 HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.284+125C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 4/22 | chr1 | 224317569 | |||||||
| chr1:224317812 | C | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0130 |
2 | HG02683.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.185-19G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 3/22 | chr1 | 224317812 | |||||||
| chr1:224317816 | A | G | 1 | a0001c0003t0002g0242 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.185-23T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 3/22 | chr1 | 224317816 | |||||||
| chr1:224317827 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.185-34G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 3/22 | chr1 | 224317827 | |||||||
| chr1:224318017 | T | G | 280 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(277): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.132-87A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224318017 | |||||||
| chr1:224318182 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.132-252A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224318182 | |||||||
| chr1:224318831 | A | T | 1 | a0001c0002t0002g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.132-901T>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224318831 | |||||||
| chr1:224318914 | A | G | 3 | a0002c0004t0001g0075 a0002c0004t0001g0076 a0002c0004t0001g0077 |
3 | NA18961.hp1 NA18971.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.132-984T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224318914 | |||||||
| chr1:224318977 | G | A | 242 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.132-1047C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224318977 | |||||||
| chr1:224318988 | C | CA | 41 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0072 others(38): Show |
42 | HG00323.hp1 HG00597.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.132-1059dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224318988 | |||||||
| chr1:224319080 | A | G | 6 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(3): Show |
6 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.132-1150T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224319080 | |||||||
| chr1:224319120 | A | T | 1 | a0001c0001t0001g0026 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.132-1190T>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224319120 | |||||||
| chr1:224319149 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.132-1219C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224319149 | |||||||
| chr1:224319153 | C | CA | 11 | a0001c0001t0001g0023 a0001c0001t0001g0137 a0001c0001t0001g0138 others(8): Show |
11 | HG00673.hp2 HG01361.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.132-1224dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224319153 | |||||||
| chr1:224319153 | C | CAA | 15 | a0001c0002t0002g0249 a0001c0002t0002g0251 a0001c0002t0002g0252 others(12): Show |
15 | HG00140.hp2 HG02083.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.132-1225_132-1224d others(4): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224319153 | |||||||
| chr1:224319153 | C | CAAA | 6 | a0001c0002t0002g0258 a0001c0002t0002g0259 a0001c0002t0002g0260 others(3): Show |
6 | HG02027.hp2 HG03927.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.132-1226_132-1224d others(5): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224319153 | |||||||
| chr1:224319153 | CA | C | 102 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(99): Show |
103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.132-1224delT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224319153 | |||||||
| chr1:224319153 | CAA | C | 11 | a0001c0001t0001g0033 a0001c0001t0001g0052 a0001c0002t0001g0011 others(8): Show |
11 | HG01168.hp2 HG02486.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.132-1225_132-1224d others(4): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224319153 | |||||||
| chr1:224319339 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.132-1409C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224319339 | |||||||
| chr1:224319355 | T | C | 1 | a0001c0012t0001g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.132-1425A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224319355 | |||||||
| chr1:224319393 | C | G | 3 | a0001c0001t0001g0029 a0001c0001t0001g0049 a0001c0001t0001g0050 |
3 | HG02630.hp2 HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.132-1463G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224319393 | |||||||
| chr1:224319400 | G | A | 1 | a0001c0002t0002g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.132-1470C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224319400 | |||||||
| chr1:224319440 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.132-1510A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224319440 | |||||||
| chr1:224319452 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.132-1522G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224319452 | |||||||
| chr1:224319938 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.132-2008G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224319938 | |||||||
| chr1:224319939 | C | G | 242 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.132-2009G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224319939 | |||||||
| chr1:224320338 | T | C | 1 | a0001c0001t0001g0154 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.132-2408A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224320338 | |||||||
| chr1:224320373 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.132-2443C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224320373 | |||||||
| chr1:224320422 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.132-2492C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224320422 | |||||||
| chr1:224320476 | A | C | 1 | a0001c0001t0001g0018 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.132-2546T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224320476 | |||||||
| chr1:224320533 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.132-2603C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224320533 | |||||||
| chr1:224320566 | G | C | 242 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.132-2636C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224320566 | |||||||
| chr1:224320646 | C | CA | 22 | a0001c0001t0001g0023 a0001c0001t0001g0143 a0001c0001t0001g0153 others(19): Show |
23 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.132-2717dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224320646 | |||||||
| chr1:224320724 | T | G | 1 | a0001c0002t0002g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.132-2794A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224320724 | |||||||
| chr1:224320825 | T | C | 1 | a0007c0013t0002g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.132-2895A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224320825 | |||||||
