Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 338917 |
| ensemblid | ENSG00000119614.3 |
| hgncid | 1975 |
| symbol | VSX2 |
| name | visual system homeobox 2 |
| refseq_nuc | NM_182894.3 |
| refseq_prot | NP_878314.1 |
| ensembl_nuc | ENST00000261980.3 |
| ensembl_prot | ENSP00000261980.2 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 74239449 |
| end | 74262738 |
| strand | + |
| ver | v1.2 |
| region | chr14:74239449-74262738 |
| region5000 | chr14:74234449-74267738 |
| regionname0 | VSX2_chr14_74239449_74262738 |
| regionname5000 | VSX2_chr14_74234449_74267738 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 361 | 402 | 87 | 66 | 186 | 14 | 47 | 149 | VSX2_chr14_74234449_74267738 | VSX2 | MTGKA others(356): Show |
chr14 | 74234449 | 74267738 |
| a0002 | 0/0 | 361 | 11 | 0 | 8 | 2 | 0 | 1 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | MTGKA others(356): Show |
chr14 | 74234449 | 74267738 |
| a0003 | 0/0 | 362 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | MTGKA others(357): Show |
chr14 | 74234449 | 74267738 |
| a0004 | 0/0 | 361 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | MTGKA others(356): Show |
chr14 | 74234449 | 74267738 |
| a0005 | 0/0 | 361 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | MTGKA others(356): Show |
chr14 | 74234449 | 74267738 |
| a0006 | 0/0 | 361 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | MTGKA others(356): Show |
chr14 | 74234449 | 74267738 |
| a0007 | 0/0 | 361 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | MTGKA others(356): Show |
chr14 | 74234449 | 74267738 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1083 | 313 | 80 | 35 | 160 | 8 | 28 | VSX2_chr14_74234449_74267738 | VSX2 | ATGAC others(1078): Show |
chr14 | 74234449 | 74267738 | ||
| a0001c0002 | 0/0 | 1083 | 79 | 6 | 29 | 22 | 6 | 16 | VSX2_chr14_74234449_74267738 | VSX2 | ATGAC others(1078): Show |
chr14 | 74234449 | 74267738 | ||
| a0001c0004 | 0/0 | 1083 | 4 | 0 | 2 | 0 | 0 | 2 | VSX2_chr14_74234449_74267738 | VSX2 | ATGAC others(1078): Show |
chr14 | 74234449 | 74267738 | ||
| a0001c0006 | 0/0 | 1083 | 3 | 0 | 0 | 3 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | ATGAC others(1078): Show |
chr14 | 74234449 | 74267738 | ||
| a0001c0007 | 0/0 | 1083 | 2 | 1 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | ATGAC others(1078): Show |
chr14 | 74234449 | 74267738 | ||
| a0001c0010 | 0/0 | 1083 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | ATGAC others(1078): Show |
chr14 | 74234449 | 74267738 | ||
| a0002c0003 | 0/0 | 1083 | 11 | 0 | 8 | 2 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | ATGAC others(1078): Show |
chr14 | 74234449 | 74267738 | ||
| a0003c0005 | 0/0 | 1086 | 4 | 4 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | ATGAC others(1081): Show |
chr14 | 74234449 | 74267738 | ||
| a0003c0012 | 0/0 | 1086 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | ATGAC others(1081): Show |
chr14 | 74234449 | 74267738 | ||
| a0004c0013 | 0/0 | 1083 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | ATGAC others(1078): Show |
chr14 | 74234449 | 74267738 | ||
| a0005c0008 | 0/0 | 1083 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | ATGAC others(1078): Show |
chr14 | 74234449 | 74267738 | ||
| a0006c0011 | 0/0 | 1083 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | ATGAC others(1078): Show |
chr14 | 74234449 | 74267738 | ||
| a0007c0009 | 0/0 | 1083 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | ATGAC others(1078): Show |
chr14 | 74234449 | 74267738 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3018 | 151 | 20 | 16 | 97 | 4 | 12 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3013): Show |
chr14 | 74234449 | 74267738 |
| a0001c0001t0002 | 0/0 | 3018 | 63 | 20 | 6 | 27 | 0 | 10 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3013): Show |
chr14 | 74234449 | 74267738 |
| a0001c0001t0003 | 0/0 | 3018 | 23 | 0 | 1 | 17 | 1 | 4 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3013): Show |
chr14 | 74234449 | 74267738 |
| a0001c0001t0004 | 0/0 | 3016 | 16 | 0 | 0 | 16 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3011): Show |
chr14 | 74234449 | 74267738 |
| a0001c0001t0005 | 0/0 | 3016 | 15 | 12 | 2 | 0 | 1 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3011): Show |
chr14 | 74234449 | 74267738 |
| a0001c0001t0006 | 0/0 | 3018 | 10 | 9 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3013): Show |
chr14 | 74234449 | 74267738 |
| a0001c0001t0007 | 0/0 | 3016 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3011): Show |
chr14 | 74234449 | 74267738 |
| a0001c0001t0008 | 0/0 | 3018 | 7 | 0 | 5 | 0 | 2 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3013): Show |
chr14 | 74234449 | 74267738 |
| a0001c0001t0009 | 0/0 | 3016 | 7 | 5 | 2 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3011): Show |
chr14 | 74234449 | 74267738 |
| a0001c0001t0011 | 0/0 | 3016 | 3 | 3 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3011): Show |
chr14 | 74234449 | 74267738 |
| a0001c0001t0012 | 0/0 | 3018 | 3 | 3 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3013): Show |
chr14 | 74234449 | 74267738 |
| a0001c0001t0013 | 0/0 | 3018 | 3 | 2 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3013): Show |
chr14 | 74234449 | 74267738 |
| a0001c0001t0014 | 0/0 | 3016 | 2 | 2 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3011): Show |
chr14 | 74234449 | 74267738 |
| a0001c0001t0015 | 0/0 | 3018 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3013): Show |
chr14 | 74234449 | 74267738 |
| a0001c0001t0016 | 0/0 | 3018 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3013): Show |
chr14 | 74234449 | 74267738 |
| a0001c0001t0017 | 0/0 | 3018 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3013): Show |
chr14 | 74234449 | 74267738 |
| a0001c0001t0019 | 0/0 | 3018 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3013): Show |
chr14 | 74234449 | 74267738 |
| a0001c0001t0020 | 0/0 | 3018 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3013): Show |
chr14 | 74234449 | 74267738 |
| a0001c0001t0021 | 0/0 | 3018 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3013): Show |
chr14 | 74234449 | 74267738 |
| a0001c0001t0022 | 0/0 | 3018 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3013): Show |
chr14 | 74234449 | 74267738 |
| a0001c0001t0023 | 0/0 | 3018 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3013): Show |
chr14 | 74234449 | 74267738 |
| a0001c0001t0024 | 0/0 | 3018 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3013): Show |
chr14 | 74234449 | 74267738 |
| a0001c0002t0001 | 0/0 | 3018 | 74 | 6 | 29 | 17 | 6 | 16 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3013): Show |
chr14 | 74234449 | 74267738 |
| a0001c0002t0010 | 0/0 | 3018 | 4 | 0 | 0 | 4 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3013): Show |
chr14 | 74234449 | 74267738 |
| a0001c0002t0018 | 0/0 | 3018 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3013): Show |
chr14 | 74234449 | 74267738 |
| a0001c0004t0002 | 0/0 | 3018 | 4 | 0 | 2 | 0 | 0 | 2 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3013): Show |
chr14 | 74234449 | 74267738 |
| a0001c0006t0003 | 0/0 | 3018 | 3 | 0 | 0 | 3 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3013): Show |
chr14 | 74234449 | 74267738 |
| a0001c0007t0001 | 0/0 | 3018 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3013): Show |
chr14 | 74234449 | 74267738 |
| a0001c0007t0007 | 0/0 | 3016 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3011): Show |
chr14 | 74234449 | 74267738 |
| a0001c0010t0002 | 0/0 | 3018 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3013): Show |
chr14 | 74234449 | 74267738 |
| a0002c0003t0001 | 0/0 | 3018 | 11 | 0 | 8 | 2 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3013): Show |
chr14 | 74234449 | 74267738 |
| a0003c0005t0007 | 0/0 | 3019 | 4 | 4 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3014): Show |
chr14 | 74234449 | 74267738 |
| a0003c0012t0007 | 0/0 | 3019 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3014): Show |
chr14 | 74234449 | 74267738 |
| a0004c0013t0001 | 0/0 | 3018 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3013): Show |
chr14 | 74234449 | 74267738 |
| a0005c0008t0011 | 0/0 | 3016 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3011): Show |
chr14 | 74234449 | 74267738 |
| a0006c0011t0001 | 0/0 | 3018 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3013): Show |
chr14 | 74234449 | 74267738 |
| a0007c0009t0003 | 0/0 | 3018 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | AGCAT others(3013): Show |
chr14 | 74234449 | 74267738 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0180 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0292 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0046 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0003g0002 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0004g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0004g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0004g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0004g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0004g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0005g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0005g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0005g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0006g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0006g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0006g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0008g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0008g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0008g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0008g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0008g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0009g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0009g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0009g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0009g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0009g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0009g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0009g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0011g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0011g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0011g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0012g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0012g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0013g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0013g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0013g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0014g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0014g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0015g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0016g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0017g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0019g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0020g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0021g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0022g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0023g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0001t0024g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0001 | 0/0 | 12 | 1 | 5 | 4 | 1 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0004 | 0/0 | 6 | 0 | 3 | 0 | 0 | 3 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0009 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0014 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0015 | 0/0 | 3 | 1 | 0 | 1 | 1 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0042 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0044 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0010g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0010g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0002t0018g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0004t0002g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0004t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0004t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0006t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0006t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0006t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0007t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0007t0007g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0001c0010t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0002c0003t0001g0008 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0002c0003t0001g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0002c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0002c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0002c0003t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0002c0003t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0002c0003t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0003c0005t0007g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0003c0005t0007g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0003c0005t0007g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0003c0005t0007g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0003c0012t0007g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0004c0013t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0005c0008t0011g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0006c0011t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| a0007c0009t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | GBR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0262 | EUR | GBR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0009 | EUR | GBR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | GBR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0234 | EUR | FIN | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00280 | hp2 | a0001 | c0001 | t0008 | g0174 | EUR | FIN | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0120 | EUR | FIN | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0195 | EUR | FIN | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00438 | hp2 | a0002 | c0003 | t0001 | g0148 | EAS | CHS | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0315 | EAS | CHS | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00639 | hp1 | a0002 | c0003 | t0001 | g0321 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0278 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00733 | hp1 | a0001 | c0001 | t0008 | g0030 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0065 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0199 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0196 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01070 | hp1 | a0002 | c0003 | t0001 | g0053 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0062 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01071 | hp2 | a0002 | c0003 | t0001 | g0053 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0280 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01081 | hp1 | a0001 | c0001 | t0006 | g0186 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0042 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0214 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0194 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01109 | hp1 | a0001 | c0001 | t0009 | g0146 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01109 | hp2 | a0001 | c0001 | t0013 | g0224 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0064 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0017 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01243 | hp2 | a0001 | c0001 | t0009 | g0106 | AMR | PUR | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0212 | AMR | CLM | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01255 | hp2 | a0001 | c0001 | t0008 | g0119 | AMR | CLM | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01256 | hp1 | a0001 | c0004 | t0002 | g0023 | AMR | CLM | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01256 | hp2 | a0002 | c0003 | t0001 | g0319 | AMR | CLM | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0205 | AMR | CLM | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01257 | hp2 | a0001 | c0001 | t0008 | g0029 | AMR | CLM | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01258 | hp1 | a0001 | c0004 | t0002 | g0023 | AMR | CLM | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01258 | hp2 | a0001 | c0001 | t0008 | g0029 | AMR | CLM | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0014 | AMR | CLM | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0207 | AMR | CLM | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0213 | AMR | CLM | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01433 | hp1 | a0001 | c0001 | t0015 | g0116 | AMR | CLM | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0202 | AMR | CLM | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0200 | EUR | IBS | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01515 | hp2 | a0001 | c0001 | t0008 | g0074 | EUR | IBS | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | IBS | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0198 | EUR | IBS | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | ACB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01884 | hp2 | a0001 | c0001 | t0011 | g0133 | AFR | ACB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PEL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01934 | hp1 | a0002 | c0003 | t0001 | g0008 | AMR | PEL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0183 | AMR | PEL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01943 | hp1 | a0002 | c0003 | t0001 | g0008 | AMR | PEL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0231 | AMR | PEL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0044 | AMR | PEL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PEL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0203 | AMR | PEL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0216 | AMR | PEL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | KHV | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0302 | EAS | KHV | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02055 | hp1 | a0001 | c0001 | t0017 | g0222 | AFR | ACB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | KHV | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0211 | EAS | KHV | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | KHV | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0314 | EAS | KHV | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0250 | AFR | ACB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02148 | hp1 | a0002 | c0003 | t0001 | g0320 | AMR | PEL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02148 | hp2 | a0001 | c0001 | t0008 | g0030 | AMR | PEL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0066 | AFR | ACB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0244 | AFR | ACB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | ACB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | ACB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0201 | AFR | ACB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02293 | hp1 | a0002 | c0003 | t0001 | g0008 | AMR | PEL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0210 | AFR | ACB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0013 | AFR | ACB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | KHV | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02572 | hp1 | a0001 | c0001 | t0009 | g0058 | AFR | GWD | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0258 | SAS | PJL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02615 | hp2 | a0001 | c0001 | t0009 | g0286 | AFR | GWD | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0188 | AFR | GWD | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0241 | AFR | GWD | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02630 | hp1 | a0001 | c0001 | t0014 | g0185 | AFR | GWD | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0272 | AFR | GWD | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0295 | AFR | GWD | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02698 | hp1 | a0001 | c0004 | t0002 | g0002 | SAS | PJL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0197 | SAS | PJL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0059 | AFR | GWD | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0189 | AFR | GWD | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02723 | hp1 | a0001 | c0001 | t0014 | g0184 | AFR | GWD | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0043 | SAS | PJL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0284 | SAS | PJL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0265 | AFR | GWD | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02818 | hp1 | a0001 | c0001 | t0011 | g0077 | AFR | GWD | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02818 | hp2 | a0003 | c0005 | t0007 | g0055 | AFR | GWD | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02886 | hp1 | a0001 | c0001 | t0009 | g0060 | AFR | GWD | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02886 | hp2 | a0001 | c0001 | t0013 | g0223 | AFR | GWD | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0240 | AFR | GWD | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0291 | AFR | GWD | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | ESN | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0276 | AFR | ESN | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02965 | hp1 | a0003 | c0012 | t0007 | g0057 | AFR | ESN | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | ESN | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0245 | AFR | ESN | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0193 | AFR | ESN | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | ESN | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0275 | AFR | ESN | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0301 | SAS | PJL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03017 | hp2 | a0001 | c0007 | t0001 | g0157 | SAS | PJL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03041 | hp1 | a0001 | c0001 | t0012 | g0192 | AFR | GWD | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0256 | AFR | GWD | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03098 | hp1 | a0001 | c0001 | t0016 | g0257 | AFR | MSL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03098 | hp2 | a0003 | c0005 | t0007 | g0266 | AFR | MSL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03130 | hp2 | a0005 | c0008 | t0011 | g0237 | AFR | ESN | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0078 | AFR | ESN | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0298 | AFR | ESN | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0238 | AFR | ESN | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0303 | AFR | ESN | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0013 | AFR | MSL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0013 | AFR | MSL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0187 | AFR | MSL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0297 | AFR | MSL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03486 | hp2 | a0003 | c0005 | t0007 | g0269 | AFR | MSL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03490 | hp1 | a0001 | c0001 | t0024 | g0096 | SAS | PJL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0063 | SAS | PJL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0215 | SAS | PJL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0270 | SAS | PJL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0009 | SAS | PJL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03516 | hp1 | a0001 | c0001 | t0011 | g0235 | AFR | ESN | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03516 | hp2 | a0001 | c0001 | t0020 | g0247 | AFR | ESN | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0190 | AFR | GWD | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0239 | AFR | GWD | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03579 | hp2 | a0001 | c0001 | t0013 | g0225 | AFR | MSL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03654 | hp2 | a0001 | c0001 | t0021 | g0168 | SAS | PJL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0067 | SAS | PJL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0204 | SAS | PJL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0046 | SAS | STU | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0255 | SAS | STU | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0274 | SAS | BEB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03834 | hp2 | a0002 | c0003 | t0001 | g0008 | SAS | BEB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0208 | SAS | BEB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0051 | SAS | STU | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0051 | SAS | STU | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0044 | SAS | BEB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG04199 | hp1 | a0001 | c0004 | t0002 | g0048 | SAS | STU | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | STU | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | STU | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | STU | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | STU | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0009 | SAS | STU | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | YRI | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | YRI | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CHB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CHB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | YRI | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0290 | AFR | YRI | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18941 | hp2 | a0001 | c0002 | t0018 | g0217 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18944 | hp1 | a0001 | c0002 | t0010 | g0012 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18949 | hp1 | a0002 | c0003 | t0001 | g0149 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18951 | hp2 | a0001 | c0001 | t0019 | g0176 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18966 | hp1 | a0001 | c0006 | t0003 | g0281 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0317 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18970 | hp2 | a0001 | c0002 | t0010 | g0001 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18972 | hp2 | a0001 | c0001 | t0004 | g0316 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18977 | hp2 | a0001 | c0006 | t0003 | g0304 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18978 | hp1 | a0001 | c0002 | t0010 | g0012 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18982 | hp2 | a0001 | c0001 | t0022 | g0296 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18988 | hp1 | a0006 | c0011 | t0001 | g0003 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18990 | hp1 | a0007 | c0009 | t0003 | g0285 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18995 | hp1 | a0001 | c0001 | t0023 | g0020 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19011 | hp2 | a0001 | c0006 | t0003 | g0002 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0246 | AFR | LWK | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19030 | hp2 | a0001 | c0007 | t0007 | g0318 | AFR | LWK | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0306 | AFR | LWK | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19058 | hp2 | a0001 | c0010 | t0002 | g0047 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19085 | hp1 | a0001 | c0002 | t0010 | g0012 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0313 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0242 | AFR | YRI | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ASW | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | ASW | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0015 | EUR | TSI | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | TSI | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0042 | SAS | GIH | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0209 | SAS | GIH | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0206 | AMR | CLM | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0043 | AMR | CLM | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02486 | hp1 | a0001 | c0001 | t0012 | g0041 | AFR | ACB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02486 | hp2 | a0004 | c0013 | t0001 | g0236 | AFR | ACB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | ACB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | ACB | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0191 | AFR | MSL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0243 | AFR | MSL | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG06807 | hp1 | a0003 | c0005 | t0007 | g0056 | AFR | USA | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| HG06807 | hp2 | a0001 | c0001 | t0009 | g0103 | AFR | USA | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | USA | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0300 | AFR | USA | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA21309 | hp1 | a0001 | c0001 | t0012 | g0041 | AFR | LWK | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0253 | AFR | LWK | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0180 | REF | REF | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0292 | REF | REF | VSX2_chr14_74234449_74267738 | VSX2 | chr14 | 74234449 | 74267738 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74239581 | A | G | 1 | a0004 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.20A>G | p.Glu7Gly | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 1/5 | 133/3018 | 20/1086 | 7/361 | chr14 | 74239581 | |||
| chr14:74239723 | C | A | 1 | a0005 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.162C>A | p.Asp54Glu | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 1/5 | 275/3018 | 162/1086 | 54/361 | chr14 | 74239723 | |||
| chr14:74239853 | T | C | 1 | a0007 | 1 | NA18990.hp1 | missense_variant | MODERATE | c.292T>C | p.Ser98Pro | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 1/5 | 405/3018 | 292/1086 | 98/361 | chr14 | 74239853 | |||
| chr14:74259695 | A | G | 1 | a0006 | 1 | NA18988.hp1 | missense_variant | MODERATE | c.673A>G | p.Met225Val | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 4/5 | 786/3018 | 673/1086 | 225/361 | chr14 | 74259695 | |||
| chr14:74260704 | G | A | 1 | a0002 | 11 | HG00438.hp2 HG00639.hp1 HG01070.hp1 others(8): Show |
missense_variant | MODERATE | c.871G>A | p.Asp291Asn | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 5/5 | 984/3018 | 871/1086 | 291/361 | chr14 | 74260704 | |||
| chr14:74260844 | A | AGAG | 1 | a0003 | 5 | HG02818.hp2 HG02965.hp1 HG03098.hp2 others(2): Show |
disruptive_inframe_insertion | MODERATE | c.1022_1024dupAGG | p.Glu341dup | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 5/5 | 1138/3018 | 1025/1086 | 342/361 | INFO_REALIGN_3_PRIME | chr14 | 74260844 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74239732 | C | G | 1 | a0001c0006 | 3 | NA18966.hp1 NA18977.hp2 NA19011.hp2 |
synonymous_variant | LOW | c.171C>G | p.Ala57Ala | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 1/5 | 284/3018 | 171/1086 | 57/361 | chr14 | 74239732 | |||
| chr14:74245180 | C | T | 1 | a0001c0002 | 79 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(76): Show |
synonymous_variant | LOW | c.471C>T | p.Ser157Ser | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/5 | 584/3018 | 471/1086 | 157/361 | chr14 | 74245180 | |||
| chr14:74245231 | C | T | 1 | a0003c0012 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.522C>T | p.Asp174Asp | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/5 | 635/3018 | 522/1086 | 174/361 | chr14 | 74245231 | |||
| chr14:74245273 | G | A | 1 | a0001c0007 | 2 | HG03017.hp2 NA19030.hp2 |
synonymous_variant | LOW | c.564G>A | p.Pro188Pro | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/5 | 677/3018 | 564/1086 | 188/361 | chr14 | 74245273 | |||
| chr14:74245288 | G | A | 1 | a0001c0010 | 1 | NA19058.hp2 | splice_region_variant&synonymous_variant | LOW | c.579G>A | p.Gln193Gln | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/5 | 692/3018 | 579/1086 | 193/361 | chr14 | 74245288 | |||
| chr14:74259772 | G | A | 1 | a0001c0010 | 1 | NA19058.hp2 | synonymous_variant | LOW | c.750G>A | p.Pro250Pro | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 4/5 | 863/3018 | 750/1086 | 250/361 | chr14 | 74259772 | |||
| chr14:74260664 | G | A | 1 | a0001c0004 | 4 | HG01256.hp1 HG01258.hp1 HG02698.hp1 others(1): Show |
synonymous_variant | LOW | c.831G>A | p.Leu277Leu | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 5/5 | 944/3018 | 831/1086 | 277/361 | chr14 | 74260664 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74239468 | G | A | 1 | a0001c0001t0015 | 1 | HG01433.hp1 | 5_prime_UTR_variant | MODIFIER | c.-94G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 1/5 | 94 | chr14 | 74239468 | ||||||
| chr14:74239507 | G | T | 1 | a0001c0001t0024 | 1 | HG03490.hp1 | 5_prime_UTR_variant | MODIFIER | c.-55G>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 1/5 | 55 | chr14 | 74239507 | ||||||
| chr14:74239516 | G | C | 1 | a0001c0001t0006 | 10 | HG01081.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-46G>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 1/5 | 46 | chr14 | 74239516 | ||||||
| chr14:74260930 | G | A | 1 | a0001c0001t0016 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 5/5 | 11 | chr14 | 74260930 | ||||||
| chr14:74260958 | C | T | 5 | a0001c0001t0003 a0001c0001t0022 a0001c0001t0023 others(2): Show |
29 | HG00099.hp2 HG01346.hp1 HG02040.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*39C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 5/5 | 39 | chr14 | 74260958 | ||||||
| chr14:74260973 | G | A | 1 | a0001c0001t0014 | 2 | HG02630.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*54G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 5/5 | 54 | chr14 | 74260973 | ||||||
| chr14:74261169 | C | T | 1 | a0001c0001t0021 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*250C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 5/5 | 250 | chr14 | 74261169 | ||||||
| chr14:74261180 | G | T | 1 | a0001c0001t0013 | 3 | HG01109.hp2 HG02886.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*261G>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 5/5 | 261 | chr14 | 74261180 | ||||||
| chr14:74261210 | A | T | 1 | a0001c0001t0014 | 2 | HG02630.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*291A>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 5/5 | 291 | chr14 | 74261210 | ||||||
| chr14:74261374 | C | T | 4 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0011 others(1): Show |
26 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*455C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 5/5 | 455 | chr14 | 74261374 | ||||||
| chr14:74261404 | T | C | 1 | a0001c0001t0017 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*485T>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 5/5 | 485 | chr14 | 74261404 | ||||||
| chr14:74261498 | C | T | 9 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0020 others(6): Show |
98 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*579C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 5/5 | 579 | chr14 | 74261498 | ||||||
| chr14:74261589 | G | A | 1 | a0001c0001t0005 | 15 | HG00280.hp1 HG01243.hp1 HG01934.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*670G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 5/5 | 670 | chr14 | 74261589 | ||||||
| chr14:74261701 | C | A | 1 | a0001c0002t0010 | 4 | NA18944.hp1 NA18970.hp2 NA18978.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*782C>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 5/5 | 782 | chr14 | 74261701 | ||||||
| chr14:74261738 | C | T | 1 | a0001c0001t0019 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*819C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 5/5 | 819 | chr14 | 74261738 | ||||||
| chr14:74261904 | C | G | 1 | a0001c0001t0023 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*985C>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 5/5 | 985 | chr14 | 74261904 | ||||||
| chr14:74261993 | C | T | 2 | a0001c0001t0008 a0001c0001t0015 |
8 | HG00280.hp2 HG00733.hp1 HG01255.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1074C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 5/5 | 1074 | chr14 | 74261993 | ||||||
| chr14:74262131 | G | A | 1 | a0001c0001t0004 | 16 | HG00408.hp1 HG00609.hp1 HG02074.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1212G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 5/5 | 1212 | chr14 | 74262131 | ||||||
| chr14:74262171 | C | T | 1 | a0001c0001t0014 | 2 | HG02630.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1252C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 5/5 | 1252 | chr14 | 74262171 | ||||||
| chr14:74262221 | G | A | 4 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0011 others(1): Show |
26 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1302G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 5/5 | 1302 | chr14 | 74262221 | ||||||
| chr14:74262230 | G | A | 1 | a0001c0001t0020 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1311G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 5/5 | 1311 | chr14 | 74262230 | ||||||
| chr14:74262296 | C | T | 1 | a0001c0001t0014 | 2 | HG02630.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1377C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 5/5 | 1377 | chr14 | 74262296 | ||||||
| chr14:74262456 | G | A | 1 | a0001c0001t0022 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1537G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 5/5 | 1537 | chr14 | 74262456 | ||||||
| chr14:74262463 | CTT | C | 10 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0007 others(7): Show |
51 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1548_*1549delTT | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 5/5 | 1548 | INFO_REALIGN_3_PRIME | chr14 | 74262463 | |||||
| chr14:74262504 | A | C | 1 | a0001c0001t0009 | 7 | HG01109.hp1 HG01243.hp2 HG02572.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1585A>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 5/5 | 1585 | chr14 | 74262504 | ||||||
| chr14:74262578 | G | T | 1 | a0001c0002t0018 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1659G>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 5/5 | 1659 | chr14 | 74262578 | ||||||
| chr14:74262722 | A | C | 2 | a0001c0001t0006 a0001c0001t0012 |
