Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9887 |
| ensemblid | ENSG00000116698.22 |
| hgncid | 16792 |
| symbol | SMG7 |
| name | SMG7 nonsense mediated mRNA decay factor |
| refseq_nuc | NM_001375584.1 |
| refseq_prot | NP_001362513.1 |
| ensembl_nuc | ENST00000688051.1 |
| ensembl_prot | ENSP00000510175.1 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 183472499 |
| end | 183554191 |
| strand | + |
| ver | v1.2 |
| region | chr1:183472499-183554191 |
| region5000 | chr1:183467499-183559191 |
| regionname0 | SMG7_chr1_183472499_183554191 |
| regionname5000 | SMG7_chr1_183467499_183559191 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1187 | 229 | 60 | 42 | 94 | 10 | 21 | 71 | SMG7_chr1_183467499_183559191 | SMG7 | MSLQS others(1182): Show |
chr1 | 183467499 | 183559191 |
| a0002 | 0/0 | 1187 | 69 | 20 | 15 | 25 | 4 | 5 | 21 | SMG7_chr1_183467499_183559191 | SMG7 | MSLQS others(1182): Show |
chr1 | 183467499 | 183559191 |
| a0003 | 0/0 | 1187 | 44 | 0 | 4 | 38 | 0 | 2 | 30 | SMG7_chr1_183467499_183559191 | SMG7 | MSLQS others(1182): Show |
chr1 | 183467499 | 183559191 |
| a0004 | 0/0 | 1188 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | MSLQS others(1183): Show |
chr1 | 183467499 | 183559191 |
| a0005 | 0/0 | 1187 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | SMG7_chr1_183467499_183559191 | SMG7 | MSLQS others(1182): Show |
chr1 | 183467499 | 183559191 |
| a0006 | 0/0 | 1187 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | MSLQS others(1182): Show |
chr1 | 183467499 | 183559191 |
| a0007 | 0/0 | 1187 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | MSLQS others(1182): Show |
chr1 | 183467499 | 183559191 |
| a0008 | 0/0 | 1187 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | MSLQS others(1182): Show |
chr1 | 183467499 | 183559191 |
| a0009 | 0/0 | 1187 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | MSLQS others(1182): Show |
chr1 | 183467499 | 183559191 |
| a0010 | 0/0 | 1187 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | MSLQS others(1182): Show |
chr1 | 183467499 | 183559191 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3561 | 212 | 57 | 37 | 92 | 6 | 19 | SMG7_chr1_183467499_183559191 | SMG7 | ATGAG others(3556): Show |
chr1 | 183467499 | 183559191 | ||
| a0001c0004 | 1/0 | 3561 | 14 | 2 | 5 | 0 | 4 | 2 | SMG7_chr1_183467499_183559191 | SMG7 | ATGAG others(3556): Show |
chr1 | 183467499 | 183559191 | ||
| a0001c0010 | 0/0 | 3561 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | ATGAG others(3556): Show |
chr1 | 183467499 | 183559191 | ||
| a0001c0012 | 0/0 | 3561 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | ATGAG others(3556): Show |
chr1 | 183467499 | 183559191 | ||
| a0001c0014 | 0/0 | 3561 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | ATGAG others(3556): Show |
chr1 | 183467499 | 183559191 | ||
| a0002c0002 | 0/0 | 3561 | 69 | 20 | 15 | 25 | 4 | 5 | SMG7_chr1_183467499_183559191 | SMG7 | ATGAG others(3556): Show |
chr1 | 183467499 | 183559191 | ||
| a0003c0003 | 0/0 | 3561 | 44 | 0 | 4 | 38 | 0 | 2 | SMG7_chr1_183467499_183559191 | SMG7 | ATGAG others(3556): Show |
chr1 | 183467499 | 183559191 | ||
| a0004c0005 | 0/0 | 3564 | 8 | 8 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | ATGAG others(3559): Show |
chr1 | 183467499 | 183559191 | ||
| a0005c0006 | 0/0 | 3561 | 3 | 0 | 0 | 3 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | ATGAG others(3556): Show |
chr1 | 183467499 | 183559191 | ||
| a0006c0007 | 0/0 | 3561 | 2 | 1 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | ATGAG others(3556): Show |
chr1 | 183467499 | 183559191 | ||
| a0007c0008 | 0/0 | 3561 | 2 | 0 | 2 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | ATGAG others(3556): Show |
chr1 | 183467499 | 183559191 | ||
| a0008c0011 | 0/0 | 3561 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | ATGAG others(3556): Show |
chr1 | 183467499 | 183559191 | ||
| a0009c0013 | 0/0 | 3561 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | ATGAG others(3556): Show |
chr1 | 183467499 | 183559191 | ||
| a0010c0009 | 0/0 | 3561 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | ATGAG others(3556): Show |
chr1 | 183467499 | 183559191 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5946 | 86 | 35 | 14 | 23 | 4 | 9 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5941): Show |
chr1 | 183467499 | 183559191 |
| a0001c0001t0003 | 0/0 | 5949 | 43 | 3 | 11 | 26 | 0 | 3 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5944): Show |
chr1 | 183467499 | 183559191 |
| a0001c0001t0004 | 0/0 | 5948 | 26 | 4 | 5 | 15 | 1 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5943): Show |
chr1 | 183467499 | 183559191 |
| a0001c0001t0005 | 0/0 | 5946 | 8 | 3 | 2 | 1 | 0 | 2 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5941): Show |
chr1 | 183467499 | 183559191 |
| a0001c0001t0006 | 0/0 | 5950 | 16 | 1 | 3 | 9 | 1 | 2 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5945): Show |
chr1 | 183467499 | 183559191 |
| a0001c0001t0007 | 0/0 | 5947 | 12 | 5 | 2 | 5 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5942): Show |
chr1 | 183467499 | 183559191 |
| a0001c0001t0009 | 0/0 | 5946 | 3 | 2 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5941): Show |
chr1 | 183467499 | 183559191 |
| a0001c0001t0010 | 0/0 | 5946 | 4 | 0 | 0 | 4 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5941): Show |
chr1 | 183467499 | 183559191 |
| a0001c0001t0011 | 0/0 | 5948 | 3 | 0 | 0 | 3 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5943): Show |
chr1 | 183467499 | 183559191 |
| a0001c0001t0013 | 0/0 | 5948 | 2 | 0 | 0 | 2 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5943): Show |
chr1 | 183467499 | 183559191 |
| a0001c0001t0014 | 0/0 | 5948 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5943): Show |
chr1 | 183467499 | 183559191 |
| a0001c0001t0015 | 0/0 | 5946 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5941): Show |
chr1 | 183467499 | 183559191 |
| a0001c0001t0016 | 0/0 | 5950 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5945): Show |
chr1 | 183467499 | 183559191 |
| a0001c0001t0017 | 0/0 | 5946 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5941): Show |
chr1 | 183467499 | 183559191 |
| a0001c0001t0018 | 0/0 | 5947 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5942): Show |
chr1 | 183467499 | 183559191 |
| a0001c0001t0019 | 0/0 | 5947 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5942): Show |
chr1 | 183467499 | 183559191 |
| a0001c0001t0020 | 0/0 | 5950 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5945): Show |
chr1 | 183467499 | 183559191 |
| a0001c0001t0021 | 0/0 | 5946 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5941): Show |
chr1 | 183467499 | 183559191 |
| a0001c0001t0022 | 0/0 | 5949 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5944): Show |
chr1 | 183467499 | 183559191 |
| a0001c0004t0001 | 1/0 | 5946 | 14 | 2 | 5 | 0 | 4 | 2 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5941): Show |
chr1 | 183467499 | 183559191 |
| a0001c0010t0009 | 0/0 | 5946 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5941): Show |
chr1 | 183467499 | 183559191 |
| a0001c0012t0006 | 0/0 | 5950 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5945): Show |
chr1 | 183467499 | 183559191 |
| a0001c0014t0001 | 0/0 | 5946 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5941): Show |
chr1 | 183467499 | 183559191 |
| a0002c0002t0002 | 0/0 | 5940 | 62 | 19 | 15 | 21 | 3 | 4 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5935): Show |
chr1 | 183467499 | 183559191 |
| a0002c0002t0005 | 0/0 | 5946 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5941): Show |
chr1 | 183467499 | 183559191 |
| a0002c0002t0008 | 0/0 | 5941 | 4 | 0 | 0 | 3 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5936): Show |
chr1 | 183467499 | 183559191 |
| a0002c0002t0012 | 0/0 | 5943 | 2 | 0 | 0 | 1 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5938): Show |
chr1 | 183467499 | 183559191 |
| a0003c0003t0001 | 0/0 | 5946 | 43 | 0 | 4 | 37 | 0 | 2 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5941): Show |
chr1 | 183467499 | 183559191 |
| a0003c0003t0004 | 0/0 | 5948 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5943): Show |
chr1 | 183467499 | 183559191 |
| a0004c0005t0005 | 0/0 | 5949 | 8 | 8 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5944): Show |
chr1 | 183467499 | 183559191 |
| a0005c0006t0001 | 0/0 | 5946 | 3 | 0 | 0 | 3 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5941): Show |
chr1 | 183467499 | 183559191 |
| a0006c0007t0005 | 0/0 | 5946 | 2 | 1 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5941): Show |
chr1 | 183467499 | 183559191 |
| a0007c0008t0001 | 0/0 | 5946 | 2 | 0 | 2 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5941): Show |
chr1 | 183467499 | 183559191 |
| a0008c0011t0001 | 0/0 | 5946 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5941): Show |
chr1 | 183467499 | 183559191 |
| a0009c0013t0001 | 0/0 | 5946 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5941): Show |
chr1 | 183467499 | 183559191 |
| a0010c0009t0007 | 0/0 | 5947 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | GAGGA others(5942): Show |
chr1 | 183467499 | 183559191 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0154 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0024 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0004g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0005g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0005g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0005g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0005g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0006g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0006g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0006g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0006g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0006g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0006g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0006g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0006g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0006g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0006g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0006g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0006g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0006g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0006g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0006g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0007g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0007g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0007g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0007g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0007g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0007g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0007g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0007g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0007g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0007g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0009g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0009g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0009g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0010g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0010g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0010g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0010g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0011g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0011g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0011g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0013g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0013g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0014g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0015g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0016g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0017g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0018g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0019g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0020g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0021g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0001t0022g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0004t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0004t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0004t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0004t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0004t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0004t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0004t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0004t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0004t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0004t0001g0097 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0004t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0004t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0010t0009g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0012t0006g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0001c0014t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0008g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0008g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0008g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0008g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0012g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0002c0002t0012g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0003c0003t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0004c0005t0005g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0004c0005t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0004c0005t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0004c0005t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0004c0005t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0004c0005t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0005c0006t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0005c0006t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0005c0006t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0006c0007t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0006c0007t0005g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0007c0008t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0007c0008t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0008c0011t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0009c0013t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| a0010c0009t0007g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0001 | g0088 | EUR | GBR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0306 | EUR | GBR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG00140 | hp1 | a0002 | c0002 | t0012 | g0060 | EUR | GBR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0022 | EUR | GBR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0323 | EUR | FIN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG00280 | hp2 | a0001 | c0004 | t0001 | g0083 | EUR | FIN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG00408 | hp1 | a0003 | c0003 | t0001 | g0181 | EAS | CHS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | CHS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG00423 | hp1 | a0003 | c0003 | t0001 | g0121 | EAS | CHS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0241 | EAS | CHS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0212 | EAS | CHS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0258 | EAS | CHS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | CHS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | CHS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0057 | EAS | CHS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG00597 | hp1 | a0003 | c0003 | t0001 | g0140 | EAS | CHS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0280 | EAS | CHS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0242 | EAS | CHS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0044 | EAS | CHS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG00735 | hp1 | a0001 | c0001 | t0007 | g0240 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0072 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG00738 | hp1 | a0001 | c0004 | t0001 | g0089 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0074 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01069 | hp2 | a0006 | c0007 | t0005 | g0167 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0198 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01081 | hp1 | a0003 | c0003 | t0001 | g0133 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0214 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0225 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0062 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0095 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01167 | hp2 | a0001 | c0004 | t0001 | g0092 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0229 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01168 | hp2 | a0003 | c0003 | t0001 | g0018 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01169 | hp1 | a0001 | c0004 | t0001 | g0091 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01169 | hp2 | a0001 | c0001 | t0006 | g0207 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0260 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01175 | hp2 | a0001 | c0004 | t0001 | g0090 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0259 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0032 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01243 | hp2 | a0003 | c0003 | t0001 | g0018 | AMR | PUR | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0191 | AMR | CLM | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01256 | hp2 | a0001 | c0004 | t0001 | g0084 | AMR | CLM | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0058 | AMR | CLM | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0192 | AMR | CLM | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0012 | AMR | CLM | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01261 | hp2 | a0007 | c0008 | t0001 | g0322 | AMR | CLM | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0012 | AMR | CLM | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | CLM | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0251 | AMR | CLM | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0209 | AMR | CLM | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0004 | EUR | IBS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0283 | EUR | IBS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01516 | hp1 | a0001 | c0004 | t0001 | g0087 | EUR | IBS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0066 | EUR | IBS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0282 | EUR | IBS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0067 | EUR | IBS | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01891 | hp1 | a0002 | c0002 | t0002 | g0042 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01891 | hp2 | a0001 | c0004 | t0001 | g0099 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0076 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0226 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0081 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01943 | hp2 | a0001 | c0001 | t0006 | g0218 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0195 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0194 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0064 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0077 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01993 | hp1 | a0001 | c0001 | t0007 | g0193 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0068 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0059 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02004 | hp2 | a0003 | c0003 | t0001 | g0119 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02015 | hp1 | a0008 | c0011 | t0001 | g0015 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02015 | hp2 | a0001 | c0001 | t0010 | g0187 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02027 | hp1 | a0001 | c0001 | t0010 | g0186 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02055 | hp1 | a0004 | c0005 | t0005 | g0162 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0039 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02056 | hp2 | a0001 | c0001 | t0010 | g0188 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02074 | hp1 | a0001 | c0001 | t0022 | g0234 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02080 | hp1 | a0001 | c0001 | t0006 | g0249 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02080 | hp2 | a0002 | c0002 | t0012 | g0080 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02132 | hp1 | a0003 | c0003 | t0001 | g0013 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02132 | hp2 | a0001 | c0001 | t0020 | g0007 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0178 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02145 | hp2 | a0004 | c0005 | t0005 | g0165 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0196 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02155 | hp1 | a0003 | c0003 | t0001 | g0026 | EAS | CDX | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02155 | hp2 | a0003 | c0003 | t0001 | g0122 | EAS | CDX | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | CDX | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02165 | hp2 | a0003 | c0003 | t0001 | g0138 | EAS | CDX | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0204 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02258 | hp1 | a0002 | c0002 | t0005 | g0041 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0264 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02280 | hp1 | a0002 | c0002 | t0002 | g0010 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02293 | hp1 | a0007 | c0008 | t0001 | g0317 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02293 | hp2 | a0001 | c0001 | t0006 | g0211 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0247 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0010 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02523 | hp1 | a0001 | c0001 | t0021 | g0286 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02523 | hp2 | a0003 | c0003 | t0001 | g0118 | EAS | KHV | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02572 | hp2 | a0004 | c0005 | t0005 | g0006 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0075 | SAS | PJL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0043 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02622 | hp1 | a0004 | c0005 | t0005 | g0164 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02698 | hp2 | a0001 | c0001 | t0006 | g0203 | SAS | PJL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0020 