| chr1:224321113 | A | C | 1 | a0001c0001t0001g0155 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.132-3183T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224321113 | |||||||
| chr1:224321143 | T | G | 1 | a0001c0001t0001g0203 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.132-3213A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224321143 | |||||||
| chr1:224321192 | C | A | 1 | a0001c0001t0001g0204 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.132-3262G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224321192 | |||||||
| chr1:224321262 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.132-3332T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224321262 | |||||||
| chr1:224321298 | G | A | 4 | a0001c0001t0001g0040 a0001c0001t0001g0144 a0001c0001t0001g0145 others(1): Show |
4 | HG01081.hp1 HG01168.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.132-3368C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224321298 | |||||||
| chr1:224321395 | T | A | 7 | a0001c0002t0002g0251 a0001c0002t0002g0252 a0001c0002t0002g0262 others(4): Show |
7 | HG02027.hp2 HG02083.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.132-3465A>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224321395 | |||||||
| chr1:224321402 | T | C | 1 | a0001c0002t0002g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.132-3472A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224321402 | |||||||
| chr1:224321584 | TTTTTAAA others(4): Show |
T | 2 | a0001c0002t0002g0250 a0001c0002t0002g0270 |
2 | HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.132-3665_132-3655d others(13): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224321584 | |||||||
| chr1:224321687 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.132-3757G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224321687 | |||||||
| chr1:224321705 | G | A | 10 | a0001c0002t0002g0250 a0001c0002t0002g0270 a0001c0002t0002g0271 others(7): Show |
10 | HG01256.hp1 HG01258.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.132-3775C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224321705 | |||||||
| chr1:224321715 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.132-3785G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224321715 | |||||||
| chr1:224321752 | C | T | 276 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(273): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.132-3822G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224321752 | |||||||
| chr1:224321755 | CA | C | 32 | a0001c0001t0001g0036 a0001c0002t0002g0250 a0001c0002t0002g0251 others(29): Show |
32 | HG00140.hp2 HG01256.hp1 HG01258.hp2 others(29): Show |
intron_variant | MODIFIER | c.132-3826delT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224321755 | |||||||
| chr1:224321755 | CAA | C | 241 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(238): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.132-3827_132-3826d others(4): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224321755 | |||||||
| chr1:224321803 | A | G | 7 | a0001c0001t0001g0028 a0001c0001t0001g0041 a0001c0001t0001g0042 others(4): Show |
7 | HG01106.hp1 HG01243.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.132-3873T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224321803 | |||||||
| chr1:224322054 | G | A | 1 | a0001c0003t0002g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.132-4124C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224322054 | |||||||
| chr1:224322126 | G | A | 9 | a0001c0003t0002g0001 a0001c0003t0002g0233 a0001c0003t0002g0234 others(6): Show |
10 | HG00733.hp2 HG02258.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.132-4196C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224322126 | |||||||
| chr1:224322215 | A | G | 276 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(273): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.131+4176T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224322215 | |||||||
| chr1:224322243 | A | AT | 42 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0153 others(39): Show |
42 | HG00323.hp1 HG01256.hp1 HG01258.hp2 others(39): Show |
intron_variant | MODIFIER | c.131+4147dupA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224322243 | |||||||
| chr1:224322243 | AT | A | 19 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0220 others(16): Show |
20 | HG00733.hp2 HG01106.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.131+4147delA | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224322243 | |||||||
| chr1:224322572 | A | G | 1 | a0001c0002t0002g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.131+3819T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224322572 | |||||||
| chr1:224322670 | A | G | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | NA18992.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.131+3721T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224322670 | |||||||
| chr1:224322779 | C | A | 1 | a0001c0001t0001g0147 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.131+3612G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224322779 | |||||||
| chr1:224322810 | C | T | 53 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 others(50): Show |
54 | HG00140.hp2 HG00733.hp2 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.131+3581G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224322810 | |||||||
| chr1:224322970 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.131+3421G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224322970 | |||||||
| chr1:224323037 | T | C | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.131+3354A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323037 | |||||||
| chr1:224323423 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG00609.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.131+2968C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323423 | |||||||
| chr1:224323447 | G | A | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG00323.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.131+2944C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323447 | |||||||
| chr1:224323505 | A | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA18956.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.131+2886T>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323505 | |||||||
| chr1:224323536 | G | A | 2 | a0001c0002t0002g0248 a0001c0002t0002g0249 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.131+2855C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323536 | |||||||
| chr1:224323611 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 |
3 | HG02970.hp2 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.131+2780G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323611 | |||||||
| chr1:224323665 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.131+2726G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323665 | |||||||
| chr1:224323675 | G | A | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2716C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323675 | |||||||