13 | HG01081.hp1 HG02451.hp2 HG02486.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1803A>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 5/5 | 1803 | chr14 | 74262722 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74239990 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.370+59G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 1/4 | chr14 | 74239990 | |||||||
| chr14:74240007 | G | T | 5 | a0002c0003t0001g0008 a0002c0003t0001g0053 a0002c0003t0001g0319 others(2): Show |
9 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.370+76G>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 1/4 | chr14 | 74240007 | |||||||
| chr14:74240062 | G | T | 1 | a0001c0007t0007g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.370+131G>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 1/4 | chr14 | 74240062 | |||||||
| chr14:74240110 | C | T | 5 | a0002c0003t0001g0008 a0002c0003t0001g0053 a0002c0003t0001g0319 others(2): Show |
9 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.370+179C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 1/4 | chr14 | 74240110 | |||||||
| chr14:74240147 | C | G | 8 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0022 others(5): Show |
16 | HG00408.hp1 HG00609.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.370+216C>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 1/4 | chr14 | 74240147 | |||||||
| chr14:74240232 | G | A | 3 | a0003c0005t0007g0055 a0003c0005t0007g0056 a0003c0012t0007g0057 |
3 | HG02818.hp2 HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.370+301G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 1/4 | chr14 | 74240232 | |||||||
| chr14:74240291 | G | A | 1 | a0001c0004t0002g0023 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.370+360G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 1/4 | chr14 | 74240291 | |||||||
| chr14:74240394 | C | A | 147 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(144): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.370+463C>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 1/4 | chr14 | 74240394 | |||||||
| chr14:74240585 | C | G | 2 | a0001c0001t0001g0311 a0001c0001t0001g0312 |
2 | HG02559.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.371-597C>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 1/4 | chr14 | 74240585 | |||||||
| chr14:74240832 | T | C | 243 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(240): Show |
319 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.371-350T>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 1/4 | chr14 | 74240832 | |||||||
| chr14:74240863 | A | C | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0238 others(6): Show |
13 | HG01243.hp1 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.371-319A>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 1/4 | chr14 | 74240863 | |||||||
| chr14:74241005 | G | A | 5 | a0002c0003t0001g0008 a0002c0003t0001g0053 a0002c0003t0001g0319 others(2): Show |
9 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.371-177G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 1/4 | chr14 | 74241005 | |||||||
| chr14:74241009 | G | C | 8 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0022 others(5): Show |
16 | HG00408.hp1 HG00609.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.371-173G>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 1/4 | chr14 | 74241009 | |||||||
| chr14:74241021 | C | A | 1 | a0001c0001t0005g0183 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.371-161C>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 1/4 | chr14 | 74241021 | |||||||
| chr14:74241083 | G | A | 3 | a0001c0001t0002g0245 a0001c0001t0002g0246 a0001c0001t0020g0247 |
3 | HG02970.hp1 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.371-99G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 1/4 | chr14 | 74241083 | |||||||
| chr14:74241149 | A | C | 6 | a0001c0001t0002g0021 a0001c0001t0002g0052 a0001c0001t0002g0307 others(3): Show |
9 | HG00438.hp1 HG00558.hp2 NA18965.hp2 others(6): Show |
intron_variant | MODIFIER | c.371-33A>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 1/4 | chr14 | 74241149 | |||||||
| chr14:74241334 | G | T | 1 | a0001c0001t0002g0306 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.455+68G>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74241334 | |||||||
| chr14:74241394 | G | A | 1 | a0001c0002t0010g0012 | 3 | NA18944.hp1 NA18978.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.455+128G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74241394 | |||||||
| chr14:74241426 | G | T | 5 | a0002c0003t0001g0008 a0002c0003t0001g0053 a0002c0003t0001g0319 others(2): Show |
9 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.455+160G>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74241426 | |||||||
| chr14:74241441 | G | C | 242 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(239): Show |
318 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.455+175G>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74241441 | |||||||
| chr14:74241446 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.455+180C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74241446 | |||||||
| chr14:74241482 | C | T | 230 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(227): Show |
303 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.455+216C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74241482 | |||||||
| chr14:74241561 | G | T | 33 | a0001c0001t0001g0233 a0001c0001t0005g0016 a0001c0001t0005g0017 others(30): Show |
44 | HG00280.hp1 HG00639.hp1 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.455+295G>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74241561 | |||||||
| chr14:74241608 | G | C | 243 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(240): Show |
319 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.455+342G>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74241608 | |||||||
| chr14:74241645 | C | T | 1 | a0001c0001t0006g0193 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.455+379C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74241645 | |||||||
| chr14:74241669 | C | T | 8 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0022 others(5): Show |
16 | HG00408.hp1 HG00609.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.455+403C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74241669 | |||||||
| chr14:74241673 | G | A | 2 | a0001c0001t0001g0233 a0001c0001t0003g0248 |
2 | HG03579.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.455+407G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74241673 | |||||||
| chr14:74241674 | C | G | 1 | a0001c0001t0003g0248 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.455+408C>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74241674 | |||||||
| chr14:74241737 | G | A | 13 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0183 others(10): Show |
17 | HG00280.hp1 HG01243.hp1 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.455+471G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74241737 | |||||||
| chr14:74241750 | G | T | 3 | a0001c0001t0001g0040 a0001c0001t0001g0181 a0001c0001t0001g0182 |
4 | NA18966.hp2 NA18989.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.455+484G>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74241750 | |||||||
| chr14:74241755 | G | T | 3 | a0001c0001t0001g0040 a0001c0001t0001g0181 a0001c0001t0001g0182 |
4 | NA18966.hp2 NA18989.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.455+489G>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74241755 | |||||||
| chr14:74241940 | G | GGTTTT | 3 | a0001c0001t0009g0058 a0001c0001t0009g0059 a0001c0001t0009g0060 |
3 | HG02572.hp1 HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.455+700_455+704dup others(5): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74241940 | ||||||
| chr14:74241940 | GGTTTTGT others(3): Show |
G | 1 | a0001c0001t0001g0305 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.455+695_455+704del others(10): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74241940 | ||||||
| chr14:74242007 | C | T | 8 | a0001c0002t0001g0005 a0001c0002t0001g0226 a0001c0002t0001g0227 others(5): Show |
11 | HG01975.hp1 NA18945.hp2 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.455+741C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74242007 | |||||||
| chr14:74242063 | G | T | 1 | a0001c0001t0001g0233 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.455+797G>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74242063 | |||||||
| chr14:74242170 | T | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(204): Show |
268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.455+904T>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74242170 | |||||||
| chr14:74242252 | G | T | 1 | a0001c0001t0002g0310 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.455+986G>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74242252 | |||||||
| chr14:74242351 | T | C | 41 | a0001c0001t0001g0233 a0001c0001t0004g0006 a0001c0001t0004g0007 others(38): Show |
60 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.455+1085T>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74242351 | |||||||
| chr14:74242370 | C | T | 1 | a0001c0006t0003g0304 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.455+1104C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74242370 | |||||||
| chr14:74242426 | C | G | 9 | a0001c0001t0001g0233 a0001c0001t0004g0006 a0001c0001t0004g0007 others(6): Show |
17 | HG00408.hp1 HG00609.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.455+1160C>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74242426 | |||||||
| chr14:74242456 | C | G | 10 | a0001c0001t0006g0013 a0001c0001t0006g0186 a0001c0001t0006g0187 others(7): Show |
13 | HG01081.hp1 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.455+1190C>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74242456 | |||||||
| chr14:74242471 | G | A | 9 | a0001c0001t0001g0233 a0001c0001t0004g0006 a0001c0001t0004g0007 others(6): Show |
17 | HG00408.hp1 HG00609.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.455+1205G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74242471 | |||||||
| chr14:74242587 | A | G | 1 | a0001c0001t0003g0248 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.455+1321A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74242587 | |||||||
| chr14:74242588 | G | A | 1 | a0001c0001t0003g0248 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.455+1322G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74242588 | |||||||
| chr14:74242592 | A | T | 1 | a0001c0001t0003g0248 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.455+1326A>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74242592 | |||||||
| chr14:74242617 | C | CT | 131 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(128): Show |
157 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.455+1367dupT | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74242617 | ||||||
| chr14:74242617 | C | CTT | 6 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0009g0058 others(3): Show |
6 | HG02572.hp1 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.455+1366_455+1367d others(4): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74242617 | ||||||
| chr14:74242617 | CT | C | 68 | a0001c0001t0001g0061 a0001c0001t0001g0233 a0001c0001t0002g0250 others(65): Show |
106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.455+1367delT | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74242617 | ||||||
| chr14:74242617 | CTT | C | 16 | a0001c0001t0002g0249 a0001c0001t0004g0313 a0001c0001t0005g0016 others(13): Show |
24 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.455+1366_455+1367d others(4): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74242617 | ||||||
| chr14:74242651 | C | T | 1 | a0004c0013t0001g0236 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.455+1385C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74242651 | |||||||
| chr14:74242783 | G | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | NA18940.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.455+1517G>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74242783 | |||||||
| chr14:74242799 | G | T | 1 | a0001c0002t0001g0231 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.455+1533G>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74242799 | |||||||
| chr14:74242894 | G | A | 1 | a0001c0001t0004g0314 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.455+1628G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74242894 | |||||||
| chr14:74242899 | G | A | 10 | a0001c0001t0006g0013 a0001c0001t0006g0186 a0001c0001t0006g0187 others(7): Show |
13 | HG01081.hp1 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.455+1633G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74242899 | |||||||
| chr14:74242922 | A | G | 1 | a0001c0001t0003g0302 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.455+1656A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74242922 | |||||||
| chr14:74242987 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.455+1721G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74242987 | |||||||
| chr14:74243046 | G | C | 30 | a0001c0001t0001g0233 a0001c0001t0004g0006 a0001c0001t0004g0007 others(27): Show |
46 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.455+1780G>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74243046 | |||||||
| chr14:74243077 | C | T | 1 | a0001c0001t0005g0243 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.455+1811C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74243077 | |||||||
| chr14:74243223 | G | GT | 3 | a0001c0001t0002g0051 a0001c0001t0002g0301 a0001c0001t0003g0051 |
3 | HG03017.hp1 HG04115.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.456-1939dupT | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74243223 | ||||||
| chr14:74243236 | C | T | 1 | a0001c0001t0008g0174 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.456-1929C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74243236 | |||||||
| chr14:74243294 | G | A | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0238 others(6): Show |
13 | HG01243.hp1 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.456-1871G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74243294 | |||||||
| chr14:74243382 | A | T | 21 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0183 others(18): Show |
29 | HG00280.hp1 HG00639.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.456-1783A>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74243382 | |||||||
| chr14:74243491 | T | C | 2 | a0001c0001t0014g0184 a0001c0001t0014g0185 |
2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.456-1674T>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74243491 | |||||||
| chr14:74243555 | CT | C | 13 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0183 others(10): Show |
17 | HG00280.hp1 HG01243.hp1 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.456-1609delT | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74243555 | |||||||
| chr14:74243585 | T | C | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0238 others(6): Show |
13 | HG01243.hp1 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.456-1580T>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74243585 | |||||||
| chr14:74243675 | C | T | 242 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(239): Show |
318 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.456-1490C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74243675 | |||||||
| chr14:74243709 | C | T | 1 | a0001c0001t0002g0300 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.456-1456C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74243709 | |||||||
| chr14:74243712 | C | G | 17 | a0001c0001t0001g0233 a0001c0001t0004g0006 a0001c0001t0004g0007 others(14): Show |
29 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.456-1453C>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74243712 | |||||||
| chr14:74243717 | GAGAAT | G | 3 | a0003c0005t0007g0055 a0003c0005t0007g0056 a0003c0012t0007g0057 |
3 | HG02818.hp2 HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.456-1445_456-1441d others(7): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74243717 | ||||||
| chr14:74243795 | C | T | 17 | a0001c0001t0001g0233 a0001c0001t0004g0006 a0001c0001t0004g0007 others(14): Show |
29 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.456-1370C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74243795 | |||||||
| chr14:74243826 | T | G | 17 | a0001c0001t0001g0233 a0001c0001t0004g0006 a0001c0001t0004g0007 others(14): Show |
29 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.456-1339T>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74243826 | |||||||
| chr14:74243869 | G | A | 1 | a0001c0002t0001g0194 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.456-1296G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74243869 | |||||||
| chr14:74243948 | G | A | 1 | a0002c0003t0001g0053 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.456-1217G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74243948 | |||||||
| chr14:74244027 | C | T | 242 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(239): Show |
318 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.456-1138C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244027 | |||||||
| chr14:74244095 | G | A | 8 | a0001c0001t0006g0013 a0001c0001t0006g0186 a0001c0001t0006g0187 others(5): Show |
10 | HG01081.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.456-1070G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244095 | |||||||
| chr14:74244161 | C | A | 218 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(215): Show |
283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.456-1004C>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244161 | |||||||
| chr14:74244220 | C | T | 1 | a0001c0001t0020g0247 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.456-945C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244220 | |||||||
| chr14:74244242 | C | G | 1 | a0001c0002t0001g0218 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.456-923C>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244242 | |||||||
| chr14:74244249 | A | G | 1 | a0001c0001t0002g0299 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.456-916A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244249 | |||||||
| chr14:74244300 | C | T | 1 | a0001c0001t0002g0298 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.456-865C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244300 | |||||||
| chr14:74244342 | T | G | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG02135.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.456-823T>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244342 | |||||||
| chr14:74244344 | G | A | 3 | a0003c0005t0007g0055 a0003c0005t0007g0056 a0003c0012t0007g0057 |
3 | HG02818.hp2 HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.456-821G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244344 | |||||||
| chr14:74244371 | G | C | 242 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(239): Show |
318 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.456-794G>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244371 | |||||||