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02717 | hp2 | a0001 | c0014 | t0001 | g0131 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02723 | hp1 | a0001 | c0001 | t0019 | g0183 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0230 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0079 | SAS | PJL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02809 | hp1 | a0002 | c0002 | t0002 | g0009 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0177 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02895 | hp1 | a0004 | c0005 | t0005 | g0161 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0028 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02896 | hp2 | a0001 | c0001 | t0009 | g0179 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02897 | hp1 | a0002 | c0002 | t0002 | g0029 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02897 | hp2 | a0004 | c0005 | t0005 | g0006 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02922 | hp1 | a0004 | c0005 | t0005 | g0163 | AFR | ESN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02922 | hp2 | a0006 | c0007 | t0005 | g0166 | AFR | ESN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02965 | hp2 | a0001 | c0004 | t0001 | g0100 | AFR | ESN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0019 | AFR | ESN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0033 | AFR | ESN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0096 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0009 | AFR | ESN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03130 | hp2 | a0004 | c0005 | t0005 | g0006 | AFR | ESN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0020 | AFR | ESN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0027 | AFR | MSL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03453 | hp1 | a0002 | c0002 | t0002 | g0035 | AFR | MSL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03491 | hp1 | a0001 | c0004 | t0001 | g0093 | SAS | PJL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03491 | hp2 | a0001 | c0001 | t0005 | g0253 | SAS | PJL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0176 | AFR | ESN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0037 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03654 | hp2 | a0003 | c0003 | t0001 | g0136 | SAS | PJL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0243 | SAS | PJL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0073 | SAS | PJL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0261 | SAS | BEB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0024 | SAS | BEB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03834 | hp2 | a0003 | c0003 | t0001 | g0144 | SAS | BEB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03927 | hp1 | a0002 | c0002 | t0008 | g0069 | SAS | BEB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03927 | hp2 | a0001 | c0001 | t0009 | g0231 | SAS | BEB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | BEB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03942 | hp2 | a0001 | c0001 | t0006 | g0007 | SAS | BEB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG04115 | hp1 | a0001 | c0001 | t0005 | g0252 | SAS | STU | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0065 | SAS | STU | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0315 | SAS | BEB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0222 | SAS | BEB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG04228 | hp1 | a0001 | c0001 | t0015 | g0128 | SAS | STU | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | STU | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18522 | hp1 | a0002 | c0002 | t0002 | g0031 | AFR | YRI | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0175 | AFR | YRI | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18612 | hp1 | a0001 | c0001 | t0017 | g0184 | EAS | CHB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | CHB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | YRI | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0034 | AFR | YRI | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0050 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18939 | hp2 | a0003 | c0003 | t0001 | g0146 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18943 | hp2 | a0003 | c0003 | t0001 | g0135 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18945 | hp2 | a0003 | c0003 | t0001 | g0015 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0200 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18947 | hp2 | a0003 | c0003 | t0001 | g0145 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18948 | hp1 | a0003 | c0003 | t0001 | g0016 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18948 | hp2 | a0001 | c0001 | t0004 | g0205 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18949 | hp2 | a0003 | c0003 | t0001 | g0148 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18951 | hp2 | a0003 | c0003 | t0001 | g0147 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18953 | hp1 | a0002 | c0002 | t0008 | g0051 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18954 | hp2 | a0001 | c0010 | t0009 | g0202 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18956 | hp2 | a0003 | c0003 | t0001 | g0143 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18961 | hp1 | a0001 | c0001 | t0006 | g0189 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18961 | hp2 | a0003 | c0003 | t0001 | g0017 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18963 | hp2 | a0003 | c0003 | t0001 | g0132 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18967 | hp1 | a0002 | c0002 | t0008 | g0056 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0217 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18971 | hp1 | a0001 | c0001 | t0013 | g0267 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18971 | hp2 | a0003 | c0003 | t0004 | g0233 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18972 | hp1 | a0003 | c0003 | t0001 | g0016 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18972 | hp2 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18973 | hp1 | a0001 | c0001 | t0006 | g0235 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18973 | hp2 | a0003 | c0003 | t0001 | g0017 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18977 | hp2 | a0001 | c0001 | t0006 | g0210 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18978 | hp2 | a0003 | c0003 | t0001 | g0155 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18983 | hp1 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18983 | hp2 | a0003 | c0003 | t0001 | g0120 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18988 | hp1 | a0005 | c0006 | t0001 | g0001 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18990 | hp1 | a0001 | c0001 | t0007 | g0262 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18990 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18991 | hp1 | a0002 | c0002 | t0008 | g0048 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18992 | hp2 | a0001 | c0001 | t0006 | g0248 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18993 | hp1 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18993 | hp2 | a0003 | c0003 | t0001 | g0137 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18998 | hp1 | a0001 | c0001 | t0006 | g0236 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0054 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19001 | hp2 | a0001 | c0001 | t0011 | g0278 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19002 | hp2 | a0001 | c0001 | t0006 | g0275 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19003 | hp1 | a0001 | c0001 | t0011 | g0272 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19003 | hp2 | a0003 | c0003 | t0001 | g0150 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19004 | hp1 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19006 | hp1 | a0001 | c0001 | t0010 | g0185 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19006 | hp2 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19007 | hp1 | a0001 | c0001 | t0013 | g0268 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19007 | hp2 | a0005 | c0006 | t0001 | g0308 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19009 | hp1 | a0001 | c0001 | t0006 | g0022 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19009 | hp2 | a0003 | c0003 | t0001 | g0153 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19010 | hp1 | a0003 | c0003 | t0001 | g0098 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19012 | hp1 | a0001 | c0001 | t0005 | g0223 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19012 | hp2 | a0003 | c0003 | t0001 | g0149 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0030 | AFR | LWK | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19030 | hp2 | a0001 | c0001 | t0016 | g0173 | AFR | LWK | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0174 | AFR | LWK | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19043 | hp2 | a0002 | c0002 | t0002 | g0040 | AFR | LWK | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19056 | hp2 | a0003 | c0003 | t0001 | g0130 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19057 | hp1 | a0001 | c0001 | t0007 | g0239 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19064 | hp1 | a0003 | c0003 | t0001 | g0124 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19066 | hp1 | a0001 | c0001 | t0006 | g0237 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19066 | hp2 | a0003 | c0003 | t0001 | g0014 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19067 | hp2 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19072 | hp1 | a0005 | c0006 | t0001 | g0309 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19072 | hp2 | a0001 | c0001 | t0007 | g0216 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19074 | hp1 | a0003 | c0003 | t0001 | g0013 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19076 | hp2 | a0003 | c0003 | t0001 | g0111 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19078 | hp1 | a0001 | c0012 | t0006 | g0266 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19078 | hp2 | a0009 | c0013 | t0001 | g0295 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19079 | hp2 | a0003 | c0003 | t0001 | g0151 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19080 | hp1 | a0003 | c0003 | t0001 | g0134 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19081 | hp1 | a0001 | c0001 | t0007 | g0219 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19082 | hp1 | a0003 | c0003 | t0001 | g0014 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19082 | hp2 | a0001 | c0001 | t0011 | g0277 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0206 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19084 | hp2 | a0003 | c0003 | t0001 | g0110 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19086 | hp2 | a0003 | c0003 | t0001 | g0123 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19089 | hp2 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0019 | AFR | YRI | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0228 | AFR | YRI | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA20129 | hp1 | a0001 | c0001 | t0007 | g0221 | AFR | ASW | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ASW | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA20805 | hp1 | a0001 | c0004 | t0001 | g0085 | EUR | TSI | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA20805 | hp2 | a0001 | c0001 | t0006 | g0215 | EUR | TSI | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA20905 | hp1 | a0001 | c0004 | t0001 | g0086 | SAS | GIH | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0301 | SAS | GIH | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | CLM | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0094 | AFR | ACB | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03471 | hp1 | a0001 | c0001 | t0014 | g0157 | AFR | MSL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG03471 | hp2 | a0002 | c0002 | t0002 | g0038 | AFR | MSL | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG06807 | hp1 | a0002 | c0002 | t0002 | g0036 | AFR | USA | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | USA | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | USA | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0199 | AFR | USA | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA21309 | hp1 | a0001 | c0001 | t0018 | g0180 | AFR | LWK | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| NA21309 | hp2 | a0010 | c0009 | t0007 | g0197 | AFR | LWK | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0154 | REF | REF | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| homoSapiens | grch38p0 | a0001 | c0004 | t0001 | g0097 | REF | REF | SMG7_chr1_183467499_183559191 | SMG7 | chr1 | 183467499 | 183559191 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:183526605 | G | A | 1 | a0009 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.322G>A | p.Glu108Lys | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 5/23 | 444/5946 | 322/3564 | 108/1187 | chr1 | 183526605 | |||
| chr1:183526677 | A | G | 1 | a0007 | 2 | HG01261.hp2 HG02293.hp1 |
missense_variant | MODERATE | c.394A>G | p.Lys132Glu | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 5/23 | 516/5946 | 394/3564 | 132/1187 | chr1 | 183526677 | |||
| chr1:183526681 | A | G | 1 | a0009 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.398A>G | p.Gln133Arg | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 5/23 | 520/5946 | 398/3564 | 133/1187 | chr1 | 183526681 | |||
| chr1:183526706 | G | C | 1 | a0009 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.423G>C | p.Lys141Asn | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 5/23 | 545/5946 | 423/3564 | 141/1187 | chr1 | 183526706 | |||
| chr1:183526707 | C | G | 1 | a0009 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.424C>G | p.Pro142Ala | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 5/23 | 546/5946 | 424/3564 | 142/1187 | chr1 | 183526707 | |||
| chr1:183529445 | C | T | 2 | a0005 a0009 |
4 | NA18988.hp1 NA19007.hp2 NA19072.hp1 others(1): Show |
missense_variant | MODERATE | c.755C>T | p.Ala252Val | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/23 | 877/5946 | 755/3564 | 252/1187 | chr1 | 183529445 | |||
| chr1:183533735 | T | TACA | 1 | a0004 | 8 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
disruptive_inframe_insertion | MODERATE | c.1068_1070dupCAA | p.Asn357dup | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/23 | 1193/5946 | 1071/3564 | 357/1187 | INFO_REALIGN_3_PRIME | chr1 | 183533735 | ||
| chr1:183546293 | G | A | 1 | a0002 | 69 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(66): Show |
missense_variant | MODERATE | c.2698G>A | p.Val900Ile | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 17/23 | 2820/5946 | 2698/3564 | 900/1187 | chr1 | 183546293 | |||
| chr1:183547106 | C | T | 2 | a0003 a0008 |
45 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(42): Show |
missense_variant | MODERATE | c.2746C>T | p.Pro916Ser | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/23 | 2868/5946 | 2746/3564 | 916/1187 | chr1 | 183547106 | |||
| chr1:183547136 | C | A | 1 | a0008 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.2776C>A | p.Leu926Met | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/23 | 2898/5946 | 2776/3564 | 926/1187 | chr1 | 183547136 | |||
| chr1:183549767 | A | G | 1 | a0010 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.2977A>G | p.Arg993Gly | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 20/23 | 3099/5946 | 2977/3564 | 993/1187 | chr1 | 183549767 | |||
| chr1:183550908 | A | C | 1 | a0006 | 2 | HG01069.hp2 HG02922.hp2 |
missense_variant | MODERATE | c.3291A>C | p.Lys1097Asn | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 21/23 | 3413/5946 | 3291/3564 | 1097/1187 | chr1 | 183550908 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:183515944 | A | G | 1 | a0001c0014 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.132A>G | p.Leu44Leu | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/23 | 254/5946 | 132/3564 | 44/1187 | chr1 | 183515944 | |||
| chr1:183517724 | G | A | 13 | a0001c0001 a0001c0010 a0001c0012 others(10): Show |
345 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(342): Show |
synonymous_variant | LOW | c.216G>A | p.Leu72Leu | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/23 | 338/5946 | 216/3564 | 72/1187 | chr1 | 183517724 | |||
| chr1:183526604 | A | G | 1 | a0009c0013 | 1 | NA19078.hp2 | synonymous_variant | LOW | c.321A>G | p.Gln107Gln | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 5/23 | 443/5946 | 321/3564 | 107/1187 | chr1 | 183526604 | |||
| chr1:183526607 | A | G | 1 | a0009c0013 | 1 | NA19078.hp2 | synonymous_variant | LOW | c.324A>G | p.Glu108Glu | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 5/23 | 446/5946 | 324/3564 | 108/1187 | chr1 | 183526607 | |||
| chr1:183526682 | G | A | 1 | a0009c0013 | 1 | NA19078.hp2 | synonymous_variant | LOW | c.399G>A | p.Gln133Gln | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 5/23 | 521/5946 | 399/3564 | 133/1187 | chr1 | 183526682 | |||
| chr1:183546058 | C | T | 1 | a0001c0012 | 1 | NA19078.hp1 | synonymous_variant | LOW | c.2463C>T | p.Tyr821Tyr | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 17/23 | 2585/5946 | 2463/3564 | 821/1187 | chr1 | 183546058 | |||
| chr1:183549216 | A | G | 1 | a0001c0010 | 1 | NA18954.hp2 | synonymous_variant | LOW | c.2901A>G | p.Leu967Leu | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 19/23 | 3023/5946 | 2901/3564 | 967/1187 | chr1 | 183549216 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:183552040 | C | T | 1 | a0001c0001t0022 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*109C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 109 | chr1 | 183552040 | ||||||
| chr1:183552086 | C | T | 1 | a0001c0001t0021 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*155C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 155 | chr1 | 183552086 | ||||||
| chr1:183552148 | C | T | 22 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(19): Show |
203 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(200): Show |
3_prime_UTR_variant | MODIFIER | c.*217C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 217 | chr1 | 183552148 | ||||||
| chr1:183552176 | G | A | 1 | a0001c0001t0014 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*245G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 245 | chr1 | 183552176 | ||||||
| chr1:183552267 | A | G | 1 | a0001c0001t0020 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*336A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 336 | chr1 | 183552267 | ||||||
| chr1:183552375 | ATTATTC | A | 3 | a0002c0002t0002 a0002c0002t0008 a0002c0002t0012 |
68 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*448_*453delTTCTTA | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 448 | INFO_REALIGN_3_PRIME | chr1 | 183552375 | |||||
| chr1:183552580 | G | C | 1 | a0001c0001t0013 | 2 | NA18971.hp1 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*649G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 649 | chr1 | 183552580 | ||||||
| chr1:183553128 | G | A | 1 | a0001c0001t0015 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1197G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 1197 | chr1 | 183553128 | ||||||
| chr1:183553406 | G | T | 1 | a0001c0001t0011 | 3 | NA19001.hp2 NA19003.hp1 NA19082.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1475G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 1475 | chr1 | 183553406 | ||||||
| chr1:183553573 | A | AT | 3 | a0001c0001t0014 a0001c0001t0018 a0001c0001t0019 |
3 | HG02723.hp1 HG03471.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1643dupT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 1644 | INFO_REALIGN_3_PRIME | chr1 | 183553573 | |||||
| chr1:183553608 | G | GC | 4 | a0001c0001t0007 a0001c0001t0014 a0002c0002t0008 others(1): Show |
18 | HG00735.hp1 HG01993.hp1 HG02970.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1685dupC | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 1686 | INFO_REALIGN_3_PRIME | chr1 | 183553608 | |||||
| chr1:183553608 | G | GCC | 4 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0013 others(1): Show |
32 | HG00140.hp2 HG00423.hp2 HG00609.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1684_*1685dupCC | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 1686 | INFO_REALIGN_3_PRIME | chr1 | 183553608 | |||||
| chr1:183553608 | G | GCCC | 3 | a0001c0001t0003 a0001c0001t0022 a0002c0002t0012 |
46 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1683_*1685dupCCC | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 1686 | INFO_REALIGN_3_PRIME | chr1 | 183553608 | |||||
| chr1:183553608 | G | GCCCC | 4 | a0001c0001t0006 a0001c0001t0016 a0001c0001t0020 others(1): Show |
19 | HG01169.hp2 HG01943.hp2 HG02080.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1682_*1685dupCCCC | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 1686 | INFO_REALIGN_3_PRIME | chr1 | 183553608 | |||||
| chr1:183553616 | C | T | 1 | a0001c0001t0017 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1685C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 1685 | chr1 | 183553616 | ||||||
| chr1:183553617 | G | C | 15 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(12): Show |
114 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*1686G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 1686 | chr1 | 183553617 | ||||||
| chr1:183553936 | A | G | 1 | a0001c0001t0010 | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2005A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 2005 | chr1 | 183553936 | ||||||
| chr1:183554068 | G | A | 1 | a0001c0001t0010 | 4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2137G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 23/23 | 2137 | chr1 | 183554068 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:183472701 | G | C | 1 | a0001c0001t0003g0025 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.29+52G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183472701 | |||||||
| chr1:183472711 | A | G | 1 | a0001c0001t0001g0324 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.29+62A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183472711 | |||||||
| chr1:183472811 | G | A | 1 | a0003c0003t0001g0026 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.29+162G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183472811 | |||||||
| chr1:183472842 | C | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0281 others(44): Show |
53 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.29+193C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183472842 | |||||||
| chr1:183472856 | G | A | 61 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0009 others(58): Show |
69 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.29+207G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183472856 | |||||||