| chr1:224323676 | G | GAAAGAGA others(29): Show |
1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2714_131+2715i others(38): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323676 | |||||||
| chr1:224323682 | C | A | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2709G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323682 | |||||||
| chr1:224323695 | G | A | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2696C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323695 | |||||||
| chr1:224323696 | G | A | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2695C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323696 | |||||||
| chr1:224323697 | C | G | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2694G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323697 | |||||||
| chr1:224323698 | T | A | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2693A>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323698 | |||||||
| chr1:224323700 | C | A | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2691G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323700 | |||||||
| chr1:224323701 | C | A | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2690G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323701 | |||||||
| chr1:224323703 | C | A | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2688G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323703 | |||||||
| chr1:224323705 | G | A | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2686C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323705 | |||||||
| chr1:224323706 | C | G | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2685G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323706 | |||||||
| chr1:224323707 | C | A | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2684G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323707 | |||||||
| chr1:224323710 | C | G | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2681G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323710 | |||||||
| chr1:224323712 | C | G | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2679G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323712 | |||||||
| chr1:224323716 | C | A | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2675G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323716 | |||||||
| chr1:224323717 | C | A | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2674G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323717 | |||||||
| chr1:224323718 | C | A | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2673G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323718 | |||||||
| chr1:224323727 | C | A | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2664G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323727 | |||||||
| chr1:224323730 | G | A | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2661C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323730 | |||||||
| chr1:224323731 | T | G | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2660A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323731 | |||||||
| chr1:224323732 | C | A | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2659G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323732 | |||||||
| chr1:224323733 | C | A | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2658G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323733 | |||||||
| chr1:224323733 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0034 |
2 | NA18978.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.131+2658G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323733 | |||||||
| chr1:224323734 | G | A | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2657C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323734 | |||||||
| chr1:224323736 | C | A | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2655G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323736 | |||||||
| chr1:224323738 | GGTGGGGC others(11): Show |
G | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2635_131+2652d others(20): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323738 | |||||||
| chr1:224323759 | G | A | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2632C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323759 | |||||||
| chr1:224323763 | C | A | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2628G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323763 | |||||||
| chr1:224323765 | G | A | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2626C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323765 | |||||||
| chr1:224323766 | G | A | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2625C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323766 | |||||||
| chr1:224323771 | G | A | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2620C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323771 | |||||||
| chr1:224323773 | T | A | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2618A>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323773 | |||||||
| chr1:224323774 | C | G | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2617G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323774 | |||||||
| chr1:224323777 | C | G | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2614G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323777 | |||||||
| chr1:224323784 | C | A | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2607G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323784 | |||||||
| chr1:224323785 | G | A | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2606C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323785 | |||||||
| chr1:224323790 | C | A | 6 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(3): Show |
6 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.131+2601G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323790 | |||||||
| chr1:224323793 | C | G | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2598G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323793 | |||||||
| chr1:224323797 | G | A | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2594C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323797 | |||||||
| chr1:224323798 | C | T | 1 | a0001c0002t0002g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.131+2593G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323798 | |||||||
| chr1:224323804 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.131+2587T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323804 | |||||||
| chr1:224323831 | T | C | 244 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(241): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.131+2560A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323831 | |||||||
| chr1:224323853 | C | T | 1 | a0001c0002t0002g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.131+2538G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323853 | |||||||