| chr14:74244383 | T | G | 175 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(172): Show |
211 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.456-782T>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244383 | |||||||
| chr14:74244438 | C | T | 8 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0022 others(5): Show |
16 | HG00408.hp1 HG00609.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.456-727C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244438 | |||||||
| chr14:74244546 | G | A | 141 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(138): Show |
168 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.456-619G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244546 | |||||||
| chr14:74244803 | C | A | 9 | a0001c0001t0001g0233 a0002c0003t0001g0008 a0002c0003t0001g0053 others(6): Show |
13 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.456-362C>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244803 | |||||||
| chr14:74244847 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.456-318G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244847 | |||||||
| chr14:74244851 | G | A | 2 | a0001c0001t0005g0238 a0001c0001t0005g0243 |
2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.456-314G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244851 | |||||||
| chr14:74244881 | A | AGT | 4 | a0001c0001t0002g0051 a0001c0001t0002g0295 a0001c0001t0003g0051 others(1): Show |
4 | HG02647.hp2 HG04115.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.456-236_456-235dup others(2): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244881 | ||||||
| chr14:74244881 | A | AGTGT | 3 | a0001c0001t0002g0297 a0001c0001t0012g0192 a0004c0013t0001g0236 |
3 | HG02486.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.456-238_456-235dup others(4): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244881 | ||||||
| chr14:74244881 | AGT | A | 85 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(82): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.456-236_456-235del others(2): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244881 | ||||||
| chr14:74244881 | AGTGT | A | 65 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(62): Show |
81 | HG00609.hp2 HG00642.hp2 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.456-238_456-235del others(4): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244881 | ||||||
| chr14:74244881 | AGTGTGT | A | 17 | a0001c0001t0001g0219 a0001c0001t0002g0047 a0001c0001t0002g0298 others(14): Show |
17 | HG00099.hp2 HG00280.hp1 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.456-240_456-235del others(6): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244881 | ||||||
| chr14:74244881 | AGTGTGTG others(1): Show |
A | 11 | a0001c0001t0001g0305 a0001c0001t0002g0046 a0001c0001t0002g0250 others(8): Show |
14 | HG01081.hp1 HG02145.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.456-242_456-235del others(8): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244881 | ||||||
| chr14:74244881 | AGTGTGTG others(3): Show |
A | 1 | a0001c0001t0003g0254 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.456-244_456-235del others(10): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244881 | ||||||
| chr14:74244881 | AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0002g0253 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.456-246_456-235del others(12): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244881 | ||||||
| chr14:74244881 | AGTGTGTG others(7): Show |
A | 1 | a0001c0001t0004g0317 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.456-248_456-235del others(14): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244881 | ||||||
| chr14:74244881 | AGTGTGTG others(9): Show |
A | 7 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0022 others(4): Show |
15 | HG00408.hp1 HG00609.hp1 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.456-250_456-235del others(16): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244881 | ||||||
| chr14:74244899 | T | TGTGTGTG others(33): Show |
1 | a0001c0002t0001g0210 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.456-253_456-252ins others(40): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244899 | ||||||
| chr14:74244899 | T | TGTGTGTG others(35): Show |
1 | a0001c0002t0018g0217 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.456-251_456-250ins others(42): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244899 | ||||||
| chr14:74244901 | T | TGTGTGTG others(29): Show |
3 | a0001c0002t0001g0194 a0001c0002t0001g0196 a0001c0002t0001g0218 |
3 | HG00741.hp2 HG01106.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.456-255_456-254ins others(36): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244901 | ||||||
| chr14:74244901 | T | TGTGTGTG others(31): Show |
21 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0042 others(18): Show |
38 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.456-253_456-252ins others(38): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244901 | ||||||
| chr14:74244901 | T | TGTGTGTG others(29): Show |
1 | a0001c0002t0001g0211 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.456-251_456-250ins others(36): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244901 | ||||||
| chr14:74244901 | T | TGTGTGTG others(33): Show |
7 | a0001c0002t0001g0004 a0001c0002t0001g0044 a0001c0002t0001g0213 others(4): Show |
13 | HG01099.hp1 HG01168.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.456-251_456-250ins others(40): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244901 | ||||||
| chr14:74244903 | T | TGTGTGTG others(27): Show |
1 | a0001c0002t0001g0195 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.456-255_456-254ins others(34): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244903 | ||||||
| chr14:74244903 | T | TGTGTGTG others(29): Show |
7 | a0001c0002t0001g0009 a0001c0002t0001g0014 a0001c0002t0001g0015 others(4): Show |
13 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.456-253_456-252ins others(36): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244903 | ||||||
| chr14:74244903 | T | TGTGTGTG others(31): Show |
3 | a0001c0002t0001g0043 a0001c0002t0001g0067 a0001c0002t0001g0212 |
4 | HG01123.hp2 HG01255.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.456-251_456-250ins others(38): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244903 | ||||||
| chr14:74244905 | T | TGTGTGTG others(27): Show |
2 | a0001c0002t0001g0062 a0001c0002t0001g0226 |
2 | HG01071.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.456-253_456-252ins others(34): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244905 | ||||||
| chr14:74244907 | T | TGTGTGAA others(25): Show |
2 | a0001c0002t0001g0197 a0001c0002t0001g0198 |
2 | HG01516.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.456-253_456-252ins others(32): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244907 | ||||||
| chr14:74244907 | T | TGTGTGAG others(23): Show |
1 | a0001c0001t0001g0233 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.456-253_456-252ins others(30): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244907 | ||||||
| chr14:74244909 | T | TGAGAGAG others(17): Show |
1 | a0001c0007t0007g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.456-255_456-254ins others(24): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244909 | ||||||
| chr14:74244915 | T | A | 1 | a0003c0005t0007g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.456-250T>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244915 | |||||||
| chr14:74244915 | TGTGTGTG others(77): Show |
T | 1 | a0001c0001t0014g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.456-248_456-165del others(84): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244915 | ||||||
| chr14:74244917 | T | A | 1 | a0003c0005t0007g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.456-248T>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244917 | |||||||
| chr14:74244917 | TGTGTGTG others(75): Show |
T | 1 | a0001c0001t0014g0185 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.456-246_456-165del others(82): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244917 | ||||||
| chr14:74244919 | T | A | 8 | a0002c0003t0001g0008 a0002c0003t0001g0053 a0002c0003t0001g0319 others(5): Show |
12 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.456-246T>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244919 | |||||||
| chr14:74244921 | T | A | 13 | a0001c0001t0001g0100 a0001c0001t0001g0131 a0001c0001t0001g0163 others(10): Show |
17 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.456-244T>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244921 | |||||||
| chr14:74244923 | T | A | 100 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0025 others(97): Show |
117 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.456-242T>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244923 | |||||||
| chr14:74244923 | T | TGA | 12 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0076 others(9): Show |
12 | HG00438.hp2 HG01074.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.456-241_456-240ins others(2): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244923 | ||||||
| chr14:74244925 | T | A | 120 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(117): Show |
139 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.456-240T>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244925 | |||||||
| chr14:74244925 | T | TGA | 5 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0136 others(2): Show |
5 | NA18747.hp2 NA18951.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.456-239_456-238ins others(2): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244925 | ||||||
| chr14:74244925 | T | TGAGA | 17 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0038 others(14): Show |
17 | HG00408.hp2 HG00673.hp1 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.456-239_456-238ins others(4): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244925 | ||||||
| chr14:74244925 | T | TGAGAGAG others(39): Show |
1 | a0001c0001t0001g0032 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.456-239_456-238ins others(46): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244925 | ||||||
| chr14:74244925 | T | TGAGAGAG others(41): Show |
1 | a0001c0001t0001g0134 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.456-239_456-238ins others(48): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244925 | ||||||
| chr14:74244927 | T | A | 145 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(142): Show |
167 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.456-238T>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244927 | |||||||
| chr14:74244927 | T | TGAGA | 4 | a0001c0001t0001g0011 a0001c0001t0001g0145 a0001c0001t0001g0175 others(1): Show |
5 | HG01943.hp2 HG01975.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.456-237_456-236ins others(4): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244927 | ||||||
| chr14:74244927 | T | TGAGAGA | 7 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0135 others(4): Show |
8 | HG00621.hp2 NA18952.hp2 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.456-237_456-236ins others(6): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244927 | ||||||
| chr14:74244927 | T | TGAGAGAG others(41): Show |
1 | a0001c0001t0001g0032 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.456-237_456-236ins others(48): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244927 | ||||||
| chr14:74244929 | T | A | 156 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(153): Show |
184 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.456-236T>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244929 | |||||||
| chr14:74244929 | T | TGAGA | 3 | a0001c0001t0001g0003 a0001c0001t0001g0144 a0001c0001t0001g0160 |
3 | HG02071.hp2 NA18965.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.456-234_456-233ins others(4): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244929 | ||||||
| chr14:74244929 | T | TGAGAGAG others(1): Show |
4 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0138 others(1): Show |
4 | HG03017.hp2 NA18977.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.456-234_456-233ins others(8): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244929 | ||||||
| chr14:74244929 | T | TGAGAGAG others(43): Show |
1 | a0001c0001t0001g0137 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.456-234_456-233ins others(50): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244929 | ||||||
| chr14:74244932 | A | G | 1 | a0001c0007t0007g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.456-233A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244932 | |||||||
| chr14:74244945 | A | AGT | 13 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(10): Show |
13 | HG01516.hp2 HG02056.hp1 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.456-184_456-183dup others(2): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244945 | ||||||
| chr14:74244945 | A | AGTGT | 8 | a0001c0001t0002g0046 a0001c0001t0002g0050 a0001c0001t0002g0264 others(5): Show |
9 | HG00140.hp1 HG01070.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.456-186_456-183dup others(4): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244945 | ||||||
| chr14:74244945 | A | AGTGTGT | 3 | a0001c0001t0002g0019 a0001c0001t0002g0249 a0001c0001t0002g0259 |
3 | NA18950.hp2 NA18961.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.456-188_456-183dup others(6): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244945 | ||||||
| chr14:74244945 | AGT | A | 16 | a0001c0001t0002g0245 a0001c0001t0002g0246 a0001c0001t0002g0290 others(13): Show |
16 | HG00323.hp2 HG00741.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.456-184_456-183del others(2): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244945 | ||||||
| chr14:74244945 | AGTGT | A | 8 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0284 others(5): Show |
11 | HG00099.hp1 HG00733.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.456-186_456-183del others(4): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244945 | ||||||
| chr14:74244945 | AGTGTGTG others(1): Show |
A | 22 | a0001c0001t0002g0295 a0001c0001t0004g0317 a0001c0001t0005g0016 others(19): Show |
29 | HG01081.hp1 HG01243.hp1 HG02258.hp1 others(26): Show |
intron_variant | MODIFIER | c.456-190_456-183del others(8): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244945 | ||||||
| chr14:74244945 | AGTGTGTG others(3): Show |
A | 8 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0022 others(5): Show |
16 | HG00408.hp1 HG00609.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.456-192_456-183del others(10): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244945 | ||||||
| chr14:74244947 | T | A | 1 | a0001c0007t0007g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.456-218T>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244947 | |||||||
| chr14:74244949 | T | A | 1 | a0001c0007t0007g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.456-216T>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244949 | |||||||
| chr14:74244951 | T | A | 1 | a0001c0007t0007g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.456-214T>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244951 | |||||||
| chr14:74244953 | T | A | 1 | a0001c0007t0007g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.456-212T>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244953 | |||||||
| chr14:74244955 | T | A | 1 | a0001c0007t0007g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.456-210T>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244955 | |||||||
| chr14:74244956 | G | A | 1 | a0001c0007t0007g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.456-209G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244956 | |||||||
| chr14:74244957 | T | A | 1 | a0001c0007t0007g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.456-208T>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244957 | |||||||
| chr14:74244957 | T | TGTGTGTG others(27): Show |
1 | a0005c0008t0011g0237 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.456-201_456-200ins others(34): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244957 | ||||||
| chr14:74244957 | T | TGTGTGTG others(29): Show |
11 | a0001c0001t0001g0036 a0001c0001t0001g0070 a0001c0001t0001g0071 others(8): Show |
11 | HG01175.hp2 HG01496.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.456-199_456-198ins others(36): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244957 | ||||||
| chr14:74244959 | T | TGTGAGAG others(23): Show |
4 | a0001c0001t0008g0030 a0001c0001t0008g0074 a0001c0001t0008g0119 others(1): Show |
5 | HG00280.hp2 HG00733.hp1 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.456-203_456-202ins others(30): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244959 | ||||||
| chr14:74244959 | T | TGTGTGAG others(25): Show |
8 | a0001c0001t0001g0031 a0001c0001t0001g0054 a0001c0001t0001g0110 others(5): Show |
8 | HG01109.hp2 HG02818.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.456-201_456-200ins others(32): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244959 | ||||||
| chr14:74244959 | T | TGTGTGTG others(25): Show |
2 | a0001c0001t0001g0035 a0001c0001t0001g0162 |
2 | NA19072.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.456-199_456-198ins others(32): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244959 | ||||||
| chr14:74244959 | T | TGTGTGTG others(27): Show |
116 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(113): Show |
135 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.456-199_456-198ins others(34): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244959 | ||||||
| chr14:74244959 | T | TGTGTGTG others(29): Show |
6 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0219 others(3): Show |
7 | HG02055.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.456-197_456-196ins others(36): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244959 | ||||||
| chr14:74244961 | T | TGTGTGAG others(25): Show |
1 | a0001c0001t0001g0010 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.456-199_456-198ins others(32): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244961 | ||||||
| chr14:74244963 | T | TGTGAGAG others(23): Show |
1 | a0001c0001t0001g0126 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.456-199_456-198ins others(30): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244963 | ||||||
| chr14:74244963 | T | TGTGTGAG others(25): Show |
2 | a0001c0001t0001g0311 a0001c0001t0001g0312 |
2 | HG02559.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.456-197_456-196ins others(32): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244963 | ||||||
| chr14:74244973 | TGTGTGTG others(5): Show |
T | 3 | a0001c0001t0001g0032 a0001c0001t0005g0183 a0001c0001t0005g0234 |
3 | HG00280.hp1 HG01934.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.456-190_456-179del others(12): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244973 | ||||||
| chr14:74244973 | TGTGTGTG others(7): Show |
T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0134 a0001c0001t0001g0137 others(2): Show |