| chr1:183472932 | G | C | 1 | a0002c0002t0002g0027 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.29+283G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183472932 | |||||||
| chr1:183472962 | C | T | 103 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0023 others(100): Show |
106 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.29+313C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183472962 | |||||||
| chr1:183472967 | A | G | 1 | a0001c0001t0003g0280 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.29+318A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183472967 | |||||||
| chr1:183472999 | G | A | 1 | a0001c0001t0006g0189 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.29+350G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183472999 | |||||||
| chr1:183473015 | C | A | 1 | a0001c0001t0001g0082 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.29+366C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183473015 | |||||||
| chr1:183473040 | G | A | 4 | a0002c0002t0002g0009 a0002c0002t0002g0028 a0002c0002t0002g0029 others(1): Show |
5 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.29+391G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183473040 | |||||||
| chr1:183473185 | G | C | 1 | a0001c0001t0003g0190 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.29+536G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183473185 | |||||||
| chr1:183473189 | A | C | 42 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0011 others(39): Show |
48 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.29+540A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183473189 | |||||||
| chr1:183473362 | T | G | 16 | a0002c0002t0002g0003 a0002c0002t0002g0011 a0002c0002t0002g0044 others(13): Show |
19 | HG00558.hp2 HG00609.hp2 HG02129.hp2 others(16): Show |
intron_variant | MODIFIER | c.29+713T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183473362 | |||||||
| chr1:183473402 | G | A | 11 | a0001c0004t0001g0083 a0001c0004t0001g0084 a0001c0004t0001g0085 others(8): Show |
11 | HG00099.hp1 HG00280.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.29+753G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183473402 | |||||||
| chr1:183473659 | T | TG | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.29+1014dupG | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183473659 | ||||||
| chr1:183473973 | A | T | 10 | a0001c0001t0003g0025 a0001c0001t0003g0190 a0001c0001t0003g0274 others(7): Show |
10 | HG00408.hp2 HG02056.hp1 NA19001.hp2 others(7): Show |
intron_variant | MODIFIER | c.29+1324A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183473973 | |||||||
| chr1:183474039 | C | T | 1 | a0001c0001t0001g0021 | 2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.29+1390C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183474039 | |||||||
| chr1:183474160 | G | A | 3 | a0001c0001t0005g0094 a0001c0001t0005g0095 a0001c0001t0005g0096 |
3 | HG01109.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.29+1511G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183474160 | |||||||
| chr1:183474296 | CTCACGCC others(5): Show |
C | 1 | a0001c0001t0017g0184 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.29+1650_29+1661del others(12): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183474296 | ||||||
| chr1:183474650 | A | G | 329 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(326): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.29+2001A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183474650 | |||||||
| chr1:183474766 | C | T | 1 | a0001c0001t0019g0183 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.29+2117C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183474766 | |||||||
| chr1:183474875 | G | C | 1 | a0003c0003t0001g0098 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.29+2226G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183474875 | |||||||
| chr1:183474925 | G | A | 5 | a0001c0001t0003g0194 a0001c0001t0003g0195 a0001c0001t0003g0196 others(2): Show |
5 | HG01257.hp2 HG01952.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.29+2276G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183474925 | |||||||
| chr1:183474929 | G | A | 22 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(19): Show |
22 | HG00099.hp1 HG00280.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.29+2280G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183474929 | |||||||
| chr1:183475154 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.29+2505C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183475154 | |||||||
| chr1:183475229 | G | A | 2 | a0003c0003t0001g0110 a0003c0003t0001g0111 |
2 | NA19076.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.29+2580G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183475229 | |||||||
| chr1:183475313 | A | G | 8 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.29+2664A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183475313 | |||||||
| chr1:183475445 | G | T | 1 | a0003c0003t0001g0181 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.29+2796G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183475445 | |||||||
| chr1:183475879 | GA | G | 39 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0024 others(36): Show |
41 | HG00544.hp1 HG00597.hp2 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.29+3238delA | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183475879 | ||||||
| chr1:183476147 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.29+3498G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183476147 | |||||||
| chr1:183476233 | T | C | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.29+3584T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183476233 | |||||||
| chr1:183476728 | A | G | 1 | a0001c0001t0003g0271 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.29+4079A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183476728 | |||||||
| chr1:183476745 | TTTG | T | 56 | a0001c0001t0001g0082 a0001c0001t0001g0114 a0001c0001t0001g0115 others(53): Show |
61 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.29+4099_29+4101del others(3): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183476745 | ||||||
| chr1:183476969 | G | A | 61 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0009 others(58): Show |
69 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.29+4320G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183476969 | |||||||
| chr1:183477242 | T | C | 1 | a0001c0001t0014g0157 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.29+4593T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477242 | |||||||
| chr1:183477398 | T | TTG | 118 | a0001c0001t0001g0156 a0001c0001t0003g0002 a0001c0001t0003g0007 others(115): Show |
121 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.29+4769_29+4770dup others(2): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477398 | ||||||
| chr1:183477398 | TTGTG | T | 40 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0011 others(37): Show |
46 | HG00140.hp1 HG00609.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.29+4767_29+4770del others(4): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477398 | ||||||
| chr1:183477400 | G | T | 2 | a0001c0001t0014g0157 a0001c0001t0018g0180 |
2 | HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.29+4751G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477400 | |||||||
| chr1:183477402 | G | T | 1 | a0001c0001t0014g0157 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.29+4753G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477402 | |||||||
| chr1:183477416 | G | A | 1 | a0002c0002t0002g0057 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.29+4767G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477416 | |||||||
| chr1:183477419 | T | TGTGCATA others(21): Show |
1 | a0002c0002t0002g0057 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.29+4770_29+4771ins others(28): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477419 | |||||||
| chr1:183477420 | A | G | 1 | a0001c0001t0001g0323 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.29+4771A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477420 | |||||||
| chr1:183477442 | A | G | 1 | a0002c0002t0002g0057 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.29+4793A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477442 | |||||||
| chr1:183477452 | A | ATGTGTGC others(27): Show |
84 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0023 others(81): Show |
87 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.29+4835_29+4836ins others(34): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477452 | ||||||
| chr1:183477452 | A | ATGTGTGC others(61): Show |
13 | a0001c0001t0003g0025 a0001c0001t0003g0190 a0001c0001t0003g0274 others(10): Show |
13 | HG00408.hp2 HG01891.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.29+4835_29+4836ins others(68): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477452 | ||||||
| chr1:183477452 | A | ATGTGTGC others(27): Show |
4 | a0001c0001t0003g0269 a0001c0001t0003g0270 a0001c0001t0013g0267 others(1): Show |
4 | NA18971.hp1 NA19007.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.29+4832_29+4833ins others(34): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477452 | ||||||
| chr1:183477457 | T | TGCATATG others(27): Show |
1 | a0001c0010t0009g0202 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.29+4835_29+4836ins others(34): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477457 | ||||||
| chr1:183477485 | C | CGTGTGTG others(27): Show |
1 | a0001c0001t0004g0191 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.29+4869_29+4902dup others(34): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477485 | ||||||
| chr1:183477485 | C | T | 319 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(316): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.29+4836C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477485 | |||||||
| chr1:183477496 | A | ATGTGTAT others(27): Show |
1 | a0001c0001t0003g0247 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.29+4880_29+4881ins others(34): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477496 | ||||||
| chr1:183477519 | T | TGTGTGTG others(25): Show |
17 | a0001c0001t0001g0005 a0001c0001t0001g0102 a0001c0001t0001g0104 others(14): Show |
19 | HG00099.hp1 HG00738.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.29+5041_29+5072dup others(32): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477519 | ||||||
| chr1:183477519 | T | TGTGTGTG others(59): Show |
5 | a0001c0001t0003g0201 a0001c0001t0004g0198 a0001c0001t0004g0199 others(2): Show |
5 | HG00280.hp2 HG01070.hp1 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.29+4902_29+4903ins others(66): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477519 | ||||||
| chr1:183477519 | T | TGTGTGTG others(57): Show |
2 | a0001c0001t0001g0103 a0001c0001t0001g0114 |
2 | HG01433.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.29+5009_29+5072dup others(64): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477519 | ||||||
| chr1:183477519 | TGTGTGTG others(25): Show |
T | 6 | a0001c0001t0001g0172 a0001c0001t0010g0185 a0001c0001t0010g0186 others(3): Show |
6 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.29+5041_29+5072del others(32): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477519 | ||||||
| chr1:183477580 | A | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0281 others(44): Show |
53 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.29+4931A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477580 | |||||||
| chr1:183477612 | A | G | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | HG01123.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.29+4963A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477612 | |||||||
| chr1:183477630 | G | T | 2 | a0001c0001t0003g0245 a0001c0001t0004g0246 |
2 | HG00558.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.29+4981G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477630 | |||||||
| chr1:183477644 | A | G | 1 | a0001c0001t0001g0319 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.29+4995A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477644 | |||||||
| chr1:183477655 | CAT | C | 5 | a0001c0001t0003g0194 a0001c0001t0003g0195 a0001c0001t0003g0196 others(2): Show |
5 | HG01257.hp2 HG01952.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.29+5009_29+5010del others(2): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477655 | ||||||
| chr1:183477679 | CGTGTGTG others(57): Show |
C | 1 | a0001c0001t0001g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.29+5047_29+5110del others(64): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477679 | ||||||
| chr1:183477712 | G | GTGTGTGC others(25): Show |
1 | a0001c0001t0004g0256 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.29+5072_29+5073ins others(32): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477712 | ||||||
| chr1:183477712 | G | GTGTGTGC others(55): Show |
1 | a0002c0002t0012g0080 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.29+5072_29+5073ins others(62): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477712 | ||||||
| chr1:183477719 | C | CAT | 6 | a0001c0001t0003g0177 a0001c0001t0004g0175 a0001c0001t0004g0178 others(3): Show |
7 | HG02145.hp1 HG02809.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.29+5071_29+5072dup others(2): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477719 | ||||||
| chr1:183477719 | C | CATATGTG others(59): Show |
1 | a0001c0001t0001g0108 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.29+5072_29+5073ins others(66): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477719 | ||||||
| chr1:183477741 | C | CGTGTGTG others(23): Show |
6 | a0001c0001t0003g0177 a0001c0001t0004g0175 a0001c0001t0004g0178 others(3): Show |
7 | HG02145.hp1 HG02809.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.29+5092_29+5093ins others(30): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477741 | |||||||
| chr1:183477742 | A | G | 2 | a0001c0001t0001g0108 a0003c0003t0001g0124 |
2 | HG02451.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.29+5093A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477742 | |||||||
| chr1:183477743 | T | C | 6 | a0001c0001t0003g0177 a0001c0001t0004g0175 a0001c0001t0004g0178 others(3): Show |
7 | HG02145.hp1 HG02809.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.29+5094T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477743 | |||||||
| chr1:183477776 | G | A | 325 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(322): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.29+5127G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477776 | |||||||
| chr1:183477787 | T | A | 103 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0023 others(100): Show |
106 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.29+5138T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477787 | |||||||
| chr1:183477810 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.29+5161C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477810 | |||||||
| chr1:183477810 | CTA | C | 7 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.29+5163_29+5164del others(2): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183477810 | ||||||
| chr1:183477871 | G | A | 3 | a0001c0001t0005g0094 a0001c0001t0005g0095 a0001c0001t0005g0096 |
3 | HG01109.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.29+5222G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477871 | |||||||
| chr1:183477885 | G | T | 1 | a0002c0002t0005g0041 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.29+5236G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183477885 | |||||||
| chr1:183478129 | A | G | 1 | a0001c0001t0003g0265 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.29+5480A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183478129 | |||||||
| chr1:183478474 | G | A | 3 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0182 |
3 | HG01099.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.29+5825G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183478474 | |||||||
| chr1:183478590 | T | C | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.29+5941T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183478590 | |||||||
| chr1:183478593 | G | A | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.29+5944G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183478593 | |||||||
| chr1:183478752 | AT | A | 11 | a0001c0004t0001g0083 a0001c0004t0001g0084 a0001c0004t0001g0085 others(8): Show |
11 | HG00099.hp1 HG00280.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.29+6108delT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183478752 | ||||||
| chr1:183478837 | C | T | 1 | a0002c0002t0012g0080 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.29+6188C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183478837 | |||||||
| chr1:183478889 | A | G | 6 | a0001c0001t0003g0177 a0001c0001t0004g0175 a0001c0001t0004g0178 others(3): Show |
7 | HG02145.hp1 HG02809.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.29+6240A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183478889 | |||||||
| chr1:183478975 | T | C | 1 | a0001c0001t0005g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.29+6326T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183478975 | |||||||
| chr1:183479032 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.29+6383G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183479032 | |||||||
| chr1:183479039 | C | G | 1 | a0001c0001t0004g0244 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.29+6390C>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183479039 | |||||||
| chr1:183479288 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.29+6639A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183479288 | |||||||
| chr1:183479429 | G | A | 1 | a0002c0002t0002g0044 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.29+6780G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183479429 | |||||||
| chr1:183479632 | T | G | 1 | a0001c0001t0001g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.29+6983T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183479632 | |||||||
| chr1:183479981 | T | C | 3 | a0001c0001t0006g0020 a0001c0001t0009g0020 a0001c0001t0009g0179 |
3 | HG02717.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.29+7332T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183479981 | |||||||
| chr1:183480193 | G | A | 1 | a0002c0002t0002g0044 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.29+7544G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183480193 | |||||||
| chr1:183480222 | C | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0281 others(44): Show |
53 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.29+7573C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183480222 | |||||||
| chr1:183480571 | A | G | 1 | a0003c0003t0001g0018 | 2 | HG01168.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.29+7922A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183480571 | |||||||
| chr1:183480658 | A | G | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.29+8009A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183480658 | |||||||
| chr1:183480751 | A | G | 1 | a0001c0001t0004g0264 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.29+8102A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183480751 | |||||||
| chr1:183480766 | A | G | 303 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(300): Show |
330 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.29+8117A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183480766 | |||||||
| chr1:183480779 | A | G | 1 | a0002c0002t0002g0010 | 2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.29+8130A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183480779 | |||||||
| chr1:183480849 | T | C | 1 | a0001c0001t0006g0203 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.29+8200T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183480849 | |||||||
| chr1:183481124 | GGTATT | G | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.29+8478_29+8482del others(5): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183481124 | ||||||
| chr1:183481172 | G | T | 2 | a0001c0001t0003g0263 a0001c0001t0007g0262 |
2 | NA18612.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.29+8523G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183481172 | |||||||
| chr1:183481487 | G | C | 125 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0023 others(122): Show |
131 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.29+8838G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183481487 | |||||||
| chr1:183481545 | A | G | 1 | a0006c0007t0005g0167 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.29+8896A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183481545 | |||||||
| chr1:183481816 | C | A | 56 | a0001c0001t0001g0082 a0001c0001t0001g0114 a0001c0001t0001g0115 others(53): Show |
61 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.29+9167C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183481816 | |||||||
| chr1:183481866 | G | GCCCAGGC others(2792): Show |
2 | a0001c0001t0004g0192 a0001c0001t0007g0193 |
2 | HG01257.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.29+9231_29+9232ins others(2799): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183481866 | ||||||
| chr1:183481866 | G | GCCCAGGC others(2793): Show |
2 | a0001c0001t0003g0194 a0001c0001t0003g0195 |
2 | HG01952.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.29+9231_29+9232ins others(2800): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183481866 | ||||||
| chr1:183481866 | G | GCCCAGGC others(2794): Show |
1 | a0001c0001t0003g0196 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.29+9231_29+9232ins others(2801): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183481866 | ||||||
| chr1:183482111 | G | T | 1 | a0001c0001t0004g0261 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.29+9462G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183482111 | |||||||
| chr1:183482212 | A | T | 1 | a0002c0002t0002g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.29+9563A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183482212 | |||||||
| chr1:183482230 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.29+9581G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183482230 | |||||||
| chr1:183482390 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.29+9741A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183482390 | |||||||
| chr1:183482428 | C | A | 4 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 others(1): Show |
4 | HG01515.hp2 HG01517.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.29+9779C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183482428 | |||||||
