Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9410 |
| ensemblid | ENSG00000060688.13 |
| hgncid | 30857 |
| symbol | SNRNP40 |
| name | small nuclear ribonucleoprotein U5 subunit 40 |
| refseq_nuc | NM_004814.3 |
| refseq_prot | NP_004805.2 |
| ensembl_nuc | ENST00000263694.9 |
| ensembl_prot | ENSP00000263694.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 31259568 |
| end | 31296788 |
| strand | - |
| ver | v1.2 |
| region | chr1:31259568-31296788 |
| region5000 | chr1:31254568-31301788 |
| regionname0 | SNRNP40_chr1_31259568_31296788 |
| regionname5000 | SNRNP40_chr1_31254568_31301788 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1071 | 345 | 92 | 58 | 151 | 10 | 32 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | ATGAT others(1066): Show |
chr1 | 31254568 | 31301788 | ||
| a0001c0002 | 0/0 | 1071 | 8 | 0 | 0 | 8 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | ATGAT others(1066): Show |
chr1 | 31254568 | 31301788 | ||
| a0001c0003 | 0/0 | 1071 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | ATGAT others(1066): Show |
chr1 | 31254568 | 31301788 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1615 | 124 | 19 | 20 | 67 | 4 | 13 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | GCGGT others(1610): Show |
chr1 | 31254568 | 31301788 |
| a0001c0001t0002 | 0/0 | 1614 | 104 | 39 | 21 | 34 | 3 | 7 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | GCGGT others(1609): Show |
chr1 | 31254568 | 31301788 |
| a0001c0001t0003 | 0/0 | 1615 | 38 | 7 | 5 | 14 | 1 | 11 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | GCGGT others(1610): Show |
chr1 | 31254568 | 31301788 |
| a0001c0001t0004 | 0/0 | 1614 | 29 | 0 | 0 | 29 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | GCGGT others(1609): Show |
chr1 | 31254568 | 31301788 |
| a0001c0001t0005 | 0/1 | 1614 | 27 | 16 | 7 | 0 | 2 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | GCGGT others(1609): Show |
chr1 | 31254568 | 31301788 |
| a0001c0001t0006 | 0/0 | 1616 | 6 | 0 | 0 | 6 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | GCGGT others(1611): Show |
chr1 | 31254568 | 31301788 |
| a0001c0001t0007 | 0/0 | 1614 | 7 | 4 | 3 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | GCGGT others(1609): Show |
chr1 | 31254568 | 31301788 |
| a0001c0001t0008 | 0/0 | 1614 | 5 | 4 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | GCGGT others(1609): Show |
chr1 | 31254568 | 31301788 |
| a0001c0001t0009 | 0/0 | 1616 | 2 | 0 | 1 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | GCGGT others(1611): Show |
chr1 | 31254568 | 31301788 |
| a0001c0001t0010 | 0/0 | 1613 | 2 | 2 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | GCGGT others(1608): Show |
chr1 | 31254568 | 31301788 |
| a0001c0001t0011 | 0/0 | 1614 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | GCGGT others(1609): Show |
chr1 | 31254568 | 31301788 |
| a0001c0002t0003 | 0/0 | 1615 | 7 | 0 | 0 | 7 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | GCGGT others(1610): Show |
chr1 | 31254568 | 31301788 |
| a0001c0002t0006 | 0/0 | 1616 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | GCGGT others(1611): Show |
chr1 | 31254568 | 31301788 |
| a0001c0003t0001 | 0/0 | 1615 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | GCGGT others(1610): Show |
chr1 | 31254568 | 31301788 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 0 | 5 | 2 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0057 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0004g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0004g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0005g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0005g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0005g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0005g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0005g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0005g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0005g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0005g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0005g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0005g0083 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0006g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0006g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0006g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0006g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0006g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0007g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0007g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0007g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0007g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0007g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0007g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0008g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0008g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0008g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0009g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0009g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0010g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0010g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0001t0011g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0002t0003g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0002t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0002t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0002t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0002t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| a0001c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0205 | EUR | GBR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | GBR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | FIN | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG00280 | hp2 | a0001 | c0001 | t0005 | g0067 | EUR | FIN | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0025 | EUR | FIN | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0139 | EUR | FIN | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0278 | EAS | CHS | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | CHS | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | CHS | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG00597 | hp2 | a0001 | c0001 | t0006 | g0181 | EAS | CHS | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | CHS | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG00621 | hp2 | a0001 | c0002 | t0003 | g0037 | EAS | CHS | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG00639 | hp1 | a0001 | c0001 | t0007 | g0034 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0269 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0158 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0071 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01069 | hp1 | a0001 | c0001 | t0007 | g0298 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0270 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01071 | hp1 | a0001 | c0001 | t0007 | g0299 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0011 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0075 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0074 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0066 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0250 | AMR | PUR | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | CLM | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01255 | hp2 | a0001 | c0001 | t0008 | g0271 | AMR | CLM | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | CLM | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0079 | AMR | CLM | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0228 | AMR | CLM | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0177 | AMR | CLM | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | IBS | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01517 | hp2 | a0001 | c0001 | t0005 | g0078 | EUR | IBS | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | ACB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0031 | AFR | ACB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0160 | AMR | PEL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PEL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0080 | AMR | PEL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0176 | AMR | PEL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PEL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PEL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02040 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | KHV | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | KHV | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | ACB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0073 | AFR | ACB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | KHV | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02071 | hp1 | a0001 | c0002 | t0003 | g0035 | EAS | KHV | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0285 | EAS | KHV | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02074 | hp2 | a0001 | c0002 | t0003 | g0036 | EAS | KHV | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0292 | EAS | KHV | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | KHV | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | KHV | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | KHV | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02132 | hp2 | a0001 | c0001 | t0006 | g0020 | EAS | KHV | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0282 | EAS | KHV | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | ACB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0264 | AFR | ACB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | PEL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02148 | hp2 | a0001 | c0001 | t0009 | g0137 | AMR | PEL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CDX | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | ACB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0077 | AFR | ACB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | ACB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02258 | hp2 | a0001 | c0001 | t0011 | g0206 | AFR | ACB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | PEL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0081 | AFR | ACB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0297 | AFR | ACB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0175 | AMR | PEL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ACB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0155 | AFR | GWD | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02572 | hp2 | a0001 | c0001 | t0010 | g0065 | AFR | GWD | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0174 | SAS | PJL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0034 | AFR | GWD | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0069 | AFR | GWD | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0210 | SAS | PJL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0183 | SAS | PJL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0243 | AFR | GWD | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | GWD | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0255 | AFR | GWD | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0185 | SAS | PJL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0245 | AFR | GWD | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0257 | AFR | GWD | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0054 | AFR | GWD | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0062 | AFR | GWD | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02895 | hp1 | a0001 | c0001 | t0008 | g0031 | AFR | GWD | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02895 | hp2 | a0001 | c0001 | t0010 | g0064 | AFR | GWD | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0239 | AFR | GWD | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | GWD | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | GWD | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02897 | hp2 | a0001 | c0001 | t0008 | g0030 | AFR | GWD | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0240 | AFR | ESN | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | ESN | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0068 | AFR | ESN | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0261 | AFR | ESN | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0238 | AFR | ESN | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | ESN | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0242 | AFR | ESN | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0156 | AFR | GWD | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0241 | AFR | GWD | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0256 | AFR | MSL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0262 | AFR | ESN | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | ESN | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | ESN | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0252 | AFR | ESN | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ESN | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ESN | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | MSL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0072 | AFR | MSL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0053 | SAS | PJL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03453 | hp1 | a0001 | c0001 | t0008 | g0030 | AFR | MSL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | MSL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0021 | SAS | PJL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0246 | AFR | GWD | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | MSL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0244 | AFR | MSL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0184 | SAS | PJL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | STU | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0157 | SAS | STU | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0052 | SAS | PJL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0268 | SAS | PJL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0027 | SAS | BEB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0187 | SAS | STU | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | STU | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0236 | SAS | BEB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | STU | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0201 | SAS | STU | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0224 | SAS | STU | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0076 | SAS | STU | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | STU | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0182 | SAS | STU | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | YRI | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | CHB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | CHB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | CHB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0290 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0294 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0275 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18952 | hp2 | a0001 | c0001 | t0006 | g0161 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0281 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18962 | hp2 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0280 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0293 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0284 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18970 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18972 | hp1 | a0001 | c0001 | t0009 | g0085 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0283 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0286 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18987 | hp2 | a0001 | c0001 | t0004 | g0288 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18989 | hp1 | a0001 | c0003 | t0001 | g0039 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0287 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18993 | hp2 | a0001 | c0001 | t0006 | g0020 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0295 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0291 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18999 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19001 | hp1 | a0001 | c0001 | t0006 | g0265 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0263 | AFR | LWK | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | LWK | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0061 | AFR | LWK | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0082 | AFR | LWK | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0289 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0277 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19066 | hp2 | a0001 | c0001 | t0006 | g0159 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0279 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19078 | hp2 | a0001 | c0002 | t0006 | g0038 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19084 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0249 | AFR | YRI | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | YRI | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA20129 | hp1 | a0001 | c0001 | t0007 | g0296 | AFR | ASW | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ASW | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0222 | EUR | TSI | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0172 | EUR | TSI | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0186 | SAS | GIH | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | GIH | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0070 | AFR | ACB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0247 | AFR | ACB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0251 | AFR | ACB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0300 | AFR | MSL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0040 | AFR | MSL | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0258 | AFR | USA | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0248 | AFR | USA | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | USA | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | USA | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0266 | AFR | LWK | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | LWK | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0083 | REF | REF | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0057 | REF | REF | SNRNP40_chr1_31254568_31301788 | SNRNP40 | chr1 | 31254568 | 31301788 |
| 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 |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:31296676 | A | G | 1 | a0001c0003 | 1 | NA18989.hp1 | synonymous_variant | LOW | c.76T>C | p.Leu26Leu | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/10 | 113/1615 | 76/1074 | 26/357 | chr1 | 31296676 | |||
| chr1:31296713 | C | G | 1 | a0001c0002 | 8 | HG00621.hp2 HG02040.hp1 HG02071.hp1 others(5): Show |
synonymous_variant | LOW | c.39G>C | p.Pro13Pro | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/10 | 76/1615 | 39/1074 | 13/357 | chr1 | 31296713 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:31259677 | G | C | 1 | a0001c0001t0011 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*395C>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 10/10 | 395 | chr1 | 31259677 | ||||||
| chr1:31259755 | C | CA | 3 | a0001c0001t0006 a0001c0001t0009 a0001c0002t0006 |
9 | HG00597.hp2 HG02132.hp2 HG02148.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*316dupT | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 10/10 | 316 | chr1 | 31259755 | ||||||
| chr1:31259755 | CA | C | 5 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(2): Show |
167 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*316delT | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 10/10 | 316 | chr1 | 31259755 | ||||||
| chr1:31259755 | CAA | C | 2 | a0001c0001t0008 a0001c0001t0010 |
7 | HG01255.hp2 HG01891.hp2 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*315_*316delTT | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 10/10 | 315 | chr1 | 31259755 | ||||||
| chr1:31259841 | A | AG | 1 | a0001c0001t0008 | 5 | HG01255.hp2 HG01891.hp2 HG02895.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*230_*231insC | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 10/10 | 230 | chr1 | 31259841 | ||||||
| chr1:31259941 | C | T | 1 | a0001c0001t0004 | 29 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*131G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 10/10 | 131 | chr1 | 31259941 | ||||||
| chr1:31260045 | G | A | 6 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(3): Show |
80 | HG00280.hp2 HG00597.hp2 HG00621.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*27C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 10/10 | 27 | chr1 | 31260045 | ||||||
| chr1:31296762 | G | A | 1 | a0001c0001t0007 | 7 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(4): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-11C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/10 | chr1 | 31296762 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:31260141 | T | C | 1 | a0001c0001t0005g0062 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1025-20A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 9/9 | chr1 | 31260141 | |||||||
| chr1:31260306 | T | C | 9 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 others(6): Show |
10 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.1025-185A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 9/9 | chr1 | 31260306 | |||||||
| chr1:31260373 | C | T | 10 | a0001c0001t0002g0041 a0001c0001t0002g0046 a0001c0001t0002g0047 others(7): Show |
11 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1025-252G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 9/9 | chr1 | 31260373 | |||||||
| chr1:31260473 | A | T | 1 | a0001c0001t0006g0265 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1025-352T>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 9/9 | chr1 | 31260473 | |||||||
| chr1:31260551 | A | G | 26 | a0001c0001t0004g0009 a0001c0001t0004g0033 a0001c0001t0004g0272 others(23): Show |
29 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1025-430T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 9/9 | chr1 | 31260551 | |||||||
| chr1:31260754 | T | G | 3 | a0001c0001t0008g0030 a0001c0001t0008g0031 a0001c0001t0008g0271 |
5 | HG01255.hp2 HG01891.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1025-633A>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 9/9 | chr1 | 31260754 | |||||||
| chr1:31260827 | C | A | 19 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0066 others(16): Show |
21 | HG00280.hp2 HG00741.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1024+702G>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 9/9 | chr1 | 31260827 | |||||||
| chr1:31260863 | C | CA | 7 | a0001c0001t0001g0084 a0001c0001t0001g0091 a0001c0001t0001g0105 others(4): Show |
7 | HG01496.hp1 HG02135.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1024+665dupT | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 9/9 | chr1 | 31260863 | |||||||
| chr1:31260863 | C | CAA | 100 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 others(97): Show |
114 | HG00280.hp2 HG00408.hp2 HG00597.hp2 others(111): Show |
intron_variant | MODIFIER | c.1024+664_1024+665d others(4): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 9/9 | chr1 | 31260863 | |||||||
| chr1:31260874 | A | AAAG | 96 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(93): Show |
107 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1024+654_1024+655i others(5): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 9/9 | chr1 | 31260874 | |||||||
| chr1:31260910 | G | A | 1 | a0001c0001t0004g0278 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1024+619C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 9/9 | chr1 | 31260910 | |||||||
| chr1:31260935 | T | A | 97 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(94): Show |
108 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1024+594A>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 9/9 | chr1 | 31260935 | |||||||
| chr1:31260983 | T | C | 26 | a0001c0001t0004g0009 a0001c0001t0004g0033 a0001c0001t0004g0272 others(23): Show |
29 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1024+546A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 9/9 | chr1 | 31260983 | |||||||
| chr1:31261079 | A | G | 205 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0221 others(202): Show |
230 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.1024+450T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 9/9 | chr1 | 31261079 | |||||||
| chr1:31261128 | G | A | 1 | a0001c0001t0002g0222 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1024+401C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 9/9 | chr1 | 31261128 | |||||||
| chr1:31261169 | C | T | 2 | a0001c0001t0002g0046 a0001c0001t0002g0047 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1024+360G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 9/9 | chr1 | 31261169 | |||||||
| chr1:31261186 | CA | C | 119 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(116): Show |
133 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1024+342delT | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 9/9 | chr1 | 31261186 | |||||||
| chr1:31261336 | G | A | 1 | a0001c0001t0002g0244 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1024+193C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 9/9 | chr1 | 31261336 | |||||||
| chr1:31261364 | C | T | 4 | a0001c0001t0005g0061 a0001c0001t0005g0062 a0001c0001t0005g0155 others(1): Show |
4 | HG02572.hp1 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024+165G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 9/9 | chr1 | 31261364 | |||||||
| chr1:31261388 | A | C | 1 | a0001c0002t0003g0037 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1024+141T>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 9/9 | chr1 | 31261388 | |||||||
| chr1:31261506 | C | T | 1 | a0001c0001t0002g0027 | 2 | HG01081.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1024+23G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 9/9 | chr1 | 31261506 | |||||||
| chr1:31261861 | G | T | 46 | a0001c0001t0003g0008 a0001c0001t0003g0010 a0001c0001t0003g0021 others(43): Show |
54 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.921-229C>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31261861 | |||||||
| chr1:31261901 | G | T | 23 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0061 others(20): Show |
25 | HG00280.hp2 HG00741.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.921-269C>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31261901 | |||||||
| chr1:31261994 | C | T | 97 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(94): Show |
108 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.921-362G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31261994 | |||||||
| chr1:31262094 | G | A | 7 | a0001c0001t0002g0032 a0001c0001t0002g0257 a0001c0001t0002g0258 others(4): Show |
8 | HG01884.hp2 HG02818.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.921-462C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31262094 | |||||||
| chr1:31262460 | G | A | 6 | a0001c0001t0007g0034 a0001c0001t0007g0296 a0001c0001t0007g0297 others(3): Show |
7 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.921-828C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31262460 | |||||||
| chr1:31262521 | C | CA | 30 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0092 others(27): Show |
32 | HG00280.hp2 HG00741.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.921-890dupT | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31262521 | |||||||
| chr1:31262521 | CA | C | 6 | a0001c0001t0001g0100 a0001c0001t0002g0041 a0001c0001t0002g0048 others(3): Show |
6 | HG01070.hp2 HG02080.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.921-890delT | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31262521 | |||||||
| chr1:31262521 | CAA | C | 44 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0003g0008 others(41): Show |
52 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.921-891_921-890del others(2): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31262521 | |||||||
| chr1:31262542 | AAAGAG | A | 56 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(53): Show |
61 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.921-915_921-911del others(5): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31262542 | |||||||
| chr1:31262543 | AAG | A | 7 | a0001c0001t0002g0240 a0001c0001t0002g0250 a0001c0001t0004g0009 others(4): Show |
8 | HG01243.hp2 HG02922.hp1 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.921-913_921-912del others(2): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31262543 | |||||||
| chr1:31262543 | AAGAG | A | 7 | a0001c0001t0002g0027 a0001c0001t0002g0163 a0001c0001t0002g0203 others(4): Show |
10 | HG00609.hp1 HG01081.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.921-915_921-912del others(4): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31262543 | |||||||
| chr1:31262544 | AGAG | A | 54 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0032 others(51): Show |
57 | HG00408.hp2 HG00639.hp2 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.921-915_921-913del others(3): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31262544 | |||||||
| chr1:31262547 | G | A | 7 | a0001c0001t0002g0240 a0001c0001t0002g0250 a0001c0001t0004g0009 others(4): Show |
8 | HG01243.hp2 HG02922.hp1 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.921-915C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31262547 | |||||||
| chr1:31262570 | C | G | 1 | a0001c0001t0001g0059 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.921-938G>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31262570 | |||||||
| chr1:31262657 | G | T | 2 | a0001c0001t0002g0046 a0001c0001t0002g0047 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.921-1025C>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31262657 | |||||||
| chr1:31262665 | C | A | 121 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(118): Show |
134 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.921-1033G>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31262665 | |||||||
| chr1:31262696 | T | TA | 44 | a0001c0001t0003g0008 a0001c0001t0003g0010 a0001c0001t0003g0021 others(41): Show |
52 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.921-1065dupT | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31262696 | |||||||
| chr1:31262726 | A | G | 1 | a0001c0001t0005g0079 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.921-1094T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31262726 | |||||||
| chr1:31262733 | T | C | 1 | a0001c0001t0002g0197 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.921-1101A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31262733 | |||||||
| chr1:31262736 | G | A | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG02486.hp2 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.921-1104C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31262736 | |||||||
| chr1:31262792 | T | A | 26 | a0001c0001t0004g0009 a0001c0001t0004g0033 a0001c0001t0004g0272 others(23): Show |
29 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.921-1160A>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31262792 | |||||||
| chr1:31263004 | G | GA | 97 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(94): Show |
108 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.921-1373dupT | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31263004 | |||||||