5 | HG02818.hp2 HG06807.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.456-190_456-177del others(14): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244973 | ||||||
| chr14:74244977 | TGTGTGA | T | 5 | a0002c0003t0001g0008 a0002c0003t0001g0053 a0002c0003t0001g0319 others(2): Show |
9 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.456-186_456-181del others(6): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244977 | ||||||
| chr14:74244977 | TGTGTGAG others(3): Show |
T | 1 | a0003c0012t0007g0057 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.456-186_456-177del others(10): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244977 | ||||||
| chr14:74244979 | TGTGA | T | 3 | a0001c0002t0001g0064 a0001c0002t0001g0065 a0001c0002t0001g0066 |
3 | HG00735.hp1 HG01192.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.456-184_456-181del others(4): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244979 | ||||||
| chr14:74244981 | T | A | 15 | a0001c0001t0002g0253 a0001c0001t0002g0290 a0001c0001t0002g0297 others(12): Show |
22 | HG02451.hp2 HG02486.hp1 HG02622.hp1 others(19): Show |
intron_variant | MODIFIER | c.456-184T>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244981 | |||||||
| chr14:74244981 | T | TGA | 3 | a0001c0001t0002g0258 a0001c0001t0002g0278 a0001c0001t0003g0251 |
3 | HG00642.hp2 HG02602.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.456-159_456-158dup others(2): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244981 | ||||||
| chr14:74244981 | TGA | T | 8 | a0001c0001t0002g0265 a0001c0001t0002g0272 a0001c0001t0002g0273 others(5): Show |
8 | HG01074.hp1 HG02559.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.456-159_456-158del others(2): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74244981 | ||||||
| chr14:74244983 | A | T | 156 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(153): Show |
184 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.456-182A>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244983 | |||||||
| chr14:74244985 | A | T | 150 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(147): Show |
176 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.456-180A>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244985 | |||||||
| chr14:74244987 | A | T | 148 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(145): Show |
174 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.456-178A>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244987 | |||||||
| chr14:74244989 | A | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0111 |
2 | HG02015.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.456-176A>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244989 | |||||||
| chr14:74244994 | G | C | 1 | a0001c0001t0001g0152 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.456-171G>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74244994 | |||||||
| chr14:74245000 | G | C | 1 | a0001c0002t0001g0232 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.456-165G>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74245000 | |||||||
| chr14:74245002 | G | C | 41 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0009 others(38): Show |
64 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.456-163G>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74245002 | |||||||
| chr14:74245002 | G | GAC | 7 | a0001c0002t0001g0004 a0001c0002t0001g0042 a0001c0002t0001g0043 others(4): Show |
14 | HG01081.hp2 HG01123.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.456-162_456-161ins others(2): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 74245002 | ||||||
| chr14:74245006 | G | C | 26 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0022 others(23): Show |
42 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.456-159G>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74245006 | |||||||
| chr14:74245008 | C | G | 77 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0022 others(74): Show |
123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.456-157C>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74245008 | |||||||
| chr14:74245016 | G | C | 2 | a0001c0001t0014g0184 a0001c0001t0014g0185 |
2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.456-149G>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74245016 | |||||||
| chr14:74245024 | G | C | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0238 others(6): Show |
13 | HG01243.hp1 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.456-141G>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74245024 | |||||||
| chr14:74245028 | G | T | 1 | a0001c0001t0011g0235 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.456-137G>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74245028 | |||||||
| chr14:74245054 | A | C | 1 | a0001c0001t0004g0313 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.456-111A>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74245054 | |||||||
| chr14:74245069 | C | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0173 |
2 | HG01358.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.456-96C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 2/4 | chr14 | 74245069 | |||||||
| chr14:74245374 | G | A | 1 | a0001c0001t0002g0306 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.579+86G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74245374 | |||||||
| chr14:74245465 | C | T | 1 | a0004c0013t0001g0236 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.579+177C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74245465 | |||||||
| chr14:74245466 | G | A | 1 | a0001c0001t0002g0271 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.579+178G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74245466 | |||||||
| chr14:74245564 | G | A | 149 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(146): Show |
179 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.579+276G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74245564 | |||||||
| chr14:74245566 | G | T | 1 | a0001c0001t0001g0172 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.579+278G>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74245566 | |||||||
| chr14:74245728 | C | T | 5 | a0002c0003t0001g0008 a0002c0003t0001g0053 a0002c0003t0001g0319 others(2): Show |
9 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.579+440C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74245728 | |||||||
| chr14:74245731 | C | T | 1 | a0001c0002t0001g0216 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.579+443C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74245731 | |||||||
| chr14:74245767 | C | A | 2 | a0001c0001t0007g0078 a0001c0001t0011g0077 |
2 | HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.579+479C>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74245767 | |||||||
| chr14:74245835 | G | C | 10 | a0001c0001t0006g0013 a0001c0001t0006g0186 a0001c0001t0006g0187 others(7): Show |
13 | HG01081.hp1 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.579+547G>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74245835 | |||||||
| chr14:74245841 | C | T | 1 | a0001c0001t0003g0263 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.579+553C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74245841 | |||||||
| chr14:74245920 | G | A | 4 | a0001c0002t0001g0014 a0001c0002t0001g0197 a0001c0002t0001g0201 others(1): Show |
6 | HG00639.hp2 HG01255.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.579+632G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74245920 | |||||||
| chr14:74245993 | C | T | 202 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(199): Show |
262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.579+705C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74245993 | |||||||
| chr14:74246201 | C | T | 1 | a0001c0001t0002g0280 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.579+913C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74246201 | |||||||
| chr14:74246504 | G | A | 1 | a0001c0001t0003g0260 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.579+1216G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74246504 | |||||||
| chr14:74246512 | T | A | 1 | a0001c0001t0001g0132 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.579+1224T>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74246512 | |||||||
| chr14:74246570 | T | A | 201 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(198): Show |
261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.579+1282T>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74246570 | |||||||
| chr14:74246612 | C | T | 5 | a0001c0001t0004g0007 a0001c0001t0004g0022 a0001c0001t0004g0313 others(2): Show |
10 | NA18967.hp1 NA18972.hp2 NA19003.hp2 others(7): Show |
intron_variant | MODIFIER | c.579+1324C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74246612 | |||||||
| chr14:74246716 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.579+1428G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74246716 | |||||||
| chr14:74246757 | C | T | 3 | a0001c0001t0013g0223 a0001c0001t0013g0224 a0001c0001t0013g0225 |
3 | HG01109.hp2 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.579+1469C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74246757 | |||||||
| chr14:74246758 | G | A | 1 | a0001c0001t0002g0298 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.579+1470G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74246758 | |||||||
| chr14:74246775 | A | T | 1 | a0001c0001t0001g0130 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.579+1487A>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74246775 | |||||||
| chr14:74246831 | G | A | 150 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(147): Show |
180 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.579+1543G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74246831 | |||||||
| chr14:74246979 | A | C | 200 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(197): Show |
260 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.579+1691A>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74246979 | |||||||
| chr14:74247087 | C | T | 5 | a0002c0003t0001g0008 a0002c0003t0001g0053 a0002c0003t0001g0319 others(2): Show |
9 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.579+1799C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74247087 | |||||||
| chr14:74247100 | A | G | 244 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(241): Show |
321 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.579+1812A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74247100 | |||||||
| chr14:74247105 | G | C | 49 | a0001c0001t0001g0129 a0001c0002t0001g0001 a0001c0002t0001g0004 others(46): Show |
79 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.579+1817G>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74247105 | |||||||
| chr14:74247210 | C | T | 2 | a0001c0001t0001g0311 a0001c0001t0001g0312 |
2 | HG02559.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.579+1922C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74247210 | |||||||
| chr14:74247305 | A | C | 5 | a0002c0003t0001g0008 a0002c0003t0001g0053 a0002c0003t0001g0319 others(2): Show |
9 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.579+2017A>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74247305 | |||||||
| chr14:74247325 | G | A | 10 | a0001c0001t0006g0013 a0001c0001t0006g0186 a0001c0001t0006g0187 others(7): Show |
13 | HG01081.hp1 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.579+2037G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74247325 | |||||||
| chr14:74247340 | G | A | 1 | a0001c0001t0011g0077 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.579+2052G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74247340 | |||||||
| chr14:74247389 | G | A | 5 | a0002c0003t0001g0008 a0002c0003t0001g0053 a0002c0003t0001g0319 others(2): Show |
9 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.579+2101G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74247389 | |||||||
| chr14:74247407 | G | C | 1 | a0001c0001t0011g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.579+2119G>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74247407 | |||||||
| chr14:74247456 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0024g0096 |
3 | HG01168.hp1 HG01346.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.579+2168G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74247456 | |||||||
| chr14:74247500 | C | T | 5 | a0001c0001t0001g0045 a0001c0001t0001g0219 a0001c0001t0001g0220 others(2): Show |
6 | HG02055.hp1 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.579+2212C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74247500 | |||||||
| chr14:74247502 | G | T | 2 | a0001c0001t0014g0184 a0001c0001t0014g0185 |
2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.579+2214G>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74247502 | |||||||
| chr14:74247716 | G | T | 1 | a0003c0012t0007g0057 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.579+2428G>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74247716 | |||||||
| chr14:74247717 | G | C | 1 | a0001c0001t0007g0078 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.579+2429G>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74247717 | |||||||
| chr14:74247724 | T | C | 8 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0022 others(5): Show |
16 | HG00408.hp1 HG00609.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.579+2436T>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74247724 | |||||||
| chr14:74247800 | T | TA | 61 | a0001c0001t0001g0129 a0001c0001t0002g0249 a0001c0001t0014g0184 others(58): Show |
95 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.579+2525dupA | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74247800 | ||||||
| chr14:74247801 | A | T | 3 | a0001c0001t0006g0186 a0001c0001t0006g0190 a0001c0001t0006g0191 |
3 | HG01081.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.579+2513A>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74247801 | |||||||
| chr14:74247855 | G | A | 3 | a0003c0005t0007g0055 a0003c0005t0007g0056 a0003c0012t0007g0057 |
3 | HG02818.hp2 HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.579+2567G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74247855 | |||||||
| chr14:74247965 | CA | C | 5 | a0001c0001t0001g0045 a0001c0001t0001g0219 a0001c0001t0001g0220 others(2): Show |
6 | HG02055.hp1 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.579+2678delA | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74247965 | |||||||
| chr14:74248064 | A | G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0094 |
5 | HG02572.hp2 HG02809.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+2776A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74248064 | |||||||
| chr14:74248118 | C | T | 1 | a0001c0001t0003g0302 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.579+2830C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74248118 | |||||||
| chr14:74248334 | T | TA | 75 | a0001c0001t0001g0129 a0001c0001t0002g0249 a0001c0001t0002g0264 others(72): Show |
112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.579+3063dupA | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74248334 | ||||||
| chr14:74248334 | T | TAA | 6 | a0001c0001t0001g0162 a0001c0001t0001g0177 a0001c0001t0019g0176 others(3): Show |
6 | HG02129.hp1 NA18951.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.579+3062_579+3063d others(4): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74248334 | ||||||
| chr14:74248334 | T | TAAA | 36 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0028 others(33): Show |
47 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.579+3061_579+3063d others(5): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74248334 | ||||||
| chr14:74248334 | T | TAAAA | 25 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0027 others(22): Show |
29 | HG00558.hp1 HG00673.hp1 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.579+3060_579+3063d others(6): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74248334 | ||||||
| chr14:74248334 | T | TAAAAA | 10 | a0001c0001t0001g0032 a0001c0001t0001g0069 a0001c0001t0001g0085 others(7): Show |
11 | HG00741.hp1 HG01175.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.579+3059_579+3063d others(7): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74248334 | ||||||
| chr14:74248351 | AC | A | 6 | a0001c0001t0001g0045 a0001c0001t0001g0219 a0001c0001t0001g0220 others(3): Show |
7 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.579+3064delC | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74248351 | |||||||
| chr14:74248352 | C | A | 143 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(140): Show |
169 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.579+3064C>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74248352 | |||||||
| chr14:74248357 | A | AAAC | 35 | a0001c0001t0001g0031 a0001c0001t0001g0036 a0001c0001t0001g0037 others(32): Show |
42 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.579+3071_579+3072i others(5): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74248357 | ||||||
| chr14:74248357 | A | AAC | 7 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0094 others(4): Show |
9 | HG01515.hp2 HG02572.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.579+3070_579+3071i others(4): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74248357 | ||||||
| chr14:74248357 | A | C | 1 | a0001c0001t0001g0028 | 2 | HG02129.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.579+3069A>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74248357 | |||||||
| chr14:74248361 | C | A | 188 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(185): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.579+3073C>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74248361 | |||||||
| chr14:74248361 | C | CAAAA | 14 | a0001c0001t0001g0040 a0001c0001t0001g0079 a0001c0001t0001g0080 others(11): Show |
15 | HG02015.hp1 HG02135.hp1 HG02683.hp2 others(12): Show |
intron_variant | MODIFIER | c.579+3073_579+3074i others(6): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74248361 | |||||||
| chr14:74248362 | C | A | 5 | a0001c0001t0001g0032 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
6 | NA18941.hp1 NA18960.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.579+3074C>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74248362 | |||||||
| chr14:74248465 | T | C | 1 | a0001c0001t0011g0235 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.579+3177T>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74248465 | |||||||
| chr14:74248547 | C | T | 200 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(197): Show |
260 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.579+3259C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74248547 | |||||||
| chr14:74248646 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.579+3358G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74248646 | |||||||
| chr14:74248698 | A | C | 1 | a0001c0001t0004g0317 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.579+3410A>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74248698 | |||||||
| chr14:74248701 | G | T | 1 | a0001c0001t0004g0317 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.579+3413G>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74248701 | |||||||