| chr1:183482476 | G | T | 1 | a0001c0001t0003g0260 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.29+9827G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183482476 | |||||||
| chr1:183482630 | C | T | 1 | a0002c0002t0002g0039 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.29+9981C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183482630 | |||||||
| chr1:183482842 | G | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 |
3 | HG01123.hp1 HG01192.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.29+10193G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183482842 | |||||||
| chr1:183482880 | T | A | 2 | a0001c0001t0005g0095 a0001c0001t0005g0096 |
2 | HG01109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.29+10231T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183482880 | |||||||
| chr1:183482950 | G | T | 1 | a0001c0001t0001g0182 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.29+10301G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183482950 | |||||||
| chr1:183483410 | G | A | 125 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0023 others(122): Show |
131 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.29+10761G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183483410 | |||||||
| chr1:183483523 | C | T | 1 | a0001c0001t0001g0324 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.29+10874C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183483523 | |||||||
| chr1:183484049 | G | C | 325 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(322): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.29+11400G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183484049 | |||||||
| chr1:183484113 | A | T | 1 | a0001c0001t0003g0259 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.29+11464A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183484113 | |||||||
| chr1:183484203 | A | G | 1 | a0001c0001t0003g0024 | 2 | HG03834.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.29+11554A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183484203 | |||||||
| chr1:183484213 | G | A | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.29+11564G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183484213 | |||||||
| chr1:183484360 | A | AT | 52 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0101 others(49): Show |
58 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.29+11728dupT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183484360 | ||||||
| chr1:183484360 | A | T | 122 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0023 others(119): Show |
128 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.29+11711A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183484360 | |||||||
| chr1:183484389 | G | T | 1 | a0001c0001t0001g0318 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.29+11740G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183484389 | |||||||
| chr1:183484417 | G | A | 1 | a0001c0004t0001g0084 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.29+11768G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183484417 | |||||||
| chr1:183484760 | C | T | 1 | a0001c0001t0003g0243 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.29+12111C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183484760 | |||||||
| chr1:183485053 | A | G | 61 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0009 others(58): Show |
69 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.29+12404A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183485053 | |||||||
| chr1:183485835 | A | G | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 |
3 | HG01123.hp1 HG01192.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.29+13186A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183485835 | |||||||
| chr1:183486267 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
6 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.29+13618G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183486267 | |||||||
| chr1:183486316 | G | A | 1 | a0003c0003t0001g0118 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.29+13667G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183486316 | |||||||
| chr1:183486423 | T | G | 3 | a0001c0001t0005g0094 a0001c0001t0005g0095 a0001c0001t0005g0096 |
3 | HG01109.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.29+13774T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183486423 | |||||||
| chr1:183486576 | G | A | 3 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0182 |
3 | HG01099.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.29+13927G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183486576 | |||||||
| chr1:183486584 | T | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0108 |
2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.29+13935T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183486584 | |||||||
| chr1:183486689 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.29+14040G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183486689 | |||||||
| chr1:183486848 | C | T | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 |
3 | HG01123.hp1 HG01192.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.29+14199C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183486848 | |||||||
| chr1:183486884 | G | A | 61 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0009 others(58): Show |
69 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.29+14235G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183486884 | |||||||
| chr1:183487297 | A | G | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.29+14648A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183487297 | |||||||
| chr1:183487341 | C | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0281 others(42): Show |
51 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.29+14692C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183487341 | |||||||
| chr1:183487376 | C | T | 1 | a0001c0001t0004g0242 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.29+14727C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183487376 | |||||||
| chr1:183487462 | T | A | 1 | a0001c0010t0009g0202 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.29+14813T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183487462 | |||||||
| chr1:183487610 | C | T | 2 | a0006c0007t0005g0166 a0006c0007t0005g0167 |
2 | HG01069.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.29+14961C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183487610 | |||||||
| chr1:183487955 | T | C | 1 | a0001c0001t0003g0204 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.29+15306T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183487955 | |||||||
| chr1:183488063 | A | G | 125 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0023 others(122): Show |
131 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.29+15414A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183488063 | |||||||
| chr1:183488261 | A | G | 113 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0023 others(110): Show |
117 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.29+15612A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183488261 | |||||||
| chr1:183488403 | A | G | 1 | a0002c0002t0002g0055 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.29+15754A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183488403 | |||||||
| chr1:183488597 | A | G | 1 | a0001c0001t0019g0183 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.29+15948A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183488597 | |||||||
| chr1:183488682 | C | CT | 23 | a0001c0001t0001g0112 a0001c0001t0001g0152 a0001c0001t0001g0282 others(20): Show |
23 | HG01069.hp1 HG01081.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.29+16056dupT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183488682 | ||||||
| chr1:183488682 | CT | C | 194 | a0001c0001t0001g0005 a0001c0001t0001g0102 a0001c0001t0001g0103 others(191): Show |
208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.29+16056delT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183488682 | ||||||
| chr1:183488684 | T | C | 8 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.29+16035T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183488684 | |||||||
| chr1:183488710 | C | T | 1 | a0002c0002t0002g0012 | 2 | HG01261.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.29+16061C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183488710 | |||||||
| chr1:183488766 | C | A | 1 | a0001c0001t0003g0201 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.29+16117C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183488766 | |||||||
| chr1:183488806 | C | T | 1 | a0001c0001t0016g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.29+16157C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183488806 | |||||||
| chr1:183488831 | C | A | 1 | a0003c0003t0001g0148 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.29+16182C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183488831 | |||||||
| chr1:183488949 | G | T | 1 | a0001c0004t0001g0083 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.29+16300G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183488949 | |||||||
| chr1:183489057 | C | T | 1 | a0001c0001t0003g0201 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.29+16408C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183489057 | |||||||
| chr1:183489078 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.29+16429G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183489078 | |||||||
| chr1:183489094 | A | G | 8 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.29+16445A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183489094 | |||||||
| chr1:183489302 | C | T | 1 | a0001c0001t0004g0238 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.29+16653C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183489302 | |||||||
| chr1:183489324 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.29+16675G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183489324 | |||||||
| chr1:183489500 | C | T | 1 | a0001c0001t0003g0260 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.29+16851C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183489500 | |||||||
| chr1:183489508 | T | C | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.29+16859T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183489508 | |||||||
| chr1:183489535 | C | T | 1 | a0002c0002t0002g0076 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.29+16886C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183489535 | |||||||
| chr1:183489583 | A | G | 2 | a0001c0001t0001g0109 a0002c0002t0002g0075 |
2 | HG02602.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.29+16934A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183489583 | |||||||
| chr1:183489657 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.29+17008A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183489657 | |||||||
| chr1:183489665 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.29+17016G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183489665 | |||||||
| chr1:183489822 | A | G | 61 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0009 others(58): Show |
69 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.29+17173A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183489822 | |||||||
| chr1:183489905 | A | G | 1 | a0001c0001t0003g0177 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.29+17256A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183489905 | |||||||
| chr1:183490074 | G | A | 1 | a0001c0001t0003g0204 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.29+17425G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183490074 | |||||||
| chr1:183490177 | A | G | 4 | a0001c0001t0001g0102 a0001c0001t0001g0105 a0001c0001t0001g0106 others(1): Show |
4 | HG02109.hp2 HG02622.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.29+17528A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183490177 | |||||||
| chr1:183490442 | T | A | 1 | a0001c0001t0006g0249 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.29+17793T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183490442 | |||||||
| chr1:183490479 | G | T | 1 | a0002c0002t0002g0075 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.29+17830G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183490479 | |||||||
| chr1:183490535 | G | A | 112 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0023 others(109): Show |
116 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.29+17886G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183490535 | |||||||
| chr1:183490825 | G | A | 7 | a0002c0002t0002g0075 a0003c0003t0001g0018 a0003c0003t0001g0120 others(4): Show |
8 | HG00423.hp1 HG01168.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.29+18176G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183490825 | |||||||
| chr1:183490911 | A | G | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.29+18262A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183490911 | |||||||
| chr1:183491147 | T | C | 1 | a0001c0001t0019g0183 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.29+18498T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183491147 | |||||||
| chr1:183491194 | G | A | 3 | a0001c0001t0005g0094 a0001c0001t0005g0095 a0001c0001t0005g0096 |
3 | HG01109.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.29+18545G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183491194 | |||||||
| chr1:183491217 | G | C | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.29+18568G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183491217 | |||||||
| chr1:183491391 | G | T | 2 | a0007c0008t0001g0317 a0007c0008t0001g0322 |
2 | HG01261.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.29+18742G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183491391 | |||||||
| chr1:183491435 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.29+18786G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183491435 | |||||||
| chr1:183491550 | G | A | 1 | a0003c0003t0001g0124 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.29+18901G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183491550 | |||||||
| chr1:183491559 | A | T | 1 | a0003c0003t0001g0147 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.29+18910A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183491559 | |||||||
| chr1:183491595 | C | T | 1 | a0006c0007t0005g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.29+18946C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183491595 | |||||||
| chr1:183491983 | G | C | 2 | a0002c0002t0002g0031 a0002c0002t0002g0032 |
2 | HG01243.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.29+19334G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183491983 | |||||||
| chr1:183492136 | A | G | 3 | a0001c0001t0006g0235 a0001c0001t0006g0236 a0001c0001t0006g0237 |
3 | NA18973.hp1 NA18998.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.29+19487A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183492136 | |||||||
| chr1:183492441 | A | G | 1 | a0001c0001t0016g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.29+19792A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183492441 | |||||||
| chr1:183492715 | A | G | 1 | a0001c0001t0016g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.29+20066A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183492715 | |||||||
| chr1:183492988 | G | T | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.30-19849G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183492988 | |||||||
| chr1:183493149 | C | CT | 113 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0023 others(110): Show |
117 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.30-19682dupT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183493149 | ||||||
| chr1:183493171 | T | C | 6 | a0004c0005t0005g0006 a0004c0005t0005g0161 a0004c0005t0005g0162 others(3): Show |
8 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.30-19666T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183493171 | |||||||
| chr1:183493177 | A | G | 3 | a0001c0001t0005g0094 a0001c0001t0005g0095 a0001c0001t0005g0096 |
3 | HG01109.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.30-19660A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183493177 | |||||||
| chr1:183493378 | A | T | 126 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0023 others(123): Show |
132 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.30-19459A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183493378 | |||||||
| chr1:183493494 | A | C | 1 | a0001c0001t0001g0160 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.30-19343A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183493494 | |||||||
| chr1:183493601 | A | T | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.30-19236A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183493601 | |||||||
| chr1:183493642 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.30-19195C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183493642 | |||||||
| chr1:183493657 | T | C | 1 | a0001c0001t0001g0005 | 3 | HG02258.hp2 HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.30-19180T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183493657 | |||||||
| chr1:183493749 | T | G | 2 | a0001c0001t0001g0290 a0001c0001t0001g0291 |
2 | NA18970.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.30-19088T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183493749 | |||||||
| chr1:183493876 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG01123.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.30-18961G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183493876 | |||||||
| chr1:183493999 | C | T | 189 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0023 others(186): Show |
203 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.30-18838C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183493999 | |||||||
| chr1:183494136 | C | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0281 others(42): Show |
51 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.30-18701C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183494136 | |||||||
| chr1:183494211 | T | C | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.30-18626T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183494211 | |||||||
| chr1:183494277 | C | A | 1 | a0001c0001t0001g0082 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.30-18560C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183494277 | |||||||
| chr1:183494368 | GT | G | 8 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.30-18459delT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183494368 | ||||||
| chr1:183494472 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
6 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.30-18365G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183494472 | |||||||
| chr1:183494652 | G | A | 303 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(300): Show |
330 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.30-18185G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183494652 | |||||||
| chr1:183494756 | C | CT | 63 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0101 others(60): Show |
69 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.30-18053dupT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183494756 | ||||||
| chr1:183494756 | C | CTT | 13 | a0001c0001t0001g0310 a0001c0001t0001g0316 a0001c0001t0001g0318 others(10): Show |
13 | HG00099.hp1 HG00280.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.30-18054_30-18053d others(4): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183494756 | ||||||
| chr1:183494756 | CT | C | 147 | a0001c0001t0001g0103 a0001c0001t0001g0108 a0001c0001t0003g0002 others(144): Show |
160 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.30-18053delT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183494756 | ||||||
| chr1:183494756 | CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02647.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.30-18064_30-18053d others(14): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183494756 | ||||||
| chr1:183494789 | TGGTGTCT others(56): Show |
T | 4 | a0002c0002t0002g0009 a0002c0002t0002g0028 a0002c0002t0002g0029 others(1): Show |
5 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.30-17984_30-17922d others(65): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183494789 | ||||||
| chr1:183494987 | C | T | 1 | a0005c0006t0001g0308 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.30-17850C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183494987 | |||||||
| chr1:183495079 | G | A | 1 | a0001c0001t0001g0312 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.30-17758G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183495079 | |||||||
| chr1:183495157 | A | G | 61 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0009 others(58): Show |
69 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.30-17680A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183495157 | |||||||
| chr1:183495193 | G | A | 325 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(322): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.30-17644G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183495193 | |||||||
| chr1:183495229 | T | C | 3 | a0001c0001t0005g0094 a0001c0001t0005g0095 a0001c0001t0005g0096 |
3 | HG01109.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.30-17608T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183495229 | |||||||
| chr1:183495268 | G | A | 6 | a0004c0005t0005g0006 a0004c0005t0005g0161 a0004c0005t0005g0162 others(3): Show |
8 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.30-17569G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183495268 | |||||||
| chr1:183495454 | A | G | 1 | a0002c0002t0002g0043 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.30-17383A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183495454 | |||||||
| chr1:183495489 | G | A | 1 | a0001c0001t0003g0250 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.30-17348G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183495489 | |||||||
| chr1:183495583 | A | C | 1 | a0002c0002t0002g0037 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30-17254A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183495583 | |||||||
| chr1:183495596 | C | T | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.30-17241C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183495596 | |||||||
| chr1:183495804 | G | T | 1 | a0001c0001t0003g0260 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.30-17033G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183495804 | |||||||