| chr1:31263015 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(83): Show |
115 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.921-1383A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31263015 | |||||||
| chr1:31263033 | T | C | 70 | a0001c0001t0003g0008 a0001c0001t0003g0010 a0001c0001t0003g0021 others(67): Show |
80 | HG00280.hp2 HG00597.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.921-1401A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31263033 | |||||||
| chr1:31263058 | CTA | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(83): Show |
115 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.921-1428_921-1427d others(4): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31263058 | |||||||
| chr1:31263155 | GAATA | G | 26 | a0001c0001t0004g0009 a0001c0001t0004g0033 a0001c0001t0004g0272 others(23): Show |
29 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.921-1527_921-1524d others(6): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31263155 | |||||||
| chr1:31263161 | A | G | 3 | a0001c0001t0002g0263 a0001c0001t0002g0269 a0001c0001t0002g0270 |
3 | HG00639.hp2 HG01070.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.921-1529T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31263161 | |||||||
| chr1:31263198 | G | A | 1 | a0001c0001t0002g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.921-1566C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31263198 | |||||||
| chr1:31263276 | T | C | 60 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(57): Show |
66 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.921-1644A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31263276 | |||||||
| chr1:31263335 | C | A | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.921-1703G>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31263335 | |||||||
| chr1:31263341 | A | AT | 6 | a0001c0001t0001g0063 a0001c0001t0001g0098 a0001c0001t0001g0099 others(3): Show |
6 | HG01517.hp1 HG02109.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.921-1710dupA | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31263341 | |||||||
| chr1:31263341 | AT | A | 82 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0023 others(79): Show |
89 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.921-1710delA | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31263341 | |||||||
| chr1:31263341 | ATT | A | 15 | a0001c0001t0002g0022 a0001c0001t0002g0024 a0001c0001t0002g0192 others(12): Show |
19 | HG00597.hp1 HG01255.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.921-1711_921-1710d others(4): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31263341 | |||||||
| chr1:31263345 | T | G | 9 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 others(6): Show |
10 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.921-1713A>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31263345 | |||||||
| chr1:31263401 | A | G | 123 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(120): Show |
137 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.921-1769T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31263401 | |||||||
| chr1:31263465 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.921-1833G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31263465 | |||||||
| chr1:31263913 | T | TA | 165 | a0001c0001t0001g0122 a0001c0001t0001g0221 a0001c0001t0002g0022 others(162): Show |
187 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.921-2282dupT | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31263913 | |||||||
| chr1:31263913 | T | TAA | 8 | a0001c0001t0002g0048 a0001c0001t0002g0194 a0001c0001t0002g0196 others(5): Show |
8 | HG00735.hp1 HG02129.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.921-2283_921-2282d others(4): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31263913 | |||||||
| chr1:31263953 | T | C | 123 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(120): Show |
137 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.921-2321A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31263953 | |||||||
| chr1:31264009 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.921-2377A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31264009 | |||||||
| chr1:31264372 | C | T | 1 | a0001c0001t0005g0040 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.921-2740G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31264372 | |||||||
| chr1:31264553 | T | C | 2 | a0001c0001t0005g0011 a0001c0001t0005g0066 |
3 | HG01109.hp1 HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.921-2921A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31264553 | |||||||
| chr1:31264556 | A | C | 26 | a0001c0001t0004g0009 a0001c0001t0004g0033 a0001c0001t0004g0272 others(23): Show |
29 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.921-2924T>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31264556 | |||||||
| chr1:31264725 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0116 a0001c0001t0001g0117 |
5 | HG02135.hp2 NA18947.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.921-3093G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31264725 | |||||||
| chr1:31264846 | G | A | 1 | a0001c0001t0003g0008 | 3 | NA18747.hp2 NA18940.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.920+3025C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31264846 | |||||||
| chr1:31264893 | G | C | 1 | a0001c0002t0006g0038 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.920+2978C>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31264893 | |||||||
| chr1:31264949 | G | C | 3 | a0001c0001t0008g0030 a0001c0001t0008g0031 a0001c0001t0008g0271 |
5 | HG01255.hp2 HG01891.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.920+2922C>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31264949 | |||||||
| chr1:31265111 | C | T | 26 | a0001c0001t0004g0009 a0001c0001t0004g0033 a0001c0001t0004g0272 others(23): Show |
29 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.920+2760G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31265111 | |||||||
| chr1:31265130 | GT | G | 97 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(94): Show |
108 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.920+2740delA | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31265130 | |||||||
| chr1:31265176 | G | A | 1 | a0001c0001t0003g0174 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.920+2695C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31265176 | |||||||
| chr1:31265310 | TA | T | 26 | a0001c0001t0004g0009 a0001c0001t0004g0033 a0001c0001t0004g0272 others(23): Show |
29 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.920+2560delT | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31265310 | |||||||
| chr1:31265382 | A | G | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.920+2489T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31265382 | |||||||
| chr1:31265474 | T | A | 2 | a0001c0001t0002g0046 a0001c0001t0002g0047 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.920+2397A>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31265474 | |||||||
| chr1:31265569 | A | G | 123 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(120): Show |
137 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.920+2302T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31265569 | |||||||
| chr1:31265701 | G | A | 46 | a0001c0001t0003g0008 a0001c0001t0003g0010 a0001c0001t0003g0021 others(43): Show |
54 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.920+2170C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31265701 | |||||||
| chr1:31265733 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(83): Show |
115 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.920+2138C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31265733 | |||||||
| chr1:31265849 | C | CAA | 123 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(120): Show |
137 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.920+2020_920+2021d others(4): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31265849 | |||||||
| chr1:31266010 | G | A | 97 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(94): Show |
108 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.920+1861C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31266010 | |||||||
| chr1:31266041 | T | C | 6 | a0001c0001t0002g0188 a0001c0001t0002g0197 a0001c0001t0002g0199 others(3): Show |
6 | NA18747.hp1 NA18983.hp1 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.920+1830A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31266041 | |||||||
| chr1:31266201 | T | C | 203 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(200): Show |
228 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.920+1670A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31266201 | |||||||
| chr1:31266327 | T | C | 34 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0032 others(31): Show |
37 | HG00639.hp2 HG01069.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.920+1544A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31266327 | |||||||
| chr1:31266580 | C | T | 26 | a0001c0001t0004g0009 a0001c0001t0004g0033 a0001c0001t0004g0272 others(23): Show |
29 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.920+1291G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31266580 | |||||||
| chr1:31266631 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.920+1240G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31266631 | |||||||
| chr1:31266757 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.920+1114G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31266757 | |||||||
| chr1:31267576 | G | A | 1 | a0001c0001t0003g0053 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.920+295C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31267576 | |||||||
| chr1:31267606 | G | A | 27 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0032 others(24): Show |
30 | HG01069.hp2 HG01243.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.920+265C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31267606 | |||||||
| chr1:31267613 | G | A | 1 | a0001c0001t0002g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.920+258C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31267613 | |||||||
| chr1:31267793 | A | G | 44 | a0001c0001t0003g0008 a0001c0001t0003g0010 a0001c0001t0003g0021 others(41): Show |
52 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.920+78T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31267793 | |||||||
| chr1:31267820 | C | T | 3 | a0001c0001t0002g0163 a0001c0001t0002g0164 a0001c0001t0002g0165 |
3 | HG02083.hp2 NA18972.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.920+51G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31267820 | |||||||
| chr1:31267821 | C | T | 60 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(57): Show |
66 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.920+50G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31267821 | |||||||
| chr1:31267859 | A | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(84): Show |
116 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.920+12T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 8/9 | chr1 | 31267859 | |||||||
| chr1:31268286 | G | GT | 51 | a0001c0001t0001g0016 a0001c0001t0001g0088 a0001c0001t0001g0115 others(48): Show |
59 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.859-355dupA | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 7/9 | chr1 | 31268286 | |||||||
| chr1:31268300 | TG | T | 6 | a0001c0001t0002g0200 a0001c0001t0002g0203 a0001c0001t0002g0230 others(3): Show |
6 | HG01106.hp2 HG02486.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.859-369delC | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 7/9 | chr1 | 31268300 | |||||||
| chr1:31268300 | TGA | T | 91 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(88): Show |
102 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.859-370_859-369del others(2): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 7/9 | chr1 | 31268300 | |||||||
| chr1:31268302 | A | T | 6 | a0001c0001t0002g0200 a0001c0001t0002g0203 a0001c0001t0002g0230 others(3): Show |
6 | HG01106.hp2 HG02486.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.859-370T>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 7/9 | chr1 | 31268302 | |||||||
| chr1:31268730 | G | A | 122 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(119): Show |
136 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.858+428C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 7/9 | chr1 | 31268730 | |||||||
| chr1:31268782 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.858+376G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 7/9 | chr1 | 31268782 | |||||||
| chr1:31268845 | A | G | 1 | a0001c0001t0002g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.858+313T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 7/9 | chr1 | 31268845 | |||||||
| chr1:31268896 | G | A | 1 | a0001c0001t0003g0187 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.858+262C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 7/9 | chr1 | 31268896 | |||||||
| chr1:31268930 | C | T | 19 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0066 others(16): Show |
21 | HG00280.hp2 HG00741.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.858+228G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 7/9 | chr1 | 31268930 | |||||||
| chr1:31268969 | A | G | 202 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(199): Show |
227 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.858+189T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 7/9 | chr1 | 31268969 | |||||||
| chr1:31269482 | A | G | 1 | a0001c0001t0005g0074 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.776-242T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 6/9 | chr1 | 31269482 | |||||||
| chr1:31269782 | T | A | 19 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0066 others(16): Show |
21 | HG00280.hp2 HG00741.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.776-542A>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 6/9 | chr1 | 31269782 | |||||||
| chr1:31269858 | T | A | 26 | a0001c0001t0004g0009 a0001c0001t0004g0033 a0001c0001t0004g0272 others(23): Show |
29 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.776-618A>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 6/9 | chr1 | 31269858 | |||||||
| chr1:31269918 | T | C | 1 | a0001c0001t0005g0040 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.776-678A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 6/9 | chr1 | 31269918 | |||||||
| chr1:31269965 | T | C | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.776-725A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 6/9 | chr1 | 31269965 | |||||||
| chr1:31270029 | A | T | 1 | a0001c0001t0002g0190 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.776-789T>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 6/9 | chr1 | 31270029 | |||||||
| chr1:31270126 | C | T | 1 | a0001c0001t0005g0068 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.776-886G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 6/9 | chr1 | 31270126 | |||||||
| chr1:31270212 | A | G | 1 | a0001c0001t0005g0082 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.776-972T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 6/9 | chr1 | 31270212 | |||||||
| chr1:31270319 | T | C | 1 | a0001c0001t0001g0018 | 2 | HG00735.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.775+1060A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 6/9 | chr1 | 31270319 | |||||||
| chr1:31270405 | A | T | 9 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 others(6): Show |
10 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.775+974T>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 6/9 | chr1 | 31270405 | |||||||
| chr1:31270511 | G | T | 1 | a0001c0001t0002g0192 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.775+868C>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 6/9 | chr1 | 31270511 | |||||||