| chr14:74248703 | A | G | 1 | a0001c0001t0004g0317 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.579+3415A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74248703 | |||||||
| chr14:74248704 | C | A | 1 | a0001c0001t0004g0317 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.579+3416C>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74248704 | |||||||
| chr14:74248704 | C | CA | 232 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(229): Show |
297 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.579+3428dupA | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74248704 | ||||||
| chr14:74248704 | C | CAA | 19 | a0001c0001t0001g0164 a0001c0001t0004g0006 a0001c0001t0004g0007 others(16): Show |
30 | HG00408.hp1 HG00609.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.579+3427_579+3428d others(4): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74248704 | ||||||
| chr14:74248705 | A | T | 1 | a0001c0001t0004g0317 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.579+3417A>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74248705 | |||||||
| chr14:74248706 | A | C | 1 | a0001c0001t0004g0317 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.579+3418A>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74248706 | |||||||
| chr14:74248707 | A | G | 1 | a0001c0001t0004g0317 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.579+3419A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74248707 | |||||||
| chr14:74248708 | A | C | 1 | a0001c0001t0004g0317 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.579+3420A>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74248708 | |||||||
| chr14:74248709 | A | G | 1 | a0001c0001t0004g0317 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.579+3421A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74248709 | |||||||
| chr14:74248710 | A | T | 1 | a0001c0001t0004g0317 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.579+3422A>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74248710 | |||||||
| chr14:74248711 | A | G | 1 | a0001c0001t0004g0317 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.579+3423A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74248711 | |||||||
| chr14:74248712 | A | T | 1 | a0001c0001t0004g0317 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.579+3424A>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74248712 | |||||||
| chr14:74248713 | A | T | 1 | a0001c0001t0004g0317 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.579+3425A>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74248713 | |||||||
| chr14:74248773 | C | T | 2 | a0001c0001t0002g0264 a0001c0001t0002g0277 |
2 | NA19009.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.579+3485C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74248773 | |||||||
| chr14:74248978 | C | G | 8 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0022 others(5): Show |
16 | HG00408.hp1 HG00609.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.579+3690C>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74248978 | |||||||
| chr14:74248996 | T | C | 8 | a0001c0001t0006g0013 a0001c0001t0006g0186 a0001c0001t0006g0187 others(5): Show |
10 | HG01081.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.579+3708T>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74248996 | |||||||
| chr14:74249004 | C | G | 1 | a0001c0001t0005g0234 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.579+3716C>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74249004 | |||||||
| chr14:74249193 | C | T | 241 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(238): Show |
317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.579+3905C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74249193 | |||||||
| chr14:74249201 | T | C | 1 | a0001c0001t0011g0235 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.579+3913T>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74249201 | |||||||
| chr14:74249243 | A | C | 45 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0032 others(42): Show |
56 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.579+3955A>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74249243 | |||||||
| chr14:74249421 | C | T | 1 | a0001c0001t0011g0077 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.579+4133C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74249421 | |||||||
| chr14:74249427 | T | C | 50 | a0001c0001t0001g0129 a0001c0002t0001g0001 a0001c0002t0001g0004 others(47): Show |
80 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.579+4139T>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74249427 | |||||||
| chr14:74249459 | G | A | 1 | a0001c0002t0001g0064 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.579+4171G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74249459 | |||||||
| chr14:74249533 | G | T | 1 | a0001c0001t0002g0259 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.579+4245G>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74249533 | |||||||
| chr14:74249556 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0161 |
2 | NA19009.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.579+4268C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74249556 | |||||||
| chr14:74249619 | C | T | 2 | a0001c0001t0014g0184 a0001c0001t0014g0185 |
2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.579+4331C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74249619 | |||||||
| chr14:74249800 | A | G | 244 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(241): Show |
321 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.579+4512A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74249800 | |||||||
| chr14:74249860 | G | C | 3 | a0001c0001t0006g0013 a0001c0001t0006g0187 a0001c0001t0006g0193 |
5 | HG02451.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+4572G>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74249860 | |||||||
| chr14:74249950 | T | TTAAA | 5 | a0002c0003t0001g0008 a0002c0003t0001g0053 a0002c0003t0001g0319 others(2): Show |
9 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.579+4679_579+4682d others(6): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74249950 | ||||||
| chr14:74249972 | C | T | 241 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(238): Show |
317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.579+4684C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74249972 | |||||||
| chr14:74250146 | A | G | 1 | a0001c0002t0001g0207 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.579+4858A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74250146 | |||||||
| chr14:74250150 | T | A | 1 | a0001c0002t0001g0213 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.579+4862T>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74250150 | |||||||
| chr14:74250235 | TCA | T | 4 | a0001c0001t0011g0133 a0003c0005t0007g0055 a0003c0005t0007g0056 others(1): Show |
4 | HG01884.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+4948_579+4949d others(4): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74250235 | |||||||
| chr14:74250236 | CA | C | 84 | a0001c0001t0001g0305 a0001c0001t0002g0002 a0001c0001t0002g0018 others(81): Show |
97 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.579+4961delA | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74250236 | ||||||
| chr14:74250248 | AAT | A | 222 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(219): Show |
297 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.579+4961_579+4962d others(4): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74250248 | |||||||
| chr14:74250248 | AATT | A | 8 | a0001c0001t0001g0045 a0001c0001t0001g0219 a0001c0001t0001g0220 others(5): Show |
9 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.579+4961_579+4963d others(5): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74250248 | |||||||
| chr14:74250249 | A | T | 3 | a0001c0006t0003g0002 a0001c0006t0003g0281 a0001c0006t0003g0304 |
3 | NA18966.hp1 NA18977.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.579+4961A>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74250249 | |||||||
| chr14:74250250 | T | A | 4 | a0001c0001t0011g0133 a0003c0005t0007g0055 a0003c0005t0007g0056 others(1): Show |
4 | HG01884.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+4962T>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74250250 | |||||||
| chr14:74250468 | G | A | 3 | a0001c0001t0003g0251 a0001c0001t0003g0267 a0001c0001t0003g0283 |
3 | NA19002.hp2 NA19005.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.579+5180G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74250468 | |||||||
| chr14:74250554 | T | C | 1 | a0001c0004t0002g0023 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.579+5266T>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74250554 | |||||||
| chr14:74250560 | T | G | 1 | a0001c0001t0001g0147 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.579+5272T>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74250560 | |||||||
| chr14:74250562 | CCTCTTCT others(7): Show |
C | 1 | a0001c0001t0001g0147 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.579+5276_579+5289d others(16): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74250562 | ||||||
| chr14:74250601 | A | G | 202 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(199): Show |
263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.579+5313A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74250601 | |||||||
| chr14:74250675 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.579+5387C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74250675 | |||||||
| chr14:74250704 | A | AT | 51 | a0001c0001t0001g0129 a0001c0001t0004g0317 a0001c0002t0001g0001 others(48): Show |
81 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.579+5426dupT | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74250704 | ||||||
| chr14:74250706 | T | G | 146 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(143): Show |
177 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.579+5418T>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74250706 | |||||||
| chr14:74250771 | C | T | 1 | a0001c0002t0001g0206 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.579+5483C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74250771 | |||||||
| chr14:74250802 | C | A | 202 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(199): Show |
263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.579+5514C>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74250802 | |||||||
| chr14:74250868 | C | G | 5 | a0002c0003t0001g0008 a0002c0003t0001g0053 a0002c0003t0001g0319 others(2): Show |
9 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.579+5580C>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74250868 | |||||||
| chr14:74250919 | T | C | 5 | a0002c0003t0001g0008 a0002c0003t0001g0053 a0002c0003t0001g0319 others(2): Show |
9 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.579+5631T>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74250919 | |||||||
| chr14:74250996 | C | A | 209 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(206): Show |
273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.579+5708C>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74250996 | |||||||
| chr14:74251124 | G | A | 8 | a0001c0001t0006g0013 a0001c0001t0006g0186 a0001c0001t0006g0187 others(5): Show |
10 | HG01081.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.579+5836G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74251124 | |||||||
| chr14:74251189 | C | T | 6 | a0001c0001t0001g0076 a0001c0001t0001g0109 a0001c0001t0001g0124 others(3): Show |
6 | HG01074.hp2 HG01099.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.579+5901C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74251189 | |||||||
| chr14:74251199 | C | T | 241 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(238): Show |
317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.579+5911C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74251199 | |||||||
| chr14:74251211 | A | T | 3 | a0001c0001t0013g0223 a0001c0001t0013g0224 a0001c0001t0013g0225 |
3 | HG01109.hp2 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.579+5923A>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74251211 | |||||||
| chr14:74251217 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.579+5929A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74251217 | |||||||
| chr14:74251231 | C | T | 9 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0022 others(6): Show |
19 | HG00408.hp1 HG00609.hp1 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.579+5943C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74251231 | |||||||
| chr14:74251403 | T | C | 1 | a0001c0007t0007g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.579+6115T>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74251403 | |||||||
| chr14:74251407 | G | T | 1 | a0001c0001t0011g0077 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.579+6119G>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74251407 | |||||||
| chr14:74251434 | G | C | 1 | a0001c0001t0001g0117 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.579+6146G>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74251434 | |||||||
| chr14:74251486 | C | T | 49 | a0001c0001t0001g0129 a0001c0002t0001g0001 a0001c0002t0001g0004 others(46): Show |
79 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.579+6198C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74251486 | |||||||
| chr14:74251543 | G | C | 1 | a0001c0001t0005g0239 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.579+6255G>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74251543 | |||||||
| chr14:74251577 | G | C | 200 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(197): Show |
260 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.579+6289G>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74251577 | |||||||
| chr14:74251819 | CAG | C | 136 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(133): Show |
162 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.579+6534_579+6535d others(4): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74251819 | ||||||
| chr14:74252037 | T | C | 1 | a0001c0001t0001g0163 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.579+6749T>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74252037 | |||||||
| chr14:74252096 | T | G | 241 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(238): Show |
317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.579+6808T>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74252096 | |||||||
| chr14:74252138 | T | A | 1 | a0001c0001t0002g0268 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.579+6850T>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74252138 | |||||||
| chr14:74252138 | T | C | 8 | a0001c0001t0006g0013 a0001c0001t0006g0186 a0001c0001t0006g0187 others(5): Show |
10 | HG01081.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.579+6850T>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74252138 | |||||||
| chr14:74252389 | TC | T | 72 | a0001c0001t0001g0129 a0001c0001t0001g0311 a0001c0001t0001g0312 others(69): Show |
107 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.579+7102delC | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74252389 | |||||||
| chr14:74252390 | C | T | 169 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(166): Show |
210 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.579+7102C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74252390 | |||||||
| chr14:74252394 | C | CT | 15 | a0001c0001t0001g0035 a0001c0001t0002g0246 a0001c0001t0005g0016 others(12): Show |
20 | HG00280.hp1 HG01243.hp1 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.579+7120dupT | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74252394 | ||||||
| chr14:74252394 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.579+7106C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74252394 | |||||||
| chr14:74252394 | CT | C | 34 | a0001c0001t0001g0099 a0001c0001t0001g0150 a0001c0001t0001g0311 others(31): Show |
41 | HG00438.hp2 HG00639.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.579+7120delT | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74252394 | ||||||
| chr14:74252395 | T | C | 1 | a0001c0001t0001g0182 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.579+7107T>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74252395 | |||||||
| chr14:74252467 | T | C | 1 | a0001c0007t0007g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.580-7135T>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74252467 | |||||||
| chr14:74252498 | CTCCTGCC others(13): Show |
C | 160 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(157): Show |
199 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.580-7102_580-7083d others(22): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74252498 | ||||||
| chr14:74252680 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0108 a0001c0001t0001g0160 |
5 | HG01928.hp2 HG01943.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-6922C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74252680 | |||||||
| chr14:74252715 | G | A | 5 | a0001c0001t0001g0035 a0001c0001t0001g0147 a0001c0001t0001g0150 others(2): Show |
6 | NA18747.hp2 NA18993.hp1 NA19063.hp2 others(3): Show |
intron_variant | MODIFIER | c.580-6887G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74252715 | |||||||
| chr14:74252738 | G | A | 1 | a0001c0007t0007g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.580-6864G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74252738 | |||||||
| chr14:74252822 | C | T | 20 | a0001c0001t0009g0058 a0001c0001t0009g0059 a0001c0001t0009g0060 others(17): Show |
25 | HG00438.hp2 HG00639.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.580-6780C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74252822 | |||||||
| chr14:74252823 | G | A | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0178 others(1): Show |
4 | HG00597.hp1 HG02027.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-6779G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74252823 | |||||||
| chr14:74253048 | C | CA | 121 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(118): Show |
148 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.580-6535dupA | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74253048 | ||||||
| chr14:74253048 | C | CAA | 19 | a0001c0001t0001g0082 a0001c0001t0001g0152 a0001c0001t0001g0165 others(16): Show |
27 | HG00408.hp1 HG00609.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.580-6536_580-6535d others(4): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74253048 | ||||||
| chr14:74253048 | C | CAAA | 14 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0183 others(11): Show |
18 | HG00280.hp1 HG01243.hp1 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.580-6537_580-6535d others(5): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74253048 | ||||||
| chr14:74253048 | CA | C | 109 | a0001c0001t0001g0305 a0001c0001t0002g0002 a0001c0001t0002g0018 others(106): Show |
129 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.580-6535delA | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74253048 | ||||||