| chr1:183495872 | A | G | 1 | a0001c0001t0007g0193 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.30-16965A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183495872 | |||||||
| chr1:183495909 | T | C | 1 | a0002c0002t0002g0044 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.30-16928T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183495909 | |||||||
| chr1:183496543 | G | A | 2 | a0001c0001t0001g0313 a0001c0001t0001g0318 |
2 | HG01099.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.30-16294G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183496543 | |||||||
| chr1:183496546 | A | G | 1 | a0001c0001t0016g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.30-16291A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183496546 | |||||||
| chr1:183496672 | T | C | 1 | a0001c0001t0001g0319 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.30-16165T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183496672 | |||||||
| chr1:183496806 | A | G | 3 | a0003c0003t0001g0017 a0003c0003t0001g0140 a0003c0003t0001g0146 |
4 | HG00597.hp1 NA18939.hp2 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.30-16031A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183496806 | |||||||
| chr1:183497150 | A | G | 17 | a0002c0002t0002g0003 a0002c0002t0002g0011 a0002c0002t0002g0044 others(14): Show |
20 | HG00558.hp2 HG00609.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.30-15687A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183497150 | |||||||
| chr1:183497170 | T | C | 42 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0011 others(39): Show |
48 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.30-15667T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183497170 | |||||||
| chr1:183497494 | T | C | 1 | a0001c0001t0010g0185 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.30-15343T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183497494 | |||||||
| chr1:183497673 | G | A | 1 | a0001c0001t0015g0128 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.30-15164G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183497673 | |||||||
| chr1:183497724 | C | T | 1 | a0002c0002t0002g0036 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.30-15113C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183497724 | |||||||
| chr1:183497725 | G | A | 1 | a0004c0005t0005g0162 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.30-15112G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183497725 | |||||||
| chr1:183497776 | G | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0168 a0001c0001t0001g0169 others(2): Show |
6 | HG02109.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.30-15061G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183497776 | |||||||
| chr1:183497833 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0129 |
2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.30-15004G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183497833 | |||||||
| chr1:183497960 | G | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0112 a0001c0001t0001g0113 others(4): Show |
9 | HG01099.hp1 HG01884.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.30-14877G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183497960 | |||||||
| chr1:183498175 | A | G | 1 | a0001c0001t0005g0228 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.30-14662A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183498175 | |||||||
| chr1:183498374 | C | A | 1 | a0006c0007t0005g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.30-14463C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183498374 | |||||||
| chr1:183498437 | G | A | 61 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0009 others(58): Show |
69 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.30-14400G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183498437 | |||||||
| chr1:183498534 | T | C | 2 | a0001c0001t0004g0205 a0001c0001t0004g0206 |
2 | NA18948.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.30-14303T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183498534 | |||||||
| chr1:183498618 | A | G | 1 | a0003c0003t0001g0123 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.30-14219A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183498618 | |||||||
| chr1:183498767 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30-14070C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183498767 | |||||||
| chr1:183499007 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.30-13830A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183499007 | |||||||
| chr1:183499120 | G | C | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.30-13717G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183499120 | |||||||
| chr1:183499172 | T | C | 1 | a0001c0001t0001g0292 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.30-13665T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183499172 | |||||||
| chr1:183499285 | T | G | 42 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0011 others(39): Show |
48 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.30-13552T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183499285 | |||||||
| chr1:183499400 | T | C | 2 | a0001c0001t0003g0229 a0001c0001t0006g0207 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.30-13437T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183499400 | |||||||
| chr1:183499405 | A | T | 1 | a0001c0001t0001g0307 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.30-13432A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183499405 | |||||||
| chr1:183499737 | C | A | 1 | a0001c0001t0001g0293 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.30-13100C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183499737 | |||||||
| chr1:183500036 | G | C | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.30-12801G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183500036 | |||||||
| chr1:183500551 | A | G | 1 | a0001c0001t0019g0183 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.30-12286A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183500551 | |||||||
| chr1:183500791 | G | T | 2 | a0002c0002t0002g0028 a0002c0002t0002g0029 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.30-12046G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183500791 | |||||||
| chr1:183500968 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.30-11869A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183500968 | |||||||
| chr1:183500974 | G | T | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.30-11863G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183500974 | |||||||
| chr1:183500981 | G | T | 6 | a0004c0005t0005g0006 a0004c0005t0005g0161 a0004c0005t0005g0162 others(3): Show |
8 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.30-11856G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183500981 | |||||||
| chr1:183501048 | A | G | 2 | a0002c0002t0002g0027 a0002c0002t0002g0035 |
2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.30-11789A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183501048 | |||||||
| chr1:183501112 | A | C | 3 | a0001c0001t0005g0094 a0001c0001t0005g0095 a0001c0001t0005g0096 |
3 | HG01109.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.30-11725A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183501112 | |||||||
| chr1:183501377 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.30-11460C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183501377 | |||||||
| chr1:183501462 | C | T | 2 | a0002c0002t0002g0027 a0002c0002t0002g0035 |
2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.30-11375C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183501462 | |||||||
| chr1:183501890 | A | G | 5 | a0001c0001t0003g0258 a0001c0001t0003g0269 a0001c0001t0003g0270 others(2): Show |
5 | HG00544.hp1 NA18971.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.30-10947A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183501890 | |||||||
| chr1:183502160 | G | T | 317 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(314): Show |
345 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(342): Show |
intron_variant | MODIFIER | c.30-10677G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183502160 | |||||||
| chr1:183503287 | T | C | 1 | a0001c0001t0004g0264 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.30-9550T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183503287 | |||||||
| chr1:183503390 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.30-9447C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183503390 | |||||||
| chr1:183503538 | T | A | 1 | a0002c0002t0002g0030 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.30-9299T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183503538 | |||||||
| chr1:183503671 | A | G | 2 | a0002c0002t0002g0070 a0002c0002t0002g0071 |
2 | NA18998.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.30-9166A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183503671 | |||||||
| chr1:183503742 | C | A | 2 | a0006c0007t0005g0166 a0006c0007t0005g0167 |
2 | HG01069.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.30-9095C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183503742 | |||||||
| chr1:183503778 | G | T | 2 | a0001c0001t0003g0269 a0001c0001t0003g0270 |
2 | NA19011.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.30-9059G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183503778 | |||||||
| chr1:183503937 | A | G | 1 | a0001c0001t0003g0195 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.30-8900A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183503937 | |||||||
| chr1:183503970 | C | G | 1 | a0001c0001t0005g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.30-8867C>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183503970 | |||||||
| chr1:183504103 | A | G | 5 | a0002c0002t0002g0009 a0002c0002t0002g0028 a0002c0002t0002g0029 others(2): Show |
6 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.30-8734A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183504103 | |||||||
| chr1:183504233 | A | G | 1 | a0001c0001t0003g0023 | 2 | NA18943.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.30-8604A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183504233 | |||||||
| chr1:183504286 | T | C | 1 | a0001c0001t0003g0201 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.30-8551T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183504286 | |||||||
| chr1:183504304 | G | A | 61 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0009 others(58): Show |
69 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.30-8533G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183504304 | |||||||
| chr1:183504324 | G | GATTT | 18 | a0001c0001t0001g0021 a0001c0001t0001g0168 a0001c0001t0001g0169 others(15): Show |
19 | HG01099.hp2 HG01167.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.30-8484_30-8481dup others(4): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183504324 | ||||||
| chr1:183504324 | G | GATTTATT others(1): Show |
4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.30-8488_30-8481dup others(8): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183504324 | ||||||
| chr1:183504324 | G | T | 2 | a0001c0001t0001g0182 a0001c0001t0016g0173 |
2 | HG01099.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.30-8513G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183504324 | |||||||
| chr1:183504324 | GATTTATT others(5): Show |
G | 1 | a0001c0001t0001g0102 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.30-8492_30-8481del others(12): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183504324 | ||||||
| chr1:183504501 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.30-8336C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183504501 | |||||||
| chr1:183504513 | A | G | 1 | a0001c0001t0001g0320 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30-8324A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183504513 | |||||||
| chr1:183504629 | G | A | 2 | a0002c0002t0002g0028 a0002c0002t0002g0029 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.30-8208G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183504629 | |||||||
| chr1:183504763 | C | T | 1 | a0001c0001t0003g0227 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.30-8074C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183504763 | |||||||
| chr1:183504775 | C | T | 1 | a0001c0001t0007g0176 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.30-8062C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183504775 | |||||||
| chr1:183504931 | C | T | 1 | a0002c0002t0008g0069 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.30-7906C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183504931 | |||||||
| chr1:183505147 | G | A | 1 | a0001c0001t0001g0311 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.30-7690G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183505147 | |||||||
| chr1:183505224 | C | A | 1 | a0001c0001t0004g0246 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.30-7613C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183505224 | |||||||
| chr1:183505266 | A | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
6 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.30-7571A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183505266 | |||||||
| chr1:183505552 | C | G | 1 | a0006c0007t0005g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.30-7285C>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183505552 | |||||||
| chr1:183505559 | C | T | 6 | a0004c0005t0005g0006 a0004c0005t0005g0161 a0004c0005t0005g0162 others(3): Show |
8 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.30-7278C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183505559 | |||||||
| chr1:183505626 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.30-7211C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183505626 | |||||||
| chr1:183505711 | C | G | 1 | a0001c0004t0001g0089 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.30-7126C>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183505711 | |||||||
| chr1:183505715 | G | C | 113 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0023 others(110): Show |
117 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.30-7122G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183505715 | |||||||
| chr1:183505783 | G | A | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.30-7054G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183505783 | |||||||
| chr1:183505852 | G | GT | 4 | a0001c0001t0001g0005 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
6 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.30-6980dupT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183505852 | ||||||
| chr1:183505895 | A | C | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.30-6942A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183505895 | |||||||
| chr1:183506101 | G | A | 2 | a0001c0004t0001g0091 a0001c0004t0001g0092 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.30-6736G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183506101 | |||||||
| chr1:183506288 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.30-6549C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183506288 | |||||||
| chr1:183506395 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.30-6442T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183506395 | |||||||
| chr1:183506602 | A | G | 1 | a0003c0003t0001g0026 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.30-6235A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183506602 | |||||||
| chr1:183506653 | T | TA | 62 | a0001c0001t0001g0082 a0001c0001t0001g0114 a0001c0001t0001g0115 others(59): Show |
67 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.30-6170dupA | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183506653 | ||||||
| chr1:183506653 | TA | T | 6 | a0001c0001t0001g0312 a0001c0001t0003g0194 a0001c0001t0004g0244 others(3): Show |
6 | HG01081.hp2 HG01975.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.30-6170delA | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183506653 | ||||||
| chr1:183506670 | C | T | 1 | a0006c0007t0005g0167 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.30-6167C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183506670 | |||||||
| chr1:183506706 | A | C | 6 | a0004c0005t0005g0006 a0004c0005t0005g0161 a0004c0005t0005g0162 others(3): Show |
8 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.30-6131A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183506706 | |||||||
| chr1:183506875 | C | CT | 120 | a0001c0001t0001g0117 a0001c0001t0001g0156 a0001c0001t0001g0172 others(117): Show |
125 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.30-5942dupT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183506875 | ||||||
| chr1:183506875 | CT | C | 6 | a0001c0001t0005g0095 a0002c0002t0002g0027 a0002c0002t0002g0035 others(3): Show |
6 | HG01109.hp2 HG01891.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.30-5942delT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183506875 | ||||||
| chr1:183507036 | G | A | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.30-5801G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183507036 | |||||||
| chr1:183507254 | C | G | 2 | a0003c0003t0001g0118 a0003c0003t0001g0138 |
2 | HG02165.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.30-5583C>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183507254 | |||||||
| chr1:183507483 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.30-5354C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183507483 | |||||||
| chr1:183507563 | A | G | 1 | a0001c0004t0001g0100 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.30-5274A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183507563 | |||||||
| chr1:183507794 | G | A | 112 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0023 others(109): Show |
116 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.30-5043G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183507794 | |||||||
| chr1:183507953 | C | T | 1 | a0002c0002t0002g0044 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.30-4884C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183507953 | |||||||
| chr1:183508059 | T | C | 1 | a0001c0001t0003g0243 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.30-4778T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183508059 | |||||||
| chr1:183508096 | G | A | 254 | a0001c0001t0001g0005 a0001c0001t0001g0082 a0001c0001t0001g0112 others(251): Show |
275 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.30-4741G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183508096 | |||||||
| chr1:183508110 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
6 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.30-4727G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183508110 | |||||||
| chr1:183508389 | T | G | 5 | a0002c0002t0002g0045 a0002c0002t0002g0046 a0002c0002t0002g0052 others(2): Show |
5 | NA18960.hp1 NA18978.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.30-4448T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183508389 | |||||||
| chr1:183508457 | A | C | 6 | a0004c0005t0005g0006 a0004c0005t0005g0161 a0004c0005t0005g0162 others(3): Show |
8 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.30-4380A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183508457 | |||||||
| chr1:183508483 | T | C | 1 | a0002c0002t0002g0045 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.30-4354T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183508483 | |||||||
| chr1:183508517 | A | C | 3 | a0001c0001t0001g0285 a0001c0001t0001g0305 a0001c0001t0001g0306 |
3 | HG00099.hp2 HG01070.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.30-4320A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183508517 | |||||||
| chr1:183508912 | T | G | 1 | a0001c0001t0019g0183 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.30-3925T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183508912 | |||||||
| chr1:183509160 | A | G | 6 | a0001c0001t0003g0177 a0001c0001t0004g0175 a0001c0001t0004g0178 others(3): Show |
7 | HG02145.hp1 HG02809.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.30-3677A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183509160 | |||||||
| chr1:183509328 | G | T | 53 | a0001c0001t0001g0082 a0001c0001t0001g0114 a0001c0001t0001g0125 others(50): Show |
58 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.30-3509G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183509328 | |||||||
| chr1:183509524 | G | A | 1 | a0001c0001t0003g0024 | 2 | HG03834.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.30-3313G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183509524 | |||||||
| chr1:183509562 | C | A | 2 | a0002c0002t0002g0027 a0002c0002t0002g0035 |
2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.30-3275C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183509562 | |||||||
| chr1:183509586 | A | G | 1 | a0003c0003t0001g0119 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.30-3251A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183509586 | |||||||
| chr1:183509847 | A | T | 1 | a0001c0001t0003g0226 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.30-2990A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183509847 | |||||||
| chr1:183509951 | A | T | 1 | a0001c0001t0001g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.30-2886A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183509951 | |||||||
| chr1:183509955 | T | C | 125 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0023 others(122): Show |
131 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.30-2882T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183509955 | |||||||
| chr1:183509967 | A | G | 1 | a0001c0010t0009g0202 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.30-2870A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183509967 | |||||||
| chr1:183510151 | G | A | 1 | a0001c0001t0006g0210 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.30-2686G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183510151 | |||||||
| chr1:183510228 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.30-2609A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183510228 | |||||||
| chr1:183510307 | C | T | 9 | a0001c0001t0003g0225 a0001c0001t0003g0247 a0001c0001t0003g0250 others(6): Show |
9 | HG01106.hp2 HG01192.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.30-2530C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183510307 | |||||||
| chr1:183510471 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.30-2366G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183510471 | |||||||
| chr1:183510860 | A | G | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.30-1977A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183510860 | |||||||