| chr1:31270680 | ATATT | A | 97 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(94): Show |
108 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.775+695_775+698del others(4): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 6/9 | chr1 | 31270680 | |||||||
| chr1:31270715 | T | C | 1 | a0001c0001t0005g0040 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.775+664A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 6/9 | chr1 | 31270715 | |||||||
| chr1:31270721 | T | C | 2 | a0001c0001t0003g0158 a0001c0001t0003g0160 |
2 | HG00642.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.775+658A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 6/9 | chr1 | 31270721 | |||||||
| chr1:31271182 | TG | T | 3 | a0001c0001t0003g0167 a0001c0001t0003g0168 a0001c0001t0003g0169 |
3 | NA18991.hp2 NA18995.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.775+196delC | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 6/9 | chr1 | 31271182 | |||||||
| chr1:31271295 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.775+84G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 6/9 | chr1 | 31271295 | |||||||
| chr1:31271321 | G | A | 60 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(57): Show |
66 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.775+58C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 6/9 | chr1 | 31271321 | |||||||
| chr1:31271534 | T | C | 37 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0032 others(34): Show |
42 | HG00639.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.655-35A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31271534 | |||||||
| chr1:31271658 | A | AT | 186 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(183): Show |
209 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.655-160dupA | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31271658 | |||||||
| chr1:31271668 | T | TG | 16 | a0001c0001t0002g0023 a0001c0001t0002g0026 a0001c0001t0002g0188 others(13): Show |
18 | HG00423.hp2 HG02129.hp2 HG02132.hp1 others(15): Show |
intron_variant | MODIFIER | c.655-170dupC | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31271668 | |||||||
| chr1:31271677 | G | A | 3 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 |
3 | NA18983.hp2 NA19062.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.655-178C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31271677 | |||||||
| chr1:31271737 | G | A | 9 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 others(6): Show |
10 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.655-238C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31271737 | |||||||
| chr1:31271938 | C | G | 1 | a0001c0001t0001g0127 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.655-439G>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31271938 | |||||||
| chr1:31272118 | A | C | 1 | a0001c0001t0001g0127 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.655-619T>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31272118 | |||||||
| chr1:31272119 | G | C | 1 | a0001c0001t0001g0127 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.655-620C>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31272119 | |||||||
| chr1:31272225 | T | G | 1 | a0001c0001t0001g0058 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.655-726A>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31272225 | |||||||
| chr1:31272228 | T | A | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.655-729A>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31272228 | |||||||
| chr1:31272338 | G | A | 1 | a0001c0001t0002g0197 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.655-839C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31272338 | |||||||
| chr1:31272438 | T | C | 46 | a0001c0001t0003g0008 a0001c0001t0003g0010 a0001c0001t0003g0021 others(43): Show |
54 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.655-939A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31272438 | |||||||
| chr1:31272466 | T | C | 2 | a0001c0001t0001g0123 a0001c0001t0001g0130 |
2 | NA18954.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.655-967A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31272466 | |||||||
| chr1:31272650 | G | A | 1 | a0001c0001t0005g0070 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.655-1151C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31272650 | |||||||
| chr1:31272780 | T | A | 1 | a0001c0001t0003g0184 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.655-1281A>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31272780 | |||||||
| chr1:31273100 | A | G | 8 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0087 others(5): Show |
10 | NA18943.hp1 NA18972.hp1 NA18998.hp1 others(7): Show |
intron_variant | MODIFIER | c.655-1601T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31273100 | |||||||
| chr1:31273186 | T | A | 1 | a0001c0001t0005g0040 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.655-1687A>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31273186 | |||||||
| chr1:31273219 | A | G | 3 | a0001c0001t0002g0245 a0001c0001t0002g0247 a0001c0001t0002g0256 |
3 | HG02486.hp1 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.655-1720T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31273219 | |||||||
| chr1:31273423 | CCTGAGGT others(8): Show |
C | 46 | a0001c0001t0003g0008 a0001c0001t0003g0010 a0001c0001t0003g0021 others(43): Show |
54 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.655-1939_655-1925d others(17): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31273423 | |||||||
| chr1:31273514 | C | G | 2 | a0001c0001t0002g0046 a0001c0001t0002g0047 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.655-2015G>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31273514 | |||||||
| chr1:31273562 | C | T | 1 | a0001c0001t0002g0263 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.655-2063G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31273562 | |||||||
| chr1:31273600 | A | G | 60 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(57): Show |
66 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.655-2101T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31273600 | |||||||
| chr1:31273640 | C | CA | 144 | a0001c0001t0001g0124 a0001c0001t0001g0221 a0001c0001t0001g0267 others(141): Show |
163 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.655-2142dupT | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31273640 | |||||||
| chr1:31273904 | G | A | 1 | a0001c0001t0002g0264 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.655-2405C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31273904 | |||||||
| chr1:31273975 | T | G | 30 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0102 others(27): Show |
33 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(30): Show |
intron_variant | MODIFIER | c.655-2476A>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31273975 | |||||||
| chr1:31274168 | G | T | 1 | a0001c0001t0003g0052 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.655-2669C>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31274168 | |||||||
| chr1:31274195 | T | G | 1 | a0001c0001t0001g0148 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.655-2696A>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31274195 | |||||||
| chr1:31274250 | T | C | 1 | a0001c0001t0007g0034 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.655-2751A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31274250 | |||||||
| chr1:31274347 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.655-2848G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31274347 | |||||||
| chr1:31274383 | C | T | 1 | a0001c0001t0002g0190 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.655-2884G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31274383 | |||||||
| chr1:31274438 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.655-2939A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31274438 | |||||||
| chr1:31274486 | C | A | 23 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0061 others(20): Show |
25 | HG00280.hp2 HG00741.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.655-2987G>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31274486 | |||||||
| chr1:31274489 | C | T | 8 | a0001c0001t0002g0032 a0001c0001t0002g0252 a0001c0001t0002g0257 others(5): Show |
9 | HG01884.hp2 HG02818.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.655-2990G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31274489 | |||||||
| chr1:31274532 | C | T | 1 | a0001c0001t0003g0008 | 3 | NA18747.hp2 NA18940.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.655-3033G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31274532 | |||||||
| chr1:31274546 | T | C | 204 | a0001c0001t0001g0063 a0001c0001t0001g0221 a0001c0001t0001g0267 others(201): Show |
229 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.655-3047A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31274546 | |||||||
| chr1:31274645 | T | TA | 35 | a0001c0001t0001g0094 a0001c0001t0001g0125 a0001c0001t0001g0129 others(32): Show |
38 | HG00597.hp1 HG00609.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.655-3147dupT | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31274645 | |||||||
| chr1:31274645 | T | TAA | 113 | a0001c0001t0001g0063 a0001c0001t0001g0221 a0001c0001t0002g0023 others(110): Show |
130 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.655-3148_655-3147d others(4): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31274645 | |||||||
| chr1:31274645 | T | TAAA | 33 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0032 others(30): Show |
36 | HG01069.hp2 HG01243.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.655-3149_655-3147d others(5): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31274645 | |||||||
| chr1:31274645 | TA | T | 8 | a0001c0001t0001g0143 a0001c0001t0002g0048 a0001c0001t0007g0034 others(5): Show |
9 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.655-3147delT | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31274645 | |||||||
| chr1:31274682 | T | A | 2 | a0001c0001t0002g0269 a0001c0001t0002g0270 |
2 | HG00639.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.655-3183A>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31274682 | |||||||
| chr1:31274831 | C | T | 1 | a0001c0001t0002g0201 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.655-3332G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31274831 | |||||||
| chr1:31274885 | G | T | 9 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 others(6): Show |
10 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.655-3386C>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31274885 | |||||||
| chr1:31274922 | GC | G | 26 | a0001c0001t0004g0009 a0001c0001t0004g0033 a0001c0001t0004g0272 others(23): Show |
29 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.655-3424delG | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31274922 | |||||||
| chr1:31274975 | A | G | 1 | a0001c0001t0002g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.655-3476T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31274975 | |||||||
| chr1:31275048 | C | T | 1 | a0001c0001t0002g0045 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.655-3549G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31275048 | |||||||
| chr1:31275062 | GTTAA | G | 4 | a0001c0001t0003g0010 a0001c0001t0003g0049 a0001c0001t0003g0050 others(1): Show |
5 | HG02622.hp1 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.655-3567_655-3564d others(6): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31275062 | |||||||
| chr1:31275435 | T | TCCAGG | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.655-3937_655-3936i others(7): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31275435 | |||||||
| chr1:31275914 | A | C | 4 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0055 others(1): Show |
4 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.655-4415T>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31275914 | |||||||
| chr1:31275974 | T | C | 1 | a0001c0001t0002g0201 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.655-4475A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31275974 | |||||||
| chr1:31276172 | T | C | 5 | a0001c0002t0003g0004 a0001c0002t0003g0035 a0001c0002t0003g0036 others(2): Show |
8 | HG00621.hp2 HG02040.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.655-4673A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31276172 | |||||||
| chr1:31276245 | C | G | 97 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(94): Show |
108 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.655-4746G>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31276245 | |||||||
| chr1:31276259 | A | G | 23 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0061 others(20): Show |
25 | HG00280.hp2 HG00741.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.655-4760T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31276259 | |||||||
| chr1:31276269 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.655-4770A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31276269 | |||||||
| chr1:31276315 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.655-4816G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31276315 | |||||||
| chr1:31276353 | C | T | 9 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 others(6): Show |
10 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.655-4854G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31276353 | |||||||
| chr1:31276358 | C | T | 1 | a0001c0001t0002g0259 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.655-4859G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31276358 | |||||||
| chr1:31276455 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.654+4919C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31276455 | |||||||
| chr1:31276468 | A | T | 204 | a0001c0001t0001g0063 a0001c0001t0001g0221 a0001c0001t0001g0267 others(201): Show |
229 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.654+4906T>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31276468 | |||||||
| chr1:31276533 | T | G | 1 | a0001c0001t0002g0258 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.654+4841A>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31276533 | |||||||
| chr1:31276552 | G | A | 2 | a0001c0001t0010g0064 a0001c0001t0010g0065 |
2 | HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.654+4822C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31276552 | |||||||
| chr1:31276687 | A | C | 23 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0061 others(20): Show |
25 | HG00280.hp2 HG00741.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.654+4687T>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31276687 | |||||||
| chr1:31276807 | C | T | 1 | a0001c0001t0002g0209 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.654+4567G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31276807 | |||||||
| chr1:31276889 | T | C | 123 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(120): Show |
137 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.654+4485A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31276889 | |||||||
| chr1:31276894 | C | T | 34 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0032 others(31): Show |
37 | HG00639.hp2 HG01069.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.654+4480G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31276894 | |||||||
| chr1:31276907 | G | A | 123 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(120): Show |
137 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.654+4467C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31276907 | |||||||
| chr1:31276927 | G | A | 1 | a0001c0001t0005g0079 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.654+4447C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31276927 | |||||||