| chr14:74253048 | CAA | C | 8 | a0001c0001t0002g0276 a0001c0001t0002g0288 a0001c0001t0003g0254 others(5): Show |
8 | HG01081.hp1 HG02818.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.580-6536_580-6535d others(4): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74253048 | ||||||
| chr14:74253130 | G | A | 127 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(124): Show |
153 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.580-6472G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74253130 | |||||||
| chr14:74253243 | C | A | 1 | a0001c0001t0017g0222 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.580-6359C>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74253243 | |||||||
| chr14:74253245 | T | A | 1 | a0001c0001t0001g0153 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.580-6357T>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74253245 | |||||||
| chr14:74253262 | C | G | 2 | a0001c0001t0014g0184 a0001c0001t0014g0185 |
2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.580-6340C>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74253262 | |||||||
| chr14:74253348 | G | T | 1 | a0001c0001t0001g0182 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.580-6254G>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74253348 | |||||||
| chr14:74253351 | T | G | 1 | a0001c0001t0001g0182 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.580-6251T>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74253351 | |||||||
| chr14:74253352 | G | T | 1 | a0001c0001t0001g0182 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.580-6250G>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74253352 | |||||||
| chr14:74253396 | G | T | 8 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0022 others(5): Show |
16 | HG00408.hp1 HG00609.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.580-6206G>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74253396 | |||||||
| chr14:74253433 | T | A | 1 | a0001c0001t0001g0182 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.580-6169T>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74253433 | |||||||
| chr14:74253495 | A | T | 1 | a0001c0001t0001g0182 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.580-6107A>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74253495 | |||||||
| chr14:74253554 | C | T | 7 | a0002c0003t0001g0008 a0002c0003t0001g0053 a0002c0003t0001g0148 others(4): Show |
11 | HG00438.hp2 HG00639.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.580-6048C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74253554 | |||||||
| chr14:74253558 | C | T | 5 | a0001c0001t0001g0045 a0001c0001t0001g0219 a0001c0001t0001g0220 others(2): Show |
6 | HG02055.hp1 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.580-6044C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74253558 | |||||||
| chr14:74253619 | G | A | 7 | a0001c0001t0001g0028 a0001c0001t0001g0117 a0001c0001t0001g0118 others(4): Show |
8 | HG00597.hp2 HG02027.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.580-5983G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74253619 | |||||||
| chr14:74253697 | G | A | 5 | a0001c0001t0001g0045 a0001c0001t0001g0219 a0001c0001t0001g0220 others(2): Show |
6 | HG02055.hp1 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.580-5905G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74253697 | |||||||
| chr14:74253730 | A | T | 1 | a0001c0001t0001g0182 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.580-5872A>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74253730 | |||||||
| chr14:74253743 | C | A | 1 | a0001c0001t0001g0182 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.580-5859C>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74253743 | |||||||
| chr14:74253848 | C | A | 1 | a0001c0001t0007g0078 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.580-5754C>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74253848 | |||||||
| chr14:74253887 | G | A | 1 | a0001c0001t0002g0265 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.580-5715G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74253887 | |||||||
| chr14:74253908 | C | A | 1 | a0001c0007t0007g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.580-5694C>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74253908 | |||||||
| chr14:74253918 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.580-5684G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74253918 | |||||||
| chr14:74253941 | T | A | 8 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0022 others(5): Show |
16 | HG00408.hp1 HG00609.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.580-5661T>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74253941 | |||||||
| chr14:74253971 | C | T | 8 | a0001c0001t0006g0013 a0001c0001t0006g0186 a0001c0001t0006g0187 others(5): Show |
10 | HG01081.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.580-5631C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74253971 | |||||||
| chr14:74254070 | A | G | 279 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(276): Show |
338 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.580-5532A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74254070 | |||||||
| chr14:74254080 | C | T | 2 | a0001c0001t0014g0184 a0001c0001t0014g0185 |
2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.580-5522C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74254080 | |||||||
| chr14:74254131 | C | T | 13 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0183 others(10): Show |
17 | HG00280.hp1 HG01243.hp1 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.580-5471C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74254131 | |||||||
| chr14:74254132 | A | G | 271 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(268): Show |
328 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.580-5470A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74254132 | |||||||
| chr14:74254171 | A | G | 8 | a0001c0001t0006g0013 a0001c0001t0006g0186 a0001c0001t0006g0187 others(5): Show |
10 | HG01081.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.580-5431A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74254171 | |||||||
| chr14:74254271 | C | T | 1 | a0001c0007t0007g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.580-5331C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74254271 | |||||||
| chr14:74254341 | G | T | 7 | a0002c0003t0001g0008 a0002c0003t0001g0053 a0002c0003t0001g0148 others(4): Show |
11 | HG00438.hp2 HG00639.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.580-5261G>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74254341 | |||||||
| chr14:74254360 | A | G | 278 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(275): Show |
337 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.580-5242A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74254360 | |||||||
| chr14:74254389 | CGACA | C | 8 | a0001c0001t0006g0013 a0001c0001t0006g0186 a0001c0001t0006g0187 others(5): Show |
10 | HG01081.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.580-5206_580-5203d others(6): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74254389 | ||||||
| chr14:74254402 | G | A | 1 | a0001c0001t0002g0284 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.580-5200G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74254402 | |||||||
| chr14:74254421 | A | T | 1 | a0005c0008t0011g0237 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.580-5181A>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74254421 | |||||||
| chr14:74254571 | T | C | 8 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0022 others(5): Show |
16 | HG00408.hp1 HG00609.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.580-5031T>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74254571 | |||||||
| chr14:74254654 | C | T | 1 | a0001c0001t0002g0282 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.580-4948C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74254654 | |||||||
| chr14:74254655 | G | T | 8 | a0001c0001t0006g0013 a0001c0001t0006g0186 a0001c0001t0006g0187 others(5): Show |
10 | HG01081.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.580-4947G>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74254655 | |||||||
| chr14:74254658 | T | C | 259 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(256): Show |
313 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.580-4944T>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74254658 | |||||||
| chr14:74254784 | A | AT | 18 | a0001c0001t0001g0233 a0001c0001t0009g0058 a0001c0001t0009g0059 others(15): Show |
23 | HG00438.hp2 HG00639.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.580-4805dupT | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74254784 | ||||||
| chr14:74254784 | A | ATT | 11 | a0001c0001t0006g0013 a0001c0001t0006g0186 a0001c0001t0006g0187 others(8): Show |
13 | HG01081.hp1 HG02451.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.580-4806_580-4805d others(4): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74254784 | ||||||
| chr14:74254784 | A | ATTTTTT | 5 | a0001c0001t0002g0050 a0001c0001t0002g0253 a0001c0001t0002g0256 others(2): Show |
6 | HG01070.hp2 HG01192.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.580-4810_580-4805d others(8): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74254784 | ||||||
| chr14:74254784 | A | ATTTTTTT | 79 | a0001c0001t0001g0132 a0001c0001t0001g0305 a0001c0001t0002g0002 others(76): Show |
91 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.580-4811_580-4805d others(9): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74254784 | ||||||
| chr14:74254784 | A | ATTTTTTT others(1): Show |
8 | a0001c0001t0002g0275 a0001c0001t0002g0279 a0001c0001t0002g0287 others(5): Show |
8 | HG00280.hp1 HG00735.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.580-4812_580-4805d others(10): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74254784 | ||||||
| chr14:74254784 | A | ATTTTTTT others(3): Show |
2 | a0001c0001t0001g0134 a0001c0001t0001g0139 |
2 | NA18974.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.580-4814_580-4805d others(12): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74254784 | ||||||
| chr14:74254784 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0001g0219 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.580-4817_580-4805d others(15): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74254784 | ||||||
| chr14:74254784 | A | ATTTTTTT others(8): Show |
8 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0313 others(5): Show |
14 | HG00408.hp1 HG00609.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.580-4805_580-4804i others(17): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74254784 | ||||||
| chr14:74254784 | A | ATTTTTTT others(9): Show |
2 | a0001c0001t0001g0091 a0001c0001t0004g0022 |
4 | HG03831.hp1 NA19010.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-4805_580-4804i others(18): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74254784 | ||||||
| chr14:74254784 | A | ATTTTTTT others(10): Show |
2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG02109.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.580-4805_580-4804i others(19): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74254784 | ||||||
| chr14:74254784 | A | ATTTTTTT others(11): Show |
1 | a0001c0001t0007g0078 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.580-4805_580-4804i others(20): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74254784 | ||||||
| chr14:74254784 | A | ATTTTTTT others(13): Show |
1 | a0003c0012t0007g0057 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.580-4805_580-4804i others(22): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74254784 | ||||||
| chr14:74254784 | A | ATTTTTTT others(14): Show |
1 | a0001c0001t0008g0074 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.580-4805_580-4804i others(23): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74254784 | ||||||
| chr14:74254784 | A | ATTTTTTT others(15): Show |
3 | a0001c0001t0001g0094 a0001c0001t0008g0029 a0003c0005t0007g0055 |
4 | HG01257.hp2 HG01258.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-4805_580-4804i others(24): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74254784 | ||||||
| chr14:74254784 | A | ATTTTTTT others(16): Show |
21 | a0001c0001t0001g0025 a0001c0001t0001g0036 a0001c0001t0001g0040 others(18): Show |
25 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.580-4805_580-4804i others(25): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74254784 | ||||||
| chr14:74254784 | A | ATTTTTTT others(17): Show |
57 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0028 others(54): Show |
68 | HG00558.hp1 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.580-4805_580-4804i others(26): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74254784 | ||||||
| chr14:74254784 | A | ATTTTTTT others(18): Show |
41 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0027 others(38): Show |
55 | HG00140.hp2 HG00408.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.580-4805_580-4804i others(27): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74254784 | ||||||
| chr14:74254784 | A | ATTTTTTT others(19): Show |
8 | a0001c0001t0001g0024 a0001c0001t0001g0081 a0001c0001t0001g0108 others(5): Show |
9 | HG01168.hp1 HG01346.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.580-4805_580-4804i others(28): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74254784 | ||||||
| chr14:74254784 | A | ATTTTTTT others(20): Show |
3 | a0001c0001t0001g0090 a0001c0001t0001g0102 a0001c0001t0001g0165 |
3 | HG02683.hp1 HG04199.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.580-4805_580-4804i others(29): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74254784 | ||||||
| chr14:74254784 | A | ATTTTTTT others(21): Show |
1 | a0001c0001t0001g0147 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.580-4805_580-4804i others(30): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74254784 | ||||||
| chr14:74254784 | A | ATTTTTTT others(22): Show |
3 | a0001c0001t0001g0115 a0001c0001t0013g0223 a0001c0001t0013g0225 |
3 | HG02683.hp2 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.580-4805_580-4804i others(31): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74254784 | ||||||
| chr14:74254784 | A | ATTTTTTT others(27): Show |
1 | a0001c0001t0013g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.580-4805_580-4804i others(36): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74254784 | ||||||
| chr14:74254830 | A | G | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0178 others(1): Show |
4 | HG00597.hp1 HG02027.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-4772A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74254830 | |||||||
| chr14:74254841 | A | G | 2 | a0001c0001t0001g0092 a0001c0001t0001g0122 |
2 | HG00673.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.580-4761A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74254841 | |||||||
| chr14:74254923 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.580-4679G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74254923 | |||||||
| chr14:74254938 | C | A | 3 | a0001c0001t0013g0223 a0001c0001t0013g0224 a0001c0001t0013g0225 |
3 | HG01109.hp2 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.580-4664C>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74254938 | |||||||
| chr14:74254970 | C | T | 8 | a0001c0001t0001g0134 a0002c0003t0001g0008 a0002c0003t0001g0053 others(5): Show |
12 | HG00438.hp2 HG00639.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.580-4632C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74254970 | |||||||
| chr14:74254982 | G | A | 1 | a0001c0007t0007g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.580-4620G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74254982 | |||||||
| chr14:74254989 | C | A | 250 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(247): Show |
302 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.580-4613C>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74254989 | |||||||
| chr14:74255029 | C | T | 1 | a0001c0001t0003g0262 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.580-4573C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74255029 | |||||||
| chr14:74255033 | G | T | 1 | a0001c0002t0001g0213 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.580-4569G>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74255033 | |||||||
| chr14:74255034 | C | T | 1 | a0001c0002t0001g0213 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.580-4568C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74255034 | |||||||
| chr14:74255081 | G | A | 1 | a0001c0001t0011g0077 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.580-4521G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74255081 | |||||||
| chr14:74255183 | A | C | 1 | a0001c0007t0007g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.580-4419A>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74255183 | |||||||
| chr14:74255239 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.580-4363G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74255239 | |||||||
| chr14:74255282 | G | A | 1 | a0001c0001t0011g0077 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.580-4320G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74255282 | |||||||
| chr14:74255327 | A | G | 1 | a0001c0001t0011g0077 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.580-4275A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74255327 | |||||||
| chr14:74255455 | G | A | 1 | a0001c0007t0007g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.580-4147G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74255455 | |||||||
| chr14:74255480 | C | T | 1 | a0001c0001t0002g0274 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.580-4122C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74255480 | |||||||
| chr14:74255510 | G | C | 1 | a0001c0001t0002g0265 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.580-4092G>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74255510 | |||||||
| chr14:74255587 | C | A | 1 | a0001c0001t0005g0234 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.580-4015C>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74255587 | |||||||
| chr14:74255676 | C | T | 8 | a0001c0001t0006g0013 a0001c0001t0006g0186 a0001c0001t0006g0187 others(5): Show |
10 | HG01081.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.580-3926C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74255676 | |||||||
| chr14:74255766 | CTCTG | C | 13 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0183 others(10): Show |
17 | HG00280.hp1 HG01243.hp1 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.580-3832_580-3829d others(6): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74255766 | ||||||
| chr14:74255883 | C | T | 1 | a0002c0003t0001g0319 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.580-3719C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74255883 | |||||||
| chr14:74255962 | G | A | 1 | a0001c0001t0002g0291 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.580-3640G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74255962 | |||||||