| chr1:224323875 | T | A | 1 | a0001c0001t0001g0148 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.131+2516A>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224323875 | |||||||
| chr1:224324007 | G | C | 1 | a0001c0002t0002g0278 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.131+2384C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224324007 | |||||||
| chr1:224324223 | T | C | 2 | a0001c0002t0002g0279 a0001c0002t0002g0280 |
2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.131+2168A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224324223 | |||||||
| chr1:224324297 | T | C | 19 | a0001c0003t0002g0001 a0001c0003t0002g0233 a0001c0003t0002g0234 others(16): Show |
20 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.131+2094A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224324297 | |||||||
| chr1:224324427 | T | C | 1 | a0001c0003t0002g0242 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.131+1964A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224324427 | |||||||
| chr1:224324506 | G | A | 1 | a0001c0001t0004g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.131+1885C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224324506 | |||||||
| chr1:224324551 | C | T | 1 | a0001c0002t0002g0244 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.131+1840G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224324551 | |||||||
| chr1:224324689 | T | C | 280 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(277): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.131+1702A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224324689 | |||||||
| chr1:224324702 | G | C | 2 | a0001c0002t0002g0279 a0001c0002t0002g0280 |
2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.131+1689C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224324702 | |||||||
| chr1:224324719 | C | G | 1 | a0007c0013t0002g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.131+1672G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224324719 | |||||||
| chr1:224324837 | T | C | 62 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0150 others(59): Show |
62 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.131+1554A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224324837 | |||||||
| chr1:224324909 | C | G | 10 | a0001c0002t0002g0250 a0001c0002t0002g0270 a0001c0002t0002g0271 others(7): Show |
10 | HG01256.hp1 HG01258.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.131+1482G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224324909 | |||||||
| chr1:224324917 | C | T | 10 | a0001c0002t0002g0250 a0001c0002t0002g0270 a0001c0002t0002g0271 others(7): Show |
10 | HG01256.hp1 HG01258.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.131+1474G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224324917 | |||||||
| chr1:224325087 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.131+1304G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224325087 | |||||||
| chr1:224325091 | T | G | 1 | a0001c0003t0002g0242 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.131+1300A>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224325091 | |||||||
| chr1:224325190 | A | G | 1 | a0001c0001t0001g0031 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.131+1201T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224325190 | |||||||
| chr1:224325312 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.131+1079C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224325312 | |||||||
| chr1:224325319 | C | G | 1 | a0001c0001t0001g0027 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.131+1072G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224325319 | |||||||
| chr1:224325379 | C | G | 1 | a0004c0014t0002g0283 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.131+1012G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224325379 | |||||||
| chr1:224325434 | TA | T | 6 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(3): Show |
6 | HG02896.hp1 HG02896.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.131+956delT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224325434 | |||||||
| chr1:224325435 | A | T | 20 | a0001c0002t0002g0252 a0001c0002t0002g0254 a0001c0002t0002g0255 others(17): Show |
20 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.131+956T>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224325435 | |||||||
| chr1:224325436 | A | T | 1 | a0001c0002t0002g0251 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.131+955T>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224325436 | |||||||
| chr1:224325475 | T | C | 31 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 others(28): Show |
31 | HG00140.hp2 HG01256.hp1 HG01258.hp2 others(28): Show |
intron_variant | MODIFIER | c.131+916A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224325475 | |||||||
| chr1:224325532 | G | A | 1 | a0001c0002t0002g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.131+859C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224325532 | |||||||
| chr1:224325836 | G | C | 19 | a0001c0003t0002g0001 a0001c0003t0002g0233 a0001c0003t0002g0234 others(16): Show |
20 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.131+555C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224325836 | |||||||
| chr1:224326018 | G | A | 2 | a0001c0002t0002g0250 a0001c0002t0002g0270 |
2 | HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.131+373C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224326018 | |||||||
| chr1:224326166 | T | C | 6 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(3): Show |
6 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.131+225A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224326166 | |||||||
| chr1:224326270 | T | C | 12 | a0001c0001t0001g0022 a0001c0001t0001g0210 a0001c0001t0001g0211 others(9): Show |
12 | HG00438.hp1 HG00735.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.131+121A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224326270 | |||||||
| chr1:224326282 | C | T | 4 | a0001c0003t0002g0001 a0001c0003t0002g0235 a0001c0003t0002g0236 others(1): Show |
5 | HG00733.hp2 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.131+109G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 2/22 | chr1 | 224326282 | |||||||
| chr1:224326514 | G | T | 1 | a0001c0002t0002g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.58-50C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224326514 | |||||||
| chr1:224326740 | A | G | 6 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(3): Show |
6 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.58-276T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224326740 | |||||||
| chr1:224326888 | G | C | 21 | a0001c0002t0002g0251 a0001c0002t0002g0252 a0001c0002t0002g0254 others(18): Show |
21 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.58-424C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224326888 | |||||||
| chr1:224327007 | G | A | 1 | a0001c0002t0002g0279 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.58-543C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224327007 | |||||||