| chr1:31276995 | T | C | 1 | a0001c0001t0002g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.654+4379A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31276995 | |||||||
| chr1:31277246 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.654+4128G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31277246 | |||||||
| chr1:31277296 | T | G | 2 | a0001c0001t0010g0064 a0001c0001t0010g0065 |
2 | HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.654+4078A>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31277296 | |||||||
| chr1:31277417 | A | G | 5 | a0001c0001t0003g0010 a0001c0001t0003g0049 a0001c0001t0003g0050 others(2): Show |
6 | HG02622.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.654+3957T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31277417 | |||||||
| chr1:31277710 | T | C | 1 | a0001c0001t0005g0077 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.654+3664A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31277710 | |||||||
| chr1:31277819 | T | C | 1 | a0001c0001t0003g0051 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.654+3555A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31277819 | |||||||
| chr1:31278099 | T | C | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.654+3275A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31278099 | |||||||
| chr1:31278642 | A | G | 1 | a0001c0001t0007g0297 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.654+2732T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31278642 | |||||||
| chr1:31278665 | G | A | 97 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(94): Show |
108 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.654+2709C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31278665 | |||||||
| chr1:31278925 | T | C | 97 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(94): Show |
108 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.654+2449A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31278925 | |||||||
| chr1:31278952 | G | A | 1 | a0001c0001t0005g0040 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.654+2422C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31278952 | |||||||
| chr1:31279049 | C | CAAAAAAA others(319): Show |
3 | a0001c0001t0007g0297 a0001c0001t0007g0298 a0001c0001t0007g0300 |
3 | HG01069.hp1 HG02280.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.654+2324_654+2325i others(328): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31279049 | |||||||
| chr1:31279049 | C | CAAAAAAA others(320): Show |
3 | a0001c0001t0007g0034 a0001c0001t0007g0296 a0001c0001t0007g0299 |
4 | HG00639.hp1 HG01071.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+2324_654+2325i others(329): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31279049 | |||||||
| chr1:31279049 | CA | C | 121 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(118): Show |
135 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.654+2324delT | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31279049 | |||||||
| chr1:31279060 | A | C | 7 | a0001c0001t0005g0067 a0001c0001t0005g0071 a0001c0001t0005g0074 others(4): Show |
7 | HG00280.hp2 HG00741.hp2 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.654+2314T>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31279060 | |||||||
| chr1:31279218 | C | T | 3 | a0001c0001t0008g0030 a0001c0001t0008g0031 a0001c0001t0008g0271 |
5 | HG01255.hp2 HG01891.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.654+2156G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31279218 | |||||||
| chr1:31279229 | C | T | 2 | a0001c0001t0002g0269 a0001c0001t0002g0270 |
2 | HG00639.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.654+2145G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31279229 | |||||||
| chr1:31279330 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.654+2044C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31279330 | |||||||
| chr1:31279340 | A | G | 123 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(120): Show |
137 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.654+2034T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31279340 | |||||||
| chr1:31279413 | A | G | 97 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(94): Show |
108 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.654+1961T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31279413 | |||||||
| chr1:31279469 | G | A | 97 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(94): Show |
108 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.654+1905C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31279469 | |||||||
| chr1:31279642 | G | A | 1 | a0001c0001t0005g0077 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.654+1732C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31279642 | |||||||
| chr1:31279746 | C | CA | 5 | a0001c0001t0001g0130 a0001c0001t0002g0216 a0001c0001t0002g0220 others(2): Show |
5 | HG00741.hp1 HG01928.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.654+1627dupT | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31279746 | |||||||
| chr1:31279905 | G | A | 19 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0066 others(16): Show |
21 | HG00280.hp2 HG00741.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.654+1469C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31279905 | |||||||
| chr1:31279935 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.654+1439A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31279935 | |||||||
| chr1:31279967 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.654+1407C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31279967 | |||||||
| chr1:31280009 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.654+1365C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31280009 | |||||||
| chr1:31280113 | C | CA | 42 | a0001c0001t0001g0063 a0001c0001t0001g0114 a0001c0001t0001g0267 others(39): Show |
49 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.654+1260dupT | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31280113 | |||||||
| chr1:31280113 | C | CAA | 20 | a0001c0001t0001g0221 a0001c0001t0002g0165 a0001c0001t0002g0189 others(17): Show |
20 | HG00597.hp1 HG01099.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.654+1259_654+1260d others(4): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31280113 | |||||||
| chr1:31280113 | CA | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
172 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.654+1260delT | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31280113 | |||||||
| chr1:31280113 | CAAA | C | 24 | a0001c0001t0004g0009 a0001c0001t0004g0033 a0001c0001t0004g0272 others(21): Show |
27 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.654+1258_654+1260d others(5): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31280113 | |||||||
| chr1:31280170 | C | CT | 74 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0063 others(71): Show |
84 | HG00280.hp2 HG00597.hp2 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.654+1203dupA | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31280170 | |||||||
| chr1:31280241 | G | A | 1 | a0001c0001t0005g0062 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.654+1133C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31280241 | |||||||
| chr1:31280310 | A | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0144 a0001c0001t0001g0146 others(1): Show |
6 | HG02615.hp2 HG02630.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.654+1064T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31280310 | |||||||
| chr1:31280335 | T | C | 4 | a0001c0001t0002g0202 a0001c0001t0002g0214 a0001c0001t0002g0215 others(1): Show |
4 | HG02273.hp1 NA18947.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+1039A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31280335 | |||||||
| chr1:31280408 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.654+966G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31280408 | |||||||
| chr1:31280498 | G | T | 26 | a0001c0001t0004g0009 a0001c0001t0004g0033 a0001c0001t0004g0272 others(23): Show |
29 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.654+876C>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31280498 | |||||||
| chr1:31280506 | G | A | 97 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(94): Show |
108 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.654+868C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31280506 | |||||||
| chr1:31280558 | G | GTATT | 123 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(120): Show |
137 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.654+815_654+816ins others(4): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31280558 | |||||||
| chr1:31280559 | T | G | 1 | a0001c0001t0001g0096 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.654+815A>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31280559 | |||||||
| chr1:31280608 | C | T | 9 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 others(6): Show |
10 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.654+766G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31280608 | |||||||
| chr1:31280659 | G | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0144 a0001c0001t0001g0146 others(1): Show |
6 | HG02615.hp2 HG02630.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.654+715C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31280659 | |||||||
| chr1:31280758 | G | A | 9 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 others(6): Show |
10 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.654+616C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31280758 | |||||||
| chr1:31280767 | G | GT | 79 | a0001c0001t0001g0058 a0001c0001t0001g0063 a0001c0001t0002g0163 others(76): Show |
88 | HG00280.hp2 HG00597.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.654+606dupA | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31280767 | |||||||
| chr1:31280767 | G | GTT | 10 | a0001c0001t0002g0041 a0001c0001t0002g0046 a0001c0001t0002g0048 others(7): Show |
11 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.654+605_654+606dup others(2): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31280767 | |||||||
| chr1:31280772 | T | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(83): Show |
115 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.654+602A>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31280772 | |||||||
| chr1:31281037 | A | G | 23 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0061 others(20): Show |
25 | HG00280.hp2 HG00741.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.654+337T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31281037 | |||||||
| chr1:31281111 | C | G | 1 | a0001c0001t0001g0097 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.654+263G>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31281111 | |||||||
| chr1:31281332 | C | T | 2 | a0001c0001t0007g0298 a0001c0001t0007g0299 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.654+42G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 5/9 | chr1 | 31281332 | |||||||
| chr1:31281520 | T | C | 23 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0061 others(20): Show |
25 | HG00280.hp2 HG00741.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.532-24A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31281520 | |||||||
| chr1:31281616 | A | G | 2 | a0001c0001t0005g0011 a0001c0001t0005g0066 |
3 | HG01109.hp1 HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.532-120T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31281616 | |||||||
| chr1:31281661 | T | A | 1 | a0001c0001t0005g0073 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.532-165A>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31281661 | |||||||
| chr1:31281664 | G | C | 123 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(120): Show |
137 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.532-168C>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31281664 | |||||||
| chr1:31281758 | T | C | 5 | a0001c0001t0003g0010 a0001c0001t0003g0049 a0001c0001t0003g0050 others(2): Show |
6 | HG02622.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.532-262A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31281758 | |||||||
| chr1:31281840 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.532-344C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31281840 | |||||||
| chr1:31281858 | G | C | 13 | a0001c0001t0004g0009 a0001c0001t0004g0033 a0001c0001t0004g0273 others(10): Show |
16 | HG00408.hp2 HG00609.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.532-362C>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31281858 | |||||||
| chr1:31281963 | C | A | 1 | a0001c0001t0002g0227 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.532-467G>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31281963 | |||||||
| chr1:31281981 | A | G | 26 | a0001c0001t0004g0009 a0001c0001t0004g0033 a0001c0001t0004g0272 others(23): Show |
29 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.532-485T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31281981 | |||||||
| chr1:31282130 | G | A | 3 | a0001c0001t0002g0263 a0001c0001t0002g0269 a0001c0001t0002g0270 |
3 | HG00639.hp2 HG01070.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.532-634C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282130 | |||||||
| chr1:31282444 | G | A | 9 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 others(6): Show |
10 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.532-948C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282444 | |||||||
| chr1:31282466 | GCTATCTA others(13): Show |
G | 5 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0004g0289 others(2): Show |
5 | HG01952.hp1 HG02300.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.532-990_532-971del others(20): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282466 | |||||||
| chr1:31282466 | GCTATCTA others(17): Show |
G | 1 | a0001c0001t0003g0177 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.532-994_532-971del others(24): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282466 | |||||||
| chr1:31282467 | CTATCTAT others(9): Show |
C | 29 | a0001c0001t0002g0026 a0001c0001t0002g0249 a0001c0001t0002g0263 others(26): Show |
30 | HG00597.hp2 HG00621.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.532-987_532-972del others(16): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282467 | |||||||
| chr1:31282471 | CTATCTAT others(5): Show |
C | 44 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0041 others(41): Show |
46 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.532-987_532-976del others(12): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282471 | |||||||
| chr1:31282475 | CTATCTAT others(1): Show |
C | 73 | a0001c0001t0001g0221 a0001c0001t0002g0022 a0001c0001t0002g0023 others(70): Show |
80 | HG00423.hp2 HG00639.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.532-987_532-980del others(8): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282475 | |||||||
| chr1:31282479 | CTATG | C | 47 | a0001c0001t0001g0267 a0001c0001t0002g0022 a0001c0001t0002g0024 others(44): Show |
47 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.532-987_532-984del others(4): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282479 | |||||||
| chr1:31282483 | G | C | 19 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0163 others(16): Show |
19 | HG00099.hp1 HG00597.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.532-987C>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282483 | |||||||
| chr1:31282483 | G | GTATC | 7 | a0001c0001t0001g0060 a0001c0001t0001g0063 a0001c0001t0001g0086 others(4): Show |
7 | HG02109.hp2 HG02135.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.532-991_532-988dup others(4): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282483 | |||||||
| chr1:31282483 | G | GTATCTAT others(1): Show |