| chr1:183511129 | T | G | 1 | a0001c0001t0001g0182 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.30-1708T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183511129 | |||||||
| chr1:183511304 | T | C | 1 | a0001c0001t0003g0226 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.30-1533T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183511304 | |||||||
| chr1:183511576 | G | A | 1 | a0002c0002t0002g0037 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.30-1261G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183511576 | |||||||
| chr1:183511967 | C | A | 64 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(61): Show |
72 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.30-870C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183511967 | |||||||
| chr1:183512203 | G | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0168 a0001c0001t0001g0169 others(2): Show |
6 | HG02109.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.30-634G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183512203 | |||||||
| chr1:183512655 | C | A | 1 | a0001c0001t0001g0182 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.30-182C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | chr1 | 183512655 | |||||||
| chr1:183512808 | C | CT | 108 | a0001c0001t0001g0306 a0001c0001t0003g0002 a0001c0001t0003g0007 others(105): Show |
111 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(108): Show |
splice_region_variant&intron_variant | LOW | c.30-9dupT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183512808 | ||||||
| chr1:183512808 | CT | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0112 a0001c0001t0001g0113 others(8): Show |
13 | HG01099.hp1 HG01884.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.30-9delT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 183512808 | ||||||
| chr1:183512950 | A | G | 1 | a0001c0001t0004g0246 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.61+82A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183512950 | |||||||
| chr1:183512974 | G | A | 1 | a0001c0001t0001g0321 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.61+106G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183512974 | |||||||
| chr1:183513060 | G | A | 3 | a0001c0004t0001g0083 a0001c0004t0001g0086 a0001c0004t0001g0090 |
3 | HG00280.hp2 HG01175.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.61+192G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183513060 | |||||||
| chr1:183513369 | C | CT | 9 | a0001c0001t0001g0005 a0001c0001t0001g0104 a0001c0001t0001g0158 others(6): Show |
11 | HG01192.hp2 HG01516.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.61+521dupT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 183513369 | ||||||
| chr1:183513369 | C | CTT | 57 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0009 others(54): Show |
65 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.61+520_61+521dupTT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 183513369 | ||||||
| chr1:183513369 | CT | C | 8 | a0001c0001t0003g0177 a0001c0001t0003g0243 a0001c0001t0004g0230 others(5): Show |
8 | HG01891.hp2 HG02723.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.61+521delT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 183513369 | ||||||
| chr1:183513433 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.61+565G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183513433 | |||||||
| chr1:183513465 | T | C | 3 | a0002c0002t0002g0058 a0002c0002t0002g0068 a0002c0002t0002g0077 |
3 | HG01257.hp1 HG01978.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.61+597T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183513465 | |||||||
| chr1:183513520 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0129 |
2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.61+652C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183513520 | |||||||
| chr1:183513577 | G | C | 1 | a0001c0001t0011g0272 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.61+709G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183513577 | |||||||
| chr1:183513650 | G | A | 61 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0009 others(58): Show |
69 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.61+782G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183513650 | |||||||
| chr1:183513717 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.61+849G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183513717 | |||||||
| chr1:183513756 | G | T | 1 | a0001c0001t0017g0184 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.61+888G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183513756 | |||||||
| chr1:183513758 | G | A | 2 | a0002c0002t0002g0040 a0002c0002t0005g0041 |
2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.61+890G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183513758 | |||||||
| chr1:183513768 | G | C | 1 | a0004c0005t0005g0162 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.61+900G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183513768 | |||||||
| chr1:183513875 | C | G | 1 | a0003c0003t0001g0137 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.61+1007C>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183513875 | |||||||
| chr1:183513880 | AT | A | 9 | a0002c0002t0002g0003 a0002c0002t0002g0011 a0002c0002t0002g0045 others(6): Show |
12 | HG00558.hp2 HG02129.hp2 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.61+1014delT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 183513880 | ||||||
| chr1:183514029 | C | CA | 17 | a0001c0001t0001g0021 a0001c0001t0001g0101 a0001c0001t0001g0168 others(14): Show |
18 | HG00438.hp1 HG00438.hp2 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.61+1182dupA | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 183514029 | ||||||
| chr1:183514029 | CA | C | 19 | a0001c0001t0001g0005 a0001c0001t0001g0158 a0001c0001t0001g0159 others(16): Show |
21 | HG01070.hp1 HG01070.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.61+1182delA | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 183514029 | ||||||
| chr1:183514029 | CAA | C | 6 | a0004c0005t0005g0006 a0004c0005t0005g0161 a0004c0005t0005g0162 others(3): Show |
8 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.61+1181_61+1182del others(2): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 183514029 | ||||||
| chr1:183514044 | A | T | 12 | a0001c0001t0003g0002 a0001c0001t0003g0194 a0001c0001t0003g0195 others(9): Show |
13 | HG01257.hp2 HG01952.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.61+1176A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183514044 | |||||||
| chr1:183514095 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.61+1227C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183514095 | |||||||
| chr1:183514119 | C | T | 1 | a0002c0002t0002g0034 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.61+1251C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183514119 | |||||||
| chr1:183514216 | C | CA | 52 | a0001c0001t0001g0082 a0001c0001t0001g0115 a0001c0001t0001g0116 others(49): Show |
58 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.61+1365dupA | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 183514216 | ||||||
| chr1:183514216 | C | CAAA | 6 | a0001c0001t0001g0114 a0001c0001t0001g0125 a0001c0001t0001g0141 others(3): Show |
6 | HG01433.hp2 HG01978.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+1363_61+1365dup others(3): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 183514216 | ||||||
| chr1:183514216 | CA | C | 83 | a0001c0001t0001g0106 a0001c0001t0001g0293 a0001c0001t0003g0177 others(80): Show |
94 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.61+1365delA | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 183514216 | ||||||
| chr1:183514643 | C | A | 1 | a0001c0001t0001g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.62-1231C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183514643 | |||||||
| chr1:183514780 | G | T | 1 | a0001c0001t0001g0304 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.62-1094G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183514780 | |||||||
| chr1:183515038 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.62-836G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183515038 | |||||||
| chr1:183515048 | T | C | 1 | a0001c0001t0001g0293 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.62-826T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183515048 | |||||||
| chr1:183515106 | T | G | 2 | a0001c0001t0005g0095 a0001c0001t0005g0096 |
2 | HG01109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.62-768T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183515106 | |||||||
| chr1:183515132 | T | C | 1 | a0002c0002t0002g0031 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.62-742T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183515132 | |||||||
| chr1:183515145 | C | G | 1 | a0002c0002t0002g0031 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.62-729C>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183515145 | |||||||
| chr1:183515161 | G | T | 1 | a0001c0001t0001g0152 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.62-713G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183515161 | |||||||
| chr1:183515162 | A | T | 1 | a0001c0001t0001g0152 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.62-712A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183515162 | |||||||
| chr1:183515195 | C | A | 1 | a0003c0003t0001g0119 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.62-679C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183515195 | |||||||
| chr1:183515270 | CTT | C | 42 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0011 others(39): Show |
48 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.62-603_62-602delTT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183515270 | |||||||
| chr1:183515288 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.62-586G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183515288 | |||||||
| chr1:183515527 | T | C | 1 | a0001c0001t0016g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.62-347T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183515527 | |||||||
| chr1:183515605 | C | CT | 64 | a0001c0001t0001g0152 a0001c0001t0003g0254 a0001c0001t0003g0269 others(61): Show |
71 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.62-251dupT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 183515605 | ||||||
| chr1:183515605 | CT | C | 11 | a0001c0001t0001g0172 a0001c0001t0001g0285 a0001c0001t0004g0198 others(8): Show |
11 | HG01069.hp2 HG01070.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.62-251delT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 183515605 | ||||||
| chr1:183515676 | A | AACCAGAC | 17 | a0003c0003t0001g0013 a0003c0003t0001g0014 a0003c0003t0001g0018 others(14): Show |
20 | HG00408.hp1 HG00423.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.62-197_62-191dupAC others(5): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 183515676 | ||||||
| chr1:183515851 | A | G | 2 | a0006c0007t0005g0166 a0006c0007t0005g0167 |
2 | HG01069.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.62-23A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 2/22 | chr1 | 183515851 | |||||||
| chr1:183516224 | G | T | 1 | a0001c0001t0001g0182 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.179+233G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/22 | chr1 | 183516224 | |||||||
| chr1:183516259 | C | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 |
3 | HG01123.hp1 HG01192.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.179+268C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/22 | chr1 | 183516259 | |||||||
| chr1:183516314 | C | A | 2 | a0001c0001t0014g0157 a0001c0001t0018g0180 |
2 | HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.179+323C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/22 | chr1 | 183516314 | |||||||
| chr1:183516482 | A | G | 3 | a0001c0001t0005g0094 a0001c0001t0005g0095 a0001c0001t0005g0096 |
3 | HG01109.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.179+491A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/22 | chr1 | 183516482 | |||||||
| chr1:183516758 | C | T | 1 | a0002c0002t0002g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.179+767C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/22 | chr1 | 183516758 | |||||||
| chr1:183516890 | A | G | 1 | a0002c0002t0002g0039 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.180-798A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/22 | chr1 | 183516890 | |||||||
| chr1:183516908 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.180-780A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/22 | chr1 | 183516908 | |||||||
| chr1:183516969 | A | G | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.180-719A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/22 | chr1 | 183516969 | |||||||
| chr1:183517253 | G | A | 1 | a0001c0001t0003g0213 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.180-435G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/22 | chr1 | 183517253 | |||||||
| chr1:183517285 | C | T | 1 | a0006c0007t0005g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.180-403C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/22 | chr1 | 183517285 | |||||||
| chr1:183517480 | T | C | 1 | a0002c0002t0002g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.180-208T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/22 | chr1 | 183517480 | |||||||
| chr1:183517499 | G | T | 1 | a0001c0001t0005g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.180-189G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/22 | chr1 | 183517499 | |||||||
| chr1:183517523 | T | C | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02647.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.180-165T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 3/22 | chr1 | 183517523 | |||||||
| chr1:183517919 | A | G | 2 | a0001c0001t0004g0175 a0001c0001t0007g0174 |
2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.312+99A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183517919 | |||||||
| chr1:183517929 | T | A | 1 | a0003c0003t0001g0143 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.312+109T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183517929 | |||||||
| chr1:183517948 | T | C | 1 | a0004c0005t0005g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.312+128T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183517948 | |||||||
| chr1:183518002 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.312+182T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183518002 | |||||||
| chr1:183518129 | G | A | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.312+309G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183518129 | |||||||
| chr1:183518173 | C | T | 1 | a0001c0001t0014g0157 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.312+353C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183518173 | |||||||
| chr1:183518261 | C | T | 1 | a0003c0003t0001g0144 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.312+441C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183518261 | |||||||
| chr1:183518270 | A | G | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0303 |
3 | NA18970.hp2 NA18992.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.312+450A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183518270 | |||||||
| chr1:183518445 | C | T | 1 | a0001c0001t0001g0321 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.312+625C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183518445 | |||||||
| chr1:183518445 | CTA | C | 6 | a0004c0005t0005g0006 a0004c0005t0005g0161 a0004c0005t0005g0162 others(3): Show |
8 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.312+628_312+629del others(2): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr1 | 183518445 | ||||||
| chr1:183518714 | A | G | 1 | a0001c0001t0019g0183 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.312+894A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183518714 | |||||||
| chr1:183518836 | T | A | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.312+1016T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183518836 | |||||||
| chr1:183518909 | A | G | 1 | a0001c0004t0001g0088 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.312+1089A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183518909 | |||||||
| chr1:183519246 | A | G | 1 | a0001c0001t0004g0224 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.312+1426A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183519246 | |||||||
| chr1:183519356 | C | T | 2 | a0003c0003t0001g0135 a0003c0003t0001g0155 |
2 | NA18943.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.312+1536C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183519356 | |||||||
| chr1:183519392 | C | T | 57 | a0001c0001t0001g0082 a0001c0001t0001g0114 a0001c0001t0001g0115 others(54): Show |
62 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.312+1572C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183519392 | |||||||
| chr1:183519780 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.312+1960G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183519780 | |||||||
| chr1:183520025 | A | AT | 40 | a0001c0001t0019g0183 a0002c0002t0002g0076 a0003c0003t0001g0013 others(37): Show |
45 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.312+2218dupT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr1 | 183520025 | ||||||
| chr1:183520068 | G | A | 111 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0023 others(108): Show |
115 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.312+2248G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183520068 | |||||||
| chr1:183520143 | G | A | 111 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0023 others(108): Show |
115 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.312+2323G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183520143 | |||||||
| chr1:183520164 | C | A | 2 | a0006c0007t0005g0166 a0006c0007t0005g0167 |
2 | HG01069.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.312+2344C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183520164 | |||||||
| chr1:183520547 | A | C | 1 | a0002c0002t0002g0065 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.312+2727A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183520547 | |||||||
| chr1:183520862 | G | C | 2 | a0001c0001t0003g0201 a0001c0001t0004g0200 |
2 | NA18946.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.312+3042G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183520862 | |||||||
| chr1:183520911 | G | C | 1 | a0001c0001t0001g0312 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.312+3091G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183520911 | |||||||
| chr1:183521004 | G | A | 1 | a0001c0001t0003g0259 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.312+3184G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183521004 | |||||||
| chr1:183521015 | C | T | 2 | a0001c0001t0004g0230 a0010c0009t0007g0197 |
2 | HG02723.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.312+3195C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183521015 | |||||||
| chr1:183521072 | C | CT | 8 | a0001c0001t0001g0291 a0001c0001t0003g0201 a0001c0001t0006g0210 others(5): Show |
8 | HG04228.hp1 NA18906.hp2 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.312+3270dupT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr1 | 183521072 | ||||||
| chr1:183521072 | CT | C | 13 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(10): Show |
13 | HG02027.hp1 HG02056.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.312+3270delT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr1 | 183521072 | ||||||
| chr1:183521168 | C | T | 2 | a0001c0001t0014g0157 a0001c0001t0018g0180 |
2 | HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.312+3348C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183521168 | |||||||
| chr1:183521327 | G | C | 1 | a0003c0003t0001g0026 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.312+3507G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183521327 | |||||||
| chr1:183521481 | C | G | 57 | a0001c0001t0001g0082 a0001c0001t0001g0114 a0001c0001t0001g0115 others(54): Show |
62 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.312+3661C>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183521481 | |||||||
| chr1:183521495 | G | T | 1 | a0001c0001t0006g0189 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.312+3675G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183521495 | |||||||
| chr1:183521562 | G | A | 1 | a0001c0001t0007g0239 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.312+3742G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183521562 | |||||||
| chr1:183521858 | C | CA | 241 | a0001c0001t0001g0082 a0001c0001t0001g0114 a0001c0001t0001g0115 others(238): Show |
259 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.312+4054dupA | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr1 | 183521858 | ||||||
| chr1:183521875 | G | A | 1 | a0001c0001t0001g0296 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.312+4055G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183521875 | |||||||
| chr1:183521878 | G | A | 1 | a0001c0001t0001g0296 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.312+4058G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183521878 | |||||||
| chr1:183522030 | A | G | 1 | a0001c0001t0005g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.312+4210A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183522030 | |||||||
| chr1:183522256 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.313-4340A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183522256 | |||||||
| chr1:183522268 | T | G | 2 | a0001c0001t0003g0279 a0001c0001t0004g0273 |
2 | NA19006.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.313-4328T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183522268 | |||||||
| chr1:183522271 | T | C | 1 | a0001c0001t0003g0243 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.313-4325T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183522271 | |||||||
| chr1:183523070 | A | G | 1 | a0001c0001t0003g0204 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.313-3526A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183523070 | |||||||
| chr1:183523072 | A | G | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.313-3524A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183523072 | |||||||
| chr1:183523117 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.313-3479G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183523117 | |||||||
| chr1:183523417 | A | G | 1 | a0001c0004t0001g0093 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.313-3179A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183523417 | |||||||