| chr14:74256015 | A | G | 9 | a0001c0001t0009g0058 a0001c0001t0009g0059 a0001c0001t0009g0060 others(6): Show |
10 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.580-3587A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74256015 | |||||||
| chr14:74256206 | G | A | 8 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0022 others(5): Show |
16 | HG00408.hp1 HG00609.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.580-3396G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74256206 | |||||||
| chr14:74256288 | C | T | 5 | a0001c0001t0001g0045 a0001c0001t0001g0219 a0001c0001t0001g0220 others(2): Show |
6 | HG02055.hp1 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.580-3314C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74256288 | |||||||
| chr14:74256339 | G | A | 90 | a0001c0001t0001g0305 a0001c0001t0002g0002 a0001c0001t0002g0018 others(87): Show |
103 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.580-3263G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74256339 | |||||||
| chr14:74256353 | T | G | 1 | a0001c0001t0002g0252 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.580-3249T>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74256353 | |||||||
| chr14:74256401 | A | C | 13 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0183 others(10): Show |
17 | HG00280.hp1 HG01243.hp1 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.580-3201A>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74256401 | |||||||
| chr14:74256523 | A | T | 279 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(276): Show |
338 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.580-3079A>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74256523 | |||||||
| chr14:74256530 | C | G | 8 | a0001c0001t0006g0013 a0001c0001t0006g0186 a0001c0001t0006g0187 others(5): Show |
10 | HG01081.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.580-3072C>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74256530 | |||||||
| chr14:74256601 | G | A | 1 | a0001c0001t0021g0168 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.580-3001G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74256601 | |||||||
| chr14:74256669 | CT | C | 222 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(219): Show |
261 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.580-2911delT | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74256669 | ||||||
| chr14:74256669 | CTT | C | 11 | a0001c0001t0001g0088 a0001c0001t0001g0099 a0001c0001t0001g0109 others(8): Show |
11 | HG02897.hp2 HG03098.hp2 HG03486.hp2 others(8): Show |
intron_variant | MODIFIER | c.580-2912_580-2911d others(4): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74256669 | ||||||
| chr14:74256669 | CTTT | C | 9 | a0001c0001t0006g0013 a0001c0001t0006g0186 a0001c0001t0006g0187 others(6): Show |
11 | HG01081.hp1 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.580-2913_580-2911d others(5): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74256669 | ||||||
| chr14:74256669 | CTTTT | C | 19 | a0001c0001t0009g0058 a0001c0001t0009g0059 a0001c0001t0009g0060 others(16): Show |
24 | HG00438.hp2 HG00639.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.580-2914_580-2911d others(6): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74256669 | ||||||
| chr14:74256734 | C | T | 135 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(132): Show |
162 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.580-2868C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74256734 | |||||||
| chr14:74256735 | A | G | 135 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(132): Show |
162 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.580-2867A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74256735 | |||||||
| chr14:74256736 | C | T | 135 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(132): Show |
162 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.580-2866C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74256736 | |||||||
| chr14:74256762 | C | T | 1 | a0001c0002t0001g0205 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.580-2840C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74256762 | |||||||
| chr14:74256822 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.580-2780C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74256822 | |||||||
| chr14:74256917 | A | G | 90 | a0001c0001t0001g0305 a0001c0001t0002g0002 a0001c0001t0002g0018 others(87): Show |
103 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.580-2685A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74256917 | |||||||
| chr14:74256935 | A | G | 8 | a0001c0001t0006g0013 a0001c0001t0006g0186 a0001c0001t0006g0187 others(5): Show |
10 | HG01081.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.580-2667A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74256935 | |||||||
| chr14:74256937 | C | T | 7 | a0002c0003t0001g0008 a0002c0003t0001g0053 a0002c0003t0001g0148 others(4): Show |
11 | HG00438.hp2 HG00639.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.580-2665C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74256937 | |||||||
| chr14:74256954 | A | G | 266 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(263): Show |
324 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.580-2648A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74256954 | |||||||
| chr14:74257053 | C | G | 90 | a0001c0001t0001g0305 a0001c0001t0002g0002 a0001c0001t0002g0018 others(87): Show |
103 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.580-2549C>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74257053 | |||||||
| chr14:74257066 | G | C | 1 | a0007c0009t0003g0285 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.580-2536G>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74257066 | |||||||
| chr14:74257086 | C | T | 7 | a0002c0003t0001g0008 a0002c0003t0001g0053 a0002c0003t0001g0148 others(4): Show |
11 | HG00438.hp2 HG00639.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.580-2516C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74257086 | |||||||
| chr14:74257145 | G | A | 8 | a0001c0001t0006g0013 a0001c0001t0006g0186 a0001c0001t0006g0187 others(5): Show |
10 | HG01081.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.580-2457G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74257145 | |||||||
| chr14:74257150 | C | G | 1 | a0001c0007t0007g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.580-2452C>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74257150 | |||||||
| chr14:74257169 | A | C | 1 | a0001c0001t0011g0077 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.580-2433A>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74257169 | |||||||
| chr14:74257282 | C | T | 1 | a0001c0007t0001g0157 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.580-2320C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74257282 | |||||||
| chr14:74257296 | G | T | 161 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(158): Show |
200 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.580-2306G>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74257296 | |||||||
| chr14:74257309 | T | C | 330 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(327): Show |
419 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(416): Show |
intron_variant | MODIFIER | c.580-2293T>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74257309 | |||||||
| chr14:74257557 | A | G | 228 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(225): Show |
268 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.580-2045A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74257557 | |||||||
| chr14:74257564 | T | C | 1 | a0001c0002t0001g0202 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.580-2038T>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74257564 | |||||||
| chr14:74257591 | C | A | 2 | a0001c0001t0014g0184 a0001c0001t0014g0185 |
2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.580-2011C>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74257591 | |||||||
| chr14:74257709 | A | AC | 161 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(158): Show |
207 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.580-1887dupC | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74257709 | ||||||
| chr14:74257709 | A | ACC | 71 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0038 others(68): Show |
77 | HG00099.hp2 HG00408.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.580-1888_580-1887d others(4): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74257709 | ||||||
| chr14:74257715 | C | CG | 8 | a0001c0001t0006g0013 a0001c0001t0006g0186 a0001c0001t0006g0187 others(5): Show |
10 | HG01081.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.580-1887_580-1886i others(3): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74257715 | |||||||
| chr14:74257716 | A | C | 242 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(239): Show |
286 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.580-1886A>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74257716 | |||||||
| chr14:74257716 | A | G | 17 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0094 others(14): Show |
27 | HG00408.hp1 HG00609.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.580-1886A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74257716 | |||||||
| chr14:74257813 | G | C | 1 | a0005c0008t0011g0237 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.580-1789G>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74257813 | |||||||
| chr14:74257883 | A | T | 87 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(84): Show |
100 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.580-1719A>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74257883 | |||||||
| chr14:74257897 | C | G | 6 | a0001c0001t0002g0021 a0001c0001t0002g0052 a0001c0001t0002g0307 others(3): Show |
9 | HG00438.hp1 HG00558.hp2 NA18965.hp2 others(6): Show |
intron_variant | MODIFIER | c.580-1705C>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74257897 | |||||||
| chr14:74258031 | G | A | 2 | a0001c0001t0005g0183 a0001c0001t0005g0234 |
2 | HG00280.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.580-1571G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74258031 | |||||||
| chr14:74258057 | G | C | 1 | a0001c0001t0002g0280 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.580-1545G>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74258057 | |||||||
| chr14:74258120 | A | G | 5 | a0003c0005t0007g0055 a0003c0005t0007g0056 a0003c0005t0007g0266 others(2): Show |
5 | HG02818.hp2 HG02965.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-1482A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74258120 | |||||||
| chr14:74258170 | T | C | 278 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(275): Show |
337 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.580-1432T>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74258170 | |||||||
| chr14:74258196 | C | A | 1 | a0001c0001t0002g0309 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.580-1406C>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74258196 | |||||||
| chr14:74258207 | C | T | 1 | a0001c0002t0001g0066 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.580-1395C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74258207 | |||||||
| chr14:74258394 | G | C | 6 | a0001c0001t0001g0081 a0001c0001t0001g0085 a0001c0001t0001g0086 others(3): Show |
6 | HG00741.hp1 HG01175.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.580-1208G>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74258394 | |||||||
| chr14:74258564 | CGAGAA | C | 8 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0022 others(5): Show |
16 | HG00408.hp1 HG00609.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.580-1036_580-1032d others(7): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74258564 | ||||||
| chr14:74258655 | G | A | 1 | a0001c0007t0007g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.580-947G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74258655 | |||||||
| chr14:74258816 | G | A | 2 | a0001c0001t0014g0184 a0001c0001t0014g0185 |
2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.580-786G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74258816 | |||||||
| chr14:74258875 | C | T | 10 | a0001c0001t0006g0013 a0001c0001t0006g0186 a0001c0001t0006g0187 others(7): Show |
13 | HG01081.hp1 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.580-727C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74258875 | |||||||
| chr14:74259138 | C | T | 2 | a0001c0001t0002g0250 a0001c0001t0002g0272 |
2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.580-464C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74259138 | |||||||
| chr14:74259162 | C | T | 7 | a0002c0003t0001g0008 a0002c0003t0001g0053 a0002c0003t0001g0148 others(4): Show |
11 | HG00438.hp2 HG00639.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.580-440C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74259162 | |||||||
| chr14:74259178 | G | A | 1 | a0001c0001t0011g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.580-424G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74259178 | |||||||
| chr14:74259338 | T | C | 10 | a0001c0001t0006g0013 a0001c0001t0006g0186 a0001c0001t0006g0187 others(7): Show |
13 | HG01081.hp1 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.580-264T>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74259338 | |||||||
| chr14:74259357 | A | C | 1 | a0001c0001t0001g0167 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.580-245A>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74259357 | |||||||
| chr14:74259416 | T | TAAGACTG others(322): Show |
2 | a0001c0001t0006g0186 a0001c0001t0006g0191 |
2 | HG01081.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.580-170_580-169ins others(329): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74259416 | ||||||
| chr14:74259416 | T | TAAGACTG others(323): Show |
2 | a0001c0001t0006g0189 a0001c0001t0006g0190 |
2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.580-170_580-169ins others(330): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74259416 | ||||||
| chr14:74259416 | T | TAAGACTG others(324): Show |
5 | a0001c0001t0006g0013 a0001c0001t0006g0187 a0001c0001t0006g0188 others(2): Show |
8 | HG02451.hp2 HG02486.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.580-170_580-169ins others(331): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74259416 | ||||||
| chr14:74259416 | T | TAAGACTG others(326): Show |
1 | a0001c0001t0006g0193 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.580-170_580-169ins others(333): Show |
VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 74259416 | ||||||
| chr14:74259447 | T | G | 1 | a0001c0001t0014g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.580-155T>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74259447 | |||||||
| chr14:74259498 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.580-104G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74259498 | |||||||
| chr14:74259500 | A | G | 2 | a0001c0001t0005g0239 a0001c0001t0005g0240 |
2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.580-102A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74259500 | |||||||
| chr14:74259523 | C | T | 2 | a0003c0005t0007g0266 a0003c0005t0007g0269 |
2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.580-79C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74259523 | |||||||
| chr14:74259557 | A | C | 3 | a0001c0001t0014g0184 a0001c0001t0014g0185 a0001c0007t0007g0318 |
3 | HG02630.hp1 HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.580-45A>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74259557 | |||||||
| chr14:74259558 | G | A | 3 | a0001c0001t0014g0184 a0001c0001t0014g0185 a0001c0007t0007g0318 |
3 | HG02630.hp1 HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.580-44G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 3/4 | chr14 | 74259558 | |||||||
| chr14:74259856 | C | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0108 |
4 | HG01928.hp2 HG01943.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.760+74C>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 4/4 | chr14 | 74259856 | |||||||
| chr14:74259868 | G | A | 20 | a0001c0001t0006g0013 a0001c0001t0006g0186 a0001c0001t0006g0187 others(17): Show |
23 | HG01081.hp1 HG01109.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.760+86G>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 4/4 | chr14 | 74259868 | |||||||
| chr14:74259879 | C | T | 1 | a0001c0001t0004g0315 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.760+97C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 4/4 | chr14 | 74259879 | |||||||
| chr14:74259931 | C | T | 20 | a0001c0001t0006g0013 a0001c0001t0006g0186 a0001c0001t0006g0187 others(17): Show |
23 | HG01081.hp1 HG01109.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.760+149C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 4/4 | chr14 | 74259931 | |||||||
| chr14:74259937 | G | T | 1 | a0001c0001t0021g0168 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.760+155G>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 4/4 | chr14 | 74259937 | |||||||
| chr14:74259948 | G | C | 1 | a0001c0001t0002g0049 | 2 | HG01884.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.760+166G>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 4/4 | chr14 | 74259948 | |||||||
| chr14:74259991 | A | C | 10 | a0001c0001t0006g0013 a0001c0001t0006g0186 a0001c0001t0006g0187 others(7): Show |
13 | HG01081.hp1 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.760+209A>C | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 4/4 | chr14 | 74259991 | |||||||
| chr14:74260007 | A | G | 257 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(254): Show |
313 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.760+225A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 4/4 | chr14 | 74260007 | |||||||
| chr14:74260125 | C | T | 1 | a0001c0001t0002g0271 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.760+343C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 4/4 | chr14 | 74260125 | |||||||
| chr14:74260173 | T | A | 140 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(137): Show |
167 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.760+391T>A | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 4/4 | chr14 | 74260173 | |||||||
| chr14:74260241 | C | T | 1 | a0001c0002t0001g0204 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.761-353C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 4/4 | chr14 | 74260241 | |||||||
| chr14:74260256 | A | G | 2 | a0001c0002t0001g0203 a0001c0002t0001g0206 |
2 | HG01123.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.761-338A>G | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 4/4 | chr14 | 74260256 | |||||||
| chr14:74260278 | C | T | 264 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(261): Show |
315 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.761-316C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 4/4 | chr14 | 74260278 | |||||||
| chr14:74260496 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.761-98C>T | VSX2 | ENSG00000119614.3 | transcript | ENST00000261980.3 | protein_coding | 4/4 | chr14 | 74260496 |