3 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0107 |
3 | HG01884.hp1 HG02559.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.532-995_532-988dup others(8): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282483 | |||||||
| chr1:31282483 | GTATC | G | 43 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(40): Show |
59 | HG00408.hp1 HG00423.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.532-991_532-988del others(4): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282483 | |||||||
| chr1:31282483 | GTATCTAT others(1): Show |
G | 17 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(14): Show |
20 | HG00323.hp2 HG00673.hp1 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.532-995_532-988del others(8): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282483 | |||||||
| chr1:31282483 | GTATCTAT others(5): Show |
G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0100 |
4 | HG00099.hp2 HG00642.hp1 HG01070.hp2 others(1): Show |
intron_variant | MODIFIER | c.532-999_532-988del others(12): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282483 | |||||||
| chr1:31282518 | T | C | 4 | a0001c0001t0002g0202 a0001c0001t0002g0214 a0001c0001t0002g0215 others(1): Show |
4 | HG02273.hp1 NA18947.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.532-1022A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282518 | |||||||
| chr1:31282521 | A | G | 3 | a0001c0001t0002g0263 a0001c0001t0002g0269 a0001c0001t0002g0270 |
3 | HG00639.hp2 HG01070.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.532-1025T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282521 | |||||||
| chr1:31282549 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.532-1053C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282549 | |||||||
| chr1:31282558 | G | GCTAT | 82 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0013 others(79): Show |
92 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.532-1066_532-1063d others(6): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282558 | |||||||
| chr1:31282558 | G | GCTATCTA others(1): Show |
28 | a0001c0001t0001g0003 a0001c0001t0001g0056 a0001c0001t0001g0086 others(25): Show |
33 | HG00408.hp2 HG00673.hp2 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.532-1070_532-1063d others(10): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282558 | |||||||
| chr1:31282558 | G | GCTATCTA others(5): Show |
2 | a0001c0001t0001g0139 a0001c0001t0002g0192 |
2 | HG00323.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.532-1074_532-1063d others(14): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282558 | |||||||
| chr1:31282558 | GCTAT | G | 47 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0055 others(44): Show |
50 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.532-1066_532-1063d others(6): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282558 | |||||||
| chr1:31282558 | GCTATCTA others(1): Show |
G | 21 | a0001c0001t0001g0043 a0001c0001t0001g0059 a0001c0001t0001g0132 others(18): Show |
25 | HG01167.hp2 HG01175.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.532-1070_532-1063d others(10): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282558 | |||||||
| chr1:31282558 | GCTATCTA others(5): Show |
G | 10 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0141 others(7): Show |
10 | HG01255.hp2 HG01346.hp1 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.532-1074_532-1063d others(14): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282558 | |||||||
| chr1:31282558 | GCTATCTA others(9): Show |
G | 5 | a0001c0001t0002g0027 a0001c0001t0002g0222 a0001c0001t0002g0223 others(2): Show |
6 | HG01081.hp2 HG02965.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.532-1078_532-1063d others(18): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282558 | |||||||
| chr1:31282558 | GCTATCTA others(17): Show |
G | 1 | a0001c0001t0001g0107 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.532-1086_532-1063d others(26): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282558 | |||||||
| chr1:31282605 | ATCTATCT others(5): Show |
A | 1 | a0001c0001t0001g0060 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.532-1121_532-1110d others(14): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282605 | |||||||
| chr1:31282654 | G | A | 199 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(196): Show |
224 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.532-1158C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282654 | |||||||
| chr1:31282673 | C | CTCTA | 26 | a0001c0001t0004g0009 a0001c0001t0004g0033 a0001c0001t0004g0272 others(23): Show |
29 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.532-1181_532-1178d others(6): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282673 | |||||||
| chr1:31282700 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.532-1204C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282700 | |||||||
| chr1:31282910 | A | C | 27 | a0001c0001t0002g0244 a0001c0001t0004g0009 a0001c0001t0004g0033 others(24): Show |
30 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(27): Show |
intron_variant | MODIFIER | c.532-1414T>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282910 | |||||||
| chr1:31282955 | C | T | 1 | a0001c0001t0004g0291 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.532-1459G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31282955 | |||||||
| chr1:31283127 | T | C | 7 | a0001c0001t0001g0018 a0001c0001t0001g0133 a0001c0001t0001g0134 others(4): Show |
8 | HG00735.hp2 HG01099.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.532-1631A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31283127 | |||||||
| chr1:31283138 | C | A | 37 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0032 others(34): Show |
42 | HG00639.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.532-1642G>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31283138 | |||||||
| chr1:31283468 | T | G | 4 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
4 | NA18940.hp1 NA18983.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.532-1972A>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31283468 | |||||||
| chr1:31283536 | G | C | 1 | a0001c0001t0005g0062 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.532-2040C>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31283536 | |||||||
| chr1:31283722 | A | C | 1 | a0001c0001t0009g0085 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.532-2226T>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31283722 | |||||||
| chr1:31283893 | A | G | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG02486.hp2 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.532-2397T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31283893 | |||||||
| chr1:31283898 | T | C | 2 | a0001c0001t0003g0052 a0001c0001t0003g0053 |
2 | HG03239.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.532-2402A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31283898 | |||||||
| chr1:31283982 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.532-2486G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31283982 | |||||||
| chr1:31284014 | CAG | C | 4 | a0001c0001t0003g0183 a0001c0001t0003g0184 a0001c0001t0003g0185 others(1): Show |
4 | HG02698.hp2 HG02735.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.532-2520_532-2519d others(4): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31284014 | |||||||
| chr1:31284023 | C | T | 4 | a0001c0001t0004g0274 a0001c0001t0004g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG02080.hp1 NA18952.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.532-2527G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31284023 | |||||||
| chr1:31284138 | G | A | 1 | a0001c0001t0004g0291 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.532-2642C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31284138 | |||||||
| chr1:31284298 | G | A | 97 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(94): Show |
108 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.532-2802C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31284298 | |||||||
| chr1:31284321 | C | G | 203 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(200): Show |
228 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.532-2825G>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31284321 | |||||||
| chr1:31284330 | G | A | 2 | a0001c0001t0005g0080 a0001c0001t0005g0081 |
2 | HG01934.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.532-2834C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31284330 | |||||||
| chr1:31284331 | A | T | 123 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(120): Show |
137 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.532-2835T>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31284331 | |||||||
| chr1:31284340 | G | A | 1 | a0001c0001t0003g0054 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.532-2844C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31284340 | |||||||
| chr1:31284449 | C | T | 1 | a0001c0001t0009g0085 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.532-2953G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31284449 | |||||||
| chr1:31284596 | G | A | 6 | a0001c0001t0007g0034 a0001c0001t0007g0296 a0001c0001t0007g0297 others(3): Show |
7 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.532-3100C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31284596 | |||||||
| chr1:31284647 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.532-3151C>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31284647 | |||||||
| chr1:31284677 | G | A | 3 | a0001c0001t0008g0030 a0001c0001t0008g0031 a0001c0001t0008g0271 |
5 | HG01255.hp2 HG01891.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.532-3181C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31284677 | |||||||
| chr1:31284696 | T | C | 3 | a0001c0001t0001g0084 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | NA18963.hp2 NA18999.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.532-3200A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31284696 | |||||||
| chr1:31284867 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.532-3371C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31284867 | |||||||
| chr1:31284902 | C | T | 26 | a0001c0001t0004g0009 a0001c0001t0004g0033 a0001c0001t0004g0272 others(23): Show |
29 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.532-3406G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31284902 | |||||||
| chr1:31284982 | A | G | 1 | a0001c0001t0002g0239 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.532-3486T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31284982 | |||||||
| chr1:31285119 | C | A | 1 | a0001c0001t0005g0082 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.532-3623G>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31285119 | |||||||
| chr1:31285210 | G | C | 1 | a0001c0001t0005g0082 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.532-3714C>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31285210 | |||||||
| chr1:31285242 | C | CTT | 118 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(115): Show |
132 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.532-3748_532-3747d others(4): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31285242 | |||||||
| chr1:31285257 | G | C | 1 | a0001c0001t0002g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.532-3761C>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31285257 | |||||||
| chr1:31285261 | T | C | 4 | a0001c0001t0002g0028 a0001c0001t0002g0239 a0001c0001t0002g0242 others(1): Show |
5 | HG02717.hp1 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.532-3765A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31285261 | |||||||
| chr1:31285313 | C | T | 2 | a0001c0001t0002g0229 a0001c0001t0002g0237 |
2 | NA18960.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.532-3817G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31285313 | |||||||
| chr1:31285374 | G | C | 26 | a0001c0001t0004g0009 a0001c0001t0004g0033 a0001c0001t0004g0272 others(23): Show |
29 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.532-3878C>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31285374 | |||||||
| chr1:31285430 | G | A | 1 | a0001c0001t0002g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.531+3824C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31285430 | |||||||
| chr1:31285466 | C | T | 9 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 others(6): Show |
10 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.531+3788G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31285466 | |||||||
| chr1:31285518 | C | G | 44 | a0001c0001t0003g0008 a0001c0001t0003g0010 a0001c0001t0003g0021 others(41): Show |
52 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.531+3736G>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31285518 | |||||||
| chr1:31285620 | C | T | 70 | a0001c0001t0003g0008 a0001c0001t0003g0010 a0001c0001t0003g0021 others(67): Show |
80 | HG00280.hp2 HG00597.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.531+3634G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31285620 | |||||||
| chr1:31285898 | G | A | 1 | a0001c0001t0005g0040 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.531+3356C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31285898 | |||||||
| chr1:31286017 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.531+3237A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31286017 | |||||||
| chr1:31286022 | T | TGTGAAAG others(10): Show |
26 | a0001c0001t0004g0009 a0001c0001t0004g0033 a0001c0001t0004g0272 others(23): Show |
29 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.531+3231_531+3232i others(19): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31286022 | |||||||
| chr1:31286025 | C | G | 26 | a0001c0001t0004g0009 a0001c0001t0004g0033 a0001c0001t0004g0272 others(23): Show |
29 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.531+3229G>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31286025 | |||||||
| chr1:31286026 | T | TG | 26 | a0001c0001t0004g0009 a0001c0001t0004g0033 a0001c0001t0004g0272 others(23): Show |
29 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.531+3227dupC | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31286026 | |||||||
| chr1:31286140 | G | A | 1 | a0001c0001t0002g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.531+3114C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31286140 | |||||||
| chr1:31286165 | T | TAC | 63 | a0001c0001t0001g0152 a0001c0001t0001g0221 a0001c0001t0001g0267 others(60): Show |
69 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.531+3087_531+3088d others(4): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31286165 | |||||||
| chr1:31286211 | T | A | 1 | a0001c0001t0001g0113 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.531+3043A>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31286211 | |||||||
| chr1:31286430 | A | G | 4 | a0001c0001t0002g0028 a0001c0001t0002g0239 a0001c0001t0002g0242 others(1): Show |
5 | HG02717.hp1 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.531+2824T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31286430 | |||||||
| chr1:31286641 | C | T | 1 | a0001c0001t0002g0268 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.531+2613G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31286641 | |||||||
| chr1:31286649 | C | T | 1 | a0001c0001t0002g0268 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.531+2605G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31286649 | |||||||
| chr1:31286650 | G | A | 1 | a0001c0001t0002g0224 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.531+2604C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31286650 | |||||||
| chr1:31286823 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.531+2431C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31286823 | |||||||