| chr1:183523771 | T | A | 1 | a0001c0001t0019g0183 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.313-2825T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183523771 | |||||||
| chr1:183523786 | T | C | 1 | a0001c0001t0009g0231 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.313-2810T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183523786 | |||||||
| chr1:183523864 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.313-2732A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183523864 | |||||||
| chr1:183523874 | G | T | 1 | a0001c0001t0005g0223 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.313-2722G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183523874 | |||||||
| chr1:183523897 | A | G | 1 | a0006c0007t0005g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.313-2699A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183523897 | |||||||
| chr1:183523977 | T | A | 6 | a0004c0005t0005g0006 a0004c0005t0005g0161 a0004c0005t0005g0162 others(3): Show |
8 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.313-2619T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183523977 | |||||||
| chr1:183524086 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.313-2510T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183524086 | |||||||
| chr1:183524198 | C | T | 2 | a0003c0003t0001g0134 a0003c0003t0001g0145 |
2 | NA18947.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.313-2398C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183524198 | |||||||
| chr1:183524251 | T | G | 1 | a0001c0001t0018g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.313-2345T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183524251 | |||||||
| chr1:183524401 | A | G | 1 | a0003c0003t0001g0181 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.313-2195A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183524401 | |||||||
| chr1:183524681 | C | T | 2 | a0003c0003t0001g0016 a0003c0003t0001g0132 |
3 | NA18948.hp1 NA18963.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.313-1915C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183524681 | |||||||
| chr1:183524827 | C | G | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.313-1769C>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183524827 | |||||||
| chr1:183525079 | A | G | 113 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0023 others(110): Show |
117 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.313-1517A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183525079 | |||||||
| chr1:183525119 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.313-1477A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183525119 | |||||||
| chr1:183525134 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.313-1462G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183525134 | |||||||
| chr1:183525200 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.313-1396C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183525200 | |||||||
| chr1:183525285 | G | T | 9 | a0003c0003t0001g0014 a0003c0003t0001g0018 a0003c0003t0001g0120 others(6): Show |
11 | HG00423.hp1 HG01168.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.313-1311G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183525285 | |||||||
| chr1:183525318 | G | A | 190 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0023 others(187): Show |
204 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.313-1278G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183525318 | |||||||
| chr1:183525391 | A | G | 317 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(314): Show |
345 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(342): Show |
intron_variant | MODIFIER | c.313-1205A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183525391 | |||||||
| chr1:183525409 | G | A | 1 | a0001c0001t0005g0095 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.313-1187G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183525409 | |||||||
| chr1:183525813 | T | C | 1 | a0001c0001t0004g0238 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.313-783T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183525813 | |||||||
| chr1:183525884 | T | C | 1 | a0009c0013t0001g0295 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.313-712T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183525884 | |||||||
| chr1:183525885 | C | T | 1 | a0009c0013t0001g0295 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.313-711C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183525885 | |||||||
| chr1:183525932 | T | G | 1 | a0002c0002t0008g0069 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.313-664T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183525932 | |||||||
| chr1:183525968 | TTTGC | T | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02647.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.313-621_313-618del others(4): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr1 | 183525968 | ||||||
| chr1:183525999 | C | G | 1 | a0001c0001t0001g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.313-597C>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183525999 | |||||||
| chr1:183526153 | TA | T | 4 | a0001c0001t0001g0104 a0001c0001t0003g0229 a0001c0001t0006g0207 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.313-442delA | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526153 | |||||||
| chr1:183526154 | A | T | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.313-442A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526154 | |||||||
| chr1:183526155 | TA | T | 185 | a0001c0001t0001g0021 a0001c0001t0001g0082 a0001c0001t0001g0102 others(182): Show |
197 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.313-440delA | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526155 | |||||||
| chr1:183526156 | A | AT | 5 | a0001c0001t0001g0005 a0001c0001t0001g0158 a0001c0001t0001g0159 others(2): Show |
7 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.313-429dupT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr1 | 183526156 | ||||||
| chr1:183526156 | A | ATTT | 55 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0009 others(52): Show |
63 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.313-431_313-429dup others(3): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr1 | 183526156 | ||||||
| chr1:183526156 | A | T | 8 | a0001c0001t0001g0104 a0001c0001t0003g0229 a0001c0001t0006g0207 others(5): Show |
8 | HG01168.hp1 HG01169.hp2 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.313-440A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526156 | |||||||
| chr1:183526156 | AT | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0281 others(44): Show |
53 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.313-429delT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr1 | 183526156 | ||||||
| chr1:183526159 | T | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0293 |
4 | HG03654.hp1 NA18946.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.313-437T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526159 | |||||||
| chr1:183526278 | A | G | 2 | a0001c0001t0003g0190 a0001c0001t0003g0276 |
2 | HG02056.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.313-318A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526278 | |||||||
| chr1:183526311 | G | C | 1 | a0009c0013t0001g0295 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.313-285G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526311 | |||||||
| chr1:183526312 | C | G | 1 | a0009c0013t0001g0295 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.313-284C>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526312 | |||||||
| chr1:183526397 | G | A | 1 | a0001c0001t0018g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.313-199G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526397 | |||||||
| chr1:183526496 | T | G | 1 | a0009c0013t0001g0295 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.313-100T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526496 | |||||||
| chr1:183526531 | G | A | 1 | a0002c0002t0008g0069 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.313-65G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526531 | |||||||
| chr1:183526539 | A | C | 1 | a0009c0013t0001g0295 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.313-57A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526539 | |||||||
| chr1:183526540 | C | T | 1 | a0009c0013t0001g0295 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.313-56C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526540 | |||||||
| chr1:183526548 | T | G | 1 | a0003c0003t0001g0018 | 2 | HG01168.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.313-48T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526548 | |||||||
| chr1:183526578 | T | C | 9 | a0001c0001t0003g0177 a0001c0001t0004g0175 a0001c0001t0004g0178 others(6): Show |
10 | HG02145.hp1 HG02717.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.313-18T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 4/22 | chr1 | 183526578 | |||||||
| chr1:183527235 | G | A | 1 | a0002c0002t0002g0059 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.484+468G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 5/22 | chr1 | 183527235 | |||||||
| chr1:183527246 | A | T | 3 | a0001c0001t0005g0094 a0001c0001t0005g0095 a0001c0001t0005g0096 |
3 | HG01109.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.484+479A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 5/22 | chr1 | 183527246 | |||||||
| chr1:183527523 | A | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0281 others(42): Show |
51 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.485-433A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 5/22 | chr1 | 183527523 | |||||||
| chr1:183527854 | A | G | 3 | a0001c0001t0005g0094 a0001c0001t0005g0095 a0001c0001t0005g0096 |
3 | HG01109.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.485-102A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 5/22 | chr1 | 183527854 | |||||||
| chr1:183528492 | G | A | 56 | a0001c0001t0001g0082 a0001c0001t0001g0114 a0001c0001t0001g0115 others(53): Show |
61 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.557-400G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 6/22 | chr1 | 183528492 | |||||||
| chr1:183528553 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.557-339C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 6/22 | chr1 | 183528553 | |||||||
| chr1:183528672 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.557-220G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 6/22 | chr1 | 183528672 | |||||||
| chr1:183528724 | C | G | 1 | a0001c0001t0001g0182 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.557-168C>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 6/22 | chr1 | 183528724 | |||||||
| chr1:183529183 | A | G | 2 | a0001c0001t0001g0113 a0001c0001t0003g0190 |
2 | HG03516.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.707+141A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 7/22 | chr1 | 183529183 | |||||||
| chr1:183530013 | C | T | 1 | a0001c0001t0003g0222 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.843+480C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183530013 | |||||||
| chr1:183530028 | T | A | 1 | a0001c0001t0001g0113 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.843+495T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183530028 | |||||||
| chr1:183530129 | A | T | 1 | a0003c0003t0001g0119 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.843+596A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183530129 | |||||||
| chr1:183530159 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.843+626C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183530159 | |||||||
| chr1:183530389 | C | T | 2 | a0002c0002t0002g0031 a0002c0002t0002g0032 |
2 | HG01243.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.843+856C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183530389 | |||||||
| chr1:183530424 | T | C | 1 | a0001c0001t0001g0324 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.843+891T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183530424 | |||||||
| chr1:183530514 | A | G | 1 | a0001c0001t0003g0204 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.843+981A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183530514 | |||||||
| chr1:183530696 | C | T | 1 | a0007c0008t0001g0317 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.843+1163C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183530696 | |||||||
| chr1:183530697 | G | A | 1 | a0001c0001t0003g0227 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.843+1164G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183530697 | |||||||
| chr1:183530975 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.843+1442A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183530975 | |||||||
| chr1:183531025 | T | C | 1 | a0001c0001t0005g0095 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.843+1492T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183531025 | |||||||
| chr1:183531044 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.843+1511C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183531044 | |||||||
| chr1:183531212 | T | G | 2 | a0002c0002t0002g0040 a0002c0002t0005g0041 |
2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.843+1679T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183531212 | |||||||
| chr1:183531235 | G | T | 1 | a0001c0001t0015g0128 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.843+1702G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183531235 | |||||||
| chr1:183531270 | A | G | 1 | a0002c0002t0002g0034 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.843+1737A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183531270 | |||||||
| chr1:183531445 | C | T | 1 | a0002c0002t0002g0043 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.844-1719C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183531445 | |||||||
| chr1:183531814 | A | G | 1 | a0002c0002t0002g0064 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.844-1350A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183531814 | |||||||
| chr1:183531834 | G | A | 6 | a0004c0005t0005g0006 a0004c0005t0005g0161 a0004c0005t0005g0162 others(3): Show |
8 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.844-1330G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183531834 | |||||||
| chr1:183531835 | C | T | 6 | a0004c0005t0005g0006 a0004c0005t0005g0161 a0004c0005t0005g0162 others(3): Show |
8 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.844-1329C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183531835 | |||||||
| chr1:183532104 | G | A | 1 | a0003c0003t0001g0136 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.844-1060G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183532104 | |||||||
| chr1:183532187 | G | A | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.844-977G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183532187 | |||||||
| chr1:183532215 | C | T | 3 | a0001c0001t0004g0191 a0001c0001t0006g0203 a0001c0001t0007g0221 |
3 | HG01256.hp1 HG02698.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.844-949C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183532215 | |||||||
| chr1:183532316 | G | T | 3 | a0001c0001t0005g0094 a0001c0001t0005g0095 a0001c0001t0005g0096 |
3 | HG01109.hp2 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.844-848G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183532316 | |||||||
| chr1:183532355 | T | G | 1 | a0001c0001t0019g0183 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.844-809T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183532355 | |||||||
| chr1:183532526 | C | T | 1 | a0001c0001t0004g0191 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.844-638C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183532526 | |||||||
| chr1:183532639 | A | C | 41 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0024 others(38): Show |
43 | HG00544.hp1 HG00597.hp2 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.844-525A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183532639 | |||||||
| chr1:183532845 | G | A | 2 | a0001c0001t0004g0199 a0001c0001t0007g0240 |
2 | HG00735.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.844-319G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183532845 | |||||||
| chr1:183532995 | G | A | 1 | a0001c0004t0001g0090 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.844-169G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183532995 | |||||||
| chr1:183533060 | A | G | 1 | a0001c0001t0004g0224 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.844-104A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | chr1 | 183533060 | |||||||
| chr1:183533098 | AT | A | 65 | a0001c0001t0006g0236 a0001c0001t0010g0185 a0001c0001t0010g0186 others(62): Show |
73 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.844-63delT | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr1 | 183533098 | ||||||
| chr1:183533486 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1006+160T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 9/22 | chr1 | 183533486 | |||||||
| chr1:183533596 | G | C | 1 | a0002c0002t0012g0060 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1007-80G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 9/22 | chr1 | 183533596 | |||||||
| chr1:183533928 | C | A | 5 | a0002c0002t0002g0045 a0002c0002t0002g0046 a0002c0002t0002g0052 others(2): Show |
5 | NA18960.hp1 NA18978.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.1163+96C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183533928 | |||||||
| chr1:183534043 | A | T | 1 | a0001c0001t0001g0152 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1163+211A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183534043 | |||||||
| chr1:183534138 | T | C | 3 | a0001c0001t0006g0020 a0001c0001t0009g0020 a0001c0001t0009g0179 |
3 | HG02717.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1163+306T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183534138 | |||||||
| chr1:183534177 | A | AG | 58 | a0001c0001t0001g0082 a0001c0001t0001g0114 a0001c0001t0001g0115 others(55): Show |
63 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.1163+348dupG | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr1 | 183534177 | ||||||
| chr1:183534302 | A | G | 2 | a0006c0007t0005g0166 a0006c0007t0005g0167 |
2 | HG01069.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1163+470A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183534302 | |||||||
| chr1:183534367 | A | G | 1 | a0001c0004t0001g0100 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1163+535A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183534367 | |||||||
| chr1:183534529 | A | G | 37 | a0001c0001t0003g0023 a0001c0001t0003g0201 a0001c0001t0003g0208 others(34): Show |
38 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1163+697A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183534529 | |||||||
| chr1:183534800 | G | C | 7 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1163+968G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183534800 | |||||||
| chr1:183534803 | G | A | 39 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0024 others(36): Show |
41 | HG00544.hp1 HG00597.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.1163+971G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183534803 | |||||||
| chr1:183534807 | C | T | 9 | a0001c0001t0003g0177 a0001c0001t0004g0175 a0001c0001t0004g0178 others(6): Show |
10 | HG02145.hp1 HG02717.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1163+975C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183534807 | |||||||
| chr1:183534823 | C | T | 4 | a0001c0001t0003g0220 a0001c0001t0004g0238 a0001c0001t0004g0257 others(1): Show |
4 | NA18960.hp2 NA19012.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.1163+991C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183534823 | |||||||
| chr1:183535013 | G | T | 1 | a0001c0001t0021g0286 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1163+1181G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183535013 | |||||||
| chr1:183535020 | G | A | 7 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1163+1188G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183535020 | |||||||
| chr1:183535126 | ATATAT | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0290 a0001c0001t0001g0291 others(9): Show |
16 | HG02523.hp1 NA18953.hp2 NA18954.hp1 others(13): Show |
intron_variant | MODIFIER | c.1163+1300_1163+130 others(9): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr1 | 183535126 | ||||||
| chr1:183535236 | T | G | 6 | a0004c0005t0005g0006 a0004c0005t0005g0161 a0004c0005t0005g0162 others(3): Show |
8 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1163+1404T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183535236 | |||||||
| chr1:183535750 | T | C | 58 | a0001c0001t0001g0082 a0001c0001t0001g0114 a0001c0001t0001g0115 others(55): Show |
63 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.1164-1395T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183535750 | |||||||
| chr1:183535811 | G | A | 1 | a0002c0002t0002g0039 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1164-1334G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183535811 | |||||||
| chr1:183535862 | T | C | 1 | a0001c0001t0001g0298 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1164-1283T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183535862 | |||||||
| chr1:183535909 | C | T | 1 | a0001c0001t0004g0191 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1164-1236C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183535909 | |||||||
| chr1:183536102 | T | G | 1 | a0001c0001t0001g0105 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1164-1043T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183536102 | |||||||
| chr1:183536121 | T | C | 3 | a0001c0001t0001g0299 a0001c0001t0001g0307 a0001c0001t0001g0311 |
3 | HG00544.hp2 NA18966.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1164-1024T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183536121 | |||||||
| chr1:183536210 | A | T | 1 | a0001c0001t0001g0288 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1164-935A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 10/22 | chr1 | 183536210 | |||||||
| chr1:183537707 | A | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0168 a0001c0001t0001g0169 others(2): Show |
6 | HG02109.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1234+492A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 11/22 | chr1 | 183537707 | |||||||
| chr1:183537944 | A | G | 2 | a0001c0001t0014g0157 a0001c0001t0018g0180 |
2 | HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1235-436A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 11/22 | chr1 | 183537944 | |||||||