| chr1:224327165 | G | A | 223 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(220): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.58-701C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224327165 | |||||||
| chr1:224327241 | G | A | 242 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.58-777C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224327241 | |||||||
| chr1:224327369 | C | T | 21 | a0001c0002t0002g0251 a0001c0002t0002g0252 a0001c0002t0002g0254 others(18): Show |
21 | HG00140.hp2 HG02027.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.58-905G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224327369 | |||||||
| chr1:224327437 | A | C | 1 | a0001c0001t0001g0026 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.58-973T>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224327437 | |||||||
| chr1:224327700 | A | G | 1 | a0001c0002t0002g0271 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.58-1236T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224327700 | |||||||
| chr1:224328074 | C | A | 242 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.58-1610G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224328074 | |||||||
| chr1:224328119 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02148.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.58-1655G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224328119 | |||||||
| chr1:224328173 | C | A | 1 | a0001c0002t0002g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.58-1709G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224328173 | |||||||
| chr1:224328274 | C | A | 2 | a0001c0002t0002g0279 a0001c0002t0002g0280 |
2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.57+1797G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224328274 | |||||||
| chr1:224328317 | C | T | 2 | a0001c0002t0002g0250 a0001c0002t0002g0270 |
2 | HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.57+1754G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224328317 | |||||||
| chr1:224328371 | G | T | 244 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(241): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.57+1700C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224328371 | |||||||
| chr1:224328389 | A | G | 1 | a0001c0001t0001g0023 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.57+1682T>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224328389 | |||||||
| chr1:224328417 | G | A | 2 | a0001c0003t0002g0233 a0001c0003t0002g0234 |
2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.57+1654C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224328417 | |||||||
| chr1:224328469 | G | GA | 235 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0024 others(232): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.57+1601dupT | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224328469 | |||||||
| chr1:224328656 | AC | A | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | NA18956.hp1 NA18989.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.57+1414delG | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224328656 | |||||||
| chr1:224328734 | C | G | 1 | a0001c0012t0001g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.57+1337G>C | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224328734 | |||||||
| chr1:224328776 | G | A | 1 | a0001c0002t0001g0016 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.57+1295C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224328776 | |||||||
| chr1:224328978 | C | T | 2 | a0001c0002t0002g0279 a0001c0002t0002g0280 |
2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.57+1093G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224328978 | |||||||
| chr1:224328983 | G | A | 1 | a0001c0002t0002g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.57+1088C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224328983 | |||||||
| chr1:224329014 | G | A | 8 | a0001c0002t0002g0271 a0001c0002t0002g0272 a0001c0002t0002g0273 others(5): Show |
8 | HG01256.hp1 HG01258.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.57+1057C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224329014 | |||||||
| chr1:224329029 | C | A | 2 | a0001c0002t0002g0279 a0001c0002t0002g0280 |
2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.57+1042G>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224329029 | |||||||
| chr1:224329032 | G | A | 31 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 others(28): Show |
31 | HG00140.hp2 HG01256.hp1 HG01258.hp2 others(28): Show |
intron_variant | MODIFIER | c.57+1039C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224329032 | |||||||
| chr1:224329040 | AAAT | A | 6 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(3): Show |
6 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.57+1028_57+1030del others(3): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224329040 | |||||||
| chr1:224329058 | T | A | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.57+1013A>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224329058 | |||||||
| chr1:224329142 | C | T | 242 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.57+929G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224329142 | |||||||
| chr1:224329207 | G | C | 2 | a0001c0002t0002g0279 a0001c0002t0002g0280 |
2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.57+864C>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224329207 | |||||||
| chr1:224329279 | T | C | 2 | a0001c0002t0002g0281 a0001c0002t0002g0282 |
2 | NA18959.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.57+792A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224329279 | |||||||
| chr1:224329346 | AGAG | A | 216 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.57+722_57+724delCT others(1): Show |
NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224329346 | |||||||
| chr1:224329362 | G | A | 6 | a0001c0001t0001g0227 a0001c0001t0001g0229 a0001c0001t0001g0230 others(3): Show |
6 | HG00323.hp1 HG00733.hp1 HG00735.hp1 others(3): Show |
intron_variant | MODIFIER | c.57+709C>T | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224329362 | |||||||
| chr1:224329475 | G | T | 242 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.57+596C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224329475 | |||||||
| chr1:224329476 | T | C | 242 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.57+595A>G | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224329476 | |||||||
| chr1:224329576 | G | T | 1 | a0001c0001t0001g0010 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.57+495C>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224329576 | |||||||
| chr1:224329695 | C | T | 19 | a0001c0003t0002g0001 a0001c0003t0002g0233 a0001c0003t0002g0234 others(16): Show |
20 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.57+376G>A | NVL | ENSG00000143748.18 | transcript | ENST00000281701.11 | protein_coding | 1/22 | chr1 | 224329695 |