| chr1:31286841 | A | G | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+2413T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31286841 | |||||||
| chr1:31286904 | T | A | 37 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0032 others(34): Show |
42 | HG00639.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.531+2350A>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31286904 | |||||||
| chr1:31286946 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.531+2308A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31286946 | |||||||
| chr1:31287014 | G | A | 37 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0032 others(34): Show |
42 | HG00639.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.531+2240C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31287014 | |||||||
| chr1:31287144 | T | C | 23 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0061 others(20): Show |
25 | HG00280.hp2 HG00741.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.531+2110A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31287144 | |||||||
| chr1:31287186 | C | G | 1 | a0001c0001t0002g0227 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.531+2068G>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31287186 | |||||||
| chr1:31287193 | C | T | 9 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 others(6): Show |
10 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.531+2061G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31287193 | |||||||
| chr1:31287241 | A | C | 1 | a0001c0001t0002g0236 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.531+2013T>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31287241 | |||||||
| chr1:31287247 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.531+2007C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31287247 | |||||||
| chr1:31287281 | G | A | 123 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(120): Show |
137 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.531+1973C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31287281 | |||||||
| chr1:31287327 | T | C | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.531+1927A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31287327 | |||||||
| chr1:31287503 | G | C | 1 | a0001c0001t0005g0040 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.531+1751C>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31287503 | |||||||
| chr1:31287566 | C | T | 26 | a0001c0001t0004g0009 a0001c0001t0004g0033 a0001c0001t0004g0272 others(23): Show |
29 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.531+1688G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31287566 | |||||||
| chr1:31287768 | G | A | 1 | a0001c0001t0002g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.531+1486C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31287768 | |||||||
| chr1:31287818 | T | C | 17 | a0001c0001t0005g0012 a0001c0001t0005g0067 a0001c0001t0005g0068 others(14): Show |
18 | HG00280.hp2 HG00741.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.531+1436A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31287818 | |||||||
| chr1:31287917 | A | T | 60 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(57): Show |
66 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.531+1337T>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31287917 | |||||||
| chr1:31288044 | T | A | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1210A>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288044 | |||||||
| chr1:31288048 | A | T | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1206T>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288048 | |||||||
| chr1:31288053 | C | T | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1201G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288053 | |||||||
| chr1:31288056 | A | T | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1198T>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288056 | |||||||
| chr1:31288058 | G | T | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1196C>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288058 | |||||||
| chr1:31288059 | A | T | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1195T>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288059 | |||||||
| chr1:31288062 | C | T | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1192G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288062 | |||||||
| chr1:31288063 | T | A | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1191A>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288063 | |||||||
| chr1:31288068 | C | A | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1186G>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288068 | |||||||
| chr1:31288069 | T | G | 37 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0032 others(34): Show |
42 | HG00639.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.531+1185A>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288069 | |||||||
| chr1:31288074 | A | T | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1180T>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288074 | |||||||
| chr1:31288075 | A | T | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1179T>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288075 | |||||||
| chr1:31288088 | G | A | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1166C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288088 | |||||||
| chr1:31288093 | G | C | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1161C>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288093 | |||||||
| chr1:31288102 | A | G | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1152T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288102 | |||||||
| chr1:31288108 | A | G | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1146T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288108 | |||||||
| chr1:31288109 | G | C | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1145C>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288109 | |||||||
| chr1:31288110 | C | G | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1144G>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288110 | |||||||
| chr1:31288114 | G | T | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1140C>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288114 | |||||||
| chr1:31288115 | A | C | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1139T>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288115 | |||||||
| chr1:31288117 | T | C | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1137A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288117 | |||||||
| chr1:31288118 | G | A | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1136C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288118 | |||||||
| chr1:31288119 | T | G | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1135A>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288119 | |||||||
| chr1:31288120 | G | C | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1134C>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288120 | |||||||
| chr1:31288121 | C | T | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1133G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288121 | |||||||
| chr1:31288131 | C | A | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1123G>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288131 | |||||||
| chr1:31288133 | A | C | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1121T>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288133 | |||||||
| chr1:31288134 | G | T | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1120C>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288134 | |||||||
| chr1:31288144 | T | C | 44 | a0001c0001t0003g0008 a0001c0001t0003g0010 a0001c0001t0003g0021 others(41): Show |
52 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.531+1110A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288144 | |||||||
| chr1:31288146 | G | C | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1108C>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288146 | |||||||
| chr1:31288148 | G | A | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1106C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288148 | |||||||
| chr1:31288149 | C | G | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1105G>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288149 | |||||||
| chr1:31288150 | A | C | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1104T>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288150 | |||||||
| chr1:31288153 | A | T | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1101T>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288153 | |||||||
| chr1:31288159 | T | C | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+1095A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288159 | |||||||
| chr1:31288166 | GA | G | 72 | a0001c0001t0001g0063 a0001c0001t0001g0084 a0001c0001t0003g0008 others(69): Show |
82 | HG00280.hp2 HG00597.hp2 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.531+1087delT | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288166 | |||||||
| chr1:31288209 | A | G | 23 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0061 others(20): Show |
25 | HG00280.hp2 HG00741.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.531+1045T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288209 | |||||||
| chr1:31288666 | C | CCTTT | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
205 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.531+584_531+587dup others(4): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288666 | |||||||
| chr1:31288667 | C | CTTTCT | 123 | a0001c0001t0001g0118 a0001c0001t0001g0221 a0001c0001t0001g0267 others(120): Show |
137 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.531+586_531+587ins others(5): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288667 | |||||||
| chr1:31288762 | A | G | 123 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(120): Show |
137 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.531+492T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288762 | |||||||
| chr1:31288802 | A | G | 204 | a0001c0001t0001g0063 a0001c0001t0001g0221 a0001c0001t0001g0267 others(201): Show |
229 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.531+452T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288802 | |||||||
| chr1:31288824 | C | T | 2 | a0001c0001t0004g0274 a0001c0001t0004g0275 |
2 | NA18952.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.531+430G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288824 | |||||||
| chr1:31288825 | G | A | 2 | a0001c0001t0005g0155 a0001c0001t0005g0156 |
2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.531+429C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288825 | |||||||
| chr1:31288856 | C | A | 71 | a0001c0001t0001g0063 a0001c0001t0003g0008 a0001c0001t0003g0010 others(68): Show |
81 | HG00280.hp2 HG00597.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.531+398G>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288856 | |||||||
| chr1:31288878 | C | T | 97 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(94): Show |
108 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.531+376G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288878 | |||||||
| chr1:31288921 | C | G | 1 | a0001c0002t0006g0038 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.531+333G>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288921 | |||||||
| chr1:31288921 | C | T | 27 | a0001c0001t0003g0008 a0001c0001t0003g0021 a0001c0001t0003g0167 others(24): Show |
33 | HG00597.hp2 HG00621.hp2 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.531+333G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288921 | |||||||
| chr1:31288982 | C | T | 26 | a0001c0001t0004g0009 a0001c0001t0004g0033 a0001c0001t0004g0272 others(23): Show |
29 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.531+272G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288982 | |||||||
| chr1:31288998 | T | C | 2 | a0001c0001t0010g0064 a0001c0001t0010g0065 |
2 | HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.531+256A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31288998 | |||||||
| chr1:31289013 | A | G | 123 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(120): Show |
137 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.531+241T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31289013 | |||||||
| chr1:31289089 | T | A | 123 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(120): Show |
137 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.531+165A>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31289089 | |||||||
| chr1:31289142 | G | A | 292 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(289): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.531+112C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31289142 | |||||||
| chr1:31289228 | C | T | 1 | a0001c0001t0002g0191 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.531+26G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 4/9 | chr1 | 31289228 | |||||||
| chr1:31289527 | C | T | 204 | a0001c0001t0001g0063 a0001c0001t0001g0221 a0001c0001t0001g0267 others(201): Show |
229 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.366-108G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31289527 | |||||||
| chr1:31289535 | C | T | 1 | a0001c0001t0005g0040 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366-116G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31289535 | |||||||
| chr1:31289684 | G | A | 1 | a0001c0001t0002g0262 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.366-265C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31289684 | |||||||
| chr1:31289780 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.366-361C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31289780 | |||||||
| chr1:31289885 | T | C | 1 | a0001c0001t0002g0264 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.366-466A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31289885 | |||||||
| chr1:31289895 | T | A | 1 | a0001c0002t0006g0038 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.366-476A>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31289895 | |||||||
| chr1:31289906 | T | C | 7 | a0001c0001t0002g0032 a0001c0001t0002g0257 a0001c0001t0002g0258 others(4): Show |
8 | HG01884.hp2 HG02818.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.366-487A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31289906 | |||||||
| chr1:31290134 | T | C | 97 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(94): Show |
108 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.366-715A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31290134 | |||||||
| chr1:31290237 | G | T | 26 | a0001c0001t0004g0009 a0001c0001t0004g0033 a0001c0001t0004g0272 others(23): Show |
29 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.366-818C>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31290237 | |||||||
| chr1:31290323 | C | A | 1 | a0001c0001t0001g0138 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.366-904G>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31290323 | |||||||
| chr1:31290603 | T | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(71): Show |
100 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.366-1184A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31290603 | |||||||
| chr1:31290605 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(71): Show |
100 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.366-1186G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31290605 | |||||||
| chr1:31290648 | C | T | 1 | a0001c0001t0002g0190 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.366-1229G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31290648 | |||||||
| chr1:31290649 | G | A | 123 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(120): Show |