| chr1:183537945 | A | G | 1 | a0002c0002t0012g0080 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1235-435A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 11/22 | chr1 | 183537945 | |||||||
| chr1:183537970 | G | A | 10 | a0003c0003t0001g0015 a0003c0003t0001g0098 a0003c0003t0001g0110 others(7): Show |
10 | HG02015.hp1 NA18945.hp2 NA18949.hp2 others(7): Show |
intron_variant | MODIFIER | c.1235-410G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 11/22 | chr1 | 183537970 | |||||||
| chr1:183538029 | A | G | 1 | a0001c0001t0001g0171 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1235-351A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 11/22 | chr1 | 183538029 | |||||||
| chr1:183538204 | A | G | 1 | a0002c0002t0008g0048 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1235-176A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 11/22 | chr1 | 183538204 | |||||||
| chr1:183538270 | G | A | 6 | a0004c0005t0005g0006 a0004c0005t0005g0161 a0004c0005t0005g0162 others(3): Show |
8 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1235-110G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 11/22 | chr1 | 183538270 | |||||||
| chr1:183538704 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1295+264C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 12/22 | chr1 | 183538704 | |||||||
| chr1:183538911 | G | A | 1 | a0001c0001t0019g0183 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1295+471G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 12/22 | chr1 | 183538911 | |||||||
| chr1:183538926 | A | G | 1 | a0007c0008t0001g0317 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1295+486A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 12/22 | chr1 | 183538926 | |||||||
| chr1:183539184 | T | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
6 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1295+744T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 12/22 | chr1 | 183539184 | |||||||
| chr1:183539634 | G | T | 1 | a0001c0001t0004g0178 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1295+1194G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 12/22 | chr1 | 183539634 | |||||||
| chr1:183539662 | A | G | 2 | a0002c0002t0002g0027 a0002c0002t0002g0035 |
2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1295+1222A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 12/22 | chr1 | 183539662 | |||||||
| chr1:183539822 | A | G | 54 | a0001c0001t0001g0082 a0001c0001t0001g0114 a0001c0001t0001g0125 others(51): Show |
59 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.1296-1162A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 12/22 | chr1 | 183539822 | |||||||
| chr1:183539917 | A | G | 2 | a0006c0007t0005g0166 a0006c0007t0005g0167 |
2 | HG01069.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1296-1067A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 12/22 | chr1 | 183539917 | |||||||
| chr1:183540103 | A | C | 194 | a0001c0001t0001g0021 a0001c0001t0001g0168 a0001c0001t0001g0169 others(191): Show |
208 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.1296-881A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 12/22 | chr1 | 183540103 | |||||||
| chr1:183540419 | TA | T | 8 | a0001c0001t0001g0172 a0001c0001t0001g0283 a0001c0001t0001g0314 others(5): Show |
8 | HG01069.hp1 HG01515.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.1296-552delA | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr1 | 183540419 | ||||||
| chr1:183540719 | A | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0168 a0001c0001t0001g0169 others(2): Show |
6 | HG02109.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1296-265A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 12/22 | chr1 | 183540719 | |||||||
| chr1:183541162 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1415+59G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 13/22 | chr1 | 183541162 | |||||||
| chr1:183541164 | GCA | G | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1415+65_1415+66del others(2): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 183541164 | ||||||
| chr1:183541410 | A | G | 2 | a0001c0001t0004g0238 a0001c0001t0005g0223 |
2 | NA18960.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1415+307A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 13/22 | chr1 | 183541410 | |||||||
| chr1:183541523 | T | A | 8 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1415+420T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 13/22 | chr1 | 183541523 | |||||||
| chr1:183541630 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1416-446C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 13/22 | chr1 | 183541630 | |||||||
| chr1:183541691 | A | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0168 a0001c0001t0001g0169 others(2): Show |
6 | HG02109.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1416-385A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 13/22 | chr1 | 183541691 | |||||||
| chr1:183541907 | C | G | 1 | a0002c0002t0002g0062 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1416-169C>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 13/22 | chr1 | 183541907 | |||||||
| chr1:183541923 | C | A | 1 | a0001c0001t0019g0183 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1416-153C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 13/22 | chr1 | 183541923 | |||||||
| chr1:183541990 | A | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
6 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1416-86A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 13/22 | chr1 | 183541990 | |||||||
| chr1:183542021 | T | C | 1 | a0001c0001t0001g0300 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1416-55T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 13/22 | chr1 | 183542021 | |||||||
| chr1:183542599 | G | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 |
3 | HG01123.hp1 HG01192.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1842+97G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183542599 | |||||||
| chr1:183542681 | A | G | 2 | a0006c0007t0005g0166 a0006c0007t0005g0167 |
2 | HG01069.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1842+179A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183542681 | |||||||
| chr1:183542908 | T | C | 2 | a0001c0001t0004g0242 a0001c0001t0007g0216 |
2 | HG00609.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.1842+406T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183542908 | |||||||
| chr1:183542916 | A | AAT | 3 | a0001c0001t0001g0298 a0001c0001t0001g0301 a0001c0001t0001g0315 |
3 | HG04184.hp1 HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1842+425_1842+426d others(4): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 183542916 | ||||||
| chr1:183542916 | AAT | A | 13 | a0001c0001t0001g0168 a0001c0001t0001g0182 a0001c0001t0005g0094 others(10): Show |
14 | HG00423.hp1 HG01099.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.1842+425_1842+426d others(4): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 183542916 | ||||||
| chr1:183542925 | A | ATG | 28 | a0001c0001t0001g0021 a0001c0001t0001g0114 a0001c0001t0001g0116 others(25): Show |
31 | HG00408.hp1 HG01081.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.1842+424_1842+425i others(4): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 183542925 | ||||||
| chr1:183542925 | A | ATGTG | 20 | a0001c0001t0001g0141 a0002c0002t0002g0027 a0002c0002t0002g0058 others(17): Show |
22 | HG01257.hp1 HG01978.hp2 HG01993.hp2 others(19): Show |
intron_variant | MODIFIER | c.1842+424_1842+425i others(6): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 183542925 | ||||||
| chr1:183542925 | ATATG | A | 14 | a0001c0001t0001g0324 a0001c0001t0005g0095 a0001c0001t0005g0096 others(11): Show |
17 | HG00140.hp1 HG01109.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1842+425_1842+428d others(6): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 183542925 | ||||||
| chr1:183542925 | ATATGTGT others(3): Show |
A | 1 | a0006c0007t0005g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1842+425_1842+434d others(12): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 183542925 | ||||||
| chr1:183542925 | ATATGTGT others(7): Show |
A | 13 | a0001c0001t0003g0190 a0001c0001t0003g0196 a0001c0001t0007g0262 others(10): Show |
16 | HG00558.hp2 HG01069.hp2 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.1842+425_1842+438d others(16): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 183542925 | ||||||
| chr1:183542925 | ATATGTGT others(9): Show |
A | 104 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0023 others(101): Show |
108 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1842+425_1842+440d others(18): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 183542925 | ||||||
| chr1:183542925 | ATATGTGT others(11): Show |
A | 4 | a0001c0001t0006g0020 a0001c0001t0006g0203 a0001c0001t0009g0020 others(1): Show |
4 | HG02698.hp2 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1842+425_1842+442d others(20): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 183542925 | ||||||
| chr1:183542927 | A | ATGTGTGT others(9): Show |
1 | a0001c0001t0018g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1842+453_1842+468d others(18): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 183542927 | ||||||
| chr1:183542927 | A | G | 99 | a0001c0001t0001g0021 a0001c0001t0001g0082 a0001c0001t0001g0114 others(96): Show |
108 | HG00408.hp1 HG00597.hp1 HG00735.hp2 others(105): Show |
intron_variant | MODIFIER | c.1842+425A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183542927 | |||||||
| chr1:183542927 | ATG | A | 22 | a0001c0001t0001g0104 a0001c0001t0001g0106 a0001c0001t0001g0107 others(19): Show |
22 | HG00099.hp1 HG00280.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.1842+467_1842+468d others(4): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 183542927 | ||||||
| chr1:183542927 | ATGTG | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0101 a0001c0001t0001g0102 others(5): Show |
9 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1842+465_1842+468d others(6): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 183542927 | ||||||
| chr1:183542927 | ATGTGTG | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0158 a0001c0001t0001g0172 others(1): Show |
4 | HG02257.hp1 HG02486.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1842+463_1842+468d others(8): Show |
SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 183542927 | ||||||
| chr1:183542931 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1842+429G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183542931 | |||||||
| chr1:183542933 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1842+431G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183542933 | |||||||
| chr1:183542950 | T | C | 44 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0281 others(41): Show |
50 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.1842+448T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183542950 | |||||||
| chr1:183543091 | G | C | 1 | a0001c0001t0001g0300 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1842+589G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183543091 | |||||||
| chr1:183543470 | A | T | 1 | a0001c0001t0001g0304 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1843-883A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183543470 | |||||||
| chr1:183543487 | GA | G | 14 | a0001c0001t0001g0103 a0001c0001t0001g0108 a0001c0001t0001g0297 others(11): Show |
16 | HG02055.hp1 HG02145.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1843-855delA | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | 183543487 | ||||||
| chr1:183543690 | C | T | 1 | a0003c0003t0001g0124 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1843-663C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183543690 | |||||||
| chr1:183543705 | T | C | 316 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(313): Show |
344 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(341): Show |
intron_variant | MODIFIER | c.1843-648T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183543705 | |||||||
| chr1:183543706 | G | A | 1 | a0001c0001t0007g0176 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1843-647G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183543706 | |||||||
| chr1:183543807 | G | A | 7 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1843-546G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183543807 | |||||||
| chr1:183544048 | C | T | 9 | a0003c0003t0001g0014 a0003c0003t0001g0018 a0003c0003t0001g0120 others(6): Show |
11 | HG00423.hp1 HG01168.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1843-305C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183544048 | |||||||
| chr1:183544310 | A | C | 1 | a0001c0001t0007g0239 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1843-43A>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 14/22 | chr1 | 183544310 | |||||||
| chr1:183544511 | G | A | 8 | a0002c0002t0002g0058 a0002c0002t0002g0061 a0002c0002t0002g0063 others(5): Show |
8 | HG01257.hp1 HG01978.hp2 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.1987+14G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 15/22 | chr1 | 183544511 | |||||||
| chr1:183544857 | A | T | 2 | a0006c0007t0005g0166 a0006c0007t0005g0167 |
2 | HG01069.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1988-73A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 15/22 | chr1 | 183544857 | |||||||
| chr1:183545396 | C | A | 16 | a0002c0002t0002g0009 a0002c0002t0002g0010 a0002c0002t0002g0027 others(13): Show |
18 | HG01891.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.2370+84C>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 16/22 | chr1 | 183545396 | |||||||
| chr1:183545727 | T | A | 1 | a0001c0001t0004g0217 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2371-239T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 16/22 | chr1 | 183545727 | |||||||
| chr1:183545896 | A | T | 3 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 |
3 | HG02109.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2371-70A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 16/22 | chr1 | 183545896 | |||||||
| chr1:183545957 | C | T | 2 | a0001c0001t0001g0101 a0001c0001t0013g0268 |
2 | HG03098.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.2371-9C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 16/22 | chr1 | 183545957 | |||||||
| chr1:183546376 | G | A | 1 | a0002c0002t0002g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2742+39G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 17/22 | chr1 | 183546376 | |||||||
| chr1:183546386 | T | C | 1 | a0001c0001t0007g0174 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2742+49T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 17/22 | chr1 | 183546386 | |||||||
| chr1:183546505 | A | G | 2 | a0001c0001t0001g0284 a0001c0001t0001g0324 |
2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2742+168A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 17/22 | chr1 | 183546505 | |||||||
| chr1:183546642 | A | G | 66 | a0001c0001t0001g0021 a0001c0001t0001g0168 a0001c0001t0001g0169 others(63): Show |
75 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.2742+305A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 17/22 | chr1 | 183546642 | |||||||
| chr1:183546965 | G | C | 193 | a0001c0001t0001g0021 a0001c0001t0001g0168 a0001c0001t0001g0169 others(190): Show |
208 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.2743-138G>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 17/22 | chr1 | 183546965 | |||||||
| chr1:183547033 | A | G | 1 | a0002c0002t0002g0047 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2743-70A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 17/22 | chr1 | 183547033 | |||||||
| chr1:183547073 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2743-30G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 17/22 | chr1 | 183547073 | |||||||
| chr1:183547296 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2892+44T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183547296 | |||||||
| chr1:183547305 | G | A | 102 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0023 others(99): Show |
105 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.2892+53G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183547305 | |||||||
| chr1:183547367 | T | C | 3 | a0001c0001t0003g0214 a0001c0001t0006g0211 a0001c0001t0006g0218 |
3 | HG01106.hp1 HG01943.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.2892+115T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183547367 | |||||||
| chr1:183547631 | T | C | 1 | a0001c0001t0005g0096 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2892+379T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183547631 | |||||||
| chr1:183547850 | T | A | 102 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0023 others(99): Show |
105 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.2892+598T>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183547850 | |||||||
| chr1:183547854 | A | T | 111 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0023 others(108): Show |
115 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.2892+602A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183547854 | |||||||
| chr1:183547942 | G | A | 1 | a0003c0003t0001g0098 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2892+690G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183547942 | |||||||
| chr1:183548025 | G | T | 2 | a0006c0007t0005g0166 a0006c0007t0005g0167 |
2 | HG01069.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2892+773G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183548025 | |||||||
| chr1:183548146 | C | T | 1 | a0001c0001t0006g0275 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2892+894C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183548146 | |||||||
| chr1:183548293 | G | T | 2 | a0001c0001t0014g0157 a0001c0001t0018g0180 |
2 | HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2893-915G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183548293 | |||||||
| chr1:183548389 | T | C | 2 | a0002c0002t0002g0066 a0002c0002t0002g0067 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2893-819T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183548389 | |||||||
| chr1:183548398 | C | T | 16 | a0001c0001t0001g0021 a0001c0001t0001g0168 a0001c0001t0001g0169 others(13): Show |
18 | HG01891.hp1 HG02109.hp1 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.2893-810C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183548398 | |||||||
| chr1:183548447 | T | G | 9 | a0001c0001t0004g0217 a0001c0001t0004g0224 a0001c0001t0004g0232 others(6): Show |
9 | HG00423.hp2 HG00609.hp1 NA18954.hp2 others(6): Show |
intron_variant | MODIFIER | c.2893-761T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183548447 | |||||||
| chr1:183548546 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2893-662A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183548546 | |||||||
| chr1:183548700 | T | C | 1 | a0001c0001t0006g0203 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2893-508T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183548700 | |||||||
| chr1:183548731 | A | G | 1 | a0001c0001t0003g0222 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2893-477A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183548731 | |||||||
| chr1:183548836 | T | C | 124 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0023 others(121): Show |
130 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.2893-372T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183548836 | |||||||
| chr1:183548837 | G | A | 1 | a0001c0001t0005g0253 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2893-371G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183548837 | |||||||
| chr1:183548871 | A | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0168 a0001c0001t0001g0169 others(2): Show |
6 | HG02109.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2893-337A>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183548871 | |||||||
| chr1:183548902 | C | G | 4 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0284 others(1): Show |
4 | HG01884.hp1 HG02970.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2893-306C>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183548902 | |||||||
| chr1:183548979 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2893-229T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183548979 | |||||||
| chr1:183549106 | C | T | 1 | a0002c0002t0002g0074 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2893-102C>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183549106 | |||||||
| chr1:183549107 | G | A | 1 | a0002c0002t0002g0039 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2893-101G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 18/22 | chr1 | 183549107 | |||||||
| chr1:183549434 | G | T | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.2973+146G>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 19/22 | chr1 | 183549434 | |||||||
| chr1:183550024 | G | A | 4 | a0001c0001t0010g0185 a0001c0001t0010g0186 a0001c0001t0010g0187 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.3133+101G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 20/22 | chr1 | 183550024 | |||||||
| chr1:183550060 | T | C | 1 | a0002c0002t0008g0069 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3133+137T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 20/22 | chr1 | 183550060 | |||||||
| chr1:183550074 | GA | G | 7 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.3133+162delA | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 183550074 | ||||||
| chr1:183550269 | G | A | 56 | a0001c0001t0001g0082 a0001c0001t0001g0114 a0001c0001t0001g0115 others(53): Show |
61 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.3133+346G>A | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 20/22 | chr1 | 183550269 | |||||||
| chr1:183550286 | A | T | 2 | a0003c0003t0001g0118 a0003c0003t0001g0138 |
2 | HG02165.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.3133+363A>T | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 20/22 | chr1 | 183550286 | |||||||
| chr1:183550608 | T | G | 1 | a0003c0003t0001g0119 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3134-143T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 20/22 | chr1 | 183550608 | |||||||
| chr1:183550622 | T | C | 1 | a0001c0001t0005g0252 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3134-129T>C | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 20/22 | chr1 | 183550622 | |||||||
| chr1:183551495 | T | G | 2 | a0001c0001t0014g0157 a0001c0001t0018g0180 |
2 | HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3450+305T>G | SMG7 | ENSG00000116698.22 | transcript | ENST00000688051.1 | protein_coding | 22/22 | chr1 | 183551495 |