137 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.366-1230C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31290649 | |||||||
| chr1:31290693 | C | T | 43 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(40): Show |
54 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.365+1220G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31290693 | |||||||
| chr1:31290746 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.365+1167G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31290746 | |||||||
| chr1:31290747 | G | A | 1 | a0001c0001t0002g0226 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.365+1166C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31290747 | |||||||
| chr1:31290827 | G | A | 1 | a0001c0001t0002g0227 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.365+1086C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31290827 | |||||||
| chr1:31290850 | A | C | 123 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(120): Show |
137 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.365+1063T>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31290850 | |||||||
| chr1:31290940 | T | C | 123 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(120): Show |
137 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.365+973A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31290940 | |||||||
| chr1:31290955 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.365+958C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31290955 | |||||||
| chr1:31291075 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.365+838C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31291075 | |||||||
| chr1:31291178 | T | C | 204 | a0001c0001t0001g0063 a0001c0001t0001g0221 a0001c0001t0001g0267 others(201): Show |
229 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.365+735A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31291178 | |||||||
| chr1:31291201 | A | T | 123 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(120): Show |
137 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.365+712T>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31291201 | |||||||
| chr1:31291207 | G | C | 1 | a0001c0001t0002g0228 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.365+706C>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31291207 | |||||||
| chr1:31291288 | C | CAAAAAAA others(2): Show |
33 | a0001c0001t0001g0267 a0001c0001t0002g0028 a0001c0001t0002g0029 others(30): Show |
38 | HG01069.hp2 HG01070.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.365+616_365+624dup others(9): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31291288 | |||||||
| chr1:31291288 | C | CAAAAAAA others(3): Show |
56 | a0001c0001t0001g0221 a0001c0001t0002g0022 a0001c0001t0002g0023 others(53): Show |
62 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.365+615_365+624dup others(10): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31291288 | |||||||
| chr1:31291288 | C | CAAAAAAA others(4): Show |
27 | a0001c0001t0002g0229 a0001c0001t0002g0230 a0001c0001t0002g0231 others(24): Show |
30 | HG00408.hp2 HG00609.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.365+614_365+624dup others(11): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31291288 | |||||||
| chr1:31291288 | C | CAAAAAAA others(5): Show |
3 | a0001c0001t0004g0292 a0001c0001t0004g0293 a0001c0001t0004g0294 |
3 | HG02080.hp1 NA18950.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.365+613_365+624dup others(12): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31291288 | |||||||
| chr1:31291313 | A | G | 97 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(94): Show |
108 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.365+600T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31291313 | |||||||
| chr1:31291325 | G | A | 1 | a0001c0001t0003g0187 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.365+588C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31291325 | |||||||
| chr1:31291772 | T | C | 1 | a0001c0001t0005g0040 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.365+141A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31291772 | |||||||
| chr1:31291846 | G | A | 60 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(57): Show |
66 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.365+67C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31291846 | |||||||
| chr1:31291866 | C | CAAG | 123 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(120): Show |
137 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.365+44_365+46dupCT others(1): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 3/9 | chr1 | 31291866 | |||||||
| chr1:31292083 | T | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(287): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.272-77A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 2/9 | chr1 | 31292083 | |||||||
| chr1:31292090 | C | T | 1 | a0001c0001t0002g0238 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.272-84G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 2/9 | chr1 | 31292090 | |||||||
| chr1:31292170 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.272-164C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 2/9 | chr1 | 31292170 | |||||||
| chr1:31292317 | G | A | 22 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0055 others(19): Show |
24 | HG00280.hp2 HG00741.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.272-311C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 2/9 | chr1 | 31292317 | |||||||
| chr1:31292442 | G | C | 19 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0066 others(16): Show |
21 | HG00280.hp2 HG00741.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.272-436C>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 2/9 | chr1 | 31292442 | |||||||
| chr1:31292553 | C | T | 1 | a0001c0001t0005g0061 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.272-547G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 2/9 | chr1 | 31292553 | |||||||
| chr1:31292610 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.272-604A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 2/9 | chr1 | 31292610 | |||||||
| chr1:31292639 | TGATTTTT others(5): Show |
T | 1 | a0001c0001t0006g0265 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.271+568_271+579del others(12): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 2/9 | chr1 | 31292639 | |||||||
| chr1:31292674 | A | G | 1 | a0001c0001t0003g0158 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.271+545T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 2/9 | chr1 | 31292674 | |||||||
| chr1:31292777 | A | G | 1 | a0001c0001t0002g0045 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.271+442T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 2/9 | chr1 | 31292777 | |||||||
| chr1:31292838 | T | C | 71 | a0001c0001t0001g0063 a0001c0001t0003g0008 a0001c0001t0003g0010 others(68): Show |
81 | HG00280.hp2 HG00597.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.271+381A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 2/9 | chr1 | 31292838 | |||||||
| chr1:31292840 | G | T | 1 | a0001c0001t0004g0033 | 2 | NA19010.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.271+379C>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 2/9 | chr1 | 31292840 | |||||||
| chr1:31293121 | C | T | 60 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(57): Show |
66 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.271+98G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 2/9 | chr1 | 31293121 | |||||||
| chr1:31293359 | G | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0055 |
3 | HG01884.hp1 HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.142-11C>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31293359 | |||||||
| chr1:31293464 | C | T | 1 | a0001c0001t0003g0157 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.142-116G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31293464 | |||||||
| chr1:31293644 | T | C | 97 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(94): Show |
108 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.142-296A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31293644 | |||||||
| chr1:31293738 | T | A | 37 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0032 others(34): Show |
42 | HG00639.hp2 HG01069.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.142-390A>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31293738 | |||||||
| chr1:31293913 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.142-565G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31293913 | |||||||
| chr1:31293941 | A | G | 26 | a0001c0001t0004g0009 a0001c0001t0004g0033 a0001c0001t0004g0272 others(23): Show |
29 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.142-593T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31293941 | |||||||
| chr1:31294043 | A | G | 44 | a0001c0001t0003g0008 a0001c0001t0003g0010 a0001c0001t0003g0021 others(41): Show |
52 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.142-695T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31294043 | |||||||
| chr1:31294051 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.142-703A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31294051 | |||||||
| chr1:31294052 | G | T | 1 | a0001c0001t0001g0151 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.142-704C>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31294052 | |||||||
| chr1:31294082 | C | T | 2 | a0001c0001t0002g0046 a0001c0001t0002g0047 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.142-734G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31294082 | |||||||
| chr1:31294109 | A | G | 97 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(94): Show |
108 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.142-761T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31294109 | |||||||
| chr1:31294114 | C | T | 1 | a0001c0001t0002g0188 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.142-766G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31294114 | |||||||
| chr1:31294278 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.142-930A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31294278 | |||||||
| chr1:31294315 | T | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(83): Show |
115 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.142-967A>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31294315 | |||||||
| chr1:31294339 | A | G | 2 | a0001c0001t0002g0234 a0001c0001t0002g0235 |
2 | HG01069.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.142-991T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31294339 | |||||||
| chr1:31294406 | A | G | 9 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 others(6): Show |
10 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-1058T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31294406 | |||||||
| chr1:31294448 | A | ATATT | 58 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(55): Show |
64 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.142-1104_142-1101d others(6): Show |
SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31294448 | |||||||
| chr1:31294521 | G | A | 1 | a0001c0001t0005g0040 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.142-1173C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31294521 | |||||||
| chr1:31294621 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.142-1273C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31294621 | |||||||
| chr1:31294735 | T | G | 1 | a0001c0001t0001g0151 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.142-1387A>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31294735 | |||||||
| chr1:31294980 | C | A | 1 | a0001c0001t0002g0268 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.141+1631G>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31294980 | |||||||
| chr1:31294986 | G | A | 1 | a0001c0001t0002g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.141+1625C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31294986 | |||||||
| chr1:31295003 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.141+1608G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31295003 | |||||||
| chr1:31295077 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.141+1534A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31295077 | |||||||
| chr1:31295087 | T | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | NA18963.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.141+1524A>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31295087 | |||||||
| chr1:31295147 | T | G | 2 | a0001c0001t0005g0155 a0001c0001t0005g0156 |
2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.141+1464A>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31295147 | |||||||
| chr1:31295151 | A | G | 26 | a0001c0001t0004g0009 a0001c0001t0004g0033 a0001c0001t0004g0272 others(23): Show |
29 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.141+1460T>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31295151 | |||||||
| chr1:31295260 | G | A | 7 | a0001c0001t0003g0157 a0001c0001t0003g0158 a0001c0001t0003g0160 others(4): Show |
8 | HG00642.hp2 HG01928.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.141+1351C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31295260 | |||||||
| chr1:31295350 | C | CA | 99 | a0001c0001t0001g0166 a0001c0001t0001g0221 a0001c0001t0001g0267 others(96): Show |
110 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.141+1260dupT | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31295350 | |||||||
| chr1:31295358 | G | T | 1 | a0001c0001t0001g0044 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.141+1253C>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31295358 | |||||||
| chr1:31295392 | G | C | 28 | a0001c0001t0003g0008 a0001c0001t0003g0021 a0001c0001t0003g0167 others(25): Show |
34 | HG00597.hp2 HG00621.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.141+1219C>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31295392 | |||||||
| chr1:31295477 | G | C | 2 | a0001c0001t0002g0269 a0001c0001t0002g0270 |
2 | HG00639.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.141+1134C>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31295477 | |||||||
| chr1:31295928 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.141+683G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31295928 | |||||||
| chr1:31296094 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.141+517G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31296094 | |||||||
| chr1:31296178 | T | C | 121 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0002g0022 others(118): Show |
135 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.141+433A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31296178 | |||||||
| chr1:31296203 | C | T | 1 | a0001c0001t0005g0040 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.141+408G>A | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31296203 | |||||||
| chr1:31296475 | T | A | 1 | a0001c0001t0004g0295 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.141+136A>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31296475 | |||||||
| chr1:31296509 | T | C | 1 | a0001c0001t0008g0271 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.141+102A>G | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31296509 | |||||||
| chr1:31296516 | C | G | 26 | a0001c0001t0004g0009 a0001c0001t0004g0033 a0001c0001t0004g0272 others(23): Show |
29 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.141+95G>C | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31296516 | |||||||
| chr1:31296567 | G | A | 26 | a0001c0001t0004g0009 a0001c0001t0004g0033 a0001c0001t0004g0272 others(23): Show |
29 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.141+44C>T | SNRNP40 | ENSG00000060688.13 | transcript | ENST00000263694.9 | protein_coding | 1/9 | chr1 | 31296567 |